Crystallography Open Database
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Searching journal of publication like 'Organic & Biomolecular Chemistry' volume of publication is 10
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
7152101 | CIF | C16 H11 Cl2 N O3 | P 1 21/n 1 | 6.393; 9.37; 26.44 90; 92.38; 90 | 1582 | Lu, Shen-Ci; Wang, Wei-Xia; Gao, Pan-Liang; Zhang, Wei; Tu, Zhi-Feng Photoinduced chlorine atom-transfer cyclization/photohydrolysis of 3-acyl-2-chloro-N-(ω-phenylalkynyl)pyrroles: a one-pot synthesis of benzoyl-substituted fused pyrroles. Organic & biomolecular chemistry, 2012, 10, 232-235 |
7152102 | CIF | C53 H54 N10 O13 | P -1 | 14.3728; 14.5231; 14.9321 66.097; 62.095; 73.914 | 2503.44 | Klein, Jörg M; Saggiomo, Vittorio; Reck, Lisa; Lüning, Ulrich; Sanders, Jeremy K. M. Dynamic combinatorial libraries for the recognition of heavy metal ions. Organic & biomolecular chemistry, 2012, 10, 60-66 |
7152103 | CIF | C27 H31 N5 O8 | C 1 c 1 | 8.0009; 25.2757; 12.9386 90; 92.918; 90 | 2613.16 | Klein, Jörg M; Saggiomo, Vittorio; Reck, Lisa; Lüning, Ulrich; Sanders, Jeremy K. M. Dynamic combinatorial libraries for the recognition of heavy metal ions. Organic & biomolecular chemistry, 2012, 10, 60-66 |
7152104 | CIF | C22 H15 N O S2 | P 1 21/c 1 | 11.8038; 16.2989; 19.3777 90; 105.682; 90 | 3589.3 | Maurya, Hardesh K.; Tandon, Vishnu K.; Kumar, Brijesh; Kumar, Abhinav; Huch, Volker; Ram, Vishnu Ji Non-catalytic approach to the synthesis of partially reduced 'S' shaped dioxathia- and oxadithiahelicenes through base induced inter- and intramolecular C-C bond formation. Organic & biomolecular chemistry, 2012, 10, 605-613 |
7152105 | CIF | C17 H13 Cl N2 O2 S | P c a 21 | 8.7105; 8.3893; 41.097 90; 90; 90 | 3003.2 | Maurya, Hardesh K.; Tandon, Vishnu K.; Kumar, Brijesh; Kumar, Abhinav; Huch, Volker; Ram, Vishnu Ji Non-catalytic approach to the synthesis of partially reduced 'S' shaped dioxathia- and oxadithiahelicenes through base induced inter- and intramolecular C-C bond formation. Organic & biomolecular chemistry, 2012, 10, 605-613 |
7152106 | CIF | C23 H17 N O2 S | P 1 21/n 1 | 7.723; 9.374; 24.947 90; 95.26; 90 | 1798.4 | Maurya, Hardesh K.; Tandon, Vishnu K.; Kumar, Brijesh; Kumar, Abhinav; Huch, Volker; Ram, Vishnu Ji Non-catalytic approach to the synthesis of partially reduced 'S' shaped dioxathia- and oxadithiahelicenes through base induced inter- and intramolecular C-C bond formation. Organic & biomolecular chemistry, 2012, 10, 605-613 |
7152107 | CIF | C31 H58 Cl3 Dy N8 O10 | P -1 | 10.8844; 14.3626; 15.4658 113.395; 103.121; 99.252 | 2074.15 | Milne, Mark; Chicas, Kirby; Li, Alex; Bartha, Robert; Hudson, Robert H. E. ParaCEST MRI contrast agents capable of derivatization via"click" chemistry. Organic & biomolecular chemistry, 2012, 10, 287-292 |
7152108 | CIF | C31 H58 Cl3 N8 Nd O10 | P -1 | 11.1524; 13.9136; 15.2106 110.878; 103.133; 100.034 | 2061.4 | Milne, Mark; Chicas, Kirby; Li, Alex; Bartha, Robert; Hudson, Robert H. E. ParaCEST MRI contrast agents capable of derivatization via"click" chemistry. Organic & biomolecular chemistry, 2012, 10, 287-292 |
7152109 | CIF | C31 H57 Cl3 N8 O10 Tb | P -1 | 10.8916; 14.362; 15.4604 113.338; 103.205; 99.22 | 2075 | Milne, Mark; Chicas, Kirby; Li, Alex; Bartha, Robert; Hudson, Robert H. E. ParaCEST MRI contrast agents capable of derivatization via"click" chemistry. Organic & biomolecular chemistry, 2012, 10, 287-292 |
7152110 | CIF | C31 H53 Cl3 N8 O10 Yb | P -1 | 10.8858; 14.3185; 15.4483 113.484; 102.767; 99.404 | 2067 | Milne, Mark; Chicas, Kirby; Li, Alex; Bartha, Robert; Hudson, Robert H. E. ParaCEST MRI contrast agents capable of derivatization via"click" chemistry. Organic & biomolecular chemistry, 2012, 10, 287-292 |
7152111 | CIF | C30 H22 F2 N2 O | C 1 c 1 | 12.828; 11.141; 16.665 90; 103.208; 90 | 2318.7 | Zhou, Rong; Wang, Jianfang; Tian, Junjun; He, Zhengjie Phosphine-catalyzed [4 + 2] annulation and vinylogous addition reactions between 1,4-dien-3-ones and 1,1-dicyanoalkenes. Organic & biomolecular chemistry, 2012, 10, 773-781 |
7152113 | CIF | C10 H8 N2 O | P 1 21/c 1 | 10.3225; 11.2447; 16.7681 90; 114.116; 90 | 1776.5 | Li, Ping; Teng, Bo-Tao; Jin, Fa-Gen; Li, Xin-Sheng; Zhu, Wei-Dong; Xie, Jian-Wu Synthesis of functionalized 2,3-dihydroisoxazoles by domino reactions in water and unexpected ring-opening reactions of 2,3-dihydroisoxazoles. Organic & biomolecular chemistry, 2012, 10, 244-247 |
7152114 | CIF | C6 H8 O4 | P 21 21 21 | 6.2773; 9.4898; 10.1036 90; 90; 90 | 601.87 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152115 | CIF | C6 H8 O4 | P 21 21 21 | 6.7114; 10.2593; 17.4506 90; 90; 90 | 1201.55 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152116 | CIF | C6 H8 O4 | P 1 21 1 | 5.0789; 11.0036; 10.9164 90; 90.128; 90 | 610.07 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152117 | CIF | C6 H8 O4 | P 21 21 21 | 5.6736; 9.5781; 10.7239 90; 90; 90 | 582.76 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152118 | CIF | C6 H8 O4 | P 21 21 21 | 6.4573; 9.4912; 10.0281 90; 90; 90 | 614.6 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152119 | CIF | C6 H8 O4 | P 21 21 21 | 6.1219; 8.5353; 11.8539 90; 90; 90 | 619.39 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152120 | CIF | C6 H8 O4 | P 1 21 1 | 6.6936; 7.0452; 6.707 90; 99.357; 90 | 312.08 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152121 | CIF | C6 H8 O4 | P 1 21 1 | 6.1357; 5.1847; 9.4064 90; 93.064; 90 | 298.81 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152122 | CIF | C6 H7 F O3 | P 1 21 1 | 7.698; 8.773; 8.885 90; 94.976; 90 | 597.78 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152123 | CIF | C6 H7 F O3 | P 1 21 1 | 8.193; 7.164; 10.941 90; 109.287; 90 | 606.14 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152124 | CIF | C6 H7 F O3 | P 21 21 21 | 6.3628; 9.2072; 10.1628 90; 90; 90 | 595.37 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152125 | CIF | C6 H7 F O3 | P 21 21 21 | 5.7591; 6.2197; 16.2984 90; 90; 90 | 583.81 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152126 | CIF | C6 H7 F O3 | P 1 21 1 | 6.1181; 7.1297; 6.9272 90; 94.628; 90 | 301.18 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152127 | CIF | C6 H7 F O3 | P 21 21 21 | 6.271; 7.6812; 12.1999 90; 90; 90 | 587.65 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152128 | CIF | C6 H7 F O3 | P 21 21 21 | 6.3457; 7.8536; 12.1288 90; 90; 90 | 604.46 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152129 | CIF | C6 H7 F O3 | P 21 21 21 | 7.2178; 8.7675; 9.5 90; 90; 90 | 601.18 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152130 | CIF | C6 H7 F O3 | P 1 | 5.1716; 5.2806; 6.082 68.403; 67.501; 80.743 | 142.64 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152131 | CIF | C6 H7 F O3 | P 21 21 21 | 6.7058; 8.1556; 10.7504 90; 90; 90 | 587.94 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152132 | CIF | C13 H13 F O4 | P 1 21 1 | 6.224; 10.6879; 8.8554 90; 106.7; 90 | 564.23 | Karban, Jindřich; Císařová, Ivana; Strašák, Tomáš; Šťastná, Lucie Červenková; Sýkora, Jan Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with diethylaminosulphur trifluoride. Organic & biomolecular chemistry, 2012, 10, 394-403 |
7152133 | CIF | C17 H16 N4 O | P 1 21/c 1 | 6.203; 13.362; 18.973 90; 106.802; 90 | 1505.4 | Han, Feng; Yang, Lei; Li, Zhen; Xia, Chungu Acidic-functionalized ionic liquid as an efficient, green and reusable catalyst for hetero-Michael addition of nitrogen, sulfur and oxygen nucleophiles to α,β-unsaturated ketones. Organic & biomolecular chemistry, 2012, 10, 346-354 |
7152134 | CIF | C16 H15 N3 O | P 1 21/c 1 | 9.912; 13.636; 10.633 90; 104.257; 90 | 1392.9 | Han, Feng; Yang, Lei; Li, Zhen; Xia, Chungu Acidic-functionalized ionic liquid as an efficient, green and reusable catalyst for hetero-Michael addition of nitrogen, sulfur and oxygen nucleophiles to α,β-unsaturated ketones. Organic & biomolecular chemistry, 2012, 10, 346-354 |
7152135 | CIF | C42 H57 N3 O21 | P -1 | 13.063; 13.707; 13.95 99.713; 99.524; 99.393 | 2380.7 | Nieto-García, Olaia; Lago-Santomé, Hugo; Cagide-Fagín, Fernando; Ortiz-Lara, Juan Carlos; Alonso, Ricardo A formal [3+3]-annulation-based approach to pancratistatins: total synthesis of (±)-7-deoxy-pancratistatin and its 2-epi and 2,4-diepi analogues. Organic & biomolecular chemistry, 2012, 10, 825-834 |
7152136 | CIF | C15 H23 N O2 | P -1 | 8.9268; 8.9385; 9.3112 68.989; 78.429; 74.952 | 665 | Gignoux, Camille; Newton, Annabella F.; Barthelme, Alexandre; Lewis, William; Alcaraz, Marie-Lyne; Stockman, Robert A. Combining two-directional synthesis and tandem reactions: a short formal synthesis of halichlorine. Organic & biomolecular chemistry, 2012, 10, 67-69 |
7152137 | CIF | C87 H111 Br2 Cl9 N4 O9 | P 1 21/c 1 | 15.9979; 29.8312; 20.5629 90; 105.044; 90 | 9477 | El Moll, Hani; Sémeril, David; Matt, Dominique; Toupet, Loïc; Harrowfield, Jean-Jacques Resorcin[4]arene-derived mono-, bis- and tetra-imidazolium salts as ligand precursors for Suzuki-Miyaura cross-coupling. Organic & biomolecular chemistry, 2012, 10, 372-382 |
7152138 | CIF | C15 H15 Cl N2 O | P 1 21/n 1 | 8.466; 7.2644; 22.2712 90; 95.081; 90 | 1364.31 | Hardin Narayan, Alison R.; Sarpong, Richmond Indolizinones as synthetic scaffolds: fundamental reactivity and the relay of stereochemical information. Organic & biomolecular chemistry, 2012, 10, 70-78 |
7152139 | CIF | C16 H15 N O4 | C 1 2/c 1 | 22.2396; 12.8939; 10.309 90; 110.568; 90 | 2767.7 | Hardin Narayan, Alison R.; Sarpong, Richmond Indolizinones as synthetic scaffolds: fundamental reactivity and the relay of stereochemical information. Organic & biomolecular chemistry, 2012, 10, 70-78 |
7152140 | CIF | C27 H20 | P 1 21/c 1 | 13.908; 11.0651; 12.376 90; 91.176; 90 | 1904.2 | Peng, Shiyong; Wang, Lei; Wang, Jian Iron-catalyzed ene-type propargylation of diarylethylenes with propargyl alcohols. Organic & biomolecular chemistry, 2012, 10, 225-228 |
7152141 | CIF | C26 H24 N4 S6 | P b c a | 16.337; 9.364; 36.071 90; 90; 90 | 5518.1 | Rivadehi, Shadi; Reid, Ellen F.; Hogan, Conor F.; Bhosale, Sheshanath V.; Langford, Steven J. Fluoride-selective optical sensor based on the dipyrrolyl-tetrathiafulvalene chromophore. Organic & biomolecular chemistry, 2012, 10, 705-709 |
7152142 | CIF | C42 H36 O3 | P -1 | 13.215; 14.889; 17.81 89.02; 85.32; 65.87 | 3186.9 | Yu, Jin-Tao; Huang, Zhi-Tang; Zheng, Qi-Yu Synthesis, structure, fullerene-binding and resolution of C(3)-symmetric cavitands with rigid and deep cavities. Organic & biomolecular chemistry, 2012, 10, 1359-1364 |
7152143 | CIF | C15 H9 N O2 | P 1 21/c 1 | 12.237; 7.6556; 12.237 90; 108.92; 90 | 1084.4 | Xia, Ziming; Wang, Kuo; Zheng, Jiening; Ma, Zheyong; Jiang, Zhanguo; Wang, Xiaoxia; Lv, Xin Copper-catalyzed domino intramolecular cyclization: a facile and efficient approach to polycyclic indole derivatives. Organic & biomolecular chemistry, 2012, 10, 1602-1611 |
7152144 | CIF | C20 H22 O2 | P 1 21/c 1 | 18.554; 6.256; 13.851 90; 100.778; 90 | 1579.4 | Subba Reddy, B. V.; Borkar, Prashant; Yadav, J. S.; Purushotham Reddy, P.; Kunwar, A. C.; Sridhar, B.; Grée, René Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C-H activation. Organic & biomolecular chemistry, 2012, 10, 1349-1358 |
7152145 | CIF | C18 H13 N3 O2 | P 21 21 21 | 6.1634; 11.2748; 19.9532 90; 90; 90 | 1386.6 | Iaroshenko, Viktor O.; Mkrtchyan, Satenik; Gevorgyan, Ashot; Miliutina, Mariia; Villinger, Alexander; Volochnyuk, Dmytro; Sosnovskikh, Vyacheslav Ya; Langer, Peter 2,3-unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines. Organic & biomolecular chemistry, 2012, 10, 890-894 |
7152146 | CIF | C18 H12 Cl N3 O2 | P 1 21/c 1 | 13.5897; 11.4742; 10.2062 90; 110.969; 90 | 1486.07 | Iaroshenko, Viktor O.; Mkrtchyan, Satenik; Gevorgyan, Ashot; Miliutina, Mariia; Villinger, Alexander; Volochnyuk, Dmytro; Sosnovskikh, Vyacheslav Ya; Langer, Peter 2,3-unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines. Organic & biomolecular chemistry, 2012, 10, 890-894 |
7152147 | CIF | C19 H15 N3 O2 | P 1 21/c 1 | 13.5332; 11.4883; 10.268 90; 111.013; 90 | 1490.24 | Iaroshenko, Viktor O.; Mkrtchyan, Satenik; Gevorgyan, Ashot; Miliutina, Mariia; Villinger, Alexander; Volochnyuk, Dmytro; Sosnovskikh, Vyacheslav Ya; Langer, Peter 2,3-unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines. Organic & biomolecular chemistry, 2012, 10, 890-894 |
7152148 | CIF | C20 H17 N3 O | P 1 21/c 1 | 12.7467; 16.7588; 7.5184 90; 105.053; 90 | 1550.97 | Iaroshenko, Viktor O.; Mkrtchyan, Satenik; Gevorgyan, Ashot; Miliutina, Mariia; Villinger, Alexander; Volochnyuk, Dmytro; Sosnovskikh, Vyacheslav Ya; Langer, Peter 2,3-unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines. Organic & biomolecular chemistry, 2012, 10, 890-894 |
7152149 | CIF | C17 H16 Cl N3 O S | P 1 21/n 1 | 7.0888; 24.91; 8.8454 90; 101.728; 90 | 1529.33 | Iaroshenko, Viktor O.; Mkrtchyan, Satenik; Gevorgyan, Ashot; Miliutina, Mariia; Villinger, Alexander; Volochnyuk, Dmytro; Sosnovskikh, Vyacheslav Ya; Langer, Peter 2,3-unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines. Organic & biomolecular chemistry, 2012, 10, 890-894 |
7152150 | CIF | C18 H19 N3 O S | P 21 21 21 | 6.3395; 7.8493; 31.3577 90; 90; 90 | 1560.38 | Iaroshenko, Viktor O.; Mkrtchyan, Satenik; Gevorgyan, Ashot; Miliutina, Mariia; Villinger, Alexander; Volochnyuk, Dmytro; Sosnovskikh, Vyacheslav Ya; Langer, Peter 2,3-unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines. Organic & biomolecular chemistry, 2012, 10, 890-894 |
7152151 | CIF | C29 H25 N O7 S2 | P 1 21 1 | 9.934; 9.0722; 14.812 90; 104.519; 90 | 1292.3 | Du, Zhiyun; Zhou, Chenggang; Gao, Yaojun; Ren, Qiao; Zhang, Kun; Cheng, Hansong; Wang, Wei; Wang, Jian Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst. Organic & biomolecular chemistry, 2012, 10, 36-39 |
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