Crystallography Open Database
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Searching year of publication is 2016
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| 1542545 | CIF | C14 H3.5 F10.5 N7 | P 41 3 2 | 15.8427; 15.8427; 15.8427 90; 90; 90 | 3976.4 | Zhou, 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 | CIF | C32 H50 Cu Na O8 S2 | P 1 21/c 1 | 10.5883; 21.967; 14.4286 90; 95.682; 90 | 3339.5 | Johnson, 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 | CIF | C18 H16 B2 F8 N4 | P -1 | 7.547; 7.886; 8.992 66.005; 85.305; 83.508 | 485.4 | Leblanc, 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 | CIF | C18 H17 B F4 N4 | P 1 21/n 1 | 7.133; 20.036; 11.526 90; 99.454; 90 | 1624.9 | Leblanc, 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 | CIF | C18 H16 Cd Cl2 N4 | P -1 | 7.4683; 10.4739; 11.3249 80.15; 82.274; 81.982 | 858.7 | Leblanc, 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 | CIF | C40 H44 Fe N6 O6 | P 1 21/c 1 | 12.5879; 20.8699; 13.6448 90; 93.531; 90 | 3577.8 | Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L. Non-cyclic formylated dipyrromethanes as phosphate anion receptors Chem. Sci., 2016, 7, 3843 |
| 1542551 | CIF | C44 H38 Cl6 N6 O6 | P -1 | 10.1932; 12.318; 19.654 72.773; 77.793; 81.49 | 2294.1 | Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L. Non-cyclic formylated dipyrromethanes as phosphate anion receptors Chem. Sci., 2016, 7, 3843 |
| 1542552 | CIF | C62.5 H99 Cl N6 O11 P2 | P 1 21/n 1 | 19.5077; 15.3419; 22.1726 90; 95.401; 90 | 6606.47 | Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L. Non-cyclic formylated dipyrromethanes as phosphate anion receptors Chem. Sci., 2016, 7, 3843 |
| 1542553 | CIF | C46.5 H64.5 Cl1.5 N5 O8 P | P -1 | 9.9599; 14.6932; 16.4802 81.05; 75.273; 88.017 | 2304.1 | Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L. Non-cyclic formylated dipyrromethanes as phosphate anion receptors Chem. Sci., 2016, 7, 3843 |
| 1542554 | CIF | C119 H151 Cl9 N14 O20 P2 | P -1 | 16.0755; 18.9299; 24.4976 93.415; 96.103; 111.261 | 6869.2 | Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L. Non-cyclic formylated dipyrromethanes as phosphate anion receptors Chem. Sci., 2016, 7, 3843 |
| 1542555 | CIF | C69 H62.5 Cl6 I6 N12 Zn3 | C 1 2/c 1 | 35.7365; 15.061; 30.9345 90; 104.141; 90 | 16145.3 | Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto Structure determination of microbial metabolites by the crystalline sponge method Chem. Sci., 2016, 7, 3910 |
| 1542556 | CIF | C132.77 H131.15 I12 N24 O15.14 Zn6 | C 1 2 1 | 36.3783; 14.6755; 31.2278 90; 103.184; 90 | 16232.2 | Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto Structure determination of microbial metabolites by the crystalline sponge method Chem. Sci., 2016, 7, 3910 |
| 1542557 | CIF | C134.29 H138.92 I12 N24 O8.41 Zn6 | C 1 2 1 | 34.7707; 14.8406; 31.2152 90; 102.601; 90 | 15719.6 | Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto Structure determination of microbial metabolites by the crystalline sponge method Chem. Sci., 2016, 7, 3910 |
| 1542558 | CIF | C68 H74 N Ni O3 P3 S3 Si3 | P b c a | 27.4702; 17.1432; 27.9778 90; 90; 90 | 13175.5 | Chiou, 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 | CIF | C68 H74 N2 Ni O2 P3 S3 Si3 | P b c a | 27.5733; 17.0409; 27.8585 90; 90; 90 | 13090 | Chiou, 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 | CIF | C67 H78 N3 Ni O P3 S3 Si3 | P 1 21/n 1 | 14.316; 26.0756; 18.0992 90; 97.069; 90 | 6705 | Chiou, 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 | CIF | C50 H68 O4 | P -1 | 9.1934; 13.5122; 18.2252 76.83; 75.995; 86.625 | 2138.9 | Wang, 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 | CIF | C17 H21.3 N O4.15 | P 21 21 21 | 9.7421; 9.7391; 16.0471 90; 90; 90 | 1522.54 | Zhan, 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 | CIF | C16 H22 N O4.5 | P 21 21 21 | 8.0372; 15.6818; 22.5648 90; 90; 90 | 2844.02 | Zhan, 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 | CIF | C23 H30.01 N2 O4 | P 1 21 1 | 9.4965; 11.4906; 9.9133 90; 95.247; 90 | 1077.21 | Zhan, 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 | CIF | C23 H30 N2 O4 | P 1 21 1 | 9.6195; 11.6392; 9.6441 90; 94.229; 90 | 1076.85 | Zhan, 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 | CIF | C18 H27 N O5 | P 21 21 21 | 7.9947; 8.6002; 24.7362 90; 90; 90 | 1700.76 | Zhan, 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 | CIF | C21 H17 N3 O | C 1 2/c 1 | 17.9422; 9.9101; 19.1301 90; 99.879; 90 | 3351.1 | Chen, 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 | CIF | C38 H30 N4 S3 | P b c n | 29.6046; 11.8388; 17.1781 90; 90; 90 | 6020.6 | Zhang, 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 | CIF | C88 H64 N12 S6 | P -1 | 10.6919; 11.6399; 14.4791 90.178; 104.4; 95.311 | 1737.22 | Zhang, 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 | CIF | C13 H10 Cl N O2 | P 1 | 7.02512; 8.17982; 10.0807 104.135; 104.019; 91.6954 | 542.58 | Sanchez-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 | CIF | C8 H11 N O4 S | P -1 | 6.4922; 8.38; 9.896 74.212; 73.241; 80.346 | 493.74 | Mommer, 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 | CIF | C23 H18 O3 | P 1 c 1 | 5.82646; 9.44106; 15.616 90; 100.11; 90 | 845.67 | Han, 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 | CIF | C26 H19 N3 O2 | P 1 21/c 1 | 10.0072; 23.043; 9.4047 90; 110.772; 90 | 2027.7 | Cai, 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 | CIF | C28 H22 Cl3 N3 O3 | P 1 21/c 1 | 12.2576; 19.07; 11.4688 90; 97.837; 90 | 2655.8 | Cai, 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 | CIF | C21 H15 Br N4 | P b c a | 13.3161; 7.7509; 33.992 90; 90; 90 | 3508.4 | Cai, 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 | CIF | C14 H16 O4 | P 21 21 21 | 7.2935; 8.8494; 19.329 90; 90; 90 | 1247.55 | Sun, 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 | CIF | C14 H16 O4 | P 21 21 21 | 5.5435; 7.7426; 27.879 90; 90; 90 | 1196.6 | Sun, 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 | CIF | C16 H11 F3 Mo O3 | P -1 | 7.1145; 7.6417; 15.3159 93.275; 97.569; 113.744 | 749.96 | Reich, 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 | CIF | C16 H11 F3 Mo O3 | P 1 21/c 1 | 7.2471; 31.8822; 6.7406 90; 104.266; 90 | 1509.41 | Reich, 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 | CIF | C16 H11 F3 Mo O3 | P 1 21/c 1 | 8.9791; 12.3295; 13.7453 90; 100.651; 90 | 1495.49 | Reich, 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 | CIF | C17 H10 F6 Mo O3 | P -1 | 8.4202; 10.2245; 10.5319 101.377; 102.663; 103.044 | 832.29 | Reich, 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 | CIF | C32 H33 N3 Ni O3 | P 1 21 1 | 11.0798; 21.9977; 11.88015 90; 102.003; 90 | 2832.25 | Miles, 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 | CIF | C16 H11 Fe3 N O7 S2 | P -1 | 7.7263; 11.203; 11.9 94.504; 108.019; 93.687 | 972.2 | Lunsford, 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 | CIF | C40 H35 Fe3 N O5 P2 S2 | P -1 | 11.3103; 12.9416; 15.479 105.449; 100.216; 110.921 | 1944.2 | Lunsford, 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 | CIF | C20.2 H22.23 B F4 Fe3 N4.6 O6.72 S2 | P -1 | 10.4593; 11.6085; 12.256 76.988; 85.341; 81.75 | 1433.02 | Lunsford, 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 | CIF | C80 H75 B F24 Fe3 N O4 P4 S2 | P -1 | 13.352; 13.623; 24.074 92.828; 94.41; 99.584 | 4296 | Lunsford, 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 | CIF | C25 H23 N5 O8 | P -1 | 7.856; 11.799; 14.315 66.98; 77.401; 74.377 | 1166.6 | Biswas, 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 | CIF | C25 H25 N O | P 1 21/c 1 | 11.1357; 10.6585; 17.1362 90; 90.608; 90 | 2033.8 | Wang, 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 | CIF | C26 H21 Cl O | P 1 21 1 | 13.2144; 5.6194; 14.8801 90; 111.914; 90 | 1025.11 | Wang, 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 | CIF | C79.27 H80.86 N5.59 Zn | P -1 | 10.0013; 14.5831; 24.366 75.428; 87.017; 71.26 | 3255.5 | Fukui, 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 | CIF | C64.5 H68 Cl7.5 N5 Ni O2 | P b c n | 11.0983; 34.992; 32.965 90; 90; 90 | 12802 | Fukui, 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 | CIF | C69 H77 N5 Ni O2 | P -1 | 14.734; 20.554; 20.788 90.073; 103.209; 109.518 | 5756 | Fukui, 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 | CIF | C74 H77 N4 Ni O P | P 1 21/n 1 | 12.3714; 28.233; 41.36 90; 96.168; 90 | 14363 | Fukui, 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 | CIF | C44 H36 Br N O P2 Pd | P -1 | 11.12; 12.074; 15.487 69.218; 72.309; 70.811 | 1794.3 | Wu, Jiang; Liu, Yafei; Lu, Changhui; Shen, Qilong Palladium-catalyzed difluoromethylthiolation of heteroaryl bromides, iodides, triflates and aryl iodides Chem. Sci., 2016, 7, 3757 |
| 1542596 | CIF | C18 H27 Cl N2 O12 S | P 1 21 1 | 7.2371; 9.8802; 15.9674 90; 97.002; 90 | 1133.2 | Liang, 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 | CIF | C23 H24 N2 O4 S2 | P 1 21/n 1 | 8.2793; 22.107; 12.8092 90; 105.304; 90 | 2261.3 | Liang, 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 | CIF | C41 H32 N2 O | P 1 21/c 1 | 17.751; 6.9635; 26.097 90; 107.904; 90 | 3069.6 | Jiang, 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 | CIF | C37 H30 N2 O | P 1 21/n 1 | 20.5458; 14.0737; 20.9813 90; 108.671; 90 | 5747.6 | Jiang, 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 | CIF | C41 H32 N2 O | P 1 21/c 1 | 19.0371; 9.7457; 18.7726 90; 114.993; 90 | 3156.7 | Jiang, 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 O | P -1 | 6.4998; 7.4286; 14.8289 84.859; 86.707; 83.313 | 707.47 | Maheswari, 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 O3 | P 1 21/c 1 | 9.9339; 10.6614; 12.6802 90; 105.863; 90 | 1291.8 | Avezov, 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 | CIF | C13 H9 N5 O2 | P 1 21/c 1 | 3.8512; 19.078; 21.23 90; 91.015; 90 | 1559.6 | Kaloo, 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 | CIF | C14 H23 O5 Rh | P 1 21/n 1 | 7.2023; 13.3209; 16.1663 90; 93.426; 90 | 1548.24 | Jardim, 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 | CIF | C20 H24 Cl4 F6 Rh2 | R -3 | 28.1638; 28.1638; 8.1635 90; 90; 120 | 5607.8 | Jardim, 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 | CIF | C24 H38 Cl4 Rh2 | P -1 | 8.2993; 8.9088; 9.3961 102.335; 106.607; 94.5603 | 643 | Jardim, 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 | CIF | C10 H5 I O2 | P -1 | 7.7536; 8.2731; 14.2858 73.2168; 78.223; 85.339 | 858.63 | Jardim, 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 | CIF | C11 H7 I O3 | P 1 21/c 1 | 8.1168; 7.9198; 15.1553 90; 93.0671; 90 | 972.84 | Jardim, 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 | CIF | C12 H9 I O3 | P 1 21/c 1 | 17.2465; 16.7627; 7.5137 90; 91.9216; 90 | 2170.97 | Jardim, 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 | CIF | C10 H4 I N O4 | P 1 21/c 1 | 7.7794; 9.0897; 13.9834 90; 99.5625; 90 | 975.06 | Jardim, 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 | CIF | C10 H4 Br I O2 | P 21 21 21 | 5.0752; 6.1752; 30.9217 90; 90; 90 | 969.1 | Jardim, 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 | CIF | C10 H3 Br2 I O2 | P -1 | 7.1805; 8.2069; 10.2503 67.006; 88.761; 69.374 | 515.67 | Jardim, 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 | CIF | C10 H5 I O2 | P 1 21/c 1 | 14.1706; 4.1298; 15.9165 90; 106.661; 90 | 892.36 | Jardim, 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 | CIF | C10 H4 I2 O2 | P 1 21/n 1 | 13.9652; 4.4527; 16.4351 90; 102.327; 90 | 998.42 | Jardim, 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 | CIF | C10 H5 Br O2 | P 1 21/c 1 | 7.7808; 8.1027; 12.8379 90; 94.413; 90 | 806.97 | Jardim, 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 | CIF | C57 H38 Cl3 | P 1 21/c 1 | 9.65924; 9.12014; 50.6162 90; 91.6555; 90 | 4457.1 | Zhang, 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 | CIF | C9 H10 N3 O5 | C 1 2 1 | 15.791; 5.0056; 16.133 90; 122.52; 90 | 1075.3 | Dixit, 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 | CIF | C27 H32 O8 | P 1 21 1 | 7.5013; 11.6919; 14.619 90; 103.882; 90 | 1244.7 | Wang, 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 | CIF | C27 H34 O8 | P 1 21 1 | 7.4553; 12.0869; 28.1295 90; 90.18; 90 | 2534.78 | Wang, 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 | CIF | C27 H43 O5.5 | C 1 2 1 | 11.4484; 18.1806; 25.8417 90; 98.082; 90 | 5325.2 | Liu, 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 | CIF | C26 H28 N3 O7.5 | P -1 | 10.42; 11.567; 12.233 60.629; 74.155; 87.858 | 1227.9 | Yang, 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 | CIF | C14 H9 Cl N4 O7 | P 1 21/n 1 | 8.8587; 18.447; 9.759 90; 110.87; 90 | 1490.1 | Yang, 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 | CIF | C33 H34 F N3 O7 | P -1 | 8.201; 11.187; 17.705 91.352; 103.004; 105.472 | 1519.3 | Yang, 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 | CIF | C30 H29 N3 O5 | P -1 | 10.485; 10.4852; 13.306 79.14; 67.26; 76.51 | 1304 | Yang, 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 | CIF | C23 H16 N2 O | C 1 c 1 | 5.5058; 26.046; 11.867 90; 97.83; 90 | 1685.9 | Yang, 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 | CIF | C29 H27 N3 O5 | P 1 21/c 1 | 13.4022; 10.939; 16.5069 90; 91.481; 90 | 2419.2 | Yang, 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 | CIF | C23 H25 N2 O6 Re | P -1 | 9.569; 9.937; 12.748 89.068; 68.454; 84.701 | 1122.4 | Li, 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 | CIF | C63 H39 B F24 N3 P Pd | P -1 | 12.7129; 13.3917; 17.6166 93.824; 90.923; 93.204 | 2987.2 | Ojwach, 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 | CIF | C16 H12 N2 O2 | P 1 21/c 1 | 9.0373; 6.9446; 20.7426 90; 100.138; 90 | 1281.49 | Dhanasekaran, 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 | CIF | C19 H20 N2 O3 | P 1 21/n 1 | 8.4076; 9.6355; 20.2875 90; 98.838; 90 | 1624.01 | Dhanasekaran, 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 | CIF | C17 H22 N2 O5 | P b c a | 8.5688; 19.141; 21.222 90; 90; 90 | 3480.7 | Izumi, Sanae; Kobayashi, Yusuke; Takemoto, Yoshiji Catalytic Asymmetric Synthesis of anti-α,β-Diamino Acid Derivatives. Organic letters, 2016, 18, 696-699 |
| 1542632 | CIF | C19 H15 Br O4 | P 1 21 1 | 10.8044; 6.7767; 12.3031 90; 113.354; 90 | 827 | Sun, 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 | CIF | C23 H28 O5 | P 1 21 1 | 7.1955; 19.2595; 7.6395 90; 101.353; 90 | 1037.98 | Wang, 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 | CIF | C15 H25 N O2 | P 1 21/c 1 | 10.6087; 12.4575; 10.8471 90; 104.219; 90 | 1389.6 | Song, 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 | CIF | C31 H31 N3 O3 | P -1 | 10.139; 11.268; 11.71 92.64; 97.053; 92.437 | 1324.7 | Tian, 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 | CIF | C30 H29 N3 O3 | P 1 21/c 1 | 11.499; 25.987; 18.929 90; 115.027; 90 | 5125 | Tian, 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 | CIF | C33 H26 Br N3 O | P -1 | 7.873; 11.346; 15.84 80.449; 77.035; 74.443 | 1319.9 | Tian, 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 | CIF | C16 H11 N O | P 1 21/c 1 | 9.9587; 12.7222; 9.7025 90; 94.493; 90 | 1225.5 | Zhang, 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 | CIF | C16 H28 F N O5 | P 21 21 21 | 32.528; 6.026; 9.305 90; 90; 90 | 1823.9 | Hu, 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 | CIF | C28 H22 N2 O5 S | P -1 | 8.28533; 11.53237; 14.1641 111.2; 94.4487; 93.4599 | 1252.27 | Wang, 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 | CIF | C26 H21 N O4 S | P 1 21/n 1 | 15.5173; 9.24556; 15.6647 90; 90.404; 90 | 2247.3 | Wang, 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 | CIF | C28 H24 N2 O5 S | P 21 21 21 | 8.797; 12.2522; 22.914 90; 90; 90 | 2469.7 | Wang, 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 | CIF | C24 H21 B F2 N2 | P n a 21 | 16.262; 8.2789; 15.194 90; 90; 90 | 2045.6 | Zhou, 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 | CIF | C25 H23 B F2 N2 O | P n a 21 | 17.9538; 8.2467; 14.4494 90; 90; 90 | 2139.4 | Zhou, 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 | CIF | C30 H25 B F2 N2 | P -1 | 13.143; 13.3965; 15.473 67.831; 78.64; 87.648 | 2471.8 | Zhou, 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 |
| 1542646 | CIF | C43 H28 N4 | P 1 21/n 1 | 11.523; 16.7116; 17.0577 90; 106.759; 90 | 3145.2 | Huang, Jau-Jiun; Hung, Yu-Hsiang; Ting, Pei-Ling; Tsai, Yu-Ning; Gao, Huan-Jie; Chiu, Tien-Lung; Lee, Jiun-Haw; Chen, Chi-Lin; Chou, Pi-Tai; Leung, Man-Kit Orthogonally Substituted Benzimidazole-Carbazole Benzene As Universal Hosts for Phosphorescent Organic Light-Emitting Diodes. Organic letters, 2016, 18, 672-675 |
| 1542647 | CIF | C31 H23 N3 O0.5 | P 1 21/n 1 | 9.8285; 13.81; 17.3341 90; 91.02; 90 | 2352.41 | Huang, Jau-Jiun; Hung, Yu-Hsiang; Ting, Pei-Ling; Tsai, Yu-Ning; Gao, Huan-Jie; Chiu, Tien-Lung; Lee, Jiun-Haw; Chen, Chi-Lin; Chou, Pi-Tai; Leung, Man-Kit Orthogonally Substituted Benzimidazole-Carbazole Benzene As Universal Hosts for Phosphorescent Organic Light-Emitting Diodes. Organic letters, 2016, 18, 672-675 |
| 1542648 | CIF | C16 H8 Ag Br F8 N2 | P 1 21/n 1 | 6.8291; 15.1012; 16.8892 90; 100.705; 90 | 1711.4 | Kaplan, Peter T.; Vicic, David A. Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks. Organic letters, 2016, 18, 884-886 |
| 1542649 | CIF | C16 H8 Br Cu F8 N2 | P 1 21/c 1 | 6.598; 17.1674; 14.6901 90; 95.676; 90 | 1655.8 | Kaplan, Peter T.; Vicic, David A. Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks. Organic letters, 2016, 18, 884-886 |
| 1542650 | CIF | C10 H4 Br F8 N O2 | P -1 | 6.1276; 8.3737; 12.5585 108.992; 90.118; 90.223 | 609.3 | Kaplan, Peter T.; Vicic, David A. Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks. Organic letters, 2016, 18, 884-886 |
| 1542651 | CIF | C11 H4 Br F8 N | P 1 21/c 1 | 5.9092; 15.55; 13.5414 90; 91.044; 90 | 1244.09 | Kaplan, Peter T.; Vicic, David A. Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks. Organic letters, 2016, 18, 884-886 |
| 1542652 | CIF | C12 H4 Br F12 N O2 | P -1 | 6.0576; 8.4076; 15.1254 73.883; 89.304; 89.536 | 739.99 | Kaplan, Peter T.; Vicic, David A. Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks. Organic letters, 2016, 18, 884-886 |
| 1542653 | CIF | C13 H4 Br F12 N | P -1 | 5.9088; 8.397; 15.6935 105.477; 90.42; 91.565 | 750.05 | Kaplan, Peter T.; Vicic, David A. Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks. Organic letters, 2016, 18, 884-886 |
| 1542654 | CIF | C17 H15 N O4 | P 21 21 21 | 5.9263; 14.358; 17.7263 90; 90; 90 | 1508.33 | Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo Anti-Selective Asymmetric Nitro-Michael Reaction of Furanones: Diastereocontrol by Catalyst. Organic letters, 2016, 18, 646-649 |
| 1542655 | CIF | C24 H26 N4 O4 | P -1 | 9.715; 10.003; 13.038 105.483; 98.771; 111.44 | 1091.5 | Zhao, Hong-Wu; Li, Bo; Pang, Hai-Liang; Tian, Ting; Chen, Xiao-Qin; Song, Xiu-Qing; Meng, Wei; Yang, Zhao; Zhao, Yu-Di; Liu, Yue-Yang Diastereoselective 1,3-Dipolar Cycloadditions of N,N'-Cyclic Azomethine Imines with Iminooxindoles for Access to Oxindole Spiro-N,N-bicyclic Heterocycles. Organic letters, 2016, 18, 848-851 |
| 1542656 | CIF | C20 H11 Cl6 O2 P S2 | P 1 21/n 1 | 11.338; 11.077; 18.981 90; 106.186; 90 | 2289.4 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542657 | CIF | C18 H9 O3 P S | P 1 21/n 1 | 8.3936; 15.6127; 10.697 90; 100.496; 90 | 1378.35 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542658 | CIF | C18 H9 P S3 | P -1 | 3.9829; 10.6559; 17.2702 86.043; 89.121; 81.767 | 723.68 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542659 | CIF | C18 H9 O2 P S | P c c n | 16.762; 22.071; 7.4782 90; 90; 90 | 2766.6 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542660 | CIF | C21 H16 F2 N O4 P S | P 1 21/c 1 | 11.099; 11.479; 14.854 90; 95.89; 90 | 1882.5 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542661 | CIF | C18 H9 O P S3 | P 1 21/n 1 | 9.166; 10.699; 15.212 90; 101.527; 90 | 1461.7 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542662 | CIF | C18 H9 O P S2 | P b c a | 8.0119; 20.775; 34.265 90; 90; 90 | 5703.3 | Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms. Organic letters, 2016, 18, 816-819 |
| 1542663 | CIF | C30 H28 N O3 P | P 1 21/c 1 | 8.675; 19.74; 15.454 90; 106.49; 90 | 2538 | Jiang, Jin; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun Diethyl Phosphite Initiated Coupling of α-Ketoesters with Imines for Synthesis of α-Phosphonyloxy-β-amino Acid Derivatives and Aziridine-2-carboxylates. Organic letters, 2016, 18, 880-883 |
| 1542664 | CIF | C29 H36 N O9 P S | P 1 21/a 1 | 16.58; 10.731; 17.82 90; 104.369; 90 | 3071 | Jiang, Jin; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun Diethyl Phosphite Initiated Coupling of α-Ketoesters with Imines for Synthesis of α-Phosphonyloxy-β-amino Acid Derivatives and Aziridine-2-carboxylates. Organic letters, 2016, 18, 880-883 |
| 1542665 | CIF | C19 H26 Cl3 N2 Rh | P 1 21/c 1 | 11.0944; 14.838; 13.848 90; 105.603; 90 | 2195.6 | Qi, Zisong; Yu, Songjie; Li, Xingwei Rh(III)-Catalyzed Synthesis of N-Unprotected Indoles from Imidamides and Diazo Ketoesters via C-H Activation and C-C/C-N Bond Cleavage. Organic letters, 2016, 18, 700-703 |
| 1542666 | CIF | C17 H13 Br N2 O2 | P 1 21/c 1 | 4.4677; 16.8234; 20.1968 90; 92.566; 90 | 1516.51 | Ma, Haichao; Li, Dianjun; Yu, Wei Synthesis of Quinoxaline Derivatives via Tandem Oxidative Azidation/Cyclization Reaction of N-Arylenamines. Organic letters, 2016, 18, 868-871 |
| 1542667 | CIF | C26 H34 O8 | P 21 21 21 | 7.8754; 9.4243; 32.1424 90; 90; 90 | 2385.61 | Wan, Luo-Sheng; Shao, Li-Dong; Fu, Liangbing; Xu, Jun; Zhu, Guo-Lei; Peng, Xing-Rong; Li, Xiao-Nian; Li, Yan; Qiu, Ming-Hua One-Step Semisynthesis of a Segetane Diterpenoid from a Jatrophane Precursor via a Diels-Alder Reaction. Organic letters, 2016, 18, 496-499 |
| 1542668 | CIF | C42 H32 S | P -1 | 8.317; 16.04; 23.373 108.62; 98.945; 90.295 | 2913.9 | Bhanuchandra, M.; Yorimitsu, Hideki; Osuka, Atsuhiro Synthesis of Spirocyclic Diarylfluorenes by One-Pot Twofold SNAr Reactions of Diaryl Sulfones with Diarylmethanes. Organic letters, 2016, 18, 384-387 |
| 1542669 | CIF | C26 H15 F3 S | P -1 | 7.4947; 10.4244; 12.3741 83; 82.694; 81.603 | 943.36 | Bhanuchandra, M.; Yorimitsu, Hideki; Osuka, Atsuhiro Synthesis of Spirocyclic Diarylfluorenes by One-Pot Twofold SNAr Reactions of Diaryl Sulfones with Diarylmethanes. Organic letters, 2016, 18, 384-387 |
| 1542670 | CIF | C24 H32 N2 O3 S | P 1 21 1 | 16.9083; 5.97938; 23.1232 90; 103.885; 90 | 2269.47 | Yoshizaki, Soichi; Nakamura, Yu; Masutomi, Koji; Yoshida, Tomoka; Noguchi, Keiichi; Shibata, Yu; Tanaka, Ken Rhodium-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of 1,6-Enynes with Cyclopropylideneacetamides. Organic letters, 2016, 18, 388-391 |
| 1542671 | CIF | C28 H20 N2 O6 S | P b c a | 13.7519; 14.9993; 22.6562 90; 90; 90 | 4673.27 | Kumar, N. N. Bhuvan; Kutateladze, Andrei G. Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications. Organic letters, 2016, 18, 460-463 |
| 1542672 | CIF | C17 H14 N2 O4 | P 1 21/n 1 | 9.1645; 8.7385; 18.3694 90; 104.426; 90 | 1424.71 | Kumar, N. N. Bhuvan; Kutateladze, Andrei G. Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications. Organic letters, 2016, 18, 460-463 |
| 1542673 | CIF | C19 H13 Cl N2 O3 | C 1 2/c 1 | 17.6228; 12.8352; 14.1014 90; 91.786; 90 | 3188.08 | Kumar, N. N. Bhuvan; Kutateladze, Andrei G. Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications. Organic letters, 2016, 18, 460-463 |
| 1542674 | CIF | C36 H50 S4 Si2 | P -1 | 12.2329; 17.7221; 19.3408 69.034; 72.015; 72.867 | 3643.1 | Chang, Shao-Ling; Lu, Chih-Wen; Lai, Yu-Ying; Hsu, Jhih-Yang; Cheng, Yen-Ju Synthesis and Molecular Properties of Two Isomeric Dialkylated Tetrathienonaphthalenes. Organic letters, 2016, 18, 368-371 |
| 1542675 | CIF | C34 H44 S4 Si2 | P -1 | 11.715; 12.209; 15.564 76.856; 75.796; 79.474 | 2082.4 | Chang, Shao-Ling; Lu, Chih-Wen; Lai, Yu-Ying; Hsu, Jhih-Yang; Cheng, Yen-Ju Synthesis and Molecular Properties of Two Isomeric Dialkylated Tetrathienonaphthalenes. Organic letters, 2016, 18, 368-371 |
| 1542676 | CIF | C24 H18 O3 | P 1 21/n 1 | 9.9595; 12.5319; 14.6208 90; 97.484; 90 | 1809.3 | More, Atul A.; Ramana, Chepuri V. o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic letters, 2016, 18, 612-615 |
| 1542677 | CIF | C16 H12 O3 | P -1 | 7.6359; 8.6199; 10.087 80.935; 79.666; 69.242 | 607.6 | More, Atul A.; Ramana, Chepuri V. o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic letters, 2016, 18, 612-615 |
| 1542678 | CIF | C19 H18 O4 | P 1 21/c 1 | 9.4895; 8.7747; 19.062 90; 101.174; 90 | 1557.2 | More, Atul A.; Ramana, Chepuri V. o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic letters, 2016, 18, 612-615 |
| 1542679 | CIF | C17 H14 O3 | P 1 21/n 1 | 9.3485; 13.5764; 10.5947 90; 101.444; 90 | 1317.94 | More, Atul A.; Ramana, Chepuri V. o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic letters, 2016, 18, 612-615 |
| 1542680 | CIF | C16 H12 O3 | P b c a | 10.0417; 18.527; 26.755 90; 90; 90 | 4977.6 | More, Atul A.; Ramana, Chepuri V. o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic letters, 2016, 18, 612-615 |
| 1542681 | CIF | C22 H22 O5 | P -1 | 9.3342; 10.9832; 19.0771 103.527; 91.081; 99.292 | 1873.3 | More, Atul A.; Ramana, Chepuri V. o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic letters, 2016, 18, 612-615 |
| 1542682 | CIF | C12 H11 Cl F3 N O | P 1 21/n 1 | 10.761; 5.854; 19.673 90; 102.693; 90 | 1209 | Fu, Mingyang; Chen, Long; Jiang, Yongpeng; Jiang, Zhong-Xing; Yang, Zhigang Copper-Catalyzed Intermolecular Chloro- and Bromotrifluoromethylation of Alkenes. Organic letters, 2016, 18, 348-351 |
| 1542683 | CIF | C36 H36 Br N2 O4.5 S | C 1 2 1 | 27.2716; 10.7113; 11.2422 90; 90.5644; 90 | 3283.85 | Wang, Shoulei; Rodriguez-Escrich, Carles; Pericàs, Miquel A H-Bond-Directing Organocatalyst for Enantioselective [4 + 2] Cycloadditions via Dienamine Catalysis. Organic letters, 2016, 18, 556-559 |
| 1542684 | CIF | C13 H10 N2 S | P -1 | 3.9105; 10.8964; 12.403 97.328; 94.957; 92.265 | 521.54 | Sharma, Shivani; Pathare, Ramdas S.; Maurya, Antim K.; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M.; Pardasani, Ram T. Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight. Organic letters, 2016, 18, 356-359 |
| 1542685 | CIF | C14 H12 N2 O S | P 1 21/c 1 | 13.1514; 12.8014; 7.2224 90; 105.094; 90 | 1173.99 | Sharma, Shivani; Pathare, Ramdas S.; Maurya, Antim K.; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M.; Pardasani, Ram T. Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight. Organic letters, 2016, 18, 356-359 |
| 1542686 | CIF | C26 H22 Cl2 N2 O4 | P 1 21/c 1 | 9.921; 17.9238; 12.9555 90; 90.022; 90 | 2303.8 | Zhou, Yunfei; Zhu, Jianming; Li, Bo; Zhang, Yong; Feng, Jia; Hall, Adrian; Shi, Jiye; Zhu, Weiliang Access to Different Isomeric Dibenzoxazepinones through Copper-Catalyzed C-H Etherification and C-N Bond Construction with Controllable Smiles Rearrangement. Organic letters, 2016, 18, 380-383 |
| 1542687 | CIF | C24 H17 Cl N2 O3 | P 1 21/c 1 | 14.8316; 16.4395; 7.8011 90; 93.277; 90 | 1898.99 | Zhou, Yunfei; Zhu, Jianming; Li, Bo; Zhang, Yong; Feng, Jia; Hall, Adrian; Shi, Jiye; Zhu, Weiliang Access to Different Isomeric Dibenzoxazepinones through Copper-Catalyzed C-H Etherification and C-N Bond Construction with Controllable Smiles Rearrangement. Organic letters, 2016, 18, 380-383 |
| 1542688 | CIF | C32 H16 Br8 O8 | C 1 2/c 1 | 21.0972; 15.0686; 14.2085 90; 128.249; 90 | 3547.3 | Kumar, Yogendra; Kumar, Sharvan; Kumar Keshri, Sudhir; Shukla, Jyoti; Singh, Shiv Shankar; Thakur, Tejender S.; Denti, Mitchell; Facchetti, Antonio; Mukhopadhyay, Pritam Synthesis of Octabromoperylene Dianhydride and Diimides: Evidence of Halogen Bonding and Semiconducting Properties. Organic letters, 2016, 18, 472-475 |
| 1542689 | CIF | C11 H10 N4 O3 | P b c a | 10.487; 13.0919; 16.145 90; 90; 90 | 2216.6 | Pawar, Govind Goroba; Brahmanandan, Abhilashamole; Kapur, Manmohan Palladium(II)-Catalyzed, Heteroatom-Directed, Regioselective C-H Nitration of Anilines Using Pyrimidine as a Removable Directing Group. Organic letters, 2016, 18, 448-451 |
| 1542690 | CIF | C34 H35 Br N2 O | P 21 21 21 | 10.839; 23.282; 24.36 90; 90; 90 | 6147 | Li, Xuanyi; Xu, Xiuyan; Wei, Weiwei; Lin, Aijun; Yao, Hequan Organocatalyzed Asymmetric 1,6-Conjugate Addition of para-Quinone Methides with Dicyanoolefins. Organic letters, 2016, 18, 428-431 |
| 1542691 | CIF | C14 H17 F N2 O2 S | P 1 21 1 | 5.8834; 11.064; 11.101 90; 102.611; 90 | 705.2 | Hajra, Saumen; Aziz, Sk Mohammad; Jana, Bibekananda; Mahish, Prosenjit; Das, Dhiraj Synthesis of Chiral Spiro-Aziridine Oxindoles via Aza-Corey-Chaykovsky Reaction of Isatin Derived N-tert-Butanesulfinyl Ketimines. Organic letters, 2016, 18, 532-535 |
| 1542692 | CIF | C32 H31 N O5 | P 1 21/c 1 | 10.3073; 11.8581; 21.8138 90; 94.816; 90 | 2656.8 | Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines. Organic letters, 2016, 18, 600-603 |
| 1542693 | CIF | C26 H20 F3 N O | I 1 2/a 1 | 18.3718; 5.6809; 40.089 90; 100.975; 90 | 4107.5 | Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines. Organic letters, 2016, 18, 600-603 |
| 1542694 | CIF | C29 H25 F2 N O3 | P -1 | 10.2357; 10.5168; 12.7893 71.454; 71.195; 73.002 | 1207.61 | Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines. Organic letters, 2016, 18, 600-603 |
| 1542695 | CIF | C18 H24 O3 | P 21 21 21 | 7.8269; 8.7254; 23.407 90; 90; 90 | 1598.5 | Liu, Chenguang; Zeng, Zhixiong; Chen, Renzhi; Jiang, Xunjin; Wang, Yinglu; Zhang, Yandong Total Synthesis of (+)-Fusarisetin A Driven by a One-Pot Four-Reaction Process. Organic letters, 2016, 18, 624-627 |
| 1542696 | CIF | C18 H12 Br2 O2 S | P -1 | 7.9582; 8.0654; 13.665 82.257; 84.908; 72.622 | 828.3 | Wang, Miao; Xiang, Jia-Chen; Cheng, Yan; Wu, Yan-Dong; Wu, An-Xin Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit. Organic letters, 2016, 18, 524-527 |
| 1542697 | CIF | C19 H16 O4 S2 | P -1 | 7.573; 8.012; 15.475 77.359; 78.217; 86.315 | 896.7 | Wang, Miao; Xiang, Jia-Chen; Cheng, Yan; Wu, Yan-Dong; Wu, An-Xin Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit. Organic letters, 2016, 18, 524-527 |
| 1542698 | CIF | C23.5 H14.5 Cl4.5 N3 O8 | P -1 | 9.645; 11.531; 23.18 92.059; 90.249; 95.534 | 2564.25 | Yoon, Ina; Suh, Sung-Eun; Barros, Stephanie A.; Chenoweth, David M. Synthesis of 9-Substituted Triptycene Building Blocks for Solid-Phase Diversification and Nucleic Acid Junction Targeting. Organic letters, 2016, 18, 1096 |
| 1542699 | CIF | C17 H16 F N O | P -1 | 5.5492; 10.9097; 11.6094 102.644; 93.799; 96.078 | 679.03 | Wang, Yi-Feng; Hu, Ming; Hayashi, Hirohito; Xing, Bengang; Chiba, Shunsuke Linking of Alcohols with Vinyl Azides. Organic letters, 2016, 18, 992 |
| 1542700 | CIF | C22 H17 Cl2 F3 N2 O3 | P 21 21 21 | 7.6378; 15.9147; 18.2712 90; 90; 90 | 2220.9 | Li, Xiaoyuan; Su, Jinhuan; Liu, Zhourujun; Zhu, Yuanyuan; Dong, Zhenghao; Qiu, Shuai; Wang, Jiayi; Lin, Li; Shen, Zhiqiang; Yan, Wenjin; Wang, Kairong; Wang, Rui Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block". Organic letters, 2016, 18, 956 |
| 1542701 | CIF | C26 H20 Cl F3 N2 O3 | P 1 21 1 | 10.2811; 11.149; 11.3115 90; 115.56; 90 | 1169.7 | Li, Xiaoyuan; Su, Jinhuan; Liu, Zhourujun; Zhu, Yuanyuan; Dong, Zhenghao; Qiu, Shuai; Wang, Jiayi; Lin, Li; Shen, Zhiqiang; Yan, Wenjin; Wang, Kairong; Wang, Rui Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block". Organic letters, 2016, 18, 956 |
| 1542702 | CIF | C10 H6 F3 N3 O | P -1 | 7.0244; 7.2782; 10.394 99.34; 92.323; 91.732 | 523.55 | Pieber, Bartholomäus; Kappe, C. Oliver Generation and Synthetic Application of Trifluoromethyl Diazomethane Utilizing Continuous Flow Technologies. Organic letters, 2016, 18, 1076 |
| 1542703 | CIF | C16 H15 F5 O3 S | P -1 | 5.584; 11.7071; 12.0947 85.184; 83.294; 87.881 | 782.18 | Friese, Florian W.; Dreier, Anna-Lena; Matsnev, Andrej V.; Daniliuc, Constantin G.; Thrasher, Joseph S.; Haufe, Günter Anti-Selective Aldol Reactions of Pentafluorosulfanylacetic Acid Esters with Aldehydes Mediated by Dicyclohexylchloroborane. Organic letters, 2016, 18, 1012 |
| 1542704 | CIF | C17 H23 Cl2 F5 O3 S | P -1 | 10.0879; 13.4704; 16.5159 66.318; 85.001; 89.698 | 2046.4 | Friese, Florian W.; Dreier, Anna-Lena; Matsnev, Andrej V.; Daniliuc, Constantin G.; Thrasher, Joseph S.; Haufe, Günter Anti-Selective Aldol Reactions of Pentafluorosulfanylacetic Acid Esters with Aldehydes Mediated by Dicyclohexylchloroborane. Organic letters, 2016, 18, 1012 |
| 1542705 | CIF | C19 H19 N O3 | P 1 21 1 | 9.2196; 6.1859; 14.23 90; 94.59; 90 | 809 | Wang, Jie; Wang, Mingyang; Chen, Kehao; Zha, Shanke; Song, Chao; Zhu, Jin C-H Activation-Based Traceless Synthesis via Electrophilic Removal of a Directing Group. Rhodium(III)-Catalyzed Entry into Indoles from N-Nitroso and α-Diazo-β-keto Compounds. Organic letters, 2016, 18, 1178 |
| 1542706 | CIF | C12 H14 N2 O5 | P 1 21/c 1 | 8.922; 19.474; 8.18 90; 111.49; 90 | 1322.4 | Wang, Jie; Wang, Mingyang; Chen, Kehao; Zha, Shanke; Song, Chao; Zhu, Jin C-H Activation-Based Traceless Synthesis via Electrophilic Removal of a Directing Group. Rhodium(III)-Catalyzed Entry into Indoles from N-Nitroso and α-Diazo-β-keto Compounds. Organic letters, 2016, 18, 1178 |
| 1542707 | CIF | C21 H29 N O6 | P 1 21/n 1 | 15.7725; 9.1679; 16.4313 90; 115.84; 90 | 2138.41 | Shen, Xin-Yue; Peng, Xiao-Shui; Wong, Henry N. C. Total Synthesis of (±)-Gracilioether F. Organic letters, 2016, 18, 1032 |
| 1542708 | CIF | C14 H18 F N O4 S | P 21 21 21 | 7.0953; 12.6329; 16.757 90; 90; 90 | 1502 | Wu, Liang; Chen, Pinhong; Liu, Guosheng Pd(II)-Catalyzed Aminofluorination of Alkenes in Total Synthesis 6-(R)-Fluoroswainsonine and 5-(R)-Fluorofebrifugine. Organic letters, 2016, 18, 960 |
| 1542709 | CIF | C22 H17 N3 O2 | P -1 | 3.8508; 12.3597; 18.3893 82.341; 88.727; 87.157 | 866.25 | Kumar, Gangam Srikanth; Kapur, Manmohan Ruthenium-Catalyzed, Site-Selective C-H Allylation of Indoles with Allyl Alcohols as Coupling Partners. Organic letters, 2016, 18, 1112 |
| 1542710 | CIF | C22 H18 Br N O | P 21 21 21 | 9.7821; 10.3912; 35.968 90; 90; 90 | 3656.1 | Liu, Zhen-Ting; Wang, Ya-Hui; Zhu, Fu-Lin; Hu, Xiang-Ping Enantioselective Copper-Catalyzed Formal [4 + 2] Cycloaddition of o-Aminophenol Derivatives with Propargylic Esters for Synthesis of Optically Active 3,4-Dihydro-2H-1,4-benzoxazines. Organic letters, 2016, 18, 1190 |
| 1542711 | CIF | C15 H10 Br I O | P 1 21/n 1 | 7.603; 10.723; 16.702 90; 91.919; 90 | 1360.9 | Sasaki, Teppei; Miyagi, Kotaro; Moriyama, Katsuhiko; Togo, Hideo Direct Preparation of 3-Iodochromenes from 3-Aryl- and 3-Alkyl-2-propyn-1-ols with Diaryliodonium Salts and NIS. Organic letters, 2016, 18, 944 |
| 1542712 | CIF | C18 H16 F N O4 | P 1 21/n 1 | 11.161; 9.295; 15.244 90; 94.06; 90 | 1577.5 | Yang, Chen; Liu, Yang; Yang, Jin-Dong; Li, Yi-He; Li, Xin; Cheng, Jin-Pei Amination of 3-Substituted Benzofuran-2(3H)-ones Triggered by Single-Electron Transfer. Organic letters, 2016, 18, 1036 |
| 1542713 | CIF | C79 H72 N6 O10 | C 1 2/c 1 | 38.088; 12.3446; 34.909 90; 107.222; 90 | 15678 | Bi, Jiahai; Zeng, Xiangfei; Tian, Demei; Li, Haibing Temperature-Responsive Switch Constructed from an Anthracene-Functionalized Pillar[5]arene-Based Host-Guest System. Organic letters, 2016, 18, 1092 |
| 1542714 | CIF | C30 H44 O4 | P 21 21 21 | 8.0564; 12.2225; 28.0933 90; 90; 90 | 2766.33 | Coffinier, Romain; Assal, Mourad El; Peixoto, Philippe A.; Bosset, Cyril; Miqueu, Karinne; Sotiropoulos, Jean-Marc; Pouységu, Laurent; Quideau, Stéphane Total Synthesis of (-)-Bacchopetiolone via an Asymmetric Hydroxylative Phenol Dearomatization/[4+2]-Dimerization Cascade Promoted by a Novel Salen-Type Chiral Iodane. Organic letters, 2016, 18, 1120 |
| 1542715 | CIF | C14 H10 N2 O2 | P 1 21/c 1 | 15.2095; 5.9093; 12.9247 90; 102.997; 90 | 1131.88 | Bhat, Shreesha V.; Robinson, David; Moses, John E.; Sharma, Pallavi Synthesis of Oxadiazol-5-imines via the Cyclizative Capture of in Situ Generated Cyanamide Ions and Nitrile Oxides. Organic letters, 2016, 18, 1100 |
| 1542716 | CIF | C114 H105 Br7 Cl9 N16 O19 | P 1 21/n 1 | 19.423; 23.548; 30.226 90; 98.09; 90 | 13687 | Li, Xuesong; Qi, Ting; Srinivas, Kolupula; Massip, Stéphane; Maurizot, Victor; Huc, Ivan Synthesis and Multibromination of Nanosized Helical Aromatic Amide Foldamers via Segment-Doubling Condensation. Organic letters, 2016, 18, 1044 |
| 1542717 | CIF | C699.6 H691.6 Br14 Cl64.8 N96 O101 | P 1 21/c 1 | 59.25; 37.63; 38.83 90; 104.6; 90 | 83779 | Li, Xuesong; Qi, Ting; Srinivas, Kolupula; Massip, Stéphane; Maurizot, Victor; Huc, Ivan Synthesis and Multibromination of Nanosized Helical Aromatic Amide Foldamers via Segment-Doubling Condensation. Organic letters, 2016, 18, 1044 |
| 1542718 | CIF | C19 H23 N O3 S | P 21 21 21 | 6.101; 15.371; 19.086 90; 90; 90 | 1789.9 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542719 | CIF | C16 H19 N O3 S | P 1 21 1 | 5.804; 22.592; 6.639 90; 115.905; 90 | 783.1 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542720 | CIF | C18 H18 Br N O5 S | P 21 21 21 | 8.115; 11.495; 19.441 90; 90; 90 | 1813.5 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542721 | CIF | C16 H19 N O4 S | P 21 21 21 | 7.758; 10.373; 19.137 90; 90; 90 | 1540 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542722 | CIF | C17 H13 Br F3 N O4 S | P 21 21 21 | 14.6; 14.941; 16.318 90; 90; 90 | 3559.6 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542723 | CIF | C16 H18 Br N O3 S | P 1 21 1 | 5.9781; 19.198; 7.657 90; 108.46; 90 | 833.6 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542724 | CIF | C16 H18 N4 O3 S | P 21 21 21 | 5.4849; 12.639; 24.563 90; 90; 90 | 1702.8 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542725 | CIF | C17 H16 Br N O4 S | P 1 21 1 | 7.819; 11.246; 9.64 90; 94.539; 90 | 845 | Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules. Organic letters, 2016, 18, 896 |
| 1542726 | CIF HKL Paper | C14 H16 O3 | C 1 2/c 1 | 16.401; 6.9386; 20.666 90; 97.089; 90 | 2333.8 | Lough, Alan J.; Carlson, Emily; Tam, William (1a<i>R</i>*,2<i>R</i>*,7<i>S</i>*,7a<i>S</i>*)-<i>rel</i>-3,6-Dimethoxy-2-methyl-1a,2,7,7a-tetrahydro-2,7-epoxy-1<i>H</i>-cyclopropa[<i>b</i>]naphthalene IUCrData, 2016, 1, x160341 |
| 1542727 | CIF HKL Paper | C76 H72 Ag2 Cl N O5 P4 S2 | P -1 | 12.44; 13.07; 13.579 93.489; 117.157; 115.354 | 1682.6 | Li, Yun-Hua; Shao, Yong-Liang μ-Chlorido-bis[(dimethyl sulfoxide-κ<i>O</i>)bis(triphenylphosphane-κ<i>P</i>)silver(I)] nitrate IUCrData, 2016, 1, x160332 |
| 1542728 | CIF HKL Paper | C13 H19 N O3 | P -1 | 5.2542; 10.374; 11.341 94.937; 102.429; 102.811 | 582.8 | Moriguchi, Tetsuji; Kamoto, Ryota; Jalli, Venkataprasad; Tsuge, Akihiko <i>N</i>-Hexyl-3,4-dihydroxybenzamide IUCrData, 2016, 1, x160346 |
| 1542729 | CIF HKL Paper | C32 H48 Cl4 Cu2 N6 O20 | P 1 21/n 1 | 15.262; 9.355; 15.832 90; 92.858; 90 | 2257.6 | Zhu, Xian-Hong; Li, Peng; Chen, Xiao-Wei; Ke, Wen-Shan; Chen, Fei; Zhang, Hua-Xin [μ-<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-Tetrakis(pyridin-2-ylmethyl)butane-1,4-diamine]bis[(dimethanol-κ<i>O</i>)(perchlorato-κ<i>O</i>)copper(II)] bis(perchlorate) IUCrData, 2016, 1, x160344 |
| 1542730 | CIF | C22 H18 | P n a 21 | 22.283; 10.1485; 6.7864 90; 90; 90 | 1534.7 | Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min Divergent reaction pathways in gold-catalyzed cycloisomerization of 1,5-enynes containing a cyclopropane ring: dramatic ortho substituent and temperature effects Chem. Sci., 2016, 7, 4318 |
| 1542731 | CIF | C24 H18 | P 1 21/n 1 | 7.4014; 11.2513; 19.726 90; 91.021; 90 | 1642.4 | Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min Divergent reaction pathways in gold-catalyzed cycloisomerization of 1,5-enynes containing a cyclopropane ring: dramatic ortho substituent and temperature effects Chem. Sci., 2016, 7, 4318 |
| 1542732 | CIF | C19 H18 O | P 1 21/n 1 | 9.9373; 5.8477; 23.768 90; 98.064; 90 | 1367.5 | Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min Divergent reaction pathways in gold-catalyzed cycloisomerization of 1,5-enynes containing a cyclopropane ring: dramatic ortho substituent and temperature effects Chem. Sci., 2016, 7, 4318 |
| 1542733 | CIF | C19 H19 Cl O5 | P -1 | 7.9475; 10.528; 11.586 93.439; 108.109; 96.394 | 911.1 | Che, Chao; Huang, Qianwen; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed cascade annulation of unsaturated α-bromocarbonyls with enynals: a facile access to ketones from aldehydes Chem. Sci., 2016, 7, 4134 |
| 1542734 | CIF | C20 H22 O5 | P -1 | 8.172; 9.085; 13.302 85.887; 79.292; 63.379 | 867.4 | Che, Chao; Huang, Qianwen; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed cascade annulation of unsaturated α-bromocarbonyls with enynals: a facile access to ketones from aldehydes Chem. Sci., 2016, 7, 4134 |
| 1542735 | CIF | C19 H19 Cl O6 | P -1 | 9.9793; 11.954; 15.515 90.309; 90.735; 101.28 | 1814.9 | Che, Chao; Huang, Qianwen; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed cascade annulation of unsaturated α-bromocarbonyls with enynals: a facile access to ketones from aldehydes Chem. Sci., 2016, 7, 4134 |
| 1542736 | CIF | C22 H19 F6 N4 O8 Os S2 | P 1 21/n 1 | 14.8667; 23.2445; 16.5946 90; 91.203; 90 | 5733.31 | Sugimoto, Hideki; Kanetake, Takayuki; Maeda, Kazuki; Itoh, Shinobu Oxidative Cyclization of 1,5-Dienes with Hydrogen Peroxide Catalyzed by an Osmium(III) Complex: Synthesis of cis-Tetrahydrofurans. Organic letters, 2016, 18, 1246-1249 |
| 1542737 | CIF | C15 H15 N O5 | C 1 2/c 1 | 28.1106; 5.872; 21.0927 90; 130.543; 90 | 2645.79 | Wendler, Felix; Rudolph, Tobias; Görls, Helmar; Jasinski, Nils; Trouillet, Vanessa; Barner-Kowollik, Christopher; Schacher, Felix H. Maleimide-functionalized poly(2-ethyl-2-oxazoline): synthesis and reactivity Polym. Chem., 2016, 7, 2419 |
| 1542741 | CIF | C27 H19 N3 O | P 1 21/c 1 | 4.832; 30.042; 13.79 90; 90.81; 90 | 2001.6 | Wang, Fen; Wang, He; Wang, Qiang; Yu, Songjie; Li, Xingwei Co(III)-Catalyzed Synthesis of Quinazolines via C-H Activation of N-Sulfinylimines and Benzimidates. Organic letters, 2016, 18, 1306-1309 |
| 1542742 | CIF | C33 H40 O7 S | P 1 21 1 | 11.0077; 9.7685; 14.9709 90; 103.216; 90 | 1567.17 | Vibhute, Amol M.; Dhaka, Arun; Athiyarath, Vignesh; Sureshan, Kana M. A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors Chem. Sci., 2016, 7, 4259 |
| 1542743 | CIF | C22 H16 Cl N O2 S | P 1 21/c 1 | 10.375; 16.767; 10.757 90; 97.534; 90 | 1855.1 | Zhang, Liangliang; Chen, Su; Gao, Yuzhen; Zhang, Pengbo; Wu, Yile; Tang, Guo; Zhao, Yufen tert-Butyl Hydroperoxide Mediated Cascade Synthesis of 3-Arylsulfonylquinolines. Organic letters, 2016, 18, 1286-1289 |
| 1542744 | CIF | C14 H17 N O3 | P b c a | 9.1055; 9.4967; 30.8939 90; 90; 90 | 2671.46 | Zhu, Chuanle; Li, Jiawei; Chen, Pengquan; Wu, Wanqing; Ren, Yanwei; Jiang, Huanfeng Transition-Metal-Free Cyclopropanation of 2-Aminoacrylates with N-Tosylhydrazones: A General Route to Cyclopropane α-Amino Acid with Contiguous Quaternary Carbon Centers. Organic letters, 2016, 18, 1470-1473 |
| 1542745 | CIF | C16 H19 N O5 | P 1 21/c 1 | 8.8082; 19.624; 9.7487 90; 95.42; 90 | 1677.5 | Zhu, Chuanle; Li, Jiawei; Chen, Pengquan; Wu, Wanqing; Ren, Yanwei; Jiang, Huanfeng Transition-Metal-Free Cyclopropanation of 2-Aminoacrylates with N-Tosylhydrazones: A General Route to Cyclopropane α-Amino Acid with Contiguous Quaternary Carbon Centers. Organic letters, 2016, 18, 1470-1473 |
| 1542746 | CIF | C48 H191 Co5 N40 O126 Sb9 W24 | P 21 3 | 27.1499; 27.1499; 27.1499 90; 90; 90 | 20012.7 | Zhang, Zhi-Ming; Duan, Xiaopin; Yao, Shuang; Wang, Zhishu; Lin, Zekai; Li, Yang-Guang; Long, La-Sheng; Wang, En-Bo; Lin, Wenbin Cation-mediated optical resolution and anticancer activity of chiral polyoxometalates built from entirely achiral building blocks Chem. Sci., 2016, 7, 4220 |
| 1542747 | CIF | C60 H235 Cl Co4 N49 O133 Sb9 W24 | P 1 21/c 1 | 21.9241; 26.104; 42.1665 90; 119.618; 90 | 20979 | Zhang, Zhi-Ming; Duan, Xiaopin; Yao, Shuang; Wang, Zhishu; Lin, Zekai; Li, Yang-Guang; Long, La-Sheng; Wang, En-Bo; Lin, Wenbin Cation-mediated optical resolution and anticancer activity of chiral polyoxometalates built from entirely achiral building blocks Chem. Sci., 2016, 7, 4220 |
| 1542748 | CIF | C48 H47 N10 O10.5 S2 | P -1 | 16.853; 17.211; 18.087 99.16; 91.7; 96.78 | 5136.9 | Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L. Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening Chem. Sci., 2016, 7, 4148 |
| 1542749 | CIF | C48 H52 N10 O13 S2 | P 1 21/n 1 | 13.49; 18.126; 20.197 90; 101.26; 90 | 4843.5 | Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L. Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening Chem. Sci., 2016, 7, 4148 |
| 1542750 | CIF | C54 H68 F12 N10 O10 P2 | P -1 | 10.032; 10.288; 15.459 80.45; 80.06; 80.81 | 1535.6 | Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L. Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening Chem. Sci., 2016, 7, 4148 |
| 1542751 | CIF | C40 H39 F12 N11 O2 P2 | P 1 21/n 1 | 11.353; 20.065; 19.117 90; 98.58; 90 | 4306.1 | Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L. Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening Chem. Sci., 2016, 7, 4148 |
| 1542752 | CIF | C40 H41 F12 N11 O3 P2 | C 1 2/c 1 | 28.552; 13.685; 22.641 90; 103.63; 90 | 8597 | Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L. Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening Chem. Sci., 2016, 7, 4148 |
| 1542753 | CIF | C20 H18 O6 | P 1 21/c 1 | 11.2187; 15.6963; 9.3981 90; 90.354; 90 | 1654.9 | Do, Lien T. M.; Aree, Thammarat; Siripong, Pongpun; Pham, Tuyen N. K.; Nguyen, Phung K. P.; Tip-pyang, Santi Bougainvinones A–H, Peltogynoids from the Stem Bark of PurpleBougainvillea spectabilisand Their Cytotoxic Activity Journal of Natural Products, 2016 |
| 1542754 | CIF HKL Paper | C14 H8 I N3 O2 | P 1 21/c 1 | 11.962; 9.0103; 13.2047 90; 109.893; 90 | 1338.29 | Moreno-Fuquen, Rodolfo; Garcia, Andres C.; Abonia, Rodrigo; Jaramillo-Gómez, Luz M.; Kennedy, Alan R. (<i>Z</i>)-<i>N</i>-(2-Iodophenyl)-4-nitrobenzimidoyl cyanide IUCrData, 2016, 1, x160315 |
| 1542755 | CIF HKL Paper | C12 H16 O3 | P 1 21/c 1 | 4.5856; 14.2281; 8.3312 90; 98.515; 90 | 537.57 | Wickramasinhage, Ravindra; McAdam, C. John; Simpson, Jim 2,5-Dimethoxy-3,4,6-trimethylbenzaldehyde IUCrData, 2016, 1, x160307 |
| 1542756 | CIF HKL Paper | C74 H91 Ge2 N5 S2 Si2 | P -1 | 11.0447; 13.4587; 13.9291 64.297; 82.371; 85.629 | 1848.74 | Guo, Wenzhen; Ma, Fengle; Zheng, Wenjun 1,3,7,9-Tetrakis[2,6-bis(1-methylethyl)phenyl]-2,2,8,8-tetraphenyl-5,10-dithia-1,3,7,9-tetraaza-2,8-disila-4,6-digermadispiro[3.1.3.1]decane acetonitrile monosolvate IUCrData, 2016, 1, x160299 |
| 1542757 | CIF HKL Paper | C32 H78 Bi4 Cl16 N14 | P 1 21/c 1 | 12.6427; 18.8486; 15.1377 90; 112.782; 90 | 3325.8 | Tiritiris, Ioannis; Knobloch, Georg; Saur, Stefan; Kantlehner, Willi <i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>',<i>N</i>'',<i>N</i>''-Hexamethylguanidinium di-μ~3~-chlorido-tetra-μ~2~-chlorido-decachloridotetrabismuthate acetonitrile disolvate IUCrData, 2016, 1, x160317 |
| 1542758 | CIF | C17.5 H16 Cl N O2 | P -1 | 5.98282; 11.5033; 22.3942 83.2783; 89.5639; 85.3431 | 1525.57 | García-Domínguez, Patricia; Fehr, Lorenz; Rusconi, Giulia; Nevado, Cristina Palladium-catalyzed incorporation of atmospheric CO2: efficient synthesis of functionalized oxazolidinones Chem. Sci., 2016, 7, 3914 |
| 1542759 | CIF | C10 H9 N O2 | P 1 21/n 1 | 7.498; 5.69208; 19.4188 90; 90.668; 90 | 828.72 | García-Domínguez, Patricia; Fehr, Lorenz; Rusconi, Giulia; Nevado, Cristina Palladium-catalyzed incorporation of atmospheric CO2: efficient synthesis of functionalized oxazolidinones Chem. Sci., 2016, 7, 3914 |
| 1542760 | CIF | C20 H19 N O4 | P -1 | 12.43088; 15.8294; 18.0723 92.4918; 101.882; 100.546 | 3408.97 | García-Domínguez, Patricia; Fehr, Lorenz; Rusconi, Giulia; Nevado, Cristina Palladium-catalyzed incorporation of atmospheric CO2: efficient synthesis of functionalized oxazolidinones Chem. Sci., 2016, 7, 3914 |
| 1542761 | CIF | C15 H19 Br2 Cl O3 | P 1 21 1 | 15.775; 7.137; 16.382 90; 107.97; 90 | 1754.4 | Gutiérrez-Cepeda, Adrián; Fernández, José J; Norte, Manuel; López-Rodríguez, Matías; Brito, Iván; Muller, Christian D.; Souto, María L Additional Insights into the Obtusallene Family: Components of Laurencia marilzae. Journal of natural products, 2016, 79, 1184-1188 |
| 1542762 | CIF | C20 H31 N3 O | P 21 21 21 | 5.3218; 14.7425; 21.8252 90; 90; 90 | 1712.33 | Li, Xiao-Hui; Zhang, Yu; Zhang, Jia-Hui; Li, Xiao-Nian; Cao, Ming-Ming; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Hao, Xiao-Jiang Myritonines A-C, Alkaloids from Myrioneuron tonkinensis Based on a Novel Hexacyclic Skeleton. Journal of natural products, 2016, 79, 1203-1207 |
| 1542763 | CIF | C20 H33 N3 | P 21 21 21 | 5.4602; 17.7085; 18.1951 90; 90; 90 | 1759.3 | Li, Xiao-Hui; Zhang, Yu; Zhang, Jia-Hui; Li, Xiao-Nian; Cao, Ming-Ming; Di, Ying-Tong; Peng, Zong-Gen; Jiang, Jian-Dong; Hao, Xiao-Jiang Myritonines A-C, Alkaloids from Myrioneuron tonkinensis Based on a Novel Hexacyclic Skeleton. Journal of natural products, 2016, 79, 1203-1207 |
| 1542764 | CIF | C50 H45 Cl F12 N10 O3 P2 Ru2 | C 1 2/c 1 | 36.067; 15.5582; 18.7893 90; 92.869; 90 | 10530.2 | Roeser, Stephan; Bozoglian, Fernando; Richmond, Craig J.; League, Aaron B.; Ertem, Mehmed Z.; Francàs, Laia; Miró, Pere; Benet-Buchholz, Jordi; Cramer, Christopher J.; Llobet, Antoni Water oxidation catalysis with ligand substituted Ru‒bpp type complexes Catal. Sci. Technol., 2016, 6, 5088 |
| 1542765 | CIF | C50.5 H43.25 Cl2 N13.75 O10 Ru2 | P 1 21/n 1 | 15.1819; 26.556; 15.5336 90; 112.382; 90 | 5790.9 | Roeser, Stephan; Bozoglian, Fernando; Richmond, Craig J.; League, Aaron B.; Ertem, Mehmed Z.; Francàs, Laia; Miró, Pere; Benet-Buchholz, Jordi; Cramer, Christopher J.; Llobet, Antoni Water oxidation catalysis with ligand substituted Ru‒bpp type complexes Catal. Sci. Technol., 2016, 6, 5088 |
| 1542766 | CIF | C14 H15 N O S | P 1 21/c 1 | 17.501; 5.6716; 12.6807 90; 104.641; 90 | 1217.8 | Gu, Zheng-Yang; Cao, Jia-Jia; Wang, Shun-Yi; Ji, Shun-Jun The involvement of the trisulfur radical anion in electron-catalyzed sulfur insertion reactions: facile synthesis of benzothiazine derivatives under transition metal-free conditions Chem. Sci., 2016, 7, 4067 |
| 1542767 | CIF | C45 H56 Cl4 Cs2 N20 O13 Zn | C 1 c 1 | 16.17; 15.723; 22.381 90; 98.896; 90 | 5621.7 | Wei, Lian Tong; Zhang, Yun Qian; Zhou, Kai Zhi; Zhan, Lin Ling; Qu, Yun Xia; Tao, Zhu; Ma, Pei Hua Coordination of fully substituted cyclopentano cucurbit[5]uril with alkali cation in the presence of tetrachloridezicate anion Inorganica Chimica Acta, 2016, 445, 1-7 |
| 1542768 | CIF | C45 H77 Cl5 K2 N20 O23 Zn | P 21 21 21 | 11.478; 15.141; 34.706 90; 90; 90 | 6032 | Wei, Lian Tong; Zhang, Yun Qian; Zhou, Kai Zhi; Zhan, Lin Ling; Qu, Yun Xia; Tao, Zhu; Ma, Pei Hua Coordination of fully substituted cyclopentano cucurbit[5]uril with alkali cation in the presence of tetrachloridezicate anion Inorganica Chimica Acta, 2016, 445, 1-7 |
| 1542769 | CIF | C45 H75 Cl5 N20 Na2 O22 Zn | P 21 21 21 | 11.522; 15.252; 35.056 90; 90; 90 | 6160.5 | Wei, Lian Tong; Zhang, Yun Qian; Zhou, Kai Zhi; Zhan, Lin Ling; Qu, Yun Xia; Tao, Zhu; Ma, Pei Hua Coordination of fully substituted cyclopentano cucurbit[5]uril with alkali cation in the presence of tetrachloridezicate anion Inorganica Chimica Acta, 2016, 445, 1-7 |
| 1542770 | CIF | C45 H56 Cl4 N20 O13 Rb2 Zn | C 1 c 1 | 16.032; 15.689; 22.294 90; 99.974; 90 | 5522.8 | Wei, Lian Tong; Zhang, Yun Qian; Zhou, Kai Zhi; Zhan, Lin Ling; Qu, Yun Xia; Tao, Zhu; Ma, Pei Hua Coordination of fully substituted cyclopentano cucurbit[5]uril with alkali cation in the presence of tetrachloridezicate anion Inorganica Chimica Acta, 2016, 445, 1-7 |
| 1542862 | CIF | C19 H20 Cl2 Cu N4 O9 | P 1 | 8.8284; 10.076; 14.925 76.39; 78.81; 66.84 | 1178.7 | Hallett, Andrew J.; O'Brien, Thomas M.; Carter, Emma; Kariuki, Benson M.; Murphy, Damien M.; Ward, Benjamin D. Copper(II) complexes of pyridine-oxazoline (Pyox) ligands: Coordination chemistry, ligand stability, and catalysis Inorganica Chimica Acta, 2016, 441, 86-94 |
| 1542863 | CIF | C18 H14 Cl Cu2 N3 O11 | P -1 | 8.5615; 10.268; 12.907 101.62; 100.94; 98.19 | 1071.8 | Hallett, Andrew J.; O'Brien, Thomas M.; Carter, Emma; Kariuki, Benson M.; Murphy, Damien M.; Ward, Benjamin D. Copper(II) complexes of pyridine-oxazoline (Pyox) ligands: Coordination chemistry, ligand stability, and catalysis Inorganica Chimica Acta, 2016, 441, 86-94 |
| 1542876 | CIF HKL Paper | C11 H6 Cl N O2 | C 1 2/c 1 | 15.0004; 7.9035; 16.888 90; 101.057; 90 | 1965 | Bargavi, Srinivasan; Kandhasamy, Subramani; Perumal, Paramasivam T.; Lakshmi, Srinivasakannan 5-Chloro-1-(prop-2-ynyl)indoline-2,3-dione IUCrData, 2016, 1, x160397 |
| 1542877 | CIF HKL Paper | C5 H12 F3 N O3 S | P 1 21/m 1 | 10.216; 8.507; 11.445 90; 101.807; 90 | 973.6 | Bourque, Jeremy L.; Baines, Kim M. Tetramethylammonium trifluoromethanesulfonate IUCrData, 2016, 1, x160370 |
| 1542878 | CIF HKL Paper | C39 H90 Bi3 I12 N9 | R -3 | 18.7962; 18.7962; 36.666 90; 90; 120 | 11218.5 | Tiritiris, Ioannis; Knobloch, Georg; Saur, Stefan; Kantlehner, Willi Tris(<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>',<i>N</i>'',<i>N</i>''-hexaethylguanidinium) dodecaiodidotribismuthate(III) IUCrData, 2016, 1, x160391 |
| 1542879 | CIF HKL | C16 H20 Br N O2 | P -1 | 4.5284; 13.2044; 25.9133 96.663; 90.728; 95.393 | 1531.77 | Kharbach, Yassine; Kandri Rodi, Youssef; Capet, Frédéric; Essassi, El Mokhtar; El Ammari, Lahcen 5-Bromo-1-octylindoline-2,3-dione IUCrData, 2016, 1, x160371 |
| 1542880 | CIF HKL Paper | C8 H4 I N O2 | P 1 21/c 1 | 4.0896; 13.2139; 15.1946 90; 92.325; 90 | 820.43 | Golen, James A.; Manke, David R. 7-Iodo-1<i>H</i>-indole-2,3-dione IUCrData, 2016, 1, x160412 |
| 1542881 | CIF HKL Paper | C7 H5 Br O3 | P -1 | 3.9283; 5.9578; 15.1246 92.925; 90.62; 94.71 | 352.28 | Suchetan, P. A.; Suneetha, V.; Naveen, S.; Lokanath, N. K.; Krishna Murthy, P. 4-Bromo-2-hydroxybenzoic acid IUCrData, 2016, 1, x160325 |
| 1542882 | CIF HKL Paper | C9 H14 N2 | P 1 21/c 1 | 8.1735; 12.9313; 8.73 90; 105.803; 90 | 887.83 | Brihi, Ouarda; Hamdouni, Noudjoud; Boulcina, Raouf; Medjani, Meriem; Meinnel, Jean; Boudjada, Ali Diaminomesitylene IUCrData, 2016, 1, x160351 |
| 1542883 | CIF HKL Paper | C33 H68 Li N9 Si6 | P 1 21/c 1 | 23.077; 18.798; 11.169 90; 98.744; 90 | 4789 | Rave, Justin A.; Garcia, Diego A.; Hillesheim, Patrick C.; Guillet, Gary L. Bis[2,6-bis(trimethylsilylamino)pyridine-κ<i>N</i>^1^]{[6-bis(trimethylsilylamino)pyridin-2-yl-κ<i>N</i>^1^](trimethylsilyl)azanido-κ<i>N</i>}lithium IUCrData, 2016, 1, x160338 |
| 1542884 | CIF HKL Paper | C5 H9 Cl3 Ga N | P 1 21/c 1 | 6.517; 19.393; 8.5991 90; 102.287; 90 | 1061.9 | Bourque, Jeremy L.; Tashkandi, Nada Y.; Baines, Kim M. (<i>tert</i>-Butyl isocyanide-κ<i>C</i>)trichloridogallium(III) IUCrData, 2016, 1, x160389 |
| 1542885 | CIF HKL | C19 H16 O | C 1 c 1 | 31.27; 5.672; 7.8812 90; 99.271; 90 | 1379.58 | Adam, Farook; Ameram, Nadiah; Kamath, Shevgoor Dhiraj; Pallavi; Samshuddin, Seranthimata 4-Benzyloxy-1,1'-biphenyl IUCrData, 2016, 1, x160398 |
| 1542886 | CIF HKL Paper | C14 H20 O3 S | P 1 21/c 1 | 11.39; 10.9935; 12.5613 90; 113.79; 90 | 1439.2 | Paquin, Cyrenus T.; Boerth, Donald W.; Golen, James A.; Manke, David R. 4-Methylcyclohexyl <i>p</i>-toluenesulfonate IUCrData, 2016, 1, x160390 |
| 1542887 | CIF HKL | C16 H13 N O2 | P b c a | 14.6122; 8.3882; 20.911 90; 90; 90 | 2563.1 | Sharmila, N.; Sundar, T. V.; Satish, G.; Venkatesan, P. 1-Benzyl-5-methylindoline-2,3-dione IUCrData, 2016, 1, x160381 |
| 1542888 | CIF | C31 H34 N2 O4 P2 Ru | I -4 | 19.4893; 19.4893; 21.1331 90; 90; 90 | 8027 | Tan, Xuefeng; Wang, Guozhen; Zhu, Ziyue; Ren, Conghui; Zhou, Jinping; Lv, Hui; Zhang, Xiaoyong; Chung, Lung Wa; Zhang, Lina; Zhang, Xumu Hydrogenation of Aldehydes Catalyzed by an Available Ruthenium Complex. Organic letters, 2016, 18, 1518-1521 |
| 1542889 | CIF | C14 H18 O6 | P 1 21/c 1 | 6.2663; 14.1771; 16.226 90; 97.633; 90 | 1428.7 | Cao, Tao; Ma, Shengming Highly Stereo- and Regioselective Hydrocarboxylation of Diynes with Carbon Dioxide. Organic letters, 2016, 18, 1510-1513 |
| 1542890 | CIF | C14 H18 O6 | P -1 | 7.9442; 9.3857; 10.6485 68.342; 77.473; 84.276 | 720.18 | Cao, Tao; Ma, Shengming Highly Stereo- and Regioselective Hydrocarboxylation of Diynes with Carbon Dioxide. Organic letters, 2016, 18, 1510-1513 |
| 1542891 | CIF | C23 H18 N2 O | P -1 | 9.556; 10.061; 10.958 73.61; 65.525; 68.71 | 882.6 | Zhang, Jingjing; Gao, Qinghe; Wu, Xia; Geng, Xiao; Wu, Yan-Dong; Wu, Anxin Dual Roles of Methyl Ketones in Radziszewski-Type Reaction: Formal [2 + 1 + 1 + 1] Synthesis of 1,2,5-Trisubstituted Imidazoles. Organic letters, 2016, 18, 1686-1689 |
| 1542892 | CIF | C22 H28 Br2 Cl Fe N4 O6 | P b c n | 10.3027; 14.2644; 18.1624 90; 90; 90 | 2669.18 | Vicente, Ana I.; Joseph, Abhinav; Ferreira, Liliana P.; de Deus Carvalho, Maria; Rodrigues, Vítor H. N.; Duttine, Mathieu; Diogo, Hermínio P.; Minas da Piedade, Manuel E.; Calhorda, Maria José; Martinho, Paulo N. Dynamic spin interchange in a tridentate Fe(iii) Schiff-base compound Chem. Sci., 2016, 7, 4251 |
| 1542893 | CIF | C22 H28 Br2 Cl Fe N4 O6 | P b c n | 11.931; 12.17; 19.166 90; 90; 90 | 2782.9 | Vicente, Ana I.; Joseph, Abhinav; Ferreira, Liliana P.; de Deus Carvalho, Maria; Rodrigues, Vítor H. N.; Duttine, Mathieu; Diogo, Hermínio P.; Minas da Piedade, Manuel E.; Calhorda, Maria José; Martinho, Paulo N. Dynamic spin interchange in a tridentate Fe(iii) Schiff-base compound Chem. Sci., 2016, 7, 4251 |
| 1542894 | CIF | C17 H10.5 N P0.5 | P n m a | 15.8239; 19.3822; 7.8312 90; 90; 90 | 2401.8 | Ren, Yi; Sezen, Melda; Guo, Fang; Jäkle, Frieder; Loo, Yueh-Lin [d]-Carbon‒carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines Chem. Sci., 2016, 7, 4211 |
| 1542895 | CIF | C34.5 H21.5 Cl1.5 N2 O P | P -1 | 11.925; 12.375; 18.662 87.764; 76.46; 83.562 | 2660 | Ren, Yi; Sezen, Melda; Guo, Fang; Jäkle, Frieder; Loo, Yueh-Lin [d]-Carbon‒carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines Chem. Sci., 2016, 7, 4211 |
| 1542896 | CIF | C28 H17 N4 P S | P c c n | 17.008; 32.243; 7.688 90; 90; 90 | 4216 | Ren, Yi; Sezen, Melda; Guo, Fang; Jäkle, Frieder; Loo, Yueh-Lin [d]-Carbon–carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines Chem. Sci., 2016, 7, 4211 |
| 1542897 | CIF | C28 H19 N2 P | P 1 21/n 1 | 8.5379; 12.3661; 20.2417 90; 99.918; 90 | 2105.19 | Ren, Yi; Sezen, Melda; Guo, Fang; Jäkle, Frieder; Loo, Yueh-Lin [d]-Carbon–carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines Chem. Sci., 2016, 7, 4211 |
| 1542898 | CIF | C27 H18 N3 O3 P | P -1 | 10.2381; 13.0126; 17.4162 89.311; 88.175; 67.825 | 2147.6 | Ren, Yi; Sezen, Melda; Guo, Fang; Jäkle, Frieder; Loo, Yueh-Lin [d]-Carbon–carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines Chem. Sci., 2016, 7, 4211 |
| 1542899 | CIF HKL Paper | C23 H18 Cl N5 O4 S | P -1 | 8.1828; 12.1541; 12.3654 114.474; 93.681; 96.949 | 1102.14 | Mague, Joel T.; Mohamed, Shaaban K.; Akkurt, Mehmet; Ahmed, Gamal A.-W.; Bakhite, Etify A.; Albayati, Mustafa R. 2-{[5-(4-Chlorophenoxymethyl)-4-phenyl-4<i>H</i>-1,2,4-triazol-3-yl]sulfanyl}-<i>N</i>-(4-nitrophenyl)acetamide IUCrData, 2016, 1, x160452 |
| 1542900 | CIF HKL Paper | C12 H12 O | P c a 21 | 9.8022; 14.9047; 12.643 90; 90; 90 | 1847.13 | Garozzo, Lee Ann; Nazarenko, Alexander Y. 2-(Naphthalen-1-yl)ethanol IUCrData, 2016, 1, x160423 |
| 1542901 | CIF HKL Paper | C16 H16 N2 O2 | P 1 21/c 1 | 11.7678; 13.0072; 9.9025 90; 112.371; 90 | 1401.66 | Maheswari, R.; Manjula, J.; Gunasekaran, B. (<i>E</i>)-4-Methoxy-<i>N</i>'-(4-methylbenzylidene)benzohydrazide IUCrData, 2016, 1, x160431 |
| 1542902 | CIF HKL Paper | C18 H18 O3 | P b c a | 16.1115; 7.704; 23.873 90; 90; 90 | 2963.2 | Queiroz, Jaqueline Evangelista; Vila Verde, Giuliana Muniz; Pereira, Mariette Miguens; Ramos Silva, Manuela; Aquino, Gilberto L. B. 4-(4-Methoxyphenyl)-5,7-dimethylchroman-2-one IUCrData, 2016, 1, x160430 |
| 1542903 | CIF HKL Paper | C38 H119 O83.5 P2 S17 W18 Zn3 | P -1 | 17.377; 18.889; 19.705 94.766; 90.035; 104.681 | 6233 | Hammami, Imen; Ghandour, Yassine; Belkhiria, Mohamed Salah Hexakis(dimethyl sulfoxide-κ<i>O</i>)zinc <i>mer</i>-aquatris(dimethyl sulfoxide-κ<i>O</i>)(ethanol-κ<i>O</i>)[octadecatungstodiphosphato(V)-κ<i>O</i>]zincate(II)‒dimethyl sulfoxide‒ethanol‒water (2/4/2/3) IUCrData, 2016, 1, x160406 |
| 1542904 | CIF | C24 H37 N O6 | P -1 | 8.0327; 9.3726; 16.1657 77.401; 85.464; 69.356 | 1111.49 | Hagiwara, Koichi; Tabuchi, Toshiki; Urabe, Daisuke; Inoue, Masayuki Expeditious synthesis of the fused hexacycle of puberuline C via a radical-based cyclization/translocation/cyclization process Chem. Sci., 2016, 7, 4372 |
| 1542905 | CIF | C27 H44 O7 | P 21 21 21 | 11.5247; 12.6097; 18.36 90; 90; 90 | 2668.1 | Liu, Hui; Li, Xiao-Ming; Liu, Yang; Zhang, Peng; Wang, Jia-Ning; Wang, Bin-Gui Chermesins A-D: Meroterpenoids with a Drimane-Type Spirosesquiterpene Skeleton from the Marine Algal-Derived Endophytic Fungus Penicillium chermesinum EN-480. Journal of natural products, 2016, 79, 806-811 |
| 1542906 | CIF | C24 H34 O3 | P 21 21 21 | 8.4475; 10.3954; 24.175 90; 90; 90 | 2122.9 | Liu, Hui; Li, Xiao-Ming; Liu, Yang; Zhang, Peng; Wang, Jia-Ning; Wang, Bin-Gui Chermesins A-D: Meroterpenoids with a Drimane-Type Spirosesquiterpene Skeleton from the Marine Algal-Derived Endophytic Fungus Penicillium chermesinum EN-480. Journal of natural products, 2016, 79, 806-811 |
| 1542907 | CIF | C24 H36 O3 | P 21 21 21 | 8.6259; 9.3446; 27.3784 90; 90; 90 | 2206.9 | Liu, Hui; Li, Xiao-Ming; Liu, Yang; Zhang, Peng; Wang, Jia-Ning; Wang, Bin-Gui Chermesins A-D: Meroterpenoids with a Drimane-Type Spirosesquiterpene Skeleton from the Marine Algal-Derived Endophytic Fungus Penicillium chermesinum EN-480. Journal of natural products, 2016, 79, 806-811 |
| 1542908 | CIF | C26 H38 O6 | P 21 21 21 | 8.0099; 8.5188; 35.9835 90; 90; 90 | 2455.3 | Liu, Hui; Li, Xiao-Ming; Liu, Yang; Zhang, Peng; Wang, Jia-Ning; Wang, Bin-Gui Chermesins A-D: Meroterpenoids with a Drimane-Type Spirosesquiterpene Skeleton from the Marine Algal-Derived Endophytic Fungus Penicillium chermesinum EN-480. Journal of natural products, 2016, 79, 806-811 |
| 1542909 | CIF | C17 H19 N3 O2 S3 | P 21 21 21 | 6.088; 12.5452; 23.207 90; 90; 90 | 1772.4 | Igarashi, Yasuhiro; Asano, Daisuke; Sawamura, Masashi; In, Yasuko; Ishida, Toshimasa; Imoto, Masaya Ulbactins F and G, Polycyclic Thiazoline Derivatives with Tumor Cell Migration Inhibitory Activity from Brevibacillus sp. Organic letters, 2016, 18, 1658-1661 |
| 1542910 | CIF | C17 H19 N3 O2 S3 | P 21 21 21 | 9.8806; 10.4876; 17.144 90; 90; 90 | 1776.5 | Igarashi, Yasuhiro; Asano, Daisuke; Sawamura, Masashi; In, Yasuko; Ishida, Toshimasa; Imoto, Masaya Ulbactins F and G, Polycyclic Thiazoline Derivatives with Tumor Cell Migration Inhibitory Activity from Brevibacillus sp. Organic letters, 2016, 18, 1658-1661 |
| 1542911 | CIF | C21 H17 N O7 | P 1 | 8.914; 10.559; 10.6874 82.779; 72.066; 70.261 | 900.55 | Osorio-Planes, Laura; Rodríguez-Escrich, Carles; Pericàs, Miquel A. Removing the superfluous: a supported squaramide catalyst with a minimalistic linker applied to the enantioselective flow synthesis of pyranonaphthoquinones Catal. Sci. Technol., 2016, 6, 4686 |
| 1542912 | CIF | C111 H81 Br2 F18 N15 O22 Zn5 | P -3 | 23.023; 23.023; 16.459 90; 90; 120 | 7555 | Bilbeisi, Rana A.; Prakasam, Thirumurugan; Lusi, Matteo; El Khoury, Roberto; Platas-Iglesias, Carlos; Charbonnière, Loïc J.; Olsen, John-Carl; Elhabiri, Mourad; Trabolsi, Ali [C‒H⋯anion] interactions mediate the templation and anion binding properties of topologically non-trivial metal‒organic structures in aqueous solutions Chem. Sci., 2016, 7, 2524 |
| 1542913 | CIF | C25 H16 N2 | P 1 21/c 1 | 9.94167; 11.68932; 15.15921 90; 107.862; 90 | 1676.76 | Flamholc, Rafał; Zakrzewski, Janusz; Makal, Anna; Brosseau, Arnaud; Métivier, Rémi Synthesis, regioselective aerobic Pd(ii)-catalyzed C-H bond alkenylation and the photophysical properties of pyrenylphenylpyrazoles. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2016, 15, 580-588 |
| 1542914 | CIF | C25 H16 N2 | P 1 21/n 1 | 9.13704; 8.8076; 21.4207 90; 93.0448; 90 | 1721.41 | Flamholc, Rafał; Zakrzewski, Janusz; Makal, Anna; Brosseau, Arnaud; Métivier, Rémi Synthesis, regioselective aerobic Pd(ii)-catalyzed C-H bond alkenylation and the photophysical properties of pyrenylphenylpyrazoles. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2016, 15, 580-588 |
| 1542917 | CIF HKL | C16 H26 Ca N4 O6 S2 | P b c a | 9.3535; 13.8812; 16.9106 90; 90; 90 | 2195.64 | N. Golovnev; M. Molokeev; A. Samoilo; V. Atuchin Influence of alkyl substituents in 1,3-diethyl-2-thiobarbituric acid on the coordination environment in M(H2O)2(1,3-diethyl-2-thiobarbiturate)2 M = Ca2+, Sr2+ Journal of Coordination Chemistry, 2016, 69, 957-965 |
| 1542918 | CIF HKL | C16 H26 N4 O6 S2 Sr | P b c a | 9.529; 14.161; 17.094 90; 90; 90 | 2306.7 | N. Golovnev; M. Molokeev; A. Samoilo; V. Atuchin Influence of alkyl substituents in 1,3-diethyl-2-thiobarbituric acid on the coordination environment in M(H2O)2(1,3-diethyl-2-thiobarbiturate)2 M = Ca2+, Sr2+ Journal of Coordination Chemistry, 2016, 69, 957-965 |
| 1542919 | CIF HKL | B3 Ba2.76 Eu0.24 O15 P3 | P 31 2 1 | 7.104645; 7.104645; 6.986941 90; 90; 120 | 305.424 | Lina Zhang; Minghao Fang; Zhaohui Huang; Yangai Liu; Xin Min; Hao Tang; Kai Chen; Ming Guan; Maxim S. Molokeev Preparation and Luminescence Properties of the Blue-Emitting Phosphor BaBPO5:Eu2+ Science of Advanced Materials, 2016, 8, 1086-1092 |
| 1542920 | CIF HKL | B4 Mn5.64 Ni6.36 O20 | P b a m | 9.1757; 12.3163; 2.9978 90; 90; 90 | 338.78 | Moshkina Evgeniya; Sofronova Svetlana; Veligzhanin Alexey; Molokeev Maxim; Nazarenko Ilya; Eremin Evgeniy; Bezmaternykh Leonard Magnetism and Structure of Ni2MnBO5 ludwigite Journal of Magnetism and Magnetic Materials, 2016, 402, 69-75 |
| 1542921 | CIF HKL | Al24 Eu0.12 O38 Sr1.88 | P 63/m m c | 5.568411; 5.568411; 22.00704 90; 90; 120 | 590.956 | Bin Ma; Qingfeng Guo; Maxim S. Molokeev; Zhenfei Lv; Jun Yao; Lefu Mei; Zhaohui Huang Crystal structure and luminescence properties of green-emitting Sr1-xAl12O19:xEu2+ phosphors Ceramics International, 2016, 42, 5995-5999 |
| 1542922 | CIF HKL | Al24 Eu0.16 O38 Sr1.84 | P 63/m m c | 5.568011; 5.568011; 22.00807 90; 90; 120 | 590.898 | Bin Ma; Qingfeng Guo; Maxim S. Molokeev; Zhenfei Lv; Jun Yao; Lefu Mei; Zhaohui Huang Crystal structure and luminescence properties of green-emitting Sr1-xAl12O19:xEu2+ phosphors Ceramics International, 2016, 42, 5995-5999 |
| 1542923 | CIF | C17 H26 O Si | P 1 21/c 1 | 8.7087; 31.9349; 14.3643 90; 123.574; 90 | 3328.42 | Kanno, Hiroshi; Nakamura, Kyosuke; Noguchi, Keiichi; Shibata, Yu; Tanaka, Ken Rhodium-Catalyzed Cycloisomerization of 2-Silylethynyl Phenols and Anilines via 1,2-Silicon Migration. Organic letters, 2016, 18, 1654-1657 |
| 1542924 | CIF | C18 H20 N2 O4 | P 1 21/c 1 | 16.557; 10.8619; 9.5381 90; 99.792; 90 | 1690.3 | Hu, Zhiyong; Tong, Xiaofeng; Liu, Guixia Rhodium(III) Catalyzed Carboamination of Alkenes Triggered by C-H Activation of N-Phenoxyacetamides under Redox-Neutral Conditions. Organic letters, 2016, 18, 1702-1705 |
| 1542925 | CIF | C32 H32 B N S | P 1 21/n 1 | 9.841; 15.741; 17.1529 90; 104.041; 90 | 2577.72 | Shi, Yong-Gang; Yang, Deng-Tao; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning 1,1-Hydroboration of Fused Azole-Isoindole Analogues as an Approach for Construction of B,N-Heterocycles and Azole-Fused B,N-Naphthalenes. Organic letters, 2016, 18, 1626-1629 |
| 1542926 | CIF | C34 H36 B N3 | P 1 21/c 1 | 21.303; 13.582; 9.6038 90; 95.171; 90 | 2767.4 | Shi, Yong-Gang; Yang, Deng-Tao; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning 1,1-Hydroboration of Fused Azole-Isoindole Analogues as an Approach for Construction of B,N-Heterocycles and Azole-Fused B,N-Naphthalenes. Organic letters, 2016, 18, 1626-1629 |
| 1542927 | CIF | C38 H56 N4 O2 | P 1 21/n 1 | 18.6106; 9.3237; 20.2857 90; 98.941; 90 | 3477.2 | Wezenberg, Sander J.; Croisetu, Christelle M.; Stuart, Marc C. A.; Feringa, Ben L. Reversible gel–sol photoswitching with an overcrowded alkene-based bis-urea supergelator Chem. Sci., 2016, 7, 4341 |
| 1542928 | CIF | C80 H76 Ce Li2 O11 | P 1 21/c 1 | 15.7715; 12.9851; 32.521 90; 97.852; 90 | 6597.7 | Robinson, Jerome R.; Qiao, Yusen; Gu, Jun; Carroll, Patrick J.; Walsh, Patrick J.; Schelter, Eric J. The role of dynamic ligand exchange in the oxidation chemistry of cerium(iii) Chem. Sci., 2016, 7, 4537 |
| 1542929 | CIF | C97 H112 Ce Li3 O14 | P -1 | 15.6917; 16.7884; 18.8233 111.706; 103.016; 97.558 | 4360.6 | Robinson, Jerome R.; Qiao, Yusen; Gu, Jun; Carroll, Patrick J.; Walsh, Patrick J.; Schelter, Eric J. The role of dynamic ligand exchange in the oxidation chemistry of cerium(iii) Chem. Sci., 2016, 7, 4537 |
| 1542930 | CIF | C18 H15 N O3 S | P -1 | 8.0503; 8.2338; 12.787 78.396; 73.972; 85.069 | 797.6 | Murayama, Hiroaki; Nagao, Kazunori; Ohmiya, Hirohisa; Sawamura, Masaya Phosphine-Catalyzed Vicinal Acylcyanation of Alkynoates. Organic letters, 2016, 18, 1706-1709 |
| 1542931 | CIF HKL Paper | C16 H15 N3 O4 | P 1 21/c 1 | 13.1432; 13.613; 8.3381 90; 98.495; 90 | 1475.5 | Inturi, Bharathkumar; Roopashree, K. R.; Pujar, Gurubasavaraj V.; Mohammed, Irfan Ali; Devarajegowda, H. C. 2-Methoxy-4-[3-(3-nitrophenyl)-4,5-dihydro-1<i>H</i>-pyrazol-5-yl]phenol IUCrData, 2016, 1, x160466 |
| 1542932 | CIF HKL Paper | C28 H43 N | P 1 21/c 1 | 17.7676; 13.138; 11.4852 90; 108.261; 90 | 2546 | Wang, Limin; Wang, Shengpei; Liu, Shenggao Bis[4-(2,4,4-trimethylpentan-2-yl)phenyl]amine IUCrData, 2016, 1, x160424 |
| 1542933 | CIF HKL Paper | C39 H72 Bi2 I9 N9 | C 1 2/c 1 | 14.1643; 16.7047; 24.9505 90; 91.601; 90 | 5901.2 | Tiritiris, Ioannis; Knobloch, Georg; Saur, Stefan; Kantlehner, Willi Tris(pyrrolidin-1-yl)carbenium tri-μ-iodido-bis[triiodidobismuthate(III)] IUCrData, 2016, 1, x160427 |
| 1542934 | CIF HKL | C4 H6 N2 S2 | P 1 21/c 1 | 15.2211; 12.2037; 14.4716 90; 98.788; 90 | 2656.6 | Diop, Mouhamadou Birame; Diop, Libasse; Oliver, Allen G. Dimethyl <i>N</i>-cyanodithioiminocarbonate IUCrData, 2016, 1, x160454 |
| 1542935 | CIF HKL Paper | C22 H20 Cl2 N2 O | P c a 21 | 20.9334; 10.2009; 9.0493 90; 90; 90 | 1932.4 | Adam, Farook; Ameram, Nadiah; Samshuddin, Seranthimata; Akhilesh Bairy, Kurady; Shivashankarappa Sunil, Madhugiri 1-[(7<i>E</i>)-7-(2-Chlorobenzylidene)-3-(2-chlorophenyl)-3,3a,4,5,6,7-hexahydro-2<i>H</i>-indazol-2-yl]ethanone IUCrData, 2016, 1, x160474 |
| 1542936 | CIF HKL Paper | C10 H7 N3 O2 | P 1 21/n 1 | 4.0105; 21.0705; 10.7451 90; 96.323; 90 | 902.47 | Boulhaoua, Mohammed; El Hafi, Mohamed; Benchidmi, Mohammed; Essassi, El Mokhtar; Mague, Joel T. 5-Nitro-1-(prop-2-yn-1-yl)-1<i>H</i>-indazole IUCrData, 2016, 1, x160480 |
| 1542937 | CIF HKL Paper | C14 H19 N7 | P 21 21 21 | 7.7705; 9.8189; 21.5478 90; 90; 90 | 1644.05 | Tiritiris, Ioannis; Kress, Ralf; Kantlehner, Willi <i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>',<i>N</i>'',<i>N</i>''-Hexamethylguanidinium 1,1,3,3-tetracyanoprop-2-en-1-ide IUCrData, 2016, 1, x160478 |
| 1542938 | CIF | C11 H6 N O5 Zn | C 1 2/m 1 | 11.191; 14.136; 7.975 90; 106.894; 90 | 1207.2 | Yang, Xiaogang; Yan, Dongpeng Long-afterglow metal‒organic frameworks: reversible guest-induced phosphorescence tunability Chem. Sci., 2016, 7, 4519 |
| 1542939 | CIF | C40 H60 N P2 Pd | P -1 | 9.9475; 13.7704; 14.6585 98.995; 100.851; 97.3666 | 1921.9 | Cui, Peng; Hoffbauer, Melissa R.; Vyushkova, Mariya; Iluc, Vlad M. Heterobimetallic Pd‒K carbene complexes via one-electron reductions of palladium radical carbenes Chem. Sci., 2016, 7, 4444 |
| 1542940 | CIF | C45 H62 N P2 Pd | C 1 2/c 1 | 20.2994; 17.5268; 15.9561 90; 123.775; 90 | 4718.8 | Cui, Peng; Hoffbauer, Melissa R.; Vyushkova, Mariya; Iluc, Vlad M. Heterobimetallic Pd‒K carbene complexes via one-electron reductions of palladium radical carbenes Chem. Sci., 2016, 7, 4444 |
| 1542941 | CIF | C40 H59 K P2 Pd | C 1 2/c 1 | 26.989; 12.0603; 23.568 90; 96.879; 90 | 7616.1 | Cui, Peng; Hoffbauer, Melissa R.; Vyushkova, Mariya; Iluc, Vlad M. Heterobimetallic Pd‒K carbene complexes via one-electron reductions of palladium radical carbenes Chem. Sci., 2016, 7, 4444 |
| 1542942 | CIF | C49 H72 K N O P2 Pd | P 1 21/n 1 | 10.2409; 18.169; 25.743 90; 90.553; 90 | 4789.7 | Cui, Peng; Hoffbauer, Melissa R.; Vyushkova, Mariya; Iluc, Vlad M. Heterobimetallic Pd‒K carbene complexes via one-electron reductions of palladium radical carbenes Chem. Sci., 2016, 7, 4444 |
| 1542943 | CIF | C23 H17 F4 N O | P 1 2/c 1 | 13.0334; 8.6509; 17.4221 90; 101.862; 90 | 1922.41 | Wu, Xin-Xing; Chen, Wen-Long; Shen, Yi; Chen, Si; Xu, Peng-Fei; Liang, Yong-Min Palladium-Catalyzed Domino Heck/Intermolecular C-H Bond Functionalization: Efficient Synthesis of Alkylated Polyfluoroarene Derivatives. Organic letters, 2016, 18, 1784-1787 |
| 1542944 | CIF | C16 H11 F5 O | P b c a | 22.905; 7.8263; 15.601 90; 90; 90 | 2796.7 | Wu, Xin-Xing; Chen, Wen-Long; Shen, Yi; Chen, Si; Xu, Peng-Fei; Liang, Yong-Min Palladium-Catalyzed Domino Heck/Intermolecular C-H Bond Functionalization: Efficient Synthesis of Alkylated Polyfluoroarene Derivatives. Organic letters, 2016, 18, 1784-1787 |
| 1542945 | CIF | C28 H40 O4 | P 1 21/n 1 | 11.2485; 11.2825; 20.3694 90; 100.559; 90 | 2541.33 | Yang, Xing-Wei; Li, Yan-Ping; Su, Jia; Ma, Wei-Guang; Xu, Gang Hyperjapones A-E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum. Organic letters, 2016, 18, 1876-1879 |
| 1542946 | CIF | C29 H42 O4 | P 1 21 1 | 10.7495; 10.9897; 11.3193 90; 106.928; 90 | 1279.25 | Yang, Xing-Wei; Li, Yan-Ping; Su, Jia; Ma, Wei-Guang; Xu, Gang Hyperjapones A-E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum. Organic letters, 2016, 18, 1876-1879 |
| 1542947 | CIF | C29 H42 O4 | P 1 21 1 | 11.0867; 10.5463; 11.7485 90; 109.197; 90 | 1297.29 | Yang, Xing-Wei; Li, Yan-Ping; Su, Jia; Ma, Wei-Guang; Xu, Gang Hyperjapones A-E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum. Organic letters, 2016, 18, 1876-1879 |
| 1542948 | CIF | C28 H40 O4 | P 21 21 21 | 8.6184; 16.3163; 17.7667 90; 90; 90 | 2498.36 | Yang, Xing-Wei; Li, Yan-Ping; Su, Jia; Ma, Wei-Guang; Xu, Gang Hyperjapones A-E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum. Organic letters, 2016, 18, 1876-1879 |
| 1542949 | CIF | C29 H44 O4 | P 1 21 1 | 13.38314; 6.24052; 16.58575 90; 105.584; 90 | 1334.28 | Hilario-Martínez, J Ciciolil; Zeferino-Díaz, Reyna; Muñoz-Hernández, Miguel A; Hernández-Linares, Ma Guadalupe; Cabellos, José Luis; Merino, Gabriel; Sandoval-Ramírez, Jesús; Jin, Zhendong; Fernández-Herrera, María A Regioselective Spirostan E-Ring Opening for the Synthesis of Dihydropyran Steroidal Frameworks. Organic letters, 2016, 18, 1772-1775 |
| 1542950 | CIF | C22 H22 F6 I N3 O8 S2 | P -1 | 11.2415; 12.0721; 12.4456 71.657; 70.424; 72.905 | 1476.55 | Kelley, Brandon T.; Walters, Jennifer C.; Wengryniuk, Sarah E. Access to Diverse Oxygen Heterocycles via Oxidative Rearrangement of Benzylic Tertiary Alcohols. Organic letters, 2016, 18, 1896-1899 |
| 1542951 | CIF | C20 H18 F6 O2 | P -1 | 9.2002; 9.5076; 11.4762 101.253; 101.453; 103.53 | 925.3 | Kelley, Brandon T.; Walters, Jennifer C.; Wengryniuk, Sarah E. Access to Diverse Oxygen Heterocycles via Oxidative Rearrangement of Benzylic Tertiary Alcohols. Organic letters, 2016, 18, 1896-1899 |
| 1542952 | CIF | C20 H22 N2 O3 S | P 1 21/c 1 | 13.5634; 9.094; 15.4845 90; 100.494; 90 | 1878 | Kim, Youyoung; Park, Juhyeon; Chang, Sukbok A Direct Access to 7-Aminoindoles via Iridium-Catalyzed Mild C-H Amidation of N-Pivaloylindoles with Organic Azides. Organic letters, 2016, 18, 1892-1895 |
| 1542953 | CIF | C22 H15 Br N2 O | P -1 | 7.9172; 9.9111; 12.2268 71.212; 89.404; 76.745 | 882 | Martinez-Ariza, Guillermo; McConnell, Nicholas; Hulme, Christopher One-Pot Two-Step Multicomponent Process of Indole and Other Nitrogenous Heterocycles or Amines toward α-Oxo-acetamidines. Organic letters, 2016, 18, 1864-1867 |
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