Crystallography Open Database
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Result: there are 21914 entries in the selection
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Searching year of publication is 2009
COD ID ![]() |
Links | Formula ![]() |
Space group ![]() |
Cell parameters | Cell volume ![]() |
Bibliography |
|---|---|---|---|---|---|---|
| 1503722 | CIF | C20 H18 N2 O4 | P 21 21 21 | 6.1369; 16.452; 17.008 90; 90; 90 | 1717.2 | Martins, Andrew; Lemouzy, Sébastien; Lautens, Mark Bifunctional reactivity of Cu(I): sequential ring opening/N-arylation. Organic letters, 2009, 11, 181-183 |
| 1503723 | CIF | C17 H19 N3 O6 | P 1 21/c 1 | 5.8184; 20.7156; 14.5591 90; 98.768; 90 | 1734.32 | Martins, Andrew; Lemouzy, Sébastien; Lautens, Mark Bifunctional reactivity of Cu(I): sequential ring opening/N-arylation. Organic letters, 2009, 11, 181-183 |
| 1503724 | CIF | C30 H32 N2 O8 | P -1 | 8.357; 8.9262; 9.6862 104.725; 105.038; 91.747 | 671.28 | Sánchez-García, David; Borrell, José I; Nonell, Santi One-pot synthesis of substituted 2,2'-bipyrroles. A straightforward route to aryl porphycenes. Organic letters, 2009, 11, 77-79 |
| 1503725 | CIF | C7 H7 F3 N2 O2 S | P 1 21/n 1 | 10.483; 7.23; 13.081 90; 107.27; 90 | 946.7 | Ochiai, Masahito; Kawano, Yufuko; Kaneaki, Takao; Tada, Norihiro; Miyamoto, Kazunori Direct transfer of the sulfonylimino group of imino-lambda3-bromane to N-heterocycles and trialkylamines: synthesis of N-iminoammonium ylides under metal-free conditions. Organic letters, 2009, 11, 281-284 |
| 1503726 | CIF | C10 H7 F3 N2 O2 S | P -1 | 6.808; 9.009; 10.357 65.29; 81.76; 66.58 | 529.3 | Ochiai, Masahito; Kawano, Yufuko; Kaneaki, Takao; Tada, Norihiro; Miyamoto, Kazunori Direct transfer of the sulfonylimino group of imino-lambda3-bromane to N-heterocycles and trialkylamines: synthesis of N-iminoammonium ylides under metal-free conditions. Organic letters, 2009, 11, 281-284 |
| 1503727 | CIF | C50 H53 Br N2 O4 | P -1 | 18.367; 21.913; 23.727 76.289; 78.954; 65.989 | 8426 | Zhang, Zhenjun; Ferrence, Gregory M.; Lash, Timothy D. adj-Diazuliporphyrins, a new family of dicarbaporphyrinoids with unprecedented mesoionic characteristics. Organic letters, 2009, 11, 101-104 |
| 1503728 | CIF | C46.6 H46.6 Cl1.8 N2 Pd | P -1 | 14.6447; 14.9621; 18.886 93.9934; 109.874; 90.8206 | 3879.1 | Zhang, Zhenjun; Ferrence, Gregory M.; Lash, Timothy D. adj-Diazuliporphyrins, a new family of dicarbaporphyrinoids with unprecedented mesoionic characteristics. Organic letters, 2009, 11, 101-104 |
| 1503729 | CIF | C26 H26 N O3 P S | P -1 | 15.176; 22.472; 22.477 70.58; 79.743; 89.96 | 7100 | Meng, Xiangtai; Huang, You; Chen, Ruyu Bifunctional phosphine-catalyzed domino reaction: highly stereoselective synthesis of cis-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allenes. Organic letters, 2009, 11, 137-140 |
| 1503730 | CIF | C25 H23 Br N O3 P S | P 1 21 1 | 9.291; 23.68; 11.16 90; 106.733; 90 | 2351.4 | Meng, Xiangtai; Huang, You; Chen, Ruyu Bifunctional phosphine-catalyzed domino reaction: highly stereoselective synthesis of cis-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allenes. Organic letters, 2009, 11, 137-140 |
| 1503731 | CIF | C23 H24 N O P S | P 21 21 21 | 11.549; 13.094; 14.467 90; 90; 90 | 2187.7 | Meng, Xiangtai; Huang, You; Chen, Ruyu Bifunctional phosphine-catalyzed domino reaction: highly stereoselective synthesis of cis-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allenes. Organic letters, 2009, 11, 137-140 |
| 1503732 | CIF | C26 H26 N O3 P S | P 1 21/c 1 | 15.176; 7.49; 21.198 90; 100.869; 90 | 2366.3 | Meng, Xiangtai; Huang, You; Chen, Ruyu Bifunctional phosphine-catalyzed domino reaction: highly stereoselective synthesis of cis-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allenes. Organic letters, 2009, 11, 137-140 |
| 1503733 | CIF | C15 H24 O5 | P 21 21 21 | 6.4397; 15.3604; 31.2247 90; 90; 90 | 3088.63 | Zheng, Yongbiao; Shen, Yuemao Clavicorolides A and B, sesquiterpenoids from the fermentation products of edible fungus Clavicorona pyxidata. Organic letters, 2009, 11, 109-112 |
| 1503734 | CIF | C22 H24 Br O6 | P 21 21 21 | 7.6492; 11.685; 23.902 90; 90; 90 | 2136.4 | Zheng, Yongbiao; Shen, Yuemao Clavicorolides A and B, sesquiterpenoids from the fermentation products of edible fungus Clavicorona pyxidata. Organic letters, 2009, 11, 109-112 |
| 1503735 | CIF | C44 H32 | P -1 | 9.0642; 10.2306; 10.1873 113.734; 100.374; 111.086 | 746.24 | Toyota, Shinji; Onishi, Hiroyuki; Kawai, Yoshihiro; Morimoto, Takaaki; Miyahara, Hiroaki; Iwanaga, Tetsuo; Wakamatsu, Kan Stereogenic motif consisting of rigid ring and intraannular chains: isolation and structures of stereoisomers of 9-alkyl-1,8-anthrylene-butadiynylene cyclic dimers. Organic letters, 2009, 11, 321-324 |
| 1503736 | CIF | C44 H32 | P -1 | 11.1772; 11.9076; 13.265 72.87; 72.915; 68.027 | 1530.7 | Toyota, Shinji; Onishi, Hiroyuki; Kawai, Yoshihiro; Morimoto, Takaaki; Miyahara, Hiroaki; Iwanaga, Tetsuo; Wakamatsu, Kan Stereogenic motif consisting of rigid ring and intraannular chains: isolation and structures of stereoisomers of 9-alkyl-1,8-anthrylene-butadiynylene cyclic dimers. Organic letters, 2009, 11, 321-324 |
| 1503737 | CIF | C42 H28 | P b c a | 16.753; 17.878; 18.941 90; 90; 90 | 5673 | Toyota, Shinji; Onishi, Hiroyuki; Kawai, Yoshihiro; Morimoto, Takaaki; Miyahara, Hiroaki; Iwanaga, Tetsuo; Wakamatsu, Kan Stereogenic motif consisting of rigid ring and intraannular chains: isolation and structures of stereoisomers of 9-alkyl-1,8-anthrylene-butadiynylene cyclic dimers. Organic letters, 2009, 11, 321-324 |
| 1503738 | CIF | C42 H96 Cl8 N6 O2 | I 21 3 | 17.9117; 17.9117; 17.9117 90; 90; 90 | 5746.6 | Kim, Hyunwoo; Staikova, Mima; Lough, Alan J.; Chin, Jik Stereospecific synthesis of alkyl-substituted vicinal diamines from the mother diamine: overcoming the "intrinsic barrier" to the diaza-Cope rearrangement reaction. Organic letters, 2009, 11, 157-160 |
| 1503739 | CIF | C28 H36 N2 O2 | P 21 21 21 | 5.9303; 10.3195; 39.85 90; 90; 90 | 2438.7 | Kim, Hyunwoo; Staikova, Mima; Lough, Alan J.; Chin, Jik Stereospecific synthesis of alkyl-substituted vicinal diamines from the mother diamine: overcoming the "intrinsic barrier" to the diaza-Cope rearrangement reaction. Organic letters, 2009, 11, 157-160 |
| 1503740 | CIF | C22 H28 N2 O2 | P 21 21 21 | 9.7907; 18.3356; 22.0661 90; 90; 90 | 3961.27 | Kim, Hyunwoo; Staikova, Mima; Lough, Alan J.; Chin, Jik Stereospecific synthesis of alkyl-substituted vicinal diamines from the mother diamine: overcoming the "intrinsic barrier" to the diaza-Cope rearrangement reaction. Organic letters, 2009, 11, 157-160 |
| 1503741 | CIF | C66 H80 N4 O12 | P 21 21 21 | 11.3462; 20.7132; 24.828 90; 90; 90 | 5835 | Nagase, Hiroshi; Watanabe, Akio; Harada, Masaya; Nakajima, Mayumi; Hasebe, Ko; Mochizuki, Hidenori; Yoza, Kenji; Fujii, Hideaki Novel synthesis of a 1,3,5-trioxazatriquinane skeleton using a nitrogen clamp. Organic letters, 2009, 11, 539-542 |
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