Crystallography Open Database
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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 |
|---|---|---|---|---|---|---|
| 7117715 | CIF | C15 H16 Cl3 N O3 | P -1 | 6.0347; 11.3911; 13.0283 67.611; 89.839; 85.877 | 825.64 | Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones Chem.Commun., 2015, 51, 13976 |
| 7117716 | CIF | C15 H19 N O4 | P c a 21 | 11.5083; 13.3657; 9.5834 90; 90; 90 | 1474.08 | Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones Chem.Commun., 2015, 51, 13976 |
| 7117717 | CIF | C14 H20 O2 S2 | P 21 21 21 | 10.1194; 11.6313; 12.1672 90; 90; 90 | 1432.1 | Amol P. Jadhav; V. U. Bhaskara Rao; Pradeep Singh; R. G. Gonnade; Ravi P. Singh Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans Chem.Commun., 2015, 51, 13941 |
| 7117718 | CIF | C13 H18 O2 S2 | P 21 21 21 | 6.6349; 8.9609; 21.6859 90; 90; 90 | 1289.33 | Amol P. Jadhav; V. U. Bhaskara Rao; Pradeep Singh; R. G. Gonnade; Ravi P. Singh Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans Chem.Commun., 2015, 51, 13941 |
| 7117719 | CIF | C105 H113 F27 N4 O18 P4.5 | P -1 | 14.1777; 20.5414; 24.643 71.116; 78.71; 76.663 | 6549.9 | Wei-Bo Hu; Wen-Jing Hu; Xiao-Li Zhao; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen A [2]rota[2]catenane, constructed from a pillar[5]arene-crown ether fused double-cavity macrocycle: synthesis and structural characterization Chem.Commun., 2015, 51, 13882 |
| 7117720 | CIF | C166 H205 F30 N8 O26 P5 | P -1 | 20.5486; 21.3959; 24.984 65.622; 74.313; 66.014 | 9071.3 | Wei-Bo Hu; Wen-Jing Hu; Xiao-Li Zhao; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen A [2]rota[2]catenane, constructed from a pillar[5]arene-crown ether fused double-cavity macrocycle: synthesis and structural characterization Chem.Commun., 2015, 51, 13882 |
| 7117721 | CIF | C199 H189 N23 O53 Zn11 | P 1 2/c 1 | 22.018; 20.783; 37.062 90; 94.845; 90 | 16899 | S. A. Sapchenko; D. N. Dybtsev; D. G. Samsonenko; R. V. Belosludov; V. R. Belosludov; Y. Kawazoe; M. Schroder; V. P. Fedin Selective gas adsorption in microporous metal-organic frameworks incorporating urotropine basic sites: an experimental and theoretical study Chem.Commun., 2015, 51, 13918 |
| 7117722 | CIF | C17 H15 N O2 S | P 21 21 21 | 6.2454; 7.9709; 30.185 90; 90; 90 | 1502.7 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117723 | CIF | C30 H27.5 N O5.25 S | C 1 2/c 1 | 41.536; 9.8916; 25.763 90; 93.59; 90 | 10564 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117724 | CIF | C24 H23 N O5 S | P -1 | 11.0389; 13.5784; 24.5769 87.24; 84.094; 69.682 | 3436 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117725 | CIF | C25 H25 N O5 S | C 1 c 1 | 8.4273; 18.696; 14.628 90; 96.208; 90 | 2291.2 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117726 | CIF | C24 H23 N O5 S | P b c a | 12.5654; 18.5476; 18.7414 90; 90; 90 | 4367.8 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117727 | CIF | C25 H26 N2 O4 S | P 1 21/n 1 | 12.5847; 17.5982; 20.1268 90; 92.772; 90 | 4452.2 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117728 | CIF | C31 H29 N2 O6 S2 | P 1 21/c 1 | 18.1593; 10.1358; 15.6691 90; 91.647; 90 | 2882.8 | Yin-Wei Sun; Xiang-Ying Tang; Min Shi A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles Chem.Commun., 2015, 51, 13937 |
| 7117729 | CIF | C94.5 H81.75 Eu F9 N23.25 O27 S3 | P -1 | 15.608; 15.7058; 22.744 88.97; 80.503; 77.211 | 5361.5 | Eoin P. McCarney; Joseph P. Byrne; Brendan Twamley; Miguel Martinez-Calvo; Gavin Ryan; Matthias E. Mobius; Thorfinnur Gunnlaugsson Self-assembly formation of a healable lanthanide luminescent supramolecular metallogel from 2,6-bis(1,2,3-triazol-4-yl)pyridine (btp) ligands Chem.Commun., 2015, 51, 14123 |
| 7117730 | CIF | C34 H33 Cl2 F6 Ir N7 P | P b c a | 10.918; 16.0878; 39.16 90; 90; 90 | 6878.3 | Kamrul Hasan; Amlan K. Pal; Thomas Auvray; Eli Zysman-Colman; Garry S. Hanan Blue-green emissive cationic iridium(III) complexes using partially saturated strongly-donating guanidyl-pyridine/-pyrazine ancillary ligands Chem.Commun., 2015, 51, 14060 |
| 7117731 | CIF | C96 H122.5 Cl10.5 Mg2 N13 O2.5 | P 1 21/c 1 | 13.281; 26.435; 28.814 90; 94.579; 90 | 10084 | Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers Chem.Commun., 2015, 51, 14107 |
| 7117732 | CIF | C177 H219 Cl3 Mg4 N26 | P -1 | 13.848; 16.029; 19.255 96.237; 97.714; 105.938 | 4025 | Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers Chem.Commun., 2015, 51, 14107 |
| 7117733 | CIF | C96 H121 Cl6 Mg2 N14 O2 | P 1 21/n 1 | 14.137; 26.982; 25.473 90; 105.387; 90 | 9368 | Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers Chem.Commun., 2015, 51, 14107 |
| 7117734 | CIF | C92 H121 Cl4 Mg2 N9 O4 | P -1 | 13.267; 18.521; 20.98 86.112; 73.433; 69.33 | 4620 | Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers Chem.Commun., 2015, 51, 14107 |
| 7117735 | CIF | C4 H9 B11 Cs F9 O9 S3 | P 1 21/c 1 | 12.5292; 18.424; 10.6894 90; 106.109; 90 | 2370.6 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117736 | CIF | C2 H5.94 B11 Br5.06 Cs F3 O3 S | P b c n | 11.355; 27.735; 13.353 90; 90; 90 | 4205.3 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117737 | CIF | C8 H16 B11 Cl10 F3 O3 S Si | P 1 21/n 1 | 16.213; 21.072; 17.832 90; 102.362; 90 | 5951 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117738 | CIF | C38 H61 B11 Cl11 F5 O7 P4 Pd2 S | P 1 21/n 1 | 14.477; 35.02; 26.24 90; 92.565; 90 | 13290 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117739 | CIF | C17 H27 B11 Cl10 F4 O3 S Si | P 1 21/c 1 | 9.327; 20.08; 20.281 90; 94.518; 90 | 3786.5 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117740 | CIF | C27 H21 B11 Cl10 F4 O3 S | P b c a | 12.5691; 22.529; 27.755 90; 90; 90 | 7859.4 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117741 | CIF | C26 H36 B11 Br Cl10 F4 O5 P2 Pd S | P 1 21/n 1 | 14.099; 12.676; 28.345 90; 102.072; 90 | 4954 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117742 | CIF | C20 H31 B11 Cl10 F4 O5 P2 Pd S | P -1 | 12.224; 13.31; 14.337 72.268; 74.431; 78.566 | 2123 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117743 | CIF | C19 H31 B11 Cl11 F O2 P2 Pd | P -1 | 9.1582; 12.0726; 20.864 76.534; 88.597; 78.715 | 2199.5 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117744 | CIF | C3 H B11 Cl9 Cs F6 O6 S2 | P b c a | 17.7687; 15.7898; 18.9559 90; 90; 90 | 5318.3 | Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov Triflyloxy-substituted carboranes as useful weakly coordinating anions Chem.Commun., 2015, 51, 14034 |
| 7117745 | CIF | C34 H45 B2 F N12 O U | P -1 | 10.4532; 11.0258; 18.1147 102.153; 98.067; 96.74 | 1997.41 | Christopher L. Clark; Jill J. Lockhart; Phillip E. Fanwick; Suzanne C. Bart Synthesis of low-valent uranium fluorides by C-F bond activation Chem.Commun., 2015, 51, 14084 |
| 7117746 | CIF | C30 H43 B2 F2 N12 U | P 1 21/n 1 | 11.784; 22.3831; 17.0603 90; 93.165; 90 | 4493 | Christopher L. Clark; Jill J. Lockhart; Phillip E. Fanwick; Suzanne C. Bart Synthesis of low-valent uranium fluorides by C-F bond activation Chem.Commun., 2015, 51, 14084 |
| 7117747 | CIF | C7 H14 Cl3 N O4 | P 1 21/n 1 | 12.6911; 12.471; 14.9357 90; 91.68; 90 | 2362.87 | A. J. K. Roth; M. Tretbar; C. B. W. Stark Mimicking the active site of aldehyde dehydrogenases: stabilization of carbonyl hydrates through hydrogen bonds Chem.Commun., 2015, 51, 14175 |
| 7117748 | CIF | C7 H8 Cl3 N O3 | P 1 21/c 1 | 6.1594; 12.8396; 13.3985 90; 101.56; 90 | 1038.12 | A. J. K. Roth; M. Tretbar; C. B. W. Stark Mimicking the active site of aldehyde dehydrogenases: stabilization of carbonyl hydrates through hydrogen bonds Chem.Commun., 2015, 51, 14175 |
| 7117749 | CIF | C6 H6 S0.95 Se0.05 | P b c n | 13.8535; 11.4448; 7.1913 90; 90; 90 | 1140.2 | Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row Organic alloys of room temperature liquids thiophenol and selenophenol Chem.Commun., 2015, 51, 14255 |
| 7117750 | CIF | C6 H6 S0.91 Se0.09 | P b c n | 13.856; 11.425; 7.1934 90; 90; 90 | 1138.7 | Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row Organic alloys of room temperature liquids thiophenol and selenophenol Chem.Commun., 2015, 51, 14255 |
| 7117751 | CIF | C6 H6 S0.75 Se0.25 | P n a b | 7.2109; 11.3897; 13.9705 90; 90; 90 | 1147.4 | Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row Organic alloys of room temperature liquids thiophenol and selenophenol Chem.Commun., 2015, 51, 14255 |
| 7117752 | CIF | C6 H6 Se | P n a b | 7.329; 11.226; 14.422 90; 90; 90 | 1186.6 | Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row Organic alloys of room temperature liquids thiophenol and selenophenol Chem.Commun., 2015, 51, 14255 |
| 7117753 | CIF | C6 H6 S | P n a b | 7.1905; 11.4643; 13.815 90; 90; 90 | 1138.8 | Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row Organic alloys of room temperature liquids thiophenol and selenophenol Chem.Commun., 2015, 51, 14255 |
| 7117754 | CIF | C6 H6 S0.57 Se0.43 | P n a b | 7.2621; 11.371; 14.155 90; 90; 90 | 1168.9 | Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row Organic alloys of room temperature liquids thiophenol and selenophenol Chem.Commun., 2015, 51, 14255 |
| 7117755 | CIF | C25 H28 N2 O3 S | C 1 2/c 1 | 10.9399; 21.02; 20.547 90; 98.769; 90 | 4669.7 | Dongari Yadagiri; Pazhamalai Anbarasan An iodine(III) mediated oxidative rearrangement of enamines: efficient synthesis of alpha-amino ketones Chem.Commun., 2015, 51, 14203 |
| 7117756 | CIF | C54 H18 N0 O41 Zn9 | I 2 3 | 23.503; 23.503; 23.503 90; 90; 90 | 12983 | Yun-Wu Li; Jian Xu; Da-Cheng Li; Jian-Min Dou; Hui Yan; Tong-Liang Hu; Xian-He Bu Two microporous MOFs constructed from different metal cluster SBUs for selective gas adsorption Chem.Commun., 2015, 51, 14211 |
| 7117757 | CIF | C15 H20 Cd N2 O7 | P 1 21/n 1 | 10.099; 14.363; 12.975 90; 105.69; 90 | 1811.9 | Yun-Wu Li; Jian Xu; Da-Cheng Li; Jian-Min Dou; Hui Yan; Tong-Liang Hu; Xian-He Bu Two microporous MOFs constructed from different metal cluster SBUs for selective gas adsorption Chem.Commun., 2015, 51, 14211 |
| 7117758 | CIF | C30 H26 N2 S | C 1 2/c 1 | 19.059; 5.647; 42.733 90; 93.669; 90 | 4590 | Alok Ranjan; Anupam Mandal; Swapnil G. Yerande; Dattatraya H. Dethe An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates Chem.Commun., 2015, 51, 14215 |
| 7117759 | CIF | C30 H23 Br N2 O S | P 1 | 9.724; 11.581; 11.774 75.443; 87.986; 89.04 | 1282.5 | Alok Ranjan; Anupam Mandal; Swapnil G. Yerande; Dattatraya H. Dethe An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates Chem.Commun., 2015, 51, 14215 |
| 7117760 | CIF | C88 H88 Cl2 F36 N13 O2 S6 | C 1 2/c 1 | 20.3759; 35.024; 16.9047 90; 98.951; 90 | 11917 | Hennie Valkenier; Christopher M. Dias; Kathryn L. Porter Goff; Ondrej Jurcek; Rakesh Puttreddy; Kari Rissanen; Anthony P. Davis Sterically geared tris-thioureas; transmembrane chloride transporters with unusual activity and accessibility Chem.Commun., 2015, 51, 14235 |
| 7117761 | CIF | C25 H19 N O3 | P 21 21 21 | 4.11501; 10.0552; 45.8911 90; 90; 90 | 1898.85 | Zhong-Jian Cai; Chao Yang; Shun-Yi Wang; Shun-Jun Ji Palladium-catalyzed highly regioselective 6-exo-dig cyclization and alkenylation of ortho-ethynylanilides: the synthesis of polyene-substituted benzo[d][1,3]oxazines Chem.Commun., 2015, 51, 14267 |
| 7117762 | CIF | C110 H56 Br2 | I 41/a c d | 39.709; 39.709; 39.724 90; 90; 90 | 62637 | Melanie Kitchin; Kristina Konstas; Christopher J. Sumby; Milena L. Czyz; Peter Valente; Matthew R. Hill; Anastasios Polyzos; Christian J. Doonan Continuous flow synthesis of a carbon-based molecular cage macrocycle via a three-fold homocoupling reaction Chem.Commun., 2015, 51, 14231 |
| 7117763 | CIF | C21 H20 Br2 O4 S | P 1 21 1 | 10.927; 19.507; 19.81 90; 105.742; 90 | 4064.2 | Nagamoto, Midori; Nishimura, Takahiro Stereoselective hydroacylation of bicyclic alkenes with 2-hydroxybenzaldehydes catalyzed by hydroxoiridium/diene complexes. Chemical communications (Cambridge, England), 2015, 51, 13791-13794 |
| 7117766 | CIF | C168 H162 Ag3 F18 N18 P3 | R -3 | 35.4661; 35.4661; 26.194 90; 90; 120 | 28534 | Mejuto, Carmen; Guisado-Barrios, Gregorio; Gusev, Dmitry; Peris, Eduardo First homoleptic MIC and heteroleptic NHC-MIC coordination cages from 1,3,5-triphenylbenzene-bridged tris-MIC and tris-NHC ligands. Chemical communications (Cambridge, England), 2015, 51, 13914-13917 |
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