Crystallography Open Database

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1542545 CIFC14 H3.5 F10.5 N7P 41 3 215.8427; 15.8427; 15.8427
90; 90; 90
3976.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542546 CIFC32 H50 Cu Na O8 S2P 1 21/c 110.5883; 21.967; 14.4286
90; 95.682; 90
3339.5Johnson, Miles W.; Hannoun, Kareem I.; Tan, Yichen; Fu, Gregory C.; Peters, Jonas C.
A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide.
Chemical science, 2016, 7, 4091-4100
1542547 CIFC18 H16 B2 F8 N4P -17.547; 7.886; 8.992
66.005; 85.305; 83.508
485.4Leblanc, Nicolas; Sproules, Stephen; Fink, Karin; Sanguinet, Lionel; Alévêque, Olivier; Levillain, Eric; Rosa, Patrick; Powell, Annie K.
A fascinating multifaceted redox-active chelating ligand: introducing the N,N′-dimethyl-3,3′-biquinoxalinium “methylbiquinoxen” platform
Chem. Sci., 2016, 7, 3820
1542548 CIFC18 H17 B F4 N4P 1 21/n 17.133; 20.036; 11.526
90; 99.454; 90
1624.9Leblanc, Nicolas; Sproules, Stephen; Fink, Karin; Sanguinet, Lionel; Alévêque, Olivier; Levillain, Eric; Rosa, Patrick; Powell, Annie K.
A fascinating multifaceted redox-active chelating ligand: introducing the N,N′-dimethyl-3,3′-biquinoxalinium “methylbiquinoxen” platform
Chem. Sci., 2016, 7, 3820
1542549 CIFC18 H16 Cd Cl2 N4P -17.4683; 10.4739; 11.3249
80.15; 82.274; 81.982
858.7Leblanc, Nicolas; Sproules, Stephen; Fink, Karin; Sanguinet, Lionel; Alévêque, Olivier; Levillain, Eric; Rosa, Patrick; Powell, Annie K.
A fascinating multifaceted redox-active chelating ligand: introducing the N,N′-dimethyl-3,3′-biquinoxalinium “methylbiquinoxen” platform
Chem. Sci., 2016, 7, 3820
1542550 CIFC40 H44 Fe N6 O6P 1 21/c 112.5879; 20.8699; 13.6448
90; 93.531; 90
3577.8Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542551 CIFC44 H38 Cl6 N6 O6P -110.1932; 12.318; 19.654
72.773; 77.793; 81.49
2294.1Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542552 CIFC62.5 H99 Cl N6 O11 P2P 1 21/n 119.5077; 15.3419; 22.1726
90; 95.401; 90
6606.47Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542553 CIFC46.5 H64.5 Cl1.5 N5 O8 PP -19.9599; 14.6932; 16.4802
81.05; 75.273; 88.017
2304.1Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542554 CIFC119 H151 Cl9 N14 O20 P2P -116.0755; 18.9299; 24.4976
93.415; 96.103; 111.261
6869.2Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542555 CIFC69 H62.5 Cl6 I6 N12 Zn3C 1 2/c 135.7365; 15.061; 30.9345
90; 104.141; 90
16145.3Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto
Structure determination of microbial metabolites by the crystalline sponge method
Chem. Sci., 2016, 7, 3910
1542556 CIFC132.77 H131.15 I12 N24 O15.14 Zn6C 1 2 136.3783; 14.6755; 31.2278
90; 103.184; 90
16232.2Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto
Structure determination of microbial metabolites by the crystalline sponge method
Chem. Sci., 2016, 7, 3910
1542557 CIFC134.29 H138.92 I12 N24 O8.41 Zn6C 1 2 134.7707; 14.8406; 31.2152
90; 102.601; 90
15719.6Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto
Structure determination of microbial metabolites by the crystalline sponge method
Chem. Sci., 2016, 7, 3910
1542558 CIFC68 H74 N Ni O3 P3 S3 Si3P b c a27.4702; 17.1432; 27.9778
90; 90; 90
13175.5Chiou, Tzung-Wen; Tseng, Yen-Ming; Lu, Tsai-Te; Weng, Tsu-Chien; Sokaras, Dimosthenes; Ho, Wei-Chieh; Kuo, Ting-Shen; Jang, Ling-Yun; Lee, Jyh-Fu; Liaw, Wen-Feng
[NiIII(OMe)]-mediated reductive activation of CO2affording a Ni(κ1-OCO) complex
Chem. Sci., 2016, 7, 3640
1542559 CIFC68 H74 N2 Ni O2 P3 S3 Si3P b c a27.5733; 17.0409; 27.8585
90; 90; 90
13090Chiou, Tzung-Wen; Tseng, Yen-Ming; Lu, Tsai-Te; Weng, Tsu-Chien; Sokaras, Dimosthenes; Ho, Wei-Chieh; Kuo, Ting-Shen; Jang, Ling-Yun; Lee, Jyh-Fu; Liaw, Wen-Feng
[NiIII(OMe)]-mediated reductive activation of CO2affording a Ni(κ1-OCO) complex
Chem. Sci., 2016, 7, 3640
1542560 CIFC67 H78 N3 Ni O P3 S3 Si3P 1 21/n 114.316; 26.0756; 18.0992
90; 97.069; 90
6705Chiou, Tzung-Wen; Tseng, Yen-Ming; Lu, Tsai-Te; Weng, Tsu-Chien; Sokaras, Dimosthenes; Ho, Wei-Chieh; Kuo, Ting-Shen; Jang, Ling-Yun; Lee, Jyh-Fu; Liaw, Wen-Feng
[NiIII(OMe)]-mediated reductive activation of CO2affording a Ni(κ1-OCO) complex
Chem. Sci., 2016, 7, 3640
1542561 CIFC50 H68 O4P -19.1934; 13.5122; 18.2252
76.83; 75.995; 86.625
2138.9Wang, Can; Xu, Bingjia; Li, Mengshu; Chi, Zhenguo; Xie, Yujun; Li, Qianqian; Li, Zhen
A stable tetraphenylethene derivative: aggregation-induced emission, different crystalline polymorphs, and totally different mechanoluminescence properties
Mater. Horiz., 2016, 3, 220
1542562 CIFC17 H21.3 N O4.15P 21 21 219.7421; 9.7391; 16.0471
90; 90; 90
1522.54Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542563 CIFC16 H22 N O4.5P 21 21 218.0372; 15.6818; 22.5648
90; 90; 90
2844.02Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542564 CIFC23 H30.01 N2 O4P 1 21 19.4965; 11.4906; 9.9133
90; 95.247; 90
1077.21Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542565 CIFC23 H30 N2 O4P 1 21 19.6195; 11.6392; 9.6441
90; 94.229; 90
1076.85Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542566 CIFC18 H27 N O5P 21 21 217.9947; 8.6002; 24.7362
90; 90; 90
1700.76Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542567 CIFC21 H17 N3 OC 1 2/c 117.9422; 9.9101; 19.1301
90; 99.879; 90
3351.1Chen, Zhengkai; Li, Hongli; Dong, Weipeng; Miao, Maozhong; Ren, Hongjun
I2-Catalyzed Oxidative Coupling Reactions of Hydrazones and Amines and the Application in the Synthesis of 1,3,5-Trisubstituted 1,2,4-Triazoles.
Organic letters, 2016, 18, 1334-1337
1542568 CIFC38 H30 N4 S3P b c n29.6046; 11.8388; 17.1781
90; 90; 90
6020.6Zhang, Jing; Gu, Peiyang; Long, Guankui; Ganguly, Rakesh; Li, Yongxin; Aratani, Naoki; Yamada, Hiroko; Zhang, Qichun
Switching charge-transfer characteristics from p-type to n-type through molecular “doping” (co-crystallization)
Chem. Sci., 2016, 7, 3851
1542569 CIFC88 H64 N12 S6P -110.6919; 11.6399; 14.4791
90.178; 104.4; 95.311
1737.22Zhang, Jing; Gu, Peiyang; Long, Guankui; Ganguly, Rakesh; Li, Yongxin; Aratani, Naoki; Yamada, Hiroko; Zhang, Qichun
Switching charge-transfer characteristics from p-type to n-type through molecular “doping” (co-crystallization)
Chem. Sci., 2016, 7, 3851
1542570 CIFC13 H10 Cl N O2P 17.02512; 8.17982; 10.0807
104.135; 104.019; 91.6954
542.58Sanchez-Diez, Eduardo; Vesga, Diana L.; Reyes, Efraim; Uria, Uxue; Carrillo, Luisa; Vicario, Jose L.
Organocatalytically Generated Donor-Acceptor Cyclopropanes in Domino Reactions. One-Step Enantioselective Synthesis of Pyrrolo[1,2-a]quinolines.
Organic letters, 2016, 18, 1270-1273
1542571 CIFC8 H11 N O4 SP -16.4922; 8.38; 9.896
74.212; 73.241; 80.346
493.74Mommer, Stefan; Truong, Khai-Nghi; Keul, Helmut; Möller, Martin
An epoxy thiolactone on stage: four component reactions, synthesis of poly(thioether urethane)s and the respective hydrogels
Polym. Chem., 2016, 7, 2291
1542572 CIFC23 H18 O3P 1 c 15.82646; 9.44106; 15.616
90; 100.11; 90
845.67Han, Ting; Deng, Haiqin; Yu, Chris Y. Y.; Gui, Chen; Song, Zhegang; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Tang, Ben Zhong
Functional isocoumarin-containing polymers synthesized by rhodium-catalyzed oxidative polycoupling of aryl diacid and internal diyne
Polym. Chem., 2016, 7, 2501
1542573 CIFC26 H19 N3 O2P 1 21/c 110.0072; 23.043; 9.4047
90; 110.772; 90
2027.7Cai, Qun; Li, Deng-Kui; Zhou, Rong-Rong; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Catalyzed Multicomponent Tandem Cyclizations: Access to Polyfunctional Dihydroindolizino[8,7-b]indoles.
Organic letters, 2016, 18, 1342-1345
1542574 CIFC28 H22 Cl3 N3 O3P 1 21/c 112.2576; 19.07; 11.4688
90; 97.837; 90
2655.8Cai, Qun; Li, Deng-Kui; Zhou, Rong-Rong; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Catalyzed Multicomponent Tandem Cyclizations: Access to Polyfunctional Dihydroindolizino[8,7-b]indoles.
Organic letters, 2016, 18, 1342-1345
1542575 CIFC21 H15 Br N4P b c a13.3161; 7.7509; 33.992
90; 90; 90
3508.4Cai, Qun; Li, Deng-Kui; Zhou, Rong-Rong; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Catalyzed Multicomponent Tandem Cyclizations: Access to Polyfunctional Dihydroindolizino[8,7-b]indoles.
Organic letters, 2016, 18, 1342-1345
1542576 CIFC14 H16 O4P 21 21 217.2935; 8.8494; 19.329
90; 90; 90
1247.55Sun, Wang-Bin; Wang, Xuan; Sun, Bing-Feng; Zou, Jian-Ping; Lin, Guo-Qiang
Catalytic Asymmetric Total Synthesis of Hedyosumins A, B, and C.
Organic letters, 2016, 18, 1219-1221
1542577 CIFC14 H16 O4P 21 21 215.5435; 7.7426; 27.879
90; 90; 90
1196.6Sun, Wang-Bin; Wang, Xuan; Sun, Bing-Feng; Zou, Jian-Ping; Lin, Guo-Qiang
Catalytic Asymmetric Total Synthesis of Hedyosumins A, B, and C.
Organic letters, 2016, 18, 1219-1221
1542578 CIFC16 H11 F3 Mo O3P -17.1145; 7.6417; 15.3159
93.275; 97.569; 113.744
749.96Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542579 CIFC16 H11 F3 Mo O3P 1 21/c 17.2471; 31.8822; 6.7406
90; 104.266; 90
1509.41Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542580 CIFC16 H11 F3 Mo O3P 1 21/c 18.9791; 12.3295; 13.7453
90; 100.651; 90
1495.49Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542581 CIFC17 H10 F6 Mo O3P -18.4202; 10.2245; 10.5319
101.377; 102.663; 103.044
832.29Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542582 CIFC32 H33 N3 Ni O3P 1 21 111.0798; 21.9977; 11.88015
90; 102.003; 90
2832.25Miles, Jennifer A.; Yeo, David J.; Rowell, Philip; Rodriguez-Marin, Silvia; Pask, Christopher M.; Warriner, Stuart L.; Edwards, Thomas A.; Wilson, Andrew J.
Hydrocarbon constrained peptides ‒ understanding preorganisation and binding affinity
Chem. Sci., 2016, 7, 3694
1542583 CIFC16 H11 Fe3 N O7 S2P -17.7263; 11.203; 11.9
94.504; 108.019; 93.687
972.2Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542584 CIFC40 H35 Fe3 N O5 P2 S2P -111.3103; 12.9416; 15.479
105.449; 100.216; 110.921
1944.2Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542585 CIFC20.2 H22.23 B F4 Fe3 N4.6 O6.72 S2P -110.4593; 11.6085; 12.256
76.988; 85.341; 81.75
1433.02Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542586 CIFC80 H75 B F24 Fe3 N O4 P4 S2P -113.352; 13.623; 24.074
92.828; 94.41; 99.584
4296Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542587 CIFC25 H23 N5 O8P -17.856; 11.799; 14.315
66.98; 77.401; 74.377
1166.6Biswas, Arnab; Dubey, Mrigendra; Mukhopadhyay, Sujay; Kumar, Ashish; Pandey, Daya Shankar
Anion triggered metallogels: demetalation and crystal growth inside the gel matrix and improvement in viscoelastic properties using Au-NPs.
Soft matter, 2016, 12, 2997-3003
1542589 CIFC25 H25 N OP 1 21/c 111.1357; 10.6585; 17.1362
90; 90.608; 90
2033.8Wang, Nan-Nan; Huang, Lei-Rong; Hao, Wen-Juan; Zhang, Tian-Shu; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Synergistic Rhodium/Copper Catalysis: Synthesis of 1,3-Enynes and N-Aryl Enaminones.
Organic letters, 2016, 18, 1298-1301
1542590 CIFC26 H21 Cl OP 1 21 113.2144; 5.6194; 14.8801
90; 111.914; 90
1025.11Wang, Nan-Nan; Huang, Lei-Rong; Hao, Wen-Juan; Zhang, Tian-Shu; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Synergistic Rhodium/Copper Catalysis: Synthesis of 1,3-Enynes and N-Aryl Enaminones.
Organic letters, 2016, 18, 1298-1301
1542591 CIFC79.27 H80.86 N5.59 ZnP -110.0013; 14.5831; 24.366
75.428; 87.017; 71.26
3255.5Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542592 CIFC64.5 H68 Cl7.5 N5 Ni O2P b c n11.0983; 34.992; 32.965
90; 90; 90
12802Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542593 CIFC69 H77 N5 Ni O2P -114.734; 20.554; 20.788
90.073; 103.209; 109.518
5756Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542594 CIFC74 H77 N4 Ni O PP 1 21/n 112.3714; 28.233; 41.36
90; 96.168; 90
14363Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542595 CIFC44 H36 Br N O P2 PdP -111.12; 12.074; 15.487
69.218; 72.309; 70.811
1794.3Wu, Jiang; Liu, Yafei; Lu, Changhui; Shen, Qilong
Palladium-catalyzed difluoromethylthiolation of heteroaryl bromides, iodides, triflates and aryl iodides
Chem. Sci., 2016, 7, 3757
1542596 CIFC18 H27 Cl N2 O12 SP 1 21 17.2371; 9.8802; 15.9674
90; 97.002; 90
1133.2Liang, Yong; Suzol, Sazzad H.; Wen, Zhiwei; Artiles, Alain G.; Mathivathanan, Logesh; Raptis, Raphael G.; Wnuk, Stanislaw F.
Uracil Nucleosides with Reactive Group at C5 Position: 5-(1-Halo-2-sulfonylvinyl)uridine Analogues.
Organic letters, 2016, 18, 1418-1421
1542597 CIFC23 H24 N2 O4 S2P 1 21/n 18.2793; 22.107; 12.8092
90; 105.304; 90
2261.3Liang, Yong; Suzol, Sazzad H.; Wen, Zhiwei; Artiles, Alain G.; Mathivathanan, Logesh; Raptis, Raphael G.; Wnuk, Stanislaw F.
Uracil Nucleosides with Reactive Group at C5 Position: 5-(1-Halo-2-sulfonylvinyl)uridine Analogues.
Organic letters, 2016, 18, 1418-1421
1542598 CIFC41 H32 N2 OP 1 21/c 117.751; 6.9635; 26.097
90; 107.904; 90
3069.6Jiang, Pingping; Xu, Yongbao; Sun, Fuxing; Liu, Xufei; Li, Feng; Yu, Renfu; Li, Yang; Wang, Qifeng
Pd(II)-Catalyzed ortho-C-H Olefination/Dearomatization of N-Aryl Ureas: An Approach to Imine Derivatives.
Organic letters, 2016, 18, 1426-1429
1542599 CIFC37 H30 N2 OP 1 21/n 120.5458; 14.0737; 20.9813
90; 108.671; 90
5747.6Jiang, Pingping; Xu, Yongbao; Sun, Fuxing; Liu, Xufei; Li, Feng; Yu, Renfu; Li, Yang; Wang, Qifeng
Pd(II)-Catalyzed ortho-C-H Olefination/Dearomatization of N-Aryl Ureas: An Approach to Imine Derivatives.
Organic letters, 2016, 18, 1426-1429
1542600 CIFC41 H32 N2 OP 1 21/c 119.0371; 9.7457; 18.7726
90; 114.993; 90
3156.7Jiang, Pingping; Xu, Yongbao; Sun, Fuxing; Liu, Xufei; Li, Feng; Yu, Renfu; Li, Yang; Wang, Qifeng
Pd(II)-Catalyzed ortho-C-H Olefination/Dearomatization of N-Aryl Ureas: An Approach to Imine Derivatives.
Organic letters, 2016, 18, 1426-1429
1542601 CIF
HKL
Paper
C14 H8 Cl F3 N2 OP -16.4998; 7.4286; 14.8289
84.859; 86.707; 83.313
707.47Maheswari, R.; Manjula, J.; Gunasekaran, B.
(<i>E</i>)-4-Chloro-<i>N</i>'-(2,4,5-trifluorobenzylidene)benzohydrazide
IUCrData, 2016, 1, x160304
1542602 CIF
HKL
Paper
C12 H11 F3 N2 O3P 1 21/c 19.9339; 10.6614; 12.6802
90; 105.863; 90
1291.8Avezov, Kuvondik G.; Umarov, Bako B.; Talipov, Samat A.; Kunafiev, Rishad J.; Ibragimov, Bakhtiyar T.
(5-Hydroxy-3-methyl-5-trifluoromethyl-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)(2-hydroxyphenyl)methanone
IUCrData, 2016, 1, x160316
1542603 CIFC13 H9 N5 O2P 1 21/c 13.8512; 19.078; 21.23
90; 91.015; 90
1559.6Kaloo, Masood Ayoub; Sunder Raman, Ramya; Sankar, Jeyaraman
Novel structurally tuned DAMN receptor for "in situ" diagnosis of bicarbonate in environmental waters.
The Analyst, 2016, 141, 2367-2370
1542604 CIFC14 H23 O5 RhP 1 21/n 17.2023; 13.3209; 16.1663
90; 93.426; 90
1548.24Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542605 CIFC20 H24 Cl4 F6 Rh2R -328.1638; 28.1638; 8.1635
90; 90; 120
5607.8Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542606 CIFC24 H38 Cl4 Rh2P -18.2993; 8.9088; 9.3961
102.335; 106.607; 94.5603
643Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542607 CIFC10 H5 I O2P -17.7536; 8.2731; 14.2858
73.2168; 78.223; 85.339
858.63Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542608 CIFC11 H7 I O3P 1 21/c 18.1168; 7.9198; 15.1553
90; 93.0671; 90
972.84Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542609 CIFC12 H9 I O3P 1 21/c 117.2465; 16.7627; 7.5137
90; 91.9216; 90
2170.97Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542610 CIFC10 H4 I N O4P 1 21/c 17.7794; 9.0897; 13.9834
90; 99.5625; 90
975.06Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542611 CIFC10 H4 Br I O2P 21 21 215.0752; 6.1752; 30.9217
90; 90; 90
969.1Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542612 CIFC10 H3 Br2 I O2P -17.1805; 8.2069; 10.2503
67.006; 88.761; 69.374
515.67Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542613 CIFC10 H5 I O2P 1 21/c 114.1706; 4.1298; 15.9165
90; 106.661; 90
892.36Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542614 CIFC10 H4 I2 O2P 1 21/n 113.9652; 4.4527; 16.4351
90; 102.327; 90
998.42Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542615 CIFC10 H5 Br O2P 1 21/c 17.7808; 8.1027; 12.8379
90; 94.413; 90
806.97Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542616 CIFC57 H38 Cl3P 1 21/c 19.65924; 9.12014; 50.6162
90; 91.6555; 90
4457.1Zhang, Yun; Zhao, Engui; Deng, Haiqin; Lam, Jacky W. Y.; Tang, Ben Zhong
Development of a transition metal-free polymerization route to functional conjugated polydiynes from a haloalkyne-based organic reaction
Polym. Chem., 2016, 7, 2492
1542617 CIFC9 H10 N3 O5C 1 2 115.791; 5.0056; 16.133
90; 122.52; 90
1075.3Dixit, Manish Kumar; Pandey, Vinay Kumar; Dubey, Mrigendra
Alkali base triggered intramolecular charge transfer metallogels based on symmetrical A-π-D-chiral-D-π-A type ligands.
Soft matter, 2016, 12, 3622-3630
1542618 CIFC27 H32 O8P 1 21 17.5013; 11.6919; 14.619
90; 103.882; 90
1244.7Wang, Guo-Cai; Yu, Jin-Hai; Shen, Yu; Leng, Ying; Zhang, Hua; Yue, Jian-Min
Limonoids and Triterpenoids as 11β-HSD1 Inhibitors from Walsura robusta.
Journal of natural products, 2016, 79, 899-906
1542619 CIFC27 H34 O8P 1 21 17.4553; 12.0869; 28.1295
90; 90.18; 90
2534.78Wang, Guo-Cai; Yu, Jin-Hai; Shen, Yu; Leng, Ying; Zhang, Hua; Yue, Jian-Min
Limonoids and Triterpenoids as 11β-HSD1 Inhibitors from Walsura robusta.
Journal of natural products, 2016, 79, 899-906
1542620 CIFC27 H43 O5.5C 1 2 111.4484; 18.1806; 25.8417
90; 98.082; 90
5325.2Liu, Zhaoming; Chen, Yan; Chen, Senhua; Liu, Yayue; Lu, Yongjun; Chen, Dongni; Lin, Yongcheng; Huang, Xishan; She, Zhigang
Aspterpenacids A and B, Two Sesterterpenoids from a Mangrove Endophytic Fungus Aspergillus terreus H010.
Organic letters, 2016, 18, 1406-1409
1542621 CIFC26 H28 N3 O7.5P -110.42; 11.567; 12.233
60.629; 74.155; 87.858
1227.9Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542622 CIFC14 H9 Cl N4 O7P 1 21/n 18.8587; 18.447; 9.759
90; 110.87; 90
1490.1Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542623 CIFC33 H34 F N3 O7P -18.201; 11.187; 17.705
91.352; 103.004; 105.472
1519.3Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542624 CIFC30 H29 N3 O5P -110.485; 10.4852; 13.306
79.14; 67.26; 76.51
1304Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542625 CIFC23 H16 N2 OC 1 c 15.5058; 26.046; 11.867
90; 97.83; 90
1685.9Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542626 CIFC29 H27 N3 O5P 1 21/c 113.4022; 10.939; 16.5069
90; 91.481; 90
2419.2Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542627 CIFC23 H25 N2 O6 ReP -19.569; 9.937; 12.748
89.068; 68.454; 84.701
1122.4Li, Dan; Chen, Yuanyuan; Wang, Xia; Deuther-Conrad, Winnie; Chen, Xin; Jia, Bing; Dong, Chengyan; Steinbach, Jörg; Brust, Peter; Liu, Boli; Jia, Hongmei
(99m)Tc-Cyclopentadienyl Tricarbonyl Chelate-Labeled Compounds as Selective Sigma-2 Receptor Ligands for Tumor Imaging.
Journal of medicinal chemistry, 2016, 59, 934-946
1542628 CIFC63 H39 B F24 N3 P PdP -112.7129; 13.3917; 17.6166
93.824; 90.923; 93.204
2987.2Ojwach, Stephen O.; Ogweno, Aloice O.; Akerman, Matthew P.
(Pyridyl)benzoazole palladium(ii) complexes as homogeneous catalysts in hydrogenation of alkenes and alkynes
Catal. Sci. Technol., 2016, 6, 5069
1542629 CIFC16 H12 N2 O2P 1 21/c 19.0373; 6.9446; 20.7426
90; 100.138; 90
1281.49Dhanasekaran, Sivasankaran; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Approach to Isoindolinones, Isoquinolinones, and THIQs via Lewis Acid-Catalyzed Domino Strecker-Lactamization/Alkylations.
Organic letters, 2016, 18, 634-637
1542630 CIFC19 H20 N2 O3P 1 21/n 18.4076; 9.6355; 20.2875
90; 98.838; 90
1624.01Dhanasekaran, Sivasankaran; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Approach to Isoindolinones, Isoquinolinones, and THIQs via Lewis Acid-Catalyzed Domino Strecker-Lactamization/Alkylations.
Organic letters, 2016, 18, 634-637
1542631 CIFC17 H22 N2 O5P b c a8.5688; 19.141; 21.222
90; 90; 90
3480.7Izumi, Sanae; Kobayashi, Yusuke; Takemoto, Yoshiji
Catalytic Asymmetric Synthesis of anti-α,β-Diamino Acid Derivatives.
Organic letters, 2016, 18, 696-699
1542632 CIFC19 H15 Br O4P 1 21 110.8044; 6.7767; 12.3031
90; 113.354; 90
827Sun, Xue-Li; Chen, Ying-Han; Zhu, Dan-Yang; Zhang, Yan; Liu, Yan-Kai
Substrate-Controlled, One-Pot Synthesis: Access to Chiral Chroman-2-one and Polycyclic Derivatives.
Organic letters, 2016, 18, 864-867
1542633 CIFC23 H28 O5P 1 21 17.1955; 19.2595; 7.6395
90; 101.353; 90
1037.98Wang, Peng; Li, Rui-Jun; Liu, Rui-Huan; Jian, Kai-Li; Yang, Ming-Hua; Yang, Lei; Kong, Ling-Yi; Luo, Jun
Sarglaperoxides A and B, Sesquiterpene-Normonoterpene Conjugates with a Peroxide Bridge from the Seeds of Sarcandra glabra.
Organic letters, 2016, 18, 832-835
1542634 CIFC15 H25 N O2P 1 21/c 110.6087; 12.4575; 10.8471
90; 104.219; 90
1389.6Song, Dengpeng; Wang, Zhengshen; Mei, Ruoming; Zhang, Weiwei; Ma, Donghui; Xu, Dengyu; Xie, Xingang; She, Xuegong
Short and Scalable Total Synthesis of Myrioneuron Alkaloids (±)-α,β-Myrifabral A and B.
Organic letters, 2016, 18, 669-671
1542635 CIFC31 H31 N3 O3P -110.139; 11.268; 11.71
92.64; 97.053; 92.437
1324.7Tian, Yaming; Tian, Lumin; Li, Chunju; Jia, Xueshun; Li, Jian
Temperature-Dependent Double Isocyanide Insertion Reaction To Construct a Polycyclic Skeleton.
Organic letters, 2016, 18, 840-843
1542636 CIFC30 H29 N3 O3P 1 21/c 111.499; 25.987; 18.929
90; 115.027; 90
5125Tian, Yaming; Tian, Lumin; Li, Chunju; Jia, Xueshun; Li, Jian
Temperature-Dependent Double Isocyanide Insertion Reaction To Construct a Polycyclic Skeleton.
Organic letters, 2016, 18, 840-843
1542637 CIFC33 H26 Br N3 OP -17.873; 11.346; 15.84
80.449; 77.035; 74.443
1319.9Tian, Yaming; Tian, Lumin; Li, Chunju; Jia, Xueshun; Li, Jian
Temperature-Dependent Double Isocyanide Insertion Reaction To Construct a Polycyclic Skeleton.
Organic letters, 2016, 18, 840-843
1542638 CIFC16 H11 N OP 1 21/c 19.9587; 12.7222; 9.7025
90; 94.493; 90
1225.5Zhang, Lianpeng; Peng, Zhixing; Wen, Qiaodong; Li, Xihui; Lu, Ping; Wang, Yanguang
Copper-Catalyzed Preparation of 2-Aryl-3-cyanobenzofurans with Bright Blue Photoluminescence.
Organic letters, 2016, 18, 728-731
1542639 CIFC16 H28 F N O5P 21 21 2132.528; 6.026; 9.305
90; 90; 90
1823.9Hu, Xiang-Guo; Lawer, Aggie; Peterson, Matthew B.; Iranmanesh, Hasti; Ball, Graham E.; Hunter, Luke
Diastereoselective Synthesis and Conformational Analysis of (2R)- and (2S)-Fluorostatines: An Approach Based on Organocatalytic Fluorination of a Chiral Aldehyde.
Organic letters, 2016, 18, 662-665
1542640 CIFC28 H22 N2 O5 SP -18.28533; 11.53237; 14.1641
111.2; 94.4487; 93.4599
1252.27Wang, Kai-Kai; Jin, Tian; Huang, Xin; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation.
Organic letters, 2016, 18, 872-875
1542641 CIFC26 H21 N O4 SP 1 21/n 115.5173; 9.24556; 15.6647
90; 90.404; 90
2247.3Wang, Kai-Kai; Jin, Tian; Huang, Xin; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation.
Organic letters, 2016, 18, 872-875
1542642 CIFC28 H24 N2 O5 SP 21 21 218.797; 12.2522; 22.914
90; 90; 90
2469.7Wang, Kai-Kai; Jin, Tian; Huang, Xin; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation.
Organic letters, 2016, 18, 872-875
1542643 CIFC24 H21 B F2 N2P n a 2116.262; 8.2789; 15.194
90; 90; 90
2045.6Zhou, Xin; Wu, Qinghua; Yu, Yang; Yu, Changjiang; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Metal-Free Direct α-Selective Arylation of Boron Dipyrromethenes via Base-Mediated C-H Functionalization.
Organic letters, 2016, 18, 736-739
1542644 CIFC25 H23 B F2 N2 OP n a 2117.9538; 8.2467; 14.4494
90; 90; 90
2139.4Zhou, Xin; Wu, Qinghua; Yu, Yang; Yu, Changjiang; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Metal-Free Direct α-Selective Arylation of Boron Dipyrromethenes via Base-Mediated C-H Functionalization.
Organic letters, 2016, 18, 736-739
1542645 CIFC30 H25 B F2 N2P -113.143; 13.3965; 15.473
67.831; 78.64; 87.648
2471.8Zhou, Xin; Wu, Qinghua; Yu, Yang; Yu, Changjiang; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Metal-Free Direct α-Selective Arylation of Boron Dipyrromethenes via Base-Mediated C-H Functionalization.
Organic letters, 2016, 18, 736-739

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