Crystallography Open Database
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Searching year of publication is 2009
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1504172 | CIF | C13 H20 N2 Si | P n a 21 | 10.6; 14.995; 8.7526 90; 90; 90 | 1391.2 | Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes. Organic letters, 2009, 11, 4458-4461 |
| 1504173 | CIF | C27 H30 N4 O2 Si | P -1 | 12.696; 14.502; 15.33 74.95; 71.74; 79.67 | 2573.6 | Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes. Organic letters, 2009, 11, 4458-4461 |
| 1504174 | CIF | C31 H29 Br3 N6 O4 | P -1 | 10.299; 12.584; 12.776 82.36; 88.14; 72.95 | 1568.9 | Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes. Organic letters, 2009, 11, 4458-4461 |
| 1504175 | CIF | C84 H27 Cl2 N O Si | P 1 21/n 1 | 19.1274; 13.9545; 19.5256 90; 108.304; 90 | 4947.96 | Matsuo, Keiko; Matsuo, Yutaka; Iwashita, Akihiko; Nakamura, Eiichi Synthesis of imino[60]fullerenes using nitriles and trimethylsilylmethyl triflate. Organic letters, 2009, 11, 4192-4194 |
| 1504176 | CIF | C22 H26 N2 O2 | P 1 21/c 1 | 8.816; 13.762; 31.213 90; 94.584; 90 | 3774.83 | Grant, Christopher D.; Krische, Michael J. Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution. Organic letters, 2009, 11, 4485-4487 |
| 1504177 | CIF | C22 H19 N O5 | P 21 21 21 | 5.7776; 16.337; 20.021 90; 90; 90 | 1889.8 | Li, Hongyan; Hsung, Richard P. Highly substituted 2-amido-furans from Rh(II)-catalyzed cyclopropenations of ynamides. Organic letters, 2009, 11, 4462-4465 |
| 1504178 | CIF | C79 H95 F12 N7 O16 P2 | P -1 | 14.3156; 15.2385; 21.0682 86.801; 82.424; 66.377 | 4174.1 | Yen, Ming-Liang; Chen, Nai-Chia; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien A molecular cage that selectively complexes three different guests in solution. Organic letters, 2009, 11, 4604-4607 |
| 1504179 | CIF | C28 H27 Cl Cu0.5 N9 O2 | P -1 | 9.6706; 11.7736; 12.4516 80.677; 81.72; 81.309 | 1372.5 | Ozçubukçu, Salih; Ozkal, Erhan; Jimeno, Ciril; Pericàs, Miquel A A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure. Organic letters, 2009, 11, 4680-4683 |
| 1504180 | CIF | C20 H20 O8 | P 1 21 1 | 6.547; 10.892; 12.418 90; 103.542; 90 | 860.9 | Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis. Organic letters, 2009, 11, 4838-4841 |
| 1504181 | CIF | C20 H22 O9 | P -1 | 8.6844; 14.094; 17 73.293; 87.688; 72.958 | 1903.2 | Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis. Organic letters, 2009, 11, 4838-4841 |
| 1504182 | CIF | C24 H36 Cl N2 O7 | P 21 21 21 | 9.268; 13.934; 19.073 90; 90; 90 | 2463.1 | Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong Melohenines A and B, two unprecedented alkaloids from Melodinus henryi Organic Letters, 2009, 11, 4834-4837 |
| 1504183 | CIF | C19 H24 N2 O3 | P 21 21 21 | 7.9717; 12.2181; 17.265 90; 90; 90 | 1681.6 | Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong Melohenines A and B, two unprecedented alkaloids from Melodinus henryi Organic Letters, 2009, 11, 4834-4837 |
| 1504184 | CIF | C15 H11 N3 O2 | P 1 21/c 1 | 19.1116; 4.165; 16.2443 90; 111.391; 90 | 1203.97 | Board, Johnathan; Wang, Jian-Xin; Crew, Andrew P.; Jin, Meizhong; Foreman, Kenneth; Mulvihill, Mark J.; Snieckus, Victor Synthesis of substituted imidazo[1,5-a]pyrazines via mono-, di-, and directed remote metalation strategies. Organic letters, 2009, 11, 5118-5121 |
| 1504185 | CIF | C16 H18 O4 | C 1 2 1 | 18.1933; 7.711; 12.4502 90; 129.39; 90 | 1349.87 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504186 | CIF | C16 H18 O5 | P 21 21 21 | 7.8053; 9.4883; 18.9039 90; 90; 90 | 1400 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504187 | CIF | C17 H20 O5 | C 1 2 1 | 18.1525; 7.6684; 12.0226 90; 101.178; 90 | 1641.81 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504188 | CIF | C16 H18 O5 | P 21 21 21 | 9.597; 9.9935; 14.1873 90; 90; 90 | 1360.67 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504189 | CIF | C19 H24 O4 | P 21 21 21 | 7.7249; 9.6338; 22.5067 90; 90; 90 | 1674.95 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504190 | CIF | C19 H22 O4 | P 21 21 21 | 7.7635; 9.7864; 21.0195 90; 90; 90 | 1596.99 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504191 | CIF | C17 H20 O6 | P 21 21 21 | 6.1894; 8.9465; 28.8255 90; 90; 90 | 1596.17 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504192 | CIF | C16 H18 O6 | P 21 21 21 | 8.2864; 10.0771; 17.1744 90; 90; 90 | 1434.11 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504193 | CIF | C17 H20 O6 | P 21 21 21 | 11.0321; 11.6526; 11.9913 90; 90; 90 | 1541.51 | Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic letters, 2009, 11, 4640-4643 |
| 1504194 | CIF | C15 H22 O3 | P -1 | 8.8984; 9.621; 16.7771 89.599; 85.959; 85.973 | 1429.2 | Hampel, Thomas; Brückner, Reinhard A novel cis-selective cyclohexanone annulation as the key step of a total synthesis of the sesquiterpene isoacanthodoral. Organic letters, 2009, 11, 4842-4845 |
| 1504195 | CIF | C18 H13 F3 O9 S | P 1 21/c 1 | 18.964; 13.633; 29.823 90; 92.316; 90 | 7704 | Cui, Yi; Jiang, Hao; Li, Zhengtao; Wu, Na; Yang, Zhen; Quan, Junmin Unexpected regioselectivity in the synthesis of pyranonaphthoquinone via the Diels-Alder reaction. Organic letters, 2009, 11, 4628-4631 |
| 1504196 | CIF | C9 H12 O3 S | P 1 21 1 | 7.6288; 5.445; 11.5547 90; 91.844; 90 | 479.72 | Majer, Jakub; Kwiatkowski, Piotr; Jurczak, Janusz Highly enantioselective Friedel-Crafts reaction of thiophenes with glyoxylates: formal synthesis of duloxetine. Organic letters, 2009, 11, 4636-4639 |
| 1504197 | CIF | C18 H27 N O6 | P 21 21 21 | 9.355; 11.918; 17.31 90; 90; 90 | 1929.9 | Gross, Ulrike; Nieger, Martin; Bräse, Stefan Stereoselective synthesis of the epicoccin core. Organic letters, 2009, 11, 4740-4742 |
| 1504198 | CIF | C22 H27 N O7 | P 1 21 1 | 7.715; 15.086; 9.295 90; 96.54; 90 | 1074.8 | Balthaser, Bradley R.; McDonald, Frank E. Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Organic letters, 2009, 11, 4850-4853 |
| 1504199 | CIF | C22 H27 N O7 | P 1 21 1 | 13.2879; 9.2997; 17.411 90; 100.194; 90 | 2117.57 | Balthaser, Bradley R.; McDonald, Frank E. Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Organic letters, 2009, 11, 4850-4853 |
| 1504200 | CIF | C22 H35 N O11 | P 21 21 21 | 8.1737; 10.9997; 29.222 90; 90; 90 | 2627.3 | Balthaser, Bradley R.; McDonald, Frank E. Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Organic letters, 2009, 11, 4850-4853 |
| 1504201 | CIF | C28.5 H31 Cl | C 1 2/c 1 | 25.9973; 12.3802; 13.8796 90; 93.724; 90 | 4457.74 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504202 | CIF | C30 H34 | P -1 | 11.075; 14.841; 15.693 118.089; 91.405; 92.655 | 2270 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504203 | CIF | C30 H34 O2 | P 1 21/c 1 | 10.6975; 10.0435; 10.8065 90; 101.43; 90 | 1138.03 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504204 | CIF | C30 H34 O2 | P 1 21/c 1 | 14.0575; 10.3006; 8.0732 90; 99.533; 90 | 1152.86 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504205 | CIF | C30 H34 O2.96 | R -3 :H | 21.0561; 21.0561; 14.3941 90; 90; 120 | 5526.77 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504206 | CIF | C32 H38 O4 | P 1 21/n 1 | 9.6612; 6.9042; 19.3657 90; 94.574; 90 | 1287.63 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504207 | CIF | C48 H54 | P 1 21/c 1 | 21.8162; 9.4664; 8.9027 90; 90.648; 90 | 1838.5 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504208 | CIF | C66 H86 | P 1 21/n 1 | 11.9837; 36.2583; 18.6597 90; 95.013; 90 | 8076.8 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504209 | CIF | C40 H50 Cl4 O4 | P 1 21/c 1 | 12.5705; 9.6243; 15.996 90; 106.347; 90 | 1857 | Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor. Organic letters, 2009, 11, 4656-4659 |
| 1504210 | CIF | C23 H22 Cl N O3 | P 1 21 1 | 10.185; 8.74; 12.189 90; 112.29; 90 | 1003.9 | Han, Bo; Xiao, You-Cai; He, Zhao-Quan; Chen, Ying-Chun Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis. Organic letters, 2009, 11, 4660-4663 |
| 1504211 | CIF | C12 H9 N O4 | P 1 21/n 1 | 6.0584; 19.717; 8.9513 90; 98.257; 90 | 1058.2 | Huo, Fang-Jun; Sun, Yuan-Qiang; Su, Jing; Chao, Jian-Bin; Zhi, Hai-Juan; Yin, Cai-Xia Colorimetric detection of thiols using a chromene molecule Organic letters, 2009, 11, 4918-4921 |
| 1504212 | CIF | C17 H15 B F4 O3 | P 1 21/n 1 | 12.7974; 7.6261; 17.351 90; 105.01; 90 | 1635.6 | Hu, Zhi-Long; Qian, Wen-Jian; Wang, Sheng; Wang, Shaozhong; Yao, Zhu-Jun Transformation of reactive isochromenylium intermediates to stable salts and their cascade reactions with olefins. Organic letters, 2009, 11, 4676-4679 |
| 1504213 | CIF | C21 H28 O10 | P 21 21 21 | 10.0245; 12.5364; 17.6378 90; 90; 90 | 2216.6 | Afarinkia, Kamyar; Abdullahi, Mohamed Haji; Scowen, Ian J. A new, general method for the synthesis of carbasugar-sugar pseudodisaccharides. Organic letters, 2009, 11, 5182-5184 |
| 1504214 | CIF | C25 H40 O5 Si | P 21 21 21 | 6.5381; 13.0869; 28.301 90; 90; 90 | 2421.5 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
| 1504215 | CIF | C27 H40 O7 Si | C 1 2 1 | 27.8634; 7.012; 18.3625 90; 129.332; 90 | 2774.98 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
| 1504216 | CIF | C21 H24 O6 | P 1 21/n 1 | 7.1446; 10.9191; 23.7565 90; 91.941; 90 | 1852.24 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
| 1504217 | CIF | C21 H27 O7 | C 1 2 1 | 30.4299; 7.0493; 19.6268 90; 111.309; 90 | 3922.31 | Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S. A synthesis of the carbon skeleton of maoecrystal V. Organic letters, 2009, 11, 4774-4776 |
| 1504218 | CIF | C26 H21 O3 | P 1 | 8.4452; 10.6647; 11.566 82.23; 89.149; 77.425 | 1007.26 | Yoshida, Masahiro; Higuchi, Mariko; Shishido, Kozo Stereoselective construction of substituted chromans by palladium-catalyzed cyclization of propargylic carbonates with 2-(2-hydroxyphenyl)acetates. Organic letters, 2009, 11, 4752-4755 |
| 1504219 | CIF | C26 H33 N O3 Si | P 1 | 7.718; 11.898; 14.296 96.932; 103.456; 108.338 | 1184.9 | Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process. Organic letters, 2009, 11, 5230-5233 |
| 1504220 | CIF | C18 H21 N O4 | P 1 21/n 1 | 10.762; 12.294; 11.66 90; 106.56; 90 | 1478.7 | Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process. Organic letters, 2009, 11, 5230-5233 |
| 1504221 | CIF | C29 H22 O2 | C 1 2/c 1 | 25.5017; 10.0101; 18.5411 90; 118.749; 90 | 4149.6 | Zhang, Xiaoxiang; Teo, Wan Teng; Chan, Philip Wai Hong Ytterbium(III) triflate catalyzed tandem Friedel-Crafts alkylation/hydroarylation of propargylic alcohols with phenols as an expedient route to indenols. Organic letters, 2009, 11, 4990-4993 |
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