Crystallography Open Database
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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1506293 | CIF | C9 H10 F3 N O | P 21 21 21 | 6.6648; 8.1816; 18.7439 90; 90; 90 | 1022.08 | Sterk, Damjan; Stephan, Michel; Mohar, Barbara Highly enantioselective transfer hydrogenation of fluoroalkyl ketones. Organic letters, 2006, 8, 5935-5938 |
| 1506294 | CIF | C88 H16 F40 O8 | P 1 21/c 1 | 16.871; 22.046; 22.462 90; 103.148; 90 | 8135 | Reddy, J. Sreedhar; Mandal, Sukhendu; Anand, Venkataramanarao G. Cyclic oligofurans: one-pot synthesis of 30pi and 40pi expanded porphyrinoids. Organic letters, 2006, 8, 5541-5543 |
| 1506295 | CIF | C12 H9 N3 | P 21 21 21 | 5.1126; 13.096; 14.347 90; 90; 90 | 960.6 | Shibahara, Fumitoshi; Kitagawa, Asumi; Yamaguchi, Eiji; Murai, Toshiaki Synthesis of 2-azaindolizines by using an iodine-mediated oxidative desulfurization promoted cyclization of N-2-pyridylmethyl thioamides and an investigation of their photophysical properties. Organic letters, 2006, 8, 5621-5624 |
| 1506296 | CIF | C24 H16 N6 S | P -1 | 8.049; 10.286; 12.388 90.925; 101.862; 98.595 | 991.3 | Shibahara, Fumitoshi; Kitagawa, Asumi; Yamaguchi, Eiji; Murai, Toshiaki Synthesis of 2-azaindolizines by using an iodine-mediated oxidative desulfurization promoted cyclization of N-2-pyridylmethyl thioamides and an investigation of their photophysical properties. Organic letters, 2006, 8, 5621-5624 |
| 1506297 | CIF | C17 H14 N2 O S | P -1 | 9.642; 9.953; 16.2792 97.093; 92.531; 97.689 | 1533.44 | Singh, C. B.; Murru, Siva; Kavala, Veerababurao; Patel, Bhisma K. It is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br(2)/enolizable ketone. Organic letters, 2006, 8, 5397-5399 |
| 1506298 | CIF | C22 H16 N2 O S | P 1 21/n 1 | 10.4679; 15.2299; 11.7243 90; 101.491; 90 | 1831.7 | Singh, C. B.; Murru, Siva; Kavala, Veerababurao; Patel, Bhisma K. It is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br(2)/enolizable ketone. Organic letters, 2006, 8, 5397-5399 |
| 1506299 | CIF | C17 H13 Br N2 O S | P 1 21/c 1 | 16.059; 13.4006; 7.6695 90; 98.68; 90 | 1631.6 | Singh, C. B.; Murru, Siva; Kavala, Veerababurao; Patel, Bhisma K. It is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br(2)/enolizable ketone. Organic letters, 2006, 8, 5397-5399 |
| 1506300 | CIF | C12 H15 N O3 | P 1 21/n 1 | 10.9577; 9.0799; 11.3076 90; 96.931; 90 | 1116.8 | Malona, John A.; Colbourne, Jessica M.; Frontier, Alison J. A general method for the catalytic nazarov cyclization of heteroaromatic compounds. Organic letters, 2006, 8, 5661-5664 |
| 1506301 | CIF | C21 H24 O6 | P 1 21/c 1 | 11.0511; 20.5371; 9.0441 90; 96.047; 90 | 2041.2 | Duan, Xin-Hua; Guo, Li-Na; Bi, Hai-Peng; Liu, Xue-Yuan; Liang, Yong-Min Highly regioselective synthesis of 2,3-disubstituted indenes via a novel palladium-catalyzed cyclization reaction of propargylic carbonates with carbon nucleophiles. Organic letters, 2006, 8, 5777-5780 |
| 1506302 | CIF | C15 H16 O5 | P -1 | 8.193; 8.974; 18.504 89.169; 81.157; 72.754 | 1283.2 | Pittelkow, Michael; Boas, Ulrik; Christensen, Jørn B Carbocations in action. Design, synthesis, and evaluation of a highly acid-sensitive naphthalene-based backbone amide linker for solid-phase synthesis. Organic letters, 2006, 8, 5817-5820 |
| 1506303 | CIF | C19 H16 O5 | P 1 21/c 1 | 7.764; 21.989; 8.721 90; 94.738; 90 | 1483.8 | Dahl, Bart J.; Branchaud, Bruce P. 180 degree unidirectional bond rotation in a biaryl lactone artificial molecular motor prototype. Organic letters, 2006, 8, 5841-5844 |
| 1506304 | CIF | C22 H18 F6 N4 O8 Pd2 S2 | P -1 | 7.7003; 12.9161; 14.763 87.536; 84.658; 74.544 | 1408.8 | Zhao, Baowei; Lu, Xiyan Cationic palladium(II)-catalyzed addition of arylboronic acids to nitriles. One-step synthesis of benzofurans from phenoxyacetonitriles. Organic letters, 2006, 8, 5987-5990 |
| 1506305 | CIF | C46.38 H37 Cl2.76 N10 O2 | P -1 | 16.654; 17.694; 17.91 77.62; 64.1; 89.91 | 4612 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506306 | CIF | C33.5 H27.5 Cl2 N10.5 O2.5 | P -1 | 13.477; 15.305; 16.878 76.66; 89.07; 88.22 | 3385.6 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506307 | CIF | C32 H24 Cl2 N10 | P n a 21 | 13.007; 14.042; 16.794 90; 90; 90 | 3067.3 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506308 | CIF | C51 H50 Cl2 N12 O4 | C 1 2/c 1 | 26.598; 9.4281; 20.033 90; 110.21; 90 | 4714.4 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506309 | CIF | C46 H36 Cl2 N10 O | P 1 21/n 1 | 16.54; 8.832; 30.088 90; 104.33; 90 | 4258.5 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506310 | CIF | C30 H36 N2 O3 | P 1 21/c 1 | 11.1854; 34.814; 7.0886 90; 106.175; 90 | 2651.1 | Hopkins, Chad D.; Malinakova, Helena C. Allylpalladium umpolung in the three-component coupling synthesis of homoallylic amines. Organic letters, 2006, 8, 5971-5974 |
| 1506311 | CIF | C105.5 H143 N8 O8.5 | C 1 2/c 1 | 24.468; 24.214; 19.3043 90; 102.267; 90 | 11176 | Ishibashi, Koichi; Tsue, Hirohito; Tokita, Satoshi; Matsui, Kazuhiro; Takahashi, Hiroki; Tamura, Rui Regioselectively N-methylated azacalix[8]arene octamethyl ether prepared by catalytic aryl amination reaction using a temporal N-silylation protocol. Organic letters, 2006, 8, 5991-5994 |
| 1506312 | CIF | C26 H26 N2 | P 21 21 21 | 5.762; 9.213; 38.396 90; 90; 90 | 2038.3 | Williams, Amie L.; Srinivasan, Jayasree M.; Johnston, Jeffrey N. Synthesis of an advanced intermediate en route to the mitomycin natural products. Organic letters, 2006, 8, 6047-6049 |
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