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Searching journal of publication like 'Chemical science (Royal Society of Chemistry : 2010)' volume of publication is 2

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COD ID	Links	Formula	Space group	Cell parameters	Cell volume	Bibliography
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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