Crystallography Open Database
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Searching journal of publication like 'ACS catalysis' volume of publication is 9
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 4514659 | CIF | C20 H34 Cl N2 P Ru | P 1 21/c 1 | 13.3641; 15.0206; 10.9602 90; 93.975; 90 | 2194.82 | Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B. Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes ACS Catalysis, 2019, 9, 7217 |
| 4514660 | CIF | C24 H42 F6 N2 P2 Ru | P n a 21 | 22.7385; 13.1551; 9.5634 90; 90; 90 | 2860.67 | Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B. Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes ACS Catalysis, 2019, 9, 7217 |
| 4514661 | CIF | C20 H31 Cl F3 N2 P Ru | P 1 21/c 1 | 13.915; 14.954; 10.922 90; 95.212; 90 | 2263.3 | Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B. Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes ACS Catalysis, 2019, 9, 7217 |
| 4514662 | CIF | C24.5 H0.5 Cl1.5 N2 O2 S3 | P 1 | 5.7084; 14.6112; 15.7856 72.801; 87.877; 87.344 | 1256.02 | Liang, Yaoyu; Zhao, Xiaodan Enantioselective Construction of Chiral Sulfides via Catalytic Electrophilic Azidothiolation and Oxythiolation of N-Allyl Sulfonamides ACS Catalysis, 2019, 9, 6896 |
| 4514663 | CIF | C19 H32 Fe N5 O7 S2 | P 1 21/c 1 | 11.986; 9.3819; 21.7658 90; 90; 90 | 2447.6 | Warner, Genoa R.; Somasundar, Yogesh; Jansen, Kyle C.; Kaaret, Evan Z.; Weng, Cindy; Burton, Abigail E.; Mills, Matthew R.; Shen, Longzhu Q.; Ryabov, Alexander D.; Pros, Gabrielle; Pintauer, Tomislav; Biswas, Saborni; Hendrich, Michael P.; Taylor, Julia A.; Vom Saal, Frederick S.; Collins, Terrence J. Bioinspired, Multidisciplinary, Iterative Catalyst Design Creates the Highest Performance Peroxidase Mimics and the Field of Sustainable Ultradilute Oxidation Catalysis (SUDOC) ACS Catalysis, 2019, 9, 7023 |
| 4514664 | CIF | C20 H21 N | P 1 21/c 1 | 10.3039; 11.9306; 12.985 90; 90.816; 90 | 1596.1 | Ping, Yuanyuan; Wang, Kuai; Pan, Qi; Ding, Zhengtian; Zhou, Zhijun; Guo, Ya; Kong, Wangqing Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines ACS Catalysis, 2019, 9, 7335 |
| 4514665 | CIF | C20 H21 N | P 1 21/c 1 | 10.2763; 11.8965; 12.9403 90; 90.785; 90 | 1581.83 | Ping, Yuanyuan; Wang, Kuai; Pan, Qi; Ding, Zhengtian; Zhou, Zhijun; Guo, Ya; Kong, Wangqing Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines ACS Catalysis, 2019, 9, 7335 |
| 4514666 | CIF | C108 H92 Cl12 N8 O4 | C 1 c 1 | 16.9269; 16.7619; 8.8583 90; 91.738; 90 | 2512.18 | Ping, Yuanyuan; Wang, Kuai; Pan, Qi; Ding, Zhengtian; Zhou, Zhijun; Guo, Ya; Kong, Wangqing Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines ACS Catalysis, 2019, 9, 7335 |
| 4514667 | CIF | C18 H14 Br F3 N2 O3 | P 1 21 1 | 9.89; 9.938; 18.564 90; 101.954; 90 | 1785 | Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko Enantioselective Friedel‒Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate ACS Catalysis, 2019, 9, 6903 |
| 4514668 | CIF | C38 H27 Br3 N2 O3 | P 21 21 21 | 6.8271; 16.06; 29.396 90; 90; 90 | 3223.1 | Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko Enantioselective Friedel‒Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate ACS Catalysis, 2019, 9, 6903 |
| 4514669 | CIF | C25 H25 Br N2 O2 S | P 41 | 9.7248; 9.7248; 48.32 90; 90; 90 | 4569.7 | Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko Enantioselective Friedel‒Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate ACS Catalysis, 2019, 9, 6903 |
| 4514670 | CIF | C22 H20 O2 | C 1 2/c 1 | 15.8408; 13.142; 16.3982 90; 98.987; 90 | 3371.9 | Giri, Sovan Sundar; Liu, Rai-Shung Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles ACS Catalysis, 2019, 9, 7328 |
| 4514671 | CIF | C25 H19 N O2 | P 1 21/c 1 | 15.6269; 10.8792; 22.0724 90; 100.839; 90 | 3685.5 | Giri, Sovan Sundar; Liu, Rai-Shung Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles ACS Catalysis, 2019, 9, 7328 |
| 4514672 | CIF | C18 H11 N O | P 1 21/c 1 | 8.2853; 31.984; 19.542 90; 93.546; 90 | 5168.7 | Giri, Sovan Sundar; Liu, Rai-Shung Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles ACS Catalysis, 2019, 9, 7328 |
| 4514673 | CIF | C22 H14 N4 | P 1 21/c 1 | 9.9466; 17.8664; 9.4521 90; 100.253; 90 | 1652.91 | Giri, Sovan Sundar; Liu, Rai-Shung Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles ACS Catalysis, 2019, 9, 7328 |
| 4514674 | CIF | C19 H13 N O | P -1 | 7.861; 9.282; 9.934 83.675; 72.702; 85.815 | 687.2 | Giri, Sovan Sundar; Liu, Rai-Shung Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles ACS Catalysis, 2019, 9, 7328 |
| 4514675 | CIF | C30 H22 O3 | P 1 21/c 1 | 24.6109; 12.239; 14.7299 90; 98.22; 90 | 4391.3 | Giri, Sovan Sundar; Liu, Rai-Shung Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles ACS Catalysis, 2019, 9, 7328 |
| 4514676 | CIF | C54 H55 B F4 N3 O5 P2 Rh | P -1 | 14.1394; 15.0162; 28.9031 77.688; 87.174; 78.469 | 5874.4 | Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H. Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands ACS Catalysis, 2019, 9, 7535 |
| 4514677 | CIF | C50 H49 B F4 N5 O5 P2 Rh | P -1 | 12.6207; 13.6039; 15.2008 72.598; 83.301; 76.784 | 2421.15 | Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H. Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands ACS Catalysis, 2019, 9, 7535 |
| 4514678 | CIF | C92 H86 B2 F8 N6 O10 P4 Rh2 | P 1 21/n 1 | 14.1446; 25.4077; 15.6384 90; 94.839; 90 | 5600.1 | Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H. Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands ACS Catalysis, 2019, 9, 7535 |
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