Crystallography Open Database
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Searching journal of publication like 'Chemical science (Royal Society of Chemistry : 2010)' volume of publication is 2
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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1515477 | CIF | C30 H25 Cl N2 O4 S | P 1 21/n 1 | 11.8193; 11.4475; 19.9444 90; 97.77; 90 | 2673.7 | Campbell, Matthew J.; Toste, F. Dean Enantioselective synthesis of cyclic carbamimidates via a three-component reaction of imines, terminal alkynes, and p-toluenesulfonylisocyanate using a monophosphine gold(I) catalyst(). Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1369-1378 |
1515493 | CIF | C19 H24 Br N O6 | P 21 21 21 | 6.6796; 9.2556; 31.8029 90; 90; 90 | 1966.2 | Bartelson, Keith J.; Singh, Ravi P.; Foxman, Bruce M.; Deng, Li Catalytic Asymmetric [4 + 2] Additions with Aliphatic Nitroalkenes. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1940-1944 |
1515535 | CIF | C17 H22 O3 | P b c a | 12.7496; 10.619; 22.4445 90; 90; 90 | 3038.7 | Parr, Brendan T.; Li, Zhanjie; Davies, Huw M. L. Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 2378-2382 |
1515536 | CIF | C17 H21 Br O3 | P 21 21 21 | 5.8343; 7.4644; 37.7001 90; 90; 90 | 1641.82 | Parr, Brendan T.; Li, Zhanjie; Davies, Huw M. L. Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 2378-2382 |
1515537 | CIF | C18 H24 O4 | P 1 21/n 1 | 12.1533; 35.1495; 12.2922 90; 110.684; 90 | 4912.5 | Parr, Brendan T.; Li, Zhanjie; Davies, Huw M. L. Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 2378-2382 |
1515551 | CIF | C16 H27 Cu F6 N P S3 | P 1 21/c 1 | 15.503; 13.996; 10.645 90; 109.377; 90 | 2178.9 | Chaudhry, Aneese F.; Mandal, Subrata; Hardcastle, Kenneth I.; Fahrni, Christoph J. High-contrast Cu(I)-selective fluorescent probes based on synergistic electronic and conformational switching. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1016-1024 |
1515576 | CIF | C21 H22 O2 | P n a 21 | 18.0449; 16.5511; 5.3798 90; 90; 90 | 1606.75 | Du, Juana; Espelt, Laura Ruiz; Guzei, Ilia A.; Yoon, Tehshik P. Photocatalytic Reductive Cyclizations of Enones: Divergent Reactivity of Photogenerated Radical and Radical Anion Intermediates. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 2115-2119 |
1515577 | CIF | C13 H18 F3 N O4 | P 1 21 1 | 9.548; 5.573; 13.512 90; 102.084; 90 | 703.1 | Royzen, Maksim; Taylor, Michael T.; Deangelis, Andrew; Fox, Joseph M. Total Synthesis of Hyacinthacine A2: Stereocontrolled 5-aza-cyclooctene Photoisomerization and Transannular Hydroamination with Planar-to-Point Chirality Transfer. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 2162-2165 |
1515607 | CIF | C30 H38 O4 Si | P 1 21 1 | 9.7467; 14.1261; 20.0486 90; 95.845; 90 | 2746 | Dermenci, Alpay; Selig, Philipp S.; Domaoal, Robert A.; Spasov, Krasimir A.; Anderson, Karen S.; Miller, Scott J. Quasi-Biomimetic Ring Contraction Catalyzed by a Cysteine-Based Nucleophile: Total Synthesis of Sch-642305, Some Analogs and their Putative anti-HIV Activities. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1568 |
1515608 | CIF | C14 H20 O4 | P 21 21 21 | 7.2838; 9.555; 19.3652 90; 90; 90 | 1347.8 | Dermenci, Alpay; Selig, Philipp S.; Domaoal, Robert A.; Spasov, Krasimir A.; Anderson, Karen S.; Miller, Scott J. Quasi-Biomimetic Ring Contraction Catalyzed by a Cysteine-Based Nucleophile: Total Synthesis of Sch-642305, Some Analogs and their Putative anti-HIV Activities. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1568 |
1515609 | CIF | C13 H18 O3 | P 1 21/c 1 | 12.956; 8.4492; 11.2977 90; 90.405; 90 | 1236.7 | Dermenci, Alpay; Selig, Philipp S.; Domaoal, Robert A.; Spasov, Krasimir A.; Anderson, Karen S.; Miller, Scott J. Quasi-Biomimetic Ring Contraction Catalyzed by a Cysteine-Based Nucleophile: Total Synthesis of Sch-642305, Some Analogs and their Putative anti-HIV Activities. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1568 |
1515610 | CIF | C14 H22 O4 | P 21 21 21 | 6.16325; 11.2731; 18.7642 90; 90; 90 | 1303.72 | Dermenci, Alpay; Selig, Philipp S.; Domaoal, Robert A.; Spasov, Krasimir A.; Anderson, Karen S.; Miller, Scott J. Quasi-Biomimetic Ring Contraction Catalyzed by a Cysteine-Based Nucleophile: Total Synthesis of Sch-642305, Some Analogs and their Putative anti-HIV Activities. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1568 |
1515611 | CIF | C14 H20 O4 | P 21 21 21 | 6.14187; 11.3932; 18.2633 90; 90; 90 | 1277.98 | Dermenci, Alpay; Selig, Philipp S.; Domaoal, Robert A.; Spasov, Krasimir A.; Anderson, Karen S.; Miller, Scott J. Quasi-Biomimetic Ring Contraction Catalyzed by a Cysteine-Based Nucleophile: Total Synthesis of Sch-642305, Some Analogs and their Putative anti-HIV Activities. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1568 |
1515646 | CIF | C33.25 H37.25 Cl1.5 N2 O4 Si | P 21 21 2 | 8.3338; 25.68; 15.2004 90; 90; 90 | 3253.1 | Kummer, David A.; Li, Derun; Dion, Amelie; Myers, Andrew G. A practical, convergent route to the key precursor to the tetracycline antibiotics. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1710-1718 |
1515647 | CIF | C20 H18 N2 O4 | P -1 | 8.4645; 9.265; 13.88 101.3; 98.534; 106.22 | 1000.8 | Kummer, David A.; Li, Derun; Dion, Amelie; Myers, Andrew G. A practical, convergent route to the key precursor to the tetracycline antibiotics. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1710-1718 |
1515648 | CIF | C20 H20 N2 O4 | P 21 21 21 | 6.4713; 12.2439; 21.5133 90; 90; 90 | 1704.58 | Kummer, David A.; Li, Derun; Dion, Amelie; Myers, Andrew G. A practical, convergent route to the key precursor to the tetracycline antibiotics. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1710-1718 |
1515650 | CIF | C27 H22 Cl N O5 S2 | P 1 21 1 | 11.2346; 7.9046; 14.0597 90; 94.892; 90 | 1244.02 | Atienza, Roxanne L.; Roth, Howard S.; Scheidt, Karl A. N-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones. Chemical science (Royal Society of Chemistry : 2010), 2011, 2, 1772-1776 |
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