Crystallography Open Database
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Result : There are 17 entries in the selection
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Searching journal of publication like 'Chemical science (Royal Society of Chemistry : 2010)' volume of publication is 2
COD ID: 1515477 | |
CIF file | Formula: - C30 H25 Cl N2 O4 S - Comments: 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) 2(7) (2011) 1369-1378 Space group: P 1 21/n 1 Cell volume: 2673.7 Cell parameters: 11.8193; 11.4475; 19.9444; 90; 97.77; 90; |
COD ID: 1515493 | |
CIF file | Formula: - C19 H24 Br N O6 - Comments: 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) 2(10) (2011) 1940-1944 Space group: P 21 21 21 Cell volume: 1966.2 Cell parameters: 6.6796; 9.2556; 31.8029; 90; 90; 90; |
COD ID: 1515535 | |
CIF file | Formula: - C17 H22 O3 - Comments: 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) 2(12) (2011) 2378-2382 Space group: P b c a Cell volume: 3038.7 Cell parameters: 12.7496; 10.619; 22.4445; 90; 90; 90; |
COD ID: 1515536 | |
CIF file | Formula: - C17 H21 Br O3 - Comments: 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) 2(12) (2011) 2378-2382 Space group: P 21 21 21 Cell volume: 1641.82 Cell parameters: 5.8343; 7.4644; 37.7001; 90; 90; 90; |
COD ID: 1515537 | |
CIF file | Formula: - C18 H24 O4 - Comments: 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) 2(12) (2011) 2378-2382 Space group: P 1 21/n 1 Cell volume: 4912.5 Cell parameters: 12.1533; 35.1495; 12.2922; 90; 110.684; 90; |
COD ID: 1515551 | |
CIF file | Formula: - C16 H27 Cu F6 N P S3 - Comments: 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) 2(6) (2011) 1016-1024 Space group: P 1 21/c 1 Cell volume: 2178.9 Cell parameters: 15.503; 13.996; 10.645; 90; 109.377; 90; |
COD ID: 1515576 | |
CIF file | Formula: - C21 H22 O2 - Comments: 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) 2(11) (2011) 2115-2119 Space group: P n a 21 Cell volume: 1606.75 Cell parameters: 18.0449; 16.5511; 5.3798; 90; 90; 90; |
COD ID: 1515577 | |
CIF file | Formula: - C13 H18 F3 N O4 - Comments: 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) 2(11) (2011) 2162-2165 Space group: P 1 21 1 Cell volume: 703.1 Cell parameters: 9.548; 5.573; 13.512; 90; 102.084; 90; |
COD ID: 1515607 | |
CIF file | Formula: - C30 H38 O4 Si - Comments: 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) 2(8) (2011) 1568 Space group: P 1 21 1 Cell volume: 2746 Cell parameters: 9.7467; 14.1261; 20.0486; 90; 95.845; 90; |
COD ID: 1515608 | |
CIF file | Formula: - C14 H20 O4 - Comments: 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) 2(8) (2011) 1568 Space group: P 21 21 21 Cell volume: 1347.8 Cell parameters: 7.2838; 9.555; 19.3652; 90; 90; 90; |
COD ID: 1515609 | |
CIF file | Formula: - C13 H18 O3 - Comments: 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) 2(8) (2011) 1568 Space group: P 1 21/c 1 Cell volume: 1236.7 Cell parameters: 12.956; 8.4492; 11.2977; 90; 90.405; 90; |
COD ID: 1515610 | |
CIF file | Formula: - C14 H22 O4 - Comments: 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) 2(8) (2011) 1568 Space group: P 21 21 21 Cell volume: 1303.72 Cell parameters: 6.16325; 11.2731; 18.7642; 90; 90; 90; |
COD ID: 1515611 | |
CIF file | Formula: - C14 H20 O4 - Comments: 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) 2(8) (2011) 1568 Space group: P 21 21 21 Cell volume: 1277.98 Cell parameters: 6.14187; 11.3932; 18.2633; 90; 90; 90; |
COD ID: 1515646 | |
CIF file | Formula: - C33.25 H37.25 Cl1.5 N2 O4 Si - Comments: 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) 2(9) (2011) 1710-1718 Space group: P 21 21 2 Cell volume: 3253.1 Cell parameters: 8.3338; 25.68; 15.2004; 90; 90; 90; |
COD ID: 1515647 | |
CIF file | Formula: - C20 H18 N2 O4 - Comments: 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) 2(9) (2011) 1710-1718 Space group: P -1 Cell volume: 1000.8 Cell parameters: 8.4645; 9.265; 13.88; 101.3; 98.534; 106.22; |
COD ID: 1515648 | |
CIF file | Formula: - C20 H20 N2 O4 - Comments: 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) 2(9) (2011) 1710-1718 Space group: P 21 21 21 Cell volume: 1704.58 Cell parameters: 6.4713; 12.2439; 21.5133; 90; 90; 90; |
COD ID: 1515650 | |
CIF file | Formula: - C27 H22 Cl N O5 S2 - Comments: Atienza, Roxanne L.; Roth, Howard S.; Scheidt, Karl A. N-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones. Chemical science (Royal Society of Chemistry : 2010) 2(9) (2011) 1772-1776 Space group: P 1 21 1 Cell volume: 1244.02 Cell parameters: 11.2346; 7.9046; 14.0597; 90; 94.892; 90; |
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