Crystallography Open Database

Result: there are 332 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 | archive of CIF files (ZIP)

Searching journal of publication like 'Organic Chemistry Frontiers' volume of publication is 5

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 4 | Next 100 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
1553969 CIFC23 H19 F O2P -18.9683; 9.8217; 11.353
75.074; 77.458; 63.345
857.59Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa
A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines
Organic Chemistry Frontiers, 2018, 5, 1160
1553970 CIFC64 H100 N4 Na4 O46C 1 2/c 129.1539; 14.0671; 24.2333
90; 126.156; 90
8024.4Zhang, Yao; Yu, Shang-Bo; Yang, Bo; Wang, Hui; Zhang, Dan-Wei; Li, Zhan-Ting
Ion-pair electrostatic attraction-enhanced donor‒acceptor interactions between the prototypic 1,4-dialkoxybenzene-viologen binding mode in water
Organic Chemistry Frontiers, 2018, 5, 1039
1553971 CIFC10 H9 Br F N O4 SP 1 21/n 18.7382; 5.8569; 23.8346
90; 91.141; 90
1219.58Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li
Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C–H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams
Organic Chemistry Frontiers, 2018, 5, 1411
1553972 CIFC15 H11 F O5 SP 1 21/n 18.6492; 6.7929; 25.645
90; 98.112; 90
1491.6Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li
Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C–H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams
Organic Chemistry Frontiers, 2018, 5, 1411
1553973 CIFC12 H10 Br N OP 1 21/c 112.062; 4.0452; 21.707
90; 90.12; 90
1059.2Reddy, Ganapam Manohar; Rao, Naidu Sambasiva; Maheswaran, H.
Highly meta-selective halogenation of 2-phenylpyridine with a ruthenium(i) catalyst
Organic Chemistry Frontiers, 2018, 5, 1118
1553974 CIFC24 H25 Cl2 N OP 21 21 218.799; 14.7395; 16.0279
90; 90; 90
2078.7Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
Organic Chemistry Frontiers, 2018, 5, 1366
1553975 CIFC22 H23 N O SP 21 21 215.6782; 8.5568; 38.5091
90; 90; 90
1871.05Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
Organic Chemistry Frontiers, 2018, 5, 1366
1553976 CIFC21 H20 N4 O4P 1 21/c 110.5329; 10.3187; 18.4305
90; 97.847; 90
1984.4Cao, Wen-Bin; Liu, Bei-Bei; Xu, Xiao-Ping; Ji, Shun-Jun
Cooperation of copper and dioxygen for the site-selective construction of benzo[1,5]diazocin-6(5H)-ones from indoles and enaminone analogues
Organic Chemistry Frontiers, 2018, 5, 1194
1553977 CIFC34 H28 N O6 P SP 21 21 2111.9446; 13.7058; 19.238
90; 90; 90
3149.5Gu, Zheng; Zhou, Ji; Jiang, Guo-Fang; Zhou, Yong-Gui
Synthesis of chiral γ-aminophosphonates through the organocatalytic hydrophosphonylation of azadienes with phosphites
Organic Chemistry Frontiers, 2018, 5, 1148
1553978 CIFC18 H18 O2P 21 21 217.9384; 9.9744; 17.126
90; 90; 90
1356Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1553979 CIFC18 H18 O3P 1 21/c 112.6396; 9.6186; 11.8318
90; 103.394; 90
1399.33Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1553980 CIFC14 H15 N O4P 1 21/c 113.13; 12.87; 7.8
90; 105.51; 90
1270Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1554253 CIFC25 H21 Br F3 N3 O4 SP 21 21 218.8119; 10.4134; 27.1396
90; 90; 90
2490.38Zhu, Wen-Run; Chen, Qing; Lin, Ning; Chen, Kai-Bin; Zhang, Zhen-Wei; Fang, Gang; Weng, Jiang; Lu, Gui
Organocatalytic Michael/cyclization cascade reactions of 3-isothiocyanato oxindoles with 3-trifluoroethylidene oxindoles: an approach for the synthesis of 3′-trifluoromethyl substituted 3,2′-pyrrolidinyl-bispirooxindoles
Organic Chemistry Frontiers, 2018, 5, 1375
1554254 CIFC28 H36 O8P 113.986; 14.019; 28.0285
98.119; 91.053; 90.157
5439.5Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua
Asperones A‒E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1‒15
Organic Chemistry Frontiers, 2018, 5, 2432
1554255 CIFC28 H38 O9P 21 21 218.3949; 15.0525; 22.267
90; 90; 90
2813.8Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua
Asperones A–E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1–15
Organic Chemistry Frontiers, 2018, 5, 2432
1554256 CIFC37 H42 O11P 21 21 219.34542; 14.58845; 24.65138
90; 90; 90
3360.85Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin
Lithocarpins A–D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508
Organic Chemistry Frontiers, 2018, 5, 1792
1554257 CIFC38 H43 Cl3 O11P 1 21 112.0999; 8.9388; 17.0397
90; 90.378; 90
1842.95Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin
Lithocarpins A–D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508
Organic Chemistry Frontiers, 2018, 5, 1792
1554258 CIFC21 H28 O4P 1 21 18.8203; 9.95; 11.3663
90; 104.882; 90
964.07Hu, Li-Jun; Cheng, Min-Jing; Cao, Jia-Qing; Zhong, Li-Ping; Hu, Ya-Jian; Wang, Ying; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Asymmetric total syntheses of callistrilones B, G and J
Organic Chemistry Frontiers, 2018, 5, 1506
1554259 CIFC27 H26 O5P -19.56; 10.76; 11.542
89.84; 78.84; 80.4
1148Ivanov, 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
1554260 CIFC11 H13 N O2P b c a5.565; 17.417; 19.97
90; 90; 90
1935.6Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554261 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

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 4 | Next 100 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!