Crystallography Open Database

Result: there are 527322 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Displaying all data in COD

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 528 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
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
1554761 CIFC22 H19 N3 O4P 1 21/c 18.7562; 23.4732; 8.8632
90; 92.21; 90
1820.35Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554762 CIFC21 H15 Cl F N3 O3P 1 21/c 17.3959; 19.3566; 12.7098
90; 91.147; 90
1819.2Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554763 CIFC29 H19 F6 N3 O4P 1 21/c 115.9357; 13.7866; 11.8725
90; 93.908; 90
2602.3Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554764 CIFC25 H20 B F4 N OP 1 21/n 110.72; 18.331; 12.174
90; 110.527; 90
2240.4Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554765 CIFC25 H21 B F4 N2 O2P 1 21/c 112.3471; 13.3272; 13.9786
90; 98.588; 90
2274.42Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554766 CIFC60 H78 Cl2 N4 O16P -115.267; 19.087; 24.39
87.94; 83.839; 73.08
6760Jordan, Jacobs H.; Wishard, Anthony; Mague, Joel T.; Gibb, Bruce C.
Binding properties and supramolecular polymerization of a water-soluble resorcin[4]arene
Organic Chemistry Frontiers, 2019, 6, 1236
1554767 CIFC31 H24 Cl N O3P 1 21 17.081; 19.406; 9.491
90; 98.161; 90
1290.99Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy
Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles.
Organic letters, 2015, 17, 1066-1069
1554768 CIFC6.21 H2.28 Cl0.48 N0.07 O0.28 S0P -19.9983; 16.3521; 19.4651
102.163; 90.869; 105.091
2995.41Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554769 CIFC143 H54 N2 O10 S2P 1 21/n 110.4701; 25.097; 16.2566
90; 91.218; 90
4270.8Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554770 CIFC70 H22.75 N O4.88 S2C 1 c 114.4203; 27.3088; 10.3569
90; 94.182; 90
4067.7Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554771 CIFC81 H42.7 N O5.85 S2P -110.4366; 16.3952; 16.824
110.869; 99.019; 100.619
2565.14Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554772 CIFC143 H57.4 N2 O11.7 S2P 1 21/n 110.4595; 25.0584; 16.2556
90; 91.316; 90
4259.4Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554773 CIFC49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2P -110.3083; 14.3567; 19.2355
75.287; 74.747; 84.913
2655.7Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554774 CIFC16 H19 Cl3 N P TiP -18.8951; 9.2936; 13.0036
79.226; 76.069; 64.74
939.24Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554775 CIFC19 H20 N2 SeP 1 21/c 113.3462; 10.2259; 12.0633
90; 96.466; 90
1635.89Guo, Tao; Wei, Xu-Ning; Liu, Yu; Zhang, Pan-Ke; Zhao, Yun-Hui
Oxidative dual C–H selenation of imidazoheterocycles with ethers or alkanes using selenium powder via a radical pathway
Organic Chemistry Frontiers, 2019, 6, 1414
1554776 CIFC35 H26 N1.6 O10P 21 21 2113.871; 15.1622; 64.627
90; 90; 90
13592Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong
New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family.
Organic letters, 2015, 17, 1146-1149
1554777 CIFC21 H18 N O3 PP 21 21 218.4621; 19.7458; 21.2129
90; 90; 90
3544.5Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554778 CIFC25 H23 N2 O2 PP 1 21/n 118.5757; 6.176; 18.9148
90; 98.809; 90
2144.38Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554779 CIFC22.5 H14.5 Cl1.5 F3 N2 O2 PC 1 2/c 129.394; 6.3419; 28.119
90; 121.188; 90
4484.2Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554780 CIFC21 H15 N2 O2 PC 1 2/c 124.331; 10.2408; 14.54
90; 102.686; 90
3534.5Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554781 CIFC21 H15 N2 O2 PC 1 2/c 126.4131; 9.7872; 14.9148
90; 115.7; 90
3474.22Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554782 CIFC34 H29 N5 O4 SP -19.7972; 10.509; 15.4371
72.931; 74.564; 84.268
1464.2Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang
Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles.
Organic letters, 2015, 17, 1192-1195
1554783 CIFC24 H27 N3 O2P 1 21/c 117.5333; 9.245; 13.3467
90; 107.946; 90
2058.18Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554784 CIFC13 H18 N2 O2 S2P b c a14.1538; 10.7714; 20.0319
90; 90; 90
3054Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554785 CIFC11 H12 O4 S2P -15.1535; 7.3073; 16.2864
81.694; 82.41; 74.561
582.16Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554786 CIFC36 H38 O2 S2C 1 c 119.6986; 10.9502; 16.5805
90; 122.988; 90
2999.9Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554787 CIFC40 H46 O2 S2P -19.4599; 10.4995; 17.9405
82.254; 86.522; 88.292
1762Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554788 CIFC41 H48 O2 S2P 1 21/n 111.3446; 17.747; 17.3945
90; 97.039; 90
3475.7Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554789 CIFC13 H18 N2 O2 S2P 1 21/c 110.5966; 11.0075; 13.0168
90; 103.286; 90
1477.67Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554790 CIFC37 H40 O2 S2P 1 21/c 114.4032; 9.233; 24.7181
90; 93.6338; 90
3280.5Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554791 CIFC21 H15 N3 OP 1 21/c 110.5706; 17.3802; 10.1316
90; 96.996; 90
1847.5Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554792 CIFC24 H12 F6 SeP 1 21/c 112.234; 10.9831; 14.6454
90; 111.492; 90
1831Shi, Xinzhe; Mao, Shuxin; Roisnel, Thierry; Doucet, Henri; Soulé, Jean-François
Palladium-catalyzed successive C–H bond arylations and annulations toward the π-extension of selenophene-containing aromatic skeletons
Organic Chemistry Frontiers, 2019, 6, 2398
1554793 CIFC24 H21 I N2 O3 SP 21 21 2110.7482; 12.7229; 16.152
90; 90; 90
2208.76Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas.
Organic letters, 2015, 17, 1018-1021
1554794 CIFC19 H24 N2 OP c a 2112.8993; 10.853; 11.6466
90; 90; 90
1630.5Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng
Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond.
Organic letters, 2015, 17, 1200-1203
1554795 CIFC36 H23 Br F3 N2 O3P 21 21 2111.6434; 14.186; 17.6525
90; 90; 90
2915.72Li, Boyu; Gao, Fengyun; Feng, Xing; Sun, Mengmeng; Guo, Yifei; Wen, Dongwa; Deng, Yabo; Huang, Jinqi; Wang, Kairong; Yan, Wenjin
Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition
Organic Chemistry Frontiers, 2019, 6, 1567
1554796 CIFC24 H44 B2 N2 O4P b a m12.939; 13.093; 15.573
90; 90; 90
2638.2Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554797 CIFC29 H49 B2 Co N2 O4F d d 218.923; 58.36; 11.127
90; 90; 90
12288Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554798 CIFC24 H46 B2 N2 O5P 1 21/n 110.74; 19.626; 13.066
90; 93.197; 90
2749.8Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554799 CIFC27 H40 O6P 1 21 19.8327; 16.984; 16.2007
90; 101.138; 90
2654.54Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554800 CIFC29 H44 O6P 21 21 2112.0011; 13.3921; 17.7454
90; 90; 90
2852.04Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554801 CIFC26 H38 O6P 1 21 19.6691; 16.4235; 15.94
90; 101.09; 90
2484.01Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554802 CIFC24 H41 B2 O2 PP 1 21/n 18.6014; 17.6656; 16.4517
90; 107.162; 90
2388.51Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554803 CIFC28 H33 B2 Fe O2 PP 1 21 112.674; 9.2986; 12.919
90; 113.497; 90
1396.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554804 CIFC40 H43 B2 Fe PP 21 21 2110.3874; 17.4963; 18.3521
90; 90; 90
3335.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554805 CIFC162 H174 Au4 Cl16 O8 P4P -112.983; 13.401; 29.22
81.31; 77.62; 61.97
4376Hau, Franky Ka-Wah; Cheung, Kai-Leung; Zhu, Nianyong; Yam, Vivian Wing-Wah
Calixarene-based alkynyl-bridged gold(i) isocyanide and phosphine complexes as building motifs for the construction of chemosensors and supramolecular architectures
Organic Chemistry Frontiers, 2019, 6, 1205
1554806 CIFC13 H12 O4P 1 21/n 110.5408; 14.0223; 15.567
90; 95.216; 90
2291.4Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan
Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates.
Organic letters, 2015, 17, 1228-1231
1554807 CIFC27 H23 N OP -110.4979; 10.7112; 10.8365
60.7986; 76.2796; 71.3801
1003.08Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy
Organic Chemistry Frontiers, 2019, 6, 1655
1554808 CIFC27 H23 N OP 1 21 16.7344; 18.9552; 15.1244
90; 90.856; 90
1930.4Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy
Organic Chemistry Frontiers, 2019, 6, 1655
1554809 CIFC19 H18 N O5 S2P -17.9459; 8.3713; 15.0845
98.477; 91.135; 97.754
982.54Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan
Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols.
Organic letters, 2015, 17, 1834-1837
1554810 CIFC24 H22 O3C 1 c 114.8194; 23.1341; 17.3079
90; 104.994; 90
5731.7Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc
Development of a new family of chiral auxiliaries.
Organic letters, 2015, 17, 1819-1821
1554811 CIFC34 H30 N2 O7P 21 21 219.7212; 10.3208; 28.5171
90; 90; 90
2861.14Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying
A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
Organic Chemistry Frontiers, 2019, 6, 1485
1554812 CIFC36 H32 F N3 O7P 1 21 111.7466; 12.2636; 22.7319
90; 93.091; 90
3269.89Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying
A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
Organic Chemistry Frontiers, 2019, 6, 1485
1554813 CIFC17 H16 Cl N3 OP -18.6811; 13.1015; 15.2298
66.74; 82.416; 77.876
1553.57Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping
One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides.
Organic letters, 2015, 17, 1157-1159
1554814 CIFC34 H35 N O6 SP 21 21 219.4387; 22.551; 28.131
90; 90; 90
5987.7Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R.
2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors.
Organic letters, 2015, 17, 1421-1424
1554815 CIFC19 H21 F2 N OP 1 21/c 19.9286; 17.0093; 10.0841
90; 90.259; 90
1703He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo
Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates.
Organic letters, 2015, 17, 1838-1841
1554816 CIFC17 H16 Br F3 O2P 1 21 16.2353; 7.7873; 17.3098
90; 90.759; 90
840.42Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554817 CIFC23 H21 N O7 SP 1 21 110.6202; 6.377; 16.3385
90; 98.252; 90
1095.07Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554818 CIFC18 H17 F3 O3P 21 21 216.4981; 15.2542; 17.146
90; 90; 90
1699.57Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554819 CIFC24 H31 Ag F6 N2 P2P 1 c 115.277; 8.0788; 21.7171
90; 98.481; 90
2651.01Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554820 CIFC31 H41 Ag F6 N4 P2P 1 21/c 112.7111; 17.36; 15.7081
90; 105.588; 90
3338.73Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554821 CIFC25 H31 Ag F3 N2 O PP 1 21/c 111.3702; 12.6386; 17.83
90; 103.361; 90
2492.88Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554822 CIFC16 H10 N2 OP 1 21/n 16.4176; 20.0965; 9.335
90; 98.274; 90
1191.42Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie
Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles.
Organic letters, 2015, 17, 1445-1448
1554823 CIFC27 H40 O4P 21 21 218.061; 10.8588; 27.7356
90; 90; 90
2427.77Xu, Hou-Chao; Hu, Kun; Shi, Xiao-Huo; Tang, Jian-Wei; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin
Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea
Organic Chemistry Frontiers, 2019, 6, 1619
1554824 CIFC20 H14 O5P 1 21/n 19.0391; 9.7069; 17.2285
90; 102.573; 90
1475.41Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang
Muta-mycosynthesis of naphthalene analogs.
Organic letters, 2015, 17, 1457-1460
1554825 CIFC15 H13 N3P -15.4882; 11.1825; 11.6413
62.292; 80.059; 76.727
613.82Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554826 CIFC17 H17 N3 O2C 1 2/c 115.105; 12.8664; 15.5822
90; 91.952; 90
3026.6Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554827 CIFC19 H17 B F2 N4 O2P -17.1859; 12.0427; 12.0895
93.791; 100.927; 98.538
1011.05Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554828 CIFC17 H16 N3 O2.5P 1 21/c 110.668; 24.498; 11.286
90; 93.034; 90
2945.4Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554829 CIFC17.14 H14.5 B F2 N3 O2P 1 21/c 111.1306; 11.7622; 24.0194
90; 91.217; 90
3143.92Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554830 CIFC20 H25 F3 N2 O3 SP 1 21/c 18.128; 15.344; 16.979
90; 102.44; 90
2067.8van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554831 CIFC22 H30 F3 N3 O3 SC 1 2/c 115.441; 10.924; 27.769
90; 90.9; 90
4683.4van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554832 CIFC18 H22 F3 N3 O3 SP 1 21/c 18.4815; 11.074; 21.3223
90; 93.426; 90
1999.1van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554833 CIFC21 H25 N3P -18.61; 9.179; 11.835
93.38; 95.73; 105.2
894.57van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554834 CIFC20 H26 N2P 1 21/c 18.693; 17.464; 11.525
90; 103.69; 90
1700van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554835 CIFC14 H22 N2R 3 c :H26.3163; 26.3163; 10.403
90; 90; 120
6239.3van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554836 CIFC22 H26 N4 O5P 21 21 219.5782; 11.765; 20.2153
90; 90; 90
2278.01Dai, Chuan; Ma, Jun; Li, Min; Wu, Wen; Xia, Xuefeng; Zhang, Jinqiang
Diversity-oriented submonomer synthesis of azapeptides mediated by the Mitsunobu reaction
Organic Chemistry Frontiers, 2019, 6, 2529
1554837 CIFC49 H29 B F20 N O2 RhP 1 21/c 112.2787; 24.2002; 15.5541
90; 101.818; 90
4523.9Otley, Kate D.; Ellman, Jonathan A.
An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation.
Organic letters, 2015, 17, 1332-1335
1554838 CIFC18 H18 O2P 1 21/c 114.026; 8.7035; 12.0599
90; 104.008; 90
1428.4Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin
Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process.
Organic letters, 2015, 17, 1489-1492
1554839 CIFC17 H16 O2 SeP 1 21 16.9078; 10.3981; 10.0732
90; 95.471; 90
720.24Niu, Wenxue; Yeung, Ying-Yeung
Catalytic and highly enantioselective selenolactonization.
Organic letters, 2015, 17, 1660-1663
1554840 CIFC12 H20 O4P 3213.594; 13.594; 5.7493
90; 90; 120
920.11Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John
Exo-selective reductive macrocyclization of ynals.
Organic letters, 2015, 17, 1493-1496
1554841 CIFC14 H15 Br N2 O2P 21 21 219.2455; 10.1411; 14.412
90; 90; 90
1351.3Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing
A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters.
Organic letters, 2015, 17, 1505-1508
1554842 CIFC22 H18 F N3 O2 SP 1 21/c 115.7629; 11.6907; 10.7408
90; 100.958; 90
1943.22Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554843 CIFC16 H23 Cl F6 N3 O2 PC 1 c 110.7226; 12.3939; 15.6108
90; 92.991; 90
2071.77Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554844 CIFC17 H23 Cl2 F6 N2 O2 PP 1 21/c 111.8795; 14.5176; 12.6593
90; 102.138; 90
2134.44Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554845 CIFC28 H41 F6 N4 O2 PC 1 2/c 136.485; 10.158; 16.856
90; 92.44; 90
6241Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554846 CIFC34 H49 F12 N7 O4 P2I 1 2/a 124.915; 8.8562; 19.8464
90; 105.666; 90
4216.5Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554847 CIFC26 H39.5 F9 N4.5 O5 P SP -110.7516; 12.0558; 14.8348
107.62; 93.413; 109.731
1696.8Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554848 CIFC19 H29 Cl F6 N3 O2 PP 1 21/n 17.59057; 26.3895; 12.488
90; 107.133; 90
2390.48Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554849 CIFC21 H32 F6 N4 O2 PP 1 21/c 112.3903; 16.1931; 13.6174
90; 113.783; 90
2500.1Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554850 CIFC16 H23 F12 N3 O2 P2P 1 21/n 110.5891; 16.2883; 13.903
90; 102.985; 90
2336.65Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554851 CIFC26 H41 Cl2 F6 N2 O2 PP 1 21/c 118.6093; 10.778; 15.4265
90; 101.706; 90
3029.76Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554852 CIFC30.33 H52.53 Cl2.12 F6 N3 O2.44 PP -19.5322; 18.6061; 21.1198
83.275; 88.086; 80.993
3673.7Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554853 CIFC22 H35 Cl F6 N3 O2 PP 1 21/n 112.7678; 11.6389; 36.278
90; 94.051; 90
5377.6Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554854 CIFC33 H47.66 F12 N6.5 O4.08 P2P -112.1931; 15.3991; 22.7102
95.65; 102.392; 94.7722
4120.61Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554855 CIFC18 H21 N3 O2 S2P 1 21/c 110.0095; 11.563; 16.5773
90; 99.859; 90
1890.32Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554856 CIFC20 H26 N2 O8 SiC 1 2/c 118.687; 6.709; 37.603
90; 90.534; 90
4714Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei
Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal.
Organic letters, 2015, 17, 1553-1556
1554857 CIFC19 H20 O3 SP -16.9512; 8.6039; 15.1128
102.337; 92.466; 108.002
833.95He, Fu-Sheng; Wu, Youqian; Li, Xiaofang; Xia, Hongguang; Wu, Jie
Photoredox-catalyzed sulfonylation of alkenylcyclobutanols with the insertion of sulfur dioxide through semipinacol rearrangement
Organic Chemistry Frontiers, 2019, 6, 1873
1554858 CIFC60 H85 I3 N10 O12P -114.2686; 14.6629; 17.0163
80.443; 70.781; 82.037
3301.6Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554859 CIFC17 H23 N O5 SP 1 21/n 16.0877; 10.8073; 26.052
90; 93.948; 90
1709.9Xu, Dongyang; Wei, Hongbo; Zhen, Yanxia; Gao, Yu-Qi; Li, Ruoxin; Li, Xingzhou; He, Yupeng; Zhang, Zhong; Xie, Weiqing
Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane
Organic Chemistry Frontiers, 2019, 6, 1681
1554860 CIFC60 H78 Cl6 N10 O10C 1 2/c 122.9779; 30.564; 22.926
90; 114.207; 90
14685.1Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554861 CIFC9 H11 B0.75 O2.25P 1 21/n 16.4968; 22.26; 7.1909
90; 116.2; 90
933.1Bhavanarushi, Sangepu; Xu, Yin; Khan, Imran; Luo, Zhibin; Liu, Bin; Xie, Jimin
Transition-metal-free borylation of propargylic alcohols: structurally variable synthesis in ionic liquid medium
Organic Chemistry Frontiers, 2019, 6, 1895
1554862 CIFC27 H27 F3 N2 O8P -18.5362; 11.0883; 14.8339
89.337; 75.808; 89.011
1360.96Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan
Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes.
Organic letters, 2015, 17, 1589-1592
1554863 CIFC11 H7 F3 N2 O2P 1 21/n 15.41; 17.433; 11.237
90; 93.29; 90
1058Peng, Xiaofeng; Zhang, Xiaofei; Li, Shunyao; Lu, Yunfu; Lan, Lefu; Yang, Chunhao
Silver-mediated synthesis of novel 3-CF3/CN/phosphonate-substituted pyrazoles as pyrrolomycin analogues from 3-formylchromones and diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1775
1554864 CIFC14 H11 N O7P n a 218.6933; 19.9383; 7.6281
90; 90; 90
1322.18Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study.
Organic letters, 2015, 17, 1850-1853
1554865 CIFC24 H22 N2 O9 SP 21 21 2112.2161; 12.5468; 16.7879
90; 90; 90
2573.13Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong
Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes
Organic Chemistry Frontiers, 2019, 6, 1891
1554866 CIFC24 H24 O6P 1 21/c 110.3133; 11.2328; 19.0954
90; 99.604; 90
2181.14Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong
Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes
Organic Chemistry Frontiers, 2019, 6, 1891
1554867 CIFC23 H26 Br N O4 SP 1 21 19.8067; 9.9678; 11.8916
90; 104.237; 90
1126.7Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization.
Organic letters, 2015, 17, 1720-1723
1554868 CIFC24 H19 Cl N2 O3P 21 21 215.9309; 17.47; 19.675
90; 90; 90
2038.6Chu, Ming-Ming; Qi, Suo-Suo; Wang, Yi-Feng; Wang, Biao; Jiang, Zhen-Hui; Xu, Dan-Qian; Xu, Zhen-Yuan
Organocatalytic asymmetric [4 + 1] annulation of in situ generated ortho-quinomethanes with 4-halo pyrazolones: straightforward access to chiral spiro-benzofuran pyrazolones
Organic Chemistry Frontiers, 2019, 6, 1977
1554869 CIFC28 H19 N O3 S2P -110.443; 11.228; 11.795
70.186; 87.728; 65.484
1175.6Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang
Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes.
Organic letters, 2015, 17, 1746-1749
1554870 CIFC19 H18 N2 O4P 1 21/c 19.3579; 12.566; 29.371
90; 96.6; 90
3430.9Zhang, Wei; Zheng, Han-Liang; Liu, Yang; Yu, Ao; Yang, Chen; Li, Xin; Cheng, Jin-Pei
Catalyst-free amination of α-cyanoarylacetates enabled by single-electron transfer
Organic Chemistry Frontiers, 2019, 6, 1900
1554871 CIFC15 H21 N O3P 1 21/n 15.1627; 14.8595; 17.7219
90; 96.198; 90
1351.59Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron
Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids.
Organic letters, 2015, 17, 1754-1757
1554872 CIFC28 H29 N3 O4P 1 21 17.807; 15.9924; 10.5193
90; 109.003; 90
1241.79Zhang, Yan-Ping; You, Yong; Zhao, Jian-Qiang; Zhou, Xiao-Jian; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng
A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides
Organic Chemistry Frontiers, 2019, 6, 1879
1554873 CIFC20 H16 O2P 21 21 215.9724; 14.8969; 16.4863
90; 90; 90
1466.79Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts.
Organic letters, 2015, 17, 1735-1737
1554874 CIFC23 H30 O8P 21 21 218.0029; 15.3468; 17.8042
90; 90; 90
2186.69Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554875 CIFC12 H13 Br O2P 1 21/c 16.0066; 11.7969; 16.772
90; 97.594; 90
1178Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554876 CIFC29 H27 N2 O4.5C 1 c 114.3037; 14.0845; 23.7866
90; 91.922; 90
4789.36Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554877 CIFC23 H21 NP 1 21/c 110.4176; 11.9596; 16.0413
90; 114.231; 90
1822.51Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554878 CIFC29 H36 N2 O4P 1 21 18.527; 16.7982; 9.3056
90; 102.717; 90
1300.22Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554879 CIFC28.33333 H40.33333 N O9.33333P 21 21 218.09067; 25.4976; 41.3088
90; 90; 90
8521.7Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554880 CIFC13 H22 O2C 1 c 114.0887; 10.5929; 9.0247
90; 114.771; 90
1222.92Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554881 CIFC17 H23 N O4P 1 21/c 112.0924; 16.7422; 8.278
90; 107.825; 90
1595.5Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554882 CIFC14 H13 F3 O5P -16.4241; 10.1906; 11.3167
68.951; 83.144; 83.818
684.79Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554883 CIFC17 H20 O4P 1 21/c 112.1636; 10.2486; 12.3402
90; 110.011; 90
1445.5Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554884 CIFC16 H18 O4P 1 21/c 17.6075; 9.2096; 19.424
90; 98.561; 90
1345.7Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554885 CIFC20 H20 Br2 Cl2 N2 O4P 15.0746; 14.828; 16.699
65.191; 89.579; 80.838
1123.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554886 CIFC33 H27 Cl3 N2 O5 SP 21 21 2110.9357; 11.7723; 24.8931
90; 90; 90
3204.7Ren, Xiao-Rui; Lin, Jun-Bing; Hu, Xiu-Qin; Xu, Peng-Fei
Bifunctional Brønsted base catalyzed inverse-electron-demand aza-Diels–Alder reactions of saccharin-derived 1-azadienes with azlactones
Organic Chemistry Frontiers, 2019, 6, 2280
1554887 CIFC13 H15 Br Cl N O3P 1 21 14.8035; 8.2644; 18.363
90; 94.441; 90
726.79Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554888 CIFC10 H9 N O SeP 1 21/c 15.4632; 16.8139; 10.7302
90; 98.574; 90
974.64Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua
Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates
Organic Chemistry Frontiers, 2019, 6, 1967
1554889 CIFC24 H33 N O3 SeP 1 21 110.1323; 7.4394; 15.4852
90; 100.787; 90
1146.62Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua
Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates
Organic Chemistry Frontiers, 2019, 6, 1967
1554890 CIFC13 H16 Br Cl2 N O3P 1 21 110.669; 4.7706; 15.964
90; 107.952; 90
773Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554891 CIFC21 H21 Cl O5P 21 21 217.229; 11.212; 22.921
90; 90; 90
1857.8Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554892 CIFC20 H18 O4P 1 21 110.3231; 8.3376; 10.651
90; 116.926; 90
817.35Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554893 CIFC21 H19 Cl O4P 21 21 2110.5134; 7.5193; 22.921
90; 90; 90
1812Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554894 CIFC6 H12 Cl2 O2P 1 21 14.9886; 19.578; 9.0155
90; 92.03; 90
880Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554895 CIFC16 H15 N3 O4 SP 1 21/n 114.05; 8.3338; 14.2852
90; 101.509; 90
1639Wang, Guodong; Sun, Jian; Wang, Kai; Han, Junfen; Li, Hongshuang; Duan, Guiyun; You, Guirong; Li, Furong; Xia, Chengcai
Palladium-catalyzed direct C–H nitration and intramolecular C–H functionalization for the synthesis of 3-nitro-1-(phenylsulfonyl)-1H-indazole derivatives
Organic Chemistry Frontiers, 2019, 6, 1608
1554896 CIFC13 H15 Br Cl N O3P 1 21 112.2792; 4.9357; 13.4763
90; 115.38; 90
737.92Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554897 CIFC16 H19 N O3P 1 21 17.9218; 6.5193; 13.434
90; 101.58; 90
679.67Mandzhulo, Aleksandr; Vashchenko, Iryna; Gerasov, Andrii; Vovk, Mykhaylo; Rusanov, Eduard; Fetyukhin, Volodymyr; Lukin, Oleg; Shivanyuk, Alexander
Selective synthesis of N-protected exo-spiro[oxirane-3,2′-tropanes]
Organic Chemistry Frontiers, 2019, 6, 1692
1554898 CIFC13 H15 Br Cl N O3C 1 2 116.929; 4.841; 36.446
90; 101.211; 90
2930Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554899 CIFC24 H36 O3P 21 21 218.9194; 12.8315; 18.5057
90; 90; 90
2118Zhao, Nan; Xie, Shengling; Tian, Peilin; Tong, Rongbiao; Ning, Chengqing; Xu, Jing
Asymmetric total synthesis of (+)-astellatol and (−)-astellatene
Organic Chemistry Frontiers, 2019, 6, 2014
1554900 CIFC14 H18 Cl N O8 SP 21 21 216.1403; 13.657; 20.719
90; 90; 90
1737.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554901 CIFC20 H30 O4P 21 21 219.9964; 10.5385; 17.4587
90; 90; 90
1839.22Zhang, Jing; Tang, Xuli; Han, Xiao; Feng, Danqing; Luo, Xiangchao; Ofwegen, Leen van; Li, Pinglin; Li, Guoqiang
Sarcoglaucins A-I, new antifouling cembrane-type diterpenes from the South China Sea soft coral Sarcophyton glaucum
Organic Chemistry Frontiers, 2019, 6, 2004
1554902 CIFC6 H12 Cl2 O2P 21 21 215.8932; 9.8358; 14.7998
90; 90; 90
857.86Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554903 CIFC19 H20 N2 O3P 1 21 16.5666; 16.4713; 8.0376
90; 111.405; 90
809.39Wang, Bo; Wang, Yuankai; Wang, Zixuan; Wang, Jianbo
Rh(i)-Catalyzed intramolecular [2 + 2 + 1] cycloaddition of diynes with the N-terminal of the diazo group
Organic Chemistry Frontiers, 2019, 6, 2329
1554904 CIFC18 H14 N2 OP 1 21/c 117.283; 5.72; 16.0086
90; 115.367; 90
1430Bunescu, Ala; Wang, Qian; Zhu, Jieping
Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles.
Organic letters, 2015, 17, 1890-1893
1554905 CIFC45 H42 F4 O7C 1 2/c 115.1446; 24.455; 20.982
90; 93.45; 90
7756.8Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.
Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight
Organic Chemistry Frontiers, 2019, 6, 1961
1554906 CIFC47 H45 F4 O7P -111.4709; 13.897; 14.895
107.986; 112.427; 96.387
2015.5Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.
Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight
Organic Chemistry Frontiers, 2019, 6, 1961
1554907 CIFC28 H36 N2 O10 Pd3P 1 21/c 18.2684; 13.1049; 14.9823
90; 98.209; 90
1606.8Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng
Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle.
Organic letters, 2015, 17, 1802-1805
1554908 CIFC24 H19 N OP 1 21/c 110.273; 10.178; 16.954
90; 99.61; 90
1747.8Zhao, Hong-Ping; Ma, Xiao-Pan; Nie, Shu-Min; Xiao, Yuhong; Mo, Dong-Liang
Synthesis of chromeno[4,3-b]quinolines and spirobenzofuran-3,3′-quinolines through silver-mediated Appel reaction/C–Br bond cleavage/double selective rearrangement sequence
Organic Chemistry Frontiers, 2019, 6, 2334
1554909 CIFC21 H24 B N O2P 1 21/n 19.82013; 15.1033; 12.9881
90; 93.8267; 90
1922.05Pareek, Manish; Fallon, Thomas; Oestreich, Martin
Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 2082-2085
1554910 CIFC30 H21 N O2P 1 21/n 110.5982; 10.2369; 20.9415
90; 99.629; 90
2240Wang, Jian; Cai, Panyuan; He, Yimiao; Liu, Yuan; Zhong, Ling; Ding, Shumin; Shang, Yongjia
Tuneable access to isoquinolines via a transition-metal-free C(sp3)–C(sp3) bond cleavage rearrangement reaction
Organic Chemistry Frontiers, 2019, 6, 2430
1554911 CIFC27 H29 F6 N2 O P RuP -110.7138; 10.8978; 12.099
92.748; 96.702; 90.476
1401.24Hong, Xi; Zhou, Quan; Huang, Shuang; Cui, He-Zhen; Li, Zhi-Ming; Hou, Xiu-Feng
Transition metal catalysed C7 and ortho-selective halogenation of 2-arylbenzo[d]oxazoles
Organic Chemistry Frontiers, 2019, 6, 2226
1554912 CIFC20 H41 B2 F8 N5 OP 21 21 219.9728; 10.8425; 25.575
90; 90; 90
2765.4Mirabdolbaghi, Roya; Dudding, Travis
Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination.
Organic letters, 2015, 17, 1930-1933
1554913 CIFC14 H12 N2 OP 21 21 216.8959; 7.1261; 24.02
90; 90; 90
1180.4Feng, Guang-Shou; Zhao, Zi-Biao; Shi, Lei; Zhou, Yong-Gui
Iridium-catalyzed asymmetric hydrogenation of quinazolinones
Organic Chemistry Frontiers, 2019, 6, 2250
1554914 CIFC25 H36 F3 N3 O4P -17.9555; 12.7291; 14.1773
101.894; 105.578; 101.34
1304Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554915 CIFC20 H27 F3 N2 O3P 1 21/c 19.676; 6.0187; 35.338
90; 90.313; 90
2057.9Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554916 CIFC18 H23 F3 N2 O3P -18.4082; 8.9935; 12.6932
109.241; 90.111; 102.16
883.25Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554917 CIFC18 H16 F3 N OP 21 21 215.8836; 19.2027; 26.5181
90; 90; 90
2996Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554918 CIFC35 H27 Br F3 N3 O3P 21 21 218.4795; 18.0358; 21.5437
90; 90; 90
3294.78Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Organic Chemistry Frontiers, 2019, 6, 1989
1554919 CIFC40 H31 Cl2 F4 N2 O3P 21 21 2111.9726; 16.0021; 18.2529
90; 90; 90
3497.01Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Organic Chemistry Frontiers, 2019, 6, 1989
1554920 CIFC21 H16 N2 O2 SC 1 c 113.529; 16.7566; 8.6938
90; 116.175; 90
1768.8Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554921 CIFC24 H24 N2 O2 SP 1 21/c 112.5268; 10.8502; 16.3904
90; 103.482; 90
2166.4Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554922 CIFC31 H28 N2 O5P n a 2121.4324; 13.5256; 8.8733
90; 90; 90
2572.2Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei
Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes
Organic Chemistry Frontiers, 2019, 6, 2415
1554923 CIFC30 H25 N3 O3P -18.9859; 10.004; 15.8029
97.57; 90.211; 115.564
1267.4Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei
Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes
Organic Chemistry Frontiers, 2019, 6, 2415
1554924 CIFC19 H29 F N2 O5 SiP 21 21 216.42; 8.0707; 40.1927
90; 90; 90
2082.54Istrate, Alena; Medvecky, Michal; Leumann, Christian J.
2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity.
Organic letters, 2015, 17, 1950-1953
1554925 CIFC38 H31 Br Cl3 N3 O4P 21 21 219.1965; 9.694; 38.3086
90; 90; 90
3415.2Zhang, Jing; Chan, Wai-Lun; Chen, Ligong; Ullah, Nisar; Lu, Yixin
Creation of bispiro[pyrazolone-3,3′-oxindoles] via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita–Baylis–Hillman carbonates with pyrazoloneyldiene oxindoles
Organic Chemistry Frontiers, 2019, 6, 2210
1554926 CIFC19 H16 N2 O4P 1 21 17.5248; 11.7969; 18.7512
90; 98.035; 90
1648.2Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K.
An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence.
Organic letters, 2015, 17, 2102-2105
1554927 CIFC16 H18 OR 3 :H20.961; 20.961; 7.086
90; 90; 120
2696.2Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554928 CIFC27 H34 O3 SiC 1 2/c 142.742; 10.4771; 10.9037
90; 93.609; 90
4873.1Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554929 CIFC14 H18 O5P -17.3423; 8.4321; 10.4623
85.681; 85.985; 78.332
631.55Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554930 CIFC16 H25 N O2 S3P 21 21 215.36225; 12.0412; 27.5363
90; 90; 90
1777.96Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554931 CIFC18 H19 N O4 SP b c a17.4772; 10.488; 19.6463
90; 90; 90
3601.2Huang, Guofei; Ren, Xiaoyu; Jiang, Chunhui; Wu, Jia-Hong; Gao, Guowei; Wang, Tianli
Efficient synthesis of (E)-2-nitromethylcinnamates via phosphine-catalyzed tandem α-addition and 1,3-rearrangement
Organic Chemistry Frontiers, 2019, 6, 2872
1554932 CIFC18 H19 Cl F3 N O SP 1 21 111.7646; 15.4251; 12.0356
90; 118.452; 90
1920.3Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554933 CIFC10 H8 N2 SP n a 2115.971; 4.2214; 13.319
90; 90; 90
898Peng, Yingyuan; He, Qian; Zhang, Xiaofei; Yang, Chunhao
Pd-Catalyzed intramolecular C–H activation and C–S formation to synthesize pyrazolo[5,1-b]benzothiazoles without an additional oxidant
Organic Chemistry Frontiers, 2019, 6, 3234
1554934 CIFC19 H23 Fe N O2 SP 1 21 15.84461; 11.3132; 13.829
90; 95.4227; 90
910.298Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554935 CIFC23 H17 Cl O2P 1 21/m 19.353; 7.448; 12.251
90; 93.725; 90
851.6Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong
Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones.
Organic letters, 2015, 17, 2134-2137
1554936 CIFC20 H21 N3 O4P 1 21/n 110.8238; 10.3557; 17.8199
90; 96.908; 90
1982.9Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554937 CIFC133 H116 N8 O21 S4P 1 21 110.8299; 17.8426; 16.7462
90; 105.418; 90
3119.5Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu
Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals.
Organic letters, 2015, 17, 2318-2321
1554938 CIFC20 H21 N3 O4P 42 b c21.7832; 21.7832; 8.49552
90; 90; 90
4031.19Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554939 CIFC15 H13 N3 O2P -16.9944; 7.8586; 26.1858
85.696; 89.837; 79.658
1411.87Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554940 CIFC22 H18 F3 N O3P 21 21 219.69927; 10.835; 16.94975
90; 90; 90
1781.28Rabasa-Alcañiz, Fernando; Hammerl, Daniel; Sánchez-Merino, Anabel; Tejero, Tomás; Merino, Pedro; Fustero, Santos; del Pozo, Carlos
Asymmetric synthesis of polycyclic 3-fluoroalkylproline derivatives by intramolecular azomethine ylide cycloaddition
Organic Chemistry Frontiers, 2019, 6, 2916
1554941 CIFC39 H30 Cl N OP 1 21/n 114.7817; 10.4931; 20.1054
90; 110.04; 90
2929.66Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554942 CIFC26 H20 Cu F6 PP b c n15.5529; 7.3629; 19.8862
90; 90; 90
2277.26Liu, He; Shen, Qilong
Bistrifluoromethylated organocuprate [Ph4P]+[Cu(CF3)2]−: synthesis, characterization and its application for trifluoromethylation of activated heteroaryl bromides, chlorides and iodides
Organic Chemistry Frontiers, 2019, 6, 2324
1554943 CIFC20 H22 N2 O4P 1 21/c 110.5905; 16.0282; 11.3851
90; 116.637; 90
1727.47Yakkala, Prasanna Anjaneyulu; Giri, Deepesh; Chaudhary, Bharatkumar; Auti, Prashant; Sharma, Satyasheel
Regioselective C–H alkylation and alkenylation at the C5 position of 2-amino-1,4-naphthoquinones with maleimides under Rh(iii) catalysis
Organic Chemistry Frontiers, 2019, 6, 2441
1554944 CIFC24 H24 Cl N OP 1 21/n 112.0241; 10.8634; 15.0306
90; 92.829; 90
1960.94Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554945 CIFC17 H15 Br2 N O2P -17.5896; 10.9767; 11.9609
110.338; 100.049; 106.048
856.49Wang, Yu-Chao; Wang, Rui-Xiang; Qiu, Guanyinsheng; Zhou, Hongwei; Xie, Wenlin; Liu, Jin-Biao
ortho-Amide-directed 2,4-dibromohydration of conjugated enynes
Organic Chemistry Frontiers, 2019, 6, 2471
1554946 CIFC14 H12 N2 OP -17.2536; 9.2341; 9.3515
85.065; 81.059; 68.355
574.85Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines
Organic Chemistry Frontiers, 2019, 6, 2404
1554947 CIFC25 H15 N3 OP 1 21/n 19.8811; 14.4238; 13.7948
90; 109.258; 90
1856.1Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines
Organic Chemistry Frontiers, 2019, 6, 2404
1554948 CIFC24 H24 Cl N OP 1 21/c 116.3879; 7.0026; 17.8667
90; 103.718; 90
1991.86Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554949 CIFC25 H23 F2 N O3 SP -18.0332; 8.5272; 16.9075
99.329; 99.436; 101.204
1097.99Hu, Xiao-Si; Ding, Pei-Gang; Yu, Jin-Sheng; Zhou, Jian
A Sc(OTf)3 catalyzed Mukaiyama–Mannich reaction of difluoroenoxysilanes with unactivated ketimines
Organic Chemistry Frontiers, 2019, 6, 2500
1554950 CIFC152.5 H199 B4 N7 O23P 1 21/c 111.705; 28.512; 22.406
90; 98.94; 90
7387Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554951 CIFC24 H24 O2 S2C 1 2 123.8323; 5.5909; 15.658
90; 103.617; 90
2027.7Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554952 CIFC25 H25 N O2 SP 21 21 216.07714; 13.1618; 27.1117
90; 90; 90
2168.56Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554953 CIFC32 H30.52 O4.26 SC 1 2/c 113.9336; 19.7182; 20.3209
90; 103.298; 90
5433.4Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554954 CIFC27 H24 Fe O2 SP b c a28.3482; 19.5347; 7.5873
90; 90; 90
4201.6Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554955 CIFC50 H44 F24 N4 P4P 1 21/n 113.488; 14.281; 14.287
90; 108.36; 90
2611.9Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554956 CIFC186 H168 B4 N14 O31P -116.134; 16.609; 16.766
85.82; 65.15; 75.26
3939.7Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554957 CIFC27 H22 Cl N O5 SP 21 21 2110.1603; 10.173; 23.5179
90; 90; 90
2430.83Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes
Organic Chemistry Frontiers, 2019, 6, 2452
1554958 CIFC27 H23 N O5 SP 1 21 110.0757; 10.4448; 10.8094
90; 92.786; 90
1136.2Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes
Organic Chemistry Frontiers, 2019, 6, 2452
1554959 CIFC117 H171 B4 N4 O20P 1 21/c 142.193; 8.356; 15.63
90; 90.76; 90
5510.1Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554960 CIFC180 H112 B4 D84 N4 O34 S14P -116.67; 17.44; 19.659
81.21; 74.06; 62.19
4859Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554961 CIFC30 H29 N O3 SP 1 21/n 19.8296; 13.4413; 22.608
90; 94.433; 90
2978.1Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554962 CIFC20 H27 N O2 SP 21 21 215.8832; 8.7875; 37.5443
90; 90; 90
1940.99Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554963 CIFC22 H29 N O2 SP 21 21 218.87; 10.6671; 21.508
90; 90; 90
2035Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554964 CIFC19 H23 N O2 SC 1 2/c 135.164; 8.6573; 11.5114
90; 94.241; 90
3494.8Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554965 CIFC23 H33 N O2 SP 1 21/c 119.505; 8.6857; 13.1687
90; 92.309; 90
2229.2Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554966 CIFC21 H26 Br N O2 SP 1 21 110.888; 8.651; 10.91
90; 97.5; 90
1018.8Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554967 CIFC18 H22 Br N O2 SP 1 21/c 112.551; 11.012; 14.276
90; 113.904; 90
1803.9Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554968 CIFC70 H56 N8 O8P -111.446; 13.451; 22.036
98.71; 104.3; 98.36
3189.9Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554969 CIFC32 H26 N4 O2C 1 2/c 116.098; 8.0852; 19.417
90; 103.12; 90
2461.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554970 CIFC17 H14 ClP -110.013; 12.073; 12.827
111.893; 107.027; 93.776
1348.7Fan, Xing; Liu, Ruixing; Wei, Yin; Shi, Min
Rh-Catalyzed intramolecular decarbonylative cyclization of ortho-formyl group tethered alkylidenecyclopropanes (ACPs) for the construction of 2-methylindenes
Organic Chemistry Frontiers, 2019, 6, 2667
1554971 CIFC34 H30 N4 O4P 1 21/c 17.3964; 23.302; 16.073
90; 94.05; 90
2763.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554972 CIFC20 H17 N OP b c a14.5964; 13.9382; 14.6669
90; 90; 90
2983.94Hu, Xiaoping; Wang, Gaonan; Qin, Chunxiang; Xie, Xin; Zhang, Chunli; Xu, Wei; Liu, Yuanhong
Ligandless nickel-catalyzed transfer hydrogenation of alkenes and alkynes using water as the hydrogen donor
Organic Chemistry Frontiers, 2019, 6, 2619
1554973 CIFC70 H58 Cl6 N8 O12 SC 1 c 137.78; 8.9173; 26.953
90; 133.41; 90
6596Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554974 CIFC30 H27 N3P 1 21/n 114.929; 5.74297; 27.7627
90; 104.785; 90
2301.48Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554975 CIFC17 H16 N2P 1 21/c 115.534; 6.291; 15.0837
90; 113.849; 90
1348.18Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554976 CIFC15 H13 N3P c a 2112.9687; 13.0705; 7.18
90; 90; 90
1217.06Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554977 CIFC22 H17 N3P -18.8058; 10.1568; 10.8636
112.118; 90.659; 106.96
852.87Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554978 CIFC16 H10 Br N O4P 1 21/c 112.4447; 15.6502; 7.9646
90; 105.739; 90
1493Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam
Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides.
Organic letters, 2015, 17, 2010-2013
1554979 CIFC30 H24 F2 O5P 1 21/n 114.1655; 22.469; 16.419
90; 98.419; 90
5169.6Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin
Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling
Organic Chemistry Frontiers, 2019, 6, 2788
1554980 CIFC15 H12 F O3P -19.9135; 11.2232; 13.3885
94.007; 107.02; 109.916
1315.15Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin
Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling
Organic Chemistry Frontiers, 2019, 6, 2788
1554981 CIFC70 H120 N14 O26 S8P -113.0106; 13.1402; 14.3888
80.344; 63.999; 78.993
2160.42Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554982 CIFC30 H60 N12 O16 S4C 1 2/c 113.4741; 14.6965; 22.6791
90; 92.704; 90
4485.96Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554983 CIFC19 H19 B11 Cl6 OP 1 21/c 117.251; 12.1706; 26.112
90; 91.879; 90
5479.4Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554984 CIFC20 H21 B11 Cl6 OP b c a19.0146; 13.8372; 21.2518
90; 90; 90
5591.5Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554985 CIFC25 H22 B11 Cl6 NP b c n18.70332; 18.4574; 18.4002
90; 90; 90
6352.02Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554986 CIFC25 H22 B11 Cl6 NP b c n18.015; 14.8013; 23.3476
90; 90; 90
6225.53Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554987 CIFC25 H24 B11 Cl6 NP 1 21/c 131.445; 13.6072; 32.634
90; 116.666; 90
12478.2Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554988 CIFC40 H69.97 N4 O14 S4P -111.2634; 15.966; 16.009
111.587; 100.691; 109.004
2373.6Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554989 CIFC27 H24 N4 O4 S2P 1 21/n 19.943; 19.423; 27.408
90; 94.84; 90
5274.24Wang, Lihong; Wang, Xiaomin; Zhang, Ge; Yang, Shengbiao; Li, Yan; Zhang, Qian
Copper-catalyzed 1,3-aminoazidation of arylcyclopropanes: a facile access to 1,3-diamine derivatives
Organic Chemistry Frontiers, 2019, 6, 2934
1554990 CIFC15 H13 N O4 SP 21 21 218.1609; 9.0398; 19.318
90; 90; 90
1425.1Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping
Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions.
Organic letters, 2015, 17, 2022-2025
1554991 CIFC13 H11 N O3P 1 21/c 19.4606; 8.7844; 13.698
90; 91.45; 90
1138Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554992 CIFC15 H13 N O3P 21 21 215.2776; 10.8907; 22.1326
90; 90; 90
1272.11Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554993 CIFC14 H11 N O5P 1 21/c 111.0859; 9.2256; 12.6525
90; 101.245; 90
1269.2Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554994 CIFC28 H23 N3 O4 SP 1 21/n 112.8623; 11.3355; 16.9579
90; 94.493; 90
2464.87Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei
Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines.
Organic letters, 2015, 17, 2214-2217
1554995 CIFC23 H18 Cl N O2P -19.2832; 10.0044; 11.107
87.027; 65.546; 82.335
930.61Yao, Yongqi; Yang, Wen; Lin, Qifu; Yang, Weitao; Li, Huanyong; Wang, Lin; Gu, Fenglong; Yang, Dingqiao
1,3-Dipolar cycloaddition of nitrones to oxa(aza)bicyclic alkenes
Organic Chemistry Frontiers, 2019, 6, 3360
1554996 CIFC19 H22 O7P 1 21/n 16.0808; 23.3393; 12.5225
90; 94.028; 90
1772.82Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2338-2341
1554997 CIFC21 H18 N4 O4 SP 21 21 216.0211; 16.1241; 20.634
90; 90; 90
2003.25Li, Shi-Wu; Du, Yu; Kang, Qiang
A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis
Organic Chemistry Frontiers, 2019, 6, 2775
1554998 CIFC26 H31 Br N2 O3P -19.6121; 11.761; 13.648
98.331; 109.571; 113.637
1260.2Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu
Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts.
Organic letters, 2015, 17, 2234-2237
1554999 CIFC40 H32 O6P -110.438; 10.7; 15.172
80.197; 70.129; 79.638
1556.7Wang, Wenli; Tang, Yingzhan; Liu, Yongxiang; Yuan, Lei; Wang, Jian; Lin, Bin; Zhou, Di; Sun, Lu; Huang, Renbin; Chen, Gang; Li, Ning
Isolation, structure elucidation, and synthesis of (±)-millpuline A with a suppressive effect in miR-144 expression
Organic Chemistry Frontiers, 2019, 6, 2850
1555000 CIFC38 H44 B2 F4 N4 O6P -19.7881; 13.2333; 16.5195
67.596; 77.669; 72.069
1870.86Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond
Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts.
Organic letters, 2015, 17, 2246-2249
1555001 CIFC44 H40 N4 Ni O2P 1 21/c 119.861; 13.383; 18.29
90; 117.363; 90
4318Ren, Demin; Fu, Xinliang; Li, Xiaofang; Koniarz, Sebastian; Chmielewski, Piotr J.
Reaction of antiaromatic porphyrinoid with active methylene compounds
Organic Chemistry Frontiers, 2019, 6, 2924
1555002 CIFC15 H16 N2 O4P 1 21/c 114.1112; 4.6513; 21.124
90; 99.827; 90
1366.14Mei, Xiangui; Lan, Mengmeng; Cui, Guodong; Zhang, Hongwei; Zhu, Weiming
Caerulomycins from Actinoalloteichus cyanogriseus WH1-2216-6: isolation, identification and cytotoxicity
Organic Chemistry Frontiers, 2019, 6, 3566
1555003 CIFC27 H30 F N O2P -19.3088; 9.5092; 14.5742
92.724; 104.673; 110
1159.92Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555004 CIFC28 H32 F N O2P 21 21 218.03153; 10.686; 28.3689
90; 90; 90
2434.76Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555005 CIFC28 H32 N4 O2P 32 2 111.32263; 11.32263; 35.383
90; 90; 120
3928.44Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555006 CIFC30 H35 N O4P 19.7073; 10.168; 14.0374
85.597; 85.998; 82.306
1366.53Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555007 CIFC28 H31 F2 N O2P 110.4764; 10.6867; 12.3768
85.757; 70.552; 69.477
1222.26Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555008 CIFC28 H31 F2 N O2P 1 21 17.90952; 16.3522; 9.53794
90; 95.6737; 90
1227.58Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555009 CIFC24 H20 O SP 1 21/n 115.8263; 7.7607; 15.9189
90; 106.393; 90
1875.73Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua
Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones
Organic Chemistry Frontiers, 2019, 6, 2796
1555010 CIFC22 H14 Cl F O SP -17.3464; 8.5371; 15.0907
95.337; 91.518; 104.361
911.69Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua
Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones
Organic Chemistry Frontiers, 2019, 6, 2796
1555011 CIFC23 H27 Br N2 O5P 1 21/n 18.3956; 11.6027; 23.715
90; 91.1454; 90
2309.7Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri
PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines.
Organic letters, 2015, 17, 2416-2419
1555012 CIFC8 H11 F3 N2 O SP 1 21/c 18.4044; 11.3774; 11.5451
90; 96.16; 90
1097.6Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng
Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates.
Organic letters, 2015, 17, 2438-2441
1555013 CIFC147 H132 N16 O27 ZnP 1 21/a 123.94; 28.05; 23.991
90; 119.85; 90
13973Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555014 CIFC38 H32 N2 O6P 1 21/n 112.6219; 16.3765; 16.6547
90; 100.607; 90
3383.7Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555015 CIFC15 H16 O3P 1 21/n 14.6619; 23.4349; 12.2946
90; 97.466; 90
1331.8Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555016 CIFC152 H128 N8 O24 ZnP -112.8844; 13.9073; 20.6328
98.862; 106.525; 94.899
3469.4Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555017 CIFC36 H30 N4 O6P 1 21/n 112.8709; 15.6947; 16.5272
90; 92.507; 90
3335.38Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555018 CIFC76 H112 F14 N4 Sn4P -110.7975; 11.121; 17.986
82.945; 76.059; 70.925
1978.74Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555019 CIFC32 H4 F26 N4P -16.15317; 9.3804; 13.8177
103.878; 100.265; 98.23
747.31Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555020 CIFC26 H18 OC 1 2/c 142.263; 7.4986; 12.0012
90; 93.813; 90
3794.9Han, Jian; Liu, Xinbang; Li, Yu; Lou, Zihao; Yi, Mingdong; Kong, Huihui; Luo, Jun
New synthetic approaches for hexacene and its application in thin-film transistors
Organic Chemistry Frontiers, 2019, 6, 2839
1555021 CIFC19 H18 O2P n a 2112.91; 9.664; 12.157
90; 90; 90
1516.7Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555022 CIFC17 H22 O2P 21 21 218.6511; 11.009; 15.784
90; 90; 90
1503.3Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555023 CIFC24 H17 N O2P -111.0804; 12.2799; 13.6018
75.764; 84.604; 89.194
1785.88Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie
One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes
Organic Chemistry Frontiers, 2019, 6, 2897
1555024 CIFC24 H17 N O2P 1 21/c 18.5534; 5.4976; 37.5979
90; 93.982; 90
1763.7Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie
One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes
Organic Chemistry Frontiers, 2019, 6, 2897
1555025 CIFC26 H18 F3 N O2P -16.4787; 10.7989; 16.2052
79.201; 85.566; 73.057
1065.03Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie
One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes
Organic Chemistry Frontiers, 2019, 6, 2897
1555026 CIFC22 H21 N O3P -19.724; 10.178; 10.676
62.165; 79.328; 69.089
872.6Capreti, Naylil M. R.; Jurberg, Igor D.
Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds.
Organic letters, 2015, 17, 2490-2493
1555027 CIFC28 H22 O3 SP 1 21/c 110.465; 9.797; 22.032
90; 95.834; 90
2247.1Yang, Tao; Kou, Peihao; Jin, Fengyan; Song, Xian-Rong; Bai, Jiang; Ding, Haixin; Xiao, Qiang; Liang, Yong-Min
TFA-promoted sulfonation/cascade cyclization of 2-propynolphenols with sodium sulfinates to 4-sulfonyl 2H-chromenes under metal-free conditions
Organic Chemistry Frontiers, 2019, 6, 3162
1555028 CIFC15 H13 N OR -3 :H26.4383; 26.4383; 8.6956
90; 90; 120
5263.8Zhang, Yan; Wang, Dahai; Cui, Sunliang
Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines.
Organic letters, 2015, 17, 2494-2497
1555029 CIFC17 H15 N O3 SP 1 21/n 15.9669; 11.4767; 21.9463
90; 96.78; 90
1492.38Zhu, Cheng-Zhi; Wei, Yin; Shi, Min
Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives
Organic Chemistry Frontiers, 2019, 6, 2884
1555030 CIFC21 H16 Br N O4 SP -17.1629; 10.9804; 12.5285
102.431; 97.658; 98.768
936.85Zhu, Cheng-Zhi; Wei, Yin; Shi, Min
Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives
Organic Chemistry Frontiers, 2019, 6, 2884
1555031 CIFC36 H39 N O2P 1 21/c 114.8225; 11.0736; 18.657
90; 100.056; 90
3015.3Reddy, Virsinha; Vijaya Anand, Ramasamy
Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach.
Organic letters, 2015, 17, 3390-3393
1555032 CIFC27 H20 N2 O4 SP -19.0601; 9.927; 13.5869
82.759; 78.19; 83.39
1181.56Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides
Organic Chemistry Frontiers, 2019, 6, 2968
1555033 CIFC29.25 H25.5 Cl0.5 N3 O6 S2P 1 21/c 112.7222; 31.291; 7.7018
90; 104.211; 90
2972.2Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides
Organic Chemistry Frontiers, 2019, 6, 2968
1555034 CIFC25 H27 Fe N O3 SP 1 21 115.0789; 8.6357; 18.2167
90; 106.122; 90
2278.8Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro
Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library.
Organic letters, 2015, 17, 2286-2289
1555035 CIFC88 H73 Cl10 N3 PdC 1 2/c 117.9223; 20.5932; 21.0729
90; 100.834; 90
7638.9Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou
Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination
Organic Chemistry Frontiers, 2019, 6, 3292
1555036 CIFC84 H65 Cl2 N3 O2 PdC 1 2/c 117.6466; 20.7167; 20.3473
90; 95.896; 90
7399.2Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou
Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination
Organic Chemistry Frontiers, 2019, 6, 3292
1555037 CIFC17 H14 N2 O3P 1 21/c 18.9224; 9.3813; 18.2533
90; 103.064; 90
1488.32Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho
Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid.
Organic letters, 2015, 17, 2518-2521
1555038 CIFC9 H13 N5 O4P 1 21/c 18.3117; 17.2043; 8.3018
90; 103.231; 90
1155.62Guo, Xiaowei; Wang, Jidong; Su, Can; Liu, Chongxi; Ma, Xiao-Yan; Yu, Zhiyin; Li, Jiansong; Wang, Xiangjing; Xiang, Wensheng; Huang, Sheng-Xiong
A unique spiro-β-triazinedione-γ-hydantoin type alkaloid with antiviral activity against tobacco mosaic virus from Streptomyces gamaensis
Organic Chemistry Frontiers, 2019, 6, 3215
1555039 CIFC26 H28 O5P -110.896; 11.118; 11.442
109.812; 100.766; 111.223
1137.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555040 CIFC23 H25 N O9 SP -19.3448; 11.2047; 12.9889
106.439; 97.223; 112.631
1160.92Xing, Siyang; Xia, Hanyu; Wang, Xin; Wu, Die; Xu, Xinrui; Su, Yunran; Wang, Kui; Zhu, Bolin; Guo, Junshuo
Diastereoselective access to 2-aminoindanones via the rhodium(ii)-catalyzed tandem reaction involving O–H insertion and Michael addition
Organic Chemistry Frontiers, 2019, 6, 3121
1555041 CIFC23 H24 O3P -18.428; 11.011; 11.459
65.415; 87.993; 89.668
966.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555042 CIFC33 H38 N O5P 19.1302; 9.1578; 10.226
108.986; 98.417; 114.037
698.83Freeman, Jared L.; Brimble, Margaret A.; Furkert, Daniel P.
A chiral auxiliary-based synthesis of the C5‒C17 trans-decalin framework of anthracimycin
Organic Chemistry Frontiers, 2019, 6, 2954
1555043 CIFC25 H28 O10I 1 2 111.9189; 6.5987; 26.7335
90; 100.124; 90
2069.83Pan, Dongyan; Zhang, Xuexia; Zheng, Haizhou; Zheng, Zhihui; Nong, Xuhua; Liang, Xiao; Ma, Xuan; Qi, Shuhua
Novel anthraquinone derivatives as inhibitors of protein tyrosine phosphatases and indoleamine 2,3-dioxygenase 1 from the deep-sea derived fungus Alternaria tenuissima DFFSCS013
Organic Chemistry Frontiers, 2019, 6, 3252
1555044 CIFC21 H36 O4 SiC 1 2 122.265; 7.7011; 12.8529
90; 102.095; 90
2154.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555045 CIFC12 H14 O3P 1 21/c 112.324; 7.8713; 10.6532
90; 92.217; 90
1032.65Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555046 CIFC23 H20 O6P -17.7957; 10.1827; 12.7574
79.033; 76.634; 77.369
950.96Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555047 CIFC16 H11 Br O2P 1 21/c 110.0036; 15.567; 8.7599
90; 100.953; 90
1339.3Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555048 CIFC16 H12 O2C 1 2/c 125.676; 4.1792; 24.335
90; 112.38; 90
2414.6Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555049 CIFC23 H22 O6P 1 21/c 114.7414; 8.7416; 16.409
90; 104.242; 90
2049.53Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555050 CIFC22 H17 Cl O6P 1 21/n 114.6483; 17.4042; 15.2455
90; 94.817; 90
3872.99Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555051 CIFC36 H55 N O7 Si2P -18.9128; 10.9914; 20.184
91.339; 96.624; 104.357
1899.99Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555052 CIFC15 H20 O5P 21 21 217.3936; 10.5735; 17.817
90; 90; 90
1392.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555053 CIFC21 H38 O5 SP 1 21/c 116.4753; 10.1532; 13.8282
90; 98.669; 90
2286.71Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555054 CIFC21 H22 O10P 1 21/c 18.8935; 14.433; 15.7451
90; 92.016; 90
2019.79Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A‒E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555055 CIFC20 H20 O10P -19.016; 9.3778; 10.636
93.717; 90.826; 92.317
896.52Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555056 CIFC21 H22 O11P c a 218.33914; 13.29606; 18.06836
90; 90; 90
2003.38Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555057 CIFC21 H22 O11P 21 21 218.2302; 14.4554; 16.2394
90; 90; 90
1932.01Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555058 CIFC22 H23 N O9P 1 21/n 18.26703; 13.79202; 17.73644
90; 102.392; 90
1975.18Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555059 CIFC15 H22 O6P 1 21/n 18.5281; 18.7862; 9.5185
90; 100.368; 90
1500.07Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555060 CIFC16 H17 N O4P 1 21 16.9082; 11.2913; 19.3834
90; 91.357; 90
1511.53Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555061 CIFC34 H22 Cl2 N4 O4P b c a10.6177; 21.038; 26.249
90; 90; 90
5863.4Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555062 CIFC23 H19 F3P 1 21/c 110.7304; 18.6098; 9.9301
90; 115.595; 90
1788.36Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555063 CIFC24 H21 F3 O2P -19.28774; 13.98378; 16.25245
94.589; 106.279; 98.2135
1989.34Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555064 CIFC24 H20 F4 O2P 1 21/n 18.7646; 10.6788; 20.8962
90; 94.821; 90
1948.87Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555065 CIFC24 H21 F3P -19.7671; 10.3099; 19.8876
92.41; 96.248; 107.45
1893.23Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555066 CIFC24 H21 F3 O2P -18.8501; 10.1181; 11.7209
98.214; 105.322; 103.258
961.85Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555067 CIFC23 H19 F3 OP -19.9918; 10.2089; 10.5751
91.174; 116.274; 107.926
904.65Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555068 CIFC24 H21 F3P -18.9463; 10.2875; 11.0964
70.184; 86.437; 76.947
935.84Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555069 CIFC24 H20 Cl F3 O2P -19.0216; 9.9831; 11.9107
77.527; 82.086; 74.544
1005.86Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555070 CIFC25 H23 F3P 1 21/c 110.5544; 15.4584; 12.2743
90; 102.702; 90
1953.59Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555071 CIFC24 H21 F3P 1 21/n 111.6641; 9.1396; 17.3076
90; 95.883; 90
1835.36Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555072 CIFC22 H16 Br F3P -19.02917; 9.25385; 11.1048
87.5911; 80.5904; 78.3143
896.36Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555073 CIFC24 H19 Cl2 F3 O2P -19.2224; 10.2968; 11.9735
74.791; 80.463; 72.449
1041.48Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555074 CIFC22 H15 Cl2 F3I 1 2/c 121.8668; 10.36934; 18.0539
90; 113.947; 90
3741.25Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555075 CIFC24 H21 F3P 1 21/c 110.1714; 36.8462; 10.1929
90; 103.732; 90
3710.88Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555076 CIFC25 H23 F3 O2P 1 21/c 111.5733; 18.729; 19.4741
90; 105.635; 90
4064.94Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555077 CIFC30 H22 Cl2 N4 O12P 4310.6627; 10.6627; 29.5381
90; 90; 90
3358.3Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555078 CIFC29 H20 I4 O4P -112.1779; 21.8512; 21.9539
60.52; 87.603; 86.921
5077.5Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555079 CIFC16 H13 N O3P 1 c 114.099; 5.2916; 9.1495
90; 101.496; 90
668.92He, Guangke; Li, Yuan; Yu, Zilun; Chen, Zhaoqiang; Tang, Yongming; Song, Guangliang; Loh, Teck-Peng
Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones
Organic Chemistry Frontiers, 2019, 6, 3644
1555080 CIFC38 H26 Cl2 O4P 1 21/c 113.2235; 24.195; 10.2868
90; 110.556; 90
3081.6Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555081 CIFC17 H12 I N3 SP 1 21/n 14.12; 14.2279; 26.763
90; 94.268; 90
1564.5Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling
Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals
Organic Chemistry Frontiers, 2019, 6, 3355
1555082 CIFC19 H17 N O S2P b c a10.1327; 12.0719; 28.967
90; 90; 90
3543.3Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling
Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals
Organic Chemistry Frontiers, 2019, 6, 3355
1555083 CIFC19 H21 N O4 SP 1 21/n 18.2569; 11.0688; 20.1396
90; 95.9683; 90
1830.66Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555084 CIFC26 H16 F9 N O4P 1 21/c 16.1329; 40.065; 10.6098
90; 103.811; 90
2531.6He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng
Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers
Organic Chemistry Frontiers, 2019, 6, 3575
1555085 CIFC19 H12 Cl F9 OP c a 2111.543; 10.4; 32.618
90; 90; 90
3916He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng
Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers
Organic Chemistry Frontiers, 2019, 6, 3575
1555086 CIFC27 H27 N O5 SP 1 21/n 110.98; 21.409; 11.347
90; 104.07; 90
2587.3Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555087 CIFC10 H9 F3 N2 OP 21 21 217.1385; 7.5039; 19.126
90; 90; 90
1024.5Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng
An enantioselective aza-Henry reaction of trifluoromethyl ketimines catalyzed by phase-transfer catalysts
Organic Chemistry Frontiers, 2019, 6, 3269
1555088 CIFC26 H20 Cl F3 N2 O2C 1 c 17.2179; 17.509; 18.867
90; 100.172; 90
2346.9Yu, Yang; Zhang, Yan; Wang, Zhuo; Liang, Yong-Xin; Zhao, Yu-Long
A rhodium-catalyzed three-component reaction of arylisocyanides, trifluorodiazoethane, and activated methylene isocyanides or azomethine ylides: an efficient synthesis of trifluoroethyl-substituted imidazoles
Organic Chemistry Frontiers, 2019, 6, 3657
1555089 CIFC38 H34 P2P -18.6263; 12.097; 16.023
107.86; 95.73; 104.279
1514.1Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555090 CIFC32 H32 O P2P 1 21/c 114.7596; 10.4392; 17.7877
90; 105.924; 90
2635.5Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555091 CIFC18 H23 N O2P 1 21/c 112.58; 15.83; 8.839
90; 109.551; 90
1658.7Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555092 CIFC46 H40 O8P 1 21/n 110.1647; 17.2468; 20.8692
90; 101.136; 90
3589.7Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan
Constructing bridged multifunctional calixarenes by intramolecular indole coupling
Organic Chemistry Frontiers, 2019, 6, 3327
1555093 CIFC72 H64 N10 O6P 1 21/c 116.5782; 28.2895; 17.3002
90; 93.414; 90
8099.2Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan
Constructing bridged multifunctional calixarenes by intramolecular indole coupling
Organic Chemistry Frontiers, 2019, 6, 3327
1555094 CIFC76 H68 N8 O8C 1 2/c 130.104; 23.487; 26.09
90; 121.557; 90
15719Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan
Constructing bridged multifunctional calixarenes by intramolecular indole coupling
Organic Chemistry Frontiers, 2019, 6, 3327
1555095 CIFC19 H16 O2C 1 2 117.095; 5.874; 15.476
90; 106; 90
1493.8Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555096 CIFC21 H13 Cl I3 N O2P -18.885; 11.599; 11.638
87.07; 72.279; 76.183
1109.11Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555097 CIFC18 H14 Cl N3P 1 21/n 114.445; 6.6377; 15.6545
90; 94.414; 90
1496.53Surendra Reddy, G.; Ramachary, Dhevalapally B.
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2019, 6, 3620
1555098 CIFC23 H16 N4C 1 c 113.055; 13.601; 10.697
90; 100.788; 90
1865.8Surendra Reddy, G.; Ramachary, Dhevalapally B.
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2019, 6, 3620
1555099 CIFC23 H14 F N3 O2P -19.293; 13.946; 16.068
114.567; 99.86; 93.392
1846.1Surendra Reddy, G.; Ramachary, Dhevalapally B.
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2019, 6, 3620
1555100 CIFC21 H15 Cl I N O2P 1 21/n 111.057; 13.631; 13.716
90; 110.38; 90
1937.8Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555101 CIFC25 H22 F N O5P 21 21 218.9187; 14.6101; 16.5218
90; 90; 90
2152.8Bhattacharya, Aditya; mani Shukla, Pushpendra; Kumar Kaushik, Lalit; Maji, Biswajit
Synthesis of chromans and kinetic resolution of 2-aryl-3-nitro-2H-chromenes via the NHC-bound azolium homoenolate pathway
Organic Chemistry Frontiers, 2019, 6, 3523
1555102 CIFC22 H22 OP -19.1622; 9.508; 10.568
83; 65.519; 78.417
820Manojveer, Seetharaman; Balamurugan, Rengarajan
In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes.
Organic letters, 2015, 17, 3600-3603
1555103 CIFC22 H21 N O3 SC 1 2/c 119.5977; 8.1238; 23.2996
90; 90.182; 90
3709.5Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan
Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles
Organic Chemistry Frontiers, 2019, 6, 3415
1555104 CIFC23 H22 Br3 Cl2 N O3 SP -18.199; 11.3055; 14.2419
100.441; 100.282; 91.136
1275.6Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan
Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles
Organic Chemistry Frontiers, 2019, 6, 3415
1555105 CIFC8 H10 O4P c a 2110.571; 5.838; 12.338
90; 90; 90
761.4Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555106 CIFC12 H14 O6F d d 237.2102; 18.06; 6.8155
90; 90; 90
4580.1Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555107 CIFC10 H12 O3P b c a8.8394; 8.5924; 23.437
90; 90; 90
1780.1Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555108 CIFC9 H12 O4P 21 21 216.345; 8.9881; 15.108
90; 90; 90
861.6Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555109 CIFC8 H10 O4P 1 21 15.3883; 12.812; 6.0438
90; 114.32; 90
380.21Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555110 CIFC26 H20 O3 SP 21 21 217.9759; 16.1628; 31.7213
90; 90; 90
4089.3Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan
A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds
Organic Chemistry Frontiers, 2019, 6, 3259
1555111 CIFC27 H21 N O3 SP 21 21 215.7472; 16.912; 22.0104
90; 90; 90
2139.34Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan
A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds
Organic Chemistry Frontiers, 2019, 6, 3259
1555112 CIFC19 H22 N2 OP 21 21 217.4987; 12.2482; 16.8063
90; 90; 90
1543.58Wong, Suet-Pick; Gan, Chew-Yan; Lim, Kuan-Hon; Ting, Kang-Nee; Low, Yun-Yee; Kam, Toh-Seok
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.
Organic letters, 2015, 17, 3628-3631
1555113 CIFC33 H25 Cl N2 O5P 110.596; 11.6796; 12.6988
69.855; 70.549; 88.791
1383.42Wang, Zhen-Hua; Lei, Chuan-Wen; Zhang, Xia-Yan; You, Yong; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Asymmetric domino 1,6-addition/annulation reaction of 3-cyano-4-alkenyl-2H-chromen-2-ones with isatin-derived MBH carbonates: enantioselective synthesis of 3,3′-cyclopentenylspirooxindoles bearing 2H-chromen-2-ones
Organic Chemistry Frontiers, 2019, 6, 3342
1555114 CIFC18 H23 N O5 SP 18.6291; 9.4332; 12.4474
82.659; 70.506; 68.236
887.04Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555115 CIFC33 H29 Cl N2 O3P 1 21/n 117.7343; 13.4538; 24.68
90; 94.67; 90
5868.9Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555116 CIFC44 H39 N3 O7P -19.853; 14.0452; 15.201
111.663; 93.543; 102.84
1882Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555117 CIFC33 H29 N3 O5P 1 21/n 112.847; 12.739; 20.208
90; 96.73; 90
3284.4Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555118 CIFC34 H28 Cl2 N2 O3P b c a10.1992; 17.1094; 33.448
90; 90; 90
5836.7Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555119 CIFC12 H15 F N2 O4 SP 1 21/n 16.70613; 8.92562; 21.9646
90; 91.7362; 90
1314.12Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555120 CIFC20 H40 N3 O5 PP -19.2786; 9.5213; 15.4265
75.673; 76.438; 71.3
1232.75Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide
Enzymatic triggering of C–ON bond homolysis of alkoxyamines
Organic Chemistry Frontiers, 2019, 6, 3663
1555121 CIFC20 H38 N3 O4 PP 1 21/c 18.8282; 22.0666; 12.5309
90; 96.936; 90
2423.3Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide
Enzymatic triggering of C–ON bond homolysis of alkoxyamines
Organic Chemistry Frontiers, 2019, 6, 3663
1555122 CIFC11 H14 N2 O2 SP 1 21/n 115.2033; 5.10542; 15.6074
90; 108.006; 90
1152.1Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555123 CIFC25 H24 OP 1 21/c 110.22; 9.55; 20.071
90; 93.737; 90
1954.8Li, Hexin; Zhang, Mengru; Mehfooz, Haroon; Zhu, Dongxia; Zhao, Jinbo; Zhang, Qian
Highly convergent modular access to poly-carbon substituted cyclopropanes via Cu(i)-catalyzed three-component cyclopropene carboallylation
Organic Chemistry Frontiers, 2019, 6, 3387
1555124 CIFC16 H16 N2 O2 SP 1 21/n 18.236; 21.1919; 8.4904
90; 103.856; 90
1438.76Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555125 CIFC22 H18 Br Cl3 N2 O4P 1 21 113.3229; 6.2024; 15.4655
90; 115.145; 90
1156.87Zhao, Mei-Xin; Liu, Qiang; Yu, Kun-Ming; Zhao, Xiao-Li; Shi, Min
Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives
Organic Chemistry Frontiers, 2019, 6, 3879
1555126 CIFC13 H19 N O3 SP 21 21 217.789; 11.669; 15.029
90; 90; 90
1366Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555127 CIFC13 H10 F3 N OP -15.0942; 9.6532; 11.935
91.045; 91.275; 101.201
575.43Lu, Kui; Wei, Xianfu; Li, Quan; Li, Yuxuan; Ji, Liangshuo; Hua, Erbing; Dai, Yujie; Zhao, Xia
Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent
Organic Chemistry Frontiers, 2019, 6, 3766
1555128 CIFC14 H17 Br Cl N O4 SP 1 21 19.24; 6.262; 14.504
90; 91.561; 90
838.9Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555129 CIFC15 H30 O4P 17.0302; 7.6119; 7.7844
94.191; 109.731; 97.56
385.61Song, Yin-Ping; Miao, Feng-Ping; Yin, Xiu-Li; Ji, Nai-Yun
Nitrogenous cyclonerane sesquiterpenes from an algicolous strain of Trichoderma asperellum
Organic Chemistry Frontiers, 2019, 6, 3698
1555130 CIFC20 H24 Br N O4 SP 1 21 114.656; 10.051; 14.998
90; 104.87; 90
2135.3Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555131 CIFC16 H9 N3 O2 SP 21 21 215.168; 15.6589; 15.9344
90; 90; 90
1289.49Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina
Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution
Organic Chemistry Frontiers, 2019, 6, 3300
1555132 CIFC16 H10 Br N3 O2 SP -18.3252; 9.8395; 11.1869
65.08; 71.705; 67.231
753.73Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina
Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution
Organic Chemistry Frontiers, 2019, 6, 3300
1555133 CIFC14 H18 Br N O4 SP 1 21 16.4495; 15.276; 8.0516
90; 96.47; 90
788.2Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555134 CIFC20 H23 Br Cl N O4 SP 21 21 217.6751; 12.59; 22.275
90; 90; 90
2152.4Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555135 CIFC40 H41 N O4 S2P -111.0456; 12.0988; 14.8761
68.867; 70.725; 86.448
1746.7Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555136 CIFC27 H25 N O3 SP -17.8518; 10.3592; 14.2099
80.043; 83.223; 82.438
1123.12Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555137 CIFC26 H22 Cl N O3 SP 1 21/c 15.9034; 21.165; 21.6677
90; 91.308; 90
2706.6Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555138 CIFC24 H18 Cl N O3 SP -19.3704; 10.2251; 11.2595
76.2532; 78.5679; 75.2513
1002.43Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555139 CIFC23 H17 N O4 SP 1 21/c 17.8538; 13.4956; 17.2047
90; 101.145; 90
1789.2Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555140 CIFC23 H16 N2 O5 SP 1 21/c 113.0035; 15.8463; 9.5395
90; 101.719; 90
1924.7Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555141 CIFC24 H21 N O3 SP 21 21 217.3838; 11.2551; 24.298
90; 90; 90
2019.3Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555142 CIFC24 H21 N O3 S2P 1 21/n 19.2819; 23.5334; 10.2751
90; 111.152; 90
2093.2Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555143 CIFC20 H15 N O5 SP -18.2024; 10.5566; 11.0975
68.8504; 79.7504; 71.2427
846.51Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555144 CIFC37 H30 N2 O3 S2P 1 2/n 111.095; 12.561; 24.147
90; 93.088; 90
3360.3Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555145 CIFC31 H26 N2 O4 S2P 1 21/n 18.9049; 14.0612; 22.343
90; 93.263; 90
2793.1Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555146 CIFC35 H22 Cl2 N2 O3 S2C 1 2/c 118.289; 13.2118; 24.2095
90; 91.165; 90
5848.5Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555147 CIFC32 H28 N2 O4 S2P -17.6623; 10.2269; 19.008
102.84; 91.559; 103.009
1410.29Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555148 CIFC43 H48 N O3 S2P 21 21 2111.13642; 14.74032; 46.2616
90; 90; 90
7594.04Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555149 CIFC8 H8 N2 O4P 21 21 214.888; 9.8; 18.388
90; 90; 90
880.8Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi
Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives.
Organic letters, 2015, 17, 4666-4669
1555150 CIFC25 H34.5 F3 N O1.25C 1 2 120.6626; 10.3356; 13.6724
90; 123.325; 90
2439.76Sampaio-Dias, Ivo E.; Silva-Reis, Sara C.; Pinto da Silva, Luís; García-Mera, Xerardo; Maestro, Miguel A.; Rodríguez-Borges, José E.
Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids
Organic Chemistry Frontiers, 2019, 6, 3540
1555151 CIFC21 H23 N OP 1 21/c 19.1308; 14.0389; 14.7904
90; 106.943; 90
1813.6Sinai, Ádám; Vangel, Dóra; Gáti, Tamás; Bombicz, Petra; Novák, Zoltán
Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives.
Organic letters, 2015, 17, 4136-4139
1555152 CIFC20 H21 N O3 SC 1 2/c 133.942; 11.5163; 9.4629
90; 99.03; 90
3653.1Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni
Diastereoselective bicyclization of enynols via gold catalysis
Organic Chemistry Frontiers, 2019, 6, 3584
1555153 CIFC17 H16 O2P 21 21 217.3872; 10.8747; 16.4977
90; 90; 90
1325.32Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni
Diastereoselective bicyclization of enynols via gold catalysis
Organic Chemistry Frontiers, 2019, 6, 3584
1555154 CIFC14 H11 Cl N2P 1 21/n 115.4081; 7.7461; 19.9246
90; 98.208; 90
2353.69Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555155 CIFC19 H14 Cl N2 O PP 1 21/c 111.949; 8.5662; 17.479
90; 103.621; 90
1738.8Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555156 CIFC30 H38 O7P 1 21/c 111.8298; 17.6502; 13.5929
90; 90.058; 90
2838.17Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan
A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines
Organic Chemistry Frontiers, 2019, 6, 3535
1555157 CIFC31 H38 N2 O6P 1 21/c 111.2677; 10.9396; 24.121
90; 93.117; 90
2968.86Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan
A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines
Organic Chemistry Frontiers, 2019, 6, 3535
1555158 CIFC7 H3 Cl2 N2P b c a11.4945; 7.5152; 17.4299
90; 90; 90
1505.66Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555159 CIFC20 H19 N O5P 1 21 110.0737; 6.1334; 13.8766
90; 107.776; 90
816.45Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong
Clavipines A–C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes
Organic Chemistry Frontiers, 2019, 6, 3759
1555160 CIFC16 H14 O5P 21 21 218.594; 11.8962; 13.1105
90; 90; 90
1340.36Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong
Clavipines A‒C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes
Organic Chemistry Frontiers, 2019, 6, 3759
1555161 CIFC23 H24 O4P 1 21/c 18.759; 21.523; 10.067
90; 104.55; 90
1837Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555162 CIFC18 H20 O6P 1 21/c 17.7505; 21.813; 9.5132
90; 94.65; 90
1603Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555163 CIFC16.5 H16 Cl1.5 N2 O3P 1 21/c 116.298; 11.852; 9.939
90; 90.99; 90
1919.6Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555164 CIFC11 H6 Cl2 O SP n m a11.6812; 6.6839; 13.6312
90; 90; 90
1064.3Wang, Ting; An, Zhenyu; Qi, Zhenjie; Zhuang, Daijiao; Chang, Aosheng; Yang, Yunxia; Yan, Rulong
Ring-opening/annulation reaction of cyclopropyl ethanols: concise access to thiophene aldehydes via C–S bond formation
Organic Chemistry Frontiers, 2019, 6, 3705
1555165 CIFC17 H17 Br O5P b c a11.48; 10.279; 26.181
90; 90; 90
3089.4Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555166 CIFC28 H24 Cl N3 O4 SP 1 21 19.5954; 12.6894; 11.2412
90; 112.927; 90
1260.6Zhang, Haoran; Li, Shiwu; Kang, Qiang; Du, Yu
Chiral-at-metal rhodium(iii) complex catalyzed enantioselective synthesis of C2-substituted benzofuran derivatives
Organic Chemistry Frontiers, 2019, 6, 3683
1555167 CIFC18 H20 O5P 1 21/c 110.526; 19.394; 7.8119
90; 96.58; 90
1584.2Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555168 CIFC19 H18 N2 O6 SiC 1 c 110.8289; 10.4035; 17.1866
90; 103.19; 90
1885.14Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.
Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes
Organic Chemistry Frontiers, 2019, 6, 3793
1555169 CIFC25 H22 N2 O6 SiP 21 21 215.9864; 18.2027; 21.5323
90; 90; 90
2346.35Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.
Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes
Organic Chemistry Frontiers, 2019, 6, 3793
1555170 CIFC22 H26 O7P 21 21 219.136; 10.6809; 42.2825
90; 90; 90
4126Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555171 CIFC23 H28 O7P 21 21 218.5586; 9.2119; 27.3349
90; 90; 90
2155.11Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555172 CIFC34 H30 N2 O6P 1 21/n 111.4637; 45.4434; 12.0124
90; 116.324; 90
5608.9Yan, Jianming; Tay, Guan Liang; Neo, Cuien; Lee, Bo Ra; Chan, Philip Wai Hong
Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines.
Organic letters, 2015, 17, 4176-4179
1555173 CIFC24 H32 O5C 1 2 125.9119; 7.4654; 11.5725
90; 107.999; 90
2129.06Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao
Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion
Organic Chemistry Frontiers, 2019, 6, 3839
1555174 CIFC22 H30.66667 O4.33333P 21 21 2112.7263; 18.5197; 24.0727
90; 90; 90
5673.6Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao
Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion
Organic Chemistry Frontiers, 2019, 6, 3839
1555175 CIFC26 H18 N4 O5P -19.141; 10.706; 12.0986
73.26; 68.76; 72.31
1030.1Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555176 CIFC18 H26 O6P 6520.3875; 20.3875; 7.4174
90; 90; 120
2669.99Li, Hong-Tao; Tang, Linhuan; Liu, Tao; Yang, Ruining; Yang, Yabin; Zhou, Hao; Ding, Zhong-Tao
Polyoxygenated meroterpenoids and a bioactive illudalane derivative from a co-culture of Armillaria sp. and Epicoccum sp.
Organic Chemistry Frontiers, 2019, 6, 3847
1555177 CIFC21 H15 N3 O3P 1 21/c 116.334; 13.572; 7.87
90; 104.13; 90
1691.9Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555178 CIFC34 H27.62 N2 O6P -110.4723; 12.7127; 12.7391
113.157; 97.019; 110.996
1385.7Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank
1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties
Organic Chemistry Frontiers, 2019, 6, 3731
1555179 CIFC51 H52 N2 O7P -112.287; 13.2979; 27.85
86.66; 90; 90
4542.7Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank
1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties
Organic Chemistry Frontiers, 2019, 6, 3731
1555180 CIFC32 H28 N2 O6P n a 2132.9549; 12.7486; 24.5123
90; 90; 90
10298.3Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank
1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties
Organic Chemistry Frontiers, 2019, 6, 3731
1555181 CIFC24 H19 N2 O2 S2P 1 21/c 18.3103; 22.0934; 11.8386
90; 104.267; 90
2106.56Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555182 CIFC25 H18 O5P 1 21 111.6007; 5.7368; 15.0074
90; 101.62; 90
978.29Zhang, Song; Yu, Xiaojun; Pan, Jianke; Jiang, Chunhui; Zhang, Hongsu; Wang, Tianli
Asymmetric synthesis of spiro-structural 2,3-dihydrobenzofurans via the bifunctional phosphonium salt-promoted [4 + 1] cyclization of ortho-quinone methides with α-bromoketones
Organic Chemistry Frontiers, 2019, 6, 3799
1555183 CIFC48 H38 Cl2 N4 O4 S4P 21 21 2112.652; 19.153; 22.403
90; 90; 90
5428.8Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555184 CIFC16 H19 N O3P 1 21/n 111.4043; 9.8807; 25.367
90; 93.04; 90
2854.4Zhong, Jiaxin; He, Haibing; Gao, Shuanhu
Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids
Organic Chemistry Frontiers, 2019, 6, 3781
1555185 CIFC26 H37 N O8C 1 c 124.4812; 7.9863; 25.3899
90; 103.221; 90
4832.51Zhong, Jiaxin; He, Haibing; Gao, Shuanhu
Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids
Organic Chemistry Frontiers, 2019, 6, 3781
1555186 CIFC22 H29 N O5P 1 21/c 18.3885; 24.6653; 19.7148
90; 97.294; 90
4046.08Zhong, Jiaxin; He, Haibing; Gao, Shuanhu
Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids
Organic Chemistry Frontiers, 2019, 6, 3781
1555187 CIFC19 H21 Cl2 N O2 SP 21 21 216.1472; 11.724; 27.834
90; 90; 90
2006Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555188 CIFC19 H20 Cl N O2 SP 1 21 110.133; 9.753; 19.638
90; 100.289; 90
1909.6Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555189 CIFC25 H23 N O3 SP 1 21 111.1372; 8.2426; 12.2345
90; 110.187; 90
1054.13Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai
Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals
Organic Chemistry Frontiers, 2019, 6, 3725
1555190 CIFC25 H25 N O4 SC 1 2 126.476; 9.6581; 9.1391
90; 98.974; 90
2308.3Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai
Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals
Organic Chemistry Frontiers, 2019, 6, 3725
1555191 CIFC25 H23 N O3 SP 1 21 18.784; 9.976; 12.349
90; 90.656; 90
1082.1Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai
Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals
Organic Chemistry Frontiers, 2019, 6, 3725
1555192 CIFC19 H20 Cl N O2 SP 21 21 218.434; 9.511; 23.843
90; 90; 90
1913Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555193 CIFC30 H23 N3 O2 SP 1 21/c 113.65; 9.7451; 19.194
90; 105.2; 90
2463.9Vivek Kumar, Sundaravel; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam
Rh-Catalyzed C–C/C–N bond formation via C–H activation: synthesis of 2H-indazol-2-yl-benzo[a]carbazoles
Organic Chemistry Frontiers, 2019, 6, 3885
1555194 CIFC25 H19 N3 OP 21 21 217.2944; 14.078; 19.047
90; 90; 90
1955.9Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555195 CIFC31 H29 N3 O3 SP -19.8054; 11.1916; 13.8588
102.001; 100.882; 107.337
1367.85Wang, Fei; Xu, Pei; Liu, Bei-Bei; Wang, Shun-Yi; Ji, Shun-Jun
Pd-Catalyzed multicomponent reaction of sulfonyl azides, primary amines and methyl α-isocyanoacetates: highly efficient synthesis of tetrasubstituted imidazolone derivatives
Organic Chemistry Frontiers, 2019, 6, 3754
1555196 CIFC21 H19 N3 OP b c a12.7097; 15.6515; 17.3613
90; 90; 90
3453.6Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555197 CIFC22 H34 N4 O9P -19.7492; 10.793; 12.316
106.75; 97.22; 95.45
1219.3Jia, Yan-Lai; Wei, Mei-Yan; Chen, Hai-Yan; Guan, Fei-Fei; Wang, Chang-Yun; Shao, Chang-Lun
(+)- and (-)-Pestaloxazine A, a Pair of Antiviral Enantiomeric Alkaloid Dimers with a Symmetric Spiro[oxazinane-piperazinedione] Skeleton from Pestalotiopsis sp.
Organic letters, 2015, 17, 4216-4219
1555198 CIFC17 H14 N2 O2P 1 21/c 18.4028; 8.4685; 18.8231
90; 91.121; 90
1339.18Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555199 CIFC23 H18 N2 O2P n a 2128.7181; 16.094; 7.4702
90; 90; 90
3452.65Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555200 CIFC21 H16 N2 O2P b c a8.899; 16.027; 21.774
90; 90; 90
3106Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555201 CIFC35 H24 N4 O3P 1 21/c 114.7127; 13.2097; 27.114
90; 97.327; 90
5226.6Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555202 CIFC21 H16 N2 O2P b c a16.535; 8.4288; 22.1228
90; 90; 90
3083.3Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555203 CIFC28 H19 N3 O2P -18.36; 9.772; 13.225
79.646; 71.931; 81.249
1005Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555204 CIFC23 H16 Br2 N2 O2P 1 21/n 114.667; 9.231; 15.139
90; 107.187; 90
1958.2Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555205 CIFC25 H18 N2 O2P b c n18.714; 15.974; 12.0964
90; 90; 90
3616.1Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555206 CIFC26 H24 N4 O4C 1 c 19.0718; 20.806; 12.975
90; 107.07; 90
2341.1Liu, Honglei; Yuan, Chunhao; Wu, Yang; Xiao, Yumei; Guo, Hongchao
Sc(OTf)3-Catalyzed [3 + 3] Cycloaddition of Cyclopropane 1,1-Diesters with Phthalazinium Dicyanomethanides.
Organic letters, 2015, 17, 4220-4223
1555207 CIFC42 H22 F6P -19.9256; 11.9918; 12.9082
90.335; 100.557; 103.488
1466.85Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555208 CIFC42 H22 F6P b c a9.5341; 17.1742; 34.8068
90; 90; 90
5699.3Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555209 CIFC44.4 H38.4 N1.2 S1.8P 62 2 228.8585; 28.8585; 37.617
90; 90; 120
27130.8Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K.
Core-modified 48π and 42π decaphyrins: syntheses, properties and structures
Organic Chemistry Frontiers, 2019, 6, 3746
1555210 CIFC42 H34 N4 S3P -18.69725; 10.9283; 20.5323
84.0758; 88.6243; 67.6514
1795.05Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K.
Core-modified 48π and 42π decaphyrins: syntheses, properties and structures
Organic Chemistry Frontiers, 2019, 6, 3746
1555211 CIFC65 H65 Cl3 N4 O6 ZnP 4318.5406; 18.5406; 21.1268
90; 90; 90
7262.4Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555212 CIFC24 H24 O3P 1 21/c 110.0558; 10.1395; 18.5575
90; 98.819; 90
1869.77Jiao, Meng-Jie; Liu, Dan; Hu, Xiu-Qin; Xu, Peng-Fei
Photocatalytic decarboxylative [2 + 2 + 1] annulation of 1,6-enynes with N-hydroxyphthalimide esters for the synthesis of indene-containing polycyclic compounds
Organic Chemistry Frontiers, 2019, 6, 3834
1555213 CIFC70 H77 Cl1.5 N4 O5 ZnC 1 2/c 139.3331; 14.7758; 28.6914
90; 131.696; 90
12450.8Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555214 CIFC67 H71 N4 O5 ZnP -116.9996; 24.3355; 32.7331
89.3681; 83.194; 89.522
13444.9Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555215 CIFC26 H22 Br F3 N4 O4P 1 21/c 19.2204; 24.665; 11.584
90; 105.11; 90
2543.4Zhao, Hong-Wu; Guo, Jia-Ming; Wang, Li-Ru; Ding, Wan-Qiu; Tang, Zhe; Song, Xiu-Qing; Wu, Hui-Hui; Fan, Xiao-Zu; Bi, Xiao-Fan
Diastereoselective formal [3 + 3] cycloaddition of isatin-based α-(trifluoromethyl)imines with N,N′-dialkyloxyureas
Organic Chemistry Frontiers, 2019, 6, 3891
1555216 CIFC14 H11 N3C 1 2/c 114.857; 12.127; 13.289
90; 106.898; 90
2290.9Jia, Feng-Cheng; Zhou, Zhi-Wen; Xu, Cheng; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Expeditious Synthesis of 2-Phenylquinazolin-4-amines via a Fe/Cu Relay-Catalyzed Domino Strategy.
Organic letters, 2015, 17, 4236-4239
1555217 CIFC63.25 H86 Na5 O29.95 S5P -112.15; 12.226; 26.113
99.044; 97.039; 99.079
3739.3Pisagatti, Ilenia; Barbera, Lucia; Gattuso, Giuseppe; Parisi, Melchiorre F.; Geremia, Silvano; Hickey, Neal; Notti, Anna
Guest-length driven high fidelity self-sorting in supramolecular capsule formation of calix[5]arenes in water
Organic Chemistry Frontiers, 2019, 6, 3804
1555218 CIFC33 H23 Cl3 N2 O2P 1 21 19.07268; 11.9732; 13.4535
90; 106.945; 90
1397.99Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555219 CIFC32.5 H26 N2 O3.5P 21 21 211.4574; 24.0028; 9.1294
90; 90; 90
2510.67Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555220 CIFC34 H24 O2P 21 21 211.1679; 24.1852; 9.1499
90; 90; 90
2471.37Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555221 CIFC32 H22.67 N2 O2.33P 21 21 2110.41941; 18.297; 36.8632
90; 90; 90
7027.75Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555222 CIFC32 H22 N2 O2P 21 21 217.9491; 16.7592; 18.1848
90; 90; 90
2422.6Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555223 CIFC245 H138 Cl10 F24 N8 O32 S8P -116.057; 18.336; 18.879
79.909; 74.398; 79.264
5214Węcławski, Marek K; Meiling, Till T.; Leniak, Arkadiusz; Cywiński, Piotr J; Gryko, Daniel T.
Planar, Fluorescent Push-Pull System That Comprises Benzofuran and Iminocoumarin Moieties.
Organic letters, 2015, 17, 4252-4255
1555224 CIFC41 H36 N2 O9P 1 21/c 119.0503; 11.68507; 14.8134
90; 92.939; 90
3293.19Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555225 CIFC40 H32 N2 O9P b c a13.9815; 16.6793; 26.5582
90; 90; 90
6193.4Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555226 CIFC28 H24 N2 O3 SP 21 21 218.9629; 14.1297; 18.6198
90; 90; 90
2358.1Wang, Linqing; Yang, Dongxu; Li, Dan; Liu, Xihong; Zhao, Qian; Zhu, Ranran; Zhang, Bangzhi; Wang, Rui
Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst.
Organic letters, 2015, 17, 4260-4263
1555227 CIFC24 H25 F3 I N O4 SP 1 21/c 113.4658; 20.2837; 19.439
90; 100.921; 90
5213.3Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555228 CIFC6 H13 N O3P 418.8749; 8.8749; 20.4808
90; 90; 90
1613.1Chung, Ryan; Hein, Jason E.
Automated solubility and crystallization analysis of non-UV active compounds: integration of evaporative light scattering detection (ELSD) and robotic sampling
Reaction Chemistry & Engineering, 2019, 4, 1674
1555229 CIFC24 H26 F2 I N O4 SP 1 21/n 112.121; 15.7186; 25.7853
90; 91.321; 90
4911.4Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555230 CIFC23 H25 F2 I N2 O4 SP n a 2124.1416; 10.1959; 20.5376
90; 90; 90
5055.2Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555231 CIFC16 H26 O6P 1 21 16.5502; 13.639; 9.1291
90; 91.21; 90
815.4Hwang, In Hyun; Swenson, Dale C.; Gloer, James B.; Wicklow, Donald T.
Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp.
Organic letters, 2015, 17, 4284-4287
1555232 CIFC19 H21 Br Cl N O2P 1 21 19.5181; 11.3448; 18.2344
90; 105.143; 90
1900.6Monasterolo, Claudio; Müller-Bunz, Helge; Gilheany, Declan G.
Very short highly enantioselective Grignard synthesis of 2,2-disubstituted tetrahydrofurans and tetrahydropyrans.
Chemical science, 2019, 10, 6531-6538
1555233 CIFC22 H36 O6 SiP 1 21 16.395; 46.881; 8.2621
90; 111.164; 90
2309.9Clark, J. Stephen; Romiti, Filippo; Sieng, Bora; Paterson, Laura C.; Stewart, Alister; Chaudhury, Subhabrata; Thomas, Lynne H.
Synthesis of the A-D Ring System of the Gambieric Acids.
Organic letters, 2015, 17, 4694-4697
1555234 CIFC31 H30 F3 Ir N6P -114.228; 15.407; 16.166
86.526; 65.199; 85.672
3206Na, Hanah; Cañada, Louise M; Wen, Zhili; I-Chia Wu, Judy; Teets, Thomas S.
Mixed-carbene cyclometalated iridium complexes with saturated blue luminescence.
Chemical science, 2019, 10, 6254-6260
1555235 CIFC39 H34 F3 Ir N6C 1 2/c 127.27; 20.718; 14.832
90; 116.007; 90
7531Na, Hanah; Cañada, Louise M; Wen, Zhili; I-Chia Wu, Judy; Teets, Thomas S.
Mixed-carbene cyclometalated iridium complexes with saturated blue luminescence.
Chemical science, 2019, 10, 6254-6260
1555236 CIFC14 H17 F O2P 21 21 215.8616; 11.0435; 18.6965
90; 90; 90
1210.27Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555237 CIFC23 H23 F N2 O6P -17.9045; 11.1779; 11.7527
91.21; 92.807; 94
1034.33Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555238 CIFC26 H54 N2 O2 Zn2P 42/n :212.3523; 12.3523; 19.4557
90; 90; 90
2968.54Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz
Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO.
Chemical science, 2019, 10, 7149-7155
1555239 CIFC30 H46 N2 O2 Zn2P 1 21/c 19.4169; 30.0759; 10.6586
90; 106.582; 90
2893.2Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz
Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO.
Chemical science, 2019, 10, 7149-7155
1555240 CIFC30 H46 N2 O2 ZnP 1 21/c 110.525; 22.503; 12.296
90; 95.834; 90
2897.15Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz
Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO.
Chemical science, 2019, 10, 7149-7155
1555241 CIFC76 H48 O4C 2 2 219.5716; 40.233; 14.5609
90; 90; 90
5607.3Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555242 CIFC26 H18 O2C 2 2 219.6233; 28.1324; 14.4388
90; 90; 90
3908.97Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555243 CIFC26 H18 Br2 O2C 2 2 219.5385; 16.362; 14.106
90; 90; 90
2201.5Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555244 CIFC76 H78 O16 S4P 43 21 213.3557; 13.3557; 44.138
90; 90; 90
7873.1Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555245 CIFC21 H19 Cl O3P 1 21/c 120.4519; 8.3981; 29.0733
90; 133.17; 90
3641.9Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555246 CIFC21 H19 Br O3P 1 21/c 19.2815; 26.184; 8.2635
90; 114.173; 90
1832.2Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555247 CIFC21 H19 F O3P 1 21/n 18.0324; 10.4173; 21.4761
90; 98.076; 90
1779.2Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555248 CIFC18 H12 O2P 1 21/c 111.0083; 17.6321; 6.9894
90; 98.387; 90
1342.1Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555249 CIFC40 H34 Br N3 O3P 21 21 2112.8306; 13.8096; 19.054
90; 90; 90
3376.1Jing, Changcheng; Xing, Dong; Hu, Wenhao
Catalytic Asymmetric Four-Component Reaction for the Rapid Construction of 3,3-Disubstituted 3-Indol-3'-yloxindoles.
Organic letters, 2015, 17, 4336-4339
1555250 CIFC19 H18 O2P -18.2948; 9.5359; 10.0158
75.291; 74.899; 86.594
739.79Lu, Qingquan; Mondal, Shobhan; Cembellín, Sara; Greßies, Steffen; Glorius, Frank
Site-selective C-H activation and regiospecific annulation using propargylic carbonates.
Chemical science, 2019, 10, 6560-6564
1555251 CIFC18 H16 O SP 1 21/n 15.3543; 15.615; 17.226
90; 93.57; 90
1437.4Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555252 CIFC17 H15 Co0.5 O3P 1 21/n 19.6119; 16.0078; 12.0749
90; 94.068; 90
1853.23Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Shaw, Bikash Kumar; Vaidya, Shefali; Pariyar, Anand; Vijaykumar, Gonela; Adhikari, Debashis; Mandal, Swadhin K.
Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction.
Chemical science, 2019, 10, 7433-7441
1555253 CIFC13 H8.64 O2P c c n7.379; 14.8543; 16.8845
90; 90; 90
1850.7Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Shaw, Bikash Kumar; Vaidya, Shefali; Pariyar, Anand; Vijaykumar, Gonela; Adhikari, Debashis; Mandal, Swadhin K.
Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction.
Chemical science, 2019, 10, 7433-7441
1555254 CIFC24 H16 O SP 1 21/c 19.1038; 11.532; 16.523
90; 101.54; 90
1699.6Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555255 CIFC12 H14 B2 F8 Fe N6 O2C m c e7.243; 12.882; 23.908
90; 90; 90
2230.7Resines-Urien, Esther; Burzurí, Enrique; Fernandez-Bartolome, Estefania; García García-Tuñón, Miguel Ángel; de la Presa, Patricia; Poloni, Roberta; Teat, Simon J.; Costa, Jose Sanchez
A switchable iron-based coordination polymer toward reversible acetonitrile electro-optical readout.
Chemical science, 2019, 10, 6612-6616
1555256 CIFC21 H30 O4 SiP 1 21/c 115.86; 8.9849; 32.138
90; 117.571; 90
4059.6Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555257 CIFC20 H28 O3 SiC 1 2/c 134.403; 6.7764; 16.1333
90; 92.333; 90
3758Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555258 CIFC9 H5 Cl2 N3 SP b c a6.9189; 13.8264; 21.5767
90; 90; 90
2064.1Kalogirou, Andreas S.; Manoli, Maria; Koutentis, Panayiotis A.
Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine.
Organic letters, 2015, 17, 4118-4121
1555259 CIFC14 H20 O16.75P n -3 :211.4074; 11.4074; 11.4074
90; 90; 90
1484.43Cui, Peng; McMahon, David P.; Spackman, Peter R.; Alston, Ben M.; Little, Marc A.; Day, Graeme M.; Cooper, Andrew I.
Mining predicted crystal structure landscapes with high throughput crystallisation: old molecules, new insights
Chemical Science, 2019, 10, 9988
1555260 CIFC15 H18 O8.25I 41/a :216.4008; 16.4008; 22.397
90; 90; 90
6024.5Cui, Peng; McMahon, David P.; Spackman, Peter R.; Alston, Ben M.; Little, Marc A.; Day, Graeme M.; Cooper, Andrew I.
Mining predicted crystal structure landscapes with high throughput crystallisation: old molecules, new insights
Chemical Science, 2019, 10, 9988

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 528 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!