Crystallography Open Database
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COD ID  |
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Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1554260 | CIF | C11 H13 N O2 | P b c a | 5.565; 17.417; 19.97 90; 90; 90 | 1935.6 | 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 1556101 | CIF | C52 H48 N4 O3 | P -1 | 9.935; 15.483; 15.666 66.557; 76.89; 77.978 | 2134.4 | McCarthy, Jason R.; Jenkins, Hilary A.; Brückner, Christian Free base meso-tetraaryl-morpholinochlorins and porpholactone from meso-tetraaryl-2,3-dihydroxy-chlorin. Organic letters, 2003, 5, 19-22 |
| 1556102 | CIF | C19 H18 I N O4 | P 21 21 21 | 9.2879; 9.8237; 19.8438 90; 90; 90 | 1810.6 | Li, Guigen; Xu, Xin; Chen, Dianjun; Timmons, Cody; Carducci, Michael D.; Headley, Allan D. Asymmetric halo aldol reaction (AHA). Organic letters, 2003, 5, 329-331 |
| 1556103 | CIF | C68 H92 Se10 | P -1 | 10.459; 12.983; 13.711 101.621; 96.648; 94.94 | 1799.9 | Pietschnig, Rudolf; Schäfer, Sven; Merz, Klaus Self-addition of a sterically hindered alkynylselenolate. Organic letters, 2003, 5, 1867-1869 |
| 1556104 | CIF | C19 H19 N O3 S | P 1 21/c 1 | 11.0472; 7.6308; 19.6869 90; 92.423; 90 | 1658.1 | Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince New strategy for the synthesis of tetrahydroisoquinoline alkaloids. Organic letters, 2003, 5, 2181-2184 |
| 1556105 | CIF | C13 H14 N2 O3 | P 21 21 21 | 7.572; 10.031; 15.754 90; 90; 90 | 1196.59 | Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince New strategy for the synthesis of tetrahydroisoquinoline alkaloids. Organic letters, 2003, 5, 2181-2184 |
| 1556106 | CIF | C28 H16 F6 O2 | C c c 2 | 19.3494; 20.3274; 22.3761 90; 90; 90 | 8801 | Brizius, Glen; Billingsley, Kelvin; Smith, Mark D.; Bunz, Uwe H. F. Conformational and electronic engineering of twisted diphenylacetylenes. Organic letters, 2003, 5, 3951-3954 |
| 1556107 | CIF | C27 H40 O Si2 Sn | P 1 c 1 | 11.8381; 11.6026; 22.301 90; 104.522; 90 | 2965.2 | Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R. Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne. Organic letters, 2003, 5, 3971-3974 |
| 1556108 | CIF | C24.6 H32.8 Cl O1.3 Si2 | I 41/a :2 | 33.3269; 33.3269; 9.8038 90; 90; 90 | 10888.9 | Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R. Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne. Organic letters, 2003, 5, 3971-3974 |
| 1556486 | CIF | C104 H112 F48 K8 N8 O8 | P 1 21/n 1 | 14.2195; 11.8504; 39.8155 90; 97.526; 90 | 6651.4 | Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y. K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides Inorganics, 2017, 5, 13 |
| 1556487 | CIF | C48 H64 F24 K4 N4 O4 | P -1 | 13.9764; 14.1787; 16.1077 84.831; 81.56; 80.187 | 3104.31 | Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y. K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides Inorganics, 2017, 5, 13 |
| 1556488 | CIF | C12 H16 F6 K N O | P -4 21 c | 13.5114; 13.5114; 17.556 90; 90; 90 | 3205 | Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y. K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides Inorganics, 2017, 5, 13 |
| 1556489 | CIF | C32 H48 F24 K4 N4 O4 | P 1 21/n 1 | 18.9136; 10.774; 24.7556 90; 108.265; 90 | 4790.4 | Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y. K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides Inorganics, 2017, 5, 13 |
| 1556490 | CIF | C26 H70 Be2 Cl2 O2 Si8 | P 1 21/n 1 | 10.3667; 18.8628; 11.387 90; 98.15; 90 | 2204.2 | Naglav, D.; Tobey, B.; Dzialkowski, K.; Jansen, G.; Wolper, C.; Schulz, S. Insights into Molecular Beryllium-Silicon Bonds Inorganics, 2017, 5, 22 |
| 1556491 | CIF | C26 H45 Na O3 Si | P 1 21/c 1 | 8.1123; 14.1264; 24.7662 90; 99.36; 90 | 2800.4 | Seifert, T.; Roesky, P.W. Alkali and Alkaline Earth Metal Complexes Ligated by an Ethynyl Substituted Cyclopentadienyl Ligand Inorganics, 2017, 5, 28 |
| 1556492 | CIF | C22 H37 K O2 Si | P 21 21 21 | 10.287; 11.429; 20.495 90; 90; 90 | 2409.6 | Seifert, T.; Roesky, P.W. Alkali and Alkaline Earth Metal Complexes Ligated by an Ethynyl Substituted Cyclopentadienyl Ligand Inorganics, 2017, 5, 28 |
| 1556493 | CIF | C44 H74 Ca2 I2 O4 Si2 | P 1 21/n 1 | 9.4746; 14.9924; 21.7467 90; 101.49; 90 | 3027.1 | Seifert, T.; Roesky, P.W. Alkali and Alkaline Earth Metal Complexes Ligated by an Ethynyl Substituted Cyclopentadienyl Ligand Inorganics, 2017, 5, 28 |
| 1556494 | CIF | C53 H64 Mg N2 P2 | P 1 21/c 1 | 18.7343; 11.6636; 23.279 90; 106.937; 90 | 4866 | Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A. Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide Inorganics, 2017, 5, 29 |
| 1556495 | CIF | C122 H132 Mg2 N4 P4 | C 1 2/c 1 | 20.547; 22.5; 22 90; 90.34; 90 | 10171 | Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A. Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide Inorganics, 2017, 5, 29 |
| 1556496 | CIF | C49 H57 Al N2 P2 | P 1 21/c 1 | 13.149; 18.972; 17.427 90; 99.58; 90 | 4286.8 | Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A. Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide Inorganics, 2017, 5, 29 |
| 1556497 | CIF | C134 H144 Mg2 N4 P4 | C 1 2/c 1 | 19.08; 34.382; 16.79 90; 90.56; 90 | 11014 | Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A. Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide Inorganics, 2017, 5, 29 |
| 1556498 | CIF | C114 H140 Mg2 N4 O4 P4 | P -1 | 13.51; 14.4; 29.43 100.84; 100.81; 100.62 | 5379 | Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A. Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide Inorganics, 2017, 5, 29 |
| 1556499 | CIF | C17 H25 N O | P c c n | 12.3641; 16.3858; 15.4945 90; 90; 90 | 3139.1 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556500 | CIF | C14 H19 N O | P 1 21/n 1 | 10.0068; 9.8961; 12.7933 90; 99.138; 90 | 1250.82 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556501 | CIF | C18 H27 N O | P 21 21 21 | 6.7423; 13.9706; 18.0631 90; 90; 90 | 1701.44 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556502 | CIF | C15 H21 N O | C 1 2/c 1 | 18.8762; 8.0097; 19.0037 90; 107.543; 90 | 2739.6 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556503 | CIF | C42 H64 Li2 N2 O4 | P -1 | 9.406; 10.7931; 11.9959 69.04; 73.616; 67.016 | 1032.5 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556504 | CIF | C36 H52 Li2 N2 O4 | P 1 21/c 1 | 8.0148; 15.0628; 14.5918 90; 103.855; 90 | 1710.35 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556505 | CIF | C44 H68 Li2 N2 O4 | P 1 21/n 1 | 20.843; 10.495; 21.365 90; 112.886; 90 | 4305.6 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556506 | CIF | C63 H80 Li4 N4 O4 | P 21 21 21 | 13.753; 18.3062; 24.0904 90; 90; 90 | 6065.1 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556507 | CIF | C72 H104 Li4 N4 O4 | P 1 21/n 1 | 14.3398; 27.504; 19.8735 90; 107.487; 90 | 7475.9 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556508 | CIF | C60 H80 Li4 N4 O4 | P 1 21/n 1 | 13.0543; 26.647; 16.4965 90; 91.218; 90 | 5737.1 | Gietz, T.; Boere, R.T. Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations Inorganics, 2017, 5, 30 |
| 1556509 | CIF | C49 H62 I Mg N3 O | P 1 21/n 1 | 8.9827; 23.6098; 22.1855 90; 90.818; 90 | 4704.62 | Vindus, D.; Niemeyer, M. Hetero- and Homoleptic Magnesium Triazenides Inorganics, 2017, 5, 33 |
| 1556510 | CIF | C48 H52 I Mg N3 O | P 1 21/c 1 | 19.848; 9.373; 23.033 90; 90.386; 90 | 4284.9 | Vindus, D.; Niemeyer, M. Hetero- and Homoleptic Magnesium Triazenides Inorganics, 2017, 5, 33 |
| 1556511 | CIF | C90 H104 I4 Mg3 N6 | P b c a | 20.4142; 22.2202; 39.3523 90; 90; 90 | 17850.5 | Vindus, D.; Niemeyer, M. Hetero- and Homoleptic Magnesium Triazenides Inorganics, 2017, 5, 33 |
| 1556512 | CIF | C88 H84 I4 Mg3 N6 | P -1 | 16.9933; 17.5771; 17.8005 93.427; 99.534; 109.991 | 4888.5 | Vindus, D.; Niemeyer, M. Hetero- and Homoleptic Magnesium Triazenides Inorganics, 2017, 5, 33 |
| 1556513 | CIF | C47.5 H50 Mg0.5 N3 | P 1 2/n 1 | 15.0589; 13.0937; 20.3232 90; 99.013; 90 | 3957.8 | Vindus, D.; Niemeyer, M. Hetero- and Homoleptic Magnesium Triazenides Inorganics, 2017, 5, 33 |
| 1556514 | CIF | C81.5 H84 Mg N6 | P 1 21/n 1 | 13.302; 21.531; 24.332 90; 101.877; 90 | 6819.6 | Vindus, D.; Niemeyer, M. Hetero- and Homoleptic Magnesium Triazenides Inorganics, 2017, 5, 33 |
| 1556515 | CIF | C11 H27 Li O Si2 | P 1 21/n 1 | 9.493; 9.9165; 16.7191 90; 92.527; 90 | 1572.4 | Von Pilgrim, M.; Mondeshki, M.; Klett, J. [Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands Inorganics, 2017, 5, 39 |
| 1556516 | CIF | C13 H35 Li N2 Si2 | P 1 21/c 1 | 18.7636; 13.2303; 17.7299 90; 112.04; 90 | 4079.8 | Von Pilgrim, M.; Mondeshki, M.; Klett, J. [Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands Inorganics, 2017, 5, 39 |
| 1556517 | CIF | C11 H27 Na O Si2 | P 1 21/n 1 | 11.347; 9.7379; 14.622 90; 90.876; 90 | 1615.5 | Von Pilgrim, M.; Mondeshki, M.; Klett, J. [Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands Inorganics, 2017, 5, 39 |
| 1556518 | CIF | C32 H86 N6 Na2 Si4 | P 1 21/n 1 | 10.45; 17.414; 14.258 90; 100.824; 90 | 2548.5 | Von Pilgrim, M.; Mondeshki, M.; Klett, J. [Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands Inorganics, 2017, 5, 39 |
| 1556519 | CIF | C40 H22 Fe N8 Ni O2 S4 | P -1 | 11.5777; 13.6154; 13.9687 66.134; 84.758; 65.272 | 1821 | Takahashi, K.; Sakurai, T.; Zhang, W.-M.; Okubo, S.; Ohta, H.; Yamamoto, T.; Einaga, Y.; Mori, H. Spin-Singlet Transition in the Magnetic Hybrid Compound from a Spin-Crossover Fe(III) Cation and pi-Radical Anion Inorganics, 2017, 5, 54 |
| 1556520 | CIF | C40 H22 Fe N8 Ni O2 S4 | P -1 | 11.4218; 13.7207; 13.8041 67.123; 84.938; 65.324 | 1804 | Takahashi, K.; Sakurai, T.; Zhang, W.-M.; Okubo, S.; Ohta, H.; Yamamoto, T.; Einaga, Y.; Mori, H. Spin-Singlet Transition in the Magnetic Hybrid Compound from a Spin-Crossover Fe(III) Cation and pi-Radical Anion Inorganics, 2017, 5, 54 |
| 1556521 | CIF | C40 H22 Fe N8 Ni O2 S4 | P -1 | 11.7638; 13.5893; 14.1 65.962; 85.184; 65.815 | 1868.6 | Takahashi, K.; Sakurai, T.; Zhang, W.-M.; Okubo, S.; Ohta, H.; Yamamoto, T.; Einaga, Y.; Mori, H. Spin-Singlet Transition in the Magnetic Hybrid Compound from a Spin-Crossover Fe(III) Cation and pi-Radical Anion Inorganics, 2017, 5, 54 |
| 1556522 | CIF | C20 H19 Au Cl N3 O2 | P -1 | 9.3874; 9.8339; 12.0913 69.669; 70.888; 76.465 | 979.82 | Lanoe, P.-H.; Najjari, B.; Hallez, F.; Gontard, G.; Amouri, H. N-Heterocyclic Carbene Coinage Metal Complexes Containing Naphthalimide Chromophore: Design, Structure, and Photophysical Properties Inorganics, 2017, 5, 58 |
| 1556523 | CIF | C76 H78 F12 Mn4 N8 O12 P2 | P -1 | 11.388; 11.8845; 15.3829 75.0794; 75.9749; 84.3937 | 1950.38 | Sukhikh, T.S.; Vostrikova, K.E. Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV) Inorganics, 2017, 5, 59 |
| 1556524 | CIF | C67 H64 Mn2 N11 O18 P Re | P -1 | 14.2002; 15.7993; 18.047 84.638; 82.694; 65.057 | 3637.9 | Sukhikh, T.S.; Vostrikova, K.E. Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV) Inorganics, 2017, 5, 59 |
| 1556525 | CIF | C237 H224 Cl2 F6 Mn12 N45 O30 P Re3 | P -1 | 13.813; 15.0609; 30.1361 94.447; 93.223; 94.144 | 6222.1 | Sukhikh, T.S.; Vostrikova, K.E. Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV) Inorganics, 2017, 5, 59 |
| 1556526 | CIF | C133 H160 F12 Mn6 N19 O20 P2 Re | P 1 21/n 1 | 23.738; 20.5122; 29.8804 90; 93.37; 90 | 14524.2 | Sukhikh, T.S.; Vostrikova, K.E. Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV) Inorganics, 2017, 5, 59 |
| 1556527 | CIF | C96 H100 B2 Mn2 N10 O11 | P 1 21/c 1 | 15.9891; 27.544; 21.779 90; 108.762; 90 | 9081.9 | Sukhikh, T.S.; Vostrikova, K.E. Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV) Inorganics, 2017, 5, 59 |
| 1556528 | CIF | C24 H28.5 B2 F8 Fe N10.5 P S | P 21 21 21 | 11.3421; 15.3291; 36.7355 90; 90; 90 | 6387 | Stock, P.; Wiedemann, D.; Petzold, H.; Horner, G. Structural Dynamics of Spin Crossover in Iron(II) Complexes with Extended-Tripod Ligands Inorganics, 2017, 5, 60 |
| 1556529 | CIF | C24 H28.5 Cl2 N10.5 O8 P S Zn | P 1 21/c 1 | 9.0934; 31.653; 16.281 90; 136.39; 90 | 3232.3 | Stock, P.; Wiedemann, D.; Petzold, H.; Horner, G. Structural Dynamics of Spin Crossover in Iron(II) Complexes with Extended-Tripod Ligands Inorganics, 2017, 5, 60 |
| 1556530 | CIF | C50 H32 Fe N6 S2 | I b a m | 9.602; 18.9796; 23.8123 90; 90; 90 | 4339.6 | Iwai, S.; Yoshinami, K.; Nakashima, S. Structure and Spin State of Iron(II) Assembled Complexes Using 9,10-Bis(4-pyridyl)anthracene as Bridging Ligand Inorganics, 2017, 5, 61 |
| 1556531 | CIF | C64 H54 B4 F16 Fe2 N20 O3 | P -1 | 13.837; 13.855; 20.684 77.43; 77.58; 86.73 | 3779.5 | Craze, A.R.; Sciortino, N.F.; Badbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F. Investigation of the Spin Crossover Properties of Three Dinulear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type Inorganics, 2017, 5, 62 |
| 1556532 | CIF | C65 H57 B4 F16 Fe2 N19.5 | C 1 2/c 1 | 21.131; 17.391; 21.069 90; 107; 90 | 7404 | Craze, A.R.; Sciortino, N.F.; Badbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F. Investigation of the Spin Crossover Properties of Three Dinulear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type Inorganics, 2017, 5, 62 |
| 1556533 | CIF | C64 H54 B4 F15.5 Fe2 N20 S3 | P -1 | 9.521; 16.723; 23.621 95.29; 100.29; 92.93 | 3675.9 | Craze, A.R.; Sciortino, N.F.; Badbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F. Investigation of the Spin Crossover Properties of Three Dinulear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type Inorganics, 2017, 5, 62 |
| 1556545 | CIF | C10 H22 O5 Si2 | P 1 21/c 1 | 11.5359; 6.7079; 10.1493 90; 115.83; 90 | 706.9 | Kahr, J.; Belaj, F.; Pietschnig, R. Preparation and Molecular Structure of a Cyclopentyl-Substituted Cage Hexasilsesquioxane T6 (T = cyclopentyl-SiO1.5) Starting from the Corresponding Silanetriol Inorganics, 2017, 5, 66 |
| 1556546 | CIF | C10 H22 O5 Si2 | C m c e | 10.1476; 20.7484; 6.7022 90; 90; 90 | 1411.12 | Kahr, J.; Belaj, F.; Pietschnig, R. Preparation and Molecular Structure of a Cyclopentyl-Substituted Cage Hexasilsesquioxane T6 (T = cyclopentyl-SiO1.5) Starting from the Corresponding Silanetriol Inorganics, 2017, 5, 66 |
| 1556547 | CIF | C30 H54 O9 Si6 | C c c a :2 | 16.2855; 22.346; 19.6563 90; 90; 90 | 7153.2 | Kahr, J.; Belaj, F.; Pietschnig, R. Preparation and Molecular Structure of a Cyclopentyl-Substituted Cage Hexasilsesquioxane T6 (T = cyclopentyl-SiO1.5) Starting from the Corresponding Silanetriol Inorganics, 2017, 5, 66 |
| 1556548 | CIF | C69 H45 Cl2 F18 N3 P4 Ru | C 1 2/c 1 | 21.594; 27.753; 23.938 90; 93.631; 90 | 14317 | Van de Watering, F.F.; Heijtbrink, N.; Van der Vlugt, J.I.; Dzik, W.I.; De Bruin, B.; Reek, J.N.H. 3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation Inorganics, 2017, 5, 73 |
| 1556549 | CIF | C69 H45 F18 N5 P4 Ru | P 1 21/c 1 | 14.2851; 18.909; 29.8721 90; 97.011; 90 | 8008.6 | Van de Watering, F.F.; Heijtbrink, N.; Van der Vlugt, J.I.; Dzik, W.I.; De Bruin, B.; Reek, J.N.H. 3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation Inorganics, 2017, 5, 73 |
| 1556550 | CIF | C65 H55 Cl6 N3 P4 Ru | P 1 21/n 1 | 19.1879; 18.1604; 19.7879 90; 91.012; 90 | 6894.2 | Van de Watering, F.F.; Heijtbrink, N.; Van der Vlugt, J.I.; Dzik, W.I.; De Bruin, B.; Reek, J.N.H. 3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation Inorganics, 2017, 5, 73 |
| 1556551 | CIF | C41 H39 I Ni P3 | P n a 21 | 20.526; 10.367; 17.0858 90; 90; 90 | 3635.7 | Iffland, L.; Petuker, A.; Van Gastel, M.; Apfel, U.-P. Mechanistic Implications for the Ni(I)-Catalyzed Kumada Cross-Coupling Reaction Inorganics, 2017, 5, 78 |
| 1556552 | CIF | C31.5 H27 O2.5 | P -1 | 10.337; 10.816; 12.119 72.216; 84.13; 69.554 | 1208.9 | Nguyen, H.N.; Tashima, N.; Ikariya, T.; Kuwata, S. Ruthenium-Catalyzed Dimerization of 1,1-Diphenylpropargyl Alcohol to a Hydroxybenzocyclobutene and Related Reactions Inorganics, 2017, 5, 80 |
| 1556553 | CIF | C55 H50 O3 Ru | P 1 21/c 1 | 17.089; 12.512; 20.001 90; 107.378; 90 | 4081.4 | Nguyen, H.N.; Tashima, N.; Ikariya, T.; Kuwata, S. Ruthenium-Catalyzed Dimerization of 1,1-Diphenylpropargyl Alcohol to a Hydroxybenzocyclobutene and Related Reactions Inorganics, 2017, 5, 80 |
| 1556554 | CIF | C38 H78 N4 Pd4 Si3 | P 1 21/n 1 | 10.8179; 22.0783; 22.8654 90; 92.1391; 90 | 5457.4 | Sunada, Y.; Taniyama, N.; Shimamoto, K.; Kyushin, S.; Nagashima, H. Construction of a Planar Tetrapalladium Cluster by the Reaction of Palladium(0) Bis(isocyanide) with Cyclic Tetrasilane Inorganics, 2017, 5, 84 |
| 1556555 | CIF | C51 H100 N6 Pd4 Si3 | P -1 | 14.505; 15.339; 15.655 89.593; 63.724; 81.301 | 3080.2 | Sunada, Y.; Taniyama, N.; Shimamoto, K.; Kyushin, S.; Nagashima, H. Construction of a Planar Tetrapalladium Cluster by the Reaction of Palladium(0) Bis(isocyanide) with Cyclic Tetrasilane Inorganics, 2017, 5, 84 |
| 1556556 | CIF | C36 H75 O9 P3 Pd3 Si3 | P -1 | 11.2891; 12.711; 19.549 81.516; 85.854; 64.096 | 2495.6 | Sunada, Y.; Taniyama, N.; Shimamoto, K.; Kyushin, S.; Nagashima, H. Construction of a Planar Tetrapalladium Cluster by the Reaction of Palladium(0) Bis(isocyanide) with Cyclic Tetrasilane Inorganics, 2017, 5, 84 |
| 1556557 | CIF | C13 H28 Cl2 N4 Zn | P 21 21 21 | 13.4778; 15.173; 17.57 90; 90; 90 | 3593 | Metz, A.; Heck, J.; Gohlke, C.M.; Krockert, K.; Louven, Y.; McKeown, P.; Hoffmann, A.; Jones, M.D.; Herres-Pawlis, S. Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide Inorganics, 2017, 5, 85 |
| 1556558 | CIF | C13 H26 Cl2 N4 Zn | P 1 21 1 | 9.4718; 18.095; 10.1331 90; 103.908; 90 | 1685.8 | Metz, A.; Heck, J.; Gohlke, C.M.; Krockert, K.; Louven, Y.; McKeown, P.; Hoffmann, A.; Jones, M.D.; Herres-Pawlis, S. Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide Inorganics, 2017, 5, 85 |
| 1556559 | CIF | C13 H26 Br2 N4 Zn | P 1 21 1 | 9.2972; 14.257; 13.2 90; 101.844; 90 | 1712.4 | Metz, A.; Heck, J.; Gohlke, C.M.; Krockert, K.; Louven, Y.; McKeown, P.; Hoffmann, A.; Jones, M.D.; Herres-Pawlis, S. Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide Inorganics, 2017, 5, 85 |
| 1556756 | CIF | Ni Se5 Ta2 | C m c m | 3.5029; 12.8699; 15.6768 90; 90; 90 | 706.74 | Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>. IUCrJ, 2018, 5, 158-165 |
| 1556757 | CIF | Ni Se5 Ta2 | C m c m | 3.4375; 12.375; 15.4437 90; 90; 90 | 656.96 | Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>. IUCrJ, 2018, 5, 158-165 |
| 1556758 | CIF | Ni Se5 Ta2 | P m n m :2 | 3.437; 5.861; 15.512 90; 90; 90 | 312.48 | Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>. IUCrJ, 2018, 5, 158-165 |
| 1556759 | CIF | Ni Se5 Ta2 | P 1 2/n 1 | 3.437; 5.849; 15.512 90; 90.53; 90 | 311.8 | Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>. IUCrJ, 2018, 5, 158-165 |
| 1556829 | CIF | C30 H29 Cl2 Cu2 I2 N O2 S2 | P -1 | 11.7925; 11.9665; 13.4375 93.29; 95.681; 118.683 | 1643.38 | Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes. IUCrJ, 2018, 5, 45-53 |
| 1556830 | CIF | C29 H27 Cd2 I4 N O2 S2 | C 1 2/c 1 | 23.3017; 13.4569; 26.9935 90; 102.963; 90 | 8248.6 | Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes. IUCrJ, 2018, 5, 45-53 |
| 1556831 | CIF | C58 H54 Cd4 I8 N2 O4 S4 | P -1 | 11.66; 12.147; 12.585 75.142; 87.056; 86.996 | 1719.2 | Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes. IUCrJ, 2018, 5, 45-53 |
| 1556832 | CIF | C116 H106 Cd8 I16 N4 O8 S8 | P -1 | 11.3166; 13.4404; 24.586 86.655; 89.396; 78.371 | 3656.5 | Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes. IUCrJ, 2018, 5, 45-53 |
| 1556833 | CIF | C29 H27 Cd Cu I3 N O2 S2 | P -1 | 8.9645; 14.4098; 14.8826 65.853; 73.386; 81.546 | 1680.04 | Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes. IUCrJ, 2018, 5, 45-53 |
| 1556834 | CIF | C0.26 Na0.01 O2 Si | F d -3 m :2 | 19.442; 19.442; 19.442 90; 90; 90 | 7348.9 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
| 1556835 | CIF | C0.26 Na0.01 O2 Si | F d -3 m :2 | 19.4214; 19.4214; 19.4214 90; 90; 90 | 7325.6 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
| 1556836 | CIF | C0.58 Na0.02 O4.53 Si2.27 | A 1 2/n 1 | 23.7844; 13.732; 23.784 90; 109.47; 90 | 7324 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
| 1556837 | CIF | C0.26 Na0.01 O2 Si | F d -3 m :2 | 19.4199; 19.4199; 19.4199 90; 90; 90 | 7323.9 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
| 1556838 | CIF | C0.58 Na0.02 O4.53 Si2.27 | A 1 2/n 1 | 23.834; 13.76; 23.833 90; 109.47; 90 | 7369 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
| 1556839 | CIF | C0.26 Na0.01 O2 Si | F d -3 m :2 | 19.3944; 19.3944; 19.3944 90; 90; 90 | 7295.1 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
| 1556840 | CIF | C0.58 Na0.02 O4.53 Si2.27 | A 1 2/n 1 | 23.834; 13.76; 23.833 90; 109.47; 90 | 7369 | Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature. IUCrJ, 2018, 5, 595-607 |
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