Crystallography Open Database
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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
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|---|---|---|---|---|---|---|
| 4514406 | CIF | C52 H49 Cl2 I O2 P2 Pd | P 1 21 1 | 11.6182; 17.9333; 12.329 90; 115.788; 90 | 2312.95 | Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines ACS Catalysis, 2019, 9, 5268 |
| 4514407 | CIF | C37 H36 Cr N O5 P | P 21 21 21 | 7.15; 19.5691; 24.0399 90; 90; 90 | 3363.6 | Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines ACS Catalysis, 2019, 9, 5268 |
| 4514408 | CIF | C62 H74.56 Ag O4.78 P2 | I 1 2 1 | 11.7485; 26.0007; 18.5841 90; 106.036; 90 | 5456 | Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines ACS Catalysis, 2019, 9, 5268 |
| 4514409 | CIF | C31 H31 N O3 S | P 1 21/c 1 | 6.4182; 21.7785; 19.0994 90; 96.787; 90 | 2651 | Li, Man-Bo; Grape, Erik Svensson; Bäckvall, Jan-E. Palladium-Catalyzed Stereospecific Oxidative Cascade Reaction of Allenes for the Construction of Pyrrole Rings: Control of Reactivity and Selectivity ACS Catalysis, 2019, 9, 5184 |
| 4514412 | CIF | C20 H26 Cl Rh | P 1 21/c 1 | 7.4511; 12.8249; 18.6937 90; 94.11; 90 | 1781.8 | Burman, Jacob S.; Harris, Robert J.; B. Farr, Caitlin M.; Bacsa, John; Blakey, Simon B. Rh(III) and Ir(III)Cp* Complexes Provide Complementary Regioselectivity Profiles in Intermolecular Allylic C‒H Amidation Reactions ACS Catalysis, 2019, 9, 5474 |
| 4514413 | CIF | C20 H26 Cl Ir | P 1 21/c 1 | 7.46343; 12.81878; 18.68909 90; 93.9187; 90 | 1783.84 | Burman, Jacob S.; Harris, Robert J.; B. Farr, Caitlin M.; Bacsa, John; Blakey, Simon B. Rh(III) and Ir(III)Cp* Complexes Provide Complementary Regioselectivity Profiles in Intermolecular Allylic C‒H Amidation Reactions ACS Catalysis, 2019, 9, 5474 |
| 4514414 | CIF | C15 H27 Br2 Co N3 | P 1 21/c 1 | 10.8842; 11.4192; 15.8101 90; 104.557; 90 | 1901.94 | Pattanaik, Sandip; Gunanathan, Chidambaram Cobalt-Catalyzed Selective Synthesis of Disiloxanes and Hydrodisiloxanes ACS Catalysis, 2019, 9, 5552 |
| 4514415 | CIF | C17 H15 N3 O2 | P 1 21/c 1 | 11.1449; 12.2086; 11.4303 90; 107.468; 90 | 1483.5 | Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters ACS Catalysis, 2019, 9, 5545 |
| 4514416 | CIF | C22 H25 N3 O4 | P -1 | 8.7858; 9.9521; 13.706 100.933; 94.003; 112.813 | 1070.9 | Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters ACS Catalysis, 2019, 9, 5545 |
| 4514417 | CIF | C18 H15 N3 O2 | P b c a | 15.251; 10.6393; 19.017 90; 90; 90 | 3085.7 | Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters ACS Catalysis, 2019, 9, 5545 |
| 4514418 | CIF | C15 H11 N3 O2 | C 1 2/c 1 | 19.26; 6.4425; 20.274 90; 100.533; 90 | 2473.3 | Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters ACS Catalysis, 2019, 9, 5545 |
| 4514419 | CIF | C12 H10 I N O | P 1 21/c 1 | 16.093; 9.8036; 6.9586 90; 93.02; 90 | 1096.33 | Chen, Fumin; He, Dongxu; Chen, Li; Chang, Xiaoyong; Wang, David Zhigang; Xu, Chen; Xing, Xiangyou Chirality-Economy Catalysis: Asymmetric Transfer Hydrogenation of Ketones by Ru-Catalysts of Minimal Stereogenicity ACS Catalysis, 2019, 9, 5562 |
| 4514420 | CIF | C59 H60 Cl2 N2 P2 Ru | P 21 21 21 | 10.9656; 11.9509; 38.4007 90; 90; 90 | 5032.4 | Chen, Fumin; He, Dongxu; Chen, Li; Chang, Xiaoyong; Wang, David Zhigang; Xu, Chen; Xing, Xiangyou Chirality-Economy Catalysis: Asymmetric Transfer Hydrogenation of Ketones by Ru-Catalysts of Minimal Stereogenicity ACS Catalysis, 2019, 9, 5562 |
| 4514611 | CIF | C29 H33 B O4 Si | P 1 | 6.264; 9.621; 11.639 91.385; 96.47; 100.453 | 684.7 | Zhao, Zhi-Yuan; Nie, Yi-Xue; Tang, Ren-He; Yin, Guan-Wu; Cao, Jian; Xu, Zheng; Cui, Yu-Ming; Zheng, Zhan-Jiang; Xu, Li-Wen Enantioselective Rhodium-Catalyzed Desymmetric Hydrosilylation of Cyclopropenes ACS Catalysis, 2019, 9, 9110 |
| 4514612 | CIF | C72 H63 Ir N2 O6 P2 | P 21 21 21 | 15.155; 17.531; 22.268 90; 90; 90 | 5916.2 | Kim, Seung Wook; Meyer, Cole C.; Mai, Binh Khanh; Liu, Peng; Krische, Michael J. Inversion of Enantioselectivity in Allene Gas versus Allyl Acetate Reductive Aldehyde Allylation Guided by Metal-Centered Stereogenicity: An Experimental and Computational Study ACS Catalysis, 2019, 9, 9158 |
| 4514613 | CIF | C23 H29 B O3 | P 21 21 21 | 11.8365; 12.8133; 13.5157 90; 90; 90 | 2049.85 | Whyte, Andrew; Mirabi, Bijan; Torelli, Alexa; Prieto, Liher; Bajohr, Jonathan; Lautens, Mark Asymmetric Synthesis of Boryl-Functionalized Cyclobutanols ACS Catalysis, 2019, 9, 9253 |
| 4514614 | CIF | C14 H14 Br F2 N O | P -1 | 9.6165; 11.7307; 12.572 93.33; 100.541; 92.151 | 1390.3 | Chen, Yuanjin; Li, Liangkui; He, Xiao; Li, Zhiping Four-Component Reactions for the Synthesis of Perfluoroalkyl Isoxazoles ACS Catalysis, 2019, 9, 9098 |
| 4514615 | CIF | C20 H17 N3 O Pd | P 65 | 22.1057; 22.1057; 6.7305 90; 90; 120 | 2848.31 | Agasti, Soumitra; Mondal, Bhaskar; Achar, Tapas Kumar; Sinha, Soumya Kumar; Sarala Suseelan, Anjana; Szabo, Kalman J.; Schoenebeck, Franziska; Maiti, Debabrata Orthogonal Selectivity in C‒H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution ACS Catalysis, 2019, 9, 9606 |
| 4514616 | CIF | C23 N3 O Pd | P -1 | 9.6348; 10.7198; 11.5837 105.639; 103.125; 104.695 | 1056.88 | Agasti, Soumitra; Mondal, Bhaskar; Achar, Tapas Kumar; Sinha, Soumya Kumar; Sarala Suseelan, Anjana; Szabo, Kalman J.; Schoenebeck, Franziska; Maiti, Debabrata Orthogonal Selectivity in C‒H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution ACS Catalysis, 2019, 9, 9606 |
| 4514617 | CIF | C24 H25 N2 O2 | P -1 | 8.8691; 10.1304; 12.2386 105.617; 100.765; 93.916 | 1032.17 | Agasti, Soumitra; Mondal, Bhaskar; Achar, Tapas Kumar; Sinha, Soumya Kumar; Sarala Suseelan, Anjana; Szabo, Kalman J.; Schoenebeck, Franziska; Maiti, Debabrata Orthogonal Selectivity in C‒H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution ACS Catalysis, 2019, 9, 9606 |
| 4514618 | CIF | C20 H26 I N O2 S | P 1 21/c 1 | 12.2416; 20.4922; 7.9382 90; 91.862; 90 | 1990.3 | Nugent, Jeremy; Arroniz, Carlos; Shire, Bethany R.; Sterling, Alistair J.; Pickford, Helena D.; Wong, Marie L. J.; Mansfield, Steven J.; Caputo, Dimitri F. J.; Owen, Benjamin; Mousseau, James J.; Duarte, Fernanda; Anderson, Edward A. A General Route to Bicyclo[1.1.1]pentanes through Photoredox Catalysis ACS Catalysis, 2019, 9, 9568 |
| 4514619 | CIF | C24 H35 I O | P 21 21 21 | 6.30332; 11.85008; 28.71209 90; 90; 90 | 2144.65 | Nugent, Jeremy; Arroniz, Carlos; Shire, Bethany R.; Sterling, Alistair J.; Pickford, Helena D.; Wong, Marie L. J.; Mansfield, Steven J.; Caputo, Dimitri F. J.; Owen, Benjamin; Mousseau, James J.; Duarte, Fernanda; Anderson, Edward A. A General Route to Bicyclo[1.1.1]pentanes through Photoredox Catalysis ACS Catalysis, 2019, 9, 9568 |
| 4514620 | CIF | C21 H25 B O2 | P -1 | 10.2291; 13.3412; 13.527 87.464; 88.582; 80.599 | 1819.14 | Léonard, Nadia G.; Palmer, W. Neil; Friedfeld, Max R.; Bezdek, Máté J.; Chirik, Paul J. Remote, Diastereoselective Cobalt-Catalyzed Alkene Isomerization‒Hydroboration: Access to Stereodefined 1,3-Difunctionalized Indanes ACS Catalysis, 2019, 9, 9034 |
| 4514621 | CIF | C18 H16 N2 O3 | P 1 c 1 | 11.4615; 5.5002; 12.6887 90; 105.131; 90 | 772.17 | Yang, Hui; Wei, Guo; Jiang, Zhiyong Access to Isoxazolidines through Visible-Light-Induced Difunctionalization of Alkenes ACS Catalysis, 2019, 9, 9599 |
| 4514622 | CIF | C44 H57 F6 N5 O6 | I 1 2/a 1 | 17.95158; 10.14969; 23.05206 90; 98.418; 90 | 4154.9 | Zhang, Yunfei; Jermaks, Janis; MacMillan, Samantha N.; Lambert, Tristan H. Synthesis of 2H-Chromenes via Hydrazine-Catalyzed Ring-Closing Carbonyl-Olefin Metathesis ACS Catalysis, 2019, 9, 9259 |
| 4514623 | CIF | C28 H46 Cl2 F3 Ir O5 P2 S | P n m a | 15.492; 24.393; 18.535 90; 90; 90 | 7004 | Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I. Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System ACS Catalysis, 2019, 9, 9317 |
| 4514624 | CIF | C44 H43 F3 O4 P4 Ru S | P b c a | 23.1713; 14.6301; 24.6604 90; 90; 90 | 8359.8 | Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I. Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System ACS Catalysis, 2019, 9, 9317 |
| 4514625 | CIF | C46 H45 F6 N O6 P4 Ru S2 | P 1 21/c 1 | 17.445; 19.175; 28.449 90; 95.41; 90 | 9474 | Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I. Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System ACS Catalysis, 2019, 9, 9317 |
| 4514626 | CIF | C27 H46 Cl2 F3 Ir O4 P2 S | P 1 21/n 1 | 16.5246; 12.6284; 17.54 90; 116.553; 90 | 3274.16 | Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I. Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System ACS Catalysis, 2019, 9, 9317 |
| 4514627 | CIF | C15 H12 O2 S | C 1 2/c 1 | 20.5001; 9.8972; 14.0168 90; 114.293; 90 | 2592.1 | Liu, Can; Fang, Yi; Wang, Shun-Yi; Ji, Shun-Jun RhCl3·3H2O-Catalyzed Ligand-Enabled Highly Regioselective Thiolation of Acrylic Acids ACS Catalysis, 2019, 9, 8910 |
| 4514628 | CIF | C9 H6 F6 O9 S2 U | P -1 | 8.7768; 9.4553; 11.5011 75.998; 71.713; 79.448 | 873.34 | Monsigny, Louis; Thuéry, Pierre; Berthet, Jean-Claude; Cantat, Thibault Breaking C‒O Bonds with Uranium: Uranyl Complexes as Selective Catalysts in the Hydrosilylation of Aldehydes ACS Catalysis, 2019, 9, 9025 |
| 4514629 | CIF | C32 H24 F12 O20 S4 U2 | P -1 | 5.6883; 12.7612; 16.5764 102.634; 94.632; 96.374 | 1160.02 | Monsigny, Louis; Thuéry, Pierre; Berthet, Jean-Claude; Cantat, Thibault Breaking C‒O Bonds with Uranium: Uranyl Complexes as Selective Catalysts in the Hydrosilylation of Aldehydes ACS Catalysis, 2019, 9, 9025 |
| 4514630 | CIF | C29 H33 F6 N3 O11 S2 U | P 1 21/c 1 | 9.2981; 22.059; 18.3163 90; 102.709; 90 | 3664.8 | Monsigny, Louis; Thuéry, Pierre; Berthet, Jean-Claude; Cantat, Thibault Breaking C‒O Bonds with Uranium: Uranyl Complexes as Selective Catalysts in the Hydrosilylation of Aldehydes ACS Catalysis, 2019, 9, 9025 |
| 4514631 | CIF | C25 H22 F N O | P 21 21 21 | 6.9609; 9.0105; 32.0299 90; 90; 90 | 2008.95 | Ma, Teng; Chen, Yate; Li, Yuxiu; Ping, Yuanyuan; Kong, Wangqing Nickel-Catalyzed Enantioselective Reductive Aryl Fluoroalkenylation of Alkenes ACS Catalysis, 2019, 9, 9127 |
| 4514632 | CIF | C24 H43.5 O4.75 | P 1 21 1 | 12.5451; 25.5594; 15.6511 90; 110.747; 90 | 4693.02 | Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V. Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass ACS Catalysis, 2019, 9, 9485 |
| 4514633 | CIF | C15 H17 N3 O4 S | P 1 21/n 1 | 13.3181; 6.9639; 17.0635 90; 90.091; 90 | 1582.6 | Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V. Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass ACS Catalysis, 2019, 9, 9485 |
| 4514634 | CIF | C21 H17 N | C 1 2/c 1 | 18.1884; 10.5558; 25.3027 90; 108.216; 90 | 4614.5 | Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V. Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass ACS Catalysis, 2019, 9, 9485 |
| 4514635 | CIF | C22 H19 N | P 1 21/c 1 | 8.8592; 22.189; 8.984 90; 114.717; 90 | 1604.25 | Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V. Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass ACS Catalysis, 2019, 9, 9485 |
| 4514636 | CIF | C51 H57 Cl Ni O2 P2 | P 1 21/n 1 | 13.151; 15.965; 21.319 90; 91.921; 90 | 4474 | McGuire, Ryan T.; Paffile, Julia F. J.; Zhou, Yuqiao; Stradiotto, Mark Nickel-Catalyzed C‒N Cross-Coupling of Ammonia, (Hetero)anilines, and Indoles with Activated (Hetero)aryl Chlorides Enabled by Ligand Design ACS Catalysis, 2019, 9, 9292 |
| 4514637 | CIF | C159 H188 Cl4 N12 Rh4 | P 1 21/n 1 | 22.2298; 14.0027; 23.0551 90; 102.788; 90 | 6998.5 | Azpíroz, Ramón; Di Giuseppe, Andrea; Urriolabeitia, Asier; Passarelli, Vincenzo; Polo, Victor; Pérez-Torrente, Jesús J.; Oro, Luis A.; Castarlenas, Ricardo Hydride‒Rhodium(III)-N-Heterocyclic Carbene Catalyst for Tandem Alkylation/Alkenylation via C‒H Activation ACS Catalysis, 2019, 9, 9372 |
| 4514638 | CIF | C34 H36 Fe N O3 P S | P 1 21 1 | 11.5035; 10.7831; 13.3149 90; 110.777; 90 | 1544.22 | Han, Jie; Zhou, Wei; Zhang, Pei-Chao; Wang, Huamin; Zhang, Ronghua; Wu, Hai-Hong; Zhang, Junliang Design and Synthesis of WJ-Phos, and Application in Cu-Catalyzed Enantioselective Boroacylation of 1,1-Disubstituted Allenes ACS Catalysis, 2019, 9, 6890 |
| 4514639 | CIF | C24 H29 B O3 | P 21 21 21 | 8.8534; 12.6813; 18.9601 90; 90; 90 | 2128.7 | Han, Jie; Zhou, Wei; Zhang, Pei-Chao; Wang, Huamin; Zhang, Ronghua; Wu, Hai-Hong; Zhang, Junliang Design and Synthesis of WJ-Phos, and Application in Cu-Catalyzed Enantioselective Boroacylation of 1,1-Disubstituted Allenes ACS Catalysis, 2019, 9, 6890 |
| 4514640 | CIF | C38 H37 Cl3 Fe N O2 P S | P 1 21 1 | 10.5036; 11.7796; 15.6619 90; 106.748; 90 | 1855.62 | Han, Jie; Zhou, Wei; Zhang, Pei-Chao; Wang, Huamin; Zhang, Ronghua; Wu, Hai-Hong; Zhang, Junliang Design and Synthesis of WJ-Phos, and Application in Cu-Catalyzed Enantioselective Boroacylation of 1,1-Disubstituted Allenes ACS Catalysis, 2019, 9, 6890 |
| 4514641 | CIF | C50 H60 N4 O4 Rh2 | P 1 21/c 1 | 19.9451; 11.5613; 20.0794 90; 94.241; 90 | 4617.5 | Zhu, Weihao; Luo, Zhongwen; Chen, Junqi; Liu, Chang; Yang, Lu; Dickie, Diane A.; Liu, Naiming; Zhang, Sen; Davis, Robert J.; Gunnoe, T. Brent Mechanistic Studies of Single-Step Styrene Production Catalyzed by Rh Complexes with Diimine Ligands: An Evaluation of the Role of Ligands and Induction Period ACS Catalysis, 2019, 9, 7457 |
| 4514642 | CIF | C40 H26 F20 N4 O5 Rh2 | P 1 21/c 1 | 23.889; 9.9822; 19.624 90; 110.013; 90 | 4397.1 | Zhu, Weihao; Luo, Zhongwen; Chen, Junqi; Liu, Chang; Yang, Lu; Dickie, Diane A.; Liu, Naiming; Zhang, Sen; Davis, Robert J.; Gunnoe, T. Brent Mechanistic Studies of Single-Step Styrene Production Catalyzed by Rh Complexes with Diimine Ligands: An Evaluation of the Role of Ligands and Induction Period ACS Catalysis, 2019, 9, 7457 |
| 4514643 | CIF | C103 H224 Ni4 O32 Si8 | P 1 21/c 1 | 24.2076; 27.078; 21.532 90; 106.288; 90 | 13547.6 | Moroz, Ilia B.; Lund, Alicia; Kaushik, Monu; Severy, Laurent; Gajan, David; Fedorov, Alexey; Lesage, Anne; Copéret, Christophe Specific Localization of Aluminum Sites Favors Ethene-to-Propene Conversion on (Al)MCM-41-Supported Ni(II) Single Sites ACS Catalysis, 2019, 9, 7476 |
| 4514644 | CIF | C48 H60 Co Li N2 O | P m n 21 | 17.4715; 10.5472; 10.9763 90; 90; 90 | 2022.66 | Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates ACS Catalysis, 2019, 9, 7596 |
| 4514645 | CIF | C45 H53 Co N2 | P -1 | 12.3103; 12.6855; 13.5302 69.519; 77.844; 79.251 | 1920.22 | Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates ACS Catalysis, 2019, 9, 7596 |
| 4514646 | CIF | C36 H40 Br2 Co N2 | P 1 21/c 1 | 27.0266; 12.0329; 22.8033 90; 113.047; 90 | 6823.9 | Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates ACS Catalysis, 2019, 9, 7596 |
| 4514648 | CIF | C90 H121 Co2 Li N4 O4.5 | P b c a | 25.0102; 21.4146; 30.8908 90; 90; 90 | 16544.6 | Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates ACS Catalysis, 2019, 9, 7596 |
| 4514649 | CIF | C92 H123 Co2 Li N4 O5 | P 1 21/n 1 | 21.4917; 13.0279; 29.987 90; 101.086; 90 | 8239.4 | Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates ACS Catalysis, 2019, 9, 7596 |
| 4514650 | CIF | C48 H44 B Br N2 P4 | P -1 | 10.551; 12.062; 18.905 82.63; 81.72; 66.18 | 2171.5 | Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis ACS Catalysis, 2019, 9, 7300 |
| 4514651 | CIF | C54.5 H51 B Br Cl5 Fe O2 P4 | P -1 | 11.496; 12.374; 20.858 97.02; 94.81; 111.71 | 2709 | Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis ACS Catalysis, 2019, 9, 7300 |
| 4514652 | CIF | C18 H44 B Br Fe N2 O2 P4 | P 1 21/c 1 | 12.7253; 10.5434; 21.3482 90; 102.389; 90 | 2797.5 | Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis ACS Catalysis, 2019, 9, 7300 |
| 4514653 | CIF | C19 H43 B Br Fe N2 O3 P4 | P n a 21 | 14.623; 15.131; 12.874 90; 90; 90 | 2848.5 | Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis ACS Catalysis, 2019, 9, 7300 |
| 4514654 | CIF | C18 H21 N O5 S | P 1 21/n 1 | 9.7666; 7.7835; 22.574 90; 94.062; 90 | 1711.73 | Zhou, Kehan; Zhu, Yan; Fan, Weitai; Chen, Yujie; Xu, Xu; Zhang, Jingyu; Zhao, Yingsheng Late-Stage Functionalization of Aromatic Acids with Aliphatic Aziridines: Direct Approach to Form β-Branched Arylethylamine Backbones ACS Catalysis, 2019, 9, 6738 |
| 4514655 | CIF | C18 H23 N O6 S | P 1 21 1 | 8.1162; 11.0214; 10.5496 90; 91.17; 90 | 943.48 | Zhou, Kehan; Zhu, Yan; Fan, Weitai; Chen, Yujie; Xu, Xu; Zhang, Jingyu; Zhao, Yingsheng Late-Stage Functionalization of Aromatic Acids with Aliphatic Aziridines: Direct Approach to Form β-Branched Arylethylamine Backbones ACS Catalysis, 2019, 9, 6738 |
| 4514656 | CIF | C27 H48 Cl N2 P Ru | P 41 | 13.2477; 13.2477; 32.623 90; 90; 90 | 5725.4 | 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 |
| 4514657 | CIF | C24 H39 F9 N2 P2 Ru | P 1 21/c 1 | 22.5581; 12.7798; 22.1335 90; 113.18; 90 | 5865.7 | 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 |
| 4514658 | CIF | C40 H48 Cl4 F12 Ru4 | P -1 | 11.6853; 20.7278; 21.1082 114.576; 96.847; 99.355 | 4487.1 | 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 |
| 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 |
| 4514679 | CIF | C17 H21 B Br N O2 | P 1 21 1 | 11.3502; 7.45; 20.6376 90; 91.376; 90 | 1744.59 | Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J. Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes ACS Catalysis, 2019, 9, 6744 |
| 4514680 | CIF | C20 H16 Br N O2 | P 1 21 1 | 14.62776; 8.05742; 15.00218 90; 97.0979; 90 | 1754.64 | Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J. Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes ACS Catalysis, 2019, 9, 6744 |
| 4514681 | CIF | C11 H10 I0.96 N O | P 1 21 1 | 9.8268; 5.6439; 9.8652 90; 99.353; 90 | 539.86 | Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J. Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes ACS Catalysis, 2019, 9, 6744 |
| 4514682 | CIF | C14 H24 N2 O4 Pd | P 1 21/c 1 | 9.3121; 10.7025; 8.4772 90; 97.201; 90 | 838.2 | Feng, Wenhui; Wang, Tianyang; Liu, Dongzhi; Wang, Xiaotai; Dang, Yanfeng Mechanism of the Palladium-Catalyzed C(sp3)‒H Arylation of Aliphatic Amines: Unraveling the Crucial Role of Silver(I) Additives ACS Catalysis, 2019, 9, 6672 |
| 4514683 | CIF | C42 H35 F12 N11 P2 Pd2 | P -1 | 12.0088; 12.3492; 17.137 101.431; 106.142; 105.372 | 2250.17 | Zhu, Jiancheng; Lindsay, Vincent N. G. Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions ACS Catalysis, 2019, 9, 6993 |
| 4514684 | CIF | C25 H20 Cl F6 N4 O P Pd | P -1 | 8.7896; 12.4079; 13.433 108.517; 105.407; 103.424 | 1256.4 | Zhu, Jiancheng; Lindsay, Vincent N. G. Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions ACS Catalysis, 2019, 9, 6993 |
| 4514685 | CIF | C45 H48 F12 N8 O3 P2 Pd2 | C 1 2/c 1 | 25.202; 8.3844; 24.157 90; 108.454; 90 | 4842 | Zhu, Jiancheng; Lindsay, Vincent N. G. Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions ACS Catalysis, 2019, 9, 6993 |
| 4514686 | CIF | C12 H11 Br F3 N3 O2 | P 1 21/c 1 | 10.3636; 10.0648; 28.9197 90; 99.7; 90 | 2973.4 | Chen, Zhen; Ren, Nan; Ma, Xiaoxiao; Nie, Jing; Zhang, Fa-Guang; Ma, Jun-An Silver-Catalyzed [3 + 3] Dipolar Cycloaddition of Trifluorodiazoethane and Glycine Imines: Access to Highly Functionalized Trifluoromethyl-Substituted Triazines and Pyridines ACS Catalysis, 2019, 9, 4600 |
| 4514687 | CIF | C15 H11 Cl F3 N O2 | P 1 21/n 1 | 17.29; 4.519; 20.77 90; 111.24; 90 | 1513 | Chen, Zhen; Ren, Nan; Ma, Xiaoxiao; Nie, Jing; Zhang, Fa-Guang; Ma, Jun-An Silver-Catalyzed [3 + 3] Dipolar Cycloaddition of Trifluorodiazoethane and Glycine Imines: Access to Highly Functionalized Trifluoromethyl-Substituted Triazines and Pyridines ACS Catalysis, 2019, 9, 4600 |
| 4514688 | CIF | C34 H26 N2 | P 1 21/n 1 | 11.5593; 7.8828; 27.35 90; 98.043; 90 | 2467.6 | Noto, Naoki; Koike, Takashi; Akita, Munetaka Visible-Light-Triggered Monofluoromethylation of Alkenes by Strongly Reducing 1,4-Bis(diphenylamino)naphthalene Photoredox Catalysis ACS Catalysis, 2019, 9, 4382 |
| 4514689 | CIF | C21 H20 F3 N O5 S | P 1 | 9.0328; 9.506; 13.9771 90.165; 95.249; 115.51 | 1077.42 | He, Xiao-Long; Zhao, Hui-Ru; Song, Xue; Jiang, Bo; Du, Wei; Chen, Ying-Chun Asymmetric Barton‒Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons ACS Catalysis, 2019, 9, 4374 |
| 4514690 | CIF | C24 H25 N3 O4 | P 21 21 21 | 9.2464; 10.0773; 23.4808 90; 90; 90 | 2187.91 | He, Xiao-Long; Zhao, Hui-Ru; Song, Xue; Jiang, Bo; Du, Wei; Chen, Ying-Chun Asymmetric Barton‒Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons ACS Catalysis, 2019, 9, 4374 |
| 4514691 | CIF | C25 H17 N O | P 1 21/n 1 | 8.618; 11.775; 18.166 90; 103.293; 90 | 1794 | Yuan, Hairui; Guo, Lirong; Liu, Fengting; Miao, Zechen; Feng, Lei; Gao, Hongyin Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles ACS Catalysis, 2019, 9, 3906 |
| 4514692 | CIF | C31 H21 N O | P 21 21 21 | 8.1125; 12.1517; 23.1044 90; 90; 90 | 2277.65 | Yuan, Hairui; Guo, Lirong; Liu, Fengting; Miao, Zechen; Feng, Lei; Gao, Hongyin Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles ACS Catalysis, 2019, 9, 3906 |
| 4514693 | CIF | C24 H46 N6 Ni O6 | P 21 21 21 | 8.7123; 16.0813; 20.4271 90; 90; 90 | 2861.9 | Garrido-Barros, Pablo; Grau, Sergi; Drouet, Samuel; Benet-Buchholz, Jordi; Gimbert-Suriñach, Carolina; Llobet, Antoni Can Ni Complexes Behave as Molecular Water Oxidation Catalysts? ACS Catalysis, 2019, 9, 3936 |
| 4514694 | CIF | C21 H44 N6 Ni O9 | C 1 2/c 1 | 55.552; 6.2616; 15.8906 90; 100.323; 90 | 5438 | Garrido-Barros, Pablo; Grau, Sergi; Drouet, Samuel; Benet-Buchholz, Jordi; Gimbert-Suriñach, Carolina; Llobet, Antoni Can Ni Complexes Behave as Molecular Water Oxidation Catalysts? ACS Catalysis, 2019, 9, 3936 |
| 4514695 | CIF | C26 H29 N O | P 1 21/c 1 | 6.2208; 18.757; 17.484 90; 93.268; 90 | 2036.8 | Han, Chunhua; Fu, Zhiyuan; Guo, Songjin; Fang, Xinxin; Lin, Aijun; Yao, Hequan Palladium-Catalyzed Remote 1,n-Arylamination of Unactivated Terminal Alkenes ACS Catalysis, 2019, 9, 4196 |
| 4514696 | CIF | C58 H84 F7 N2 O4 P Pd S | P 1 21/c 1 | 20.138; 13.1828; 24.998 90; 106.912; 90 | 6349.4 | Dennis, Joseph M.; White, Nicholas A.; Liu, Richard Y.; Buchwald, Stephen L. Pd-Catalyzed C‒N Coupling Reactions Facilitated by Organic Bases: Mechanistic Investigation Leads to Enhanced Reactivity in the Arylation of Weakly Binding Amines ACS Catalysis, 2019, 9, 3822 |
| 4514697 | CIF | C43 H73.5 P2 Ru S | P -1 | 13.159; 15.396; 21.596 90.092; 92.283; 101.727 | 4280.3 | Zhou, Xiaoguang; Malakar, Santanu; Zhou, Tian; Murugesan, Sathiyamoorthy; Huang, Carlos; Emge, Thomas J.; Krogh-Jespersen, Karsten; Goldman, Alan S. Catalytic Alkane Transfer Dehydrogenation by PSP-Pincer-Ligated Ruthenium. Deactivation of an Extremely Reactive Fragment by Formation of Allyl Hydride Complexes ACS Catalysis, 2019, 9, 4072 |
| 4514698 | CIF | C38 H62 P2 Ru S | P 1 21/c 1 | 13.2907; 15.6689; 18.8836 90; 105.176; 90 | 3795.4 | Zhou, Xiaoguang; Malakar, Santanu; Zhou, Tian; Murugesan, Sathiyamoorthy; Huang, Carlos; Emge, Thomas J.; Krogh-Jespersen, Karsten; Goldman, Alan S. Catalytic Alkane Transfer Dehydrogenation by PSP-Pincer-Ligated Ruthenium. Deactivation of an Extremely Reactive Fragment by Formation of Allyl Hydride Complexes ACS Catalysis, 2019, 9, 4072 |
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