Crystallography Open Database
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Result: there are 1796 entries in the selection
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Searching journal of publication like 'Chem.Commun.' volume of publication is 51
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7116446 | CIF | C66 H86 Er N13 O20 Rh4 | P 1 21/c 1 | 13.8619; 18.8672; 28.1155 90; 93.687; 90 | 7338 | Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion Chem.Commun., 2015, 51, 1889 |
| 7116447 | CIF | C57 H48 B Cl2 F24 Ir N P S | P 41 21 2 | 12.9489; 12.9489; 70.484 90; 90; 90 | 11818.3 | Areli Flores-Gaspar; Silvia Orgue; Arnald Grabulosa; Antoni Riera; Xavier Verdaguer Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines Chem.Commun., 2015, 51, 1941 |
| 7116448 | CIF | C12 H21 B N P | P 21 21 21 | 10.793; 11.0539; 11.3385 90; 90; 90 | 1352.7 | Areli Flores-Gaspar; Silvia Orgue; Arnald Grabulosa; Antoni Riera; Xavier Verdaguer Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines Chem.Commun., 2015, 51, 1941 |
| 7116449 | CIF | C34 H34 N2 O4 S4 | A b a 2 | 28.621; 26.533; 9.756 90; 90; 90 | 7409 | Yu Jiang; Xiang-Ying Tang; Min Shi A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles Chem.Commun., 2015, 51, 2122 |
| 7116450 | CIF | C36 H38 N2 O4 S4 | P -1 | 9.597; 13.9714; 14.765 105.066; 107.053; 97.126 | 1784.1 | Yu Jiang; Xiang-Ying Tang; Min Shi A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles Chem.Commun., 2015, 51, 2122 |
| 7116451 | CIF | C18 H19 N O2 S2 | P 1 21/c 1 | 9.6224; 14.3505; 13.0206 90; 102.158; 90 | 1757.6 | Yu Jiang; Xiang-Ying Tang; Min Shi A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles Chem.Commun., 2015, 51, 2122 |
| 7116453 | CIF | C20 H17 N3 O3 | P 1 21 1 | 5.3666; 14.0877; 11.0289 90; 94.065; 90 | 831.72 | Daniel Hack; Pankaj Chauhan; Kristina Deckers; Yusuke Mizutani; Gerhard Raabe; Dieter Enders Combining silver- and organocatalysis: an enantioselective sequential catalytic approach towards pyrano-annulated pyrazoles Chem.Commun., 2015, 51, 2266 |
| 7116454 | CIF | C15 H18 O4 | P 1 21/c 1 | 8.5618; 8.4049; 18.442 90; 93.163; 90 | 1325.1 | Fiene Horeischi; Claudia Guttroff; Bernd Plietker The enantioselective total synthesis of (+)-clusianone Chem.Commun., 2015, 51, 2259 |
| 7116455 | CIF | C16 H17 I | P 1 21/n 1 | 10.6651; 14.1041; 17.531 90; 101.441; 90 | 2584.6 | Stephen J. Murray; Hasim Ibrahim Asymmetric Kita spirolactonisation catalysed by anti-dimethanoanthracene-based iodoarenes Chem.Commun., 2015, 51, 2376 |
| 7116456 | CIF | C26 H27 N3 O8 | P 21 21 21 | 10.6406; 11.0802; 21.8683 90; 90; 90 | 2578.27 | Pankaj Chauhan; Suruchi Mahajan; Gerhard Raabe; Dieter Enders Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters Chem.Commun., 2015, 51, 2270 |
| 7116457 | CIF | C229 H308 Cl3 Eu2 N20 O16 | P -1 | 19.854; 24.158; 25.212 99.59; 106.63; 106.33 | 10710 | Guifen Lu; Sen Yan; Mengying Shi; Wenhan Yu; Jing Li; Weihua Zhu; Zhongping Ou; Karl M. Kadish A new class of rare earth tetrapyrrole sandwich complexes containing corrole and phthalocyanine macrocycles: synthesis, physicochemical characterization and X-ray analysis Chem.Commun., 2015, 51, 2411 |
| 7116458 | CIF | C21 H18 N2 | P b c a | 15.517; 8.4691; 23.518 90; 90; 90 | 3090.6 | Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines. Chemical communications (Cambridge, England), 2015, 51, 2532-2535 |
| 7116459 | CIF | C25 H34 N2 Si | P -1 | 7.7419; 14.8215; 21.0488 75.571; 80.3817; 85.172 | 2303.92 | Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines. Chemical communications (Cambridge, England), 2015, 51, 2532-2535 |
| 7116460 | CIF | C24 H27 Cl4 N2 Rh | P 1 21/c 1 | 26.7294; 8.902; 20.8098 90; 90.4289; 90 | 4951.5 | Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines. Chemical communications (Cambridge, England), 2015, 51, 2532-2535 |
| 7116461 | CIF | C16 H11 B F2 N2 O | P -1 | 6.9566; 8.3315; 23.1202 95.844; 90.57; 96.433 | 1324.35 | Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties. Chemical communications (Cambridge, England), 2015, 51, 2656-2659 |
| 7116462 | CIF | C17 H13 B F2 N2 O | P -1 | 7.0915; 10.1014; 10.3857 86.948; 70.988; 86.697 | 701.75 | Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties. Chemical communications (Cambridge, England), 2015, 51, 2656-2659 |
| 7116463 | CIF | C29 H22 B F2 N3 O | P 1 21/n 1 | 18.0013; 6.9212; 20.263 90; 116.034; 90 | 2268.42 | Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties. Chemical communications (Cambridge, England), 2015, 51, 2656-2659 |
| 7116464 | CIF | C22 H15 B F2 N2 O | P -1 | 7.1054; 11.1114; 11.9627 96.493; 106.301; 105.521 | 855.17 | Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties. Chemical communications (Cambridge, England), 2015, 51, 2656-2659 |
| 7116465 | CIF | C34 H24 B F2 N3 O | P 1 2/n 1 | 14.9332; 11.3243; 17.9422 90; 94.526; 90 | 3024.71 | Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties. Chemical communications (Cambridge, England), 2015, 51, 2656-2659 |
| 7116466 | CIF | C20 H15 N O | P b c a | 13.099; 9.359; 24.26 90; 90; 90 | 2974 | Yan, Rulong; Li, Xiaoni; Yang, Xiaodong; Kang, Xing; Xiang, Likui; Huang, Guosheng A novel one-pot method for the synthesis of substituted furopyridines: iodine-mediated oxidation of enaminones by tandem metal-free cyclization. Chemical communications (Cambridge, England), 2015, 51, 2573-2576 |
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