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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1550392 | CIF | Co Li0.5 O2 | R -3 m :H | 2.8127; 2.8127; 14.2754 90; 90; 120 | 97.806 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550393 | CIF | Co Li0.58 O2 | R -3 m :H | 2.8145; 2.8145; 14.2475 90; 90; 120 | 97.74 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550394 | CIF | Co Li0.79 O2 | R -3 m :H | 2.8165; 2.8165; 14.093 90; 90; 120 | 96.817 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550395 | CIF | Co Li0.89 O2 | R -3 m :H | 2.8175; 2.8175; 14.0598 90; 90; 120 | 96.658 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550396 | CIF | Co Li0.98 O2 | R -3 m :H | 2.8178; 2.8178; 14.0621 90; 90; 120 | 96.694 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550397 | CIF | Co Li O2 | R -3 m :H | 2.8185; 2.8185; 14.0664 90; 90; 120 | 96.772 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550398 | CIF | Co Li1.16 O2 | R -3 m :H | 2.8176; 2.8176; 14.061 90; 90; 120 | 96.673 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1550399 | CIF | Co Li1.43 O2 | R -3 m :H | 2.8503; 2.8503; 14.139 90; 90; 120 | 99.48 | Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements Ionics, 1997, 3, 345-354 |
| 1552859 | CIF HKL Paper | C36 H38 Cl4 Cu2 N6 O2 | P 1 21/n 1 | 12.004; 9.7942; 17.4116 90; 107.633; 90 | 1950.9 | Naugle, Mercedes S.; Keller, Brittany T.; Zeller, Matthias; Zaleski, Curtis M. Di-μ-chlorido-bis[chlorido(dimethylformamide-κ<i>N</i>)(3,5-diphenyl-1<i>H</i>-pyrazole-κ<i>N</i>^2^)copper(II)] IUCrData, 2018, 3, x181186 |
| 1552860 | CIF HKL Paper | C34 H45 Li Mo N4 O4 P2 | P -1 | 11.7633; 12.5731; 13.7249 87.283; 75.537; 67.45 | 1812.66 | Höhne, Martha; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe Tetracarbonyl-2κ^4^<i>C</i>-[μ-5-methyl-1,1,3-triphenyl-2-(propan-2-yl)-2,4-diaza-1,3-diphosphahexan-4-ido-1κ<i>N</i>^4^:2κ<i>P</i>^1^,<i>P</i>^3^](<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-tetramethylethane-1,2-diamine-1κ^2^<i>N</i>,<i>N</i>')lithiummolybdenum IUCrData, 2018, 3, x181149 |
| 1553182 | CIF | C20 H19 N O7 | P 1 21/c 1 | 11.3454; 13.013; 12.3899 90; 91.009; 90 | 1828.93 | Kulkarni, Anand M.; Srinivas, Kolluru; Deshpande, Mukund V.; Ramana, Chepuri V. Cu-catalyzed sequential C–N bond formations: expeditious synthesis of tetracyclic indoloindol-3-ones Organic Chemistry Frontiers, 2016, 3, 43 |
| 1553195 | CIF | C24 H22 N4 O4 | P 21 21 21 | 7.6889; 15.5382; 16.4272 90; 90; 90 | 1962.58 | Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach Organic Chemistry Frontiers, 2016, 3, 24 |
| 1553196 | CIF | C24 H26 N4 O6 | P -1 | 9.32; 10.5489; 12.1772 95.818; 90.49; 111.805 | 1104.44 | Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach Organic Chemistry Frontiers, 2016, 3, 24 |
| 1553197 | CIF | C15 H24 Br N O5 | P -1 | 8.8508; 10.0352; 10.7879 116.066; 107.114; 90.5266 | 811.83 | Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S. Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates Organic Chemistry Frontiers, 2016, 3, 330 |
| 1553198 | CIF | C14 H23 Cl2 N O5 | P 1 21/n 1 | 11.7775; 8.7429; 16.8595 90; 105.852; 90 | 1670 | Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S. Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates Organic Chemistry Frontiers, 2016, 3, 330 |
| 1553199 | CIF | C13 H19 N O4 | P 1 21/n 1 | 11.3134; 9.429; 12.7345 90; 110.991; 90 | 1268.29 | Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S. Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates Organic Chemistry Frontiers, 2016, 3, 330 |
| 1553200 | CIF | C15 H21 N O4 | P 1 21/c 1 | 17.0197; 16.271; 10.1414 90; 99.0774; 90 | 2773.26 | Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S. Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates Organic Chemistry Frontiers, 2016, 3, 330 |
| 1553201 | CIF | C13 H19 N O5 | P 1 21/n 1 | 10.9816; 9.2222; 13.0751 90; 107.689; 90 | 1261.57 | Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S. Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates Organic Chemistry Frontiers, 2016, 3, 330 |
| 1553202 | CIF | C25 H32 Cl Ir N2 | P 1 21/n 1 | 13.083; 9.848; 18.876 90; 93.26; 90 | 2428.1 | Tang, Guo-Dong; Pan, Cheng-Ling; Li, Xingwei Iridium(iii)- and rhodium(iii)-catalyzed coupling of anilines with α-diazoesters via chelation-assisted C‒H activation Organic Chemistry Frontiers, 2016, 3, 87 |
| 1553203 | CIF | C27 H29 N O2 | P 1 21/c 1 | 15.5737; 12.7774; 11.4615 90; 91.399; 90 | 2280.06 | Roy, Tony; Bhojgude, Sachin Suresh; Kaicharla, Trinadh; Thangaraj, Manikandan; Garai, Bikash; Biju, Akkattu T. Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines Organic Chemistry Frontiers, 2016, 3, 71 |
| 1553204 | CIF | C12 H14 O2 | P 1 21/c 1 | 9.8964; 7.7982; 13.421 90; 91.267; 90 | 1035.5 | Ling, Jesse; Lam, Sze Kui; Lo, Brian; Lam, Sarah; Wong, Wing-Tak; Sun, Jian; Chen, Guanhua; Chiu, Pauline Epoxy and aziridinyl enolsilanes in diastereoselective inter- and intramolecular Friedel–Crafts alkylations Organic Chemistry Frontiers, 2016, 3, 457 |
| 1553205 | CIF | C22 H20 Cl N O2 S | I 1 a 1 | 11.4861; 14.0594; 13.486 90; 111.393; 90 | 2027.77 | Prabagar, B.; Nayak, Sanatan; Mallick, Rajendra K.; Prasad, Rangu; Sahoo, Akhila K. Triphenylphosphine promoted regio and stereoselective α-halogenation of ynamides Organic Chemistry Frontiers, 2016, 3, 110 |
| 1553206 | CIF | C27 H28 Br N3 O7 S | P 1 21 1 | 11.0065; 8.788; 14.4392 90; 99.424; 90 | 1377.78 | Gerten, Anthony L.; Stanley, Levi M. Enantioselective dearomative [3 + 2] cycloadditions of indoles with azomethine ylides derived from alanine imino esters Organic Chemistry Frontiers, 2016, 3, 339 |
| 1553207 | CIF | C36 H29 Cl O6 | P 21 21 21 | 6.2154; 20.2473; 22.9882 90; 90; 90 | 2893 | Fu, Zhenqian; Wu, Xingxing; Chi, Yonggui Robin Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters Organic Chemistry Frontiers, 2016, 3, 145 |
| 1553208 | CIF | C24 H25 N3 O2 | P -1 | 7.1121; 8.5933; 18.426 94.339; 100.719; 105.418 | 1057.3 | Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes Organic Chemistry Frontiers, 2016, 3, 184 |
| 1553209 | CIF | C28 H26 N2 O3 | P 1 21/c 1 | 15.8733; 11.8466; 12.3385 90; 99.402; 90 | 2289 | Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes Organic Chemistry Frontiers, 2016, 3, 184 |
| 1553210 | CIF | C22 H24 Br2 N2 | P -1 | 9.1241; 10.2171; 11.3635 78.194; 82.379; 72.418 | 985.63 | Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I) Organic Chemistry Frontiers, 2016, 3, 324 |
| 1553211 | CIF | C20 H22 N2 | P -1 | 7.4987; 7.9073; 14.5997 77.721; 79.566; 69.529 | 787.06 | Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I) Organic Chemistry Frontiers, 2016, 3, 324 |
| 1553212 | CIF | C22 H32 N2 O4 | P 21 21 21 | 10.016; 10.025; 21.596 90; 90; 90 | 2168.5 | Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine Organic Chemistry Frontiers, 2016, 3, 62 |
| 1553213 | CIF | C17 H25 Cl N2 O2 | C 2 2 21 | 10.351; 11.942; 26.963 90; 90; 90 | 3332.9 | Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine Organic Chemistry Frontiers, 2016, 3, 62 |
| 1553214 | CIF | C23 H27 Cl6 I N2 | P 1 21/n 1 | 12.0005; 9.4272; 25.9285 90; 101.178; 90 | 2877.7 | Desens, Willi; Kohrt, Christina; Spannenberg, Anke; Werner, Thomas A novel zinc based binary catalytic system for CO2utilization under mild conditions Organic Chemistry Frontiers, 2016, 3, 156 |
| 1553215 | CIF | C16 H17 Cl2 N O4 | P 21 21 21 | 8.3061; 9.701; 20.7173 90; 90; 90 | 1669.35 | Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis Organic Chemistry Frontiers, 2016, 3, 319 |
| 1553216 | CIF | C16 H17 Br2 N O4 | P 1 21 1 | 8.3327; 9.5492; 11.4501 90; 108.133; 90 | 865.84 | Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis Organic Chemistry Frontiers, 2016, 3, 319 |
| 1553217 | CIF | C20 H16 O5 | P -1 | 7.1154; 11.1585; 11.1645 107.811; 95.51; 91.238 | 838.83 | Zhang, Wen-Zhen; Yang, Ming-Wang; Yang, Xu-Tong; Shi, Ling-Long; Wang, Hui-Bo; Lu, Xiao-Bing Double carboxylation of o-alkynyl acetophenone with carbon dioxide Organic Chemistry Frontiers, 2016, 3, 217 |
| 1553218 | CIF | C25 H27 N O2 S | P 1 21/n 1 | 8.6446; 10.8046; 24.326 90; 99.922; 90 | 2238.1 | Li, Jiawen; Qin, Guiping; Liu, Yang; Huang, Hanmin Palladium-catalysed coupling reaction of aminals with N-sulfonyl hydrazones to give allylic sulfones Organic Chemistry Frontiers, 2016, 3, 259 |
| 1553219 | CIF | C20 H28 O2 Si | P 1 21/n 1 | 7.5687; 30.831; 8.0907 90; 90.916; 90 | 1887.7 | Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures Organic Chemistry Frontiers, 2016, 3, 354 |
| 1553220 | CIF | C14 H11 F3 O | P -1 | 7.3733; 11.2959; 14.9182 109.524; 92.663; 101.436 | 1139.24 | Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures Organic Chemistry Frontiers, 2016, 3, 354 |
| 1553221 | CIF | C14 H12 O3 | P 1 2/c 1 | 15.9874; 10.2887; 13.7969 90; 108.28; 90 | 2154.92 | Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures Organic Chemistry Frontiers, 2016, 3, 354 |
| 1553222 | CIF | C14 H13 F O | P b c a | 34.01; 9.158; 7.196 90; 90; 90 | 2241 | Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures Organic Chemistry Frontiers, 2016, 3, 354 |
| 1553223 | CIF | C34 H24 N P | P -1 | 9.9764; 11.8382; 12.5698 115.716; 100.125; 93.876 | 1299.22 | Fu, Wai Chung; Zhou, Zhongyuan; Kwong, Fuk Yee A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses Organic Chemistry Frontiers, 2016, 3, 273 |
| 1553224 | CIF | C19 H16 F N O5 S | P 21 21 21 | 10.342; 12.672; 13.549 90; 90; 90 | 1775.6 | Yu, Jin-Sheng; Zhou, Jian Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines Organic Chemistry Frontiers, 2016, 3, 298 |
| 1553225 | CIF | C17 H14 F2 N2 O4 S | P 21 21 21 | 7.1956; 9.6833; 23.2873 90; 90; 90 | 1622.59 | Yu, Jin-Sheng; Zhou, Jian Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines Organic Chemistry Frontiers, 2016, 3, 298 |
| 1553226 | CIF | C23 H14 Cl2 N2 O | P 1 21/c 1 | 8.9936; 20.9137; 10.6975 90; 112.585; 90 | 1857.78 | Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives Organic Chemistry Frontiers, 2016, 3, 344 |
| 1553227 | CIF | C24 H14 Cl2 N2 O2 | P -1 | 6.3775; 12.1686; 13.4121 80.819; 88.955; 75.537 | 994.7 | Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives Organic Chemistry Frontiers, 2016, 3, 344 |
| 1553228 | CIF | C24 H14 Cl2 N2 O2 | P -1 | 5.2005; 13.556; 15.6215 73.584; 85.49; 87.12 | 1052.7 | Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives Organic Chemistry Frontiers, 2016, 3, 344 |
| 1553229 | CIF | C24 H17 Cl N2 O2 | P 21 21 21 | 8.0462; 9.2337; 26.6656 90; 90; 90 | 1981.2 | Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives Organic Chemistry Frontiers, 2016, 3, 344 |
| 1553230 | CIF | C20 H15 N3 O3 | I 1 2/a 1 | 13.6461; 10.723; 22.268 90; 90.915; 90 | 3258 | Nack, W. A.; Wang, B.; Wu, X.; Jiao, R.; He, G.; Chen, G. Palladium-catalyzed arylation of β-methylene C(sp3)–H bonds at room temperature: desymmetrization of simple cycloalkyl carboxylic acids Organic Chemistry Frontiers, 2016, 3, 561 |
| 1553231 | CIF | C23 H18 N2 O5 | P 1 21 1 | 7.6839; 11.0556; 12.4153 90; 106.486; 90 | 1011.32 | Jiao, Lihui; Zhao, Xiaowei; Liu, Huixin; Ye, Xinyi; Li, Yun; Jiang, Zhiyong Organocatalytic asymmetric conjugate addition of diaryloxazolidin-2,4-diones to nitroolefins: an efficient approach to chiral α-aryl-α-hydroxy carboxylic acids Organic Chemistry Frontiers, 2016, 3, 470 |
| 1553232 | CIF | C38 H34 N O4 P S | P 1 21/c 1 | 13.83; 21.2702; 14.1309 90; 119.452; 90 | 3619.6 | Zhu, Yi-Long; Wang, De-Cai; Jiang, Bo; Hao, Wen-Juan; Wei, Ping; Wang, Ai-Fang; Qiu, Jiang-Kai; Tu, Shu-Jiang Metal-free oxidative hydrophosphinylation of 1,7-enynes Organic Chemistry Frontiers, 2016, 3, 385 |
| 1553233 | CIF | C13 H14 Br N O3 S | P 1 21/c 1 | 20.218; 9.2121; 15.306 90; 95.315; 90 | 2838.5 | Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins Organic Chemistry Frontiers, 2016, 3, 447 |
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