Crystallography Open Database
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Result: there are 591 entries in the selection
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Searching journal of publication like 'Organic & biomolecular chemistry' volume of publication is 16
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7156026 | CIF | C19 H19 N3 O9 S | P 1 21 1 | 5.9946; 13.3006; 13.1317 90; 93.111; 90 | 1045.47 | Moczulski, Marek; Drelich, Piotr; Albrecht, Łukasz Bifunctional catalysis in the stereocontrolled synthesis of tetrahydro-1,2-oxazines. Organic & biomolecular chemistry, 2018, 16, 376-379 |
| 7156027 | CIF | C30 H24 Cl2 O2 | P 1 21/c 1 | 15.2712; 11.6024; 14.692 90; 107.143; 90 | 2487.51 | Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps. Organic & biomolecular chemistry, 2018, 16, 750-755 |
| 7156028 | CIF | C24 H30 O2 | P 1 21/c 1 | 14.8423; 16.4382; 12.546 90; 97.066; 90 | 3037.73 | Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps. Organic & biomolecular chemistry, 2018, 16, 750-755 |
| 7156029 | CIF | C30 H26 O2 | P -1 | 8.2432; 10.4558; 13.9905 89.46; 73.266; 88.81 | 1154.51 | Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps. Organic & biomolecular chemistry, 2018, 16, 750-755 |
| 7156030 | CIF | C30 H24 F2 O2 | P -1 | 8.2454; 10.3667; 14.2973 90.201; 104.558; 90.585 | 1182.78 | Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps. Organic & biomolecular chemistry, 2018, 16, 750-755 |
| 7156031 | CIF | C30 H24 Cl2 O2 | P -1 | 6.164; 8.847; 12.0067 106.131; 92.963; 101.467 | 612.44 | Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps. Organic & biomolecular chemistry, 2018, 16, 750-755 |
| 7156034 | CIF | C48 H30 F5 N O2 | C 1 2/c 1 | 29.898; 12.7893; 24.928 90; 123.131; 90 | 7982.2 | Muthusamy, Sengodagounder; Balasubramani, Alagesan; Suresh, Eringathodi A BF<sub>3</sub>·Et<sub>2</sub>O catalyzed atom-economical approach to highly substituted indole-3-carbinols from nitrosobenzenes and propargylic alcohols. Organic & biomolecular chemistry, 2018, 16, 756-764 |
| 7156035 | CIF | C27 H25 Br N O3.5 S | P -1 | 12.813; 14.49; 16.225 108.147; 98.12; 116.118 | 2429.6 | Wang, Shengzheng; Chen, Shuqiang; Guo, Zhongjie; He, Shipeng; Zhang, Fan; Liu, Xueying; Chen, Weiping; Zhang, Shengyong; Sheng, Chunquan Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael-aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity. Organic & biomolecular chemistry, 2018, 16, 625-634 |
| 7156036 | CIF | C19 H14 Cl N3 O | P 1 21/c 1 | 12.6542; 6.7364; 18.7735 90; 103.364; 90 | 1556.99 | Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects. Organic & biomolecular chemistry, 2018, 16, 717-732 |
| 7156037 | CIF | C16 H16 Cl N3 O4 S | P -1 | 7.2883; 7.8141; 15.5616 78.263; 86.775; 76.922 | 845.17 | Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects. Organic & biomolecular chemistry, 2018, 16, 717-732 |
| 7156038 | CIF | C20 H15 N3 O | C 1 2/c 1 | 32.653; 4.8634; 21.787 90; 119.984; 90 | 2996.8 | Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects. Organic & biomolecular chemistry, 2018, 16, 717-732 |
| 7156039 | CIF | C21 H20 Cl N3 O3 S | P 1 21/c 1 | 20.255; 7.228; 14.842 90; 107.35; 90 | 2074 | Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects. Organic & biomolecular chemistry, 2018, 16, 717-732 |
| 7156040 | CIF | C23 H20 O3 | P 1 21/c 1 | 14.4555; 5.39; 22.7358 90; 100.038; 90 | 1744.35 | Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties. Organic & biomolecular chemistry, 2018, 16, 480-489 |
| 7156041 | CIF | C24 H20 O4 | P -1 | 6.7449; 11.3462; 12.9292 67.033; 83.287; 88.921 | 904.39 | Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties. Organic & biomolecular chemistry, 2018, 16, 480-489 |
| 7156042 | CIF | C21 H13 I O4 | P -1 | 7.76154; 14.0693; 16.6303 103.626; 100.792; 99.5738 | 1691.05 | Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties. Organic & biomolecular chemistry, 2018, 16, 480-489 |
| 7156043 | CIF | C24 H19 I O4 | P 1 21/c 1 | 12.5028; 9.0127; 17.7036 90; 103.877; 90 | 1936.69 | Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties. Organic & biomolecular chemistry, 2018, 16, 480-489 |
| 7156044 | CIF | C25 H21 I O4 | P -1 | 6.7649; 12.8471; 24.6221 82.354; 86.293; 88.097 | 2115.77 | Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties. Organic & biomolecular chemistry, 2018, 16, 480-489 |
| 7156045 | CIF | C24 H22 O3 | P 1 21/c 1 | 27.2601; 10.403; 26.2305 90; 90.833; 90 | 7437.8 | Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties. Organic & biomolecular chemistry, 2018, 16, 480-489 |
| 7156046 | CIF | C14 H23 N O2 | P 21 21 21 | 7.7672; 9.3611; 19.2665 90; 90; 90 | 1400.86 | Liu, Yi-Wen; Ma, Rui-Jun; Yan, Jia-Hang; Zhou, Zhu; Wei, Bang-Guo Asymmetric synthesis of (-)-sedacryptine through a diastereoselective Mannich reaction of N,O-acetals with ketones. Organic & biomolecular chemistry, 2018, 16, 771-779 |
| 7156047 | CIF | C27 H43 N O4 Si | C 1 2 1 | 33.616; 7.9053; 11.1852 90; 91.38; 90 | 2971.5 | Liu, Yi-Wen; Ma, Rui-Jun; Yan, Jia-Hang; Zhou, Zhu; Wei, Bang-Guo Asymmetric synthesis of (-)-sedacryptine through a diastereoselective Mannich reaction of N,O-acetals with ketones. Organic & biomolecular chemistry, 2018, 16, 771-779 |
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