Crystallography Open Database
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| 1554261 | CIF | C15 H21 N O2 | P -1 | 10.139; 10.399; 14.357 80.36; 69.86; 89.98 | 1398.4 | Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M. Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans Organic Chemistry Frontiers, 2018, 5, 1655 |
| 1554262 | CIF | C13 H15 Br O3 | P 1 21/c 1 | 9.9233; 15.1382; 8.9089 90; 105.815; 90 | 1287.64 | Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M. Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans Organic Chemistry Frontiers, 2018, 5, 1655 |
| 1554263 | CIF | C12 H14 O3 | P 1 21/c 1 | 8.638; 15.409; 8.594 90; 111.43; 90 | 1064.8 | Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M. Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans Organic Chemistry Frontiers, 2018, 5, 1655 |
| 1554264 | CIF | C13 H14 O3 | P 1 21/c 1 | 9.944; 16.675; 15.179 90; 108.38; 90 | 2389 | Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M. Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans Organic Chemistry Frontiers, 2018, 5, 1655 |
| 1554265 | CIF | C27 H26 O5 | P -1 | 7.1922; 9.9323; 16.0391 78.066; 84.732; 86.302 | 1115.04 | Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M. Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans Organic Chemistry Frontiers, 2018, 5, 1655 |
| 1554266 | CIF | C15 H18 O5 | P 1 21/c 1 | 9.9599; 6.7335; 20.4059 90; 93.522; 90 | 1365.94 | Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M. Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans Organic Chemistry Frontiers, 2018, 5, 1655 |
| 1554267 | CIF | C23 H32 O6 | P -1 | 8.2403; 11.2635; 11.6154 80.692; 75.701; 83.849 | 1028.38 | Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system Organic Chemistry Frontiers, 2018, 5, 1502 |
| 1554268 | CIF | C13 H20 O4 | P 1 21/c 1 | 10.8545; 11.1988; 10.9655 90; 117.846; 90 | 1178.59 | Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system Organic Chemistry Frontiers, 2018, 5, 1502 |
| 1554269 | CIF | C76 H104 O26 S3 | P 1 21 1 | 13.7347; 21.989; 13.7372 90; 110.63; 90 | 3882.8 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554270 | CIF | C78 H96 N4 O22 | C 2 2 21 | 10.70154; 27.4281; 26.4591 90; 90; 90 | 7766.35 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554271 | CIF | C35 H44 O12 | P 21 21 21 | 9.18292; 12.4621; 28.4369 90; 90; 90 | 3254.28 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554272 | CIF | C74 H90 Cl12 O24 | P 21 21 21 | 15.8696; 16.1185; 32.0556 90; 90; 90 | 8199.6 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554273 | CIF | C77.37 H93.1 N4 O24 | P 1 | 10.54064; 14.6009; 14.9312 62.0192; 84.9082; 68.8864 | 1884.1 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554274 | CIF | C74 H91 N2 O24 | P 21 21 21 | 15.2487; 16.1229; 29.1352 90; 90; 90 | 7163 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554275 | CIF | C70 H84 O24 | P 65 | 14.7018; 14.7018; 53.2893 90; 90; 120 | 9974.97 | Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity Organic Chemistry Frontiers, 2018, 5, 1079 |
| 1554276 | CIF | C42 H49 Cl2 N3 O3 Ru S | P 1 21/n 1 | 13.3662; 19.3514; 18.2778 90; 107.451; 90 | 4510 | Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect Organic Chemistry Frontiers, 2018, 5, 1532 |
| 1554277 | CIF | C33 H46 Cl2 N2 O Ru | P 1 21/c 1 | 14.573; 14.783; 16.116 90; 104.49; 90 | 3361 | Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect Organic Chemistry Frontiers, 2018, 5, 1532 |
| 1554278 | CIF | C36 H44 Cl2 N2 O Ru | C 1 2/c 1 | 26.317; 17.57; 17.431 90; 110.1; 90 | 7569 | Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect Organic Chemistry Frontiers, 2018, 5, 1532 |
| 1554279 | CIF | C16 H9 N5 | P 1 21/c 1 | 17.5111; 18.0998; 8.8623 90; 98.023; 90 | 2781.39 | Xin, Jing-Rui; He, Yan-Hong; Guan, Zhi Metal-free aerobic oxidative direct C–H amination of electron-deficient alkenes via photoredox catalysis Organic Chemistry Frontiers, 2018, 5, 1684 |
| 1554280 | CIF | C20 H14 N2 O2 | P c a 21 | 16.9028; 16.5253; 9.9901 90; 90; 90 | 2790.5 | Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives Organic Chemistry Frontiers, 2018, 5, 1679 |
| 1554281 | CIF | C9 H6 N O | C 1 2/c 1 | 13.3145; 13.4792; 7.0709 90; 93.942; 90 | 1266 | Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives Organic Chemistry Frontiers, 2018, 5, 1679 |
| 1554282 | CIF | C20 H16 N2 O2 | P c a 21 | 17.23; 8.7235; 9.6499 90; 90; 90 | 1450.4 | Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives Organic Chemistry Frontiers, 2018, 5, 1679 |
| 1554283 | CIF | C24 H20 N2 O2 | P 1 21/n 1 | 8.0334; 24.561; 9.1052 90; 105.603; 90 | 1730.3 | Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives Organic Chemistry Frontiers, 2018, 5, 1679 |
| 1554284 | CIF | C32 H22 N2 O2 | P -1 | 5.3397; 12.5882; 17.165 95.56; 94.461; 101.447 | 1119.93 | Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives Organic Chemistry Frontiers, 2018, 5, 1679 |
| 1554285 | CIF | C21 H14 O | P 1 21/c 1 | 9.533; 17.215; 11.031 90; 122.95; 90 | 1519.1 | Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones Organic Chemistry Frontiers, 2018, 5, 1613 |
| 1554286 | CIF | C17 H14 O | P -1 | 8.166; 9.066; 9.404 85.402; 75.824; 71.601 | 640.5 | Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones Organic Chemistry Frontiers, 2018, 5, 1613 |
| 1554287 | CIF | C27 H18 O | P -1 | 9.603; 10.694; 10.7294 70.55; 64.18; 81.02 | 935.2 | Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones Organic Chemistry Frontiers, 2018, 5, 1613 |
| 1554288 | CIF | C31 H20 O | P -1 | 8.4085; 9.35; 14.153 105.907; 95.411; 97.753 | 1050.2 | Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones Organic Chemistry Frontiers, 2018, 5, 1613 |
| 1554289 | CIF | C30 H25 Br N2 O2 | P 1 21/c 1 | 23.315; 11.3915; 18.4957 90; 93.135; 90 | 4905 | Wang, Chao-Ming; Song, Dan; Xia, Peng-Ju; Ye, Zhi-Peng; Xiao, Jun-An; Xiang, Hao-Yue; Chen, Xiao-Qing; Yang, Hua Photoredox-catalyzed direct aminoalkylation of isatins: diastereoselective access to 3-hydroxy-3-aminoalkylindolin-2-ones analogues Organic Chemistry Frontiers, 2018, 5, 1608 |
| 1554290 | CIF | C26 H21 N3 O2 | P 1 21/n 1 | 7.6842; 19.978; 13.7517 90; 98.473; 90 | 2088 | Chen, Wei; Ji, Dong-Sheng; Luo, Yong-Chun; Wang, Zhu-Yin; Xu, Peng-Fei Directing group assisted ZnI2-catalyzed cyclopropanation of indoles via 2-furylcarbenoids Organic Chemistry Frontiers, 2018, 5, 1768 |
| 1554291 | CIF | C11 H14 O2 S2 | C 1 2 1 | 27.4221; 5.1994; 19.0212 90; 121.717; 90 | 2306.99 | Liu, Yan; Zeng, Jing; Sun, Jiuchang; Cai, Lei; Zhao, Yueqi; Fang, Jing; Hu, Bo; Shu, Penghua; Meng, Lingkui; Wan, Qian 1,4-Dithiothreitol mediated cleavage of the acetal and ketal type of diol protecting groups Organic Chemistry Frontiers, 2018, 5, 2427 |
| 1554292 | CIF | C25 H20 N2 O3 | P -1 | 9.0455; 9.948; 11.7172 94.495; 95.25; 98.331 | 1034.4 | Li, Bingnan; Mai, Shaoyu; Song, Qiuling Synthesis of fused benzimidazoles via successive nucleophilic additions of benzimidazole derivatives to arynes under transition metal-free conditions Organic Chemistry Frontiers, 2018, 5, 1639 |
| 1554293 | CIF | C34 H31 N O5 | P 1 21/n 1 | 10.3357; 23.6593; 11.6006 90; 104.704; 90 | 2743.9 | Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines Organic Chemistry Frontiers, 2018, 5, 2020 |
| 1554294 | CIF | C36 H36 N2 O4 | P 1 21/c 1 | 10.9629; 9.8209; 27.4846 90; 91.397; 90 | 2958.3 | Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines Organic Chemistry Frontiers, 2018, 5, 2020 |
| 1554295 | CIF | C44 H44 Cl2 N2 O6 S | P c a 21 | 18.1688; 18.3501; 11.8464 90; 90; 90 | 3949.6 | Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines Organic Chemistry Frontiers, 2018, 5, 2020 |
| 1554296 | CIF | C23 H24 N2 O4 S2 | P 1 21/c 1 | 12.143; 10.204; 18.499 90; 94.972; 90 | 2283.5 | Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo Reductive ortho C–H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles Organic Chemistry Frontiers, 2018, 5, 1756 |
| 1554297 | CIF | C21 H22 N2 O2 S2 | P 1 21/c 1 | 9.0286; 24.083; 10.3285 90; 114.965; 90 | 2036 | Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo Reductive ortho C–H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles Organic Chemistry Frontiers, 2018, 5, 1756 |
| 1554298 | CIF | C26 H39 Cl2 Co N3 O12 | P 21 21 21 | 10.4066; 26.417; 12.0692 90; 90; 90 | 3318 | Zhang, Heyi; Lu, Zhan Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation Organic Chemistry Frontiers, 2018, 5, 1763 |
| 1554299 | CIF | C26 H39 Cl2 N3 Ni O12 | P 21 21 21 | 10.3907; 11.9429; 26.537 90; 90; 90 | 3293.1 | Zhang, Heyi; Lu, Zhan Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation Organic Chemistry Frontiers, 2018, 5, 1763 |
| 1554300 | CIF | C22 H18 O | P 1 21 1 | 6.96436; 7.91974; 15.2392 90; 92.2266; 90 | 839.9 | Zhang, Heyi; Lu, Zhan Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation Organic Chemistry Frontiers, 2018, 5, 1763 |
| 1554301 | CIF | C26 H41 Cl2 Fe N3 O12 | P 21 21 21 | 10.3081; 11.98; 26.1548 90; 90; 90 | 3229.88 | Zhang, Heyi; Lu, Zhan Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation Organic Chemistry Frontiers, 2018, 5, 1763 |
| 1554302 | CIF | C15 H19 N O3 S | P 1 21/c 1 | 10.0093; 14.3918; 10.7208 90; 104.176; 90 | 1497.32 | Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives Organic Chemistry Frontiers, 2018, 5, 2040 |
| 1554303 | CIF | C15 H19 N O3 S | P 1 21/c 1 | 6.54242; 22.4359; 10.03319 90; 102.165; 90 | 1439.65 | Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives Organic Chemistry Frontiers, 2018, 5, 2040 |
| 1554304 | CIF | C17 H18 Cl N O2 | P 1 21 1 | 5.9758; 8.5937; 15.7695 90; 93.352; 90 | 808.45 | Hu, Yang; Yin, Xuguang; Chen, Ziyi; Dong, Xiu-Qin; Zhang, Xumu Highly enantioselective Ir/f-amphox-catalyzed hydrogenation of ketoamides: efficient access to chiral hydroxy amides Organic Chemistry Frontiers, 2018, 5, 2000 |
| 1554305 | CIF | C32 H7 Cl4 F10 N3 O2 | P 1 21/m 1 | 6.4792; 25.1943; 10.1094 90; 106.673; 90 | 1580.87 | Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence Organic Chemistry Frontiers, 2018, 5, 1877 |
| 1554306 | CIF | C36 H11 Cl2 F10 N5 O2.5 | P 1 21/m 1 | 6.3689; 19.2075; 14.4005 90; 96.153; 90 | 1751.5 | Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence Organic Chemistry Frontiers, 2018, 5, 1877 |
| 1554307 | CIF | C38 H7 Br2 F10 N5 O3 | P n m a | 18.5573; 18.3335; 14.8419 90; 90; 90 | 5049.5 | Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence Organic Chemistry Frontiers, 2018, 5, 1877 |
| 1554308 | CIF | C28 H26 F N O8 S | P b c a | 8.2423; 18.2962; 34.5544 90; 90; 90 | 5210.9 | Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction Organic Chemistry Frontiers, 2018, 5, 1950 |
| 1554309 | CIF | C28.8 H27.6 N2 O10 S | P 1 21/c 1 | 21.4204; 21.5628; 14.5587 90; 97.091; 90 | 6673 | Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction Organic Chemistry Frontiers, 2018, 5, 1950 |
| 1554310 | CIF | C17 H14 O2 | P 1 21/c 1 | 10.5915; 15.1258; 9.0257 90; 109.468; 90 | 1363.29 | Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming 2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols Organic Chemistry Frontiers, 2018, 5, 1900 |
| 1554311 | CIF | C15 H18 O2 | P -1 | 5.6491; 11.5037; 11.5175 111.795; 99.48; 90.087 | 683.87 | Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming 2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols Organic Chemistry Frontiers, 2018, 5, 1900 |
| 1554312 | CIF | C16 H17 Br O4 | P 1 21 1 | 10.573; 7.311; 11.35 90; 115.216; 90 | 793.7 | Li, Sujia; Lv, Jian; Luo, Sanzhong Enantioselective indium(i)-catalyzed [4 + 2] annulation of alkoxyallenes and β,γ-unsaturated α-keto esters Organic Chemistry Frontiers, 2018, 5, 1787 |
| 1554313 | CIF | C20 H18 N4 O2 | P -1 | 8.46; 9.59; 11.8 97.55; 104.24; 108.51 | 857 | Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata Metal-free direct oxidative C–C bond coupling of pyrazolones and quinoxalinones Organic Chemistry Frontiers, 2018, 5, 1928 |
| 1554314 | CIF | C15 H16 N4 O2 | P 1 21/n 1 | 9.998; 9.281; 14.416 90; 95.77; 90 | 1330.9 | Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata Metal-free direct oxidative C–C bond coupling of pyrazolones and quinoxalinones Organic Chemistry Frontiers, 2018, 5, 1928 |
| 1554315 | CIF | C20 H40.5 O3.25 Si | P 1 21 1 | 7.3563; 46.699; 12.909 90; 92.798; 90 | 4429.4 | Santalla, Hugo; Garrido, Fátima; Gómez, Generosa; Fall, Yagamare A more reliable synthesis of a Gemini vitamin D analog, a potentially effective chemotherapeutic agent for the treatment of colorectal carcinomas Organic Chemistry Frontiers, 2018, 5, 2016 |
| 1554316 | CIF | C32 H31 N O5 | P 21 21 21 | 10.1535; 10.5316; 25.565 90; 90; 90 | 2733.73 | Duan, Chuan-Qi; He, Xiao-Long; Du, Wei; Chen, Ying-Chun Asymmetric [4 + 2] cycloadditions with 3-furfural derivatives and α-cyano-α,β-unsaturated ketones Organic Chemistry Frontiers, 2018, 5, 2057 |
| 1554317 | CIF | C23 H20 Br N O2 S | P -1 | 10.0726; 10.735; 19.604 82.045; 86.428; 81.212 | 2072.9 | Jiang, Bo; Wei, Yin; Shi, Min Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2091 |
| 1554318 | CIF | C26 H23 N O2 S | P -1 | 9.447; 10.559; 12.512 76.431; 77.755; 64.585 | 1087 | Jiang, Bo; Wei, Yin; Shi, Min Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2091 |
| 1554319 | CIF | C26 H23 N O2 S | P 1 21/n 1 | 11.7526; 13.4984; 13.5265 90; 92.44; 90 | 2143.9 | Jiang, Bo; Wei, Yin; Shi, Min Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2091 |
| 1554320 | CIF | C38 H28 N2 O3 S | P 21 21 21 | 9.00774; 11.44511; 29.0288 90; 90; 90 | 2992.71 | Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives Organic Chemistry Frontiers, 2018, 5, 2126 |
| 1554321 | CIF | C38 H28 N2 O4 S | C 1 2 1 | 14.8962; 11.3205; 20.153 90; 102.279; 90 | 3320.7 | Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives Organic Chemistry Frontiers, 2018, 5, 2126 |
| 1554322 | CIF | C26 H21 N O4 S | P 1 21 1 | 6.3467; 16.1435; 10.7987 90; 96.301; 90 | 1099.73 | Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives Organic Chemistry Frontiers, 2018, 5, 2126 |
| 1554323 | CIF | C30 H22 Cl N O2 S | P 1 21 1 | 10.4185; 15.4927; 15.8277 90; 95.756; 90 | 2541.9 | Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives Organic Chemistry Frontiers, 2018, 5, 2126 |
| 1554324 | CIF | C31 H56 F6 Mg N4 O14 S2 | P 1 | 9.2007; 9.2791; 14.237 97.598; 91.193; 97.349 | 1194.02 | Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives Organic Chemistry Frontiers, 2018, 5, 2126 |
| 1554325 | CIF | C25 H19 N3 O | P -1 | 8.2339; 14.7918; 17.1794 101.33; 95.203; 106.126 | 1947.28 | Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines Organic Chemistry Frontiers, 2018, 5, 2303 |
| 1554326 | CIF | C25 H16 F3 N3 O2 | P 1 21/c 1 | 19.5242; 8.4475; 25.582 90; 107.178; 90 | 4031.04 | Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines Organic Chemistry Frontiers, 2018, 5, 2303 |
| 1554327 | CIF | C26 H21 F2 N3 | I 41/a :2 | 18.7671; 18.7671; 24.2076 90; 90; 90 | 8526.01 | Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines Organic Chemistry Frontiers, 2018, 5, 2303 |
| 1554328 | CIF | C16 H15 Cl O | P b c n | 57.5837; 5.8021; 8.0527 90; 90; 90 | 2690.46 | Chen, Mintao; Wei, Yin; Shi, Min A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2030 |
| 1554329 | CIF | C12 H13 F3 O2 S | P -1 | 10.0641; 10.4692; 12.4244 90.033; 93.737; 96.649 | 1297.46 | Chen, Mintao; Wei, Yin; Shi, Min A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2030 |
| 1554330 | CIF | C66 H78 O2 | P -1 | 12.134; 13.857; 17.116 70.214; 75.507; 73.496 | 2558.3 | Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A. Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation Organic Chemistry Frontiers, 2018, 5, 2288 |
| 1554331 | CIF | C68 H74 | P -1 | 9.3311; 9.8219; 16.1042 103.794; 94.992; 112.566 | 1297.14 | Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A. Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation Organic Chemistry Frontiers, 2018, 5, 2288 |
| 1554332 | CIF | C95.5 H118 Cl4.5 O4.93 | P 1 21 1 | 15.3329; 18.3488; 15.6332 90; 99.6319; 90 | 4336.2 | Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A. Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation Organic Chemistry Frontiers, 2018, 5, 2288 |
| 1554333 | CIF | C127.75 H123 O1.75 | C 1 2/c 1 | 32.048; 25.4121; 26.3829 90; 102.865; 90 | 20947 | Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A. Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation Organic Chemistry Frontiers, 2018, 5, 2288 |
| 1554334 | CIF | C34 H34 Cl3 Fe N3 O4 | P 21 21 21 | 9.5467; 13.5703; 26.06 90; 90; 90 | 3376.1 | Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone–ferrocene hybrids as novel RalA inhibitors Organic Chemistry Frontiers, 2018, 5, 2229 |
| 1554335 | CIF | C34 H35 Cl2 Fe N3 O4 | P 41 21 2 | 12.0535; 12.0535; 43.8649 90; 90; 90 | 6373 | Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone‒ferrocene hybrids as novel RalA inhibitors Organic Chemistry Frontiers, 2018, 5, 2229 |
| 1554336 | CIF | C20.57 H26.27 Cl N O3.57 | C 1 2 1 | 18.4603; 16.6736; 13.8087 90; 103.239; 90 | 4137.4 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554337 | CIF | C20 H24 Cl N O3 | P -1 | 11.4568; 11.4834; 14.2866 94.508; 106.183; 90.764 | 1798.31 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554338 | CIF | C20 H25 N O4 | P 1 21/c 1 | 17.0841; 18.7193; 11.1858 90; 100.62; 90 | 3516 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554339 | CIF | C20 H24 Cl N O5 | P 1 21/n 1 | 11.3027; 7.2512; 23.102 90; 98.784; 90 | 1871.19 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554340 | CIF | C20 H24 Cl N O3 | P 21 21 21 | 7.508; 11.2397; 21.9828 90; 90; 90 | 1855.08 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554341 | CIF | C20 H22 Cl N O4 | P 1 21/n 1 | 17.278; 12.6989; 17.255 90; 102.191; 90 | 3700.6 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554342 | CIF | C20 H26 Cl N O4 | P 1 21/n 1 | 16.127; 7.209; 16.3705 90; 91.08; 90 | 1902.89 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554343 | CIF | C20 H23 N O2 | P 1 21/n 1 | 10.2096; 12.8487; 12.9425 90; 107.01; 90 | 1623.53 | Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S. Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines Organic Chemistry Frontiers, 2018, 5, 2171 |
| 1554344 | CIF | C24 H24 O5 S | P -1 | 5.5872; 13.9109; 14.4106 112.533; 98.978; 94.422 | 1010.3 | Cui, Zhiming; Zhu, Baofu; Li, Xuechen; Cao, Hua Access to sulfonylated furans or imidazo[1,2-a]pyridines via a metal-free three-component, domino reaction Organic Chemistry Frontiers, 2018, 5, 2219 |
| 1554345 | CIF | C20 H19 N O4 | P 1 21/n 1 | 10.194; 14.232; 12.523 90; 106.045; 90 | 1746.1 | Jia, Xiaodong; Hou, Wentao; Chen, Qian; Yuan, Yu; Sun, Jing; He, Kaixuan Oxidation of active sp3C–H bonds initiated consecutive intermolecular/intramolecular cyclization between glycine derivatives ando-vinylphenols: construction of a polycyclic benzofuroquinoline skeleton Organic Chemistry Frontiers, 2018, 5, 2479 |
| 1554346 | CIF | C20 H20 N2 O5 | P -1 | 9.1376; 9.5813; 10.8392 105.957; 95.789; 98.506 | 892.32 | Jia, Xiaodong; Hou, Wentao; Chen, Qian; Yuan, Yu; Sun, Jing; He, Kaixuan Oxidation of active sp3C–H bonds initiated consecutive intermolecular/intramolecular cyclization between glycine derivatives ando-vinylphenols: construction of a polycyclic benzofuroquinoline skeleton Organic Chemistry Frontiers, 2018, 5, 2479 |
| 1554347 | CIF | C11 H10 N O | P 1 21/n 1 | 21.194; 8.4619; 27.57 90; 109.98; 90 | 4647 | Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect Organic Chemistry Frontiers, 2018, 5, 2296 |
| 1554348 | CIF | C24 H21 N O2 | P 1 21/n 1 | 10.9697; 16.013; 13.031 90; 105.898; 90 | 2201.4 | Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect Organic Chemistry Frontiers, 2018, 5, 2296 |
| 1554349 | CIF | C5.5 H5.62 N0.12 O0.5 | F d d d :2 | 24.1341; 25.4123; 26.638 90; 90; 90 | 16337.2 | Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect Organic Chemistry Frontiers, 2018, 5, 2296 |
| 1554350 | CIF | C34 H33 N O3 | P -1 | 9.4355; 10.2231; 17.9161 87.132; 84.213; 68.822 | 1603.09 | Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect Organic Chemistry Frontiers, 2018, 5, 2296 |
| 1554351 | CIF | C45 H68 N2 O2 | I 41/a :2 | 40.9015; 40.9015; 9.3338 90; 90; 90 | 15614.8 | Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes Organic Chemistry Frontiers, 2018, 5, 2073 |
| 1554352 | CIF | C56 H78 B2 F8 Fe N2 O2 | C 1 2/c 1 | 21.6194; 10.6383; 26.8304 90; 95.299; 90 | 6144.4 | Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes Organic Chemistry Frontiers, 2018, 5, 2073 |
| 1554353 | CIF | C47 H71 B2 F8 N3 O2 | P 1 21/n 1 | 21.3381; 10.2919; 24.6126 90; 111.615; 90 | 5025.1 | Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes Organic Chemistry Frontiers, 2018, 5, 2073 |
| 1554354 | CIF | C19 H28 O7 | P 1 21 1 | 6.4711; 15.6577; 9.2786 90; 90.334; 90 | 940.12 | Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong Structurally diverse diterpenoids from Isodon pharicus Organic Chemistry Frontiers, 2018, 5, 2379 |
| 1554355 | CIF | C20 H32 O5 | P 21 21 21 | 6.6084; 11.8396; 22.9114 90; 90; 90 | 1792.61 | Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong Structurally diverse diterpenoids from Isodon pharicus Organic Chemistry Frontiers, 2018, 5, 2379 |
| 1554356 | CIF | C14 H11 N S2 | P 1 21/n 1 | 7.2615; 11.8328; 14.2292 90; 94.546; 90 | 1218.78 | Tan, Wei; Wang, Cuihong; Jiang, Xuefeng Green carbon disulfide surrogateviaa combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction Organic Chemistry Frontiers, 2018, 5, 2390 |
| 1554357 | CIF | C15 H13 N S2 | P 1 21/c 1 | 8.3766; 6.2895; 25.7206 90; 95.618; 90 | 1348.57 | Tan, Wei; Wang, Cuihong; Jiang, Xuefeng Green carbon disulfide surrogateviaa combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction Organic Chemistry Frontiers, 2018, 5, 2390 |
| 1554358 | CIF | C20 H22 O5 | P 1 21 1 | 12.874; 4.9; 13.9299 90; 93.36; 90 | 877.22 | Cheng, Yuyu; Fang, Zhiqiang; Li, Wenjun; Li, Pengfei Phosphine-mediated enantioselective [4 + 1] annulations between ortho-quinone methides and Morita–Baylis–Hillman carbonates Organic Chemistry Frontiers, 2018, 5, 2728 |
| 1554359 | CIF | C21 H31 B2 N O4 | P -1 | 9.6906; 10.9669; 11.5436 70.045; 86.183; 84.832 | 1147.6 | Gao, Guoliang; Kuang, Zhijie; Song, Qiuling Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2 Organic Chemistry Frontiers, 2018, 5, 2249 |
| 1554360 | CIF | C30 H42 B2 O5 | P -1 | 10.0513; 15.5408; 19.0622 88.904; 83.3; 87.795 | 2954.8 | Gao, Guoliang; Kuang, Zhijie; Song, Qiuling Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2 Organic Chemistry Frontiers, 2018, 5, 2249 |
| 1554361 | CIF | C28 H31 Cl3 N2 Pd | P 1 21/n 1 | 10.3174; 12.4692; 20.4932 90; 96.89; 90 | 2617.4 | Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides Organic Chemistry Frontiers, 2018, 5, 2484 |
| 1554362 | CIF | C28 H31 Cl N2 O Pd | P -1 | 10.0241; 11.2921; 11.727 92.4; 105.358; 106.802 | 1215.24 | Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides Organic Chemistry Frontiers, 2018, 5, 2484 |
| 1554363 | CIF | C28 H28 Cl F3 N2 Pd | P b c a | 18.6245; 13.7023; 22.6048 90; 90; 90 | 5768.7 | Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides Organic Chemistry Frontiers, 2018, 5, 2484 |
| 1554364 | CIF | C48 H39 Cl N2 Pd | P b c a | 18.9753; 19.6328; 20.1865 90; 90; 90 | 7520.2 | Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides Organic Chemistry Frontiers, 2018, 5, 2484 |
| 1554365 | CIF | C35 H32 Br N3 O3 | P 1 21 1 | 12.6497; 9.0221; 14.1532 90; 113.568; 90 | 1480.53 | Mei, Hongjiang; Lin, Lili; Shen, Bin; Liu, Xiaohua; Feng, Xiaoming Highly enantioselective desymmetrization of prochiral cyclic α,α-dicyanoalkenes via the direct vinylogous Michael/cyclization domino reaction Organic Chemistry Frontiers, 2018, 5, 2505 |
| 1554366 | CIF | C18 H15 N O2 S | P 1 21/c 1 | 18.6922; 5.447; 14.5323 90; 92.936; 90 | 1477.68 | Shen, Wen-Bo; Zhou, Bo; Zhang, Zhi-Xin; Yuan, Han; Fang, Wei; Ye, Long-Wu Gold-catalyzed cascade cyclization of N-propargyl ynamides: rapid access to functionalized indeno[1,2-c]pyrroles Organic Chemistry Frontiers, 2018, 5, 2468 |
| 1554367 | CIF | C10 H9 N O | P 1 21 1 | 7.5235; 5.5446; 10.2976 90; 99.85; 90 | 423.23 | Wu, Qi; Li, Yabo; Wang, Chenyang; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie 1,4-Refunctionalization of β-diketones to γ-keto nitriles via C–C single bond cleavage Organic Chemistry Frontiers, 2018, 5, 2496 |
| 1554368 | CIF | C28 H17 F3 N2 O1.01 | P -1 | 7.933; 11.1848; 13.1762 72.919; 73.841; 84.499 | 1073.26 | Vivek Kumar, Sundaravel; Ellairaja, Sundaram; Satheesh, Vanaparthi; Sivasamy Vasantha, Vairathevar; Punniyamurthy, Tharmalingam Rh-Catalyzed regioselective C‒H activation and C‒C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines Organic Chemistry Frontiers, 2018, 5, 2630 |
| 1554369 | CIF | C43 H37 Cl3 N2 O2 | P 1 21 1 | 10.757; 12.558; 14.389 90; 99.306; 90 | 1918 | Lu, Yi-Nan; Ma, Chun; Lan, Jin-Ping; Zhu, Caiqiang; Mao, Yu-Jia; Mei, Guang-Jian; Zhang, Shu; Shi, Feng Catalytic enantioselective and regioselective substitution of 2,3-indolyldimethanols with enaminones Organic Chemistry Frontiers, 2018, 5, 2657 |
| 1554370 | CIF | C20 H18 O4 | C 1 2/c 1 | 22.7223; 5.7888; 25.159 90; 95.416; 90 | 3294.5 | Ma, Dengke; Song, Yulong; Fu, Chunling; Zhang, Fang; Guo, Yinlong; Huang, Xin; Ma, Shengming E-Selective N-heterocyclic carbene-catalyzed reaction of aldehydes and butadienoates: effect of water and chloroform as the proton shuttle Organic Chemistry Frontiers, 2018, 5, 2560 |
| 1554371 | CIF | C25 H22 Cl N O3 S | P -1 | 10.2719; 10.4262; 11.7012 69.168; 73.012; 86.849 | 1118.45 | Wang, Hepan; Wang, Bingbing; Sun, Song; Cheng, Jiang Copper-catalyzed radical Heck type cyclization: a three-component reaction of DABCO·(SO2)2, aryldiazonium tetrafluoroborates and dienes toward sulfonated benzo- seven-membered nitrogen heterocycles Organic Chemistry Frontiers, 2018, 5, 2547 |
| 1554372 | CIF | C21 H19 Cl F N O6 | P -1 | 9.5372; 10.0615; 11.5029 74.116; 83.655; 71.87 | 1008.56 | Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L. Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals Organic Chemistry Frontiers, 2018, 5, 2588 |
| 1554373 | CIF | C16 H14 Cl F N2 O6 | P 1 21/c 1 | 16.4649; 6.9417; 15.0372 90; 93.483; 90 | 1715.5 | Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L. Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals Organic Chemistry Frontiers, 2018, 5, 2588 |
| 1554374 | CIF | C23 H31 N O2 S | P -1 | 6.812; 11.371; 13.441 80.287; 84.84; 77.986 | 1002.1 | Han, Yulin; Ma, Shengming Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes Organic Chemistry Frontiers, 2018, 5, 2680 |
| 1554375 | CIF | C18 H23 N O2 S | P 1 21/c 1 | 10.6868; 20.2; 8.0112 90; 101.747; 90 | 1693.2 | Han, Yulin; Ma, Shengming Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes Organic Chemistry Frontiers, 2018, 5, 2680 |
| 1554376 | CIF | C24 H30 O4 | P 1 21/c 1 | 8.9632; 26.894; 9.2793 90; 110.151; 90 | 2099.9 | Han, Yulin; Ma, Shengming Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes Organic Chemistry Frontiers, 2018, 5, 2680 |
| 1554377 | CIF | C36 H34 N O6 | P 1 21 1 | 11.0672; 24.0508; 11.3892 90; 91.3083; 90 | 3030.73 | Yue, Jing-Fei; Ran, Guang-Yao; Yang, Xing-Xing; Du, Wei; Chen, Ying-Chun Asymmetric Diels–Alder cycloadditions of benzofulvene-based 2,4-dienals via trienamine activation Organic Chemistry Frontiers, 2018, 5, 2676 |
| 1554378 | CIF | C24 H26 N2 O3 | P 1 21 1 | 10.2146; 11.7243; 10.2644 90; 119.315; 90 | 1071.84 | Zhang, Zi-Jing; Song, Jin An isothiourea-catalyzed asymmetric formal [4 + 2] cycloaddition of in situ generated azoalkenes with C1 ammonium enolates Organic Chemistry Frontiers, 2018, 5, 2578 |
| 1554379 | CIF | C32 H27 N O5 S | P -1 | 10.276; 12.5669; 13.0463 66.455; 73.203; 66.317 | 1397.8 | Zhang, Changyuan; Chen, Lianfen; Chen, Kai; Wang, Chuntao; Xu, Zurong; Jiang, Huanfeng; Zhu, Shifa Cu(i)-Catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition reaction Organic Chemistry Frontiers, 2018, 5, 2510 |
| 1554380 | CIF | C29 H28 Cl N3 O7 | P 21 21 21 | 8.611; 11.3415; 28.819 90; 90; 90 | 2814.5 | Wei, Qinghua; Ma, Xiaochu; Chen, Jianghui; Niu, Li; Yang, Xi; Xia, Fei; Liu, Shunying A triple-functionalised metal centre-catalyzed enantioselective multicomponent reaction Organic Chemistry Frontiers, 2018, 5, 2799 |
| 1554381 | CIF | C29 H43 I Mg N2 O | P -1 | 8.4477; 11.883; 15.889 97.79; 90.12; 96.968 | 1568.3 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554382 | CIF | C50 H66 Mg2 N4 | P 1 21/c 1 | 12.5799; 19.2069; 20.3357 90; 102.473; 90 | 4797.6 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554383 | CIF | C50 H66 Mg2 N4 | P n a 21 | 21.9804; 19.3508; 11.283 90; 90; 90 | 4799.1 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554384 | CIF | C46 H58 Mg N4 | P -1 | 11.0139; 11.3202; 18.565 75.316; 83.401; 62.905 | 1993.3 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554385 | CIF | C54 H53 Mg N2 | P 1 21/c 1 | 11.4271; 17.954; 20.908 90; 93.495; 90 | 4281.6 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554386 | CIF | C48 H49 Cl2 N2 | P c c n | 21.607; 13.2782; 14.0261 90; 90; 90 | 4024.1 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554387 | CIF | C51 H55 I Mg N2 O | C 1 2/c 1 | 25.689; 11.0511; 32.698 90; 105.996; 90 | 8923.3 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554388 | CIF | C58 H76 Cl2 Mg2 N4 | P 1 21/c 1 | 11.9804; 15.2444; 15.0882 90; 95.298; 90 | 2743.8 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554389 | CIF | C68 H96 B2 Mg2 N4 O6 | P -4 | 13.2295; 13.2295; 19.2267 90; 90; 90 | 3365.1 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554390 | CIF | C18 H36 B2 O6 | P 1 21/c 1 | 10.58; 10.4047; 10.785 90; 118.687; 90 | 1041.5 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554391 | CIF | C52 H70 Mg2 N4 | P c c n | 17.7085; 33.2898; 17.0054 90; 90; 90 | 10024.9 | Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds Organic Chemistry Frontiers, 2018, 5, 3538 |
| 1554392 | CIF | C30 H21 Cl N2 O2 | P -1 | 8.5511; 10.4286; 14.3935 88.875; 87.601; 68.209 | 1190.78 | Xu, Hui; Chen, Kuan; Liu, Hong-Wei; Wang, Guan-Wu Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions Organic Chemistry Frontiers, 2018, 5, 2864 |
| 1554393 | CIF | C22 H24 Cl3 F6 N4 P Ru | P 1 21/n 1 | 8.1716; 30.1115; 10.9853 90; 95.159; 90 | 2692.1 | Wu, Qiang; Pan, Le; Du, Guangming; Zhang, Chi; Wang, Dawei Preparation of pyridyltriazole ruthenium complexes as effective catalysts for the selective alkylation and one-pot C‒H hydroxylation of 2-oxindole with alcohols and mechanism exploration Organic Chemistry Frontiers, 2018, 5, 2668 |
| 1554394 | CIF | C17 H13 F2 N O2 | P b c a | 8.3324; 18.0049; 18.9382 90; 90; 90 | 2841.2 | Ma, Xingxing; Deng, Shuilin; Song, Qiuling Halodifluoroacetates as formylation reagents for various amines via unprecedented quadruple cleavage Organic Chemistry Frontiers, 2018, 5, 3505 |
| 1554395 | CIF | C14 H17 N O | P -1 | 6.32; 11.047; 16.999 90.548; 95.825; 90.542 | 1180.6 | Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study Organic Chemistry Frontiers, 2018, 5, 3231 |
| 1554396 | CIF | C12 H26 Cl2 N2 Ni O7 | P -1 | 6.9966; 12.0579; 12.9998 63.724; 88.61; 86.344 | 981.4 | Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study Organic Chemistry Frontiers, 2018, 5, 3231 |
| 1554397 | CIF | C22 H25 N O6 | P 1 21/c 1 | 10.9821; 9.771; 21.137 90; 119.629; 90 | 1971.56 | Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V. Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes Organic Chemistry Frontiers, 2018, 5, 2829 |
| 1554398 | CIF | C23 H29 N O7 | P 1 c 1 | 7.0556; 15.3824; 10.7866 90; 108.471; 90 | 1110.38 | Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V. Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes Organic Chemistry Frontiers, 2018, 5, 2829 |
| 1554399 | CIF | C22 H25 N O6 | P 1 21/c 1 | 15.7969; 8.7827; 14.6012 90; 103.801; 90 | 1967.28 | Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V. Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes Organic Chemistry Frontiers, 2018, 5, 2829 |
| 1554400 | CIF | C43 H26 N2 O2 | P -1 | 9.516; 11.551; 13.616 91.24; 106.05; 99.94 | 1412.9 | Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin Organic Chemistry Frontiers, 2018, 5, 3068 |
| 1554401 | CIF | C61 H45 B F4 N2 O2 | P 1 21/n 1 | 14.154; 17.553; 19.832 90; 106.78; 90 | 4717.4 | Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin Organic Chemistry Frontiers, 2018, 5, 3068 |
| 1554402 | CIF | C86 H54 B8 F22 N4 O7 | P -1 | 8.09; 12.074; 24.254 82.58; 89.11; 70.85 | 2218.3 | Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin Organic Chemistry Frontiers, 2018, 5, 3068 |
| 1554403 | CIF | C14 H18 N2 O S | P -1 | 5.5091; 7.2665; 16.992 80.823; 83.934; 78.863 | 656.9 | Dutta, Soumya; Mondal, Manas; Ghosh, Tubai; Saha, Amit Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas Organic Chemistry Frontiers, 2019, 6, 70 |
| 1554404 | CIF | C29 H37 N O7 | P 1 21 1 | 12.2892; 11.6999; 19.3795 90; 103.521; 90 | 2709.2 | Fan, Yaqin; Wang, Yi; Fu, Peng; Chairoungdua, Arthit; Piyachaturawat, Pawinee; Zhu, Weiming Secopaxilline A, an indole-diterpenoid derivative from an aciduric Penicillium fungus, its identification and semisynthesis Organic Chemistry Frontiers, 2018, 5, 2835 |
| 1554405 | CIF | C28 H24 O5 | P 1 21/n 1 | 9.5523; 9.8572; 23.9209 90; 99.141; 90 | 2223.76 | Zhao, Yinsong; Zheng, Qinze; Yu, Chuangui; Liu, Zheng; Wang, Deping; You, Jingsong; Gao, Ge Rh(iii)-Catalyzed regioselective C–H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes Organic Chemistry Frontiers, 2018, 5, 2875 |
| 1554406 | CIF | C30 H31 Br N2 O3 | P 1 21 1 | 13.248; 7.6262; 27.213 90; 97.298; 90 | 2727.1 | Yuan, Yang; Zheng, Zhan-Jiang; Ye, Fei; Ma, Jun-Han; Xu, Zheng; Bai, Xing-Feng; Li, Li; Xu, Li-Wen Highly efficient desymmetrization of cyclopropenes to azabicyclo[3.1.0]hexanes with five continuous stereogenic centers by copper-catalyzed [3 + 2] cycloadditions Organic Chemistry Frontiers, 2018, 5, 2759 |
| 1554407 | CIF | C23 H28 O6 | P 1 21 1 | 7.3005; 12.1224; 11.9121 90; 105.259; 90 | 1017.05 | Zhang, Xun; Li, Zhongle; Yong, Huaya; Xie, Zhixiang Biomimetic syntheses of C23 terpenoids: structural revision of salyunnanin A and confirmation of hassanane Organic Chemistry Frontiers, 2018, 5, 3469 |
| 1554408 | CIF | C14 H10 Br N O4 | P b c a | 7.5983; 16.424; 20.8458 90; 90; 90 | 2601.44 | Maezono, Shizuka Mei Bautista; Kim, Sung Hong; Lee, Yong Rok Copper-catalyzed [3 + 2 + 1] annulation for functionalized pyridines as potent and dynamic UV absorbers Organic Chemistry Frontiers, 2018, 5, 3368 |
| 1554409 | CIF | C18 H18 O2 | P 1 21/n 1 | 9.0575; 12.288; 12.993 90; 94.793; 90 | 1441 | Yang, Binmiao; Zhai, Xuejie; Feng, Shubo; Shao, Zhihui Dearomatization of naphthols using oxy-allyl cations: efficient construction of α-all-carbon quaternary center-containing 2-(2-oxocycloalkyl)cycloalkyl diketones Organic Chemistry Frontiers, 2018, 5, 2794 |
| 1554410 | CIF | C44 H42 Cl N5 O8 | P -1 | 17.135; 17.343; 20.802 106.696; 98.131; 118.106 | 4934.7 | Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo Domino aza/oxa-hetero-Diels–Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine] Organic Chemistry Frontiers, 2018, 5, 2754 |
| 1554411 | CIF | C42 H38 Cl N5 O6 | P -1 | 12.086; 12.455; 17.13 96.558; 109.996; 107.812 | 2236.9 | Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo Domino aza/oxa-hetero-Diels–Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine] Organic Chemistry Frontiers, 2018, 5, 2754 |
| 1554412 | CIF | C28 H22 | P -1 | 9.7638; 10.0633; 10.6246 100.341; 103.17; 95.285 | 990.28 | Chuskit, Deachen; Chaudhary, Renu; Venugopalan, Paloth; König, Burkhard; Natarajan, Palani Oxidative homodimerization of substituted olefins by DDQ visible light photocatalysis Organic Chemistry Frontiers, 2018, 5, 3553 |
| 1554413 | CIF | C18 H25 N O7 S | P 1 21/c 1 | 10; 14.827; 13.344 90; 101.939; 90 | 1935.7 | Lei, Meng; Li, Yanjun; Cao, Shi; Hou, Xinyi; Gong, Lei Alkylation–peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3–H functionalization Organic Chemistry Frontiers, 2018, 5, 3083 |
| 1554414 | CIF | C19 H24 F3 N O2 | P -1 | 12.1127; 13.1333; 13.1505 76.939; 79.228; 63.194 | 1810.2 | Long, Hao; Song, Jinshuai; Xu, Hai-Chao Electrochemical synthesis of 7-membered carbocycles through cascade 5-exo-trig/7-endo-trig radical cyclization Organic Chemistry Frontiers, 2018, 5, 3129 |
| 1554415 | CIF | C30 H29 N3 O4 S | P 1 21 1 | 8.6306; 10.9636; 14.5139 90; 90.644; 90 | 1373.25 | Huang, Qiuhong; Cheng, Yuyu; Yuan, Huijun; Chang, Xiaoyong; Li, Pengfei; Li, Wenjun Organocatalytic enantioselective Mannich-type addition of 5H-thiazol-4-ones to isatin-derived imines: access to 3-substituted 3-amino-2-oxindoles featured by vicinal sulfur-containing tetrasubstituted stereocenters Organic Chemistry Frontiers, 2018, 5, 3226 |
| 1554416 | CIF | C24 H22 N4 O4 | P 1 21/c 1 | 18.2546; 9.1982; 13.3199 90; 108.231; 90 | 2124.27 | Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors Organic Chemistry Frontiers, 2018, 5, 3206 |
| 1554417 | CIF | C12 H12 N2 O3 | P 1 21/c 1 | 11.2278; 13.7389; 7.4364 90; 107.173; 90 | 1095.98 | Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors Organic Chemistry Frontiers, 2018, 5, 3206 |
| 1554418 | CIF | C24 H20 N4 O5 | P 1 21/c 1 | 13.145; 14.0218; 12.9264 90; 114.416; 90 | 2169.47 | Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors Organic Chemistry Frontiers, 2018, 5, 3206 |
| 1554419 | CIF | C20 H18 | P n a 21 | 15.853; 12.375; 7.3639 90; 90; 90 | 1444.7 | Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K. Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism Organic Chemistry Frontiers, 2019, 6, 134 |
| 1554420 | CIF | C20 H14 O4 | P 1 21/c 1 | 8.0844; 19.8817; 10.2123 90; 109.061; 90 | 1551.44 | Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K. Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism Organic Chemistry Frontiers, 2019, 6, 134 |
| 1554421 | CIF | C24 H19 Cl N2 O | P 1 21/c 1 | 5.628; 19.385; 17.569 90; 91.36; 90 | 1916.2 | Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines Organic Chemistry Frontiers, 2018, 5, 2945 |
| 1554422 | CIF | C24 H19 Cl N2 O | P -1 | 5.7976; 9.4263; 17.097 87.715; 87.737; 86.465 | 931.2 | Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines Organic Chemistry Frontiers, 2018, 5, 2945 |
| 1554423 | CIF | C17 H0.25 N O | P 21 21 21 | 6.229; 13.6065; 14.6177 90; 90; 90 | 1238.92 | Xu, Xin-Ming; Lei, Chuan-Hu; Tong, Shuo; Zhu, Jieping; Wang, Mei-Xiang Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides Organic Chemistry Frontiers, 2018, 5, 3138 |
| 1554424 | CIF | C27 H25 F N2 O5 S | P 1 21 1 | 13.42; 5.3749; 17.821 90; 105.381; 90 | 1239.4 | Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F⋯H–N interactions on reactivity Organic Chemistry Frontiers, 2018, 5, 2960 |
| 1554425 | CIF | C18 H16 Br F O2 | P 1 | 6.6841; 8.7074; 14.4482 87.391; 81.591; 78.532 | 815.14 | Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F⋯H–N interactions on reactivity Organic Chemistry Frontiers, 2018, 5, 2960 |
| 1554426 | CIF | C14 H13 N O3 | P 1 21 1 | 10.0137; 10.3706; 11.987 90; 109.801; 90 | 1171.23 | Kim, Simon J.; Batey, Robert A. Enantioselective isoquinuclidine synthesis via sequential Diels–Alder/visible-light photoredox C–C bond cleavage: a formal synthesis of the indole alkaloid catharanthine Organic Chemistry Frontiers, 2018, 5, 2934 |
| 1554427 | CIF | C42 H50 O2 Si2 | P -1 | 7.6019; 7.7795; 17.7908 94.036; 92.577; 114.867 | 948.98 | Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs Organic Chemistry Frontiers, 2018, 5, 2912 |
| 1554428 | CIF | C48 H50 N4 Si2 | C 1 2/c 1 | 39.755; 10.0294; 11.4351 90; 102.874; 90 | 4444.8 | Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs Organic Chemistry Frontiers, 2018, 5, 2912 |
| 1554429 | CIF | C33 H35 N O6 | P 1 21/n 1 | 17.45405; 8.11896; 19.929 90; 91.5647; 90 | 2823.06 | Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction Organic Chemistry Frontiers, 2018, 5, 3003 |
| 1554430 | CIF | C30 H26 Cl3 N O3 | P 1 21/c 1 | 11.083; 21.629; 12.241 90; 116.92; 90 | 2616 | Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction Organic Chemistry Frontiers, 2018, 5, 3003 |
| 1554431 | CIF | C36 H37 O4 P S | P 1 21/c 1 | 8.7333; 32.515; 11.3552 90; 92.555; 90 | 3221.3 | Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation Organic Chemistry Frontiers, 2018, 5, 3567 |
| 1554432 | CIF | C45 H41 O4 P S | P -1 | 10.244; 13.1272; 15.4443 85.216; 77.319; 69.981 | 1903.71 | Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation Organic Chemistry Frontiers, 2018, 5, 3567 |
| 1554433 | CIF | C40 H39 O3 P S | P 1 21/c 1 | 10.9576; 24.0001; 13.0509 90; 94.036; 90 | 3423.7 | Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation Organic Chemistry Frontiers, 2018, 5, 3567 |
| 1554434 | CIF | C37 H35 O3 P S | P 1 21/c 1 | 12.3705; 13.8788; 19.1238 90; 106.702; 90 | 3144.8 | Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation Organic Chemistry Frontiers, 2018, 5, 3567 |
| 1554435 | CIF | C22 H24 N2 | P 1 21/c 1 | 22.09; 8.574; 9.447 90; 101.6; 90 | 1752.7 | Liu, Siyuan; Zhang, Wenzhu; Qu, Jingping; Wang, Baomin Engaging 2-methyl indolenines in a tandem condensation/1,5-hydride transfer/cyclization process: construction of a novel indolenine–tetrahydroquinoline assembly Organic Chemistry Frontiers, 2018, 5, 3008 |
| 1554436 | CIF | C21 H21 Br N O7 P S | P 21 21 21 | 8.8385; 14.3341; 17.8495 90; 90; 90 | 2261.4 | Sun, Jun; Mou, Chengli; Liu, Changyi; Huang, Ruoyan; Zhang, Shupeng; Zheng, Pengcheng; Chi, Yonggui Robin Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines Organic Chemistry Frontiers, 2018, 5, 2992 |
| 1554437 | CIF | C13 H13 N O4 S | P 1 21/c 1 | 9.1009; 17.5658; 8.1862 90; 103.294; 90 | 1273.61 | Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones Organic Chemistry Frontiers, 2019, 6, 183 |
| 1554438 | CIF | C13 H15 N O5 S | P -1 | 7.2268; 9.0737; 10.4696 80.813; 84.674; 88.958 | 674.8 | Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones Organic Chemistry Frontiers, 2019, 6, 183 |
| 1554439 | CIF | C13 H19 N O8 S | P -1 | 7.2412; 9.7236; 11.4552 85.64; 87.406; 77.183 | 783.86 | Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones Organic Chemistry Frontiers, 2019, 6, 183 |
| 1554440 | CIF | C16 H13 N O5 S | P 1 21/n 1 | 6.6266; 18.2993; 11.8645 90; 99.67; 90 | 1418.3 | Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones Organic Chemistry Frontiers, 2019, 6, 183 |
| 1554441 | CIF | C28 H29 Co P S | P 1 21/n 1 | 9.0319; 18.9034; 14.4632 90; 96.64; 90 | 2452.8 | Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives Organic Chemistry Frontiers, 2018, 5, 2997 |
| 1554442 | CIF | C22 H18 N O2 | P 1 21/n 1 | 12.766; 7.3952; 18.2702 90; 103.067; 90 | 1680.17 | Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives Organic Chemistry Frontiers, 2018, 5, 2997 |
| 1554443 | CIF | C30 H23 N O2 | P -1 | 7.3192; 11.4476; 14.2878 109.541; 103.435; 90.85 | 1091.7 | Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives Organic Chemistry Frontiers, 2018, 5, 2997 |
| 1554444 | CIF | C26 H21 N O2 | P -1 | 7.4718; 10.17; 13.6849 80.313; 76.092; 74.405 | 966.3 | Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives Organic Chemistry Frontiers, 2018, 5, 2997 |
| 1554445 | CIF | C28 H29 Br Co P S | P n a 21 | 16.6717; 10.051; 14.516 90; 90; 90 | 2432.4 | Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives Organic Chemistry Frontiers, 2018, 5, 2997 |
| 1554446 | CIF | C31 H44 N3 P2 Rh | P 1 21/n 1 | 10.9778; 16.148; 17.5888 90; 106.231; 90 | 2993.7 | Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex Organic Chemistry Frontiers, 2019, 6, 721 |
| 1554447 | CIF | C92 H120 N6 O3 P4 Rh2 | C 1 2/c 1 | 29.2408; 13.8295; 25.4214 90; 120.925; 90 | 8818.6 | Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex Organic Chemistry Frontiers, 2019, 6, 721 |
| 1554448 | CIF | C28 H33 Br O3 | I 1 2 1 | 26.357; 7.5712; 24.9141 90; 92.458; 90 | 4967.1 | Liu, Lin; Song, Huayue; Chen, Peng; Yuan, Ziyun; Feng, Shangbiao; Zhang, Weiwei; Fang, Bowen; Xie, Xingang; She, Xuegong Total synthesis of (−)-8-epi-chromazonarol enabled by a unique N2H4·H2O promoted intramolecular oxa-Michael cyclization reaction Organic Chemistry Frontiers, 2018, 5, 3013 |
| 1554449 | CIF | C30 H37 I N2 Ru | P -1 | 12.2395; 14.363; 18.399 89.442; 89.312; 88.419 | 3232.9 | Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines Organic Chemistry Frontiers, 2019, 6, 563 |
| 1554450 | CIF | C27 H31 I N2 Ru | P 1 21/n 1 | 15.329; 7.7727; 21.254 90; 95.269; 90 | 2521.7 | Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines Organic Chemistry Frontiers, 2019, 6, 563 |
| 1554451 | CIF | C26 H23 N O2 S | C 1 c 1 | 12.1152; 14.1577; 24.768 90; 93.519; 90 | 4240.3 | Zhang, Jia-hao; Wei, Yin; Shi, Min Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2980 |
| 1554452 | CIF | C26 H23 N O2 S | P 1 21/n 1 | 10.875; 11.83; 16.54 90; 98.8; 90 | 2103 | Zhang, Jia-hao; Wei, Yin; Shi, Min Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2980 |
| 1554453 | CIF | C26 H23 N O4 S | C 1 2/c 1 | 20.5631; 27.2351; 9.3277 90; 92.088; 90 | 5220.4 | Zhang, Jia-hao; Wei, Yin; Shi, Min Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes Organic Chemistry Frontiers, 2018, 5, 2980 |
| 1554454 | CIF | C20 H11 F12 O5 P | P 1 21/c 1 | 15.787; 10.811; 13.977 90; 112.816; 90 | 2199 | Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F. Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes Organic Chemistry Frontiers, 2018, 5, 3113 |
| 1554455 | CIF | C12 H20 N O4 P | P 1 21 1 | 7.266; 11.409; 8.573 90; 96.695; 90 | 705.8 | Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F. Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes Organic Chemistry Frontiers, 2018, 5, 3113 |
| 1554456 | CIF | C6 H7 O5 P | P 21 21 21 | 4.6005; 10.122; 16.4334 90; 90; 90 | 765.24 | Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F. Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes Organic Chemistry Frontiers, 2018, 5, 3113 |
| 1554457 | CIF | C24 H21 F6 O9 P | P -1 | 10.7892; 11.1562; 11.7122 101.788; 99.647; 106.558 | 1283.93 | Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F. Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes Organic Chemistry Frontiers, 2018, 5, 3113 |
| 1554458 | CIF | C18 H13 Cl6 O5 P | I 41/a :2 | 27.972; 27.972; 11.844 90; 90; 90 | 9267 | Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F. Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes Organic Chemistry Frontiers, 2018, 5, 3113 |
| 1554459 | CIF | C40 H40 N O2 S | P -1 | 8.8009; 12.3786; 16.3465 102.889; 95.068; 108.26 | 1624.3 | Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells Organic Chemistry Frontiers, 2018, 5, 3324 |
| 1554460 | CIF | C44 H42 N O2 S | P -1 | 7.1299; 14.678; 17.037 74.911; 81.895; 89.178 | 1703.8 | Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells Organic Chemistry Frontiers, 2018, 5, 3324 |
| 1554461 | CIF | C84 H80 N2 O4 S4 | P 1 21/c 1 | 13.5245; 24.687; 20.6534 90; 102.064; 90 | 6743.4 | Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells Organic Chemistry Frontiers, 2018, 5, 3324 |
| 1554462 | CIF | C92 H81 N2 O4 S4 | P -1 | 14.3142; 16.7266; 18.5616 105.723; 109.469; 90.336 | 4010.6 | Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells Organic Chemistry Frontiers, 2018, 5, 3324 |
| 1554463 | CIF | C27 H25 N O3 S | P -1 | 8.892; 9.668; 13.91 86.33; 86.29; 67.91 | 1105 | Beltran, Frédéric; Andna, Lucile; Miesch, Laurence Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts Organic Chemistry Frontiers, 2019, 6, 373 |
| 1554464 | CIF | C22 H25 N O3 S | P -1 | 7.6023; 7.8229; 16.7412 85.307; 84.129; 85.07 | 984.06 | Beltran, Frédéric; Andna, Lucile; Miesch, Laurence Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts Organic Chemistry Frontiers, 2019, 6, 373 |
| 1554465 | CIF | C28 H27 N O3 S | P 1 21/c 1 | 10.5059; 11.5524; 19.3292 90; 99.812; 90 | 2311.6 | Beltran, Frédéric; Andna, Lucile; Miesch, Laurence Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts Organic Chemistry Frontiers, 2019, 6, 373 |
| 1554466 | CIF | C25 H29 N O3 S | P 1 21/n 1 | 8.6751; 21.9074; 12.355 90; 107.893; 90 | 2234.5 | Beltran, Frédéric; Andna, Lucile; Miesch, Laurence Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts Organic Chemistry Frontiers, 2019, 6, 373 |
| 1554467 | CIF | C19 H16 N2 O6 S | P 1 21/c 1 | 9.7218; 7.7915; 24.097 90; 99.734; 90 | 1799 | Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines Organic Chemistry Frontiers, 2018, 5, 3574 |
| 1554468 | CIF | C20 H19 N O4 S | P -1 | 6.4452; 11.7323; 12.5163 105.865; 90.612; 93.872 | 907.9 | Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines Organic Chemistry Frontiers, 2018, 5, 3574 |
| 1554469 | CIF | C33 H26 Cl N O2 S | P 1 21/n 1 | 10.2302; 24.9417; 10.532 90; 94.66; 90 | 2678.4 | Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines Organic Chemistry Frontiers, 2018, 5, 3574 |
| 1554470 | CIF | C26 H30 N4 O9 | I 1 2 1 | 9.9349; 5.4755; 25.351 90; 101.162; 90 | 1353 | Chen, Jinhong; Li, Junfang; Zhu, Longqing; Peng, Xue; Feng, Yiyue; Lu, Yingmei; Hu, Xiaoling; Liang, Jianpin; Zhao, Quanyi; Wang, Zhen Total synthesis and structure revision of chrysamide B Organic Chemistry Frontiers, 2018, 5, 3402 |
| 1554471 | CIF | C26 H30 O6 | P 1 21/n 1 | 11.6963; 8.9597; 23.096 90; 90.67; 90 | 2420.2 | Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans Organic Chemistry Frontiers, 2018, 5, 3483 |
| 1554472 | CIF | C27 H28 Cl I N2 O5 | P -1 | 10.805; 11.7571; 12.8689 106.048; 95.01; 114.103 | 1396.3 | Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans Organic Chemistry Frontiers, 2018, 5, 3483 |
| 1554473 | CIF | C14 H12 F6 N2 O4 S2 | P 1 21/n 1 | 8.4088; 17.398; 12.1982 90; 101.318; 90 | 1749.85 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554474 | CIF | C20 H15 F6 N O5 S2 | P 1 21/n 1 | 12.6441; 11.3643; 16.2034 90; 111.751; 90 | 2162.5 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554475 | CIF | C21 H19 F6 N O6 S3 | P 1 21/n 1 | 13.0371; 14.5605; 14.0643 90; 113.617; 90 | 2446.2 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554476 | CIF | C14 H11 Cl F6 N2 O5 S2 | C 1 2/c 1 | 31.442; 7.7594; 16.3435 90; 91.74; 90 | 3985.5 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554477 | CIF | C13 H8 F6 O7 S2 | P 1 21/n 1 | 5.7308; 13.6484; 21.184 90; 95.748; 90 | 1648.6 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554478 | CIF | C13 H10 F6 N2 O4 S2 | P 1 21/c 1 | 14.266; 6.0883; 18.922 90; 94.123; 90 | 1639.2 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554479 | CIF | C9 H10 F6 N2 O5 S2 | P b c a | 17.2641; 14.8304; 23.9088 90; 90; 90 | 6121.5 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554480 | CIF | C15 H14 F6 N2 O5 S2 | P n a 21 | 27.2048; 18.3507; 12.2694 90; 90; 90 | 6125.2 | Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles Organic Chemistry Frontiers, 2018, 5, 3163 |
| 1554481 | CIF | C29 H28 N2 O S2 | P 1 21/n 1 | 17.607; 5.4871; 25.7682 90; 106.169; 90 | 2391 | Weldeab, Asmerom O.; Li, Lei; Cekli, Seda; Abboud, Khalil A.; Schanze, Kirk S.; Castellano, Ronald K. Pyridine-terminated low gap π-conjugated oligomers: design, synthesis, and photophysical response to protonation and metalation Organic Chemistry Frontiers, 2018, 5, 3170 |
| 1554482 | CIF | C26 H22 Br N O9 | P 1 21/c 1 | 11.2685; 18.6581; 12.8795 90; 111.426; 90 | 2520.8 | Agafonova, Anastasiya V.; Smetanin, Ilia A.; Rostovskii, Nikolai V.; Khlebnikov, Alexander F.; Novikov, Mikhail S. Expedient synthesis of 3-hydroxypyrroles via Bu3SnH-triggered ionic 5-exo-trig-cyclization of 5-chloro-3-azamuconoate derivatives Organic Chemistry Frontiers, 2018, 5, 3396 |
| 1554483 | CIF | C16 H9 Cl F3 N O3 S | I b a 2 | 15.569; 29.973; 7.0564 90; 90; 90 | 3292.9 | Yi, Ruxia; Li, Xincheng; Wan, Boshun Ring-opening and cyclization of aziridines with aryl azides: metal-free synthesis of 6-(triflyloxy)quinolines Organic Chemistry Frontiers, 2018, 5, 3488 |
| 1554484 | CIF | C11 H9 F O2 | P 21 21 21 | 4.9693; 5.8579; 31.3863 90; 90; 90 | 913.64 | Han, Sang Hoon; Pandey, Ashok Kumar; Lee, Heeyoung; Kim, Saegun; Kang, Dahye; Jung, Young Hoon; Kim, Hyung Sik; Hong, Sungwoo; Kim, In Su One-pot synthesis of 2-naphthols from nitrones and MBH adducts via decarboxylative N–O bond cleavage Organic Chemistry Frontiers, 2018, 5, 3210 |
| 1554485 | CIF | C20 H24 O5 | P 21 21 21 | 6.1036; 12.5506; 21.976 90; 90; 90 | 1683.45 | Yang, Qian; Hu, Kun; Yan, Bing-Chao; Liu, Miao; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin Maoeriocalysins A–D, four novel ent-kaurane diterpenoids from Isodon eriocalyx and their structure determination utilizing quantum chemical calculation in conjunction with quantitative interproton distance analysis Organic Chemistry Frontiers, 2019, 6, 45 |
| 1554486 | CIF | C14 H8 N3 O | P 1 21/n 1 | 5.7918; 13.738; 13.4519 90; 101.436; 90 | 1049.09 | Li, Ping-Gui; Yan, Cheng; Zhu, Shuai; Liu, Shu-Hui; Zou, Liang-Hua Direct construction of benzimidazo[l,2-c]quinazolin-6-ones via metal-free oxidative C‒C bond cleavage Organic Chemistry Frontiers, 2018, 5, 3464 |
| 1554487 | CIF | C37 H31 N3 O4 S | P 1 21 1 | 13.6363; 8.5322; 15.2209 90; 116.205; 90 | 1588.9 | Gu, Bo-Qi; Yang, Wu-Lin; Wu, Shu-Xiao; Wang, Yan-Bing; Deng, Wei-Ping Organocatalytic asymmetric synthesis of tetrahydrocarbazoles via an inverse-electron-demand Diels–Alder reaction of 2,3-indole-dienes with enals Organic Chemistry Frontiers, 2018, 5, 3430 |
| 1554488 | CIF | C17 H18 N O5 P | P -1 | 9.5039; 10.0075; 10.6869 64.045; 69.351; 83.294 | 854.35 | Wang, Jie; Li, Jun; Wei, Yuanyuan; Yang, Jingya; Huo, Congde Copper-catalyzed oxidative phosphonation of 3,4-dihydro-1,4-benzoxazin-2-ones Organic Chemistry Frontiers, 2018, 5, 3534 |
| 1554489 | CIF | C10 H8 F N3 | P b c a | 7.4865; 11.7277; 20.913 90; 90; 90 | 1836.1 | Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives Organic Chemistry Frontiers, 2019, 6, 426 |
| 1554490 | CIF | C16 H12 F N5 O2 | P 1 21/c 1 | 8.4745; 13.483; 12.5515 90; 96.566; 90 | 1424.7 | Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives Organic Chemistry Frontiers, 2019, 6, 426 |
| 1554491 | CIF | C10 H8 F N3 | P 1 21/n 1 | 6.185; 7.487; 18.728 90; 96.138; 90 | 862.3 | Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives Organic Chemistry Frontiers, 2019, 6, 426 |
| 1554492 | CIF | C70 H56 Ag5 Cl2 N6 P4 | A e a 2 | 27.38; 26.9; 24.03 90; 90; 90 | 17699 | Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives Organic Chemistry Frontiers, 2019, 6, 426 |
| 1554493 | CIF | C20 H14 N2 | P -1 | 3.9188; 12.5127; 15.3057 101.08; 96.416; 92.665 | 730.13 | Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes Organic Chemistry Frontiers, 2019, 6, 432 |
| 1554494 | CIF | C22 H19 N3 | P 1 21/c 1 | 10.5762; 7.8869; 19.9879 90; 91.535; 90 | 1666.7 | Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes Organic Chemistry Frontiers, 2019, 6, 432 |
| 1554495 | CIF | C25 H20 N4 O2 | P -1 | 9.1577; 10.7173; 13.3021 106.893; 91.497; 91.349 | 1248.12 | Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes Organic Chemistry Frontiers, 2019, 6, 432 |
| 1554496 | CIF | C30 H25 N O3 | P 1 21 1 | 8.5256; 16.9053; 8.9274 90; 112.31; 90 | 1190.37 | Xu, Jianfeng; Peng, Jingyi; He, Chonglong; Ren, Hongjun N-Heterocyclic carbene catalyzed chemo- and enantioselective cross-benzoin reaction of aldehydes with isatins Organic Chemistry Frontiers, 2019, 6, 172 |
| 1554497 | CIF | C18 H12 Cl3 O P S3 | C 1 2/c 1 | 12.268; 8.6753; 37.965 90; 92.878; 90 | 4035.5 | Lu, Guozhang; Chen, Jun; Huangfu, Xinlei; Li, Xueyan; Fang, Meijuan; Tang, Guo; Zhao, Yufen Visible-light-mediated direct synthesis of phosphorotrithioates as potent anti-inflammatory agents from white phosphorus Organic Chemistry Frontiers, 2019, 6, 190 |
| 1554498 | CIF | C38 H42 Cl2 O7 | C 1 2 1 | 25.2058; 7.2704; 19.2306 90; 105.306; 90 | 3399.1 | Fan, Jian-Hong; Hu, Ya-Jian; Guo, Qiang; Li, Shaoping; Zhao, Jing; Li, Chuang-Chuang Asymmetric synthesis of the tetracyclic core of bufogargarizin C by an intramolecular [5 + 2] cycloaddition Organic Chemistry Frontiers, 2019, 6, 22 |
| 1554499 | CIF | C27 H22 N O2 P | P 1 21 1 | 7.8836; 12.2399; 11.1988 90; 90.174; 90 | 1080.62 | Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides Organic Chemistry Frontiers, 2019, 6, 236 |
| 1554500 | CIF | C27 H22 N O2 P | P 1 | 6.0253; 9.0011; 10.3679 75.005; 76.437; 89.09 | 527.4 | Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides Organic Chemistry Frontiers, 2019, 6, 236 |
| 1554501 | CIF | C19 H15 F3 O4 | C 1 2/c 1 | 23.47; 9.9387; 17.2934 90; 123.484; 90 | 3364.4 | Chen, Yueji; You, Yi; Weng, Zhiqiang Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities Organic Chemistry Frontiers, 2019, 6, 213 |
| 1554502 | CIF | C17 H12 Br2 F2 O2 | P 1 21/c 1 | 13.7491; 5.8303; 21.42 90; 105.814; 90 | 1652.1 | Chen, Yueji; You, Yi; Weng, Zhiqiang Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities Organic Chemistry Frontiers, 2019, 6, 213 |
| 1554503 | CIF | C22 H21 N O5 | P 21 21 2 | 21.2879; 7.5138; 11.5723 90; 90; 90 | 1851.02 | Shoji, Taku; Araki, Takanori; Iida, Nanami; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Okujima, Tetsuo Synthesis of azulenophthalimides by phosphine-mediated annulation of 1,2-diformylazulenes with maleimides Organic Chemistry Frontiers, 2019, 6, 195 |
| 1554504 | CIF | C68 H68 Cl6 N4 O10 P2 | R -3 :H | 25.2081; 25.2081; 30.11 90; 90; 120 | 16570 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554505 | CIF | C66 H66 I N2 O4 P2 | C 1 2/c 1 | 19.7346; 19.9943; 14.9829 90; 110.36; 90 | 5542.6 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554506 | CIF | C34 H34 Br Cl3 N O2 P | P 1 21/c 1 | 10.967; 15.8648; 20.3172 90; 105.084; 90 | 3413.2 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554507 | CIF | C66 H66 F6 N2 O4 P3 | C 1 2/c 1 | 19.664; 19.9512; 15.5025 90; 111.125; 90 | 5673.2 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554508 | CIF | C66 H66 Cl N2 O7.33 P2 | R -3 :H | 24.8062; 24.8062; 30.0418 90; 90; 120 | 16009.5 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554509 | CIF | C74 H86 F12 N2 O6 P4 | P b c a | 15.5817; 20.6208; 22.0566 90; 90; 90 | 7086.9 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554510 | CIF | C66 H66 N2 O4 P2 | P 1 21/c 1 | 14.2234; 15.5567; 12.5242 90; 108.744; 90 | 2624.2 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554511 | CIF | C66 H66 Br N2 O4 P2 | R -3 :H | 24.7543; 24.7543; 30.0212 90; 90; 120 | 15931.6 | Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts Organic Chemistry Frontiers, 2019, 6, 110 |
| 1554512 | CIF | C12 H17 N S | P 1 21/c 1 | 6.3585; 10.945; 17.5672 90; 92.051; 90 | 1221.78 | Lai, Miao; Wu, Zhiyong; Wang, Yizhi; Zheng, Ying; Zhao, Mingqin Selective synthesis of aryl thioamides and aryl-α-ketoamides from α-oxocarboxylic acids and tetraalkylthiuram disulfides: an unexpected chemoselectivity from aryl sulfonyl chlorides Organic Chemistry Frontiers, 2019, 6, 506 |
| 1554513 | CIF | C21 H19 Br O3 | P 21 21 21 | 10.687; 12.035; 14.902 90; 90; 90 | 1917 | Huang, Huicai; Lu, Xue; Mao, Yukang; Ye, Jinxing Asymmetric synthesis of highly functionalized furanones via direct Michael reactions mediated by a bulky primary amine Organic Chemistry Frontiers, 2019, 6, 1080 |
| 1554514 | CIF | C17 H20 O3 | P 21 21 21 | 10.4344; 11.4942; 11.5277 90; 90; 90 | 1382.58 | Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis Organic Chemistry Frontiers, 2019, 6, 290 |
| 1554515 | CIF | C20 H20 O3 | P -1 | 8.431; 8.6965; 11.7742 80.603; 87.055; 65.92 | 777.47 | Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis Organic Chemistry Frontiers, 2019, 6, 290 |
| 1554516 | CIF | C25 H21 F O3 | P 1 21/c 1 | 9.8733; 10.3877; 37.781 90; 96.893; 90 | 3846.8 | Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis Organic Chemistry Frontiers, 2019, 6, 290 |
| 1554517 | CIF | C19 H16 O2 | F d d 2 | 23.63; 42.848; 5.8546 90; 90; 90 | 5927.8 | Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)–C(sp2) bonds Organic Chemistry Frontiers, 2019, 6, 437 |
| 1554518 | CIF | C20 H18 O3 | P 1 21/c 1 | 10.476; 15.249; 11.317 90; 116.28; 90 | 1621 | Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)‒C(sp2) bonds Organic Chemistry Frontiers, 2019, 6, 437 |
| 1554519 | CIF | C23 H21 N O3 S | I 1 a 1 | 8.3257; 15.1988; 16.3404 90; 95.005; 90 | 2059.8 | Zhu, Tong-Hao; Zhang, Xiao-Chen; Zhao, Kai; Loh, Teck-Peng Cu(OTf)2-mediated C(sp2)–H arylsulfonylation of enamides via the insertion of sulfur dioxide Organic Chemistry Frontiers, 2019, 6, 94 |
| 1554520 | CIF | C23 H25 N3 O3 | P 21 21 21 | 11.8106; 12.5767; 26.9924 90; 90; 90 | 4009.4 | Luo, Xiaowei; Chen, Chunmei; Tao, Huaming; Lin, Xiuping; Yang, Bin; Zhou, Xuefeng; Liu, Yonghong Structurally diverse diketopiperazine alkaloids from the marine-derived fungus Aspergillus versicolor SCSIO 41016 Organic Chemistry Frontiers, 2019, 6, 736 |
| 1554521 | CIF | C20 H23 N2 O3 P | P -1 | 9.115; 9.448; 11.944 101.46; 91.031; 106.62 | 962.9 | Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines Organic Chemistry Frontiers, 2019, 6, 393 |
| 1554522 | CIF | C18 H20 N O3 P | P 1 c 1 | 7.6453; 11.642; 9.808 90; 102.969; 90 | 850.7 | Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines Organic Chemistry Frontiers, 2019, 6, 393 |
| 1554523 | CIF | C30 H40 N6 O12 | C 1 2/c 1 | 27.337; 6.1593; 20.343 90; 106.22; 90 | 3288.9 | Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water Organic Chemistry Frontiers, 2019, 6, 75 |
| 1554524 | CIF | C30 H36 N6 O10 | P 1 21/n 1 | 6.8698; 14.4541; 14.7842 90; 95.204; 90 | 1461.97 | Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water Organic Chemistry Frontiers, 2019, 6, 75 |
| 1554525 | CIF | C26 H38 N6 O9 S2 | P n a 21 | 15.1627; 6.4915; 29.4057 90; 90; 90 | 2894.4 | Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water Organic Chemistry Frontiers, 2019, 6, 75 |
| 1554526 | CIF | C21 H28 N2 O8 | P 1 21 1 | 11.4833; 7.3773; 13.116 90; 96.533; 90 | 1103.92 | Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921 Organic Chemistry Frontiers, 2019, 6, 773 |
| 1554527 | CIF | C32 H34 Br0 Cl N O4 | P 21 21 21 | 6.1903; 13.744; 32.103 90; 90; 90 | 2731.3 | Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921 Organic Chemistry Frontiers, 2019, 6, 773 |
| 1554528 | CIF | C5 H4 F N5 O6 | P -1 | 7.976; 8.218; 15.344 94.059; 104.85; 97.364 | 958.5 | Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B. N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design Organic Chemistry Frontiers, 2019, 6, 249 |
| 1554529 | CIF | C5 H4 F N5 O6 | P 1 21 1 | 5.4659; 10.477; 8.1322 90; 94.857; 90 | 464.03 | Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B. N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design Organic Chemistry Frontiers, 2019, 6, 249 |
| 1554530 | CIF | C3 H3 F N6 O4 | P n a 21 | 11.4331; 5.7212; 11.2434 90; 90; 90 | 735.44 | Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B. N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design Organic Chemistry Frontiers, 2019, 6, 249 |
| 1554531 | CIF | C5 H4 F N5 O6 | P b c a | 6.6055; 11.5186; 23.4809 90; 90; 90 | 1786.57 | Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B. N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design Organic Chemistry Frontiers, 2019, 6, 249 |
| 1554532 | CIF | C19 H15 N O3 | P c a 21 | 14.3845; 4.3448; 23.199 90; 90; 90 | 1449.9 | Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides Organic Chemistry Frontiers, 2019, 6, 226 |
| 1554533 | CIF | C19 H15 N O2 | P 1 c 1 | 21.0827; 8.2829; 8.2169 90; 95.222; 90 | 1428.93 | Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides Organic Chemistry Frontiers, 2019, 6, 226 |
| 1554534 | CIF | C28 H33 Au Cl O2 P | P -1 | 9.2179; 10.4777; 14.2247 100.062; 92.031; 103.287 | 1312.41 | Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides Organic Chemistry Frontiers, 2019, 6, 226 |
| 1554535 | CIF | C33 H32 Cl N O9 | P 21 21 21 | 11.0158; 12.13; 23.587 90; 90; 90 | 3151.7 | Cao, Jian; Liu, Jin-Yu; Zhang, Yi-Ming; Wang, Zhu-Yin; Xu, Peng-Fei Synergistic promotion by intramolecular hydrogen bonding: a bi-functionally catalyzed cascade reaction for the synthesis of enantiopure chromenopyrrolidines Organic Chemistry Frontiers, 2019, 6, 674 |
| 1554536 | CIF | C20 H15 Br2 N O2 | P c a 21 | 7.0667; 23.0878; 21.9663 90; 90; 90 | 3583.9 | Liu, Zhenhua; Zhu, Guangyu; Gao, Wen; Yang, Lin; Ji, Huimin; Tong, Lili; Tang, Bo Copper-catalyzed regioselective cyclization of vinyl azides by gem-difluoromethylene for trisubstituted pyridines Organic Chemistry Frontiers, 2019, 6, 468 |
| 1554537 | CIF | C17 H17 Br N4 O | P -1 | 5.2572; 12.458; 13.205 69.94; 83.57; 89.74 | 806.7 | Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G. 3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations Organic Chemistry Frontiers, 2019, 6, 335 |
| 1554538 | CIF | C27 H21 N2 O P | P 1 21/c 1 | 12.429; 10.415; 37.841 90; 90.13; 90 | 4898.4 | Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G. 3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations Organic Chemistry Frontiers, 2019, 6, 335 |
| 1554539 | CIF | C34 H44 N2 O Si | P -1 | 8.8134; 10.3559; 18.035 100.993; 95.022; 92.933 | 1605.78 | Chen, Cui-Hong; Chai, Yun; Zhou, Zheng-Xin; Rao, Wei-Hao; Liu, Bin; Liu, Li; Xu, Ran; Liu, Yue-Jin; Zeng, Ming-Hua Room-temperature Pd(ii)-catalyzed direct C–H TIPS-ethynylation of phenylacetic amides with terminal alkynes Organic Chemistry Frontiers, 2019, 6, 442 |
| 1554540 | CIF | C35 H30 | P m n 21 | 44.902; 11.1591; 10.6337 90; 90; 90 | 5328.2 | Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe [15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase Organic Chemistry Frontiers, 2019, 6, 309 |
| 1554541 | CIF | C42 H36 | P -1 | 11.372; 13.1796; 24.509 105.144; 93.375; 90.36 | 3538.8 | Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe [15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase Organic Chemistry Frontiers, 2019, 6, 309 |
| 1554542 | CIF | C42 H54 O6 S2 Se | P -1 | 14.2625; 18.0213; 31.3062 86.466; 83.674; 83.298 | 7933.2 | Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity Organic Chemistry Frontiers, 2019, 6, 263 |
| 1554543 | CIF | C42 H54 O8 S2 Se | P 1 21/n 1 | 17.4194; 8.2052; 28.3968 90; 90.166; 90 | 4058.73 | Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity Organic Chemistry Frontiers, 2019, 6, 263 |
| 1554544 | CIF | C42 H54 O6 Se Te2 | P -1 | 12.1441; 16.8305; 20.8669 98.844; 91.448; 102.981 | 4098.7 | Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity Organic Chemistry Frontiers, 2019, 6, 263 |
| 1554545 | CIF | C42 H54 O6 S Se2 | P -1 | 14.2879; 18.0394; 31.4094 86.414; 83.365; 83.373 | 7977.7 | Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity Organic Chemistry Frontiers, 2019, 6, 263 |
| 1554546 | CIF | C24 H19 Br N2 O | P 1 21/c 1 | 13.0718; 15.5471; 10.5005 90; 113.181; 90 | 1961.7 | Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles Organic Chemistry Frontiers, 2019, 6, 256 |
| 1554547 | CIF | C24 H19 Cl N2 O | P 1 21/c 1 | 12.9966; 15.5319; 10.522 90; 113.397; 90 | 1949.3 | Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles Organic Chemistry Frontiers, 2019, 6, 256 |
| 1554548 | CIF | C16 H14 Cl N O2 | P 21 21 21 | 9.5976; 10.3316; 13.9249 90; 90; 90 | 1380.8 | Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles Organic Chemistry Frontiers, 2019, 6, 256 |
| 1554549 | CIF | C19 H16 N2 O | P -1 | 8.802; 9.9463; 10.213 116.522; 100.853; 103.243 | 734.13 | Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles Organic Chemistry Frontiers, 2019, 6, 256 |
| 1554550 | CIF | C19 H19 Cl2 N O4 | C 1 2/c 1 | 33.58; 13.96; 8.0737 90; 100.506; 90 | 3721.3 | Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles Organic Chemistry Frontiers, 2019, 6, 256 |
| 1554551 | CIF | C13 H22 O2 | P b c a | 11.8513; 8.0917; 24.6768 90; 90; 90 | 2366.4 | He, Min; Yi, Jiuzhou; Zhao, Gaoyuan; Chen, Peiqi; Long, Dan; Hu, Xiaojun; Li, Huilin; Xie, Xingang; Wang, Xiaolei; She, Xuegong A concise approach to the tricyclic framework of longipinane- and ent-longipinane-type sesquiterpenoids Organic Chemistry Frontiers, 2019, 6, 383 |
| 1554552 | CIF | C25 H24 O5 S | P 1 21 1 | 9.1789; 10.574; 11.4116 90; 91.684; 90 | 1107.11 | Zhang, Nan; He, Tingting; Liu, Yidong; Li, Shan; Tan, Yu; Peng, Lei; Li, Dongmei; Shan, Chunhui; Yan, Hailong Organocatalytic atropo- and E/Z-selective Michael addition reaction of ynones with α-amido sulfones as sulfone-type nucleophile Organic Chemistry Frontiers, 2019, 6, 451 |
| 1554553 | CIF | C12 H10 F3 N O6 Se | P -1 | 9.809; 9.877; 9.925 66.084; 65.463; 64.347 | 758.1 | Ge, Hangming; Shen, Qilong Trifluoromethyl-substituted selenium ylide: a broadly applicable electrophilic trifluoromethylating reagent Organic Chemistry Frontiers, 2019, 6, 2205 |
| 1554554 | CIF | C20 H29 N O S | P 1 21 1 | 10.5315; 7.0899; 12.4878 90; 105.29; 90 | 899.43 | Qin, Shuanglin; Liu, Tongtong; Luo, Yunhao; Jiang, Shende; Yang, Guang Diastereoselective Rh-catalyzed decarboxylative allylation to form quaternary stereocenters using sulfinimine as the directing group Organic Chemistry Frontiers, 2019, 6, 732 |
| 1554555 | CIF | C26 H31 N3 Si | C 1 2/c 1 | 41.982; 8.4505; 16.3226 90; 123.085; 90 | 4851.8 | Wu, Wanqing; Fang, Songjia; Jiang, Guangbin; Li, Meng; Jiang, Huanfeng Palladium-catalyzed regioselective C–H alkynylation of indoles with bromoalkynes in water Organic Chemistry Frontiers, 2019, 6, 2200 |
| 1554556 | CIF | C30 H25 N O2 | P 1 21/c 1 | 5.7768; 26.401; 15.2336 90; 95.248; 90 | 2313.6 | Ji, Cheng-Long; Pan, Yao; Geng, Fang-Zhou; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo Synergistic silver/scandium catalytic spiroketalization of β-alkynyl ketones for the atom economical synthesis of skeletally diverse spirocyclic isochromenes Organic Chemistry Frontiers, 2019, 6, 474 |
| 1554557 | CIF | C21 H21 N O2 S | C 1 2/c 1 | 31.1655; 8.4946; 13.3472 90; 98.752; 90 | 3492.37 | Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles Organic Chemistry Frontiers, 2019, 6, 480 |
| 1554558 | CIF | C21 H18 Br N O3 S | P 1 21/n 1 | 8.6549; 18.21; 11.9124 90; 94.769; 90 | 1870.96 | Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles Organic Chemistry Frontiers, 2019, 6, 480 |
| 1554559 | CIF | C28 H36 N2 O2 Si | P -1 | 9.7904; 10.7882; 12.3517 83.891; 69.723; 84.499 | 1214.36 | Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C–H activation Organic Chemistry Frontiers, 2019, 6, 699 |
| 1554560 | CIF | C27 H31 N O4 Si | P -1 | 9.9601; 10.6766; 11.8691 74.393; 85.571; 88.958 | 1211.99 | Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C–H activation Organic Chemistry Frontiers, 2019, 6, 699 |
| 1554561 | CIF | C31 H26 Cl2 N4 O4 S2 | P 1 21/c 1 | 8.24; 10.3859; 17.7438 90; 95.373; 90 | 1511.84 | Han, Shuaijun; Gao, Xianying; Wu, Qingsong; Li, Jingya; Zou, Dapeng; Wu, Yusheng; Wu, Yangjie Nickel-promoted C(2)‒H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide Organic Chemistry Frontiers, 2019, 6, 830 |
| 1554562 | CIF | C25.5 H28 Cl N4 O2.5 Pd | P n a 21 | 25.795; 9.144; 21.256 90; 90; 90 | 5013.6 | Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides Organic Chemistry Frontiers, 2019, 6, 544 |
| 1554563 | CIF | C18 H11 Br N2 | C 1 2/c 1 | 26.203; 10.644; 30.852 90; 106.633; 90 | 8245 | Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides Organic Chemistry Frontiers, 2019, 6, 544 |
| 1554564 | CIF | C16 H18 O2 S | P 1 21 1 | 5.712; 15.28; 8.28 90; 104.192; 90 | 700.6 | Sun, Yongjie; Jiang, Jun; Guo, Xiaochong; Wen, Jialin; Zhang, Xumu Asymmetric hydrogenation of α,β-unsaturated sulfones by a rhodium/thiourea–bisphosphine complex Organic Chemistry Frontiers, 2019, 6, 1438 |
| 1554565 | CIF | C32 H27 N O4 S | P 43 21 2 | 13.6813; 13.6813; 29.053 90; 90; 90 | 5438.1 | Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones Organic Chemistry Frontiers, 2019, 6, 405 |
| 1554566 | CIF | C33 H29 N O4 S | P 21 21 21 | 11.043; 14.753; 17.258 90; 90; 90 | 2811.6 | Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones Organic Chemistry Frontiers, 2019, 6, 405 |
| 1554567 | CIF | C22 H24 O7 | P -1 | 9.1375; 13.1527; 16.354 95.187; 95.294; 103.04 | 1894.04 | Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae Organic Chemistry Frontiers, 2019, 6, 591 |
| 1554568 | CIF | C18 H17 Cl3 O5 | P 1 2 1 | 13.8718; 9.6965; 13.8978 90; 92.204; 90 | 1867.98 | Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae Organic Chemistry Frontiers, 2019, 6, 591 |
| 1554569 | CIF | C172 H203 N13 O10 P2 | C 1 2/c 1 | 21.469; 29.096; 28.543 90; 95.17; 90 | 17757 | Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers Organic Chemistry Frontiers, 2019, 6, 299 |
| 1554570 | CIF | C173 H203 N13 O10 P2 | C 1 2/c 1 | 21.505; 29.114; 28.751 90; 94.83; 90 | 17937 | Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers Organic Chemistry Frontiers, 2019, 6, 299 |
| 1554571 | CIF | C12 H12 N2 O2 S | P 1 21/c 1 | 8.968; 9.084; 14.804 90; 105.357; 90 | 1163 | Zu, Weisai; Liu, Shuai; Jia, Xin; Xu, Liang Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions Organic Chemistry Frontiers, 2019, 6, 1356 |
| 1554572 | CIF | C19 H15 N O2 S | P 1 21 1 | 8.0275; 8.0254; 12.699 90; 101.787; 90 | 800.9 | Zhao, Zi-Biao; Shi, Lei; Meng, Fan-Jie; Li, Yaming; Zhou, Yong-Gui Synthesis of chiral seven-membered cyclic sulfonamides through palladium-catalyzed arylation of cyclic imines Organic Chemistry Frontiers, 2019, 6, 1572 |
| 1554573 | CIF | C10 H13 N O3 | P 1 | 6.9308; 6.9507; 11.8464 84.194; 79.023; 64.094 | 503.84 | Yang, Wu-Lin; Sun, Zhong-Tao; Zhang, Jian; Li, Zhong; Deng, Wei-Ping Enantioselective synthesis of 3-amino-hydrobenzofuran-2,5-diones via Cu(i)-catalyzed intramolecular conjugate addition of imino esters Organic Chemistry Frontiers, 2019, 6, 579 |
| 1554574 | CIF | C116 H162 Br F3 O12 | P 1 21 1 | 15.1538; 13.5668; 27.2737 90; 92.794; 90 | 5600.5 | Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A. Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes Organic Chemistry Frontiers, 2019, 6, 603 |
| 1554575 | CIF | C116 H162 Br F3 O12 | P 1 21 1 | 15.0627; 13.3599; 27.1554 90; 94.396; 90 | 5448.6 | Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A. Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes Organic Chemistry Frontiers, 2019, 6, 603 |
| 1554576 | CIF | C10 H8 N2 Se | P 1 21/c 1 | 7.15; 11.643; 12.098 90; 95.268; 90 | 1002.9 | Cao, Yuan; Liu, Jie; Liu, Fanmin; Jiang, Lvqi; Yi, Wenbin Copper-catalyzed direct and odorless selenylation with a sodium selenite-based reagent Organic Chemistry Frontiers, 2019, 6, 825 |
| 1554577 | CIF | C9 H9 F3 N2 | P 1 21 1 | 5.799; 7.486; 10.479 90; 104.17; 90 | 441.1 | Chen, Mu-Wang; Deng, Zhihong; Yang, Qin; Huang, Jian; Peng, Yiyuan Enantioselective synthesis of trifluoromethylated dihydroquinoxalinones via palladium-catalyzed hydrogenation Organic Chemistry Frontiers, 2019, 6, 746 |
| 1554578 | CIF | C29 H24 N2 O2 | P 21 21 21 | 9.1297; 10.326; 24.127 90; 90; 90 | 2274.5 | Xu, Lubin; Chen, Haohua; Liu, Jian; Zhou, Lan; Liu, Qing; Lan, Yu; Xiao, Jian Chiral phosphoric acid-catalyzed asymmetric C(sp3)–H functionalization of biomass-derived 2,5-dimethylfuran via two sequential Cope-type rearrangements Organic Chemistry Frontiers, 2019, 6, 1162 |
| 1554579 | CIF | C31 H42 O11 | P 21 21 21 | 32.1461; 11.483; 8.0162 90; 90; 90 | 2959.05 | Zhang, Jia; He, Jun; Cheng, Yung-Chi; Zhang, Pei-Cheng; Yan, Yu; Zhang, Hao-Jun; Zhang, Wei-Ku; Xu, Jie-Kun Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana Organic Chemistry Frontiers, 2019, 6, 2312 |
| 1554580 | CIF | C35 H26 Cl N5 O | P 21 21 21 | 11.351; 11.9996; 21.215 90; 90; 90 | 2889.6 | Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions Organic Chemistry Frontiers, 2019, 6, 1842 |
| 1554581 | CIF | C33 H23 Cl N4 O | P -1 | 9.3289; 10.9229; 12.8668 87.237; 78.614; 85.681 | 1280.91 | Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions Organic Chemistry Frontiers, 2019, 6, 1842 |
| 1554582 | CIF | C16 H14 F3 N O4 S | P 21 21 21 | 7.9193; 15.3744; 16.4929 90; 90; 90 | 2008.08 | Gui, Yang; Liang, Xinping; Li, Yanan; Li, Kuiliang; Zha, Zhenggen; Wang, Zhiyong Asymmetric synthesis of fluoroalkylated N,O-ketals via an organocatalytic dehydration/aminalization/aza-Michael desymmetrization Organic Chemistry Frontiers, 2019, 6, 942 |
| 1554583 | CIF | C36 H32 Br N O4 P2 | P 21 21 21 | 28.168; 11.3424; 10.2126 90; 90; 90 | 3262.9 | Liu, Bing; Li, Wenbo; Wu, Hai-Hong; Zhang, Junliang Enantiodivergent synthesis of 1,2-bis(diphenylphosphino)ethanes via asymmetric [3 + 2]-cycloaddition Organic Chemistry Frontiers, 2019, 6, 694 |
| 1554584 | CIF | C22 H20 Br N3 O4 | P 1 21 1 | 9.2282; 9.1743; 12.829 90; 109.724; 90 | 1022.4 | Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence Organic Chemistry Frontiers, 2019, 6, 919 |
| 1554585 | CIF | C21 H24 N2 O7 | P 1 21 1 | 9.6264; 10.858; 11.2163 90; 113.736; 90 | 1073.2 | Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence Organic Chemistry Frontiers, 2019, 6, 919 |
| 1554586 | CIF | C17 H20 F3 N O3 | P 1 21/c 1 | 11.431; 5.931; 25.849 90; 94.751; 90 | 1746.5 | Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds Organic Chemistry Frontiers, 2019, 6, 1109 |
| 1554587 | CIF | C14 H14 F3 N O2 | P -1 | 11.218; 12.296; 16.82 108.32; 101.98; 102.65 | 2051.1 | Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds Organic Chemistry Frontiers, 2019, 6, 1109 |
| 1554588 | CIF | C40 H59 Cl N2 P2 Zr | P -1 | 11.9355; 12.1743; 15.3187 112.686; 97.711; 98.63 | 1984.93 | Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends. Chemical science, 2018, 9, 5223-5232 |
| 1554589 | CIF | C52 H78 Cl N3 P2 Zr | P 1 21/n 1 | 12.10234; 13.69809; 31.6606 90; 91.0656; 90 | 5247.75 | Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends. Chemical science, 2018, 9, 5223-5232 |
| 1554590 | CIF | C52 H82 Cl N5 O P2 Zr | C 1 2/c 1 | 37.6269; 12.5284; 22.9308 90; 99.4621; 90 | 10662.6 | Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends. Chemical science, 2018, 9, 5223-5232 |
| 1554591 | CIF | C57 H80 Cl N3 P2 Zr | P -1 | 12.6621; 18.1002; 23.9357 100.866; 95.4948; 103.491 | 5182.35 | Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends. Chemical science, 2018, 9, 5223-5232 |
| 1554592 | CIF | C15 H14 O7 | P 1 21 1 | 7.1336; 7.3556; 13.246 90; 102.455; 90 | 678.7 | Szwalbe, Agnieszka J.; Williams, Katherine; Song, Zhongshu; de Mattos-Shipley, Kate; Vincent, Jason L.; Bailey, Andrew M.; Willis, Christine L.; Cox, Russell J.; Simpson, Thomas J. Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi. Chemical science, 2019, 10, 233-238 |
| 1554593 | CIF | C15 H13 O6.5 | P 21 21 21 | 7.4082; 7.9771; 43.956 90; 90; 90 | 2597.6 | Szwalbe, Agnieszka J.; Williams, Katherine; Song, Zhongshu; de Mattos-Shipley, Kate; Vincent, Jason L.; Bailey, Andrew M.; Willis, Christine L.; Cox, Russell J.; Simpson, Thomas J. Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi. Chemical science, 2019, 10, 233-238 |
| 1554594 | CIF | C152 H144 Cd4 F24 N28 O24 S8 | F -4 3 c | 34.3297; 34.3297; 34.3297 90; 90; 90 | 40458.5 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554595 | CIF | C160.5 H126.25 B3 F27 N29.25 Ni4 O15.25 S5 | C 1 2/c 1 | 34.257; 18.552; 54.149 90; 97.09; 90 | 34150 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554596 | CIF | C78.83 H76.5 F17.5 K0.83 N15.5 O11.5 S3.83 Sb Zn2 | R -3 :H | 14.93; 14.93; 68.868 90; 90; 120 | 13294 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554597 | CIF | C153 H132 Cd4 F69 N32 O3 S Sb7 | P 21 3 | 26.441; 26.441; 26.441 90; 90; 90 | 18486 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554598 | CIF | C531.5 H392.25 F48 N82.25 Ni8 O53.25 S16 Zn6 | P 4/n :2 | 34.21; 34.21; 27.215 90; 90; 90 | 31850 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554599 | CIF | C70.5 H64.5 F19.5 N15.5 O4.5 S1.5 Sb2.5 Zn2 | C 1 2 1 | 32.3977; 31.639; 22.0583 90; 123.314; 90 | 18894.9 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554600 | CIF | C543 H406 Co8 F48 N83.5 O53.75 S16 Zn6 | P 4/n :2 | 34.3; 34.3; 27.428 90; 90; 90 | 32269 | Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R. Waterproof architectures through subcomponent self-assembly. Chemical science, 2019, 10, 2006-2018 |
| 1554601 | CIF | C65 H73 Ca I N11 O4 U | P 1 21/c 1 | 17.4073; 15.531; 33.3439 90; 114.157; 90 | 8225.2 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554602 | CIF | C77 H77 N15 O2 Rb U | P 21 21 21 | 13.6821; 21.8875; 24.244 90; 90; 90 | 7260.28 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554603 | CIF | C62 H62 I N12 O2 U Zn | P 21 21 21 | 13.273; 16.4368; 27.8646 90; 90; 90 | 6079.1 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554604 | CIF | C87 H87 Cl N9 O2 Ti U | P 1 21/c 1 | 20.517; 21.431; 19.018 90; 117.115; 90 | 7443 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554605 | CIF | C86.48 H86.48 Cl3 Mg N15 O2 U Zr | C 1 2/c 1 | 47.424; 14.484; 30.602 90; 127.576; 90 | 16659 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554606 | CIF | C57 H57 Cl N11 O2 U Zn | I 1 2/a 1 | 28.7327; 22.93; 24.8036 90; 102.077; 90 | 15979.9 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554607 | CIF | C82 H86 Cl N12 O3 U Zr | P 1 21/c 1 | 20.2769; 21.7767; 18.5794 90; 115.829; 90 | 7384.4 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554608 | CIF | C87 H87 Cl Mg N17 O2 U | I 1 2/a 1 | 24.852; 23.01; 28.754 90; 102.183; 90 | 16073 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554609 | CIF | C312 H312 Cs6 N60 O12 U6 | R -3 :H | 27.7671; 27.7671; 35.7644 90; 90; 120 | 23880.5 | Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L. Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study Chemical Science, 2019, 10, 9740 |
| 1554610 | CIF | C26 H28 F12 N6 Ni P2 | P 1 21/n 1 | 13.8699; 17.1455; 14.2982 90; 100.97; 90 | 3338.1 | Lieske, Lauren E.; Rheingold, Arnold L.; Machan, Charles W. Electrochemical reduction of carbon dioxide with a molecular polypyridyl nickel complex Sustainable Energy & Fuels, 2018, 2, 1269 |
| 1554611 | CIF | C63 H46 Cu F6 N4 O P3 | P -1 | 11.2628; 12.4158; 21.9828 83.055; 78.448; 87.667 | 2989.2 | Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety Sustainable Energy & Fuels, 2019, 3, 692 |
| 1554612 | CIF | C48 H28 Cu F6 N8 P | P -1 | 8.1362; 10.6863; 22.4625 86.186; 81.28; 87.085 | 1924.5 | Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety Sustainable Energy & Fuels, 2019, 3, 692 |
| 1554613 | CIF | C22.5 H28 K0.5 N6 Ni0.5 O3 | P -1 | 12.9939; 13.5751; 14.0727 78.667; 85.315; 77.907 | 2377.8 | Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E. Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex Sustainable Energy & Fuels, 2019, 3, 1172 |
| 1554614 | CIF | C36 H44 K2 N10 O3 | P 1 21/c 1 | 23.3268; 7.362; 22.2054 90; 94.794; 90 | 3800 | Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E. Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex Sustainable Energy & Fuels, 2019, 3, 1172 |
| 1554615 | CIF | C24 H20 N10 Ni | P 1 21/n 1 | 7.7492; 16.392; 8.8505 90; 101.096; 90 | 1103.2 | Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E. Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex Sustainable Energy & Fuels, 2019, 3, 1172 |
| 1554616 | CIF | C17 H22 B10 | P -1 | 6.9712; 11.7604; 12.9797 107.511; 102.996; 102.125 | 943.63 | Chaari, Mahdi; Kelemen, Zsolt; Choquesillo-Lazarte, Duane; Gaztelumendi, Nerea; Teixidor, Francesc; Viñas, Clara; Nogués, Carme; Núñez, Rosario Efficient blue light emitting materials based on m-carborane-anthracene dyads. Structure, photophysics and bioimaging studies. Biomaterials science, 2019, 7, 5324-5337 |
| 1554617 | CIF | C17 H20 B10 I2 | I m a 2 | 13.801; 25.643; 6.8626 90; 90; 90 | 2428.7 | Chaari, Mahdi; Kelemen, Zsolt; Choquesillo-Lazarte, Duane; Gaztelumendi, Nerea; Teixidor, Francesc; Viñas, Clara; Nogués, Carme; Núñez, Rosario Efficient blue light emitting materials based on m-carborane-anthracene dyads. Structure, photophysics and bioimaging studies. Biomaterials science, 2019, 7, 5324-5337 |
| 1554618 | CIF | C17 H21 B10 I | P 1 21/n 1 | 9.319; 11.7553; 18.5808 90; 94.913; 90 | 2028 | Chaari, Mahdi; Kelemen, Zsolt; Choquesillo-Lazarte, Duane; Gaztelumendi, Nerea; Teixidor, Francesc; Viñas, Clara; Nogués, Carme; Núñez, Rosario Efficient blue light emitting materials based on m-carborane-anthracene dyads. Structure, photophysics and bioimaging studies. Biomaterials science, 2019, 7, 5324-5337 |
| 1554619 | CIF | C54 H48 Cl0 F0 N0 O43.5 | C 1 2 1 | 19.1281; 24.4901; 15.6182 90; 109.513; 90 | 6896.1 | Phan, Chiuyen; Zheng, Ziyang; Wang, Jianwei; Wang, Qiwen; Hu, Xiurong; Tang, Guping; Bai, Hongzhen Enhanced antitumour effect for hepatocellular carcinoma in the advanced stage using a cyclodextrin-sorafenib-chaperoned inclusion complex. Biomaterials science, 2019, 7, 4758-4768 |
| 1554620 | CIF | C24 H38 F6 Fe P Ru S3 | C m c e | 15.867; 20.073; 18.513 90; 90; 90 | 5896.4 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554621 | CIF | C14 H23 Co S3 | P 1 21/c 1 | 13.1028; 8.6112; 14.2219 90; 101.551; 90 | 1572.17 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554622 | CIF | C30 H43 F6 Fe P Ru S4 | P 1 21/n 1 | 14.3616; 13.9373; 16.9737 90; 99.0564; 90 | 3355.1 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554623 | CIF | C26 H41 F12 Fe N P2 Ru S3 | P n m a | 11.8; 15.608; 18.603 90; 90; 90 | 3426 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554624 | CIF | C48 H58 B Co Fe S3 | P n a 21 | 20.2817; 17.2944; 12.4241 90; 90; 90 | 4357.9 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554625 | CIF | C47 H56 B Co Fe S3 | P n a 21 | 20.576; 16.9755; 12.0227 90; 90; 90 | 4199.4 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554626 | CIF | C48 H59 B Fe Ru S3 | P 1 21/c 1 | 15.5349; 15.8332; 18.3897 90; 90.694; 90 | 4522.9 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
| 1554627 | CIF | C6 H6 N8 O9 | P 1 21/c 1 | 7.6484; 16.154; 11.156 90; 106.283; 90 | 1323.1 | Huang, Qi; Guo, Zhicheng; Liao, Longyu; Hao, Shilong; Nie, Fude; Li, Hongzhen Customization of the molecular structure to modulate the crystal packing style of energetic materials Molecular Systems Design & Engineering, 2019, 4, 1032 |
| 1554628 | CIF | C8 H8 N10 O14 | P 43 21 2 | 7.0912; 7.0912; 34.097 90; 90; 90 | 1714.6 | Huang, Qi; Guo, Zhicheng; Liao, Longyu; Hao, Shilong; Nie, Fude; Li, Hongzhen Customization of the molecular structure to modulate the crystal packing style of energetic materials Molecular Systems Design & Engineering, 2019, 4, 1032 |
| 1554629 | CIF | C6 H6 N8 O8 | P b c a | 11.0661; 13.9316; 15.839 90; 90; 90 | 2441.9 | Huang, Qi; Guo, Zhicheng; Liao, Longyu; Hao, Shilong; Nie, Fude; Li, Hongzhen Customization of the molecular structure to modulate the crystal packing style of energetic materials Molecular Systems Design & Engineering, 2019, 4, 1032 |
| 1554630 | CIF | C13 H30 I N3 | P 1 21/c 1 | 8.6068; 14.9193; 14.6169 90; 110.458; 90 | 1758.5 | Xue, Boxin; Wang, Fen; Zheng, Jifu; Li, Shenghai; Zhang, Suobo Highly stable polysulfone anion exchange membranes incorporated with bulky alkyl substituted guanidinium cations Molecular Systems Design & Engineering, 2019, 4, 1039 |
| 1554631 | CIF | C13 H28 Cl N3 O2 | C 1 2/c 1 | 9.9771; 18.0751; 8.9806 90; 104.318; 90 | 1569.2 | Xue, Boxin; Wang, Fen; Zheng, Jifu; Li, Shenghai; Zhang, Suobo Highly stable polysulfone anion exchange membranes incorporated with bulky alkyl substituted guanidinium cations Molecular Systems Design & Engineering, 2019, 4, 1039 |
| 1554632 | CIF | C39 H32 F6 Ir N3 O0 S2 | C 1 2/c 1 | 26.026; 12.94; 22.386 90; 97.214; 90 | 7479.4 | Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs Materials Chemistry Frontiers, 2019, 3, 860 |
| 1554633 | CIF | C53 H42 F6 Ir N3 S2 | P -1 | 11.3; 15.22; 16.31 79.22; 79.11; 82.46 | 2693 | Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs Materials Chemistry Frontiers, 2019, 3, 860 |
| 1554634 | CIF | C45 H28 F6 Ir N3 S2 | P 1 21/c 1 | 15.5226; 12.6925; 20.61 90; 97.559; 90 | 4025.3 | Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs Materials Chemistry Frontiers, 2019, 3, 860 |
| 1554635 | CIF | C72 H46 Co6 N12 O39 | P 1 21/c 1 | 7.237; 18.371; 62.028 90; 92.02; 90 | 8242 | Li, Ang; Qian, Binbin; Zhong, Ming; Liu, Yingying; Chang, Ze; Bu, Xian-He An insight into the pyrolysis process of metal‒organic framework templates/precursors to construct metal oxide anode materials for lithium-ion batteries Materials Chemistry Frontiers, 2019, 3, 1398 |
| 1554636 | CIF | C42 H36 N4 O2 Pt2 | P 1 21/c 1 | 11.768; 17.4213; 17.5279 90; 97.615; 90 | 3561.77 | Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands Materials Chemistry Frontiers, 2019, 3, 1199 |
| 1554637 | CIF | C43 H38 Cl2 N4 O2 Pt2 | P 21 21 21 | 11.0565; 16.7748; 20.3659 90; 90; 90 | 3777.3 | Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands Materials Chemistry Frontiers, 2019, 3, 1199 |
| 1554638 | CIF | C42 H28 Cl2 N4 O2 Pt2 | P 1 21/n 1 | 9.6783; 18.7346; 19.5011 90; 100.777; 90 | 3473.6 | Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands Materials Chemistry Frontiers, 2019, 3, 1199 |
| 1554639 | CIF | C51 H35 Cl3 N4 O2 Pt2 | P 21 21 21 | 10.7354; 20.1891; 21.7815 90; 90; 90 | 4720.9 | Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands Materials Chemistry Frontiers, 2019, 3, 1199 |
| 1554640 | CIF | C43 H38 Cl2 N4 O2 Pt2 | P 21 21 21 | 11.05822; 16.7782; 20.3868 90; 90; 90 | 3782.51 | Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands Materials Chemistry Frontiers, 2019, 3, 1199 |
| 1554641 | CIF | C17 H19 N O2 S | P 1 21/n 1 | 11.377; 9.712; 13.362 90; 95.331; 90 | 1470 | Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging Materials Chemistry Frontiers, 2019, 3, 1391 |
| 1554642 | CIF | C14 H13 N O2 S | P 1 21/n 1 | 7.9027; 11.1576; 13.5298 90; 93.338; 90 | 1190.97 | Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging Materials Chemistry Frontiers, 2019, 3, 1391 |
| 1554643 | CIF | C13 H11 N O2 S | P 1 21/n 1 | 8.78316; 11.4642; 11.1048 90; 91.3006; 90 | 1117.88 | Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging Materials Chemistry Frontiers, 2019, 3, 1391 |
| 1554644 | CIF | C16 H17 N O2 S | P 1 21/c 1 | 18.9325; 9.4253; 17.2146 90; 114.976; 90 | 2784.59 | Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging Materials Chemistry Frontiers, 2019, 3, 1391 |
| 1554645 | CIF | C18 H21 N O2 S | R 3 c :H | 26.477; 26.477; 12.475 90; 90; 120 | 7574 | Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging Materials Chemistry Frontiers, 2019, 3, 1391 |
| 1554646 | CIF | C15 H15 N O2 S | P -1 | 7.7584; 9.0839; 10.0043 109.128; 97.408; 103.752 | 630.4 | Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging Materials Chemistry Frontiers, 2019, 3, 1391 |
| 1554647 | CIF | C44 H46 N2 O4 | P -1 | 6.3304; 7.2037; 20.473 89.41; 89.13; 76.08 | 906.1 | Dai, Shuangxiong; Cai, Zhengxu; Peng, Zhe; Wang, Zhi; Tong, Bin; Shi, Jianbing; Gan, Shenglong; He, Qiming; Chen, Wei; Dong, Yuping A stabilized lamellar liquid crystalline phase with aggregation-induced emission features based on pyrrolopyrrole derivatives Materials Chemistry Frontiers, 2019, 3, 1105 |
| 1554648 | CIF | C4 H14 Br3 N3 O | P b c m | 6.70475; 13.3306; 13.1204 90; 90; 90 | 1172.68 | Li, Kai; Dong, Li-Yuan; Xu, Hao-Xiang; Qin, Yan; Li, Zhi-Gang; Azeem, Muhammad; Li, Wei; Bu, Xian-He Electronic structures and elastic properties of a family of metal-free perovskites Materials Chemistry Frontiers, 2019, 3, 1678 |
| 1554649 | CIF | C4 H14 I3 N3 O | P b c m | 7.064; 14.089; 13.684 90; 90; 90 | 1361.9 | Li, Kai; Dong, Li-Yuan; Xu, Hao-Xiang; Qin, Yan; Li, Zhi-Gang; Azeem, Muhammad; Li, Wei; Bu, Xian-He Electronic structures and elastic properties of a family of metal-free perovskites Materials Chemistry Frontiers, 2019, 3, 1678 |
| 1554650 | CIF | C30 H29 N5 O | P 1 21/c 1 | 22.0567; 7.7405; 15.5138 90; 102.762; 90 | 2583.2 | Yang, Jinfeng; Gu, Kaizhi; Shi, Chuanxing; Li, Meng; Zhao, Ping; Zhu, Wei-Hong Fluorescent thermometer based on a quinolinemalononitrile copolymer with aggregation-induced emission characteristics Materials Chemistry Frontiers, 2019, 3, 1503 |
| 1554651 | CIF | C20 H22 B F2 N3 O | C 1 2/c 1 | 12.8894; 9.0135; 31.806 90; 93.146; 90 | 3689.6 | Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells Materials Chemistry Frontiers, 2019, 3, 1823 |
| 1554652 | CIF | C26 H34 B F2 N3 O | C 1 2/c 1 | 26.649; 9.8463; 19.4482 90; 101.393; 90 | 5002.5 | Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells Materials Chemistry Frontiers, 2019, 3, 1823 |
| 1554653 | CIF | C24 H30 B F2 N3 O | C 1 2/c 1 | 23.744; 12.2488; 19.0154 90; 101.276; 90 | 5423.6 | Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells Materials Chemistry Frontiers, 2019, 3, 1823 |
| 1554654 | CIF | C20 H24 | P -1 | 4.7535; 6.1267; 13.209 96.215; 96.738; 91.369 | 379.53 | Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong Drawing a clear mechanistic picture for the aggregation-induced emission process Materials Chemistry Frontiers, 2019, 3, 1143 |
| 1554655 | CIF | C24 H26 | P 1 21/c 1 | 12.9394; 8.2851; 9.083 90; 106.48; 90 | 933.73 | Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong Drawing a clear mechanistic picture for the aggregation-induced emission process Materials Chemistry Frontiers, 2019, 3, 1143 |
| 1554656 | CIF | C24 H26 | P 1 21/n 1 | 7.9294; 7.3834; 16.2178 90; 90.745; 90 | 949.41 | Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong Drawing a clear mechanistic picture for the aggregation-induced emission process Materials Chemistry Frontiers, 2019, 3, 1143 |
| 1554657 | CIF | C20 H24 | P 1 21/n 1 | 4.8732; 10.6116; 15.5489 90; 90.251; 90 | 804.06 | Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong Drawing a clear mechanistic picture for the aggregation-induced emission process Materials Chemistry Frontiers, 2019, 3, 1143 |
| 1554658 | CIF | C44 H28 S | P -1 | 9.7394; 9.8279; 16.0542 96.661; 100.097; 92.178 | 1499.99 | Kazantsev, Maxim S.; Sonina, Alina A.; Koskin, Igor P.; Sherin, Peter S.; Rybalova, Tatyana V.; Benassi, Enrico; Mostovich, Evgeny A. Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals Materials Chemistry Frontiers, 2019, 3, 1545 |
| 1554659 | CIF | C44 H28 S | P 1 21/c 1 | 15.4125; 9.8016; 20.9249 90; 105.66; 90 | 3043.7 | Kazantsev, Maxim S.; Sonina, Alina A.; Koskin, Igor P.; Sherin, Peter S.; Rybalova, Tatyana V.; Benassi, Enrico; Mostovich, Evgeny A. Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals Materials Chemistry Frontiers, 2019, 3, 1545 |
| 1554660 | CIF | C40 H28 N4 | C 1 2/c 1 | 26.013; 12.858; 10.6428 90; 104.932; 90 | 3439.5 | Peng, Zhe; Dai, Shuangxiong; Ji, Yingchun; Tong, Bin; Shi, Jianbing; Cai, Zhengxu; Zhi, Junge; Dong, Yuping Ionic liquid crystals with aggregation-induced emission properties based on pyrrolo[3,2-b]pyrrole salt compounds Materials Chemistry Frontiers, 2019, 3, 1385 |
| 1554661 | CIF | C18 H15 Au F5 N O | P 1 21/c 1 | 7.402; 19.562; 12.283 90; 97.32; 90 | 1764.1 | Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy Materials Chemistry Frontiers, 2019, 3, 1866 |
| 1554662 | CIF | C18 H15 Au F5 N O | P 1 21/c 1 | 7.3042; 19.814; 11.9572 90; 95.327; 90 | 1723 | Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy Materials Chemistry Frontiers, 2019, 3, 1866 |
| 1554663 | CIF | C18 H15 Au F5 N O | P 1 21/c 1 | 7.2889; 19.8254; 11.9641 90; 95.306; 90 | 1721.47 | Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy Materials Chemistry Frontiers, 2019, 3, 1866 |
| 1554664 | CIF | C29 H14 N4 O2 | P 1 21 1 | 5.0052; 15.6076; 14.6006 90; 91.275; 90 | 1140.3 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554665 | CIF | C30 H16 N4 O2 | C 1 2 1 | 25.4902; 8.4676; 16.9657 90; 104.889; 90 | 3538.9 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554666 | CIF | C33 H22 N4 O2 | C 2 2 21 | 12.0721; 17.9566; 12.2305 90; 90; 90 | 2651.3 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554667 | CIF | C36 H28 N4 O2 | P -1 | 8.8302; 18.7601; 19.027 110.64; 94.387; 93.845 | 2926 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554668 | CIF | C33 H22 Cl2 N4 O2 | P 1 21 1 | 7.9714; 22.5703; 9.1047 90; 115.426; 90 | 1479.42 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554669 | CIF | C48 H30 F6 N4 O2 | C 2 2 21 | 18.4373; 25.7446; 11.6266 90; 90; 90 | 5518.7 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554670 | CIF | C11.67 H8.67 N1.33 O0.67 | P 1 21/c 1 | 8.5584; 18.7684; 17.4034 90; 94.951; 90 | 2785.03 | Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives Materials Chemistry Frontiers, 2019, 3, 1613 |
| 1554671 | CIF | C33 H23 B F2 O3 | P -1 | 8.788; 10.446; 15.407 70.818; 88.67; 79.808 | 1313.8 | Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian Deep insights into polymorphism initiated by exploring multicolor conversion materials Materials Chemistry Frontiers, 2019, 3, 1661 |
| 1554672 | CIF | C33 H23 B F2 O3 | C 1 c 1 | 53.109; 7.2441; 13.687 90; 97.371; 90 | 5222 | Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian Deep insights into polymorphism initiated by exploring multicolor conversion materials Materials Chemistry Frontiers, 2019, 3, 1661 |
| 1554673 | CIF | C33 H23 B F2 O3 | P 1 21/n 1 | 15.955; 8.978; 19.823 90; 113.38; 90 | 2606.4 | Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian Deep insights into polymorphism initiated by exploring multicolor conversion materials Materials Chemistry Frontiers, 2019, 3, 1661 |
| 1554674 | CIF | C33 H23 B F2 O3 | P 1 21/c 1 | 15.958; 8.99; 19.915 90; 113.62; 90 | 2617.7 | Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian Deep insights into polymorphism initiated by exploring multicolor conversion materials Materials Chemistry Frontiers, 2019, 3, 1661 |
| 1554675 | CIF | C33 H23 B F2 O3 | P 1 21/c 1 | 15.957; 8.984; 19.969 90; 113.55; 90 | 2624.3 | Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian Deep insights into polymorphism initiated by exploring multicolor conversion materials Materials Chemistry Frontiers, 2019, 3, 1661 |
| 1554676 | CIF | C30 H22 N2 O2 S | P 1 | 12.1382; 12.8179; 15.1854 85.684; 78.373; 89.276 | 2307.59 | Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence Materials Chemistry Frontiers, 2019, 3, 1800 |
| 1554677 | CIF | C30 H22 N2 O2 S | P 1 21/c 1 | 14.4773; 12.17882; 13.40691 90; 104.925; 90 | 2284.11 | Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence Materials Chemistry Frontiers, 2019, 3, 1800 |
| 1554678 | CIF | C30 H22 N2 O2 S | P 1 | 12.135; 12.8327; 15.1864 85.785; 78.371; 89.345 | 2310.08 | Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence Materials Chemistry Frontiers, 2019, 3, 1800 |
| 1554679 | CIF | C30 H24 N4 O Pt | P -1 | 8.4381; 12.133; 23.3476 86.889; 81.757; 83.205 | 2347.31 | Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions Materials Chemistry Frontiers, 2019, 3, 2448 |
| 1554680 | CIF | C27 H18 N4 O Pt | P 21 21 21 | 7.7277; 13.36; 20.072 90; 90; 90 | 2072.3 | Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions Materials Chemistry Frontiers, 2019, 3, 2448 |
| 1554681 | CIF | C37 H28 N4 O3 | C 1 2/c 1 | 26.686; 16.726; 14.573 90; 107.7; 90 | 6197 | Ren, Fei; Shi, Jianbing; Tong, Bin; Cai, Zhengxu; Dong, Yuping Effects of fused rings linked to the 2,5-position of pyrrole derivatives with near-infrared emission on their aggregation-enhanced emission properties Materials Chemistry Frontiers, 2019, 3, 2072 |
| 1554682 | CIF | C18 H19 N3 O | P 1 21/n 1 | 16.236; 7.7124; 25.238 90; 104.08; 90 | 3065.3 | Li, Aisen; Liu, Hao; Song, Chongping; Geng, Yijia; Xu, Shuping; Zhang, Hongyu; Zhang, Houyu; Cui, Haining; Xu, Weiqing Flexible control of excited state transition under pressure/temperature: distinct stimuli-responsive behaviours of two ESIPT polymorphs Materials Chemistry Frontiers, 2019, 3, 2128 |
| 1554683 | CIF | C18 H19 N3 O | P 1 21/c 1 | 12.841; 10.286; 12.663 90; 111.023; 90 | 1561.2 | Li, Aisen; Liu, Hao; Song, Chongping; Geng, Yijia; Xu, Shuping; Zhang, Hongyu; Zhang, Houyu; Cui, Haining; Xu, Weiqing Flexible control of excited state transition under pressure/temperature: distinct stimuli-responsive behaviours of two ESIPT polymorphs Materials Chemistry Frontiers, 2019, 3, 2128 |
| 1554684 | CIF | C10 H26 Cl6 N2 Zn | P 1 21/c 1 | 24.5577; 18.3997; 18.1621 90; 92.376; 90 | 8199.6 | Zhang, Yu-Wei; Wang, Qing; Shi, Ping-Ping; Zhang, Wan-Ying; Ye, Qiong; Fu, Da-Wei Visual low-high interchange in a dielectric switch for trimethylchloroethylamine tetrachlorozincate with a large leap symmetry breaking Materials Chemistry Frontiers, 2019, 3, 2077 |
| 1554685 | CIF | C10 H26 Cl6 N2 Zn | I 41/a :2 | 12.7985; 12.7985; 25.8884 90; 90; 90 | 4240.6 | Zhang, Yu-Wei; Wang, Qing; Shi, Ping-Ping; Zhang, Wan-Ying; Ye, Qiong; Fu, Da-Wei Visual low-high interchange in a dielectric switch for trimethylchloroethylamine tetrachlorozincate with a large leap symmetry breaking Materials Chemistry Frontiers, 2019, 3, 2077 |
| 1554686 | CIF | C218 H276 O28 P2 Pt | P -1 | 12.2995; 12.7098; 38.043 80.979; 89.471; 65.725 | 5344.1 | Hu, Yang; Wang, Wei; Yao, Rui; Wang, Xu-Qing; Wang, Yu-Xuan; Sun, Bin; Chen, Li-Jun; Zhang, Ying; Zhao, Xiao-Li; Xu, Lin; Tan, Hong-Wei; Yu, Yihua; Li, Xiaopeng; Yang, Hai-Bo Facile synthesis of diverse rotaxanes via successive supramolecular transformations Materials Chemistry Frontiers, 2019, 3, 2397 |
| 1554687 | CIF | C52 H57.5 N4.5 O7 | P 1 21/c 1 | 15.215; 14.04; 23.048 90; 100.849; 90 | 4835 | Chan, Sing-Ming; Tang, Fung-Kit; Kwan, Chak-Shing; Lam, Ching-Yau; Hau, Sam C. K.; Leung, Ken Cham-Fai Water-compatible fluorescent [2]rotaxanes for Au3+ detection and bioimaging Materials Chemistry Frontiers, 2019, 3, 2388 |
| 1554688 | CIF | C37 H23 N O2 S | P -1 | 8.9754; 11.9049; 13.8094 111.039; 90.487; 95.955 | 1368.09 | Huang, Lili; Wen, Xue; Liu, Jianwei; Chen, Mingxing; Ma, Zhiyong; Jia, Xinru An AIE molecule featuring changeable triplet emission between phosphorescence and delayed fluorescence by an external force Materials Chemistry Frontiers, 2019, 3, 2151 |
| 1554689 | CIF | C43 H31 N3 | P -1 | 12.995; 14.047; 18.771 85.928; 72.336; 78.362 | 3198 | Li, Aisen; Chu, Ning; Liu, Jianwei; Liu, Hao; Wang, Jing; Xu, Shuping; Cui, Haining; Zhang, Hongyu; Xu, Weiqing; Ma, Zhiyong Pressure-induced remarkable luminescence switch of a dimer form of donor–acceptor–donor triphenylamine (TPA) derivative Materials Chemistry Frontiers, 2019, 3, 2768 |
| 1554690 | CIF | C42 H30 N4 | P 1 21/c 1 | 17.2834; 10.2606; 18.3175 90; 96.618; 90 | 3226.74 | Li, Aisen; Chu, Ning; Liu, Jianwei; Liu, Hao; Wang, Jing; Xu, Shuping; Cui, Haining; Zhang, Hongyu; Xu, Weiqing; Ma, Zhiyong Pressure-induced remarkable luminescence switch of a dimer form of donor–acceptor–donor triphenylamine (TPA) derivative Materials Chemistry Frontiers, 2019, 3, 2768 |
| 1554691 | CIF | C15 H15 N O2 | P -1 | 6.2682; 7.1504; 28.857 94.165; 90.331; 90.002 | 1289.94 | Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state Materials Chemistry Frontiers, 2019, 3, 2746 |
| 1554692 | CIF | C16 H17 N O2 | P -1 | 6.2328; 7.2129; 31.0245 92.777; 94.558; 90.014 | 1388.7 | Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state Materials Chemistry Frontiers, 2019, 3, 2746 |
| 1554693 | CIF | C17 H19 N O2 | P -1 | 6.1745; 7.0411; 33.2296 86.545; 84.929; 89.992 | 1436.38 | Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state Materials Chemistry Frontiers, 2019, 3, 2746 |
| 1554694 | CIF | C260 H202 Cu4 N16 O23 | P 1 21/n 1 | 38.372; 43.842; 41.771 90; 101.834; 90 | 68778 | Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu Tunable enforced cavities inside self-assembled capsules Organic Chemistry Frontiers, 2019, 6, 1561 |
| 1554695 | CIF | C40 H40 B Cl4 Cu F4 N4 | P -1 | 10.7588; 13.1415; 15.339 106.956; 100.938; 91.717 | 2028.3 | Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu Tunable enforced cavities inside self-assembled capsules Organic Chemistry Frontiers, 2019, 6, 1561 |
| 1554696 | CIF | C31 H29 Cl N2 O4 | P 21 21 21 | 9.0064; 9.7885; 30.9078 90; 90; 90 | 2724.81 | Chu, Ming-Ming; Qi, Suo-Suo; Ju, Wan-Zhen; Wang, Yi-Feng; Chen, Xue-Yang; Xu, Dan-Qian; Xu, Zhen-Yuan Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters Organic Chemistry Frontiers, 2019, 6, 1140 |
| 1554697 | CIF | C63.5 H60 N6 O14.5 | C 1 c 1 | 36.594; 7.353; 28.802 90; 123.87; 90 | 6435 | Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J. Reactions of 2-aza-21-carbaporphyrin with aniline derivatives Organic Chemistry Frontiers, 2019, 6, 908 |
| 1554698 | CIF | C79 H72 N6 O6 | P 1 21/c 1 | 33.74; 12.9479; 14.8229 90; 100.325; 90 | 6370.7 | Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J. Reactions of 2-aza-21-carbaporphyrin with aniline derivatives Organic Chemistry Frontiers, 2019, 6, 908 |
| 1554699 | CIF | C18 H16 Br2 F N O3 S | P -1 | 6.9921; 11.2113; 12.4434 96.443; 95.376; 95.626 | 959.19 | Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C. Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation Organic Chemistry Frontiers, 2019, 6, 1133 |
| 1554700 | CIF | C19 H20 Cl N O3 S | C 1 2/c 1 | 18.258; 13.081; 15.4466 90; 91.845; 90 | 3687.2 | Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C. Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation Organic Chemistry Frontiers, 2019, 6, 1133 |
| 1554701 | CIF | C17 H14 N2 O7 S | P 1 21/n 1 | 7.4466; 24.7338; 9.6421 90; 104.56; 90 | 1718.87 | Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C. Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation Organic Chemistry Frontiers, 2019, 6, 1133 |
| 1554702 | CIF | C21 H25 N O4 S | P -1 | 10.994; 12.052; 16.9 95.131; 99.76; 103.107 | 2130 | Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C. Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation Organic Chemistry Frontiers, 2019, 6, 1133 |
| 1554703 | CIF | C17 H16 Br3 N O2 S | P 1 21/c 1 | 8.2985; 12.4303; 19.4432 90; 101.322; 90 | 1966.59 | Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C. Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation Organic Chemistry Frontiers, 2019, 6, 1133 |
| 1554704 | CIF | C17 H14 Br3 N O3 S | P -1 | 6.9458; 10.9848; 12.6203 95.166; 94.677; 97.68 | 946.11 | Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C. Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation Organic Chemistry Frontiers, 2019, 6, 1133 |
| 1554705 | CIF | C16 H11 F3 N2 O | P 1 21/c 1 | 6.5927; 24.4163; 9.1339 90; 108.268; 90 | 1396.18 | Zhu, Chuanle; Liu, Chi; Zeng, Hao; Chen, Fulin; Jiang, Huanfeng Transition-metal free selective C(α)–C(β) bond cleavage of trifluoromethyl ketones with amidines under air: facile access to 5-trifluoromethylated Imidazol-4-ones Organic Chemistry Frontiers, 2019, 6, 858 |
| 1554706 | CIF | C21 H22 Cl N5 O8 | C 1 2 1 | 25.9456; 8.8451; 23.3704 90; 101.146; 90 | 5262.1 | Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes Organic Chemistry Frontiers, 2019, 6, 863 |
| 1554707 | CIF | C22 H26 Cl N5 O9 | P 1 21/c 1 | 14.6444; 19.027; 9.2992 90; 98.115; 90 | 2565.17 | Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes Organic Chemistry Frontiers, 2019, 6, 863 |
| 1554708 | CIF | C25 H22 Cl N5 O8 | P -1 | 8.9522; 12.3288; 12.6211 103.938; 101.104; 102.417 | 1275.71 | Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes Organic Chemistry Frontiers, 2019, 6, 863 |
| 1554709 | CIF | C21 H23 Br N2 O4 S | P 21 21 21 | 9.4007; 10.8468; 21.7267 90; 90; 90 | 2215.42 | Shen, Guoli; Khan, Ruhima; Lv, Haiping; Yang, Yong; Zhang, Xia; Zhan, Yong; Zhou, Yongyun; Fan, Baomin Palladium/silver co-catalyzed syn-stereoselective asymmetric ring-opening reactions of azabenzonorbornadienes with amides Organic Chemistry Frontiers, 2019, 6, 1423 |
| 1554710 | CIF | C14 H8 F2 S2 | P 1 21/c 1 | 7.4893; 3.8493; 19.835 90; 94.273; 90 | 570.23 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554711 | CIF | C12 H6 F N2 S2 | P 1 21/n 1 | 5.9315; 4.9497; 18.794 90; 95.89; 90 | 548.86 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554712 | CIF | C12 H6 F2 N2 S2 | P 1 21/n 1 | 5.7427; 5.5541; 17.1753 90; 90.509; 90 | 547.79 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554713 | CIF | C14 H6 F4 S2 | P 1 21/n 1 | 6.2999; 5.0655; 18.6515 90; 90.341; 90 | 595.2 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554714 | CIF | C30 H46 F N2 S2 Si2 | P 1 21/c 1 | 9.3302; 12.3529; 14.5826 90; 106.185; 90 | 1614.11 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554715 | CIF | C30 H48 N2 S2 Si2 | P 1 21/c 1 | 9.2882; 12.3511; 14.5307 90; 105.826; 90 | 1603.77 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554716 | CIF | C12 H4 F4 N2 S2 | P -1 | 5.0225; 7.1949; 17.29 84.549; 83.096; 70.873 | 584.99 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554717 | CIF | C30 H46 F2 N2 S2 Si2 | P 1 21/c 1 | 9.3622; 12.3591; 14.6437 90; 106.674; 90 | 1623.15 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554718 | CIF | C12 H5 F N2 S2 | P 1 21/c 1 | 3.8093; 6.6644; 21.5126 90; 94.338; 90 | 544.57 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554719 | CIF | C30 H44 F4 N2 S2 Si2 | P n a 21 | 19.9633; 12.2859; 13.3676 90; 90; 90 | 3278.6 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554720 | CIF | C12 H6 F2 N2 S2 | P 1 21/n 1 | 6.6214; 25.6046; 7.2049 90; 116.456; 90 | 1093.59 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554721 | CIF | C12 H4 F4 N2 S2 | P 1 21/n 1 | 3.8531; 23.868; 6.121 90; 95.29; 90 | 560.53 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554722 | CIF | C12 H8 N2 S2 | F d d 2 | 15.9825; 9.7302; 13.6524 90; 90; 90 | 2123.12 | Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives Organic Chemistry Frontiers, 2019, 6, 780 |
| 1554723 | CIF | C29 H28 O2 | P -1 | 10.2239; 11.009; 11.0538 73.729; 86.05; 65.798 | 1087.85 | Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes Organic Chemistry Frontiers, 2019, 6, 1118 |
| 1554724 | CIF | C26 H20 O3 | P 1 21/n 1 | 11.5269; 6.9766; 23.812 90; 98.369; 90 | 1894.54 | Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes Organic Chemistry Frontiers, 2019, 6, 1118 |
| 1554725 | CIF | C76 H32 F8 O8 | C 1 2/c 1 | 22.035; 15.426; 17.593 90; 121.518; 90 | 5098 | Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study Organic Chemistry Frontiers, 2019, 6, 1372 |
| 1554726 | CIF | C76 H16 Cl24 O8 | P 1 21/n 1 | 21.782; 13.957; 24.511 90; 110.66; 90 | 6972.41 | Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study Organic Chemistry Frontiers, 2019, 6, 1372 |
| 1554727 | CIF | C15 H18 Br N O4 | P 21 21 21 | 5.0429; 11.88; 25.83 90; 90; 90 | 1547.5 | Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes Organic Chemistry Frontiers, 2019, 6, 808 |
| 1554728 | CIF | C15 H18 Br N O4 | P 21 21 21 | 6.5631; 12.796; 18.385 90; 90; 90 | 1544 | Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes Organic Chemistry Frontiers, 2019, 6, 808 |
| 1554729 | CIF | C20 H17 O2 P | C 1 c 1 | 16.191; 17.7337; 8.5986 90; 137.72; 90 | 1661 | Zhao, Xiuli; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Wu, Yangjie Stepwise photosensitized C(sp3)–C(CO) bond cleavage and C–P bond formation of 1,3-dicarbonyls with arylphosphine oxides Organic Chemistry Frontiers, 2019, 6, 1433 |
| 1554730 | CIF | C34 H25 Cl O2 | P -1 | 12.1117; 15.5259; 21.575 95.307; 97.116; 101.212 | 3920.6 | Sun, Jing; Jiang, Wang; Yan, Chao-Guo Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes Organic Chemistry Frontiers, 2019, 6, 1428 |
| 1554731 | CIF | C32 H20 N2 O6 | P 1 21/n 1 | 10.7141; 20.1653; 12.3094 90; 107.329; 90 | 2538.8 | Sun, Jing; Jiang, Wang; Yan, Chao-Guo Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes Organic Chemistry Frontiers, 2019, 6, 1428 |
| 1554732 | CIF | C32 H21 Br O2 | P 1 21/c 1 | 10.602; 20.505; 12.2951 90; 114.94; 90 | 2423.6 | Sun, Jing; Jiang, Wang; Yan, Chao-Guo Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes Organic Chemistry Frontiers, 2019, 6, 1428 |
| 1554733 | CIF | C26 H19 Cl O | P -1 | 9.998; 15.063; 15.716 63.252; 83.527; 76.536 | 2055 | Sun, Jing; Jiang, Wang; Yan, Chao-Guo Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes Organic Chemistry Frontiers, 2019, 6, 1428 |
| 1554734 | CIF | C34 H25 Br O4 | P 1 21/n 1 | 13.3814; 10.6318; 19.2274 90; 92.604; 90 | 2732.6 | Sun, Jing; Jiang, Wang; Yan, Chao-Guo Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes Organic Chemistry Frontiers, 2019, 6, 1428 |
| 1554735 | CIF | C32 H33 Cl3 N4 Ni O4 | P 1 | 9.3743; 13.379; 14.9327 81.008; 89.658; 80.276 | 1822.85 | Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I. A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals Organic Chemistry Frontiers, 2019, 6, 1094 |
| 1554736 | CIF | C37 H39 N3 Ni O4 | P 1 21 1 | 9.846; 12.0451; 14.2648 90; 110.181; 90 | 1587.89 | Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I. A general synthesis of unnatural α-amino acids by iron-catalysed olefin–olefin coupling via generated radicals Organic Chemistry Frontiers, 2019, 6, 1094 |
| 1554737 | CIF | C36 H39 Cl4 N3 Ni O3 | P 21 21 21 | 11.452; 13.8346; 22.8016 90; 90; 90 | 3612.5 | Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I. A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals Organic Chemistry Frontiers, 2019, 6, 1094 |
| 1554738 | CIF | C24 H27 Br O3 | P 21 21 21 | 5.459; 7.8884; 51.7461 90; 90; 90 | 2228.33 | Xin, Xiaodong; Pan, Xinhui; Meng, Zhilin; Liu, Xigong; Liu, Lei Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2H-pyrans with aldehydes Organic Chemistry Frontiers, 2019, 6, 1448 |
| 1554739 | CIF | C23 H19 Br N2 O3 S | P 1 21/c 1 | 12.1948; 18.8246; 10.1822 90; 105.486; 90 | 2252.6 | Xu, Ze-Feng; Shan, Lihong; Zhang, Wan; Cen, Mengjie; Li, Chuan-Ying Synthesis of α-aminoketones from N-sulfonyl-1,2,3-triazoles via N-sulfinyl imines generated by intramolecular oxygen transfer Organic Chemistry Frontiers, 2019, 6, 1391 |
| 1554740 | CIF | C43 H36 N4 O9 | C 2 2 21 | 17.41181; 27.6471; 17.61491 90; 90; 90 | 8479.57 | Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles Organic Chemistry Frontiers, 2019, 6, 1603 |
| 1554741 | CIF | C40 H37.5 N4 O9 | C 1 2 1 | 29.1304; 17.2687; 17.7328 90; 103.665; 90 | 8667.88 | Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles Organic Chemistry Frontiers, 2019, 6, 1603 |
| 1554742 | CIF | C31 H26 Cl2 Hf | P 1 21/m 1 | 8.1722; 16.0848; 9.1272 90; 95.0903; 90 | 1195.02 | Amaya, Toru; Katoh, Shun; Moriuchi, Toshiyuki; Hirao, Toshikazu Synthesis of a sumanenyl hafnocene complex Organic Chemistry Frontiers, 2019, 6, 1032 |
| 1554743 | CIF | C24 H34 O6 | P 1 21 1 | 7.272; 12.369; 12.296 90; 105.99; 90 | 1063.2 | Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate Organic Chemistry Frontiers, 2019, 6, 868 |
| 1554744 | CIF | C30 H43 N O7 | P 65 | 17.407; 17.407; 17.977 90; 90; 120 | 4717.3 | Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate Organic Chemistry Frontiers, 2019, 6, 868 |
| 1554745 | CIF | C24 H34 O5 | P 1 21 1 | 7.323; 12.384; 12.233 90; 106.42; 90 | 1064.1 | Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate Organic Chemistry Frontiers, 2019, 6, 868 |
| 1554746 | CIF | C28 H35 N O3 | P 21 21 21 | 10.391; 12.429; 18.269 90; 90; 90 | 2359.4 | Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate Organic Chemistry Frontiers, 2019, 6, 868 |
| 1554747 | CIF | C25 H17 Cl3 N2 O2 S | P 1 21/c 1 | 13.0109; 11.5329; 16.1284 90; 109.629; 90 | 2279.5 | Wang, Shengzheng; Guo, Zhongjie; Wu, Ying; Liu, Wei; Liu, Xueying; Zhang, Shengyong; Sheng, Chunquan Organocatalytic asymmetric synthesis of highly functionalized spiro-thiazolone–cyclopropane-oxindoles bearing two vicinal spiro quaternary centers Organic Chemistry Frontiers, 2019, 6, 1442 |
| 1554748 | CIF | C40 H34 I3 N3 | P 41 21 2 | 13.41045; 13.41045; 40.0935 90; 90; 90 | 7210.42 | Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A. Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands Organic Chemistry Frontiers, 2019, 6, 1226 |
| 1554749 | CIF | C152 H120 B4 F16 N8 Pd2 | P 42 21 2 | 32.9899; 32.9899; 14.3593 90; 90; 90 | 15627.7 | Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A. Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands Organic Chemistry Frontiers, 2019, 6, 1226 |
| 1554750 | CIF | C280 H248 F24 N8 O27 P8 Pd4 S8 | C 1 2/c 1 | 46.6905; 26.3232; 31.9982 90; 97.75; 90 | 38968 | Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A. Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands Organic Chemistry Frontiers, 2019, 6, 1226 |
| 1554751 | CIF | C62 H74 N22 Na O21 S2 | P -1 | 12.4931; 18.1989; 20.9673 89.537; 87.89; 72.498 | 4543.3 | Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan Functionalisable acyclic cucurbiturils Organic Chemistry Frontiers, 2019, 6, 1555 |
| 1554752 | CIF | C64 H72 Cl2 N18 Na2 O19 S2 | P b c n | 19.1042; 43.808; 23.0275 90; 90; 90 | 19272.1 | Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan Functionalisable acyclic cucurbiturils Organic Chemistry Frontiers, 2019, 6, 1555 |
| 1554753 | CIF | C31 H26 Cl N O4 | P 21 21 21 | 7.9152; 11.4088; 28.388 90; 90; 90 | 2563.5 | He, Zhao-Lin; Sheong, Fu Kit; Li, Qing-Hua; Lin, Zhenyang; Wang, Chun-Jiang Exoselective 1,3-dipolar [3 + 6] cycloaddition of azomethine ylides with 2-acylcycloheptatrienes: stereoselectivity and mechanistic insight. Organic letters, 2015, 17, 1365-1368 |
| 1554754 | CIF | C108 H150 F12 N2 O18 P2 | P 1 21/n 1 | 17.6358; 25.0174; 26.064 90; 109.616; 90 | 10832.1 | Li, Dong-Hao; Yang, Liu-Pan; Chai, Hongxin; Jia, Fei; Ke, Hua; Jiang, Wei Temperature-induced large amplitude conformational change in the complex of oxatub[4]arene revealed via rotaxane synthesis Organic Chemistry Frontiers, 2019, 6, 1027 |
| 1554755 | CIF | C22 H25 O5 P | P -1 | 7.8931; 9.4542; 14.3399 89.1605; 82.9814; 69.4905 | 994.29 | Kim, Cheol-Eui; Son, Jeong-Yu; Shin, Seohyun; Seo, Boram; Lee, Phil Ho Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins. Organic letters, 2015, 17, 908-911 |
| 1554756 | CIF | C26 H23 B F4 N2 O2 | P 1 21/c 1 | 12.2068; 13.731; 14.626 90; 99.027; 90 | 2421.1 | Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts. Organic letters, 2015, 17, 924-927 |
| 1554757 | CIF | C19 H11 F5 N2 O2 | P 1 21/c 1 | 12.1293; 8.5068; 15.8667 90; 92.925; 90 | 1635.02 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554758 | CIF | C19 H20 N4 O3 | P -1 | 7.886; 9.5658; 11.4661 86.429; 79.097; 77.958 | 830.42 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554759 | CIF | C21 H16 Cl N3 O3 | P -1 | 8.0444; 10.7234; 11.5467 71.104; 70.41; 73.474 | 870.38 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554760 | CIF | C19 H20 N4 O3 | P -1 | 7.7358; 9.6039; 11.631 85.647; 76.146; 78.816 | 822.65 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554761 | CIF | C22 H19 N3 O4 | P 1 21/c 1 | 8.7562; 23.4732; 8.8632 90; 92.21; 90 | 1820.35 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554762 | CIF | C21 H15 Cl F N3 O3 | P 1 21/c 1 | 7.3959; 19.3566; 12.7098 90; 91.147; 90 | 1819.2 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554763 | CIF | C29 H19 F6 N3 O4 | P 1 21/c 1 | 15.9357; 13.7866; 11.8725 90; 93.908; 90 | 2602.3 | Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides Organic Chemistry Frontiers, 2019, 6, 1613 |
| 1554764 | CIF | C25 H20 B F4 N O | P 1 21/n 1 | 10.72; 18.331; 12.174 90; 110.527; 90 | 2240.4 | Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts. Organic letters, 2015, 17, 924-927 |
| 1554765 | CIF | C25 H21 B F4 N2 O2 | P 1 21/c 1 | 12.3471; 13.3272; 13.9786 90; 98.588; 90 | 2274.42 | Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts. Organic letters, 2015, 17, 924-927 |
| 1554766 | CIF | C60 H78 Cl2 N4 O16 | P -1 | 15.267; 19.087; 24.39 87.94; 83.839; 73.08 | 6760 | Jordan, Jacobs H.; Wishard, Anthony; Mague, Joel T.; Gibb, Bruce C. Binding properties and supramolecular polymerization of a water-soluble resorcin[4]arene Organic Chemistry Frontiers, 2019, 6, 1236 |
| 1554767 | CIF | C31 H24 Cl N O3 | P 1 21 1 | 7.081; 19.406; 9.491 90; 98.161; 90 | 1290.99 | Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles. Organic letters, 2015, 17, 1066-1069 |
| 1554768 | CIF | C6.21 H2.28 Cl0.48 N0.07 O0.28 S0 | P -1 | 9.9983; 16.3521; 19.4651 102.163; 90.869; 105.091 | 2995.41 | Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium Organic Chemistry Frontiers, 2019, 6, 1397 |
| 1554769 | CIF | C143 H54 N2 O10 S2 | P 1 21/n 1 | 10.4701; 25.097; 16.2566 90; 91.218; 90 | 4270.8 | Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium Organic Chemistry Frontiers, 2019, 6, 1397 |
| 1554770 | CIF | C70 H22.75 N O4.88 S2 | C 1 c 1 | 14.4203; 27.3088; 10.3569 90; 94.182; 90 | 4067.7 | Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium Organic Chemistry Frontiers, 2019, 6, 1397 |
| 1554771 | CIF | C81 H42.7 N O5.85 S2 | P -1 | 10.4366; 16.3952; 16.824 110.869; 99.019; 100.619 | 2565.14 | Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium Organic Chemistry Frontiers, 2019, 6, 1397 |
| 1554772 | CIF | C143 H57.4 N2 O11.7 S2 | P 1 21/n 1 | 10.4595; 25.0584; 16.2556 90; 91.316; 90 | 4259.4 | Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium Organic Chemistry Frontiers, 2019, 6, 1397 |
| 1554773 | CIF | C49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2 | P -1 | 10.3083; 14.3567; 19.2355 75.287; 74.747; 84.913 | 2655.7 | Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J. Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes. Organic letters, 2015, 17, 752-755 |
| 1554774 | CIF | C16 H19 Cl3 N P Ti | P -1 | 8.8951; 9.2936; 13.0036 79.226; 76.069; 64.74 | 939.24 | Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J. Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes. Organic letters, 2015, 17, 752-755 |
| 1554775 | CIF | C19 H20 N2 Se | P 1 21/c 1 | 13.3462; 10.2259; 12.0633 90; 96.466; 90 | 1635.89 | Guo, Tao; Wei, Xu-Ning; Liu, Yu; Zhang, Pan-Ke; Zhao, Yun-Hui Oxidative dual C–H selenation of imidazoheterocycles with ethers or alkanes using selenium powder via a radical pathway Organic Chemistry Frontiers, 2019, 6, 1414 |
| 1554776 | CIF | C35 H26 N1.6 O10 | P 21 21 21 | 13.871; 15.1622; 64.627 90; 90; 90 | 13592 | Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family. Organic letters, 2015, 17, 1146-1149 |
| 1554777 | CIF | C21 H18 N O3 P | P 21 21 21 | 8.4621; 19.7458; 21.2129 90; 90; 90 | 3544.5 | Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M. Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones Organic Chemistry Frontiers, 2019, 6, 1257 |
| 1554778 | CIF | C25 H23 N2 O2 P | P 1 21/n 1 | 18.5757; 6.176; 18.9148 90; 98.809; 90 | 2144.38 | Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M. Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones Organic Chemistry Frontiers, 2019, 6, 1257 |
| 1554779 | CIF | C22.5 H14.5 Cl1.5 F3 N2 O2 P | C 1 2/c 1 | 29.394; 6.3419; 28.119 90; 121.188; 90 | 4484.2 | Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M. Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones Organic Chemistry Frontiers, 2019, 6, 1257 |
| 1554780 | CIF | C21 H15 N2 O2 P | C 1 2/c 1 | 24.331; 10.2408; 14.54 90; 102.686; 90 | 3534.5 | Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M. Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones Organic Chemistry Frontiers, 2019, 6, 1257 |
| 1554781 | CIF | C21 H15 N2 O2 P | C 1 2/c 1 | 26.4131; 9.7872; 14.9148 90; 115.7; 90 | 3474.22 | Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M. Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones Organic Chemistry Frontiers, 2019, 6, 1257 |
| 1554782 | CIF | C34 H29 N5 O4 S | P -1 | 9.7972; 10.509; 15.4371 72.931; 74.564; 84.268 | 1464.2 | Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles. Organic letters, 2015, 17, 1192-1195 |
| 1554783 | CIF | C24 H27 N3 O2 | P 1 21/c 1 | 17.5333; 9.245; 13.3467 90; 107.946; 90 | 2058.18 | Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides. Organic letters, 2015, 17, 1184-1187 |
| 1554784 | CIF | C13 H18 N2 O2 S2 | P b c a | 14.1538; 10.7714; 20.0319 90; 90; 90 | 3054 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554785 | CIF | C11 H12 O4 S2 | P -1 | 5.1535; 7.3073; 16.2864 81.694; 82.41; 74.561 | 582.16 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554786 | CIF | C36 H38 O2 S2 | C 1 c 1 | 19.6986; 10.9502; 16.5805 90; 122.988; 90 | 2999.9 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554787 | CIF | C40 H46 O2 S2 | P -1 | 9.4599; 10.4995; 17.9405 82.254; 86.522; 88.292 | 1762 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554788 | CIF | C41 H48 O2 S2 | P 1 21/n 1 | 11.3446; 17.747; 17.3945 90; 97.039; 90 | 3475.7 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554789 | CIF | C13 H18 N2 O2 S2 | P 1 21/c 1 | 10.5966; 11.0075; 13.0168 90; 103.286; 90 | 1477.67 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554790 | CIF | C37 H40 O2 S2 | P 1 21/c 1 | 14.4032; 9.233; 24.7181 90; 93.6338; 90 | 3280.5 | Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters Organic Chemistry Frontiers, 2019, 6, 1244 |
| 1554791 | CIF | C21 H15 N3 O | P 1 21/c 1 | 10.5706; 17.3802; 10.1316 90; 96.996; 90 | 1847.5 | Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides. Organic letters, 2015, 17, 1184-1187 |
| 1554792 | CIF | C24 H12 F6 Se | P 1 21/c 1 | 12.234; 10.9831; 14.6454 90; 111.492; 90 | 1831 | Shi, Xinzhe; Mao, Shuxin; Roisnel, Thierry; Doucet, Henri; Soulé, Jean-François Palladium-catalyzed successive C–H bond arylations and annulations toward the π-extension of selenophene-containing aromatic skeletons Organic Chemistry Frontiers, 2019, 6, 2398 |
| 1554793 | CIF | C24 H21 I N2 O3 S | P 21 21 21 | 10.7482; 12.7229; 16.152 90; 90; 90 | 2208.76 | Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas. Organic letters, 2015, 17, 1018-1021 |
| 1554794 | CIF | C19 H24 N2 O | P c a 21 | 12.8993; 10.853; 11.6466 90; 90; 90 | 1630.5 | Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond. Organic letters, 2015, 17, 1200-1203 |
| 1554795 | CIF | C36 H23 Br F3 N2 O3 | P 21 21 21 | 11.6434; 14.186; 17.6525 90; 90; 90 | 2915.72 | Li, Boyu; Gao, Fengyun; Feng, Xing; Sun, Mengmeng; Guo, Yifei; Wen, Dongwa; Deng, Yabo; Huang, Jinqi; Wang, Kairong; Yan, Wenjin Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition Organic Chemistry Frontiers, 2019, 6, 1567 |
| 1554796 | CIF | C24 H44 B2 N2 O4 | P b a m | 12.939; 13.093; 15.573 90; 90; 90 | 2638.2 | Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water. Organic letters, 2015, 17, 1212-1215 |
| 1554797 | CIF | C29 H49 B2 Co N2 O4 | F d d 2 | 18.923; 58.36; 11.127 90; 90; 90 | 12288 | Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water. Organic letters, 2015, 17, 1212-1215 |
| 1554798 | CIF | C24 H46 B2 N2 O5 | P 1 21/n 1 | 10.74; 19.626; 13.066 90; 93.197; 90 | 2749.8 | Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water. Organic letters, 2015, 17, 1212-1215 |
| 1554799 | CIF | C27 H40 O6 | P 1 21 1 | 9.8327; 16.984; 16.2007 90; 101.138; 90 | 2654.54 | Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv. Organic Chemistry Frontiers, 2019, 6, 1491 |
| 1554800 | CIF | C29 H44 O6 | P 21 21 21 | 12.0011; 13.3921; 17.7454 90; 90; 90 | 2852.04 | Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv. Organic Chemistry Frontiers, 2019, 6, 1491 |
| 1554801 | CIF | C26 H38 O6 | P 1 21 1 | 9.6691; 16.4235; 15.94 90; 101.09; 90 | 2484.01 | Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv. Organic Chemistry Frontiers, 2019, 6, 1491 |
| 1554802 | CIF | C24 H41 B2 O2 P | P 1 21/n 1 | 8.6014; 17.6656; 16.4517 90; 107.162; 90 | 2388.51 | Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes. Organic letters, 2015, 17, 1216-1219 |
| 1554803 | CIF | C28 H33 B2 Fe O2 P | P 1 21 1 | 12.674; 9.2986; 12.919 90; 113.497; 90 | 1396.3 | Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes. Organic letters, 2015, 17, 1216-1219 |
| 1554804 | CIF | C40 H43 B2 Fe P | P 21 21 21 | 10.3874; 17.4963; 18.3521 90; 90; 90 | 3335.3 | Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes. Organic letters, 2015, 17, 1216-1219 |
| 1554805 | CIF | C162 H174 Au4 Cl16 O8 P4 | P -1 | 12.983; 13.401; 29.22 81.31; 77.62; 61.97 | 4376 | Hau, Franky Ka-Wah; Cheung, Kai-Leung; Zhu, Nianyong; Yam, Vivian Wing-Wah Calixarene-based alkynyl-bridged gold(i) isocyanide and phosphine complexes as building motifs for the construction of chemosensors and supramolecular architectures Organic Chemistry Frontiers, 2019, 6, 1205 |
| 1554806 | CIF | C13 H12 O4 | P 1 21/n 1 | 10.5408; 14.0223; 15.567 90; 95.216; 90 | 2291.4 | Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates. Organic letters, 2015, 17, 1228-1231 |
| 1554807 | CIF | C27 H23 N O | P -1 | 10.4979; 10.7112; 10.8365 60.7986; 76.2796; 71.3801 | 1003.08 | Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K. Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy Organic Chemistry Frontiers, 2019, 6, 1655 |
| 1554808 | CIF | C27 H23 N O | P 1 21 1 | 6.7344; 18.9552; 15.1244 90; 90.856; 90 | 1930.4 | Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K. Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy Organic Chemistry Frontiers, 2019, 6, 1655 |
| 1554809 | CIF | C19 H18 N O5 S2 | P -1 | 7.9459; 8.3713; 15.0845 98.477; 91.135; 97.754 | 982.54 | Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols. Organic letters, 2015, 17, 1834-1837 |
| 1554810 | CIF | C24 H22 O3 | C 1 c 1 | 14.8194; 23.1341; 17.3079 90; 104.994; 90 | 5731.7 | Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc Development of a new family of chiral auxiliaries. Organic letters, 2015, 17, 1819-1821 |
| 1554811 | CIF | C34 H30 N2 O7 | P 21 21 21 | 9.7212; 10.3208; 28.5171 90; 90; 90 | 2861.14 | Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones Organic Chemistry Frontiers, 2019, 6, 1485 |
| 1554812 | CIF | C36 H32 F N3 O7 | P 1 21 1 | 11.7466; 12.2636; 22.7319 90; 93.091; 90 | 3269.89 | Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones Organic Chemistry Frontiers, 2019, 6, 1485 |
| 1554813 | CIF | C17 H16 Cl N3 O | P -1 | 8.6811; 13.1015; 15.2298 66.74; 82.416; 77.876 | 1553.57 | Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides. Organic letters, 2015, 17, 1157-1159 |
| 1554814 | CIF | C34 H35 N O6 S | P 21 21 21 | 9.4387; 22.551; 28.131 90; 90; 90 | 5987.7 | Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R. 2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors. Organic letters, 2015, 17, 1421-1424 |
| 1554815 | CIF | C19 H21 F2 N O | P 1 21/c 1 | 9.9286; 17.0093; 10.0841 90; 90.259; 90 | 1703 | He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates. Organic letters, 2015, 17, 1838-1841 |
| 1554816 | CIF | C17 H16 Br F3 O2 | P 1 21 1 | 6.2353; 7.7873; 17.3098 90; 90.759; 90 | 840.42 | Chen, Daoqian; Lu, Long; Shen, Qilong [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers, 2019, 6, 1801 |
| 1554817 | CIF | C23 H21 N O7 S | P 1 21 1 | 10.6202; 6.377; 16.3385 90; 98.252; 90 | 1095.07 | Chen, Daoqian; Lu, Long; Shen, Qilong [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers, 2019, 6, 1801 |
| 1554818 | CIF | C18 H17 F3 O3 | P 21 21 21 | 6.4981; 15.2542; 17.146 90; 90; 90 | 1699.57 | Chen, Daoqian; Lu, Long; Shen, Qilong [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers, 2019, 6, 1801 |
| 1554819 | CIF | C24 H31 Ag F6 N2 P2 | P 1 c 1 | 15.277; 8.0788; 21.7171 90; 98.481; 90 | 2651.01 | Chen, Daoqian; Lu, Long; Shen, Qilong [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers, 2019, 6, 1801 |
| 1554820 | CIF | C31 H41 Ag F6 N4 P2 | P 1 21/c 1 | 12.7111; 17.36; 15.7081 90; 105.588; 90 | 3338.73 | Chen, Daoqian; Lu, Long; Shen, Qilong [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers, 2019, 6, 1801 |
| 1554821 | CIF | C25 H31 Ag F3 N2 O P | P 1 21/c 1 | 11.3702; 12.6386; 17.83 90; 103.361; 90 | 2492.88 | Chen, Daoqian; Lu, Long; Shen, Qilong [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers, 2019, 6, 1801 |
| 1554822 | CIF | C16 H10 N2 O | P 1 21/n 1 | 6.4176; 20.0965; 9.335 90; 98.274; 90 | 1191.42 | Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles. Organic letters, 2015, 17, 1445-1448 |
| 1554823 | CIF | C27 H40 O4 | P 21 21 21 | 8.061; 10.8588; 27.7356 90; 90; 90 | 2427.77 | Xu, Hou-Chao; Hu, Kun; Shi, Xiao-Huo; Tang, Jian-Wei; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea Organic Chemistry Frontiers, 2019, 6, 1619 |
| 1554824 | CIF | C20 H14 O5 | P 1 21/n 1 | 9.0391; 9.7069; 17.2285 90; 102.573; 90 | 1475.41 | Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang Muta-mycosynthesis of naphthalene analogs. Organic letters, 2015, 17, 1457-1460 |
| 1554825 | CIF | C15 H13 N3 | P -1 | 5.4882; 11.1825; 11.6413 62.292; 80.059; 76.727 | 613.82 | Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons Organic Chemistry Frontiers, 2019, 6, 2825 |
| 1554826 | CIF | C17 H17 N3 O2 | C 1 2/c 1 | 15.105; 12.8664; 15.5822 90; 91.952; 90 | 3026.6 | Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons Organic Chemistry Frontiers, 2019, 6, 2825 |
| 1554827 | CIF | C19 H17 B F2 N4 O2 | P -1 | 7.1859; 12.0427; 12.0895 93.791; 100.927; 98.538 | 1011.05 | Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons Organic Chemistry Frontiers, 2019, 6, 2825 |
| 1554828 | CIF | C17 H16 N3 O2.5 | P 1 21/c 1 | 10.668; 24.498; 11.286 90; 93.034; 90 | 2945.4 | Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons Organic Chemistry Frontiers, 2019, 6, 2825 |
| 1554829 | CIF | C17.14 H14.5 B F2 N3 O2 | P 1 21/c 1 | 11.1306; 11.7622; 24.0194 90; 91.217; 90 | 3143.92 | Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons Organic Chemistry Frontiers, 2019, 6, 2825 |
| 1554830 | CIF | C20 H25 F3 N2 O3 S | P 1 21/c 1 | 8.128; 15.344; 16.979 90; 102.44; 90 | 2067.8 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554831 | CIF | C22 H30 F3 N3 O3 S | C 1 2/c 1 | 15.441; 10.924; 27.769 90; 90.9; 90 | 4683.4 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554832 | CIF | C18 H22 F3 N3 O3 S | P 1 21/c 1 | 8.4815; 11.074; 21.3223 90; 93.426; 90 | 1999.1 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554833 | CIF | C21 H25 N3 | P -1 | 8.61; 9.179; 11.835 93.38; 95.73; 105.2 | 894.57 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554834 | CIF | C20 H26 N2 | P 1 21/c 1 | 8.693; 17.464; 11.525 90; 103.69; 90 | 1700 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554835 | CIF | C14 H22 N2 | R 3 c :H | 26.3163; 26.3163; 10.403 90; 90; 120 | 6239.3 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554836 | CIF | C22 H26 N4 O5 | P 21 21 21 | 9.5782; 11.765; 20.2153 90; 90; 90 | 2278.01 | Dai, Chuan; Ma, Jun; Li, Min; Wu, Wen; Xia, Xuefeng; Zhang, Jinqiang Diversity-oriented submonomer synthesis of azapeptides mediated by the Mitsunobu reaction Organic Chemistry Frontiers, 2019, 6, 2529 |
| 1554837 | CIF | C49 H29 B F20 N O2 Rh | P 1 21/c 1 | 12.2787; 24.2002; 15.5541 90; 101.818; 90 | 4523.9 | Otley, Kate D.; Ellman, Jonathan A. An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation. Organic letters, 2015, 17, 1332-1335 |
| 1554838 | CIF | C18 H18 O2 | P 1 21/c 1 | 14.026; 8.7035; 12.0599 90; 104.008; 90 | 1428.4 | Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process. Organic letters, 2015, 17, 1489-1492 |
| 1554839 | CIF | C17 H16 O2 Se | P 1 21 1 | 6.9078; 10.3981; 10.0732 90; 95.471; 90 | 720.24 | Niu, Wenxue; Yeung, Ying-Yeung Catalytic and highly enantioselective selenolactonization. Organic letters, 2015, 17, 1660-1663 |
| 1554840 | CIF | C12 H20 O4 | P 32 | 13.594; 13.594; 5.7493 90; 90; 120 | 920.11 | Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John Exo-selective reductive macrocyclization of ynals. Organic letters, 2015, 17, 1493-1496 |
| 1554841 | CIF | C14 H15 Br N2 O2 | P 21 21 21 | 9.2455; 10.1411; 14.412 90; 90; 90 | 1351.3 | Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters. Organic letters, 2015, 17, 1505-1508 |
| 1554842 | CIF | C22 H18 F N3 O2 S | P 1 21/c 1 | 15.7629; 11.6907; 10.7408 90; 100.958; 90 | 1943.22 | Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles. Organic letters, 2015, 17, 1521-1524 |
| 1554843 | CIF | C16 H23 Cl F6 N3 O2 P | C 1 c 1 | 10.7226; 12.3939; 15.6108 90; 92.991; 90 | 2071.77 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554844 | CIF | C17 H23 Cl2 F6 N2 O2 P | P 1 21/c 1 | 11.8795; 14.5176; 12.6593 90; 102.138; 90 | 2134.44 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554845 | CIF | C28 H41 F6 N4 O2 P | C 1 2/c 1 | 36.485; 10.158; 16.856 90; 92.44; 90 | 6241 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554846 | CIF | C34 H49 F12 N7 O4 P2 | I 1 2/a 1 | 24.915; 8.8562; 19.8464 90; 105.666; 90 | 4216.5 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554847 | CIF | C26 H39.5 F9 N4.5 O5 P S | P -1 | 10.7516; 12.0558; 14.8348 107.62; 93.413; 109.731 | 1696.8 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554848 | CIF | C19 H29 Cl F6 N3 O2 P | P 1 21/n 1 | 7.59057; 26.3895; 12.488 90; 107.133; 90 | 2390.48 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554849 | CIF | C21 H32 F6 N4 O2 P | P 1 21/c 1 | 12.3903; 16.1931; 13.6174 90; 113.783; 90 | 2500.1 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554850 | CIF | C16 H23 F12 N3 O2 P2 | P 1 21/n 1 | 10.5891; 16.2883; 13.903 90; 102.985; 90 | 2336.65 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554851 | CIF | C26 H41 Cl2 F6 N2 O2 P | P 1 21/c 1 | 18.6093; 10.778; 15.4265 90; 101.706; 90 | 3029.76 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554852 | CIF | C30.33 H52.53 Cl2.12 F6 N3 O2.44 P | P -1 | 9.5322; 18.6061; 21.1198 83.275; 88.086; 80.993 | 3673.7 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554853 | CIF | C22 H35 Cl F6 N3 O2 P | P 1 21/n 1 | 12.7678; 11.6389; 36.278 90; 94.051; 90 | 5377.6 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554854 | CIF | C33 H47.66 F12 N6.5 O4.08 P2 | P -1 | 12.1931; 15.3991; 22.7102 95.65; 102.392; 94.7722 | 4120.61 | Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David Stable dicationic dioxoliums and fate of their dioxolyl radicals Organic Chemistry Frontiers, 2019, 6, 3184 |
| 1554855 | CIF | C18 H21 N3 O2 S2 | P 1 21/c 1 | 10.0095; 11.563; 16.5773 90; 99.859; 90 | 1890.32 | Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles. Organic letters, 2015, 17, 1521-1524 |
| 1554856 | CIF | C20 H26 N2 O8 Si | C 1 2/c 1 | 18.687; 6.709; 37.603 90; 90.534; 90 | 4714 | Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal. Organic letters, 2015, 17, 1553-1556 |
| 1554857 | CIF | C19 H20 O3 S | P -1 | 6.9512; 8.6039; 15.1128 102.337; 92.466; 108.002 | 833.95 | He, Fu-Sheng; Wu, Youqian; Li, Xiaofang; Xia, Hongguang; Wu, Jie Photoredox-catalyzed sulfonylation of alkenylcyclobutanols with the insertion of sulfur dioxide through semipinacol rearrangement Organic Chemistry Frontiers, 2019, 6, 1873 |
| 1554858 | CIF | C60 H85 I3 N10 O12 | P -1 | 14.2686; 14.6629; 17.0163 80.443; 70.781; 82.037 | 3301.6 | Saha, Subrata; Santra, Saikat; Ghosh, Pradyut [2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation. Organic letters, 2015, 17, 1854-1857 |
| 1554859 | CIF | C17 H23 N O5 S | P 1 21/n 1 | 6.0877; 10.8073; 26.052 90; 93.948; 90 | 1709.9 | Xu, Dongyang; Wei, Hongbo; Zhen, Yanxia; Gao, Yu-Qi; Li, Ruoxin; Li, Xingzhou; He, Yupeng; Zhang, Zhong; Xie, Weiqing Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane Organic Chemistry Frontiers, 2019, 6, 1681 |
| 1554860 | CIF | C60 H78 Cl6 N10 O10 | C 1 2/c 1 | 22.9779; 30.564; 22.926 90; 114.207; 90 | 14685.1 | Saha, Subrata; Santra, Saikat; Ghosh, Pradyut [2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation. Organic letters, 2015, 17, 1854-1857 |
| 1554861 | CIF | C9 H11 B0.75 O2.25 | P 1 21/n 1 | 6.4968; 22.26; 7.1909 90; 116.2; 90 | 933.1 | Bhavanarushi, Sangepu; Xu, Yin; Khan, Imran; Luo, Zhibin; Liu, Bin; Xie, Jimin Transition-metal-free borylation of propargylic alcohols: structurally variable synthesis in ionic liquid medium Organic Chemistry Frontiers, 2019, 6, 1895 |
| 1554862 | CIF | C27 H27 F3 N2 O8 | P -1 | 8.5362; 11.0883; 14.8339 89.337; 75.808; 89.011 | 1360.96 | Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes. Organic letters, 2015, 17, 1589-1592 |
| 1554863 | CIF | C11 H7 F3 N2 O2 | P 1 21/n 1 | 5.41; 17.433; 11.237 90; 93.29; 90 | 1058 | Peng, Xiaofeng; Zhang, Xiaofei; Li, Shunyao; Lu, Yunfu; Lan, Lefu; Yang, Chunhao Silver-mediated synthesis of novel 3-CF3/CN/phosphonate-substituted pyrazoles as pyrrolomycin analogues from 3-formylchromones and diazo compounds Organic Chemistry Frontiers, 2019, 6, 1775 |
| 1554864 | CIF | C14 H11 N O7 | P n a 21 | 8.6933; 19.9383; 7.6281 90; 90; 90 | 1322.18 | Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J. Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study. Organic letters, 2015, 17, 1850-1853 |
| 1554865 | CIF | C24 H22 N2 O9 S | P 21 21 21 | 12.2161; 12.5468; 16.7879 90; 90; 90 | 2573.13 | Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes Organic Chemistry Frontiers, 2019, 6, 1891 |
| 1554866 | CIF | C24 H24 O6 | P 1 21/c 1 | 10.3133; 11.2328; 19.0954 90; 99.604; 90 | 2181.14 | Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes Organic Chemistry Frontiers, 2019, 6, 1891 |
| 1554867 | CIF | C23 H26 Br N O4 S | P 1 21 1 | 9.8067; 9.9678; 11.8916 90; 104.237; 90 | 1126.7 | Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization. Organic letters, 2015, 17, 1720-1723 |
| 1554868 | CIF | C24 H19 Cl N2 O3 | P 21 21 21 | 5.9309; 17.47; 19.675 90; 90; 90 | 2038.6 | Chu, Ming-Ming; Qi, Suo-Suo; Wang, Yi-Feng; Wang, Biao; Jiang, Zhen-Hui; Xu, Dan-Qian; Xu, Zhen-Yuan Organocatalytic asymmetric [4 + 1] annulation of in situ generated ortho-quinomethanes with 4-halo pyrazolones: straightforward access to chiral spiro-benzofuran pyrazolones Organic Chemistry Frontiers, 2019, 6, 1977 |
| 1554869 | CIF | C28 H19 N O3 S2 | P -1 | 10.443; 11.228; 11.795 70.186; 87.728; 65.484 | 1175.6 | Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes. Organic letters, 2015, 17, 1746-1749 |
| 1554870 | CIF | C19 H18 N2 O4 | P 1 21/c 1 | 9.3579; 12.566; 29.371 90; 96.6; 90 | 3430.9 | Zhang, Wei; Zheng, Han-Liang; Liu, Yang; Yu, Ao; Yang, Chen; Li, Xin; Cheng, Jin-Pei Catalyst-free amination of α-cyanoarylacetates enabled by single-electron transfer Organic Chemistry Frontiers, 2019, 6, 1900 |
| 1554871 | CIF | C15 H21 N O3 | P 1 21/n 1 | 5.1627; 14.8595; 17.7219 90; 96.198; 90 | 1351.59 | Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids. Organic letters, 2015, 17, 1754-1757 |
| 1554872 | CIF | C28 H29 N3 O4 | P 1 21 1 | 7.807; 15.9924; 10.5193 90; 109.003; 90 | 1241.79 | Zhang, Yan-Ping; You, Yong; Zhao, Jian-Qiang; Zhou, Xiao-Jian; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides Organic Chemistry Frontiers, 2019, 6, 1879 |
| 1554873 | CIF | C20 H16 O2 | P 21 21 21 | 5.9724; 14.8969; 16.4863 90; 90; 90 | 1466.79 | Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J. Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts. Organic letters, 2015, 17, 1735-1737 |
| 1554874 | CIF | C23 H30 O8 | P 21 21 21 | 8.0029; 15.3468; 17.8042 90; 90; 90 | 2186.69 | Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018 Organic Chemistry Frontiers, 2019, 6, 3053 |
| 1554875 | CIF | C12 H13 Br O2 | P 1 21/c 1 | 6.0066; 11.7969; 16.772 90; 97.594; 90 | 1178 | Che, Chao; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides. Organic letters, 2015, 17, 1617-1620 |
| 1554876 | CIF | C29 H27 N2 O4.5 | C 1 c 1 | 14.3037; 14.0845; 23.7866 90; 91.922; 90 | 4789.36 | Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018 Organic Chemistry Frontiers, 2019, 6, 3053 |
| 1554877 | CIF | C23 H21 N | P 1 21/c 1 | 10.4176; 11.9596; 16.0413 90; 114.231; 90 | 1822.51 | Che, Chao; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides. Organic letters, 2015, 17, 1617-1620 |
| 1554878 | CIF | C29 H36 N2 O4 | P 1 21 1 | 8.527; 16.7982; 9.3056 90; 102.717; 90 | 1300.22 | Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates. Organic letters, 2015, 17, 2054-2057 |
| 1554879 | CIF | C28.33333 H40.33333 N O9.33333 | P 21 21 21 | 8.09067; 25.4976; 41.3088 90; 90; 90 | 8521.7 | Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018 Organic Chemistry Frontiers, 2019, 6, 3053 |
| 1554880 | CIF | C13 H22 O2 | C 1 c 1 | 14.0887; 10.5929; 9.0247 90; 114.771; 90 | 1222.92 | Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates. Organic letters, 2015, 17, 2054-2057 |
| 1554881 | CIF | C17 H23 N O4 | P 1 21/c 1 | 12.0924; 16.7422; 8.278 90; 107.825; 90 | 1595.5 | Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds Organic Chemistry Frontiers, 2019, 6, 2275 |
| 1554882 | CIF | C14 H13 F3 O5 | P -1 | 6.4241; 10.1906; 11.3167 68.951; 83.144; 83.818 | 684.79 | Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds Organic Chemistry Frontiers, 2019, 6, 2275 |
| 1554883 | CIF | C17 H20 O4 | P 1 21/c 1 | 12.1636; 10.2486; 12.3402 90; 110.011; 90 | 1445.5 | Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds Organic Chemistry Frontiers, 2019, 6, 2275 |
| 1554884 | CIF | C16 H18 O4 | P 1 21/c 1 | 7.6075; 9.2096; 19.424 90; 98.561; 90 | 1345.7 | Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds Organic Chemistry Frontiers, 2019, 6, 2275 |
| 1554885 | CIF | C20 H20 Br2 Cl2 N2 O4 | P 1 | 5.0746; 14.828; 16.699 65.191; 89.579; 80.838 | 1123.5 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554886 | CIF | C33 H27 Cl3 N2 O5 S | P 21 21 21 | 10.9357; 11.7723; 24.8931 90; 90; 90 | 3204.7 | Ren, Xiao-Rui; Lin, Jun-Bing; Hu, Xiu-Qin; Xu, Peng-Fei Bifunctional Brønsted base catalyzed inverse-electron-demand aza-Diels–Alder reactions of saccharin-derived 1-azadienes with azlactones Organic Chemistry Frontiers, 2019, 6, 2280 |
| 1554887 | CIF | C13 H15 Br Cl N O3 | P 1 21 1 | 4.8035; 8.2644; 18.363 90; 94.441; 90 | 726.79 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554888 | CIF | C10 H9 N O Se | P 1 21/c 1 | 5.4632; 16.8139; 10.7302 90; 98.574; 90 | 974.64 | Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates Organic Chemistry Frontiers, 2019, 6, 1967 |
| 1554889 | CIF | C24 H33 N O3 Se | P 1 21 1 | 10.1323; 7.4394; 15.4852 90; 100.787; 90 | 1146.62 | Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates Organic Chemistry Frontiers, 2019, 6, 1967 |
| 1554890 | CIF | C13 H16 Br Cl2 N O3 | P 1 21 1 | 10.669; 4.7706; 15.964 90; 107.952; 90 | 773 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554891 | CIF | C21 H21 Cl O5 | P 21 21 21 | 7.229; 11.212; 22.921 90; 90; 90 | 1857.8 | Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways Organic Chemistry Frontiers, 2019, 6, 1972 |
| 1554892 | CIF | C20 H18 O4 | P 1 21 1 | 10.3231; 8.3376; 10.651 90; 116.926; 90 | 817.35 | Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways Organic Chemistry Frontiers, 2019, 6, 1972 |
| 1554893 | CIF | C21 H19 Cl O4 | P 21 21 21 | 10.5134; 7.5193; 22.921 90; 90; 90 | 1812 | Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways Organic Chemistry Frontiers, 2019, 6, 1972 |
| 1554894 | CIF | C6 H12 Cl2 O2 | P 1 21 1 | 4.9886; 19.578; 9.0155 90; 92.03; 90 | 880 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554895 | CIF | C16 H15 N3 O4 S | P 1 21/n 1 | 14.05; 8.3338; 14.2852 90; 101.509; 90 | 1639 | Wang, Guodong; Sun, Jian; Wang, Kai; Han, Junfen; Li, Hongshuang; Duan, Guiyun; You, Guirong; Li, Furong; Xia, Chengcai Palladium-catalyzed direct C–H nitration and intramolecular C–H functionalization for the synthesis of 3-nitro-1-(phenylsulfonyl)-1H-indazole derivatives Organic Chemistry Frontiers, 2019, 6, 1608 |
| 1554896 | CIF | C13 H15 Br Cl N O3 | P 1 21 1 | 12.2792; 4.9357; 13.4763 90; 115.38; 90 | 737.92 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554897 | CIF | C16 H19 N O3 | P 1 21 1 | 7.9218; 6.5193; 13.434 90; 101.58; 90 | 679.67 | Mandzhulo, Aleksandr; Vashchenko, Iryna; Gerasov, Andrii; Vovk, Mykhaylo; Rusanov, Eduard; Fetyukhin, Volodymyr; Lukin, Oleg; Shivanyuk, Alexander Selective synthesis of N-protected exo-spiro[oxirane-3,2′-tropanes] Organic Chemistry Frontiers, 2019, 6, 1692 |
| 1554898 | CIF | C13 H15 Br Cl N O3 | C 1 2 1 | 16.929; 4.841; 36.446 90; 101.211; 90 | 2930 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554899 | CIF | C24 H36 O3 | P 21 21 21 | 8.9194; 12.8315; 18.5057 90; 90; 90 | 2118 | Zhao, Nan; Xie, Shengling; Tian, Peilin; Tong, Rongbiao; Ning, Chengqing; Xu, Jing Asymmetric total synthesis of (+)-astellatol and (−)-astellatene Organic Chemistry Frontiers, 2019, 6, 2014 |
| 1554900 | CIF | C14 H18 Cl N O8 S | P 21 21 21 | 6.1403; 13.657; 20.719 90; 90; 90 | 1737.5 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554901 | CIF | C20 H30 O4 | P 21 21 21 | 9.9964; 10.5385; 17.4587 90; 90; 90 | 1839.22 | Zhang, Jing; Tang, Xuli; Han, Xiao; Feng, Danqing; Luo, Xiangchao; Ofwegen, Leen van; Li, Pinglin; Li, Guoqiang Sarcoglaucins A-I, new antifouling cembrane-type diterpenes from the South China Sea soft coral Sarcophyton glaucum Organic Chemistry Frontiers, 2019, 6, 2004 |
| 1554902 | CIF | C6 H12 Cl2 O2 | P 21 21 21 | 5.8932; 9.8358; 14.7998 90; 90; 90 | 857.86 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554903 | CIF | C19 H20 N2 O3 | P 1 21 1 | 6.5666; 16.4713; 8.0376 90; 111.405; 90 | 809.39 | Wang, Bo; Wang, Yuankai; Wang, Zixuan; Wang, Jianbo Rh(i)-Catalyzed intramolecular [2 + 2 + 1] cycloaddition of diynes with the N-terminal of the diazo group Organic Chemistry Frontiers, 2019, 6, 2329 |
| 1554904 | CIF | C18 H14 N2 O | P 1 21/c 1 | 17.283; 5.72; 16.0086 90; 115.367; 90 | 1430 | Bunescu, Ala; Wang, Qian; Zhu, Jieping Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles. Organic letters, 2015, 17, 1890-1893 |
| 1554905 | CIF | C45 H42 F4 O7 | C 1 2/c 1 | 15.1446; 24.455; 20.982 90; 93.45; 90 | 7756.8 | Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R. Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight Organic Chemistry Frontiers, 2019, 6, 1961 |
| 1554906 | CIF | C47 H45 F4 O7 | P -1 | 11.4709; 13.897; 14.895 107.986; 112.427; 96.387 | 2015.5 | Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R. Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight Organic Chemistry Frontiers, 2019, 6, 1961 |
| 1554907 | CIF | C28 H36 N2 O10 Pd3 | P 1 21/c 1 | 8.2684; 13.1049; 14.9823 90; 98.209; 90 | 1606.8 | Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle. Organic letters, 2015, 17, 1802-1805 |
| 1554908 | CIF | C24 H19 N O | P 1 21/c 1 | 10.273; 10.178; 16.954 90; 99.61; 90 | 1747.8 | Zhao, Hong-Ping; Ma, Xiao-Pan; Nie, Shu-Min; Xiao, Yuhong; Mo, Dong-Liang Synthesis of chromeno[4,3-b]quinolines and spirobenzofuran-3,3′-quinolines through silver-mediated Appel reaction/C–Br bond cleavage/double selective rearrangement sequence Organic Chemistry Frontiers, 2019, 6, 2334 |
| 1554909 | CIF | C21 H24 B N O2 | P 1 21/n 1 | 9.82013; 15.1033; 12.9881 90; 93.8267; 90 | 1922.05 | Pareek, Manish; Fallon, Thomas; Oestreich, Martin Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling. Organic letters, 2015, 17, 2082-2085 |
| 1554910 | CIF | C30 H21 N O2 | P 1 21/n 1 | 10.5982; 10.2369; 20.9415 90; 99.629; 90 | 2240 | Wang, Jian; Cai, Panyuan; He, Yimiao; Liu, Yuan; Zhong, Ling; Ding, Shumin; Shang, Yongjia Tuneable access to isoquinolines via a transition-metal-free C(sp3)–C(sp3) bond cleavage rearrangement reaction Organic Chemistry Frontiers, 2019, 6, 2430 |
| 1554911 | CIF | C27 H29 F6 N2 O P Ru | P -1 | 10.7138; 10.8978; 12.099 92.748; 96.702; 90.476 | 1401.24 | Hong, Xi; Zhou, Quan; Huang, Shuang; Cui, He-Zhen; Li, Zhi-Ming; Hou, Xiu-Feng Transition metal catalysed C7 and ortho-selective halogenation of 2-arylbenzo[d]oxazoles Organic Chemistry Frontiers, 2019, 6, 2226 |
| 1554912 | CIF | C20 H41 B2 F8 N5 O | P 21 21 21 | 9.9728; 10.8425; 25.575 90; 90; 90 | 2765.4 | Mirabdolbaghi, Roya; Dudding, Travis Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination. Organic letters, 2015, 17, 1930-1933 |
| 1554913 | CIF | C14 H12 N2 O | P 21 21 21 | 6.8959; 7.1261; 24.02 90; 90; 90 | 1180.4 | Feng, Guang-Shou; Zhao, Zi-Biao; Shi, Lei; Zhou, Yong-Gui Iridium-catalyzed asymmetric hydrogenation of quinazolinones Organic Chemistry Frontiers, 2019, 6, 2250 |
| 1554914 | CIF | C25 H36 F3 N3 O4 | P -1 | 7.9555; 12.7291; 14.1773 101.894; 105.578; 101.34 | 1304 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554915 | CIF | C20 H27 F3 N2 O3 | P 1 21/c 1 | 9.676; 6.0187; 35.338 90; 90.313; 90 | 2057.9 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554916 | CIF | C18 H23 F3 N2 O3 | P -1 | 8.4082; 8.9935; 12.6932 109.241; 90.111; 102.16 | 883.25 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554917 | CIF | C18 H16 F3 N O | P 21 21 21 | 5.8836; 19.2027; 26.5181 90; 90; 90 | 2996 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554918 | CIF | C35 H27 Br F3 N3 O3 | P 21 21 21 | 8.4795; 18.0358; 21.5437 90; 90; 90 | 3294.78 | Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts Organic Chemistry Frontiers, 2019, 6, 1989 |
| 1554919 | CIF | C40 H31 Cl2 F4 N2 O3 | P 21 21 21 | 11.9726; 16.0021; 18.2529 90; 90; 90 | 3497.01 | Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts Organic Chemistry Frontiers, 2019, 6, 1989 |
| 1554920 | CIF | C21 H16 N2 O2 S | C 1 c 1 | 13.529; 16.7566; 8.6938 90; 116.175; 90 | 1768.8 | Lee, Dong Jin; Yoo, Eun Jeong Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions. Organic letters, 2015, 17, 1830-1833 |
| 1554921 | CIF | C24 H24 N2 O2 S | P 1 21/c 1 | 12.5268; 10.8502; 16.3904 90; 103.482; 90 | 2166.4 | Lee, Dong Jin; Yoo, Eun Jeong Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions. Organic letters, 2015, 17, 1830-1833 |
| 1554922 | CIF | C31 H28 N2 O5 | P n a 21 | 21.4324; 13.5256; 8.8733 90; 90; 90 | 2572.2 | Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes Organic Chemistry Frontiers, 2019, 6, 2415 |
| 1554923 | CIF | C30 H25 N3 O3 | P -1 | 8.9859; 10.004; 15.8029 97.57; 90.211; 115.564 | 1267.4 | Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes Organic Chemistry Frontiers, 2019, 6, 2415 |
| 1554924 | CIF | C19 H29 F N2 O5 Si | P 21 21 21 | 6.42; 8.0707; 40.1927 90; 90; 90 | 2082.54 | Istrate, Alena; Medvecky, Michal; Leumann, Christian J. 2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity. Organic letters, 2015, 17, 1950-1953 |
| 1554925 | CIF | C38 H31 Br Cl3 N3 O4 | P 21 21 21 | 9.1965; 9.694; 38.3086 90; 90; 90 | 3415.2 | Zhang, Jing; Chan, Wai-Lun; Chen, Ligong; Ullah, Nisar; Lu, Yixin Creation of bispiro[pyrazolone-3,3′-oxindoles] via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita–Baylis–Hillman carbonates with pyrazoloneyldiene oxindoles Organic Chemistry Frontiers, 2019, 6, 2210 |
| 1554926 | CIF | C19 H16 N2 O4 | P 1 21 1 | 7.5248; 11.7969; 18.7512 90; 98.035; 90 | 1648.2 | Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K. An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence. Organic letters, 2015, 17, 2102-2105 |
| 1554927 | CIF | C16 H18 O | R 3 :H | 20.961; 20.961; 7.086 90; 90; 120 | 2696.2 | Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F Organic Chemistry Frontiers, 2019, 6, 2771 |
| 1554928 | CIF | C27 H34 O3 Si | C 1 2/c 1 | 42.742; 10.4771; 10.9037 90; 93.609; 90 | 4873.1 | Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F Organic Chemistry Frontiers, 2019, 6, 2771 |
| 1554929 | CIF | C14 H18 O5 | P -1 | 7.3423; 8.4321; 10.4623 85.681; 85.985; 78.332 | 631.55 | Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F Organic Chemistry Frontiers, 2019, 6, 2771 |
| 1554930 | CIF | C16 H25 N O2 S3 | P 21 21 21 | 5.36225; 12.0412; 27.5363 90; 90; 90 | 1777.96 | Das, Manas; O'Shea, Donal F Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines. Organic letters, 2015, 17, 1962-1965 |
| 1554931 | CIF | C18 H19 N O4 S | P b c a | 17.4772; 10.488; 19.6463 90; 90; 90 | 3601.2 | Huang, Guofei; Ren, Xiaoyu; Jiang, Chunhui; Wu, Jia-Hong; Gao, Guowei; Wang, Tianli Efficient synthesis of (E)-2-nitromethylcinnamates via phosphine-catalyzed tandem α-addition and 1,3-rearrangement Organic Chemistry Frontiers, 2019, 6, 2872 |
| 1554932 | CIF | C18 H19 Cl F3 N O S | P 1 21 1 | 11.7646; 15.4251; 12.0356 90; 118.452; 90 | 1920.3 | Das, Manas; O'Shea, Donal F Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines. Organic letters, 2015, 17, 1962-1965 |
| 1554933 | CIF | C10 H8 N2 S | P n a 21 | 15.971; 4.2214; 13.319 90; 90; 90 | 898 | Peng, Yingyuan; He, Qian; Zhang, Xiaofei; Yang, Chunhao Pd-Catalyzed intramolecular C–H activation and C–S formation to synthesize pyrazolo[5,1-b]benzothiazoles without an additional oxidant Organic Chemistry Frontiers, 2019, 6, 3234 |
| 1554934 | CIF | C19 H23 Fe N O2 S | P 1 21 1 | 5.84461; 11.3132; 13.829 90; 95.4227; 90 | 910.298 | Das, Manas; O'Shea, Donal F Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines. Organic letters, 2015, 17, 1962-1965 |
| 1554935 | CIF | C23 H17 Cl O2 | P 1 21/m 1 | 9.353; 7.448; 12.251 90; 93.725; 90 | 851.6 | Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones. Organic letters, 2015, 17, 2134-2137 |
| 1554936 | CIF | C20 H21 N3 O4 | P 1 21/n 1 | 10.8238; 10.3557; 17.8199 90; 96.908; 90 | 1982.9 | Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates Organic Chemistry Frontiers, 2019, 6, 3321 |
| 1554937 | CIF | C133 H116 N8 O21 S4 | P 1 21 1 | 10.8299; 17.8426; 16.7462 90; 105.418; 90 | 3119.5 | Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals. Organic letters, 2015, 17, 2318-2321 |
| 1554938 | CIF | C20 H21 N3 O4 | P 42 b c | 21.7832; 21.7832; 8.49552 90; 90; 90 | 4031.19 | Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates Organic Chemistry Frontiers, 2019, 6, 3321 |
| 1554939 | CIF | C15 H13 N3 O2 | P -1 | 6.9944; 7.8586; 26.1858 85.696; 89.837; 79.658 | 1411.87 | Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates Organic Chemistry Frontiers, 2019, 6, 3321 |
| 1554940 | CIF | C22 H18 F3 N O3 | P 21 21 21 | 9.69927; 10.835; 16.94975 90; 90; 90 | 1781.28 | Rabasa-Alcañiz, Fernando; Hammerl, Daniel; Sánchez-Merino, Anabel; Tejero, Tomás; Merino, Pedro; Fustero, Santos; del Pozo, Carlos Asymmetric synthesis of polycyclic 3-fluoroalkylproline derivatives by intramolecular azomethine ylide cycloaddition Organic Chemistry Frontiers, 2019, 6, 2916 |
| 1554941 | CIF | C39 H30 Cl N O | P 1 21/n 1 | 14.7817; 10.4931; 20.1054 90; 110.04; 90 | 2929.66 | Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic letters, 2015, 17, 1986-1989 |
| 1554942 | CIF | C26 H20 Cu F6 P | P b c n | 15.5529; 7.3629; 19.8862 90; 90; 90 | 2277.26 | Liu, He; Shen, Qilong Bistrifluoromethylated organocuprate [Ph4P]+[Cu(CF3)2]−: synthesis, characterization and its application for trifluoromethylation of activated heteroaryl bromides, chlorides and iodides Organic Chemistry Frontiers, 2019, 6, 2324 |
| 1554943 | CIF | C20 H22 N2 O4 | P 1 21/c 1 | 10.5905; 16.0282; 11.3851 90; 116.637; 90 | 1727.47 | Yakkala, Prasanna Anjaneyulu; Giri, Deepesh; Chaudhary, Bharatkumar; Auti, Prashant; Sharma, Satyasheel Regioselective C–H alkylation and alkenylation at the C5 position of 2-amino-1,4-naphthoquinones with maleimides under Rh(iii) catalysis Organic Chemistry Frontiers, 2019, 6, 2441 |
| 1554944 | CIF | C24 H24 Cl N O | P 1 21/n 1 | 12.0241; 10.8634; 15.0306 90; 92.829; 90 | 1960.94 | Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic letters, 2015, 17, 1986-1989 |
| 1554945 | CIF | C17 H15 Br2 N O2 | P -1 | 7.5896; 10.9767; 11.9609 110.338; 100.049; 106.048 | 856.49 | Wang, Yu-Chao; Wang, Rui-Xiang; Qiu, Guanyinsheng; Zhou, Hongwei; Xie, Wenlin; Liu, Jin-Biao ortho-Amide-directed 2,4-dibromohydration of conjugated enynes Organic Chemistry Frontiers, 2019, 6, 2471 |
| 1554946 | CIF | C14 H12 N2 O | P -1 | 7.2536; 9.2341; 9.3515 85.065; 81.059; 68.355 | 574.85 | Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines Organic Chemistry Frontiers, 2019, 6, 2404 |
| 1554947 | CIF | C25 H15 N3 O | P 1 21/n 1 | 9.8811; 14.4238; 13.7948 90; 109.258; 90 | 1856.1 | Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines Organic Chemistry Frontiers, 2019, 6, 2404 |
| 1554948 | CIF | C24 H24 Cl N O | P 1 21/c 1 | 16.3879; 7.0026; 17.8667 90; 103.718; 90 | 1991.86 | Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic letters, 2015, 17, 1986-1989 |
| 1554949 | CIF | C25 H23 F2 N O3 S | P -1 | 8.0332; 8.5272; 16.9075 99.329; 99.436; 101.204 | 1097.99 | Hu, Xiao-Si; Ding, Pei-Gang; Yu, Jin-Sheng; Zhou, Jian A Sc(OTf)3 catalyzed Mukaiyama–Mannich reaction of difluoroenoxysilanes with unactivated ketimines Organic Chemistry Frontiers, 2019, 6, 2500 |
| 1554950 | CIF | C152.5 H199 B4 N7 O23 | P 1 21/c 1 | 11.705; 28.512; 22.406 90; 98.94; 90 | 7387 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554951 | CIF | C24 H24 O2 S2 | C 1 2 1 | 23.8323; 5.5909; 15.658 90; 103.617; 90 | 2027.7 | Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties Organic Chemistry Frontiers, 2019, 6, 2801 |
| 1554952 | CIF | C25 H25 N O2 S | P 21 21 21 | 6.07714; 13.1618; 27.1117 90; 90; 90 | 2168.56 | Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties Organic Chemistry Frontiers, 2019, 6, 2801 |
| 1554953 | CIF | C32 H30.52 O4.26 S | C 1 2/c 1 | 13.9336; 19.7182; 20.3209 90; 103.298; 90 | 5433.4 | Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties Organic Chemistry Frontiers, 2019, 6, 2801 |
| 1554954 | CIF | C27 H24 Fe O2 S | P b c a | 28.3482; 19.5347; 7.5873 90; 90; 90 | 4201.6 | Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties Organic Chemistry Frontiers, 2019, 6, 2801 |
| 1554955 | CIF | C50 H44 F24 N4 P4 | P 1 21/n 1 | 13.488; 14.281; 14.287 90; 108.36; 90 | 2611.9 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554956 | CIF | C186 H168 B4 N14 O31 | P -1 | 16.134; 16.609; 16.766 85.82; 65.15; 75.26 | 3939.7 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554957 | CIF | C27 H22 Cl N O5 S | P 21 21 21 | 10.1603; 10.173; 23.5179 90; 90; 90 | 2430.83 | Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes Organic Chemistry Frontiers, 2019, 6, 2452 |
| 1554958 | CIF | C27 H23 N O5 S | P 1 21 1 | 10.0757; 10.4448; 10.8094 90; 92.786; 90 | 1136.2 | Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes Organic Chemistry Frontiers, 2019, 6, 2452 |
| 1554959 | CIF | C117 H171 B4 N4 O20 | P 1 21/c 1 | 42.193; 8.356; 15.63 90; 90.76; 90 | 5510.1 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554960 | CIF | C180 H112 B4 D84 N4 O34 S14 | P -1 | 16.67; 17.44; 19.659 81.21; 74.06; 62.19 | 4859 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554961 | CIF | C30 H29 N O3 S | P 1 21/n 1 | 9.8296; 13.4413; 22.608 90; 94.433; 90 | 2978.1 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554962 | CIF | C20 H27 N O2 S | P 21 21 21 | 5.8832; 8.7875; 37.5443 90; 90; 90 | 1940.99 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554963 | CIF | C22 H29 N O2 S | P 21 21 21 | 8.87; 10.6671; 21.508 90; 90; 90 | 2035 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554964 | CIF | C19 H23 N O2 S | C 1 2/c 1 | 35.164; 8.6573; 11.5114 90; 94.241; 90 | 3494.8 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554965 | CIF | C23 H33 N O2 S | P 1 21/c 1 | 19.505; 8.6857; 13.1687 90; 92.309; 90 | 2229.2 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554966 | CIF | C21 H26 Br N O2 S | P 1 21 1 | 10.888; 8.651; 10.91 90; 97.5; 90 | 1018.8 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554967 | CIF | C18 H22 Br N O2 S | P 1 21/c 1 | 12.551; 11.012; 14.276 90; 113.904; 90 | 1803.9 | Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2019, 6, 2506 |
| 1554968 | CIF | C70 H56 N8 O8 | P -1 | 11.446; 13.451; 22.036 98.71; 104.3; 98.36 | 3189.9 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554969 | CIF | C32 H26 N4 O2 | C 1 2/c 1 | 16.098; 8.0852; 19.417 90; 103.12; 90 | 2461.3 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554970 | CIF | C17 H14 Cl | P -1 | 10.013; 12.073; 12.827 111.893; 107.027; 93.776 | 1348.7 | Fan, Xing; Liu, Ruixing; Wei, Yin; Shi, Min Rh-Catalyzed intramolecular decarbonylative cyclization of ortho-formyl group tethered alkylidenecyclopropanes (ACPs) for the construction of 2-methylindenes Organic Chemistry Frontiers, 2019, 6, 2667 |
| 1554971 | CIF | C34 H30 N4 O4 | P 1 21/c 1 | 7.3964; 23.302; 16.073 90; 94.05; 90 | 2763.3 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554972 | CIF | C20 H17 N O | P b c a | 14.5964; 13.9382; 14.6669 90; 90; 90 | 2983.94 | Hu, Xiaoping; Wang, Gaonan; Qin, Chunxiang; Xie, Xin; Zhang, Chunli; Xu, Wei; Liu, Yuanhong Ligandless nickel-catalyzed transfer hydrogenation of alkenes and alkynes using water as the hydrogen donor Organic Chemistry Frontiers, 2019, 6, 2619 |
| 1554973 | CIF | C70 H58 Cl6 N8 O12 S | C 1 c 1 | 37.78; 8.9173; 26.953 90; 133.41; 90 | 6596 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554974 | CIF | C30 H27 N3 | P 1 21/n 1 | 14.929; 5.74297; 27.7627 90; 104.785; 90 | 2301.48 | Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons Organic Chemistry Frontiers, 2019, 6, 3071 |
| 1554975 | CIF | C17 H16 N2 | P 1 21/c 1 | 15.534; 6.291; 15.0837 90; 113.849; 90 | 1348.18 | Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons Organic Chemistry Frontiers, 2019, 6, 3071 |
| 1554976 | CIF | C15 H13 N3 | P c a 21 | 12.9687; 13.0705; 7.18 90; 90; 90 | 1217.06 | Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons Organic Chemistry Frontiers, 2019, 6, 3071 |
| 1554977 | CIF | C22 H17 N3 | P -1 | 8.8058; 10.1568; 10.8636 112.118; 90.659; 106.96 | 852.87 | Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons Organic Chemistry Frontiers, 2019, 6, 3071 |
| 1554978 | CIF | C16 H10 Br N O4 | P 1 21/c 1 | 12.4447; 15.6502; 7.9646 90; 105.739; 90 | 1493 | Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides. Organic letters, 2015, 17, 2010-2013 |
| 1554979 | CIF | C30 H24 F2 O5 | P 1 21/n 1 | 14.1655; 22.469; 16.419 90; 98.419; 90 | 5169.6 | Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling Organic Chemistry Frontiers, 2019, 6, 2788 |
| 1554980 | CIF | C15 H12 F O3 | P -1 | 9.9135; 11.2232; 13.3885 94.007; 107.02; 109.916 | 1315.15 | Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling Organic Chemistry Frontiers, 2019, 6, 2788 |
| 1554981 | CIF | C70 H120 N14 O26 S8 | P -1 | 13.0106; 13.1402; 14.3888 80.344; 63.999; 78.993 | 2160.42 | Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail New "pyrene box" cages for adaptive guest conformations. Organic letters, 2015, 17, 2178-2181 |
| 1554982 | CIF | C30 H60 N12 O16 S4 | C 1 2/c 1 | 13.4741; 14.6965; 22.6791 90; 92.704; 90 | 4485.96 | Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail New "pyrene box" cages for adaptive guest conformations. Organic letters, 2015, 17, 2178-2181 |
| 1554983 | CIF | C19 H19 B11 Cl6 O | P 1 21/c 1 | 17.251; 12.1706; 26.112 90; 91.879; 90 | 5479.4 | Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Peraryl-X-onium ions of nitrogen and oxygen Organic Chemistry Frontiers, 2019, 6, 2640 |
| 1554984 | CIF | C20 H21 B11 Cl6 O | P b c a | 19.0146; 13.8372; 21.2518 90; 90; 90 | 5591.5 | Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Peraryl-X-onium ions of nitrogen and oxygen Organic Chemistry Frontiers, 2019, 6, 2640 |
| 1554985 | CIF | C25 H22 B11 Cl6 N | P b c n | 18.70332; 18.4574; 18.4002 90; 90; 90 | 6352.02 | Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Peraryl-X-onium ions of nitrogen and oxygen Organic Chemistry Frontiers, 2019, 6, 2640 |
| 1554986 | CIF | C25 H22 B11 Cl6 N | P b c n | 18.015; 14.8013; 23.3476 90; 90; 90 | 6225.53 | Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Peraryl-X-onium ions of nitrogen and oxygen Organic Chemistry Frontiers, 2019, 6, 2640 |
| 1554987 | CIF | C25 H24 B11 Cl6 N | P 1 21/c 1 | 31.445; 13.6072; 32.634 90; 116.666; 90 | 12478.2 | Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Peraryl-X-onium ions of nitrogen and oxygen Organic Chemistry Frontiers, 2019, 6, 2640 |
| 1554988 | CIF | C40 H69.97 N4 O14 S4 | P -1 | 11.2634; 15.966; 16.009 111.587; 100.691; 109.004 | 2373.6 | Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail New "pyrene box" cages for adaptive guest conformations. Organic letters, 2015, 17, 2178-2181 |
| 1554989 | CIF | C27 H24 N4 O4 S2 | P 1 21/n 1 | 9.943; 19.423; 27.408 90; 94.84; 90 | 5274.24 | Wang, Lihong; Wang, Xiaomin; Zhang, Ge; Yang, Shengbiao; Li, Yan; Zhang, Qian Copper-catalyzed 1,3-aminoazidation of arylcyclopropanes: a facile access to 1,3-diamine derivatives Organic Chemistry Frontiers, 2019, 6, 2934 |
| 1554990 | CIF | C15 H13 N O4 S | P 21 21 21 | 8.1609; 9.0398; 19.318 90; 90; 90 | 1425.1 | Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions. Organic letters, 2015, 17, 2022-2025 |
| 1554991 | CIF | C13 H11 N O3 | P 1 21/c 1 | 9.4606; 8.7844; 13.698 90; 91.45; 90 | 1138 | Sun, Yao-Liang; Wei, Yin; Shi, Min Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion Organic Chemistry Frontiers, 2019, 6, 2420 |
| 1554992 | CIF | C15 H13 N O3 | P 21 21 21 | 5.2776; 10.8907; 22.1326 90; 90; 90 | 1272.11 | Sun, Yao-Liang; Wei, Yin; Shi, Min Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion Organic Chemistry Frontiers, 2019, 6, 2420 |
| 1554993 | CIF | C14 H11 N O5 | P 1 21/c 1 | 11.0859; 9.2256; 12.6525 90; 101.245; 90 | 1269.2 | Sun, Yao-Liang; Wei, Yin; Shi, Min Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion Organic Chemistry Frontiers, 2019, 6, 2420 |
| 1554994 | CIF | C28 H23 N3 O4 S | P 1 21/n 1 | 12.8623; 11.3355; 16.9579 90; 94.493; 90 | 2464.87 | Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines. Organic letters, 2015, 17, 2214-2217 |
| 1554995 | CIF | C23 H18 Cl N O2 | P -1 | 9.2832; 10.0044; 11.107 87.027; 65.546; 82.335 | 930.61 | Yao, Yongqi; Yang, Wen; Lin, Qifu; Yang, Weitao; Li, Huanyong; Wang, Lin; Gu, Fenglong; Yang, Dingqiao 1,3-Dipolar cycloaddition of nitrones to oxa(aza)bicyclic alkenes Organic Chemistry Frontiers, 2019, 6, 3360 |
| 1554996 | CIF | C19 H22 O7 | P 1 21/n 1 | 6.0808; 23.3393; 12.5225 90; 94.028; 90 | 1772.82 | Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I. Organic letters, 2015, 17, 2338-2341 |
| 1554997 | CIF | C21 H18 N4 O4 S | P 21 21 21 | 6.0211; 16.1241; 20.634 90; 90; 90 | 2003.25 | Li, Shi-Wu; Du, Yu; Kang, Qiang A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis Organic Chemistry Frontiers, 2019, 6, 2775 |
| 1554998 | CIF | C26 H31 Br N2 O3 | P -1 | 9.6121; 11.761; 13.648 98.331; 109.571; 113.637 | 1260.2 | Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts. Organic letters, 2015, 17, 2234-2237 |
| 1554999 | CIF | C40 H32 O6 | P -1 | 10.438; 10.7; 15.172 80.197; 70.129; 79.638 | 1556.7 | Wang, Wenli; Tang, Yingzhan; Liu, Yongxiang; Yuan, Lei; Wang, Jian; Lin, Bin; Zhou, Di; Sun, Lu; Huang, Renbin; Chen, Gang; Li, Ning Isolation, structure elucidation, and synthesis of (±)-millpuline A with a suppressive effect in miR-144 expression Organic Chemistry Frontiers, 2019, 6, 2850 |
| 1555000 | CIF | C38 H44 B2 F4 N4 O6 | P -1 | 9.7881; 13.2333; 16.5195 67.596; 77.669; 72.069 | 1870.86 | Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts. Organic letters, 2015, 17, 2246-2249 |
| 1555001 | CIF | C44 H40 N4 Ni O2 | P 1 21/c 1 | 19.861; 13.383; 18.29 90; 117.363; 90 | 4318 | Ren, Demin; Fu, Xinliang; Li, Xiaofang; Koniarz, Sebastian; Chmielewski, Piotr J. Reaction of antiaromatic porphyrinoid with active methylene compounds Organic Chemistry Frontiers, 2019, 6, 2924 |
| 1555002 | CIF | C15 H16 N2 O4 | P 1 21/c 1 | 14.1112; 4.6513; 21.124 90; 99.827; 90 | 1366.14 | Mei, Xiangui; Lan, Mengmeng; Cui, Guodong; Zhang, Hongwei; Zhu, Weiming Caerulomycins from Actinoalloteichus cyanogriseus WH1-2216-6: isolation, identification and cytotoxicity Organic Chemistry Frontiers, 2019, 6, 3566 |
| 1555003 | CIF | C27 H30 F N O2 | P -1 | 9.3088; 9.5092; 14.5742 92.724; 104.673; 110 | 1159.92 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555004 | CIF | C28 H32 F N O2 | P 21 21 21 | 8.03153; 10.686; 28.3689 90; 90; 90 | 2434.76 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555005 | CIF | C28 H32 N4 O2 | P 32 2 1 | 11.32263; 11.32263; 35.383 90; 90; 120 | 3928.44 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555006 | CIF | C30 H35 N O4 | P 1 | 9.7073; 10.168; 14.0374 85.597; 85.998; 82.306 | 1366.53 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555007 | CIF | C28 H31 F2 N O2 | P 1 | 10.4764; 10.6867; 12.3768 85.757; 70.552; 69.477 | 1222.26 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555008 | CIF | C28 H31 F2 N O2 | P 1 21 1 | 7.90952; 16.3522; 9.53794 90; 95.6737; 90 | 1227.58 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555009 | CIF | C24 H20 O S | P 1 21/n 1 | 15.8263; 7.7607; 15.9189 90; 106.393; 90 | 1875.73 | Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones Organic Chemistry Frontiers, 2019, 6, 2796 |
| 1555010 | CIF | C22 H14 Cl F O S | P -1 | 7.3464; 8.5371; 15.0907 95.337; 91.518; 104.361 | 911.69 | Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones Organic Chemistry Frontiers, 2019, 6, 2796 |
| 1555011 | CIF | C23 H27 Br N2 O5 | P 1 21/n 1 | 8.3956; 11.6027; 23.715 90; 91.1454; 90 | 2309.7 | Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines. Organic letters, 2015, 17, 2416-2419 |
| 1555012 | CIF | C8 H11 F3 N2 O S | P 1 21/c 1 | 8.4044; 11.3774; 11.5451 90; 96.16; 90 | 1097.6 | Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates. Organic letters, 2015, 17, 2438-2441 |
| 1555013 | CIF | C147 H132 N16 O27 Zn | P 1 21/a 1 | 23.94; 28.05; 23.991 90; 119.85; 90 | 13973 | Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms Organic Chemistry Frontiers, 2019, 6, 3192 |
| 1555014 | CIF | C38 H32 N2 O6 | P 1 21/n 1 | 12.6219; 16.3765; 16.6547 90; 100.607; 90 | 3383.7 | Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms Organic Chemistry Frontiers, 2019, 6, 3192 |
| 1555015 | CIF | C15 H16 O3 | P 1 21/n 1 | 4.6619; 23.4349; 12.2946 90; 97.466; 90 | 1331.8 | Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms Organic Chemistry Frontiers, 2019, 6, 3192 |
| 1555016 | CIF | C152 H128 N8 O24 Zn | P -1 | 12.8844; 13.9073; 20.6328 98.862; 106.525; 94.899 | 3469.4 | Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms Organic Chemistry Frontiers, 2019, 6, 3192 |
| 1555017 | CIF | C36 H30 N4 O6 | P 1 21/n 1 | 12.8709; 15.6947; 16.5272 90; 92.507; 90 | 3335.38 | Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms Organic Chemistry Frontiers, 2019, 6, 3192 |
| 1555018 | CIF | C76 H112 F14 N4 Sn4 | P -1 | 10.7975; 11.121; 17.986 82.945; 76.059; 70.925 | 1978.74 | Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H. Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives. Organic letters, 2015, 17, 2266-2269 |
| 1555019 | CIF | C32 H4 F26 N4 | P -1 | 6.15317; 9.3804; 13.8177 103.878; 100.265; 98.23 | 747.31 | Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H. Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives. Organic letters, 2015, 17, 2266-2269 |
| 1555020 | CIF | C26 H18 O | C 1 2/c 1 | 42.263; 7.4986; 12.0012 90; 93.813; 90 | 3794.9 | Han, Jian; Liu, Xinbang; Li, Yu; Lou, Zihao; Yi, Mingdong; Kong, Huihui; Luo, Jun New synthetic approaches for hexacene and its application in thin-film transistors Organic Chemistry Frontiers, 2019, 6, 2839 |
| 1555021 | CIF | C19 H18 O2 | P n a 21 | 12.91; 9.664; 12.157 90; 90; 90 | 1516.7 | Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J. Michael Additions of Highly Basic Enolates to ortho-Quinone Methides. Organic letters, 2015, 17, 2278-2281 |
| 1555022 | CIF | C17 H22 O2 | P 21 21 21 | 8.6511; 11.009; 15.784 90; 90; 90 | 1503.3 | Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J. Michael Additions of Highly Basic Enolates to ortho-Quinone Methides. Organic letters, 2015, 17, 2278-2281 |
| 1555023 | CIF | C24 H17 N O2 | P -1 | 11.0804; 12.2799; 13.6018 75.764; 84.604; 89.194 | 1785.88 | Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes Organic Chemistry Frontiers, 2019, 6, 2897 |
| 1555024 | CIF | C24 H17 N O2 | P 1 21/c 1 | 8.5534; 5.4976; 37.5979 90; 93.982; 90 | 1763.7 | Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes Organic Chemistry Frontiers, 2019, 6, 2897 |
| 1555025 | CIF | C26 H18 F3 N O2 | P -1 | 6.4787; 10.7989; 16.2052 79.201; 85.566; 73.057 | 1065.03 | Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes Organic Chemistry Frontiers, 2019, 6, 2897 |
| 1555026 | CIF | C22 H21 N O3 | P -1 | 9.724; 10.178; 10.676 62.165; 79.328; 69.089 | 872.6 | Capreti, Naylil M. R.; Jurberg, Igor D. Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds. Organic letters, 2015, 17, 2490-2493 |
| 1555027 | CIF | C28 H22 O3 S | P 1 21/c 1 | 10.465; 9.797; 22.032 90; 95.834; 90 | 2247.1 | Yang, Tao; Kou, Peihao; Jin, Fengyan; Song, Xian-Rong; Bai, Jiang; Ding, Haixin; Xiao, Qiang; Liang, Yong-Min TFA-promoted sulfonation/cascade cyclization of 2-propynolphenols with sodium sulfinates to 4-sulfonyl 2H-chromenes under metal-free conditions Organic Chemistry Frontiers, 2019, 6, 3162 |
| 1555028 | CIF | C15 H13 N O | R -3 :H | 26.4383; 26.4383; 8.6956 90; 90; 120 | 5263.8 | Zhang, Yan; Wang, Dahai; Cui, Sunliang Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines. Organic letters, 2015, 17, 2494-2497 |
| 1555029 | CIF | C17 H15 N O3 S | P 1 21/n 1 | 5.9669; 11.4767; 21.9463 90; 96.78; 90 | 1492.38 | Zhu, Cheng-Zhi; Wei, Yin; Shi, Min Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives Organic Chemistry Frontiers, 2019, 6, 2884 |
| 1555030 | CIF | C21 H16 Br N O4 S | P -1 | 7.1629; 10.9804; 12.5285 102.431; 97.658; 98.768 | 936.85 | Zhu, Cheng-Zhi; Wei, Yin; Shi, Min Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives Organic Chemistry Frontiers, 2019, 6, 2884 |
| 1555031 | CIF | C36 H39 N O2 | P 1 21/c 1 | 14.8225; 11.0736; 18.657 90; 100.056; 90 | 3015.3 | Reddy, Virsinha; Vijaya Anand, Ramasamy Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach. Organic letters, 2015, 17, 3390-3393 |
| 1555032 | CIF | C27 H20 N2 O4 S | P -1 | 9.0601; 9.927; 13.5869 82.759; 78.19; 83.39 | 1181.56 | Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides Organic Chemistry Frontiers, 2019, 6, 2968 |
| 1555033 | CIF | C29.25 H25.5 Cl0.5 N3 O6 S2 | P 1 21/c 1 | 12.7222; 31.291; 7.7018 90; 104.211; 90 | 2972.2 | Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides Organic Chemistry Frontiers, 2019, 6, 2968 |
| 1555034 | CIF | C25 H27 Fe N O3 S | P 1 21 1 | 15.0789; 8.6357; 18.2167 90; 106.122; 90 | 2278.8 | Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library. Organic letters, 2015, 17, 2286-2289 |
| 1555035 | CIF | C88 H73 Cl10 N3 Pd | C 1 2/c 1 | 17.9223; 20.5932; 21.0729 90; 100.834; 90 | 7638.9 | Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination Organic Chemistry Frontiers, 2019, 6, 3292 |
| 1555036 | CIF | C84 H65 Cl2 N3 O2 Pd | C 1 2/c 1 | 17.6466; 20.7167; 20.3473 90; 95.896; 90 | 7399.2 | Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination Organic Chemistry Frontiers, 2019, 6, 3292 |
| 1555037 | CIF | C17 H14 N2 O3 | P 1 21/c 1 | 8.9224; 9.3813; 18.2533 90; 103.064; 90 | 1488.32 | Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid. Organic letters, 2015, 17, 2518-2521 |
| 1555038 | CIF | C9 H13 N5 O4 | P 1 21/c 1 | 8.3117; 17.2043; 8.3018 90; 103.231; 90 | 1155.62 | Guo, Xiaowei; Wang, Jidong; Su, Can; Liu, Chongxi; Ma, Xiao-Yan; Yu, Zhiyin; Li, Jiansong; Wang, Xiangjing; Xiang, Wensheng; Huang, Sheng-Xiong A unique spiro-β-triazinedione-γ-hydantoin type alkaloid with antiviral activity against tobacco mosaic virus from Streptomyces gamaensis Organic Chemistry Frontiers, 2019, 6, 3215 |
| 1555039 | CIF | C26 H28 O5 | P -1 | 10.896; 11.118; 11.442 109.812; 100.766; 111.223 | 1137.4 | Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products. Organic letters, 2015, 17, 3446-3449 |
| 1555040 | CIF | C23 H25 N O9 S | P -1 | 9.3448; 11.2047; 12.9889 106.439; 97.223; 112.631 | 1160.92 | Xing, Siyang; Xia, Hanyu; Wang, Xin; Wu, Die; Xu, Xinrui; Su, Yunran; Wang, Kui; Zhu, Bolin; Guo, Junshuo Diastereoselective access to 2-aminoindanones via the rhodium(ii)-catalyzed tandem reaction involving O–H insertion and Michael addition Organic Chemistry Frontiers, 2019, 6, 3121 |
| 1555041 | CIF | C23 H24 O3 | P -1 | 8.428; 11.011; 11.459 65.415; 87.993; 89.668 | 966.4 | Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products. Organic letters, 2015, 17, 3446-3449 |
| 1555042 | CIF | C33 H38 N O5 | P 1 | 9.1302; 9.1578; 10.226 108.986; 98.417; 114.037 | 698.83 | Freeman, Jared L.; Brimble, Margaret A.; Furkert, Daniel P. A chiral auxiliary-based synthesis of the C5‒C17 trans-decalin framework of anthracimycin Organic Chemistry Frontiers, 2019, 6, 2954 |
| 1555043 | CIF | C25 H28 O10 | I 1 2 1 | 11.9189; 6.5987; 26.7335 90; 100.124; 90 | 2069.83 | Pan, Dongyan; Zhang, Xuexia; Zheng, Haizhou; Zheng, Zhihui; Nong, Xuhua; Liang, Xiao; Ma, Xuan; Qi, Shuhua Novel anthraquinone derivatives as inhibitors of protein tyrosine phosphatases and indoleamine 2,3-dioxygenase 1 from the deep-sea derived fungus Alternaria tenuissima DFFSCS013 Organic Chemistry Frontiers, 2019, 6, 3252 |
| 1555044 | CIF | C21 H36 O4 Si | C 1 2 1 | 22.265; 7.7011; 12.8529 90; 102.095; 90 | 2154.9 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555045 | CIF | C12 H14 O3 | P 1 21/c 1 | 12.324; 7.8713; 10.6532 90; 92.217; 90 | 1032.65 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555046 | CIF | C23 H20 O6 | P -1 | 7.7957; 10.1827; 12.7574 79.033; 76.634; 77.369 | 950.96 | Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate Organic Chemistry Frontiers, 2019, 6, 3238 |
| 1555047 | CIF | C16 H11 Br O2 | P 1 21/c 1 | 10.0036; 15.567; 8.7599 90; 100.953; 90 | 1339.3 | Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate Organic Chemistry Frontiers, 2019, 6, 3238 |
| 1555048 | CIF | C16 H12 O2 | C 1 2/c 1 | 25.676; 4.1792; 24.335 90; 112.38; 90 | 2414.6 | Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate Organic Chemistry Frontiers, 2019, 6, 3238 |
| 1555049 | CIF | C23 H22 O6 | P 1 21/c 1 | 14.7414; 8.7416; 16.409 90; 104.242; 90 | 2049.53 | Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate Organic Chemistry Frontiers, 2019, 6, 3238 |
| 1555050 | CIF | C22 H17 Cl O6 | P 1 21/n 1 | 14.6483; 17.4042; 15.2455 90; 94.817; 90 | 3872.99 | Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate Organic Chemistry Frontiers, 2019, 6, 3238 |
| 1555051 | CIF | C36 H55 N O7 Si2 | P -1 | 8.9128; 10.9914; 20.184 91.339; 96.624; 104.357 | 1899.99 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555052 | CIF | C15 H20 O5 | P 21 21 21 | 7.3936; 10.5735; 17.817 90; 90; 90 | 1392.9 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555053 | CIF | C21 H38 O5 S | P 1 21/c 1 | 16.4753; 10.1532; 13.8282 90; 98.669; 90 | 2286.71 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555054 | CIF | C21 H22 O10 | P 1 21/c 1 | 8.8935; 14.433; 15.7451 90; 92.016; 90 | 2019.79 | Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui Canescones A‒E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens Organic Chemistry Frontiers, 2019, 6, 3274 |
| 1555055 | CIF | C20 H20 O10 | P -1 | 9.016; 9.3778; 10.636 93.717; 90.826; 92.317 | 896.52 | Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens Organic Chemistry Frontiers, 2019, 6, 3274 |
| 1555056 | CIF | C21 H22 O11 | P c a 21 | 8.33914; 13.29606; 18.06836 90; 90; 90 | 2003.38 | Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens Organic Chemistry Frontiers, 2019, 6, 3274 |
| 1555057 | CIF | C21 H22 O11 | P 21 21 21 | 8.2302; 14.4554; 16.2394 90; 90; 90 | 1932.01 | Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens Organic Chemistry Frontiers, 2019, 6, 3274 |
| 1555058 | CIF | C22 H23 N O9 | P 1 21/n 1 | 8.26703; 13.79202; 17.73644 90; 102.392; 90 | 1975.18 | Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens Organic Chemistry Frontiers, 2019, 6, 3274 |
| 1555059 | CIF | C15 H22 O6 | P 1 21/n 1 | 8.5281; 18.7862; 9.5185 90; 100.368; 90 | 1500.07 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555060 | CIF | C16 H17 N O4 | P 1 21 1 | 6.9082; 11.2913; 19.3834 90; 91.357; 90 | 1511.53 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555061 | CIF | C34 H22 Cl2 N4 O4 | P b c a | 10.6177; 21.038; 26.249 90; 90; 90 | 5863.4 | Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes. Organic letters, 2015, 17, 3494-3497 |
| 1555062 | CIF | C23 H19 F3 | P 1 21/c 1 | 10.7304; 18.6098; 9.9301 90; 115.595; 90 | 1788.36 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555063 | CIF | C24 H21 F3 O2 | P -1 | 9.28774; 13.98378; 16.25245 94.589; 106.279; 98.2135 | 1989.34 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555064 | CIF | C24 H20 F4 O2 | P 1 21/n 1 | 8.7646; 10.6788; 20.8962 90; 94.821; 90 | 1948.87 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555065 | CIF | C24 H21 F3 | P -1 | 9.7671; 10.3099; 19.8876 92.41; 96.248; 107.45 | 1893.23 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555066 | CIF | C24 H21 F3 O2 | P -1 | 8.8501; 10.1181; 11.7209 98.214; 105.322; 103.258 | 961.85 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555067 | CIF | C23 H19 F3 O | P -1 | 9.9918; 10.2089; 10.5751 91.174; 116.274; 107.926 | 904.65 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555068 | CIF | C24 H21 F3 | P -1 | 8.9463; 10.2875; 11.0964 70.184; 86.437; 76.947 | 935.84 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555069 | CIF | C24 H20 Cl F3 O2 | P -1 | 9.0216; 9.9831; 11.9107 77.527; 82.086; 74.544 | 1005.86 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555070 | CIF | C25 H23 F3 | P 1 21/c 1 | 10.5544; 15.4584; 12.2743 90; 102.702; 90 | 1953.59 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555071 | CIF | C24 H21 F3 | P 1 21/n 1 | 11.6641; 9.1396; 17.3076 90; 95.883; 90 | 1835.36 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555072 | CIF | C22 H16 Br F3 | P -1 | 9.02917; 9.25385; 11.1048 87.5911; 80.5904; 78.3143 | 896.36 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555073 | CIF | C24 H19 Cl2 F3 O2 | P -1 | 9.2224; 10.2968; 11.9735 74.791; 80.463; 72.449 | 1041.48 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555074 | CIF | C22 H15 Cl2 F3 | I 1 2/c 1 | 21.8668; 10.36934; 18.0539 90; 113.947; 90 | 3741.25 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555075 | CIF | C24 H21 F3 | P 1 21/c 1 | 10.1714; 36.8462; 10.1929 90; 103.732; 90 | 3710.88 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555076 | CIF | C25 H23 F3 O2 | P 1 21/c 1 | 11.5733; 18.729; 19.4741 90; 105.635; 90 | 4064.94 | Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V. TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes Organic Chemistry Frontiers, 2019, 6, 3264 |
| 1555077 | CIF | C30 H22 Cl2 N4 O12 | P 43 | 10.6627; 10.6627; 29.5381 90; 90; 90 | 3358.3 | Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes. Organic letters, 2015, 17, 3494-3497 |
| 1555078 | CIF | C29 H20 I4 O4 | P -1 | 12.1779; 21.8512; 21.9539 60.52; 87.603; 86.921 | 5077.5 | Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes. Organic letters, 2015, 17, 3494-3497 |
| 1555079 | CIF | C16 H13 N O3 | P 1 c 1 | 14.099; 5.2916; 9.1495 90; 101.496; 90 | 668.92 | He, Guangke; Li, Yuan; Yu, Zilun; Chen, Zhaoqiang; Tang, Yongming; Song, Guangliang; Loh, Teck-Peng Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones Organic Chemistry Frontiers, 2019, 6, 3644 |
| 1555080 | CIF | C38 H26 Cl2 O4 | P 1 21/c 1 | 13.2235; 24.195; 10.2868 90; 110.556; 90 | 3081.6 | Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes. Organic letters, 2015, 17, 3494-3497 |
| 1555081 | CIF | C17 H12 I N3 S | P 1 21/n 1 | 4.12; 14.2279; 26.763 90; 94.268; 90 | 1564.5 | Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals Organic Chemistry Frontiers, 2019, 6, 3355 |
| 1555082 | CIF | C19 H17 N O S2 | P b c a | 10.1327; 12.0719; 28.967 90; 90; 90 | 3543.3 | Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals Organic Chemistry Frontiers, 2019, 6, 3355 |
| 1555083 | CIF | C19 H21 N O4 S | P 1 21/n 1 | 8.2569; 11.0688; 20.1396 90; 95.9683; 90 | 1830.66 | Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters. Organic letters, 2015, 17, 3498-3501 |
| 1555084 | CIF | C26 H16 F9 N O4 | P 1 21/c 1 | 6.1329; 40.065; 10.6098 90; 103.811; 90 | 2531.6 | He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers Organic Chemistry Frontiers, 2019, 6, 3575 |
| 1555085 | CIF | C19 H12 Cl F9 O | P c a 21 | 11.543; 10.4; 32.618 90; 90; 90 | 3916 | He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers Organic Chemistry Frontiers, 2019, 6, 3575 |
| 1555086 | CIF | C27 H27 N O5 S | P 1 21/n 1 | 10.98; 21.409; 11.347 90; 104.07; 90 | 2587.3 | Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters. Organic letters, 2015, 17, 3498-3501 |
| 1555087 | CIF | C10 H9 F3 N2 O | P 21 21 21 | 7.1385; 7.5039; 19.126 90; 90; 90 | 1024.5 | Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng An enantioselective aza-Henry reaction of trifluoromethyl ketimines catalyzed by phase-transfer catalysts Organic Chemistry Frontiers, 2019, 6, 3269 |
| 1555088 | CIF | C26 H20 Cl F3 N2 O2 | C 1 c 1 | 7.2179; 17.509; 18.867 90; 100.172; 90 | 2346.9 | Yu, Yang; Zhang, Yan; Wang, Zhuo; Liang, Yong-Xin; Zhao, Yu-Long A rhodium-catalyzed three-component reaction of arylisocyanides, trifluorodiazoethane, and activated methylene isocyanides or azomethine ylides: an efficient synthesis of trifluoroethyl-substituted imidazoles Organic Chemistry Frontiers, 2019, 6, 3657 |
| 1555089 | CIF | C38 H34 P2 | P -1 | 8.6263; 12.097; 16.023 107.86; 95.73; 104.279 | 1514.1 | Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes. Organic letters, 2015, 17, 3518-3520 |
| 1555090 | CIF | C32 H32 O P2 | P 1 21/c 1 | 14.7596; 10.4392; 17.7877 90; 105.924; 90 | 2635.5 | Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes. Organic letters, 2015, 17, 3518-3520 |
| 1555091 | CIF | C18 H23 N O2 | P 1 21/c 1 | 12.58; 15.83; 8.839 90; 109.551; 90 | 1658.7 | Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate. Organic letters, 2015, 17, 3544-3547 |
| 1555092 | CIF | C46 H40 O8 | P 1 21/n 1 | 10.1647; 17.2468; 20.8692 90; 101.136; 90 | 3589.7 | Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan Constructing bridged multifunctional calixarenes by intramolecular indole coupling Organic Chemistry Frontiers, 2019, 6, 3327 |
| 1555093 | CIF | C72 H64 N10 O6 | P 1 21/c 1 | 16.5782; 28.2895; 17.3002 90; 93.414; 90 | 8099.2 | Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan Constructing bridged multifunctional calixarenes by intramolecular indole coupling Organic Chemistry Frontiers, 2019, 6, 3327 |
| 1555094 | CIF | C76 H68 N8 O8 | C 1 2/c 1 | 30.104; 23.487; 26.09 90; 121.557; 90 | 15719 | Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan Constructing bridged multifunctional calixarenes by intramolecular indole coupling Organic Chemistry Frontiers, 2019, 6, 3327 |
| 1555095 | CIF | C19 H16 O2 | C 1 2 1 | 17.095; 5.874; 15.476 90; 106; 90 | 1493.8 | Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate. Organic letters, 2015, 17, 3544-3547 |
| 1555096 | CIF | C21 H13 Cl I3 N O2 | P -1 | 8.885; 11.599; 11.638 87.07; 72.279; 76.183 | 1109.11 | Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC. Organic letters, 2015, 17, 3576-3579 |
| 1555097 | CIF | C18 H14 Cl N3 | P 1 21/n 1 | 14.445; 6.6377; 15.6545 90; 94.414; 90 | 1496.53 | Surendra Reddy, G.; Ramachary, Dhevalapally B. Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles Organic Chemistry Frontiers, 2019, 6, 3620 |
| 1555098 | CIF | C23 H16 N4 | C 1 c 1 | 13.055; 13.601; 10.697 90; 100.788; 90 | 1865.8 | Surendra Reddy, G.; Ramachary, Dhevalapally B. Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles Organic Chemistry Frontiers, 2019, 6, 3620 |
| 1555099 | CIF | C23 H14 F N3 O2 | P -1 | 9.293; 13.946; 16.068 114.567; 99.86; 93.392 | 1846.1 | Surendra Reddy, G.; Ramachary, Dhevalapally B. Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles Organic Chemistry Frontiers, 2019, 6, 3620 |
| 1555100 | CIF | C21 H15 Cl I N O2 | P 1 21/n 1 | 11.057; 13.631; 13.716 90; 110.38; 90 | 1937.8 | Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC. Organic letters, 2015, 17, 3576-3579 |
| 1555101 | CIF | C25 H22 F N O5 | P 21 21 21 | 8.9187; 14.6101; 16.5218 90; 90; 90 | 2152.8 | Bhattacharya, Aditya; mani Shukla, Pushpendra; Kumar Kaushik, Lalit; Maji, Biswajit Synthesis of chromans and kinetic resolution of 2-aryl-3-nitro-2H-chromenes via the NHC-bound azolium homoenolate pathway Organic Chemistry Frontiers, 2019, 6, 3523 |
| 1555102 | CIF | C22 H22 O | P -1 | 9.1622; 9.508; 10.568 83; 65.519; 78.417 | 820 | Manojveer, Seetharaman; Balamurugan, Rengarajan In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes. Organic letters, 2015, 17, 3600-3603 |
| 1555103 | CIF | C22 H21 N O3 S | C 1 2/c 1 | 19.5977; 8.1238; 23.2996 90; 90.182; 90 | 3709.5 | Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles Organic Chemistry Frontiers, 2019, 6, 3415 |
| 1555104 | CIF | C23 H22 Br3 Cl2 N O3 S | P -1 | 8.199; 11.3055; 14.2419 100.441; 100.282; 91.136 | 1275.6 | Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles Organic Chemistry Frontiers, 2019, 6, 3415 |
| 1555105 | CIF | C8 H10 O4 | P c a 21 | 10.571; 5.838; 12.338 90; 90; 90 | 761.4 | Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks. Organic letters, 2015, 17, 3604-3607 |
| 1555106 | CIF | C12 H14 O6 | F d d 2 | 37.2102; 18.06; 6.8155 90; 90; 90 | 4580.1 | Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks. Organic letters, 2015, 17, 3604-3607 |
| 1555107 | CIF | C10 H12 O3 | P b c a | 8.8394; 8.5924; 23.437 90; 90; 90 | 1780.1 | Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks. Organic letters, 2015, 17, 3604-3607 |
| 1555108 | CIF | C9 H12 O4 | P 21 21 21 | 6.345; 8.9881; 15.108 90; 90; 90 | 861.6 | Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks. Organic letters, 2015, 17, 3604-3607 |
| 1555109 | CIF | C8 H10 O4 | P 1 21 1 | 5.3883; 12.812; 6.0438 90; 114.32; 90 | 380.21 | Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks. Organic letters, 2015, 17, 3604-3607 |
| 1555110 | CIF | C26 H20 O3 S | P 21 21 21 | 7.9759; 16.1628; 31.7213 90; 90; 90 | 4089.3 | Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds Organic Chemistry Frontiers, 2019, 6, 3259 |
| 1555111 | CIF | C27 H21 N O3 S | P 21 21 21 | 5.7472; 16.912; 22.0104 90; 90; 90 | 2139.34 | Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds Organic Chemistry Frontiers, 2019, 6, 3259 |
| 1555112 | CIF | C19 H22 N2 O | P 21 21 21 | 7.4987; 12.2482; 16.8063 90; 90; 90 | 1543.58 | Wong, Suet-Pick; Gan, Chew-Yan; Lim, Kuan-Hon; Ting, Kang-Nee; Low, Yun-Yee; Kam, Toh-Seok Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor. Organic letters, 2015, 17, 3628-3631 |
| 1555113 | CIF | C33 H25 Cl N2 O5 | P 1 | 10.596; 11.6796; 12.6988 69.855; 70.549; 88.791 | 1383.42 | Wang, Zhen-Hua; Lei, Chuan-Wen; Zhang, Xia-Yan; You, Yong; Zhao, Jian-Qiang; Yuan, Wei-Cheng Asymmetric domino 1,6-addition/annulation reaction of 3-cyano-4-alkenyl-2H-chromen-2-ones with isatin-derived MBH carbonates: enantioselective synthesis of 3,3′-cyclopentenylspirooxindoles bearing 2H-chromen-2-ones Organic Chemistry Frontiers, 2019, 6, 3342 |
| 1555114 | CIF | C18 H23 N O5 S | P 1 | 8.6291; 9.4332; 12.4474 82.659; 70.506; 68.236 | 887.04 | Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes. Organic letters, 2015, 17, 3632-3635 |
| 1555115 | CIF | C33 H29 Cl N2 O3 | P 1 21/n 1 | 17.7343; 13.4538; 24.68 90; 94.67; 90 | 5868.9 | Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction Organic Chemistry Frontiers, 2019, 6, 3530 |
| 1555116 | CIF | C44 H39 N3 O7 | P -1 | 9.853; 14.0452; 15.201 111.663; 93.543; 102.84 | 1882 | Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction Organic Chemistry Frontiers, 2019, 6, 3530 |
| 1555117 | CIF | C33 H29 N3 O5 | P 1 21/n 1 | 12.847; 12.739; 20.208 90; 96.73; 90 | 3284.4 | Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction Organic Chemistry Frontiers, 2019, 6, 3530 |
| 1555118 | CIF | C34 H28 Cl2 N2 O3 | P b c a | 10.1992; 17.1094; 33.448 90; 90; 90 | 5836.7 | Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction Organic Chemistry Frontiers, 2019, 6, 3530 |
| 1555119 | CIF | C12 H15 F N2 O4 S | P 1 21/n 1 | 6.70613; 8.92562; 21.9646 90; 91.7362; 90 | 1314.12 | Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes. Organic letters, 2015, 17, 3632-3635 |
| 1555120 | CIF | C20 H40 N3 O5 P | P -1 | 9.2786; 9.5213; 15.4265 75.673; 76.438; 71.3 | 1232.75 | Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide Enzymatic triggering of C–ON bond homolysis of alkoxyamines Organic Chemistry Frontiers, 2019, 6, 3663 |
| 1555121 | CIF | C20 H38 N3 O4 P | P 1 21/c 1 | 8.8282; 22.0666; 12.5309 90; 96.936; 90 | 2423.3 | Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide Enzymatic triggering of C–ON bond homolysis of alkoxyamines Organic Chemistry Frontiers, 2019, 6, 3663 |
| 1555122 | CIF | C11 H14 N2 O2 S | P 1 21/n 1 | 15.2033; 5.10542; 15.6074 90; 108.006; 90 | 1152.1 | Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes. Organic letters, 2015, 17, 3632-3635 |
| 1555123 | CIF | C25 H24 O | P 1 21/c 1 | 10.22; 9.55; 20.071 90; 93.737; 90 | 1954.8 | Li, Hexin; Zhang, Mengru; Mehfooz, Haroon; Zhu, Dongxia; Zhao, Jinbo; Zhang, Qian Highly convergent modular access to poly-carbon substituted cyclopropanes via Cu(i)-catalyzed three-component cyclopropene carboallylation Organic Chemistry Frontiers, 2019, 6, 3387 |
| 1555124 | CIF | C16 H16 N2 O2 S | P 1 21/n 1 | 8.236; 21.1919; 8.4904 90; 103.856; 90 | 1438.76 | Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes. Organic letters, 2015, 17, 3632-3635 |
| 1555125 | CIF | C22 H18 Br Cl3 N2 O4 | P 1 21 1 | 13.3229; 6.2024; 15.4655 90; 115.145; 90 | 1156.87 | Zhao, Mei-Xin; Liu, Qiang; Yu, Kun-Ming; Zhao, Xiao-Li; Shi, Min Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives Organic Chemistry Frontiers, 2019, 6, 3879 |
| 1555126 | CIF | C13 H19 N O3 S | P 21 21 21 | 7.789; 11.669; 15.029 90; 90; 90 | 1366 | Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex. Organic letters, 2015, 17, 3956-3959 |
| 1555127 | CIF | C13 H10 F3 N O | P -1 | 5.0942; 9.6532; 11.935 91.045; 91.275; 101.201 | 575.43 | Lu, Kui; Wei, Xianfu; Li, Quan; Li, Yuxuan; Ji, Liangshuo; Hua, Erbing; Dai, Yujie; Zhao, Xia Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent Organic Chemistry Frontiers, 2019, 6, 3766 |
| 1555128 | CIF | C14 H17 Br Cl N O4 S | P 1 21 1 | 9.24; 6.262; 14.504 90; 91.561; 90 | 838.9 | Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex. Organic letters, 2015, 17, 3956-3959 |
| 1555129 | CIF | C15 H30 O4 | P 1 | 7.0302; 7.6119; 7.7844 94.191; 109.731; 97.56 | 385.61 | Song, Yin-Ping; Miao, Feng-Ping; Yin, Xiu-Li; Ji, Nai-Yun Nitrogenous cyclonerane sesquiterpenes from an algicolous strain of Trichoderma asperellum Organic Chemistry Frontiers, 2019, 6, 3698 |
| 1555130 | CIF | C20 H24 Br N O4 S | P 1 21 1 | 14.656; 10.051; 14.998 90; 104.87; 90 | 2135.3 | Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex. Organic letters, 2015, 17, 3956-3959 |
| 1555131 | CIF | C16 H9 N3 O2 S | P 21 21 21 | 5.168; 15.6589; 15.9344 90; 90; 90 | 1289.49 | Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution Organic Chemistry Frontiers, 2019, 6, 3300 |
| 1555132 | CIF | C16 H10 Br N3 O2 S | P -1 | 8.3252; 9.8395; 11.1869 65.08; 71.705; 67.231 | 753.73 | Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution Organic Chemistry Frontiers, 2019, 6, 3300 |
| 1555133 | CIF | C14 H18 Br N O4 S | P 1 21 1 | 6.4495; 15.276; 8.0516 90; 96.47; 90 | 788.2 | Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex. Organic letters, 2015, 17, 3956-3959 |
| 1555134 | CIF | C20 H23 Br Cl N O4 S | P 21 21 21 | 7.6751; 12.59; 22.275 90; 90; 90 | 2152.4 | Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex. Organic letters, 2015, 17, 3956-3959 |
| 1555135 | CIF | C40 H41 N O4 S2 | P -1 | 11.0456; 12.0988; 14.8761 68.867; 70.725; 86.448 | 1746.7 | Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors. Organic letters, 2015, 17, 4128-4131 |
| 1555136 | CIF | C27 H25 N O3 S | P -1 | 7.8518; 10.3592; 14.2099 80.043; 83.223; 82.438 | 1123.12 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555137 | CIF | C26 H22 Cl N O3 S | P 1 21/c 1 | 5.9034; 21.165; 21.6677 90; 91.308; 90 | 2706.6 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555138 | CIF | C24 H18 Cl N O3 S | P -1 | 9.3704; 10.2251; 11.2595 76.2532; 78.5679; 75.2513 | 1002.43 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555139 | CIF | C23 H17 N O4 S | P 1 21/c 1 | 7.8538; 13.4956; 17.2047 90; 101.145; 90 | 1789.2 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555140 | CIF | C23 H16 N2 O5 S | P 1 21/c 1 | 13.0035; 15.8463; 9.5395 90; 101.719; 90 | 1924.7 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555141 | CIF | C24 H21 N O3 S | P 21 21 21 | 7.3838; 11.2551; 24.298 90; 90; 90 | 2019.3 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555142 | CIF | C24 H21 N O3 S2 | P 1 21/n 1 | 9.2819; 23.5334; 10.2751 90; 111.152; 90 | 2093.2 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555143 | CIF | C20 H15 N O5 S | P -1 | 8.2024; 10.5566; 11.0975 68.8504; 79.7504; 71.2427 | 846.51 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555144 | CIF | C37 H30 N2 O3 S2 | P 1 2/n 1 | 11.095; 12.561; 24.147 90; 93.088; 90 | 3360.3 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555145 | CIF | C31 H26 N2 O4 S2 | P 1 21/n 1 | 8.9049; 14.0612; 22.343 90; 93.263; 90 | 2793.1 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555146 | CIF | C35 H22 Cl2 N2 O3 S2 | C 1 2/c 1 | 18.289; 13.2118; 24.2095 90; 91.165; 90 | 5848.5 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555147 | CIF | C32 H28 N2 O4 S2 | P -1 | 7.6623; 10.2269; 19.008 102.84; 91.559; 103.009 | 1410.29 | Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones Organic Chemistry Frontiers, 2019, 6, 3555 |
| 1555148 | CIF | C43 H48 N O3 S2 | P 21 21 21 | 11.13642; 14.74032; 46.2616 90; 90; 90 | 7594.04 | Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors. Organic letters, 2015, 17, 4128-4131 |
| 1555149 | CIF | C8 H8 N2 O4 | P 21 21 21 | 4.888; 9.8; 18.388 90; 90; 90 | 880.8 | Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives. Organic letters, 2015, 17, 4666-4669 |
| 1555150 | CIF | C25 H34.5 F3 N O1.25 | C 1 2 1 | 20.6626; 10.3356; 13.6724 90; 123.325; 90 | 2439.76 | Sampaio-Dias, Ivo E.; Silva-Reis, Sara C.; Pinto da Silva, Luís; García-Mera, Xerardo; Maestro, Miguel A.; Rodríguez-Borges, José E. Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids Organic Chemistry Frontiers, 2019, 6, 3540 |
| 1555151 | CIF | C21 H23 N O | P 1 21/c 1 | 9.1308; 14.0389; 14.7904 90; 106.943; 90 | 1813.6 | Sinai, Ádám; Vangel, Dóra; Gáti, Tamás; Bombicz, Petra; Novák, Zoltán Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives. Organic letters, 2015, 17, 4136-4139 |
| 1555152 | CIF | C20 H21 N O3 S | C 1 2/c 1 | 33.942; 11.5163; 9.4629 90; 99.03; 90 | 3653.1 | Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni Diastereoselective bicyclization of enynols via gold catalysis Organic Chemistry Frontiers, 2019, 6, 3584 |
| 1555153 | CIF | C17 H16 O2 | P 21 21 21 | 7.3872; 10.8747; 16.4977 90; 90; 90 | 1325.32 | Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni Diastereoselective bicyclization of enynols via gold catalysis Organic Chemistry Frontiers, 2019, 6, 3584 |
| 1555154 | CIF | C14 H11 Cl N2 | P 1 21/n 1 | 15.4081; 7.7461; 19.9246 90; 98.208; 90 | 2353.69 | Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines. Organic letters, 2015, 17, 3998-4001 |
| 1555155 | CIF | C19 H14 Cl N2 O P | P 1 21/c 1 | 11.949; 8.5662; 17.479 90; 103.621; 90 | 1738.8 | Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines. Organic letters, 2015, 17, 3998-4001 |
| 1555156 | CIF | C30 H38 O7 | P 1 21/c 1 | 11.8298; 17.6502; 13.5929 90; 90.058; 90 | 2838.17 | Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines Organic Chemistry Frontiers, 2019, 6, 3535 |
| 1555157 | CIF | C31 H38 N2 O6 | P 1 21/c 1 | 11.2677; 10.9396; 24.121 90; 93.117; 90 | 2968.86 | Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines Organic Chemistry Frontiers, 2019, 6, 3535 |
| 1555158 | CIF | C7 H3 Cl2 N2 | P b c a | 11.4945; 7.5152; 17.4299 90; 90; 90 | 1505.66 | Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines. Organic letters, 2015, 17, 3998-4001 |
| 1555159 | CIF | C20 H19 N O5 | P 1 21 1 | 10.0737; 6.1334; 13.8766 90; 107.776; 90 | 816.45 | Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong Clavipines A–C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes Organic Chemistry Frontiers, 2019, 6, 3759 |
| 1555160 | CIF | C16 H14 O5 | P 21 21 21 | 8.594; 11.8962; 13.1105 90; 90; 90 | 1340.36 | Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong Clavipines A‒C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes Organic Chemistry Frontiers, 2019, 6, 3759 |
| 1555161 | CIF | C23 H24 O4 | P 1 21/c 1 | 8.759; 21.523; 10.067 90; 104.55; 90 | 1837 | Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons. Organic letters, 2015, 17, 4180-4183 |
| 1555162 | CIF | C18 H20 O6 | P 1 21/c 1 | 7.7505; 21.813; 9.5132 90; 94.65; 90 | 1603 | Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons. Organic letters, 2015, 17, 4180-4183 |
| 1555163 | CIF | C16.5 H16 Cl1.5 N2 O3 | P 1 21/c 1 | 16.298; 11.852; 9.939 90; 90.99; 90 | 1919.6 | Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons. Organic letters, 2015, 17, 4180-4183 |
| 1555164 | CIF | C11 H6 Cl2 O S | P n m a | 11.6812; 6.6839; 13.6312 90; 90; 90 | 1064.3 | Wang, Ting; An, Zhenyu; Qi, Zhenjie; Zhuang, Daijiao; Chang, Aosheng; Yang, Yunxia; Yan, Rulong Ring-opening/annulation reaction of cyclopropyl ethanols: concise access to thiophene aldehydes via C–S bond formation Organic Chemistry Frontiers, 2019, 6, 3705 |
| 1555165 | CIF | C17 H17 Br O5 | P b c a | 11.48; 10.279; 26.181 90; 90; 90 | 3089.4 | Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles. Organic letters, 2015, 17, 4184-4187 |
| 1555166 | CIF | C28 H24 Cl N3 O4 S | P 1 21 1 | 9.5954; 12.6894; 11.2412 90; 112.927; 90 | 1260.6 | Zhang, Haoran; Li, Shiwu; Kang, Qiang; Du, Yu Chiral-at-metal rhodium(iii) complex catalyzed enantioselective synthesis of C2-substituted benzofuran derivatives Organic Chemistry Frontiers, 2019, 6, 3683 |
| 1555167 | CIF | C18 H20 O5 | P 1 21/c 1 | 10.526; 19.394; 7.8119 90; 96.58; 90 | 1584.2 | Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles. Organic letters, 2015, 17, 4184-4187 |
| 1555168 | CIF | C19 H18 N2 O6 Si | C 1 c 1 | 10.8289; 10.4035; 17.1866 90; 103.19; 90 | 1885.14 | Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R. Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes Organic Chemistry Frontiers, 2019, 6, 3793 |
| 1555169 | CIF | C25 H22 N2 O6 Si | P 21 21 21 | 5.9864; 18.2027; 21.5323 90; 90; 90 | 2346.35 | Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R. Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes Organic Chemistry Frontiers, 2019, 6, 3793 |
| 1555170 | CIF | C22 H26 O7 | P 21 21 21 | 9.136; 10.6809; 42.2825 90; 90; 90 | 4126 | Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis. Organic letters, 2015, 17, 4940-4943 |
| 1555171 | CIF | C23 H28 O7 | P 21 21 21 | 8.5586; 9.2119; 27.3349 90; 90; 90 | 2155.11 | Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis. Organic letters, 2015, 17, 4940-4943 |
| 1555172 | CIF | C34 H30 N2 O6 | P 1 21/n 1 | 11.4637; 45.4434; 12.0124 90; 116.324; 90 | 5608.9 | Yan, Jianming; Tay, Guan Liang; Neo, Cuien; Lee, Bo Ra; Chan, Philip Wai Hong Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines. Organic letters, 2015, 17, 4176-4179 |
| 1555173 | CIF | C24 H32 O5 | C 1 2 1 | 25.9119; 7.4654; 11.5725 90; 107.999; 90 | 2129.06 | Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion Organic Chemistry Frontiers, 2019, 6, 3839 |
| 1555174 | CIF | C22 H30.66667 O4.33333 | P 21 21 21 | 12.7263; 18.5197; 24.0727 90; 90; 90 | 5673.6 | Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion Organic Chemistry Frontiers, 2019, 6, 3839 |
| 1555175 | CIF | C26 H18 N4 O5 | P -1 | 9.141; 10.706; 12.0986 73.26; 68.76; 72.31 | 1030.1 | Miura, Wataru; Hirano, Koji; Miura, Masahiro Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage. Organic letters, 2015, 17, 4034-4037 |
| 1555176 | CIF | C18 H26 O6 | P 65 | 20.3875; 20.3875; 7.4174 90; 90; 120 | 2669.99 | Li, Hong-Tao; Tang, Linhuan; Liu, Tao; Yang, Ruining; Yang, Yabin; Zhou, Hao; Ding, Zhong-Tao Polyoxygenated meroterpenoids and a bioactive illudalane derivative from a co-culture of Armillaria sp. and Epicoccum sp. Organic Chemistry Frontiers, 2019, 6, 3847 |
| 1555177 | CIF | C21 H15 N3 O3 | P 1 21/c 1 | 16.334; 13.572; 7.87 90; 104.13; 90 | 1691.9 | Miura, Wataru; Hirano, Koji; Miura, Masahiro Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage. Organic letters, 2015, 17, 4034-4037 |
| 1555178 | CIF | C34 H27.62 N2 O6 | P -1 | 10.4723; 12.7127; 12.7391 113.157; 97.019; 110.996 | 1385.7 | Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank 1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties Organic Chemistry Frontiers, 2019, 6, 3731 |
| 1555179 | CIF | C51 H52 N2 O7 | P -1 | 12.287; 13.2979; 27.85 86.66; 90; 90 | 4542.7 | Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank 1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties Organic Chemistry Frontiers, 2019, 6, 3731 |
| 1555180 | CIF | C32 H28 N2 O6 | P n a 21 | 32.9549; 12.7486; 24.5123 90; 90; 90 | 10298.3 | Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank 1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties Organic Chemistry Frontiers, 2019, 6, 3731 |
| 1555181 | CIF | C24 H19 N2 O2 S2 | P 1 21/c 1 | 8.3103; 22.0934; 11.8386 90; 104.267; 90 | 2106.56 | Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation. Organic letters, 2015, 17, 4188-4191 |
| 1555182 | CIF | C25 H18 O5 | P 1 21 1 | 11.6007; 5.7368; 15.0074 90; 101.62; 90 | 978.29 | Zhang, Song; Yu, Xiaojun; Pan, Jianke; Jiang, Chunhui; Zhang, Hongsu; Wang, Tianli Asymmetric synthesis of spiro-structural 2,3-dihydrobenzofurans via the bifunctional phosphonium salt-promoted [4 + 1] cyclization of ortho-quinone methides with α-bromoketones Organic Chemistry Frontiers, 2019, 6, 3799 |
| 1555183 | CIF | C48 H38 Cl2 N4 O4 S4 | P 21 21 21 | 12.652; 19.153; 22.403 90; 90; 90 | 5428.8 | Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation. Organic letters, 2015, 17, 4188-4191 |
| 1555184 | CIF | C16 H19 N O3 | P 1 21/n 1 | 11.4043; 9.8807; 25.367 90; 93.04; 90 | 2854.4 | Zhong, Jiaxin; He, Haibing; Gao, Shuanhu Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids Organic Chemistry Frontiers, 2019, 6, 3781 |
| 1555185 | CIF | C26 H37 N O8 | C 1 c 1 | 24.4812; 7.9863; 25.3899 90; 103.221; 90 | 4832.51 | Zhong, Jiaxin; He, Haibing; Gao, Shuanhu Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids Organic Chemistry Frontiers, 2019, 6, 3781 |
| 1555186 | CIF | C22 H29 N O5 | P 1 21/c 1 | 8.3885; 24.6653; 19.7148 90; 97.294; 90 | 4046.08 | Zhong, Jiaxin; He, Haibing; Gao, Shuanhu Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids Organic Chemistry Frontiers, 2019, 6, 3781 |
| 1555187 | CIF | C19 H21 Cl2 N O2 S | P 21 21 21 | 6.1472; 11.724; 27.834 90; 90; 90 | 2006 | Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines. Organic letters, 2015, 17, 4042-4045 |
| 1555188 | CIF | C19 H20 Cl N O2 S | P 1 21 1 | 10.133; 9.753; 19.638 90; 100.289; 90 | 1909.6 | Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines. Organic letters, 2015, 17, 4042-4045 |
| 1555189 | CIF | C25 H23 N O3 S | P 1 21 1 | 11.1372; 8.2426; 12.2345 90; 110.187; 90 | 1054.13 | Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals Organic Chemistry Frontiers, 2019, 6, 3725 |
| 1555190 | CIF | C25 H25 N O4 S | C 1 2 1 | 26.476; 9.6581; 9.1391 90; 98.974; 90 | 2308.3 | Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals Organic Chemistry Frontiers, 2019, 6, 3725 |
| 1555191 | CIF | C25 H23 N O3 S | P 1 21 1 | 8.784; 9.976; 12.349 90; 90.656; 90 | 1082.1 | Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals Organic Chemistry Frontiers, 2019, 6, 3725 |
| 1555192 | CIF | C19 H20 Cl N O2 S | P 21 21 21 | 8.434; 9.511; 23.843 90; 90; 90 | 1913 | Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines. Organic letters, 2015, 17, 4042-4045 |
| 1555193 | CIF | C30 H23 N3 O2 S | P 1 21/c 1 | 13.65; 9.7451; 19.194 90; 105.2; 90 | 2463.9 | Vivek Kumar, Sundaravel; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam Rh-Catalyzed C–C/C–N bond formation via C–H activation: synthesis of 2H-indazol-2-yl-benzo[a]carbazoles Organic Chemistry Frontiers, 2019, 6, 3885 |
| 1555194 | CIF | C25 H19 N3 O | P 21 21 21 | 7.2944; 14.078; 19.047 90; 90; 90 | 1955.9 | Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage. Organic letters, 2015, 17, 4066-4069 |
| 1555195 | CIF | C31 H29 N3 O3 S | P -1 | 9.8054; 11.1916; 13.8588 102.001; 100.882; 107.337 | 1367.85 | Wang, Fei; Xu, Pei; Liu, Bei-Bei; Wang, Shun-Yi; Ji, Shun-Jun Pd-Catalyzed multicomponent reaction of sulfonyl azides, primary amines and methyl α-isocyanoacetates: highly efficient synthesis of tetrasubstituted imidazolone derivatives Organic Chemistry Frontiers, 2019, 6, 3754 |
| 1555196 | CIF | C21 H19 N3 O | P b c a | 12.7097; 15.6515; 17.3613 90; 90; 90 | 3453.6 | Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage. Organic letters, 2015, 17, 4066-4069 |
| 1555197 | CIF | C22 H34 N4 O9 | P -1 | 9.7492; 10.793; 12.316 106.75; 97.22; 95.45 | 1219.3 | Jia, Yan-Lai; Wei, Mei-Yan; Chen, Hai-Yan; Guan, Fei-Fei; Wang, Chang-Yun; Shao, Chang-Lun (+)- and (-)-Pestaloxazine A, a Pair of Antiviral Enantiomeric Alkaloid Dimers with a Symmetric Spiro[oxazinane-piperazinedione] Skeleton from Pestalotiopsis sp. Organic letters, 2015, 17, 4216-4219 |
| 1555198 | CIF | C17 H14 N2 O2 | P 1 21/c 1 | 8.4028; 8.4685; 18.8231 90; 91.121; 90 | 1339.18 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555199 | CIF | C23 H18 N2 O2 | P n a 21 | 28.7181; 16.094; 7.4702 90; 90; 90 | 3452.65 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555200 | CIF | C21 H16 N2 O2 | P b c a | 8.899; 16.027; 21.774 90; 90; 90 | 3106 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555201 | CIF | C35 H24 N4 O3 | P 1 21/c 1 | 14.7127; 13.2097; 27.114 90; 97.327; 90 | 5226.6 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555202 | CIF | C21 H16 N2 O2 | P b c a | 16.535; 8.4288; 22.1228 90; 90; 90 | 3083.3 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555203 | CIF | C28 H19 N3 O2 | P -1 | 8.36; 9.772; 13.225 79.646; 71.931; 81.249 | 1005 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555204 | CIF | C23 H16 Br2 N2 O2 | P 1 21/n 1 | 14.667; 9.231; 15.139 90; 107.187; 90 | 1958.2 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555205 | CIF | C25 H18 N2 O2 | P b c n | 18.714; 15.974; 12.0964 90; 90; 90 | 3616.1 | Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part Organic Chemistry Frontiers, 2019, 6, 3649 |
| 1555206 | CIF | C26 H24 N4 O4 | C 1 c 1 | 9.0718; 20.806; 12.975 90; 107.07; 90 | 2341.1 | Liu, Honglei; Yuan, Chunhao; Wu, Yang; Xiao, Yumei; Guo, Hongchao Sc(OTf)3-Catalyzed [3 + 3] Cycloaddition of Cyclopropane 1,1-Diesters with Phthalazinium Dicyanomethanides. Organic letters, 2015, 17, 4220-4223 |
| 1555207 | CIF | C42 H22 F6 | P -1 | 9.9256; 11.9918; 12.9082 90.335; 100.557; 103.488 | 1466.85 | Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F. Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene. Organic letters, 2015, 17, 4224-4227 |
| 1555208 | CIF | C42 H22 F6 | P b c a | 9.5341; 17.1742; 34.8068 90; 90; 90 | 5699.3 | Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F. Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene. Organic letters, 2015, 17, 4224-4227 |
| 1555209 | CIF | C44.4 H38.4 N1.2 S1.8 | P 62 2 2 | 28.8585; 28.8585; 37.617 90; 90; 120 | 27130.8 | Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K. Core-modified 48π and 42π decaphyrins: syntheses, properties and structures Organic Chemistry Frontiers, 2019, 6, 3746 |
| 1555210 | CIF | C42 H34 N4 S3 | P -1 | 8.69725; 10.9283; 20.5323 84.0758; 88.6243; 67.6514 | 1795.05 | Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K. Core-modified 48π and 42π decaphyrins: syntheses, properties and structures Organic Chemistry Frontiers, 2019, 6, 3746 |
| 1555211 | CIF | C65 H65 Cl3 N4 O6 Zn | P 43 | 18.5406; 18.5406; 21.1268 90; 90; 90 | 7262.4 | Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme. Organic letters, 2015, 17, 4078-4081 |
| 1555212 | CIF | C24 H24 O3 | P 1 21/c 1 | 10.0558; 10.1395; 18.5575 90; 98.819; 90 | 1869.77 | Jiao, Meng-Jie; Liu, Dan; Hu, Xiu-Qin; Xu, Peng-Fei Photocatalytic decarboxylative [2 + 2 + 1] annulation of 1,6-enynes with N-hydroxyphthalimide esters for the synthesis of indene-containing polycyclic compounds Organic Chemistry Frontiers, 2019, 6, 3834 |
| 1555213 | CIF | C70 H77 Cl1.5 N4 O5 Zn | C 1 2/c 1 | 39.3331; 14.7758; 28.6914 90; 131.696; 90 | 12450.8 | Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme. Organic letters, 2015, 17, 4078-4081 |
| 1555214 | CIF | C67 H71 N4 O5 Zn | P -1 | 16.9996; 24.3355; 32.7331 89.3681; 83.194; 89.522 | 13444.9 | Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme. Organic letters, 2015, 17, 4078-4081 |
| 1555215 | CIF | C26 H22 Br F3 N4 O4 | P 1 21/c 1 | 9.2204; 24.665; 11.584 90; 105.11; 90 | 2543.4 | Zhao, Hong-Wu; Guo, Jia-Ming; Wang, Li-Ru; Ding, Wan-Qiu; Tang, Zhe; Song, Xiu-Qing; Wu, Hui-Hui; Fan, Xiao-Zu; Bi, Xiao-Fan Diastereoselective formal [3 + 3] cycloaddition of isatin-based α-(trifluoromethyl)imines with N,N′-dialkyloxyureas Organic Chemistry Frontiers, 2019, 6, 3891 |
| 1555216 | CIF | C14 H11 N3 | C 1 2/c 1 | 14.857; 12.127; 13.289 90; 106.898; 90 | 2290.9 | Jia, Feng-Cheng; Zhou, Zhi-Wen; Xu, Cheng; Cai, Qun; Li, Deng-Kui; Wu, An-Xin Expeditious Synthesis of 2-Phenylquinazolin-4-amines via a Fe/Cu Relay-Catalyzed Domino Strategy. Organic letters, 2015, 17, 4236-4239 |
| 1555217 | CIF | C63.25 H86 Na5 O29.95 S5 | P -1 | 12.15; 12.226; 26.113 99.044; 97.039; 99.079 | 3739.3 | Pisagatti, Ilenia; Barbera, Lucia; Gattuso, Giuseppe; Parisi, Melchiorre F.; Geremia, Silvano; Hickey, Neal; Notti, Anna Guest-length driven high fidelity self-sorting in supramolecular capsule formation of calix[5]arenes in water Organic Chemistry Frontiers, 2019, 6, 3804 |
| 1555218 | CIF | C33 H23 Cl3 N2 O2 | P 1 21 1 | 9.07268; 11.9732; 13.4535 90; 106.945; 90 | 1397.99 | Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads. Organic letters, 2015, 17, 4098-4101 |
| 1555219 | CIF | C32.5 H26 N2 O3.5 | P 21 21 2 | 11.4574; 24.0028; 9.1294 90; 90; 90 | 2510.67 | Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads. Organic letters, 2015, 17, 4098-4101 |
| 1555220 | CIF | C34 H24 O2 | P 21 21 2 | 11.1679; 24.1852; 9.1499 90; 90; 90 | 2471.37 | Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads. Organic letters, 2015, 17, 4098-4101 |
| 1555221 | CIF | C32 H22.67 N2 O2.33 | P 21 21 21 | 10.41941; 18.297; 36.8632 90; 90; 90 | 7027.75 | Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads. Organic letters, 2015, 17, 4098-4101 |
| 1555222 | CIF | C32 H22 N2 O2 | P 21 21 21 | 7.9491; 16.7592; 18.1848 90; 90; 90 | 2422.6 | Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads. Organic letters, 2015, 17, 4098-4101 |
| 1555223 | CIF | C245 H138 Cl10 F24 N8 O32 S8 | P -1 | 16.057; 18.336; 18.879 79.909; 74.398; 79.264 | 5214 | Węcławski, Marek K; Meiling, Till T.; Leniak, Arkadiusz; Cywiński, Piotr J; Gryko, Daniel T. Planar, Fluorescent Push-Pull System That Comprises Benzofuran and Iminocoumarin Moieties. Organic letters, 2015, 17, 4252-4255 |
| 1555224 | CIF | C41 H36 N2 O9 | P 1 21/c 1 | 19.0503; 11.68507; 14.8134 90; 92.939; 90 | 3293.19 | Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata. Organic letters, 2015, 17, 4102-4105 |
| 1555225 | CIF | C40 H32 N2 O9 | P b c a | 13.9815; 16.6793; 26.5582 90; 90; 90 | 6193.4 | Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata. Organic letters, 2015, 17, 4102-4105 |
| 1555226 | CIF | C28 H24 N2 O3 S | P 21 21 21 | 8.9629; 14.1297; 18.6198 90; 90; 90 | 2358.1 | Wang, Linqing; Yang, Dongxu; Li, Dan; Liu, Xihong; Zhao, Qian; Zhu, Ranran; Zhang, Bangzhi; Wang, Rui Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst. Organic letters, 2015, 17, 4260-4263 |
| 1555227 | CIF | C24 H25 F3 I N O4 S | P 1 21/c 1 | 13.4658; 20.2837; 19.439 90; 100.921; 90 | 5213.3 | Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate. Organic letters, 2015, 17, 4280-4283 |
| 1555228 | CIF | C6 H13 N O3 | P 41 | 8.8749; 8.8749; 20.4808 90; 90; 90 | 1613.1 | Chung, Ryan; Hein, Jason E. Automated solubility and crystallization analysis of non-UV active compounds: integration of evaporative light scattering detection (ELSD) and robotic sampling Reaction Chemistry & Engineering, 2019, 4, 1674 |
| 1555229 | CIF | C24 H26 F2 I N O4 S | P 1 21/n 1 | 12.121; 15.7186; 25.7853 90; 91.321; 90 | 4911.4 | Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate. Organic letters, 2015, 17, 4280-4283 |
| 1555230 | CIF | C23 H25 F2 I N2 O4 S | P n a 21 | 24.1416; 10.1959; 20.5376 90; 90; 90 | 5055.2 | Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate. Organic letters, 2015, 17, 4280-4283 |
| 1555231 | CIF | C16 H26 O6 | P 1 21 1 | 6.5502; 13.639; 9.1291 90; 91.21; 90 | 815.4 | Hwang, In Hyun; Swenson, Dale C.; Gloer, James B.; Wicklow, Donald T. Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp. Organic letters, 2015, 17, 4284-4287 |
| 1555232 | CIF | C19 H21 Br Cl N O2 | P 1 21 1 | 9.5181; 11.3448; 18.2344 90; 105.143; 90 | 1900.6 | Monasterolo, Claudio; Müller-Bunz, Helge; Gilheany, Declan G. Very short highly enantioselective Grignard synthesis of 2,2-disubstituted tetrahydrofurans and tetrahydropyrans. Chemical science, 2019, 10, 6531-6538 |
| 1555233 | CIF | C22 H36 O6 Si | P 1 21 1 | 6.395; 46.881; 8.2621 90; 111.164; 90 | 2309.9 | Clark, J. Stephen; Romiti, Filippo; Sieng, Bora; Paterson, Laura C.; Stewart, Alister; Chaudhury, Subhabrata; Thomas, Lynne H. Synthesis of the A-D Ring System of the Gambieric Acids. Organic letters, 2015, 17, 4694-4697 |
| 1555234 | CIF | C31 H30 F3 Ir N6 | P -1 | 14.228; 15.407; 16.166 86.526; 65.199; 85.672 | 3206 | Na, Hanah; Cañada, Louise M; Wen, Zhili; I-Chia Wu, Judy; Teets, Thomas S. Mixed-carbene cyclometalated iridium complexes with saturated blue luminescence. Chemical science, 2019, 10, 6254-6260 |
| 1555235 | CIF | C39 H34 F3 Ir N6 | C 1 2/c 1 | 27.27; 20.718; 14.832 90; 116.007; 90 | 7531 | Na, Hanah; Cañada, Louise M; Wen, Zhili; I-Chia Wu, Judy; Teets, Thomas S. Mixed-carbene cyclometalated iridium complexes with saturated blue luminescence. Chemical science, 2019, 10, 6254-6260 |
| 1555236 | CIF | C14 H17 F O2 | P 21 21 21 | 5.8616; 11.0435; 18.6965 90; 90; 90 | 1210.27 | Navuluri, Chandrasekhar; Charette, André B Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid. Organic letters, 2015, 17, 4288-4291 |
| 1555237 | CIF | C23 H23 F N2 O6 | P -1 | 7.9045; 11.1779; 11.7527 91.21; 92.807; 94 | 1034.33 | Navuluri, Chandrasekhar; Charette, André B Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid. Organic letters, 2015, 17, 4288-4291 |
| 1555238 | CIF | C26 H54 N2 O2 Zn2 | P 42/n :2 | 12.3523; 12.3523; 19.4557 90; 90; 90 | 2968.54 | Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO. Chemical science, 2019, 10, 7149-7155 |
| 1555239 | CIF | C30 H46 N2 O2 Zn2 | P 1 21/c 1 | 9.4169; 30.0759; 10.6586 90; 106.582; 90 | 2893.2 | Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO. Chemical science, 2019, 10, 7149-7155 |
| 1555240 | CIF | C30 H46 N2 O2 Zn | P 1 21/c 1 | 10.525; 22.503; 12.296 90; 95.834; 90 | 2897.15 | Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO. Chemical science, 2019, 10, 7149-7155 |
| 1555241 | CIF | C76 H48 O4 | C 2 2 21 | 9.5716; 40.233; 14.5609 90; 90; 90 | 5607.3 | Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C. Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes. Organic letters, 2015, 17, 4296-4299 |
| 1555242 | CIF | C26 H18 O2 | C 2 2 21 | 9.6233; 28.1324; 14.4388 90; 90; 90 | 3908.97 | Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C. Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes. Organic letters, 2015, 17, 4296-4299 |
| 1555243 | CIF | C26 H18 Br2 O2 | C 2 2 21 | 9.5385; 16.362; 14.106 90; 90; 90 | 2201.5 | Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C. Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes. Organic letters, 2015, 17, 4296-4299 |
| 1555244 | CIF | C76 H78 O16 S4 | P 43 21 2 | 13.3557; 13.3557; 44.138 90; 90; 90 | 7873.1 | Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C. Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes. Organic letters, 2015, 17, 4296-4299 |
| 1555245 | CIF | C21 H19 Cl O3 | P 1 21/c 1 | 20.4519; 8.3981; 29.0733 90; 133.17; 90 | 3641.9 | Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters. Chemical science, 2019, 10, 6553-6559 |
| 1555246 | CIF | C21 H19 Br O3 | P 1 21/c 1 | 9.2815; 26.184; 8.2635 90; 114.173; 90 | 1832.2 | Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters. Chemical science, 2019, 10, 6553-6559 |
| 1555247 | CIF | C21 H19 F O3 | P 1 21/n 1 | 8.0324; 10.4173; 21.4761 90; 98.076; 90 | 1779.2 | Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters. Chemical science, 2019, 10, 6553-6559 |
| 1555248 | CIF | C18 H12 O2 | P 1 21/c 1 | 11.0083; 17.6321; 6.9894 90; 98.387; 90 | 1342.1 | Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters. Chemical science, 2019, 10, 6553-6559 |
| 1555249 | CIF | C40 H34 Br N3 O3 | P 21 21 21 | 12.8306; 13.8096; 19.054 90; 90; 90 | 3376.1 | Jing, Changcheng; Xing, Dong; Hu, Wenhao Catalytic Asymmetric Four-Component Reaction for the Rapid Construction of 3,3-Disubstituted 3-Indol-3'-yloxindoles. Organic letters, 2015, 17, 4336-4339 |
| 1555250 | CIF | C19 H18 O2 | P -1 | 8.2948; 9.5359; 10.0158 75.291; 74.899; 86.594 | 739.79 | Lu, Qingquan; Mondal, Shobhan; Cembellín, Sara; Greßies, Steffen; Glorius, Frank Site-selective C-H activation and regiospecific annulation using propargylic carbonates. Chemical science, 2019, 10, 6560-6564 |
| 1555251 | CIF | C18 H16 O S | P 1 21/n 1 | 5.3543; 15.615; 17.226 90; 93.57; 90 | 1437.4 | Zhao, Peng; Liu, Yu; Xi, Chanjuan MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones. Organic letters, 2015, 17, 4388-4391 |
| 1555252 | CIF | C17 H15 Co0.5 O3 | P 1 21/n 1 | 9.6119; 16.0078; 12.0749 90; 94.068; 90 | 1853.23 | Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Shaw, Bikash Kumar; Vaidya, Shefali; Pariyar, Anand; Vijaykumar, Gonela; Adhikari, Debashis; Mandal, Swadhin K. Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction. Chemical science, 2019, 10, 7433-7441 |
| 1555253 | CIF | C13 H8.64 O2 | P c c n | 7.379; 14.8543; 16.8845 90; 90; 90 | 1850.7 | Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Shaw, Bikash Kumar; Vaidya, Shefali; Pariyar, Anand; Vijaykumar, Gonela; Adhikari, Debashis; Mandal, Swadhin K. Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction. Chemical science, 2019, 10, 7433-7441 |
| 1555254 | CIF | C24 H16 O S | P 1 21/c 1 | 9.1038; 11.532; 16.523 90; 101.54; 90 | 1699.6 | Zhao, Peng; Liu, Yu; Xi, Chanjuan MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones. Organic letters, 2015, 17, 4388-4391 |
| 1555255 | CIF | C12 H14 B2 F8 Fe N6 O2 | C m c e | 7.243; 12.882; 23.908 90; 90; 90 | 2230.7 | Resines-Urien, Esther; Burzurí, Enrique; Fernandez-Bartolome, Estefania; García García-Tuñón, Miguel Ángel; de la Presa, Patricia; Poloni, Roberta; Teat, Simon J.; Costa, Jose Sanchez A switchable iron-based coordination polymer toward reversible acetonitrile electro-optical readout. Chemical science, 2019, 10, 6612-6616 |
| 1555256 | CIF | C21 H30 O4 Si | P 1 21/c 1 | 15.86; 8.9849; 32.138 90; 117.571; 90 | 4059.6 | Khatri, Buddha B.; Sieburth, Scott McN Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement. Organic letters, 2015, 17, 4360-4363 |
| 1555257 | CIF | C20 H28 O3 Si | C 1 2/c 1 | 34.403; 6.7764; 16.1333 90; 92.333; 90 | 3758 | Khatri, Buddha B.; Sieburth, Scott McN Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement. Organic letters, 2015, 17, 4360-4363 |
| 1555258 | CIF | C9 H5 Cl2 N3 S | P b c a | 6.9189; 13.8264; 21.5767 90; 90; 90 | 2064.1 | Kalogirou, Andreas S.; Manoli, Maria; Koutentis, Panayiotis A. Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine. Organic letters, 2015, 17, 4118-4121 |
| 1555259 | CIF | C14 H20 O16.75 | P n -3 :2 | 11.4074; 11.4074; 11.4074 90; 90; 90 | 1484.43 | Cui, Peng; McMahon, David P.; Spackman, Peter R.; Alston, Ben M.; Little, Marc A.; Day, Graeme M.; Cooper, Andrew I. Mining predicted crystal structure landscapes with high throughput crystallisation: old molecules, new insights Chemical Science, 2019, 10, 9988 |
| 1555260 | CIF | C15 H18 O8.25 | I 41/a :2 | 16.4008; 16.4008; 22.397 90; 90; 90 | 6024.5 | Cui, Peng; McMahon, David P.; Spackman, Peter R.; Alston, Ben M.; Little, Marc A.; Day, Graeme M.; Cooper, Andrew I. Mining predicted crystal structure landscapes with high throughput crystallisation: old molecules, new insights Chemical Science, 2019, 10, 9988 |
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