Crystallography Open Database

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Searching journal of publication like 'ACS Catalysis' volume of publication is 6

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4516700 CIFC38 H27 N OP -111.23; 12.753; 20.255
85.686; 80.147; 74.114
2747.7Li, Xingwei; Yang, Xifa; Qi, Zisong
Synthesis of Cyclopentadienols by Rhodium-Catalyzed C‒H Activation of 8-Formylquinolines and [2+2+1] Carbocyclization with Alkynes
ACS Catalysis, 2016, 6, 6372
4516701 CIFC26 H35 O5 PP 1 21/n 19.4338; 11.4458; 23.1231
90; 97.4269; 90
2475.83Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516702 CIFC7 H5 O4 PP 1 21/n 14.5729; 14.1363; 11.7191
90; 100.631; 90
744.57Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516703 CIFC48 H53 O12 P2 RhP -110.8599; 15.1287; 15.5406
102.742; 101.78; 100.56
2367.22Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516704 CIFC18 H19 O5 PP 1 21/c 17.9973; 11.7658; 18.4161
90; 93.7246; 90
1729.2Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516705 CIFC24 H27 N O4 SP -18.6854; 11.1584; 12.3533
110.734; 96.486; 95.657
1100.08Teske, Johannes; Plietker, Bernd
A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates
ACS Catalysis, 2016, 6, 7148
4516706 CIFC39 H32 B Cl2 F4 Fe N O3 P2P 1 21/n 116.7984; 13.6152; 16.9579
90; 103.928; 90
3764.5Teske, Johannes; Plietker, Bernd
A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates
ACS Catalysis, 2016, 6, 7148
4516707 CIFC40 H34 B Cl3 F4 Fe N2 O2 P2P -112.2695; 12.9467; 14.1404
78.636; 69.027; 83.561
2054.1Teske, Johannes; Plietker, Bernd
A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates
ACS Catalysis, 2016, 6, 7148
4516708 CIFC18 H21 F3 N4 Ni O3 SP 1 21/n 16.9941; 17.4234; 17.1188
90; 98.8919; 90
2061.04Wei, Yingfei; Liu, Shi-Xia; Mueller-Bunz, Helge; Albrecht, Martin
Synthesis of Triazolylidene Nickel Complexes and Their Catalytic Application in Selective Aldehyde Hydrosilylation
ACS Catalysis, 2016, 6, 8192
4516709 CIFC15 H16 I N3 Ni OP 1 21/c 113.4405; 10.5724; 11.268
90; 93.709; 90
1597.81Wei, Yingfei; Liu, Shi-Xia; Mueller-Bunz, Helge; Albrecht, Martin
Synthesis of Triazolylidene Nickel Complexes and Their Catalytic Application in Selective Aldehyde Hydrosilylation
ACS Catalysis, 2016, 6, 8192
4516710 CIFC18 H21 F3 N4 Ni O3 SC 1 2/c 114.416; 11.0236; 25.901
90; 98.801; 90
4067.62Wei, Yingfei; Liu, Shi-Xia; Mueller-Bunz, Helge; Albrecht, Martin
Synthesis of Triazolylidene Nickel Complexes and Their Catalytic Application in Selective Aldehyde Hydrosilylation
ACS Catalysis, 2016, 6, 8192
4516711 CIFC40 H46 Fe N4 O3P b c n24.0256; 13.1262; 22.3213
90; 90; 90
7039.4MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516712 CIFC150 H162 F12 Fe4 N12 O6 P2P 21 21 222.7811; 22.9453; 13.3383
90; 90; 90
6972.2MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516713 CIFC36 H36 Fe N6 O6P 1 21/n 18.0949; 23.7481; 17.1961
90; 97.427; 90
3278.02MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516714 CIFC42 H50 Fe N4 O5P 1 21 115.49431; 16.23501; 15.84297
90; 107.287; 90
3805.28MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516715 CIFC16 H15 N3 O4P 1 21/c 110.2029; 19.4064; 7.7687
90; 91.548; 90
1537.7Prieto, Alexis; Bouyssi, Didier; Monteiro, Nuno
Copper-Catalyzed Double C‒H Alkylation of Aldehyde-Derived N,N-Dialkylhydrazones with Polyhalomethanes: Flexible Access to 4-Functionalized Pyrazoles
ACS Catalysis, 2016, 6, 7197
4516716 CIFC33 H22 Cl3 N4 Ni O2P -19.0058; 9.3091; 17.9195
79.797; 80.388; 89.868
1457.21He, Zhiqi; Huang, Yong
Diverting C‒H Annulation Pathways: Nickel-Catalyzed Dehydrogenative Homologation of Aromatic Amides
ACS Catalysis, 2016, 6, 7814
4516717 CIFC45 H29 F4 N2 O2C 1 2 129.3161; 8.847; 16.2475
90; 122.222; 90
3564.9He, Zhiqi; Huang, Yong
Diverting C‒H Annulation Pathways: Nickel-Catalyzed Dehydrogenative Homologation of Aromatic Amides
ACS Catalysis, 2016, 6, 7814
4516718 CIFC19 H22 O5 SP 21 21 215.6343; 17.0439; 18.3976
90; 90; 90
1766.73Gutiérrez-Bonet, Álvaro; Tellis, John C.; Matsui, Jennifer K.; Vara, Brandon A.; Molander, Gary A.
1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis.
ACS catalysis, 2016, 6, 8004-8008
4516719 CIFC22 H40 Cl2 N2 Ni O5C 1 2/c 113.0843; 30.4; 6.6223
90; 92.47; 90
2631.7Gutiérrez-Bonet, Álvaro; Tellis, John C.; Matsui, Jennifer K.; Vara, Brandon A.; Molander, Gary A.
1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis.
ACS catalysis, 2016, 6, 8004-8008

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