Crystallography Open Database

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1554261 CIFC15 H21 N O2P -110.139; 10.399; 14.357
80.36; 69.86; 89.98
1398.4Ivanov, 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 CIFC13 H15 Br O3P 1 21/c 19.9233; 15.1382; 8.9089
90; 105.815; 90
1287.64Ivanov, 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 CIFC12 H14 O3P 1 21/c 18.638; 15.409; 8.594
90; 111.43; 90
1064.8Ivanov, 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 CIFC13 H14 O3P 1 21/c 19.944; 16.675; 15.179
90; 108.38; 90
2389Ivanov, 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 CIFC27 H26 O5P -17.1922; 9.9323; 16.0391
78.066; 84.732; 86.302
1115.04Ivanov, 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 CIFC15 H18 O5P 1 21/c 19.9599; 6.7335; 20.4059
90; 93.522; 90
1365.94Ivanov, 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 CIFC23 H32 O6P -18.2403; 11.2635; 11.6154
80.692; 75.701; 83.849
1028.38Liu, 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 CIFC13 H20 O4P 1 21/c 110.8545; 11.1988; 10.9655
90; 117.846; 90
1178.59Liu, 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 CIFC76 H104 O26 S3P 1 21 113.7347; 21.989; 13.7372
90; 110.63; 90
3882.8Li, 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 CIFC78 H96 N4 O22C 2 2 2110.70154; 27.4281; 26.4591
90; 90; 90
7766.35Li, 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 CIFC35 H44 O12P 21 21 219.18292; 12.4621; 28.4369
90; 90; 90
3254.28Li, 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 CIFC74 H90 Cl12 O24P 21 21 2115.8696; 16.1185; 32.0556
90; 90; 90
8199.6Li, 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 CIFC77.37 H93.1 N4 O24P 110.54064; 14.6009; 14.9312
62.0192; 84.9082; 68.8864
1884.1Li, 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 CIFC74 H91 N2 O24P 21 21 2115.2487; 16.1229; 29.1352
90; 90; 90
7163Li, 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 CIFC70 H84 O24P 6514.7018; 14.7018; 53.2893
90; 90; 120
9974.97Li, 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 CIFC42 H49 Cl2 N3 O3 Ru SP 1 21/n 113.3662; 19.3514; 18.2778
90; 107.451; 90
4510Sabbasani, 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 CIFC33 H46 Cl2 N2 O RuP 1 21/c 114.573; 14.783; 16.116
90; 104.49; 90
3361Sabbasani, 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 CIFC36 H44 Cl2 N2 O RuC 1 2/c 126.317; 17.57; 17.431
90; 110.1; 90
7569Sabbasani, 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 CIFC16 H9 N5P 1 21/c 117.5111; 18.0998; 8.8623
90; 98.023; 90
2781.39Xin, 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 CIFC20 H14 N2 O2P c a 2116.9028; 16.5253; 9.9901
90; 90; 90
2790.5Yao, 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 CIFC9 H6 N OC 1 2/c 113.3145; 13.4792; 7.0709
90; 93.942; 90
1266Yao, 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 CIFC20 H16 N2 O2P c a 2117.23; 8.7235; 9.6499
90; 90; 90
1450.4Yao, 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 CIFC24 H20 N2 O2P 1 21/n 18.0334; 24.561; 9.1052
90; 105.603; 90
1730.3Yao, 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 CIFC32 H22 N2 O2P -15.3397; 12.5882; 17.165
95.56; 94.461; 101.447
1119.93Yao, 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 CIFC21 H14 OP 1 21/c 19.533; 17.215; 11.031
90; 122.95; 90
1519.1Guo, 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 CIFC17 H14 OP -18.166; 9.066; 9.404
85.402; 75.824; 71.601
640.5Guo, 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 CIFC27 H18 OP -19.603; 10.694; 10.7294
70.55; 64.18; 81.02
935.2Guo, 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 CIFC31 H20 OP -18.4085; 9.35; 14.153
105.907; 95.411; 97.753
1050.2Guo, 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 CIFC30 H25 Br N2 O2P 1 21/c 123.315; 11.3915; 18.4957
90; 93.135; 90
4905Wang, 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 CIFC26 H21 N3 O2P 1 21/n 17.6842; 19.978; 13.7517
90; 98.473; 90
2088Chen, 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 CIFC11 H14 O2 S2C 1 2 127.4221; 5.1994; 19.0212
90; 121.717; 90
2306.99Liu, 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 CIFC25 H20 N2 O3P -19.0455; 9.948; 11.7172
94.495; 95.25; 98.331
1034.4Li, 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 CIFC34 H31 N O5P 1 21/n 110.3357; 23.6593; 11.6006
90; 104.704; 90
2743.9Alajarin, 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 CIFC36 H36 N2 O4P 1 21/c 110.9629; 9.8209; 27.4846
90; 91.397; 90
2958.3Alajarin, 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 CIFC44 H44 Cl2 N2 O6 SP c a 2118.1688; 18.3501; 11.8464
90; 90; 90
3949.6Alajarin, 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 CIFC23 H24 N2 O4 S2P 1 21/c 112.143; 10.204; 18.499
90; 94.972; 90
2283.5Luo, 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 CIFC21 H22 N2 O2 S2P 1 21/c 19.0286; 24.083; 10.3285
90; 114.965; 90
2036Luo, 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 CIFC26 H39 Cl2 Co N3 O12P 21 21 2110.4066; 26.417; 12.0692
90; 90; 90
3318Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554299 CIFC26 H39 Cl2 N3 Ni O12P 21 21 2110.3907; 11.9429; 26.537
90; 90; 90
3293.1Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554300 CIFC22 H18 OP 1 21 16.96436; 7.91974; 15.2392
90; 92.2266; 90
839.9Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554301 CIFC26 H41 Cl2 Fe N3 O12P 21 21 2110.3081; 11.98; 26.1548
90; 90; 90
3229.88Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554302 CIFC15 H19 N O3 SP 1 21/c 110.0093; 14.3918; 10.7208
90; 104.176; 90
1497.32Yu, 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 CIFC15 H19 N O3 SP 1 21/c 16.54242; 22.4359; 10.03319
90; 102.165; 90
1439.65Yu, 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 CIFC17 H18 Cl N O2P 1 21 15.9758; 8.5937; 15.7695
90; 93.352; 90
808.45Hu, 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 CIFC32 H7 Cl4 F10 N3 O2P 1 21/m 16.4792; 25.1943; 10.1094
90; 106.673; 90
1580.87Wang, 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 CIFC36 H11 Cl2 F10 N5 O2.5P 1 21/m 16.3689; 19.2075; 14.4005
90; 96.153; 90
1751.5Wang, 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 CIFC38 H7 Br2 F10 N5 O3P n m a18.5573; 18.3335; 14.8419
90; 90; 90
5049.5Wang, 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 CIFC28 H26 F N O8 SP b c a8.2423; 18.2962; 34.5544
90; 90; 90
5210.9Xing, 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 CIFC28.8 H27.6 N2 O10 SP 1 21/c 121.4204; 21.5628; 14.5587
90; 97.091; 90
6673Xing, 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 CIFC17 H14 O2P 1 21/c 110.5915; 15.1258; 9.0257
90; 109.468; 90
1363.29Zheng, 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 CIFC15 H18 O2P -15.6491; 11.5037; 11.5175
111.795; 99.48; 90.087
683.87Zheng, 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 CIFC16 H17 Br O4P 1 21 110.573; 7.311; 11.35
90; 115.216; 90
793.7Li, 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 CIFC20 H18 N4 O2P -18.46; 9.59; 11.8
97.55; 104.24; 108.51
857Toonchue, 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 CIFC15 H16 N4 O2P 1 21/n 19.998; 9.281; 14.416
90; 95.77; 90
1330.9Toonchue, 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 CIFC20 H40.5 O3.25 SiP 1 21 17.3563; 46.699; 12.909
90; 92.798; 90
4429.4Santalla, 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 CIFC32 H31 N O5P 21 21 2110.1535; 10.5316; 25.565
90; 90; 90
2733.73Duan, 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 CIFC23 H20 Br N O2 SP -110.0726; 10.735; 19.604
82.045; 86.428; 81.212
2072.9Jiang, 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 CIFC26 H23 N O2 SP -19.447; 10.559; 12.512
76.431; 77.755; 64.585
1087Jiang, 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 CIFC26 H23 N O2 SP 1 21/n 111.7526; 13.4984; 13.5265
90; 92.44; 90
2143.9Jiang, 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 CIFC38 H28 N2 O3 SP 21 21 219.00774; 11.44511; 29.0288
90; 90; 90
2992.71Zhang, 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 CIFC38 H28 N2 O4 SC 1 2 114.8962; 11.3205; 20.153
90; 102.279; 90
3320.7Zhang, 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 CIFC26 H21 N O4 SP 1 21 16.3467; 16.1435; 10.7987
90; 96.301; 90
1099.73Zhang, 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 CIFC30 H22 Cl N O2 SP 1 21 110.4185; 15.4927; 15.8277
90; 95.756; 90
2541.9Zhang, 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 CIFC31 H56 F6 Mg N4 O14 S2P 19.2007; 9.2791; 14.237
97.598; 91.193; 97.349
1194.02Zhang, 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 CIFC25 H19 N3 OP -18.2339; 14.7918; 17.1794
101.33; 95.203; 106.126
1947.28Liu, 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 CIFC25 H16 F3 N3 O2P 1 21/c 119.5242; 8.4475; 25.582
90; 107.178; 90
4031.04Liu, 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 CIFC26 H21 F2 N3I 41/a :218.7671; 18.7671; 24.2076
90; 90; 90
8526.01Liu, 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 CIFC16 H15 Cl OP b c n57.5837; 5.8021; 8.0527
90; 90; 90
2690.46Chen, 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 CIFC12 H13 F3 O2 SP -110.0641; 10.4692; 12.4244
90.033; 93.737; 96.649
1297.46Chen, 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 CIFC66 H78 O2P -112.134; 13.857; 17.116
70.214; 75.507; 73.496
2558.3Yang, 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 CIFC68 H74P -19.3311; 9.8219; 16.1042
103.794; 94.992; 112.566
1297.14Yang, 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 CIFC95.5 H118 Cl4.5 O4.93P 1 21 115.3329; 18.3488; 15.6332
90; 99.6319; 90
4336.2Yang, 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 CIFC127.75 H123 O1.75C 1 2/c 132.048; 25.4121; 26.3829
90; 102.865; 90
20947Yang, 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 CIFC34 H34 Cl3 Fe N3 O4P 21 21 219.5467; 13.5703; 26.06
90; 90; 90
3376.1Zhang, 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 CIFC34 H35 Cl2 Fe N3 O4P 41 21 212.0535; 12.0535; 43.8649
90; 90; 90
6373Zhang, 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 CIFC20.57 H26.27 Cl N O3.57C 1 2 118.4603; 16.6736; 13.8087
90; 103.239; 90
4137.4Olivon, 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 CIFC20 H24 Cl N O3P -111.4568; 11.4834; 14.2866
94.508; 106.183; 90.764
1798.31Olivon, 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 CIFC20 H25 N O4P 1 21/c 117.0841; 18.7193; 11.1858
90; 100.62; 90
3516Olivon, 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 CIFC20 H24 Cl N O5P 1 21/n 111.3027; 7.2512; 23.102
90; 98.784; 90
1871.19Olivon, 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 CIFC20 H24 Cl N O3P 21 21 217.508; 11.2397; 21.9828
90; 90; 90
1855.08Olivon, 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 CIFC20 H22 Cl N O4P 1 21/n 117.278; 12.6989; 17.255
90; 102.191; 90
3700.6Olivon, 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 CIFC20 H26 Cl N O4P 1 21/n 116.127; 7.209; 16.3705
90; 91.08; 90
1902.89Olivon, 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 CIFC20 H23 N O2P 1 21/n 110.2096; 12.8487; 12.9425
90; 107.01; 90
1623.53Olivon, 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 CIFC24 H24 O5 SP -15.5872; 13.9109; 14.4106
112.533; 98.978; 94.422
1010.3Cui, 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 CIFC20 H19 N O4P 1 21/n 110.194; 14.232; 12.523
90; 106.045; 90
1746.1Jia, 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 CIFC20 H20 N2 O5P -19.1376; 9.5813; 10.8392
105.957; 95.789; 98.506
892.32Jia, 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 CIFC11 H10 N OP 1 21/n 121.194; 8.4619; 27.57
90; 109.98; 90
4647Gong, 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 CIFC24 H21 N O2P 1 21/n 110.9697; 16.013; 13.031
90; 105.898; 90
2201.4Gong, 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 CIFC5.5 H5.62 N0.12 O0.5F d d d :224.1341; 25.4123; 26.638
90; 90; 90
16337.2Gong, 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 CIFC34 H33 N O3P -19.4355; 10.2231; 17.9161
87.132; 84.213; 68.822
1603.09Gong, 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 CIFC45 H68 N2 O2I 41/a :240.9015; 40.9015; 9.3338
90; 90; 90
15614.8Mahoney, 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 CIFC56 H78 B2 F8 Fe N2 O2C 1 2/c 121.6194; 10.6383; 26.8304
90; 95.299; 90
6144.4Mahoney, 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 CIFC47 H71 B2 F8 N3 O2P 1 21/n 121.3381; 10.2919; 24.6126
90; 111.615; 90
5025.1Mahoney, 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 CIFC19 H28 O7P 1 21 16.4711; 15.6577; 9.2786
90; 90.334; 90
940.12Hu, 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 CIFC20 H32 O5P 21 21 216.6084; 11.8396; 22.9114
90; 90; 90
1792.61Hu, 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 CIFC14 H11 N S2P 1 21/n 17.2615; 11.8328; 14.2292
90; 94.546; 90
1218.78Tan, 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 CIFC15 H13 N S2P 1 21/c 18.3766; 6.2895; 25.7206
90; 95.618; 90
1348.57Tan, 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 CIFC20 H22 O5P 1 21 112.874; 4.9; 13.9299
90; 93.36; 90
877.22Cheng, 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 CIFC21 H31 B2 N O4P -19.6906; 10.9669; 11.5436
70.045; 86.183; 84.832
1147.6Gao, Guoliang; Kuang, Zhijie; Song, Qiuling
Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2
Organic Chemistry Frontiers, 2018, 5, 2249
1554360 CIFC30 H42 B2 O5P -110.0513; 15.5408; 19.0622
88.904; 83.3; 87.795
2954.8Gao, Guoliang; Kuang, Zhijie; Song, Qiuling
Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2
Organic Chemistry Frontiers, 2018, 5, 2249
1554361 CIFC28 H31 Cl3 N2 PdP 1 21/n 110.3174; 12.4692; 20.4932
90; 96.89; 90
2617.4Jin, 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 CIFC28 H31 Cl N2 O PdP -110.0241; 11.2921; 11.727
92.4; 105.358; 106.802
1215.24Jin, 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 CIFC28 H28 Cl F3 N2 PdP b c a18.6245; 13.7023; 22.6048
90; 90; 90
5768.7Jin, 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 CIFC48 H39 Cl N2 PdP b c a18.9753; 19.6328; 20.1865
90; 90; 90
7520.2Jin, 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 CIFC35 H32 Br N3 O3P 1 21 112.6497; 9.0221; 14.1532
90; 113.568; 90
1480.53Mei, 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 CIFC18 H15 N O2 SP 1 21/c 118.6922; 5.447; 14.5323
90; 92.936; 90
1477.68Shen, 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 CIFC10 H9 N OP 1 21 17.5235; 5.5446; 10.2976
90; 99.85; 90
423.23Wu, 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 CIFC28 H17 F3 N2 O1.01P -17.933; 11.1848; 13.1762
72.919; 73.841; 84.499
1073.26Vivek 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 CIFC43 H37 Cl3 N2 O2P 1 21 110.757; 12.558; 14.389
90; 99.306; 90
1918Lu, 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 CIFC20 H18 O4C 1 2/c 122.7223; 5.7888; 25.159
90; 95.416; 90
3294.5Ma, 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 CIFC25 H22 Cl N O3 SP -110.2719; 10.4262; 11.7012
69.168; 73.012; 86.849
1118.45Wang, 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 CIFC21 H19 Cl F N O6P -19.5372; 10.0615; 11.5029
74.116; 83.655; 71.87
1008.56Motornov, 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 CIFC16 H14 Cl F N2 O6P 1 21/c 116.4649; 6.9417; 15.0372
90; 93.483; 90
1715.5Motornov, 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 CIFC23 H31 N O2 SP -16.812; 11.371; 13.441
80.287; 84.84; 77.986
1002.1Han, 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 CIFC18 H23 N O2 SP 1 21/c 110.6868; 20.2; 8.0112
90; 101.747; 90
1693.2Han, 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 CIFC24 H30 O4P 1 21/c 18.9632; 26.894; 9.2793
90; 110.151; 90
2099.9Han, 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 CIFC36 H34 N O6P 1 21 111.0672; 24.0508; 11.3892
90; 91.3083; 90
3030.73Yue, 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 CIFC24 H26 N2 O3P 1 21 110.2146; 11.7243; 10.2644
90; 119.315; 90
1071.84Zhang, 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 CIFC32 H27 N O5 SP -110.276; 12.5669; 13.0463
66.455; 73.203; 66.317
1397.8Zhang, 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 CIFC29 H28 Cl N3 O7P 21 21 218.611; 11.3415; 28.819
90; 90; 90
2814.5Wei, 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 CIFC29 H43 I Mg N2 OP -18.4477; 11.883; 15.889
97.79; 90.12; 96.968
1568.3Li, 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 CIFC50 H66 Mg2 N4P 1 21/c 112.5799; 19.2069; 20.3357
90; 102.473; 90
4797.6Li, 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 CIFC50 H66 Mg2 N4P n a 2121.9804; 19.3508; 11.283
90; 90; 90
4799.1Li, 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 CIFC46 H58 Mg N4P -111.0139; 11.3202; 18.565
75.316; 83.401; 62.905
1993.3Li, 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 CIFC54 H53 Mg N2P 1 21/c 111.4271; 17.954; 20.908
90; 93.495; 90
4281.6Li, 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 CIFC48 H49 Cl2 N2P c c n21.607; 13.2782; 14.0261
90; 90; 90
4024.1Li, 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 CIFC51 H55 I Mg N2 OC 1 2/c 125.689; 11.0511; 32.698
90; 105.996; 90
8923.3Li, 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 CIFC58 H76 Cl2 Mg2 N4P 1 21/c 111.9804; 15.2444; 15.0882
90; 95.298; 90
2743.8Li, 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 CIFC68 H96 B2 Mg2 N4 O6P -413.2295; 13.2295; 19.2267
90; 90; 90
3365.1Li, 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 CIFC18 H36 B2 O6P 1 21/c 110.58; 10.4047; 10.785
90; 118.687; 90
1041.5Li, 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 CIFC52 H70 Mg2 N4P c c n17.7085; 33.2898; 17.0054
90; 90; 90
10024.9Li, 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 CIFC30 H21 Cl N2 O2P -18.5511; 10.4286; 14.3935
88.875; 87.601; 68.209
1190.78Xu, 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 CIFC22 H24 Cl3 F6 N4 P RuP 1 21/n 18.1716; 30.1115; 10.9853
90; 95.159; 90
2692.1Wu, 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 CIFC17 H13 F2 N O2P b c a8.3324; 18.0049; 18.9382
90; 90; 90
2841.2Ma, Xingxing; Deng, Shuilin; Song, Qiuling
Halodifluoroacetates as formylation reagents for various amines via unprecedented quadruple cleavage
Organic Chemistry Frontiers, 2018, 5, 3505
1554395 CIFC14 H17 N OP -16.32; 11.047; 16.999
90.548; 95.825; 90.542
1180.6Liu, 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 CIFC12 H26 Cl2 N2 Ni O7P -16.9966; 12.0579; 12.9998
63.724; 88.61; 86.344
981.4Liu, 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 CIFC22 H25 N O6P 1 21/c 110.9821; 9.771; 21.137
90; 119.629; 90
1971.56Boichenko, 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 CIFC23 H29 N O7P 1 c 17.0556; 15.3824; 10.7866
90; 108.471; 90
1110.38Boichenko, 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 CIFC22 H25 N O6P 1 21/c 115.7969; 8.7827; 14.6012
90; 103.801; 90
1967.28Boichenko, 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 CIFC43 H26 N2 O2P -19.516; 11.551; 13.616
91.24; 106.05; 99.94
1412.9Kupietz, 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 CIFC61 H45 B F4 N2 O2P 1 21/n 114.154; 17.553; 19.832
90; 106.78; 90
4717.4Kupietz, 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 CIFC86 H54 B8 F22 N4 O7P -18.09; 12.074; 24.254
82.58; 89.11; 70.85
2218.3Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław
Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin
Organic Chemistry Frontiers, 2018, 5, 3068
1554403 CIFC14 H18 N2 O SP -15.5091; 7.2665; 16.992
80.823; 83.934; 78.863
656.9Dutta, Soumya; Mondal, Manas; Ghosh, Tubai; Saha, Amit
Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas
Organic Chemistry Frontiers, 2019, 6, 70
1554404 CIFC29 H37 N O7P 1 21 112.2892; 11.6999; 19.3795
90; 103.521; 90
2709.2Fan, 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 CIFC28 H24 O5P 1 21/n 19.5523; 9.8572; 23.9209
90; 99.141; 90
2223.76Zhao, 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 CIFC30 H31 Br N2 O3P 1 21 113.248; 7.6262; 27.213
90; 97.298; 90
2727.1Yuan, 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 CIFC23 H28 O6P 1 21 17.3005; 12.1224; 11.9121
90; 105.259; 90
1017.05Zhang, 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 CIFC14 H10 Br N O4P b c a7.5983; 16.424; 20.8458
90; 90; 90
2601.44Maezono, 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 CIFC18 H18 O2P 1 21/n 19.0575; 12.288; 12.993
90; 94.793; 90
1441Yang, 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 CIFC44 H42 Cl N5 O8P -117.135; 17.343; 20.802
106.696; 98.131; 118.106
4934.7Yang, 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 CIFC42 H38 Cl N5 O6P -112.086; 12.455; 17.13
96.558; 109.996; 107.812
2236.9Yang, 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 CIFC28 H22P -19.7638; 10.0633; 10.6246
100.341; 103.17; 95.285
990.28Chuskit, 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 CIFC18 H25 N O7 SP 1 21/c 110; 14.827; 13.344
90; 101.939; 90
1935.7Lei, 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 CIFC19 H24 F3 N O2P -112.1127; 13.1333; 13.1505
76.939; 79.228; 63.194
1810.2Long, 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 CIFC30 H29 N3 O4 SP 1 21 18.6306; 10.9636; 14.5139
90; 90.644; 90
1373.25Huang, 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 CIFC24 H22 N4 O4P 1 21/c 118.2546; 9.1982; 13.3199
90; 108.231; 90
2124.27Qiu, 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 CIFC12 H12 N2 O3P 1 21/c 111.2278; 13.7389; 7.4364
90; 107.173; 90
1095.98Qiu, 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 CIFC24 H20 N4 O5P 1 21/c 113.145; 14.0218; 12.9264
90; 114.416; 90
2169.47Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun
Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors
Organic Chemistry Frontiers, 2018, 5, 3206
1554419 CIFC20 H18P n a 2115.853; 12.375; 7.3639
90; 90; 90
1444.7Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K.
Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism
Organic Chemistry Frontiers, 2019, 6, 134
1554420 CIFC20 H14 O4P 1 21/c 18.0844; 19.8817; 10.2123
90; 109.061; 90
1551.44Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K.
Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism
Organic Chemistry Frontiers, 2019, 6, 134
1554421 CIFC24 H19 Cl N2 OP 1 21/c 15.628; 19.385; 17.569
90; 91.36; 90
1916.2Tong, 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 CIFC24 H19 Cl N2 OP -15.7976; 9.4263; 17.097
87.715; 87.737; 86.465
931.2Tong, 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 CIFC17 H0.25 N OP 21 21 216.229; 13.6065; 14.6177
90; 90; 90
1238.92Xu, 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 CIFC27 H25 F N2 O5 SP 1 21 113.42; 5.3749; 17.821
90; 105.381; 90
1239.4Cao, 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 CIFC18 H16 Br F O2P 16.6841; 8.7074; 14.4482
87.391; 81.591; 78.532
815.14Cao, 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 CIFC14 H13 N O3P 1 21 110.0137; 10.3706; 11.987
90; 109.801; 90
1171.23Kim, 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 CIFC42 H50 O2 Si2P -17.6019; 7.7795; 17.7908
94.036; 92.577; 114.867
948.98Ozdemir, 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 CIFC48 H50 N4 Si2C 1 2/c 139.755; 10.0294; 11.4351
90; 102.874; 90
4444.8Ozdemir, 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 CIFC33 H35 N O6P 1 21/n 117.45405; 8.11896; 19.929
90; 91.5647; 90
2823.06Yi, 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 CIFC30 H26 Cl3 N O3P 1 21/c 111.083; 21.629; 12.241
90; 116.92; 90
2616Yi, 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 CIFC36 H37 O4 P SP 1 21/c 18.7333; 32.515; 11.3552
90; 92.555; 90
3221.3Chen, 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 CIFC45 H41 O4 P SP -110.244; 13.1272; 15.4443
85.216; 77.319; 69.981
1903.71Chen, 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 CIFC40 H39 O3 P SP 1 21/c 110.9576; 24.0001; 13.0509
90; 94.036; 90
3423.7Chen, 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 CIFC37 H35 O3 P SP 1 21/c 112.3705; 13.8788; 19.1238
90; 106.702; 90
3144.8Chen, 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 CIFC22 H24 N2P 1 21/c 122.09; 8.574; 9.447
90; 101.6; 90
1752.7Liu, 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 CIFC21 H21 Br N O7 P SP 21 21 218.8385; 14.3341; 17.8495
90; 90; 90
2261.4Sun, Jun; Mou, Chengli; Liu, Changyi; Huang, Ruoyan; Zhang, Shupeng; Zheng, Pengcheng; Chi, Yonggui Robin
Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines
Organic Chemistry Frontiers, 2018, 5, 2992
1554437 CIFC13 H13 N O4 SP 1 21/c 19.1009; 17.5658; 8.1862
90; 103.294; 90
1273.61Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554438 CIFC13 H15 N O5 SP -17.2268; 9.0737; 10.4696
80.813; 84.674; 88.958
674.8Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554439 CIFC13 H19 N O8 SP -17.2412; 9.7236; 11.4552
85.64; 87.406; 77.183
783.86Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554440 CIFC16 H13 N O5 SP 1 21/n 16.6266; 18.2993; 11.8645
90; 99.67; 90
1418.3Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung
Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones
Organic Chemistry Frontiers, 2019, 6, 183
1554441 CIFC28 H29 Co P SP 1 21/n 19.0319; 18.9034; 14.4632
90; 96.64; 90
2452.8Liu, 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 CIFC22 H18 N O2P 1 21/n 112.766; 7.3952; 18.2702
90; 103.067; 90
1680.17Liu, 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 CIFC30 H23 N O2P -17.3192; 11.4476; 14.2878
109.541; 103.435; 90.85
1091.7Liu, 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 CIFC26 H21 N O2P -17.4718; 10.17; 13.6849
80.313; 76.092; 74.405
966.3Liu, 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 CIFC28 H29 Br Co P SP n a 2116.6717; 10.051; 14.516
90; 90; 90
2432.4Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang
Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives
Organic Chemistry Frontiers, 2018, 5, 2997
1554446 CIFC31 H44 N3 P2 RhP 1 21/n 110.9778; 16.148; 17.5888
90; 106.231; 90
2993.7Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei
Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex
Organic Chemistry Frontiers, 2019, 6, 721
1554447 CIFC92 H120 N6 O3 P4 Rh2C 1 2/c 129.2408; 13.8295; 25.4214
90; 120.925; 90
8818.6Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei
Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex
Organic Chemistry Frontiers, 2019, 6, 721
1554448 CIFC28 H33 Br O3I 1 2 126.357; 7.5712; 24.9141
90; 92.458; 90
4967.1Liu, Lin; Song, Huayue; Chen, Peng; Yuan, Ziyun; Feng, Shangbiao; Zhang, Weiwei; Fang, Bowen; Xie, Xingang; She, Xuegong
Total synthesis of (−)-8-epi-chromazonarol enabled by a unique N2H4·H2O promoted intramolecular oxa-Michael cyclization reaction
Organic Chemistry Frontiers, 2018, 5, 3013
1554449 CIFC30 H37 I N2 RuP -112.2395; 14.363; 18.399
89.442; 89.312; 88.419
3232.9Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis
Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines
Organic Chemistry Frontiers, 2019, 6, 563
1554450 CIFC27 H31 I N2 RuP 1 21/n 115.329; 7.7727; 21.254
90; 95.269; 90
2521.7Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis
Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines
Organic Chemistry Frontiers, 2019, 6, 563
1554451 CIFC26 H23 N O2 SC 1 c 112.1152; 14.1577; 24.768
90; 93.519; 90
4240.3Zhang, Jia-hao; Wei, Yin; Shi, Min
Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2980
1554452 CIFC26 H23 N O2 SP 1 21/n 110.875; 11.83; 16.54
90; 98.8; 90
2103Zhang, Jia-hao; Wei, Yin; Shi, Min
Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2980
1554453 CIFC26 H23 N O4 SC 1 2/c 120.5631; 27.2351; 9.3277
90; 92.088; 90
5220.4Zhang, Jia-hao; Wei, Yin; Shi, Min
Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2980
1554454 CIFC20 H11 F12 O5 PP 1 21/c 115.787; 10.811; 13.977
90; 112.816; 90
2199Khasiyatullina, 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 CIFC12 H20 N O4 PP 1 21 17.266; 11.409; 8.573
90; 96.695; 90
705.8Khasiyatullina, 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 CIFC6 H7 O5 PP 21 21 214.6005; 10.122; 16.4334
90; 90; 90
765.24Khasiyatullina, 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 CIFC24 H21 F6 O9 PP -110.7892; 11.1562; 11.7122
101.788; 99.647; 106.558
1283.93Khasiyatullina, 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 CIFC18 H13 Cl6 O5 PI 41/a :227.972; 27.972; 11.844
90; 90; 90
9267Khasiyatullina, 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 CIFC40 H40 N O2 SP -18.8009; 12.3786; 16.3465
102.889; 95.068; 108.26
1624.3Wu, 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 CIFC44 H42 N O2 SP -17.1299; 14.678; 17.037
74.911; 81.895; 89.178
1703.8Wu, 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 CIFC84 H80 N2 O4 S4P 1 21/c 113.5245; 24.687; 20.6534
90; 102.064; 90
6743.4Wu, 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 CIFC92 H81 N2 O4 S4P -114.3142; 16.7266; 18.5616
105.723; 109.469; 90.336
4010.6Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang
Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells
Organic Chemistry Frontiers, 2018, 5, 3324
1554463 CIFC27 H25 N O3 SP -18.892; 9.668; 13.91
86.33; 86.29; 67.91
1105Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554464 CIFC22 H25 N O3 SP -17.6023; 7.8229; 16.7412
85.307; 84.129; 85.07
984.06Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554465 CIFC28 H27 N O3 SP 1 21/c 110.5059; 11.5524; 19.3292
90; 99.812; 90
2311.6Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554466 CIFC25 H29 N O3 SP 1 21/n 18.6751; 21.9074; 12.355
90; 107.893; 90
2234.5Beltran, Frédéric; Andna, Lucile; Miesch, Laurence
Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts
Organic Chemistry Frontiers, 2019, 6, 373
1554467 CIFC19 H16 N2 O6 SP 1 21/c 19.7218; 7.7915; 24.097
90; 99.734; 90
1799Shen, 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 CIFC20 H19 N O4 SP -16.4452; 11.7323; 12.5163
105.865; 90.612; 93.872
907.9Shen, 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 CIFC33 H26 Cl N O2 SP 1 21/n 110.2302; 24.9417; 10.532
90; 94.66; 90
2678.4Shen, 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 CIFC26 H30 N4 O9I 1 2 19.9349; 5.4755; 25.351
90; 101.162; 90
1353Chen, 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 CIFC26 H30 O6P 1 21/n 111.6963; 8.9597; 23.096
90; 90.67; 90
2420.2Xiong, 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 CIFC27 H28 Cl I N2 O5P -110.805; 11.7571; 12.8689
106.048; 95.01; 114.103
1396.3Xiong, 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 CIFC14 H12 F6 N2 O4 S2P 1 21/n 18.4088; 17.398; 12.1982
90; 101.318; 90
1749.85Almendros, 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 CIFC20 H15 F6 N O5 S2P 1 21/n 112.6441; 11.3643; 16.2034
90; 111.751; 90
2162.5Almendros, 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 CIFC21 H19 F6 N O6 S3P 1 21/n 113.0371; 14.5605; 14.0643
90; 113.617; 90
2446.2Almendros, 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 CIFC14 H11 Cl F6 N2 O5 S2C 1 2/c 131.442; 7.7594; 16.3435
90; 91.74; 90
3985.5Almendros, 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 CIFC13 H8 F6 O7 S2P 1 21/n 15.7308; 13.6484; 21.184
90; 95.748; 90
1648.6Almendros, 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 CIFC13 H10 F6 N2 O4 S2P 1 21/c 114.266; 6.0883; 18.922
90; 94.123; 90
1639.2Almendros, 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 CIFC9 H10 F6 N2 O5 S2P b c a17.2641; 14.8304; 23.9088
90; 90; 90
6121.5Almendros, 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 CIFC15 H14 F6 N2 O5 S2P n a 2127.2048; 18.3507; 12.2694
90; 90; 90
6125.2Almendros, 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 CIFC29 H28 N2 O S2P 1 21/n 117.607; 5.4871; 25.7682
90; 106.169; 90
2391Weldeab, 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 CIFC26 H22 Br N O9P 1 21/c 111.2685; 18.6581; 12.8795
90; 111.426; 90
2520.8Agafonova, 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 CIFC16 H9 Cl F3 N O3 SI b a 215.569; 29.973; 7.0564
90; 90; 90
3292.9Yi, 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 CIFC11 H9 F O2P 21 21 214.9693; 5.8579; 31.3863
90; 90; 90
913.64Han, Sang Hoon; Pandey, Ashok Kumar; Lee, Heeyoung; Kim, Saegun; Kang, Dahye; Jung, Young Hoon; Kim, Hyung Sik; Hong, Sungwoo; Kim, In Su
One-pot synthesis of 2-naphthols from nitrones and MBH adducts via decarboxylative N–O bond cleavage
Organic Chemistry Frontiers, 2018, 5, 3210
1554485 CIFC20 H24 O5P 21 21 216.1036; 12.5506; 21.976
90; 90; 90
1683.45Yang, Qian; Hu, Kun; Yan, Bing-Chao; Liu, Miao; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin
Maoeriocalysins A–D, four novel ent-kaurane diterpenoids from Isodon eriocalyx and their structure determination utilizing quantum chemical calculation in conjunction with quantitative interproton distance analysis
Organic Chemistry Frontiers, 2019, 6, 45
1554486 CIFC14 H8 N3 OP 1 21/n 15.7918; 13.738; 13.4519
90; 101.436; 90
1049.09Li, 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 CIFC37 H31 N3 O4 SP 1 21 113.6363; 8.5322; 15.2209
90; 116.205; 90
1588.9Gu, 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 CIFC17 H18 N O5 PP -19.5039; 10.0075; 10.6869
64.045; 69.351; 83.294
854.35Wang, Jie; Li, Jun; Wei, Yuanyuan; Yang, Jingya; Huo, Congde
Copper-catalyzed oxidative phosphonation of 3,4-dihydro-1,4-benzoxazin-2-ones
Organic Chemistry Frontiers, 2018, 5, 3534
1554489 CIFC10 H8 F N3P b c a7.4865; 11.7277; 20.913
90; 90; 90
1836.1Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554490 CIFC16 H12 F N5 O2P 1 21/c 18.4745; 13.483; 12.5515
90; 96.566; 90
1424.7Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554491 CIFC10 H8 F N3P 1 21/n 16.185; 7.487; 18.728
90; 96.138; 90
862.3Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554492 CIFC70 H56 Ag5 Cl2 N6 P4A e a 227.38; 26.9; 24.03
90; 90; 90
17699Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming
Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives
Organic Chemistry Frontiers, 2019, 6, 426
1554493 CIFC20 H14 N2P -13.9188; 12.5127; 15.3057
101.08; 96.416; 92.665
730.13Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong
ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes
Organic Chemistry Frontiers, 2019, 6, 432
1554494 CIFC22 H19 N3P 1 21/c 110.5762; 7.8869; 19.9879
90; 91.535; 90
1666.7Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong
ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes
Organic Chemistry Frontiers, 2019, 6, 432
1554495 CIFC25 H20 N4 O2P -19.1577; 10.7173; 13.3021
106.893; 91.497; 91.349
1248.12Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong
ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes
Organic Chemistry Frontiers, 2019, 6, 432
1554496 CIFC30 H25 N O3P 1 21 18.5256; 16.9053; 8.9274
90; 112.31; 90
1190.37Xu, Jianfeng; Peng, Jingyi; He, Chonglong; Ren, Hongjun
N-Heterocyclic carbene catalyzed chemo- and enantioselective cross-benzoin reaction of aldehydes with isatins
Organic Chemistry Frontiers, 2019, 6, 172
1554497 CIFC18 H12 Cl3 O P S3C 1 2/c 112.268; 8.6753; 37.965
90; 92.878; 90
4035.5Lu, Guozhang; Chen, Jun; Huangfu, Xinlei; Li, Xueyan; Fang, Meijuan; Tang, Guo; Zhao, Yufen
Visible-light-mediated direct synthesis of phosphorotrithioates as potent anti-inflammatory agents from white phosphorus
Organic Chemistry Frontiers, 2019, 6, 190
1554498 CIFC38 H42 Cl2 O7C 1 2 125.2058; 7.2704; 19.2306
90; 105.306; 90
3399.1Fan, Jian-Hong; Hu, Ya-Jian; Guo, Qiang; Li, Shaoping; Zhao, Jing; Li, Chuang-Chuang
Asymmetric synthesis of the tetracyclic core of bufogargarizin C by an intramolecular [5 + 2] cycloaddition
Organic Chemistry Frontiers, 2019, 6, 22
1554499 CIFC27 H22 N O2 PP 1 21 17.8836; 12.2399; 11.1988
90; 90.174; 90
1080.62Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping
Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides
Organic Chemistry Frontiers, 2019, 6, 236
1554500 CIFC27 H22 N O2 PP 16.0253; 9.0011; 10.3679
75.005; 76.437; 89.09
527.4Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping
Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides
Organic Chemistry Frontiers, 2019, 6, 236
1554501 CIFC19 H15 F3 O4C 1 2/c 123.47; 9.9387; 17.2934
90; 123.484; 90
3364.4Chen, Yueji; You, Yi; Weng, Zhiqiang
Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities
Organic Chemistry Frontiers, 2019, 6, 213
1554502 CIFC17 H12 Br2 F2 O2P 1 21/c 113.7491; 5.8303; 21.42
90; 105.814; 90
1652.1Chen, Yueji; You, Yi; Weng, Zhiqiang
Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities
Organic Chemistry Frontiers, 2019, 6, 213
1554503 CIFC22 H21 N O5P 21 21 221.2879; 7.5138; 11.5723
90; 90; 90
1851.02Shoji, Taku; Araki, Takanori; Iida, Nanami; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Okujima, Tetsuo
Synthesis of azulenophthalimides by phosphine-mediated annulation of 1,2-diformylazulenes with maleimides
Organic Chemistry Frontiers, 2019, 6, 195
1554504 CIFC68 H68 Cl6 N4 O10 P2R -3 :H25.2081; 25.2081; 30.11
90; 90; 120
16570Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554505 CIFC66 H66 I N2 O4 P2C 1 2/c 119.7346; 19.9943; 14.9829
90; 110.36; 90
5542.6Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554506 CIFC34 H34 Br Cl3 N O2 PP 1 21/c 110.967; 15.8648; 20.3172
90; 105.084; 90
3413.2Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554507 CIFC66 H66 F6 N2 O4 P3C 1 2/c 119.664; 19.9512; 15.5025
90; 111.125; 90
5673.2Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554508 CIFC66 H66 Cl N2 O7.33 P2R -3 :H24.8062; 24.8062; 30.0418
90; 90; 120
16009.5Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554509 CIFC74 H86 F12 N2 O6 P4P b c a15.5817; 20.6208; 22.0566
90; 90; 90
7086.9Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554510 CIFC66 H66 N2 O4 P2P 1 21/c 114.2234; 15.5567; 12.5242
90; 108.744; 90
2624.2Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554511 CIFC66 H66 Br N2 O4 P2R -3 :H24.7543; 24.7543; 30.0212
90; 90; 120
15931.6Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan
Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts
Organic Chemistry Frontiers, 2019, 6, 110
1554512 CIFC12 H17 N SP 1 21/c 16.3585; 10.945; 17.5672
90; 92.051; 90
1221.78Lai, Miao; Wu, Zhiyong; Wang, Yizhi; Zheng, Ying; Zhao, Mingqin
Selective synthesis of aryl thioamides and aryl-α-ketoamides from α-oxocarboxylic acids and tetraalkylthiuram disulfides: an unexpected chemoselectivity from aryl sulfonyl chlorides
Organic Chemistry Frontiers, 2019, 6, 506
1554513 CIFC21 H19 Br O3P 21 21 2110.687; 12.035; 14.902
90; 90; 90
1917Huang, Huicai; Lu, Xue; Mao, Yukang; Ye, Jinxing
Asymmetric synthesis of highly functionalized furanones via direct Michael reactions mediated by a bulky primary amine
Organic Chemistry Frontiers, 2019, 6, 1080
1554514 CIFC17 H20 O3P 21 21 2110.4344; 11.4942; 11.5277
90; 90; 90
1382.58Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang
Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis
Organic Chemistry Frontiers, 2019, 6, 290
1554515 CIFC20 H20 O3P -18.431; 8.6965; 11.7742
80.603; 87.055; 65.92
777.47Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang
Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis
Organic Chemistry Frontiers, 2019, 6, 290
1554516 CIFC25 H21 F O3P 1 21/c 19.8733; 10.3877; 37.781
90; 96.893; 90
3846.8Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang
Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis
Organic Chemistry Frontiers, 2019, 6, 290
1554517 CIFC19 H16 O2F d d 223.63; 42.848; 5.8546
90; 90; 90
5927.8Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua
Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)–C(sp2) bonds
Organic Chemistry Frontiers, 2019, 6, 437
1554518 CIFC20 H18 O3P 1 21/c 110.476; 15.249; 11.317
90; 116.28; 90
1621Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua
Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)‒C(sp2) bonds
Organic Chemistry Frontiers, 2019, 6, 437
1554519 CIFC23 H21 N O3 SI 1 a 18.3257; 15.1988; 16.3404
90; 95.005; 90
2059.8Zhu, Tong-Hao; Zhang, Xiao-Chen; Zhao, Kai; Loh, Teck-Peng
Cu(OTf)2-mediated C(sp2)–H arylsulfonylation of enamides via the insertion of sulfur dioxide
Organic Chemistry Frontiers, 2019, 6, 94
1554520 CIFC23 H25 N3 O3P 21 21 2111.8106; 12.5767; 26.9924
90; 90; 90
4009.4Luo, Xiaowei; Chen, Chunmei; Tao, Huaming; Lin, Xiuping; Yang, Bin; Zhou, Xuefeng; Liu, Yonghong
Structurally diverse diketopiperazine alkaloids from the marine-derived fungus Aspergillus versicolor SCSIO 41016
Organic Chemistry Frontiers, 2019, 6, 736
1554521 CIFC20 H23 N2 O3 PP -19.115; 9.448; 11.944
101.46; 91.031; 106.62
962.9Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu
Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines
Organic Chemistry Frontiers, 2019, 6, 393
1554522 CIFC18 H20 N O3 PP 1 c 17.6453; 11.642; 9.808
90; 102.969; 90
850.7Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu
Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines
Organic Chemistry Frontiers, 2019, 6, 393
1554523 CIFC30 H40 N6 O12C 1 2/c 127.337; 6.1593; 20.343
90; 106.22; 90
3288.9Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel
Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water
Organic Chemistry Frontiers, 2019, 6, 75
1554524 CIFC30 H36 N6 O10P 1 21/n 16.8698; 14.4541; 14.7842
90; 95.204; 90
1461.97Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel
Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water
Organic Chemistry Frontiers, 2019, 6, 75
1554525 CIFC26 H38 N6 O9 S2P n a 2115.1627; 6.4915; 29.4057
90; 90; 90
2894.4Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel
Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water
Organic Chemistry Frontiers, 2019, 6, 75
1554526 CIFC21 H28 N2 O8P 1 21 111.4833; 7.3773; 13.116
90; 96.533; 90
1103.92Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang
A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921
Organic Chemistry Frontiers, 2019, 6, 773
1554527 CIFC32 H34 Br0 Cl N O4P 21 21 216.1903; 13.744; 32.103
90; 90; 90
2731.3Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang
A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921
Organic Chemistry Frontiers, 2019, 6, 773
1554528 CIFC5 H4 F N5 O6P -17.976; 8.218; 15.344
94.059; 104.85; 97.364
958.5Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554529 CIFC5 H4 F N5 O6P 1 21 15.4659; 10.477; 8.1322
90; 94.857; 90
464.03Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554530 CIFC3 H3 F N6 O4P n a 2111.4331; 5.7212; 11.2434
90; 90; 90
735.44Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554531 CIFC5 H4 F N5 O6P b c a6.6055; 11.5186; 23.4809
90; 90; 90
1786.57Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.
N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
Organic Chemistry Frontiers, 2019, 6, 249
1554532 CIFC19 H15 N O3P c a 2114.3845; 4.3448; 23.199
90; 90; 90
1449.9Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung
Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides
Organic Chemistry Frontiers, 2019, 6, 226
1554533 CIFC19 H15 N O2P 1 c 121.0827; 8.2829; 8.2169
90; 95.222; 90
1428.93Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung
Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides
Organic Chemistry Frontiers, 2019, 6, 226
1554534 CIFC28 H33 Au Cl O2 PP -19.2179; 10.4777; 14.2247
100.062; 92.031; 103.287
1312.41Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung
Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides
Organic Chemistry Frontiers, 2019, 6, 226
1554535 CIFC33 H32 Cl N O9P 21 21 2111.0158; 12.13; 23.587
90; 90; 90
3151.7Cao, Jian; Liu, Jin-Yu; Zhang, Yi-Ming; Wang, Zhu-Yin; Xu, Peng-Fei
Synergistic promotion by intramolecular hydrogen bonding: a bi-functionally catalyzed cascade reaction for the synthesis of enantiopure chromenopyrrolidines
Organic Chemistry Frontiers, 2019, 6, 674
1554536 CIFC20 H15 Br2 N O2P c a 217.0667; 23.0878; 21.9663
90; 90; 90
3583.9Liu, Zhenhua; Zhu, Guangyu; Gao, Wen; Yang, Lin; Ji, Huimin; Tong, Lili; Tang, Bo
Copper-catalyzed regioselective cyclization of vinyl azides by gem-difluoromethylene for trisubstituted pyridines
Organic Chemistry Frontiers, 2019, 6, 468
1554537 CIFC17 H17 Br N4 OP -15.2572; 12.458; 13.205
69.94; 83.57; 89.74
806.7Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G.
3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations
Organic Chemistry Frontiers, 2019, 6, 335
1554538 CIFC27 H21 N2 O PP 1 21/c 112.429; 10.415; 37.841
90; 90.13; 90
4898.4Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G.
3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations
Organic Chemistry Frontiers, 2019, 6, 335
1554539 CIFC34 H44 N2 O SiP -18.8134; 10.3559; 18.035
100.993; 95.022; 92.933
1605.78Chen, Cui-Hong; Chai, Yun; Zhou, Zheng-Xin; Rao, Wei-Hao; Liu, Bin; Liu, Li; Xu, Ran; Liu, Yue-Jin; Zeng, Ming-Hua
Room-temperature Pd(ii)-catalyzed direct C–H TIPS-ethynylation of phenylacetic amides with terminal alkynes
Organic Chemistry Frontiers, 2019, 6, 442
1554540 CIFC35 H30P m n 2144.902; 11.1591; 10.6337
90; 90; 90
5328.2Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe
[15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase
Organic Chemistry Frontiers, 2019, 6, 309
1554541 CIFC42 H36P -111.372; 13.1796; 24.509
105.144; 93.375; 90.36
3538.8Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe
[15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase
Organic Chemistry Frontiers, 2019, 6, 309
1554542 CIFC42 H54 O6 S2 SeP -114.2625; 18.0213; 31.3062
86.466; 83.674; 83.298
7933.2Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554543 CIFC42 H54 O8 S2 SeP 1 21/n 117.4194; 8.2052; 28.3968
90; 90.166; 90
4058.73Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554544 CIFC42 H54 O6 Se Te2P -112.1441; 16.8305; 20.8669
98.844; 91.448; 102.981
4098.7Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554545 CIFC42 H54 O6 S Se2P -114.2879; 18.0394; 31.4094
86.414; 83.365; 83.373
7977.7Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng
Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity
Organic Chemistry Frontiers, 2019, 6, 263
1554546 CIFC24 H19 Br N2 OP 1 21/c 113.0718; 15.5471; 10.5005
90; 113.181; 90
1961.7Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554547 CIFC24 H19 Cl N2 OP 1 21/c 112.9966; 15.5319; 10.522
90; 113.397; 90
1949.3Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554548 CIFC16 H14 Cl N O2P 21 21 219.5976; 10.3316; 13.9249
90; 90; 90
1380.8Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554549 CIFC19 H16 N2 OP -18.802; 9.9463; 10.213
116.522; 100.853; 103.243
734.13Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554550 CIFC19 H19 Cl2 N O4C 1 2/c 133.58; 13.96; 8.0737
90; 100.506; 90
3721.3Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying
Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Organic Chemistry Frontiers, 2019, 6, 256
1554551 CIFC13 H22 O2P b c a11.8513; 8.0917; 24.6768
90; 90; 90
2366.4He, Min; Yi, Jiuzhou; Zhao, Gaoyuan; Chen, Peiqi; Long, Dan; Hu, Xiaojun; Li, Huilin; Xie, Xingang; Wang, Xiaolei; She, Xuegong
A concise approach to the tricyclic framework of longipinane- and ent-longipinane-type sesquiterpenoids
Organic Chemistry Frontiers, 2019, 6, 383
1554552 CIFC25 H24 O5 SP 1 21 19.1789; 10.574; 11.4116
90; 91.684; 90
1107.11Zhang, Nan; He, Tingting; Liu, Yidong; Li, Shan; Tan, Yu; Peng, Lei; Li, Dongmei; Shan, Chunhui; Yan, Hailong
Organocatalytic atropo- and E/Z-selective Michael addition reaction of ynones with α-amido sulfones as sulfone-type nucleophile
Organic Chemistry Frontiers, 2019, 6, 451
1554553 CIFC12 H10 F3 N O6 SeP -19.809; 9.877; 9.925
66.084; 65.463; 64.347
758.1Ge, Hangming; Shen, Qilong
Trifluoromethyl-substituted selenium ylide: a broadly applicable electrophilic trifluoromethylating reagent
Organic Chemistry Frontiers, 2019, 6, 2205
1554554 CIFC20 H29 N O SP 1 21 110.5315; 7.0899; 12.4878
90; 105.29; 90
899.43Qin, Shuanglin; Liu, Tongtong; Luo, Yunhao; Jiang, Shende; Yang, Guang
Diastereoselective Rh-catalyzed decarboxylative allylation to form quaternary stereocenters using sulfinimine as the directing group
Organic Chemistry Frontiers, 2019, 6, 732
1554555 CIFC26 H31 N3 SiC 1 2/c 141.982; 8.4505; 16.3226
90; 123.085; 90
4851.8Wu, Wanqing; Fang, Songjia; Jiang, Guangbin; Li, Meng; Jiang, Huanfeng
Palladium-catalyzed regioselective C–H alkynylation of indoles with bromoalkynes in water
Organic Chemistry Frontiers, 2019, 6, 2200
1554556 CIFC30 H25 N O2P 1 21/c 15.7768; 26.401; 15.2336
90; 95.248; 90
2313.6Ji, Cheng-Long; Pan, Yao; Geng, Fang-Zhou; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Synergistic silver/scandium catalytic spiroketalization of β-alkynyl ketones for the atom economical synthesis of skeletally diverse spirocyclic isochromenes
Organic Chemistry Frontiers, 2019, 6, 474
1554557 CIFC21 H21 N O2 SC 1 2/c 131.1655; 8.4946; 13.3472
90; 98.752; 90
3492.37Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa
Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles
Organic Chemistry Frontiers, 2019, 6, 480
1554558 CIFC21 H18 Br N O3 SP 1 21/n 18.6549; 18.21; 11.9124
90; 94.769; 90
1870.96Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa
Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles
Organic Chemistry Frontiers, 2019, 6, 480
1554559 CIFC28 H36 N2 O2 SiP -19.7904; 10.7882; 12.3517
83.891; 69.723; 84.499
1214.36Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang
Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C–H activation
Organic Chemistry Frontiers, 2019, 6, 699
1554560 CIFC27 H31 N O4 SiP -19.9601; 10.6766; 11.8691
74.393; 85.571; 88.958
1211.99Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang
Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C–H activation
Organic Chemistry Frontiers, 2019, 6, 699
1554561 CIFC31 H26 Cl2 N4 O4 S2P 1 21/c 18.24; 10.3859; 17.7438
90; 95.373; 90
1511.84Han, Shuaijun; Gao, Xianying; Wu, Qingsong; Li, Jingya; Zou, Dapeng; Wu, Yusheng; Wu, Yangjie
Nickel-promoted C(2)‒H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide
Organic Chemistry Frontiers, 2019, 6, 830
1554562 CIFC25.5 H28 Cl N4 O2.5 PdP n a 2125.795; 9.144; 21.256
90; 90; 90
5013.6Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides
Organic Chemistry Frontiers, 2019, 6, 544
1554563 CIFC18 H11 Br N2C 1 2/c 126.203; 10.644; 30.852
90; 106.633; 90
8245Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides
Organic Chemistry Frontiers, 2019, 6, 544
1554564 CIFC16 H18 O2 SP 1 21 15.712; 15.28; 8.28
90; 104.192; 90
700.6Sun, Yongjie; Jiang, Jun; Guo, Xiaochong; Wen, Jialin; Zhang, Xumu
Asymmetric hydrogenation of α,β-unsaturated sulfones by a rhodium/thiourea–bisphosphine complex
Organic Chemistry Frontiers, 2019, 6, 1438
1554565 CIFC32 H27 N O4 SP 43 21 213.6813; 13.6813; 29.053
90; 90; 90
5438.1Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song
Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones
Organic Chemistry Frontiers, 2019, 6, 405
1554566 CIFC33 H29 N O4 SP 21 21 2111.043; 14.753; 17.258
90; 90; 90
2811.6Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song
Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones
Organic Chemistry Frontiers, 2019, 6, 405
1554567 CIFC22 H24 O7P -19.1375; 13.1527; 16.354
95.187; 95.294; 103.04
1894.04Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin
Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae
Organic Chemistry Frontiers, 2019, 6, 591
1554568 CIFC18 H17 Cl3 O5P 1 2 113.8718; 9.6965; 13.8978
90; 92.204; 90
1867.98Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin
Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae
Organic Chemistry Frontiers, 2019, 6, 591
1554569 CIFC172 H203 N13 O10 P2C 1 2/c 121.469; 29.096; 28.543
90; 95.17; 90
17757Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung
Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers
Organic Chemistry Frontiers, 2019, 6, 299
1554570 CIFC173 H203 N13 O10 P2C 1 2/c 121.505; 29.114; 28.751
90; 94.83; 90
17937Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung
Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers
Organic Chemistry Frontiers, 2019, 6, 299
1554571 CIFC12 H12 N2 O2 SP 1 21/c 18.968; 9.084; 14.804
90; 105.357; 90
1163Zu, Weisai; Liu, Shuai; Jia, Xin; Xu, Liang
Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions
Organic Chemistry Frontiers, 2019, 6, 1356
1554572 CIFC19 H15 N O2 SP 1 21 18.0275; 8.0254; 12.699
90; 101.787; 90
800.9Zhao, Zi-Biao; Shi, Lei; Meng, Fan-Jie; Li, Yaming; Zhou, Yong-Gui
Synthesis of chiral seven-membered cyclic sulfonamides through palladium-catalyzed arylation of cyclic imines
Organic Chemistry Frontiers, 2019, 6, 1572
1554573 CIFC10 H13 N O3P 16.9308; 6.9507; 11.8464
84.194; 79.023; 64.094
503.84Yang, Wu-Lin; Sun, Zhong-Tao; Zhang, Jian; Li, Zhong; Deng, Wei-Ping
Enantioselective synthesis of 3-amino-hydrobenzofuran-2,5-diones via Cu(i)-catalyzed intramolecular conjugate addition of imino esters
Organic Chemistry Frontiers, 2019, 6, 579
1554574 CIFC116 H162 Br F3 O12P 1 21 115.1538; 13.5668; 27.2737
90; 92.794; 90
5600.5Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A.
Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes
Organic Chemistry Frontiers, 2019, 6, 603
1554575 CIFC116 H162 Br F3 O12P 1 21 115.0627; 13.3599; 27.1554
90; 94.396; 90
5448.6Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A.
Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes
Organic Chemistry Frontiers, 2019, 6, 603
1554576 CIFC10 H8 N2 SeP 1 21/c 17.15; 11.643; 12.098
90; 95.268; 90
1002.9Cao, Yuan; Liu, Jie; Liu, Fanmin; Jiang, Lvqi; Yi, Wenbin
Copper-catalyzed direct and odorless selenylation with a sodium selenite-based reagent
Organic Chemistry Frontiers, 2019, 6, 825
1554577 CIFC9 H9 F3 N2P 1 21 15.799; 7.486; 10.479
90; 104.17; 90
441.1Chen, Mu-Wang; Deng, Zhihong; Yang, Qin; Huang, Jian; Peng, Yiyuan
Enantioselective synthesis of trifluoromethylated dihydroquinoxalinones via palladium-catalyzed hydrogenation
Organic Chemistry Frontiers, 2019, 6, 746
1554578 CIFC29 H24 N2 O2P 21 21 219.1297; 10.326; 24.127
90; 90; 90
2274.5Xu, Lubin; Chen, Haohua; Liu, Jian; Zhou, Lan; Liu, Qing; Lan, Yu; Xiao, Jian
Chiral phosphoric acid-catalyzed asymmetric C(sp3)–H functionalization of biomass-derived 2,5-dimethylfuran via two sequential Cope-type rearrangements
Organic Chemistry Frontiers, 2019, 6, 1162
1554579 CIFC31 H42 O11P 21 21 2132.1461; 11.483; 8.0162
90; 90; 90
2959.05Zhang, Jia; He, Jun; Cheng, Yung-Chi; Zhang, Pei-Cheng; Yan, Yu; Zhang, Hao-Jun; Zhang, Wei-Ku; Xu, Jie-Kun
Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana
Organic Chemistry Frontiers, 2019, 6, 2312
1554580 CIFC35 H26 Cl N5 OP 21 21 2111.351; 11.9996; 21.215
90; 90; 90
2889.6Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang
Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions
Organic Chemistry Frontiers, 2019, 6, 1842
1554581 CIFC33 H23 Cl N4 OP -19.3289; 10.9229; 12.8668
87.237; 78.614; 85.681
1280.91Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang
Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions
Organic Chemistry Frontiers, 2019, 6, 1842
1554582 CIFC16 H14 F3 N O4 SP 21 21 217.9193; 15.3744; 16.4929
90; 90; 90
2008.08Gui, Yang; Liang, Xinping; Li, Yanan; Li, Kuiliang; Zha, Zhenggen; Wang, Zhiyong
Asymmetric synthesis of fluoroalkylated N,O-ketals via an organocatalytic dehydration/aminalization/aza-Michael desymmetrization
Organic Chemistry Frontiers, 2019, 6, 942
1554583 CIFC36 H32 Br N O4 P2P 21 21 2128.168; 11.3424; 10.2126
90; 90; 90
3262.9Liu, Bing; Li, Wenbo; Wu, Hai-Hong; Zhang, Junliang
Enantiodivergent synthesis of 1,2-bis(diphenylphosphino)ethanes via asymmetric [3 + 2]-cycloaddition
Organic Chemistry Frontiers, 2019, 6, 694
1554584 CIFC22 H20 Br N3 O4P 1 21 19.2282; 9.1743; 12.829
90; 109.724; 90
1022.4Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai
Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence
Organic Chemistry Frontiers, 2019, 6, 919
1554585 CIFC21 H24 N2 O7P 1 21 19.6264; 10.858; 11.2163
90; 113.736; 90
1073.2Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai
Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence
Organic Chemistry Frontiers, 2019, 6, 919
1554586 CIFC17 H20 F3 N O3P 1 21/c 111.431; 5.931; 25.849
90; 94.751; 90
1746.5Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor
Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1109
1554587 CIFC14 H14 F3 N O2P -111.218; 12.296; 16.82
108.32; 101.98; 102.65
2051.1Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor
Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1109
1554588 CIFC40 H59 Cl N2 P2 ZrP -111.9355; 12.1743; 15.3187
112.686; 97.711; 98.63
1984.93Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H.
Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends.
Chemical science, 2018, 9, 5223-5232
1554589 CIFC52 H78 Cl N3 P2 ZrP 1 21/n 112.10234; 13.69809; 31.6606
90; 91.0656; 90
5247.75Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H.
Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends.
Chemical science, 2018, 9, 5223-5232
1554590 CIFC52 H82 Cl N5 O P2 ZrC 1 2/c 137.6269; 12.5284; 22.9308
90; 99.4621; 90
10662.6Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H.
Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends.
Chemical science, 2018, 9, 5223-5232
1554591 CIFC57 H80 Cl N3 P2 ZrP -112.6621; 18.1002; 23.9357
100.866; 95.4948; 103.491
5182.35Merz, Lukas S.; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H.
Dehydrogenative coupling of 4-substituted pyridines mediated by a zirconium(ii) synthon: reaction pathways and dead ends.
Chemical science, 2018, 9, 5223-5232
1554592 CIFC15 H14 O7P 1 21 17.1336; 7.3556; 13.246
90; 102.455; 90
678.7Szwalbe, Agnieszka J.; Williams, Katherine; Song, Zhongshu; de Mattos-Shipley, Kate; Vincent, Jason L.; Bailey, Andrew M.; Willis, Christine L.; Cox, Russell J.; Simpson, Thomas J.
Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi.
Chemical science, 2019, 10, 233-238
1554593 CIFC15 H13 O6.5P 21 21 217.4082; 7.9771; 43.956
90; 90; 90
2597.6Szwalbe, Agnieszka J.; Williams, Katherine; Song, Zhongshu; de Mattos-Shipley, Kate; Vincent, Jason L.; Bailey, Andrew M.; Willis, Christine L.; Cox, Russell J.; Simpson, Thomas J.
Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi.
Chemical science, 2019, 10, 233-238
1554594 CIFC152 H144 Cd4 F24 N28 O24 S8F -4 3 c34.3297; 34.3297; 34.3297
90; 90; 90
40458.5Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554595 CIFC160.5 H126.25 B3 F27 N29.25 Ni4 O15.25 S5C 1 2/c 134.257; 18.552; 54.149
90; 97.09; 90
34150Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554596 CIFC78.83 H76.5 F17.5 K0.83 N15.5 O11.5 S3.83 Sb Zn2R -3 :H14.93; 14.93; 68.868
90; 90; 120
13294Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554597 CIFC153 H132 Cd4 F69 N32 O3 S Sb7P 21 326.441; 26.441; 26.441
90; 90; 90
18486Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554598 CIFC531.5 H392.25 F48 N82.25 Ni8 O53.25 S16 Zn6P 4/n :234.21; 34.21; 27.215
90; 90; 90
31850Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554599 CIFC70.5 H64.5 F19.5 N15.5 O4.5 S1.5 Sb2.5 Zn2C 1 2 132.3977; 31.639; 22.0583
90; 123.314; 90
18894.9Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554600 CIFC543 H406 Co8 F48 N83.5 O53.75 S16 Zn6P 4/n :234.3; 34.3; 27.428
90; 90; 90
32269Percástegui, Edmundo G; Mosquera, Jesús; Ronson, Tanya K.; Plajer, Alex J.; Kieffer, Marion; Nitschke, Jonathan R.
Waterproof architectures through subcomponent self-assembly.
Chemical science, 2019, 10, 2006-2018
1554601 CIFC65 H73 Ca I N11 O4 UP 1 21/c 117.4073; 15.531; 33.3439
90; 114.157; 90
8225.2Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554602 CIFC77 H77 N15 O2 Rb UP 21 21 2113.6821; 21.8875; 24.244
90; 90; 90
7260.28Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554603 CIFC62 H62 I N12 O2 U ZnP 21 21 2113.273; 16.4368; 27.8646
90; 90; 90
6079.1Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554604 CIFC87 H87 Cl N9 O2 Ti UP 1 21/c 120.517; 21.431; 19.018
90; 117.115; 90
7443Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554605 CIFC86.48 H86.48 Cl3 Mg N15 O2 U ZrC 1 2/c 147.424; 14.484; 30.602
90; 127.576; 90
16659Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554606 CIFC57 H57 Cl N11 O2 U ZnI 1 2/a 128.7327; 22.93; 24.8036
90; 102.077; 90
15979.9Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554607 CIFC82 H86 Cl N12 O3 U ZrP 1 21/c 120.2769; 21.7767; 18.5794
90; 115.829; 90
7384.4Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554608 CIFC87 H87 Cl Mg N17 O2 UI 1 2/a 124.852; 23.01; 28.754
90; 102.183; 90
16073Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554609 CIFC312 H312 Cs6 N60 O12 U6R -3 :H27.7671; 27.7671; 35.7644
90; 90; 120
23880.5Zegke, Markus; Zhang, Xiaobin; Pidchenko, Ivan; Hlina, Johann A.; Lord, Rianne M.; Purkis, Jamie; Nichol, Gary S.; Magnani, Nicola; Schreckenbach, Georg; Vitova, Tonya; Love, Jason B.; Arnold, Polly L.
Differential uranyl(v) oxo-group bonding between the uranium and metal cations from groups 1, 2, 4, and 12; a high energy resolution X-ray absorption, computational, and synthetic study
Chemical Science, 2019, 10, 9740
1554610 CIFC26 H28 F12 N6 Ni P2P 1 21/n 113.8699; 17.1455; 14.2982
90; 100.97; 90
3338.1Lieske, Lauren E.; Rheingold, Arnold L.; Machan, Charles W.
Electrochemical reduction of carbon dioxide with a molecular polypyridyl nickel complex
Sustainable Energy & Fuels, 2018, 2, 1269
1554611 CIFC63 H46 Cu F6 N4 O P3P -111.2628; 12.4158; 21.9828
83.055; 78.448; 87.667
2989.2Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael
Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety
Sustainable Energy & Fuels, 2019, 3, 692
1554612 CIFC48 H28 Cu F6 N8 PP -18.1362; 10.6863; 22.4625
86.186; 81.28; 87.085
1924.5Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael
Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety
Sustainable Energy & Fuels, 2019, 3, 692
1554613 CIFC22.5 H28 K0.5 N6 Ni0.5 O3P -112.9939; 13.5751; 14.0727
78.667; 85.315; 77.907
2377.8Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554614 CIFC36 H44 K2 N10 O3P 1 21/c 123.3268; 7.362; 22.2054
90; 94.794; 90
3800Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554615 CIFC24 H20 N10 NiP 1 21/n 17.7492; 16.392; 8.8505
90; 101.096; 90
1103.2Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554616 CIFC17 H22 B10P -16.9712; 11.7604; 12.9797
107.511; 102.996; 102.125
943.63Chaari, Mahdi; Kelemen, Zsolt; Choquesillo-Lazarte, Duane; Gaztelumendi, Nerea; Teixidor, Francesc; Viñas, Clara; Nogués, Carme; Núñez, Rosario
Efficient blue light emitting materials based on m-carborane-anthracene dyads. Structure, photophysics and bioimaging studies.
Biomaterials science, 2019, 7, 5324-5337
1554617 CIFC17 H20 B10 I2I m a 213.801; 25.643; 6.8626
90; 90; 90
2428.7Chaari, Mahdi; Kelemen, Zsolt; Choquesillo-Lazarte, Duane; Gaztelumendi, Nerea; Teixidor, Francesc; Viñas, Clara; Nogués, Carme; Núñez, Rosario
Efficient blue light emitting materials based on m-carborane-anthracene dyads. Structure, photophysics and bioimaging studies.
Biomaterials science, 2019, 7, 5324-5337
1554618 CIFC17 H21 B10 IP 1 21/n 19.319; 11.7553; 18.5808
90; 94.913; 90
2028Chaari, Mahdi; Kelemen, Zsolt; Choquesillo-Lazarte, Duane; Gaztelumendi, Nerea; Teixidor, Francesc; Viñas, Clara; Nogués, Carme; Núñez, Rosario
Efficient blue light emitting materials based on m-carborane-anthracene dyads. Structure, photophysics and bioimaging studies.
Biomaterials science, 2019, 7, 5324-5337
1554619 CIFC54 H48 Cl0 F0 N0 O43.5C 1 2 119.1281; 24.4901; 15.6182
90; 109.513; 90
6896.1Phan, Chiuyen; Zheng, Ziyang; Wang, Jianwei; Wang, Qiwen; Hu, Xiurong; Tang, Guping; Bai, Hongzhen
Enhanced antitumour effect for hepatocellular carcinoma in the advanced stage using a cyclodextrin-sorafenib-chaperoned inclusion complex.
Biomaterials science, 2019, 7, 4758-4768
1554620 CIFC24 H38 F6 Fe P Ru S3C m c e15.867; 20.073; 18.513
90; 90; 90
5896.4Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554621 CIFC14 H23 Co S3P 1 21/c 113.1028; 8.6112; 14.2219
90; 101.551; 90
1572.17Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554622 CIFC30 H43 F6 Fe P Ru S4P 1 21/n 114.3616; 13.9373; 16.9737
90; 99.0564; 90
3355.1Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554623 CIFC26 H41 F12 Fe N P2 Ru S3P n m a11.8; 15.608; 18.603
90; 90; 90
3426Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554624 CIFC48 H58 B Co Fe S3P n a 2120.2817; 17.2944; 12.4241
90; 90; 90
4357.9Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554625 CIFC47 H56 B Co Fe S3P n a 2120.576; 16.9755; 12.0227
90; 90; 90
4199.4Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554626 CIFC48 H59 B Fe Ru S3P 1 21/c 115.5349; 15.8332; 18.3897
90; 90.694; 90
4522.9Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping
Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions
Catalysis Science & Technology, 2019, 9, 6492
1554627 CIFC6 H6 N8 O9P 1 21/c 17.6484; 16.154; 11.156
90; 106.283; 90
1323.1Huang, Qi; Guo, Zhicheng; Liao, Longyu; Hao, Shilong; Nie, Fude; Li, Hongzhen
Customization of the molecular structure to modulate the crystal packing style of energetic materials
Molecular Systems Design & Engineering, 2019, 4, 1032
1554628 CIFC8 H8 N10 O14P 43 21 27.0912; 7.0912; 34.097
90; 90; 90
1714.6Huang, Qi; Guo, Zhicheng; Liao, Longyu; Hao, Shilong; Nie, Fude; Li, Hongzhen
Customization of the molecular structure to modulate the crystal packing style of energetic materials
Molecular Systems Design & Engineering, 2019, 4, 1032
1554629 CIFC6 H6 N8 O8P b c a11.0661; 13.9316; 15.839
90; 90; 90
2441.9Huang, Qi; Guo, Zhicheng; Liao, Longyu; Hao, Shilong; Nie, Fude; Li, Hongzhen
Customization of the molecular structure to modulate the crystal packing style of energetic materials
Molecular Systems Design & Engineering, 2019, 4, 1032
1554630 CIFC13 H30 I N3P 1 21/c 18.6068; 14.9193; 14.6169
90; 110.458; 90
1758.5Xue, Boxin; Wang, Fen; Zheng, Jifu; Li, Shenghai; Zhang, Suobo
Highly stable polysulfone anion exchange membranes incorporated with bulky alkyl substituted guanidinium cations
Molecular Systems Design & Engineering, 2019, 4, 1039
1554631 CIFC13 H28 Cl N3 O2C 1 2/c 19.9771; 18.0751; 8.9806
90; 104.318; 90
1569.2Xue, Boxin; Wang, Fen; Zheng, Jifu; Li, Shenghai; Zhang, Suobo
Highly stable polysulfone anion exchange membranes incorporated with bulky alkyl substituted guanidinium cations
Molecular Systems Design & Engineering, 2019, 4, 1039
1554632 CIFC39 H32 F6 Ir N3 O0 S2C 1 2/c 126.026; 12.94; 22.386
90; 97.214; 90
7479.4Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860
1554633 CIFC53 H42 F6 Ir N3 S2P -111.3; 15.22; 16.31
79.22; 79.11; 82.46
2693Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860
1554634 CIFC45 H28 F6 Ir N3 S2P 1 21/c 115.5226; 12.6925; 20.61
90; 97.559; 90
4025.3Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860
1554635 CIFC72 H46 Co6 N12 O39P 1 21/c 17.237; 18.371; 62.028
90; 92.02; 90
8242Li, Ang; Qian, Binbin; Zhong, Ming; Liu, Yingying; Chang, Ze; Bu, Xian-He
An insight into the pyrolysis process of metal‒organic framework templates/precursors to construct metal oxide anode materials for lithium-ion batteries
Materials Chemistry Frontiers, 2019, 3, 1398
1554636 CIFC42 H36 N4 O2 Pt2P 1 21/c 111.768; 17.4213; 17.5279
90; 97.615; 90
3561.77Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554637 CIFC43 H38 Cl2 N4 O2 Pt2P 21 21 2111.0565; 16.7748; 20.3659
90; 90; 90
3777.3Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554638 CIFC42 H28 Cl2 N4 O2 Pt2P 1 21/n 19.6783; 18.7346; 19.5011
90; 100.777; 90
3473.6Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554639 CIFC51 H35 Cl3 N4 O2 Pt2P 21 21 2110.7354; 20.1891; 21.7815
90; 90; 90
4720.9Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554640 CIFC43 H38 Cl2 N4 O2 Pt2P 21 21 2111.05822; 16.7782; 20.3868
90; 90; 90
3782.51Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554641 CIFC17 H19 N O2 SP 1 21/n 111.377; 9.712; 13.362
90; 95.331; 90
1470Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554642 CIFC14 H13 N O2 SP 1 21/n 17.9027; 11.1576; 13.5298
90; 93.338; 90
1190.97Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554643 CIFC13 H11 N O2 SP 1 21/n 18.78316; 11.4642; 11.1048
90; 91.3006; 90
1117.88Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554644 CIFC16 H17 N O2 SP 1 21/c 118.9325; 9.4253; 17.2146
90; 114.976; 90
2784.59Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554645 CIFC18 H21 N O2 SR 3 c :H26.477; 26.477; 12.475
90; 90; 120
7574Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554646 CIFC15 H15 N O2 SP -17.7584; 9.0839; 10.0043
109.128; 97.408; 103.752
630.4Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554647 CIFC44 H46 N2 O4P -16.3304; 7.2037; 20.473
89.41; 89.13; 76.08
906.1Dai, Shuangxiong; Cai, Zhengxu; Peng, Zhe; Wang, Zhi; Tong, Bin; Shi, Jianbing; Gan, Shenglong; He, Qiming; Chen, Wei; Dong, Yuping
A stabilized lamellar liquid crystalline phase with aggregation-induced emission features based on pyrrolopyrrole derivatives
Materials Chemistry Frontiers, 2019, 3, 1105
1554648 CIFC4 H14 Br3 N3 OP b c m6.70475; 13.3306; 13.1204
90; 90; 90
1172.68Li, Kai; Dong, Li-Yuan; Xu, Hao-Xiang; Qin, Yan; Li, Zhi-Gang; Azeem, Muhammad; Li, Wei; Bu, Xian-He
Electronic structures and elastic properties of a family of metal-free perovskites
Materials Chemistry Frontiers, 2019, 3, 1678
1554649 CIFC4 H14 I3 N3 OP b c m7.064; 14.089; 13.684
90; 90; 90
1361.9Li, Kai; Dong, Li-Yuan; Xu, Hao-Xiang; Qin, Yan; Li, Zhi-Gang; Azeem, Muhammad; Li, Wei; Bu, Xian-He
Electronic structures and elastic properties of a family of metal-free perovskites
Materials Chemistry Frontiers, 2019, 3, 1678
1554650 CIFC30 H29 N5 OP 1 21/c 122.0567; 7.7405; 15.5138
90; 102.762; 90
2583.2Yang, Jinfeng; Gu, Kaizhi; Shi, Chuanxing; Li, Meng; Zhao, Ping; Zhu, Wei-Hong
Fluorescent thermometer based on a quinolinemalononitrile copolymer with aggregation-induced emission characteristics
Materials Chemistry Frontiers, 2019, 3, 1503
1554651 CIFC20 H22 B F2 N3 OC 1 2/c 112.8894; 9.0135; 31.806
90; 93.146; 90
3689.6Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung
A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells
Materials Chemistry Frontiers, 2019, 3, 1823
1554652 CIFC26 H34 B F2 N3 OC 1 2/c 126.649; 9.8463; 19.4482
90; 101.393; 90
5002.5Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung
A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells
Materials Chemistry Frontiers, 2019, 3, 1823
1554653 CIFC24 H30 B F2 N3 OC 1 2/c 123.744; 12.2488; 19.0154
90; 101.276; 90
5423.6Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung
A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells
Materials Chemistry Frontiers, 2019, 3, 1823
1554654 CIFC20 H24P -14.7535; 6.1267; 13.209
96.215; 96.738; 91.369
379.53Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554655 CIFC24 H26P 1 21/c 112.9394; 8.2851; 9.083
90; 106.48; 90
933.73Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554656 CIFC24 H26P 1 21/n 17.9294; 7.3834; 16.2178
90; 90.745; 90
949.41Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554657 CIFC20 H24P 1 21/n 14.8732; 10.6116; 15.5489
90; 90.251; 90
804.06Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554658 CIFC44 H28 SP -19.7394; 9.8279; 16.0542
96.661; 100.097; 92.178
1499.99Kazantsev, Maxim S.; Sonina, Alina A.; Koskin, Igor P.; Sherin, Peter S.; Rybalova, Tatyana V.; Benassi, Enrico; Mostovich, Evgeny A.
Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
Materials Chemistry Frontiers, 2019, 3, 1545
1554659 CIFC44 H28 SP 1 21/c 115.4125; 9.8016; 20.9249
90; 105.66; 90
3043.7Kazantsev, Maxim S.; Sonina, Alina A.; Koskin, Igor P.; Sherin, Peter S.; Rybalova, Tatyana V.; Benassi, Enrico; Mostovich, Evgeny A.
Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
Materials Chemistry Frontiers, 2019, 3, 1545
1554660 CIFC40 H28 N4C 1 2/c 126.013; 12.858; 10.6428
90; 104.932; 90
3439.5Peng, Zhe; Dai, Shuangxiong; Ji, Yingchun; Tong, Bin; Shi, Jianbing; Cai, Zhengxu; Zhi, Junge; Dong, Yuping
Ionic liquid crystals with aggregation-induced emission properties based on pyrrolo[3,2-b]pyrrole salt compounds
Materials Chemistry Frontiers, 2019, 3, 1385
1554661 CIFC18 H15 Au F5 N OP 1 21/c 17.402; 19.562; 12.283
90; 97.32; 90
1764.1Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua
Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy
Materials Chemistry Frontiers, 2019, 3, 1866
1554662 CIFC18 H15 Au F5 N OP 1 21/c 17.3042; 19.814; 11.9572
90; 95.327; 90
1723Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua
Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy
Materials Chemistry Frontiers, 2019, 3, 1866
1554663 CIFC18 H15 Au F5 N OP 1 21/c 17.2889; 19.8254; 11.9641
90; 95.306; 90
1721.47Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua
Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy
Materials Chemistry Frontiers, 2019, 3, 1866
1554664 CIFC29 H14 N4 O2P 1 21 15.0052; 15.6076; 14.6006
90; 91.275; 90
1140.3Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554665 CIFC30 H16 N4 O2C 1 2 125.4902; 8.4676; 16.9657
90; 104.889; 90
3538.9Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554666 CIFC33 H22 N4 O2C 2 2 2112.0721; 17.9566; 12.2305
90; 90; 90
2651.3Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554667 CIFC36 H28 N4 O2P -18.8302; 18.7601; 19.027
110.64; 94.387; 93.845
2926Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554668 CIFC33 H22 Cl2 N4 O2P 1 21 17.9714; 22.5703; 9.1047
90; 115.426; 90
1479.42Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554669 CIFC48 H30 F6 N4 O2C 2 2 2118.4373; 25.7446; 11.6266
90; 90; 90
5518.7Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554670 CIFC11.67 H8.67 N1.33 O0.67P 1 21/c 18.5584; 18.7684; 17.4034
90; 94.951; 90
2785.03Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554671 CIFC33 H23 B F2 O3P -18.788; 10.446; 15.407
70.818; 88.67; 79.808
1313.8Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554672 CIFC33 H23 B F2 O3C 1 c 153.109; 7.2441; 13.687
90; 97.371; 90
5222Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554673 CIFC33 H23 B F2 O3P 1 21/n 115.955; 8.978; 19.823
90; 113.38; 90
2606.4Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554674 CIFC33 H23 B F2 O3P 1 21/c 115.958; 8.99; 19.915
90; 113.62; 90
2617.7Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554675 CIFC33 H23 B F2 O3P 1 21/c 115.957; 8.984; 19.969
90; 113.55; 90
2624.3Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554676 CIFC30 H22 N2 O2 SP 112.1382; 12.8179; 15.1854
85.684; 78.373; 89.276
2307.59Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo
Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence
Materials Chemistry Frontiers, 2019, 3, 1800
1554677 CIFC30 H22 N2 O2 SP 1 21/c 114.4773; 12.17882; 13.40691
90; 104.925; 90
2284.11Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo
Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence
Materials Chemistry Frontiers, 2019, 3, 1800
1554678 CIFC30 H22 N2 O2 SP 112.135; 12.8327; 15.1864
85.785; 78.371; 89.345
2310.08Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo
Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence
Materials Chemistry Frontiers, 2019, 3, 1800
1554679 CIFC30 H24 N4 O PtP -18.4381; 12.133; 23.3476
86.889; 81.757; 83.205
2347.31Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei
High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions
Materials Chemistry Frontiers, 2019, 3, 2448
1554680 CIFC27 H18 N4 O PtP 21 21 217.7277; 13.36; 20.072
90; 90; 90
2072.3Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei
High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions
Materials Chemistry Frontiers, 2019, 3, 2448
1554681 CIFC37 H28 N4 O3C 1 2/c 126.686; 16.726; 14.573
90; 107.7; 90
6197Ren, Fei; Shi, Jianbing; Tong, Bin; Cai, Zhengxu; Dong, Yuping
Effects of fused rings linked to the 2,5-position of pyrrole derivatives with near-infrared emission on their aggregation-enhanced emission properties
Materials Chemistry Frontiers, 2019, 3, 2072
1554682 CIFC18 H19 N3 OP 1 21/n 116.236; 7.7124; 25.238
90; 104.08; 90
3065.3Li, Aisen; Liu, Hao; Song, Chongping; Geng, Yijia; Xu, Shuping; Zhang, Hongyu; Zhang, Houyu; Cui, Haining; Xu, Weiqing
Flexible control of excited state transition under pressure/temperature: distinct stimuli-responsive behaviours of two ESIPT polymorphs
Materials Chemistry Frontiers, 2019, 3, 2128
1554683 CIFC18 H19 N3 OP 1 21/c 112.841; 10.286; 12.663
90; 111.023; 90
1561.2Li, Aisen; Liu, Hao; Song, Chongping; Geng, Yijia; Xu, Shuping; Zhang, Hongyu; Zhang, Houyu; Cui, Haining; Xu, Weiqing
Flexible control of excited state transition under pressure/temperature: distinct stimuli-responsive behaviours of two ESIPT polymorphs
Materials Chemistry Frontiers, 2019, 3, 2128
1554684 CIFC10 H26 Cl6 N2 ZnP 1 21/c 124.5577; 18.3997; 18.1621
90; 92.376; 90
8199.6Zhang, Yu-Wei; Wang, Qing; Shi, Ping-Ping; Zhang, Wan-Ying; Ye, Qiong; Fu, Da-Wei
Visual low-high interchange in a dielectric switch for trimethylchloroethylamine tetrachlorozincate with a large leap symmetry breaking
Materials Chemistry Frontiers, 2019, 3, 2077
1554685 CIFC10 H26 Cl6 N2 ZnI 41/a :212.7985; 12.7985; 25.8884
90; 90; 90
4240.6Zhang, Yu-Wei; Wang, Qing; Shi, Ping-Ping; Zhang, Wan-Ying; Ye, Qiong; Fu, Da-Wei
Visual low-high interchange in a dielectric switch for trimethylchloroethylamine tetrachlorozincate with a large leap symmetry breaking
Materials Chemistry Frontiers, 2019, 3, 2077
1554686 CIFC218 H276 O28 P2 PtP -112.2995; 12.7098; 38.043
80.979; 89.471; 65.725
5344.1Hu, Yang; Wang, Wei; Yao, Rui; Wang, Xu-Qing; Wang, Yu-Xuan; Sun, Bin; Chen, Li-Jun; Zhang, Ying; Zhao, Xiao-Li; Xu, Lin; Tan, Hong-Wei; Yu, Yihua; Li, Xiaopeng; Yang, Hai-Bo
Facile synthesis of diverse rotaxanes via successive supramolecular transformations
Materials Chemistry Frontiers, 2019, 3, 2397
1554687 CIFC52 H57.5 N4.5 O7P 1 21/c 115.215; 14.04; 23.048
90; 100.849; 90
4835Chan, Sing-Ming; Tang, Fung-Kit; Kwan, Chak-Shing; Lam, Ching-Yau; Hau, Sam C. K.; Leung, Ken Cham-Fai
Water-compatible fluorescent [2]rotaxanes for Au3+ detection and bioimaging
Materials Chemistry Frontiers, 2019, 3, 2388
1554688 CIFC37 H23 N O2 SP -18.9754; 11.9049; 13.8094
111.039; 90.487; 95.955
1368.09Huang, Lili; Wen, Xue; Liu, Jianwei; Chen, Mingxing; Ma, Zhiyong; Jia, Xinru
An AIE molecule featuring changeable triplet emission between phosphorescence and delayed fluorescence by an external force
Materials Chemistry Frontiers, 2019, 3, 2151
1554689 CIFC43 H31 N3P -112.995; 14.047; 18.771
85.928; 72.336; 78.362
3198Li, Aisen; Chu, Ning; Liu, Jianwei; Liu, Hao; Wang, Jing; Xu, Shuping; Cui, Haining; Zhang, Hongyu; Xu, Weiqing; Ma, Zhiyong
Pressure-induced remarkable luminescence switch of a dimer form of donor–acceptor–donor triphenylamine (TPA) derivative
Materials Chemistry Frontiers, 2019, 3, 2768
1554690 CIFC42 H30 N4P 1 21/c 117.2834; 10.2606; 18.3175
90; 96.618; 90
3226.74Li, Aisen; Chu, Ning; Liu, Jianwei; Liu, Hao; Wang, Jing; Xu, Shuping; Cui, Haining; Zhang, Hongyu; Xu, Weiqing; Ma, Zhiyong
Pressure-induced remarkable luminescence switch of a dimer form of donor–acceptor–donor triphenylamine (TPA) derivative
Materials Chemistry Frontiers, 2019, 3, 2768
1554691 CIFC15 H15 N O2P -16.2682; 7.1504; 28.857
94.165; 90.331; 90.002
1289.94Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai
Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state
Materials Chemistry Frontiers, 2019, 3, 2746
1554692 CIFC16 H17 N O2P -16.2328; 7.2129; 31.0245
92.777; 94.558; 90.014
1388.7Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai
Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state
Materials Chemistry Frontiers, 2019, 3, 2746
1554693 CIFC17 H19 N O2P -16.1745; 7.0411; 33.2296
86.545; 84.929; 89.992
1436.38Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai
Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state
Materials Chemistry Frontiers, 2019, 3, 2746
1554694 CIFC260 H202 Cu4 N16 O23P 1 21/n 138.372; 43.842; 41.771
90; 101.834; 90
68778Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu
Tunable enforced cavities inside self-assembled capsules
Organic Chemistry Frontiers, 2019, 6, 1561
1554695 CIFC40 H40 B Cl4 Cu F4 N4P -110.7588; 13.1415; 15.339
106.956; 100.938; 91.717
2028.3Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu
Tunable enforced cavities inside self-assembled capsules
Organic Chemistry Frontiers, 2019, 6, 1561
1554696 CIFC31 H29 Cl N2 O4P 21 21 219.0064; 9.7885; 30.9078
90; 90; 90
2724.81Chu, Ming-Ming; Qi, Suo-Suo; Ju, Wan-Zhen; Wang, Yi-Feng; Chen, Xue-Yang; Xu, Dan-Qian; Xu, Zhen-Yuan
Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters
Organic Chemistry Frontiers, 2019, 6, 1140
1554697 CIFC63.5 H60 N6 O14.5C 1 c 136.594; 7.353; 28.802
90; 123.87; 90
6435Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J.
Reactions of 2-aza-21-carbaporphyrin with aniline derivatives
Organic Chemistry Frontiers, 2019, 6, 908
1554698 CIFC79 H72 N6 O6P 1 21/c 133.74; 12.9479; 14.8229
90; 100.325; 90
6370.7Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J.
Reactions of 2-aza-21-carbaporphyrin with aniline derivatives
Organic Chemistry Frontiers, 2019, 6, 908
1554699 CIFC18 H16 Br2 F N O3 SP -16.9921; 11.2113; 12.4434
96.443; 95.376; 95.626
959.19Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554700 CIFC19 H20 Cl N O3 SC 1 2/c 118.258; 13.081; 15.4466
90; 91.845; 90
3687.2Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554701 CIFC17 H14 N2 O7 SP 1 21/n 17.4466; 24.7338; 9.6421
90; 104.56; 90
1718.87Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554702 CIFC21 H25 N O4 SP -110.994; 12.052; 16.9
95.131; 99.76; 103.107
2130Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554703 CIFC17 H16 Br3 N O2 SP 1 21/c 18.2985; 12.4303; 19.4432
90; 101.322; 90
1966.59Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554704 CIFC17 H14 Br3 N O3 SP -16.9458; 10.9848; 12.6203
95.166; 94.677; 97.68
946.11Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.
Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation
Organic Chemistry Frontiers, 2019, 6, 1133
1554705 CIFC16 H11 F3 N2 OP 1 21/c 16.5927; 24.4163; 9.1339
90; 108.268; 90
1396.18Zhu, Chuanle; Liu, Chi; Zeng, Hao; Chen, Fulin; Jiang, Huanfeng
Transition-metal free selective C(α)–C(β) bond cleavage of trifluoromethyl ketones with amidines under air: facile access to 5-trifluoromethylated Imidazol-4-ones
Organic Chemistry Frontiers, 2019, 6, 858
1554706 CIFC21 H22 Cl N5 O8C 1 2 125.9456; 8.8451; 23.3704
90; 101.146; 90
5262.1Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming
Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes
Organic Chemistry Frontiers, 2019, 6, 863
1554707 CIFC22 H26 Cl N5 O9P 1 21/c 114.6444; 19.027; 9.2992
90; 98.115; 90
2565.17Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming
Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes
Organic Chemistry Frontiers, 2019, 6, 863
1554708 CIFC25 H22 Cl N5 O8P -18.9522; 12.3288; 12.6211
103.938; 101.104; 102.417
1275.71Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming
Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes
Organic Chemistry Frontiers, 2019, 6, 863
1554709 CIFC21 H23 Br N2 O4 SP 21 21 219.4007; 10.8468; 21.7267
90; 90; 90
2215.42Shen, Guoli; Khan, Ruhima; Lv, Haiping; Yang, Yong; Zhang, Xia; Zhan, Yong; Zhou, Yongyun; Fan, Baomin
Palladium/silver co-catalyzed syn-stereoselective asymmetric ring-opening reactions of azabenzonorbornadienes with amides
Organic Chemistry Frontiers, 2019, 6, 1423
1554710 CIFC14 H8 F2 S2P 1 21/c 17.4893; 3.8493; 19.835
90; 94.273; 90
570.23Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554711 CIFC12 H6 F N2 S2P 1 21/n 15.9315; 4.9497; 18.794
90; 95.89; 90
548.86Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554712 CIFC12 H6 F2 N2 S2P 1 21/n 15.7427; 5.5541; 17.1753
90; 90.509; 90
547.79Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554713 CIFC14 H6 F4 S2P 1 21/n 16.2999; 5.0655; 18.6515
90; 90.341; 90
595.2Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554714 CIFC30 H46 F N2 S2 Si2P 1 21/c 19.3302; 12.3529; 14.5826
90; 106.185; 90
1614.11Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554715 CIFC30 H48 N2 S2 Si2P 1 21/c 19.2882; 12.3511; 14.5307
90; 105.826; 90
1603.77Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554716 CIFC12 H4 F4 N2 S2P -15.0225; 7.1949; 17.29
84.549; 83.096; 70.873
584.99Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554717 CIFC30 H46 F2 N2 S2 Si2P 1 21/c 19.3622; 12.3591; 14.6437
90; 106.674; 90
1623.15Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554718 CIFC12 H5 F N2 S2P 1 21/c 13.8093; 6.6644; 21.5126
90; 94.338; 90
544.57Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554719 CIFC30 H44 F4 N2 S2 Si2P n a 2119.9633; 12.2859; 13.3676
90; 90; 90
3278.6Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554720 CIFC12 H6 F2 N2 S2P 1 21/n 16.6214; 25.6046; 7.2049
90; 116.456; 90
1093.59Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554721 CIFC12 H4 F4 N2 S2P 1 21/n 13.8531; 23.868; 6.121
90; 95.29; 90
560.53Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554722 CIFC12 H8 N2 S2F d d 215.9825; 9.7302; 13.6524
90; 90; 90
2123.12Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Organic Chemistry Frontiers, 2019, 6, 780
1554723 CIFC29 H28 O2P -110.2239; 11.009; 11.0538
73.729; 86.05; 65.798
1087.85Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa
Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes
Organic Chemistry Frontiers, 2019, 6, 1118
1554724 CIFC26 H20 O3P 1 21/n 111.5269; 6.9766; 23.812
90; 98.369; 90
1894.54Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa
Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes
Organic Chemistry Frontiers, 2019, 6, 1118
1554725 CIFC76 H32 F8 O8C 1 2/c 122.035; 15.426; 17.593
90; 121.518; 90
5098Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka
Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study
Organic Chemistry Frontiers, 2019, 6, 1372
1554726 CIFC76 H16 Cl24 O8P 1 21/n 121.782; 13.957; 24.511
90; 110.66; 90
6972.41Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka
Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study
Organic Chemistry Frontiers, 2019, 6, 1372
1554727 CIFC15 H18 Br N O4P 21 21 215.0429; 11.88; 25.83
90; 90; 90
1547.5Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang
Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes
Organic Chemistry Frontiers, 2019, 6, 808
1554728 CIFC15 H18 Br N O4P 21 21 216.5631; 12.796; 18.385
90; 90; 90
1544Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang
Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes
Organic Chemistry Frontiers, 2019, 6, 808
1554729 CIFC20 H17 O2 PC 1 c 116.191; 17.7337; 8.5986
90; 137.72; 90
1661Zhao, Xiuli; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Wu, Yangjie
Stepwise photosensitized C(sp3)–C(CO) bond cleavage and C–P bond formation of 1,3-dicarbonyls with arylphosphine oxides
Organic Chemistry Frontiers, 2019, 6, 1433
1554730 CIFC34 H25 Cl O2P -112.1117; 15.5259; 21.575
95.307; 97.116; 101.212
3920.6Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554731 CIFC32 H20 N2 O6P 1 21/n 110.7141; 20.1653; 12.3094
90; 107.329; 90
2538.8Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554732 CIFC32 H21 Br O2P 1 21/c 110.602; 20.505; 12.2951
90; 114.94; 90
2423.6Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554733 CIFC26 H19 Cl OP -19.998; 15.063; 15.716
63.252; 83.527; 76.536
2055Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554734 CIFC34 H25 Br O4P 1 21/n 113.3814; 10.6318; 19.2274
90; 92.604; 90
2732.6Sun, Jing; Jiang, Wang; Yan, Chao-Guo
Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes
Organic Chemistry Frontiers, 2019, 6, 1428
1554735 CIFC32 H33 Cl3 N4 Ni O4P 19.3743; 13.379; 14.9327
81.008; 89.658; 80.276
1822.85Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.
A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals
Organic Chemistry Frontiers, 2019, 6, 1094
1554736 CIFC37 H39 N3 Ni O4P 1 21 19.846; 12.0451; 14.2648
90; 110.181; 90
1587.89Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.
A general synthesis of unnatural α-amino acids by iron-catalysed olefin–olefin coupling via generated radicals
Organic Chemistry Frontiers, 2019, 6, 1094
1554737 CIFC36 H39 Cl4 N3 Ni O3P 21 21 2111.452; 13.8346; 22.8016
90; 90; 90
3612.5Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.
A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals
Organic Chemistry Frontiers, 2019, 6, 1094
1554738 CIFC24 H27 Br O3P 21 21 215.459; 7.8884; 51.7461
90; 90; 90
2228.33Xin, Xiaodong; Pan, Xinhui; Meng, Zhilin; Liu, Xigong; Liu, Lei
Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2H-pyrans with aldehydes
Organic Chemistry Frontiers, 2019, 6, 1448
1554739 CIFC23 H19 Br N2 O3 SP 1 21/c 112.1948; 18.8246; 10.1822
90; 105.486; 90
2252.6Xu, Ze-Feng; Shan, Lihong; Zhang, Wan; Cen, Mengjie; Li, Chuan-Ying
Synthesis of α-aminoketones from N-sulfonyl-1,2,3-triazoles via N-sulfinyl imines generated by intramolecular oxygen transfer
Organic Chemistry Frontiers, 2019, 6, 1391
1554740 CIFC43 H36 N4 O9C 2 2 2117.41181; 27.6471; 17.61491
90; 90; 90
8479.57Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying
Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles
Organic Chemistry Frontiers, 2019, 6, 1603
1554741 CIFC40 H37.5 N4 O9C 1 2 129.1304; 17.2687; 17.7328
90; 103.665; 90
8667.88Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying
Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles
Organic Chemistry Frontiers, 2019, 6, 1603
1554742 CIFC31 H26 Cl2 HfP 1 21/m 18.1722; 16.0848; 9.1272
90; 95.0903; 90
1195.02Amaya, Toru; Katoh, Shun; Moriuchi, Toshiyuki; Hirao, Toshikazu
Synthesis of a sumanenyl hafnocene complex
Organic Chemistry Frontiers, 2019, 6, 1032
1554743 CIFC24 H34 O6P 1 21 17.272; 12.369; 12.296
90; 105.99; 90
1063.2Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554744 CIFC30 H43 N O7P 6517.407; 17.407; 17.977
90; 90; 120
4717.3Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554745 CIFC24 H34 O5P 1 21 17.323; 12.384; 12.233
90; 106.42; 90
1064.1Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554746 CIFC28 H35 N O3P 21 21 2110.391; 12.429; 18.269
90; 90; 90
2359.4Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei
Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate
Organic Chemistry Frontiers, 2019, 6, 868
1554747 CIFC25 H17 Cl3 N2 O2 SP 1 21/c 113.0109; 11.5329; 16.1284
90; 109.629; 90
2279.5Wang, Shengzheng; Guo, Zhongjie; Wu, Ying; Liu, Wei; Liu, Xueying; Zhang, Shengyong; Sheng, Chunquan
Organocatalytic asymmetric synthesis of highly functionalized spiro-thiazolone–cyclopropane-oxindoles bearing two vicinal spiro quaternary centers
Organic Chemistry Frontiers, 2019, 6, 1442
1554748 CIFC40 H34 I3 N3P 41 21 213.41045; 13.41045; 40.0935
90; 90; 90
7210.42Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
Organic Chemistry Frontiers, 2019, 6, 1226
1554749 CIFC152 H120 B4 F16 N8 Pd2P 42 21 232.9899; 32.9899; 14.3593
90; 90; 90
15627.7Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
Organic Chemistry Frontiers, 2019, 6, 1226
1554750 CIFC280 H248 F24 N8 O27 P8 Pd4 S8C 1 2/c 146.6905; 26.3232; 31.9982
90; 97.75; 90
38968Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
Organic Chemistry Frontiers, 2019, 6, 1226
1554751 CIFC62 H74 N22 Na O21 S2P -112.4931; 18.1989; 20.9673
89.537; 87.89; 72.498
4543.3Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan
Functionalisable acyclic cucurbiturils
Organic Chemistry Frontiers, 2019, 6, 1555
1554752 CIFC64 H72 Cl2 N18 Na2 O19 S2P b c n19.1042; 43.808; 23.0275
90; 90; 90
19272.1Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan
Functionalisable acyclic cucurbiturils
Organic Chemistry Frontiers, 2019, 6, 1555
1554753 CIFC31 H26 Cl N O4P 21 21 217.9152; 11.4088; 28.388
90; 90; 90
2563.5He, Zhao-Lin; Sheong, Fu Kit; Li, Qing-Hua; Lin, Zhenyang; Wang, Chun-Jiang
Exoselective 1,3-dipolar [3 + 6] cycloaddition of azomethine ylides with 2-acylcycloheptatrienes: stereoselectivity and mechanistic insight.
Organic letters, 2015, 17, 1365-1368
1554754 CIFC108 H150 F12 N2 O18 P2P 1 21/n 117.6358; 25.0174; 26.064
90; 109.616; 90
10832.1Li, Dong-Hao; Yang, Liu-Pan; Chai, Hongxin; Jia, Fei; Ke, Hua; Jiang, Wei
Temperature-induced large amplitude conformational change in the complex of oxatub[4]arene revealed via rotaxane synthesis
Organic Chemistry Frontiers, 2019, 6, 1027
1554755 CIFC22 H25 O5 PP -17.8931; 9.4542; 14.3399
89.1605; 82.9814; 69.4905
994.29Kim, Cheol-Eui; Son, Jeong-Yu; Shin, Seohyun; Seo, Boram; Lee, Phil Ho
Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins.
Organic letters, 2015, 17, 908-911
1554756 CIFC26 H23 B F4 N2 O2P 1 21/c 112.2068; 13.731; 14.626
90; 99.027; 90
2421.1Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554757 CIFC19 H11 F5 N2 O2P 1 21/c 112.1293; 8.5068; 15.8667
90; 92.925; 90
1635.02Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554758 CIFC19 H20 N4 O3P -17.886; 9.5658; 11.4661
86.429; 79.097; 77.958
830.42Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554759 CIFC21 H16 Cl N3 O3P -18.0444; 10.7234; 11.5467
71.104; 70.41; 73.474
870.38Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554760 CIFC19 H20 N4 O3P -17.7358; 9.6039; 11.631
85.647; 76.146; 78.816
822.65Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613

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