Crystallography Open Database
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Result: there are 349 entries in the selection
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Searching journal of publication like 'Chemical science' volume of publication is 8
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1545095 | CIF | C18 H28 Br2 N2 P2 Pd | P 21 21 21 | 7.6802; 15.4523; 18.383 90; 90; 90 | 2181.63 | Ji, Yining; Li, Hongming; Hyde, Alan M.; Chen, Qinghao; Belyk, Kevin M.; Lexa, Katrina W.; Yin, Jingjun; Sherer, Edward C.; Williamson, R. Thomas; Brunskill, Andrew; Ren, Sumei; Campeau, Louis-Charles; Davies, Ian W.; Ruck, Rebecca T. A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions Chem. Sci., 2017, 8, 2841 |
| 1545096 | CIF | C25 H32 Br N3 O P2 Pd | C 1 2 1 | 23.434; 10.7208; 10.6091 90; 95.3448; 90 | 2653.7 | Ji, Yining; Li, Hongming; Hyde, Alan M.; Chen, Qinghao; Belyk, Kevin M.; Lexa, Katrina W.; Yin, Jingjun; Sherer, Edward C.; Williamson, R. Thomas; Brunskill, Andrew; Ren, Sumei; Campeau, Louis-Charles; Davies, Ian W.; Ruck, Rebecca T. A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions Chem. Sci., 2017, 8, 2841 |
| 1545097 | CIF | C26 H24 N2 O6 S2 | P 21 21 21 | 8.7715; 15.9157; 36.3389 90; 90; 90 | 5073.1 | Liu, Ren-Rong; Hu, Jiang-Ping; Hong, Jian-Jun; Lu, Chuan-Jun; Gao, Jian-Rong; Jia, Yi-Xia Enantioselective [2 + 2] cycloaddition of N-allenamides with cyclic N-sulfonylketimines: access to polysubstituted azetidines bearing quaternary stereocenters Chem. Sci., 2017, 8, 2811 |
| 1545143 | CIF | C31 H28 O2 | P 21 21 21 | 5.8387; 15.6232; 25.7309 90; 90; 90 | 2347.15 | Guo, Rui; Zheng, Xinxin; Zhang, Dayong; Zhang, Guozhu Rhodium(i)-catalyzed stereoselective [4+2] cycloaddition of oxetanols with alkynes through C(sp(3))-C(sp(3)) bond cleavage. Chemical science, 2017, 8, 3002-3006 |
| 1545144 | CIF | C26 H26 O3 | P 1 21 1 | 12.8937; 6.0514; 14.068 90; 107.517; 90 | 1046.75 | Guo, Rui; Zheng, Xinxin; Zhang, Dayong; Zhang, Guozhu Rhodium(i)-catalyzed stereoselective [4+2] cycloaddition of oxetanols with alkynes through C(sp(3))-C(sp(3)) bond cleavage. Chemical science, 2017, 8, 3002-3006 |
| 1545162 | CIF | C53 H90 N10 O11 | P 1 | 9.302; 9.7698; 16.9249 84.505; 86.765; 71.597 | 1452.19 | Tomsett, Michael; Maffucci, Irene; Le Bailly, Bryden A. F.; Byrne, Liam; Bijvoets, Stefan M.; Lizio, M. Giovanna; Raftery, James; Butts, Craig P.; Webb, Simon J.; Contini, Alessandro; Clayden, Jonathan A tendril perversion in a helical oligomer: trapping and characterizing a mobile screw-sense reversal. Chemical science, 2017, 8, 3007-3018 |
| 1545163 | CIF | C55 H93 N11 O11 | P 1 21 1 | 13.6336; 14.6369; 33.2755 90; 89.215; 90 | 6639.6 | Tomsett, Michael; Maffucci, Irene; Le Bailly, Bryden A. F.; Byrne, Liam; Bijvoets, Stefan M.; Lizio, M. Giovanna; Raftery, James; Butts, Craig P.; Webb, Simon J.; Contini, Alessandro; Clayden, Jonathan A tendril perversion in a helical oligomer: trapping and characterizing a mobile screw-sense reversal. Chemical science, 2017, 8, 3007-3018 |
| 1545166 | CIF | C41 H57 F7 N3 O12 P | P 1 21 1 | 9.9986; 18.897; 12.05 90; 91.502; 90 | 2276 | Saito, Fumito; Bode, Jeffrey W. Synthesis and stabilities of peptide-based [1]rotaxanes: molecular grafting onto lasso peptide scaffolds Chem. Sci., 2017, 8, 2878 |
| 1545174 | CIF | C15 H12 B Cl O3 | P 21 21 21 | 13.0121; 5.2339; 19.82 90; 90; 90 | 1349.82 | Hazra, Gurupada; Maity, Sanjay; Bhowmick, Sudipto; Ghorai, Prasanta Organocatalytic, enantioselective synthesis of benzoxaboroles via Wittig/oxa-Michael reaction Cascade of α-formyl boronic acids. Chemical science, 2017, 8, 3026-3030 |
| 1545175 | CIF | C14 H14 O4 | P 1 21 1 | 9.16074; 6.01447; 10.6243 90; 92.073; 90 | 584.984 | Orue, Ane; Uria, Uxue; Roca-López, David; Delso, Ignacio; Reyes, Efraím; Carrillo, Luisa; Merino, Pedro; Vicario, Jose L. Racemic hemiacetals as oxygen-centered pronucleophiles triggering cascade 1,4-addition/Michael reaction through dynamic kinetic resolution under iminium catalysis. Development and mechanistic insights. Chemical science, 2017, 8, 2904-2913 |
| 1545176 | CIF | C13 H20 O4 | P 21 21 21 | 5.5604; 6.6895; 33.0826 90; 90; 90 | 1230.55 | Orue, Ane; Uria, Uxue; Roca-López, David; Delso, Ignacio; Reyes, Efraím; Carrillo, Luisa; Merino, Pedro; Vicario, Jose L. Racemic hemiacetals as oxygen-centered pronucleophiles triggering cascade 1,4-addition/Michael reaction through dynamic kinetic resolution under iminium catalysis. Development and mechanistic insights. Chemical science, 2017, 8, 2904-2913 |
| 1545177 | CIF | C18 H22 O6 | P 21 21 21 | 8.9615; 10.02283; 17.71277 90; 90; 90 | 1590.95 | Orue, Ane; Uria, Uxue; Roca-López, David; Delso, Ignacio; Reyes, Efraím; Carrillo, Luisa; Merino, Pedro; Vicario, Jose L. Racemic hemiacetals as oxygen-centered pronucleophiles triggering cascade 1,4-addition/Michael reaction through dynamic kinetic resolution under iminium catalysis. Development and mechanistic insights. Chemical science, 2017, 8, 2904-2913 |
| 1545178 | CIF | C10 H11 N3 O6 S | P 1 21 1 | 6.8159; 9.972; 17.7839 90; 98.748; 90 | 1194.68 | Rovira, Alexander R.; Fin, Andrea; Tor, Yitzhak Expanding a fluorescent RNA alphabet: synthesis, photophysics and utility of isothiazole-derived purine nucleoside surrogates. Chemical science, 2017, 8, 2983-2993 |
| 1545179 | CIF | C8 H8 Br N5 O S | P 1 21/n 1 | 15.3538; 4.3958; 17.1443 90; 112.351; 90 | 1070.18 | Rovira, Alexander R.; Fin, Andrea; Tor, Yitzhak Expanding a fluorescent RNA alphabet: synthesis, photophysics and utility of isothiazole-derived purine nucleoside surrogates. Chemical science, 2017, 8, 2983-2993 |
| 1545180 | CIF | C10 H15.5 N4 O6.75 S | P 1 | 8.0883; 10.9716; 16.0771 72.07; 80.273; 86.279 | 1337.78 | Rovira, Alexander R.; Fin, Andrea; Tor, Yitzhak Expanding a fluorescent RNA alphabet: synthesis, photophysics and utility of isothiazole-derived purine nucleoside surrogates. Chemical science, 2017, 8, 2983-2993 |
| 1545181 | CIF | C2.5 H2.5 Np0.12 | I -4 2 m | 8.598; 8.598; 10.5541 90; 90; 90 | 780.22 | Dutkiewicz, Michał S.; Apostolidis, Christos; Walter, Olaf; Arnold, Polly L. Reduction chemistry of neptunium cyclopentadienide complexes: from structure to understanding Chem. Sci., 2017, 8, 2553 |
| 1545182 | CIF | C32 H35 K1.5 Np1.5 O0.5 | C 1 2 1 | 22.6093; 14.7125; 9.0155 90; 90.415; 90 | 2998.8 | Dutkiewicz, Michał S.; Apostolidis, Christos; Walter, Olaf; Arnold, Polly L. Reduction chemistry of neptunium cyclopentadienide complexes: from structure to understanding Chem. Sci., 2017, 8, 2553 |
| 1545183 | CIF | C15 H15 Np | C m c 21 | 14.1208; 8.7037; 9.5917 90; 90; 90 | 1178.85 | Dutkiewicz, Michał S.; Apostolidis, Christos; Walter, Olaf; Arnold, Polly L. Reduction chemistry of neptunium cyclopentadienide complexes: from structure to understanding Chem. Sci., 2017, 8, 2553 |
| 1545184 | CIF | C19 H21 N2 Np | P b c n | 13.6966; 8.3864; 14.6562 90; 90; 90 | 1683.5 | Dutkiewicz, Michał S.; Apostolidis, Christos; Walter, Olaf; Arnold, Polly L. Reduction chemistry of neptunium cyclopentadienide complexes: from structure to understanding Chem. Sci., 2017, 8, 2553 |
| 1545185 | CIF | C24 H39 Np Si3 | P b c a | 8.298; 22.1664; 28.917 90; 90; 90 | 5318.9 | Dutkiewicz, Michał S.; Apostolidis, Christos; Walter, Olaf; Arnold, Polly L. Reduction chemistry of neptunium cyclopentadienide complexes: from structure to understanding Chem. Sci., 2017, 8, 2553 |
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