Crystallography Open Database

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4514185 CIFC25 H21 O PP -19.8901; 10.4204; 12.056
68.572; 85.149; 69.897
1084.9Toda, Yasunori; Sakamoto, Tomoyuki; Komiyama, Yutaka; Kikuchi, Ayaka; Suga, Hiroyuki
A Phosphonium Ylide as an Ionic Nucleophilic Catalyst for Primary Hydroxyl Group Selective Acylation of Diols
ACS Catalysis, 2017, 7, 6150
4514187 CIFC22 H23 N OP b c a15.4176; 11.3505; 20.247
90; 90; 90
3543.2Li, Yang; Hu, Ming; Li, Jin-Heng
Silver-Catalyzed Intermolecular [3 + 2]/[5 + 2] Annulation of N-Arylpropiolamides with Vinyl Acids: Facile Synthesis of Fused 2H-Benzo[b]azepin-2-ones
ACS Catalysis, 2017, 7, 6757
4514188 CIFC18 H20 N2 O2P -16.3768; 10.567; 11.5596
108.484; 92.159; 106.084
703.06Mampuys, Pieter; Neumann, Helfried; Sergeyev, Sergey; Orru, Romano V. A.; Jiao, Haijun; Spannenberg, Anke; Maes, Bert U. W.; Beller, Matthias
Combining Isocyanides with Carbon Dioxide in Palladium-Catalyzed Heterocycle Synthesis: N3-Substituted Quinazoline-2,4(1H,3H)-diones via a Three-Component Reaction
ACS Catalysis, 2017, 7, 5549
4514189 CIFC16 H22 N2 O2P -110.3381; 12.1298; 12.7543
98.7084; 97.6979; 101.969
1523.79Mampuys, Pieter; Neumann, Helfried; Sergeyev, Sergey; Orru, Romano V. A.; Jiao, Haijun; Spannenberg, Anke; Maes, Bert U. W.; Beller, Matthias
Combining Isocyanides with Carbon Dioxide in Palladium-Catalyzed Heterocycle Synthesis: N3-Substituted Quinazoline-2,4(1H,3H)-diones via a Three-Component Reaction
ACS Catalysis, 2017, 7, 5549
4514190 CIFC27 H52 Cl N O P4 WP 1 21/n 113.5317; 16.7932; 14.6934
90; 95.148; 90
3325.5Rudshteyn, Benjamin; Vibbert, Hunter B.; May, Richard; Wasserman, Eric; Warnke, Ingolf; Hopkins, Michael D.; Batista, Victor S.
Thermodynamic and Structural Factors That Influence the Redox Potentials of Tungsten‒Alkylidyne Complexes
ACS Catalysis, 2017, 7, 6134
4514193 CIFC37.21 H40.41 Cl2.41 Cu I N6P 21 21 2116.9652; 19.7318; 24.8974
90; 90; 90
8334.5Wan, Kai Y.; Sung, Molly M. H.; Lough, Alan J.; Morris, Robert H.
Half-Sandwich Ruthenium Catalyst Bearing an Enantiopure Primary Amine Tethered to an N-Heterocyclic Carbene for Ketone Hydrogenation
ACS Catalysis, 2017, 7, 6827
4514194 CIFC43 H43 Cl Ni P2P 1 21/n 112.3832; 17.1052; 17.3844
90; 106.111; 90
3537.7Mifleur, Alexis; Mérel, Delphine S.; Mortreux, André; Suisse, Isabelle; Capet, Frédéric; Trivelli, Xavier; Sauthier, Mathieu; Macgregor, Stuart A.
Deciphering the Mechanism of the Nickel-Catalyzed Hydroalkoxylation Reaction: A Combined Experimental and Computational Study
ACS Catalysis, 2017, 7, 6915
4514195 CIFC32 H35 Cl Ni P2P -110.3622; 11.0841; 13.1883
100.947; 102.623; 105.014
1377.98Mifleur, Alexis; Mérel, Delphine S.; Mortreux, André; Suisse, Isabelle; Capet, Frédéric; Trivelli, Xavier; Sauthier, Mathieu; Macgregor, Stuart A.
Deciphering the Mechanism of the Nickel-Catalyzed Hydroalkoxylation Reaction: A Combined Experimental and Computational Study
ACS Catalysis, 2017, 7, 6915
4514196 CIFC39 H52 Hf N2P -19.1605; 12.4145; 15.8667
91.003; 105.64; 97.611
1719.61Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514197 CIFC28 H36 Hf N2P 1 21/n 110.3324; 14.8323; 16.0844
90; 97.923; 90
2441.5Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514198 CIFC33 H40 Hf N2P -111.0762; 11.953; 12.8362
79.555; 66.82; 67.872
1446.09Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514199 CIFC32 H38 Hf N2P -19.6947; 12.8143; 22.3108
91.516; 95.983; 93.882
2748.7Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514200 CIFC32 H36 Hf N2P -19.3898; 10.7845; 13.8529
87.005; 78.576; 86.78
1371.63Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514201 CIFC30 H30 Br N3 O4P 21 21 218.2547; 11.7633; 28.9888
90; 90; 90
2814.89Jiang, Fei; Zhao, Dan; Yang, Xue; Yuan, Fu-Ru; Mei, Guang-Jian; Shi, Feng
Catalyst-Controlled Chemoselective and Enantioselective Reactions of Tryptophols with Isatin-Derived Imines
ACS Catalysis, 2017, 7, 6984
4514202 CIFC30 H30 Cl N3 O4P -19.6201; 10.3131; 14.6525
78.547; 72.894; 89.686
1359.6Jiang, Fei; Zhao, Dan; Yang, Xue; Yuan, Fu-Ru; Mei, Guang-Jian; Shi, Feng
Catalyst-Controlled Chemoselective and Enantioselective Reactions of Tryptophols with Isatin-Derived Imines
ACS Catalysis, 2017, 7, 6984
4514205 CIFC31 H32 Fe O3P 21 21 219.6682; 10.6608; 48.1982
90; 90; 90
4967.8Larionov, Evgeny; Mastandrea, Marco M.; Pericàs, Miquel A.
Asymmetric Visible-Light Photoredox Cross-Dehydrogenative Coupling of Aldehydes with Xanthenes
ACS Catalysis, 2017, 7, 7008
4514206 CIFC20.25 H24.25 Cl0.5 O2C 1 2/c 138.935; 8.5678; 28.446
90; 133.9; 90
6837Larionov, Evgeny; Mastandrea, Marco M.; Pericàs, Miquel A.
Asymmetric Visible-Light Photoredox Cross-Dehydrogenative Coupling of Aldehydes with Xanthenes
ACS Catalysis, 2017, 7, 7008
4514207 CIFC21 H26 F6 Ir N3 O8 S2P b c a15.8414; 14.5592; 24.0253
90; 90; 90
5541.15Fujita, Ken-ichi; Tamura, Ryuichi; Tanaka, Yuhi; Yoshida, Masato; Onoda, Mitsuki; Yamaguchi, Ryohei
Dehydrogenative Oxidation of Alcohols in Aqueous Media Catalyzed by a Water-Soluble Dicationic Iridium Complex Bearing a Functional N-Heterocyclic Carbene Ligand without Using Base
ACS Catalysis, 2017, 7, 7226
4514208 CIFC20 H25 F3 Ir N3 O5 SP -19.5878; 10.2028; 11.8401
83.082; 88.989; 83.868
1143.2Fujita, Ken-ichi; Tamura, Ryuichi; Tanaka, Yuhi; Yoshida, Masato; Onoda, Mitsuki; Yamaguchi, Ryohei
Dehydrogenative Oxidation of Alcohols in Aqueous Media Catalyzed by a Water-Soluble Dicationic Iridium Complex Bearing a Functional N-Heterocyclic Carbene Ligand without Using Base
ACS Catalysis, 2017, 7, 7226
4514209 CIFC35 H32 Cl2 N6P -111.9189; 11.9269; 13.6776
89.671; 67.67; 63.388
1575.9Zhou, Xukai; Luo, Yixin; Kong, Lingheng; Xu, Youwei; Zheng, Guangfan; Lan, Yu; Li, Xingwei
Cp*CoIII-Catalyzed Branch-Selective Hydroarylation of Alkynes via C‒H Activation: Efficient Access to α-gem-Vinylindoles
ACS Catalysis, 2017, 7, 7296
4514216 CIFC42 H43 O P SiP 21 21 2110.3642; 10.71104; 30.9626
90; 90; 90
3437.2Grosheva, Daria; Cramer, Nicolai
Ketene Aminal Phosphates: Competent Substrates for Enantioselective Pd(0)-Catalyzed C‒H Functionalizations
ACS Catalysis, 2017, 7, 7417
4514217 CIFC18 H13 Cl2 N OP 21 21 214.7873; 12.3631; 25.26
90; 90; 90
1495.04Grosheva, Daria; Cramer, Nicolai
Ketene Aminal Phosphates: Competent Substrates for Enantioselective Pd(0)-Catalyzed C‒H Functionalizations
ACS Catalysis, 2017, 7, 7417
4514218 CIFC20 H6 F8 S2P b c a7.1369; 13.1737; 35.7724
90; 90; 90
3363.3Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514219 CIFC18 H25 Cl F4 Mg O3P 1 21 18.8663; 12.7576; 9.7375
90; 112.848; 90
1015.01Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514220 CIFC48 H30 F8 Ni O P2P b c n39.6323; 11.1626; 19.9766
90; 90; 90
8837.6Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514221 CIFC17 H10 F4 O2 S2P 1 21/c 17.7206; 10.8574; 19.0756
90; 90.148; 90
1599.02Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514222 CIFC36 H32 N8 O4P 21 21 215.7087; 16.28; 17.073
90; 90; 90
1586.7Liao, Yun; Lu, Qianqian; Chen, Gui; Yu, Yinghua; Li, Chunsen; Huang, Xueliang
Rhodium-Catalyzed Azide‒Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions
ACS Catalysis, 2017, 7, 7529
4514223 CIFC17 H18 N4 O2 SP 1 21/c 111.611; 19.247; 8.0285
90; 107.27; 90
1713.3Liao, Yun; Lu, Qianqian; Chen, Gui; Yu, Yinghua; Li, Chunsen; Huang, Xueliang
Rhodium-Catalyzed Azide‒Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions
ACS Catalysis, 2017, 7, 7529
4514224 CIFC10 H16 O2P 1 21/n 15.9454; 23.5638; 6.5353
90; 104.593; 90
886.03Zhu, Rui; Jiang, Ju-Long; Li, Xing-Long; Deng, Jin; Fu, Yao
A Comprehensive Study on Metal Triflate-Promoted Hydrogenolysis of Lactones to Carboxylic Acids: From Synthetic and Mechanistic Perspectives
ACS Catalysis, 2017, 7, 7520
4514225 CIFC10 H16 O2P 1 21/n 16.0866; 21.259; 7.3676
90; 106.814; 90
912.6Zhu, Rui; Jiang, Ju-Long; Li, Xing-Long; Deng, Jin; Fu, Yao
A Comprehensive Study on Metal Triflate-Promoted Hydrogenolysis of Lactones to Carboxylic Acids: From Synthetic and Mechanistic Perspectives
ACS Catalysis, 2017, 7, 7520
4514226 CIFC49 H59 Cl3 Fe2 N2 PdC 1 2/c 127.734; 9.9782; 18.5024
90; 111.932; 90
4749.7Zhao, Minhui; Chen, Changle
Accessing Multiple Catalytically Active States in Redox-Controlled Olefin Polymerization
ACS Catalysis, 2017, 7, 7490
4514231 CIFC13 H11 Br O2 SP -16.6244; 9.5477; 11.0255
69.728; 77.396; 74.138
623.31Li, Yiming; Wang, Ming; Jiang, Xuefeng
Controllable Sulfoxidation and Sulfenylation with Organic Thiosulfate Salts via Dual Electron- and Energy-Transfer Photocatalysis
ACS Catalysis, 2017, 7, 7587
4514232 CIFC26 H26 O6 SP 21 21 216.2606; 7.9157; 45.636
90; 90; 90
2261.6Wu, Zijun; Wang, Jian
Enantioselective Medium-Ring Lactone Synthesis through an NHC-Catalyzed Intramolecular Desymmetrization of Prochiral 1,3-Diols
ACS Catalysis, 2017, 7, 7647
4514233 CIFC30 H32 Fe N P SI 1 2/c 115.7631; 9.2957; 35.3175
90; 95.742; 90
5149.07Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514234 CIFC28 H32 B Fe P SP 1 21/n 118.433; 8.274; 18.909
90; 117.569; 90
2556.4Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514235 CIFC36 H44 B Fe P SP 1 21/c 112.13; 11.24; 23.29
90; 96.035; 90
3158Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514236 CIFC42 H41 Fe O P SP b c a17.451; 19.304; 20.241
90; 90; 90
6819Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514237 CIFC28 H29 Cl Fe P SP c 21 n10.13; 14.433; 16.554
90; 90; 90
2420.3Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514238 CIFC29 H29 Fe O P SP c 21 n10.1455; 14.4475; 16.7227
90; 90; 90
2451.2Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514239 CIFC20 H25 B O3P 1 21 16.468; 24.149; 12.121
90; 101.11; 90
1857.8Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514246 CIFC24 H18 O2 SP 21 21 219.5092; 12.3167; 15.9826
90; 90; 90
1871.91Lu, Hong; Zhang, Jia-Lu; Liu, Jin-Yu; Li, Hong-Yu; Xu, Peng-Fei
N-Heterocyclic Carbene-Catalyzed Atom-Economical and Enantioselective Construction of the C‒S Bond: Asymmetric Synthesis of Functionalized Thiochromans
ACS Catalysis, 2017, 7, 7797
4514247 CIFC19 H19 N O3P 1 21/n 19.3432; 12.1755; 14.6611
90; 102.176; 90
1630.3Peng, Xie-Xue; Wei, Dian; Han, Wen-Jun; Chen, Fei; Yu, Wei; Han, Bing
Dioxygen Activation via Cu-Catalyzed Cascade Radical Reaction: An Approach to Isoxazoline/Cyclic Nitrone-Featured α-Ketols
ACS Catalysis, 2017, 7, 7830
4514248 CIFC11 H11 N O2P 1 21/m 16.417; 7.0536; 10.791
90; 93.618; 90
487.46Peng, Xie-Xue; Wei, Dian; Han, Wen-Jun; Chen, Fei; Yu, Wei; Han, Bing
Dioxygen Activation via Cu-Catalyzed Cascade Radical Reaction: An Approach to Isoxazoline/Cyclic Nitrone-Featured α-Ketols
ACS Catalysis, 2017, 7, 7830
4514249 CIFC18 H17 N O3P 3210.8566; 10.8566; 11.4924
90; 90; 120
1173.08Peng, Xie-Xue; Wei, Dian; Han, Wen-Jun; Chen, Fei; Yu, Wei; Han, Bing
Dioxygen Activation via Cu-Catalyzed Cascade Radical Reaction: An Approach to Isoxazoline/Cyclic Nitrone-Featured α-Ketols
ACS Catalysis, 2017, 7, 7830
4514250 CIFC20 H20 O4P 21 21 215.6577; 8.9036; 32.5408
90; 90; 90
1639.21Su, Yong-Liang; Han, Zhi-Yong; Li, Yu-Hui; Gong, Liu-Zhu
Asymmetric Allylation of Furfural Derivatives: Synergistic Effect of Chiral Ligand and Organocatalyst on Stereochemical Control
ACS Catalysis, 2017, 7, 7917
4514251 CIFC44 H37 Cl4 Ir O3 P2P -111.127; 11.586; 16.948
85.617; 75.929; 70.932
2003Cohen, Shirel; Borin, Veniamin; Schapiro, Igor; Musa, Sanaa; De-Botton, Sophie; Belkova, Natalia V.; Gelman, Dmitri
Ir(III)-PC(sp3)P Bifunctional Catalysts for Production of H2 by Dehydrogenation of Formic Acid: Experimental and Theoretical Study
ACS Catalysis, 2017, 7, 8139
4514252 CIFC44 H32 Cl Ir N O7 P2P 1 21/c 113.554; 25.997; 13.478
90; 108.116; 90
4513.7Cohen, Shirel; Borin, Veniamin; Schapiro, Igor; Musa, Sanaa; De-Botton, Sophie; Belkova, Natalia V.; Gelman, Dmitri
Ir(III)-PC(sp3)P Bifunctional Catalysts for Production of H2 by Dehydrogenation of Formic Acid: Experimental and Theoretical Study
ACS Catalysis, 2017, 7, 8139
4514253 CIFC24 H20 N4 O3 PdP -18.323; 11.108; 11.747
95.97; 98.14; 94.164
1065Deb, Arghya; Singh, Sukriti; Seth, Kapileswar; Pimparkar, Sandeep; Bhaskararao, Bangaru; Guin, Srimanta; Sunoj, Raghavan B.; Maiti, Debabrata
Experimental and Computational Studies on Remote γ-C(sp3)‒H Silylation and Germanylation of Aliphatic Carboxamides
ACS Catalysis, 2017, 7, 8171
4514278 CIFCu2 Gd4 H104 O120 W19 Zn3P -116.3885; 16.597; 21.2038
91.749; 101.863; 113.393
5139.8Zhao, Min; Zhang, Xian-Wei; Wu, Chuan-De
Structural Transformation of Porous Polyoxometalate Frameworks and Highly Efficient Biomimetic Aerobic Oxidation of Aliphatic Alcohols
ACS Catalysis, 2017, 7, 6573
4514279 CIFCu2 Gd4 H114 O105 W19 Zn3P -112.3498; 13.2731; 16.0314
68.011; 70.892; 69.811
2226.9Zhao, Min; Zhang, Xian-Wei; Wu, Chuan-De
Structural Transformation of Porous Polyoxometalate Frameworks and Highly Efficient Biomimetic Aerobic Oxidation of Aliphatic Alcohols
ACS Catalysis, 2017, 7, 6573
4514280 CIFC26 H28 N4 O7 Ru SP 1 21/n 111.051; 15.235; 16.459
90; 105.354; 90
2672.2Matheu, Roc; Ertem, Mehmed Z.; Gimbert-Suriñach, Carolina; Benet-Buchholz, Jordi; Sala, Xavier; Llobet, Antoni
Hydrogen Bonding Rescues Overpotential in Seven-Coordinated Ru Water Oxidation Catalysts
ACS Catalysis, 2017, 7, 6525
4514281 CIFC17 H25 Ir N2 O6 SP -19.919; 10.244; 10.412
65.248; 89.25; 80.89
947Kanega, Ryoichi; Onishi, Naoya; Szalda, David J.; Ertem, Mehmed Z.; Muckerman, James T.; Fujita, Etsuko; Himeda, Yuichiro
CO2 Hydrogenation Catalysts with Deprotonated Picolinamide Ligands
ACS Catalysis, 2017, 7, 6426
4514282 CIFC102 H149 Cl In2 N4 O5P 112.1349; 12.2766; 18.6225
85.388; 74.176; 65.392
2425Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514283 CIFC96.95 H139.51 Cl In2 N4 O5P 112.196; 12.295; 18.618
86.04; 73.489; 64.932
2420.3Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514284 CIFC86 H128 In2 N4 O6P 112.0666; 12.3213; 18.3525
74.092; 87.97; 65.236
2372.91Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514285 CIFC72 H104 In2 N4 O6P 1 21/c 117.557; 19.409; 12.845
90; 99.726; 90
4314Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514286 CIFC14 H11 Br N2 OP 21 21 215.1494; 10.5103; 23.635
90; 90; 90
1279.2Hatano, Manabu; Yamakawa, Katsuya; Ishihara, Kazuaki
Enantioselective Conjugate Hydrocyanation of α,β-Unsaturated N-Acylpyrroles Catalyzed by Chiral Lithium(I) Phosphoryl Phenoxide
ACS Catalysis, 2017, 7, 6686
4514289 CIFC23 H19 F3 N4 O2P 1 21/n 18.76727; 24.7029; 9.7159
90; 100.555; 90
2068.63Ye, Jian-Heng; Zhu, Lei; Yan, Si-Shun; Miao, Meng; Zhang, Xin-Chi; Zhou, Wen-Jun; Li, Jing; Lan, Yu; Yu, Da-Gang
Radical Trifluoromethylative Dearomatization of Indoles and Furans with CO2
ACS Catalysis, 2017, 7, 8324
4514290 CIFC20 H20 Cl2 N8 RuP -19.4232; 10.4405; 14.3166
98.121; 99.958; 116.027
1208.5Telleria, Ainara; Vicent, Cristian; San Nacianceno, Virginia; Garralda, María A.; Freixa, Zoraida
Experimental Evidence Supporting Related Mechanisms for Ru(II)-Catalyzed Dehydrocoupling and Hydrolysis of Amine-Boranes
ACS Catalysis, 2017, 7, 8394
4514291 CIFC24 H22 Cl2 N2 O3.95 RuP -16.9529; 11.5712; 16.87
92.79; 99.326; 96.309
1328.14Telleria, Ainara; Vicent, Cristian; San Nacianceno, Virginia; Garralda, María A.; Freixa, Zoraida
Experimental Evidence Supporting Related Mechanisms for Ru(II)-Catalyzed Dehydrocoupling and Hydrolysis of Amine-Boranes
ACS Catalysis, 2017, 7, 8394
4514292 CIFC23 H23 Br Cl11 N5 RuP -110.6051; 10.7857; 16.5095
93.576; 102.19; 107.715
1742Telleria, Ainara; Vicent, Cristian; San Nacianceno, Virginia; Garralda, María A.; Freixa, Zoraida
Experimental Evidence Supporting Related Mechanisms for Ru(II)-Catalyzed Dehydrocoupling and Hydrolysis of Amine-Boranes
ACS Catalysis, 2017, 7, 8394
4514293 CIFC46 H48 N4 ZnP -112.1191; 13.987; 14.338
66.838; 73.267; 64.731
1999.6Lortie, John L.; Dudding, Travis; Gabidullin, Bulat M.; Nikonov, Georgii I.
Zinc-Catalyzed Hydrosilylation and Hydroboration of N-Heterocycles
ACS Catalysis, 2017, 7, 8454
4514298 CIFC34.67 H38.67 Cl0.67 N1.33 Ni0.67 P0.67P 1 21/n 113.1807; 21.777; 15.5892
90; 97.999; 90
4431.1Nazari, S. Hadi; Bourdeau, Jefferson E.; Talley, Michael R.; Valdivia-Berroeta, Gabriel A.; Smith, Stacey J.; Michaelis, David J.
Nickel-Catalyzed Suzuki Cross Couplings with Unprotected Allylic Alcohols Enabled by Bidentate N-Heterocyclic Carbene (NHC)/Phosphine Ligands
ACS Catalysis, 2017, 8, 86
4514299 CIFC18 H18 O2 S2C 1 2/c 118.468; 5.7696; 29.486
90; 91.375; 90
3140.9Lanzi, Matteo; Cañeque, Tatiana; Marchiò, Luciano; Maggi, Raimondo; Bigi, Franca; Malacria, Max; Maestri, Giovanni
Alternative Routes to Tricyclic Cyclohexenes with Trinuclear Palladium Complexes
ACS Catalysis, 2017, 8, 144
4514300 CIFC29 H29 N O3 SC 1 2/c 119.9655; 9.2515; 27.268
90; 104.314; 90
4880.3Lanzi, Matteo; Cañeque, Tatiana; Marchiò, Luciano; Maggi, Raimondo; Bigi, Franca; Malacria, Max; Maestri, Giovanni
Alternative Routes to Tricyclic Cyclohexenes with Trinuclear Palladium Complexes
ACS Catalysis, 2017, 8, 144
4514301 CIFC121 H176 O12 P2 Sc2P 1 21/n 117.6216; 14.3906; 22.3619
90; 91.6518; 90
5668.3Xu, Pengfei; Xu, Xin
Homoleptic Rare-Earth Aryloxide Based Lewis Pairs for Polymerization of Conjugated Polar Alkenes
ACS Catalysis, 2017, 8, 198
4514302 CIFC60 H86 O5 P ScP 1 21/c 113.4046; 15.1609; 28.5176
90; 103.471; 90
5636.1Xu, Pengfei; Xu, Xin
Homoleptic Rare-Earth Aryloxide Based Lewis Pairs for Polymerization of Conjugated Polar Alkenes
ACS Catalysis, 2017, 8, 198
4514315 CIFC30 H28 N2 O2 SP 19.528; 10.803; 12.452
94.682; 100.658; 98.889
1236.4Hatano, Manabu; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki
Enantioselective Aza-Friedel‒Crafts Reaction of Indoles with Ketimines Catalyzed by Chiral Potassium Binaphthyldisulfonates
ACS Catalysis, 2017, 8, 349
4514316 CIFC60 H48 Ca O10 S2P 1 21 115.348; 11.244; 17.721
90; 102.716; 90
2983Hatano, Manabu; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki
Enantioselective Aza-Friedel‒Crafts Reaction of Indoles with Ketimines Catalyzed by Chiral Potassium Binaphthyldisulfonates
ACS Catalysis, 2017, 8, 349
4514318 CIFC92 H76 Cl4 O10 Rh2P 21 21 2115.5416; 22.2438; 23.488
90; 90; 90
8119.9Liao, Kuangbiao; Liu, Wenbin; Niemeyer, Zachary L.; Ren, Zhi; Bacsa, John; Musaev, Djamaladdin G.; Sigman, Mathew S.; Davies, Huw M. L.
Site-Selective Carbene-Induced C‒H Functionalization Catalyzed by Dirhodium Tetrakis(triarylcyclopropanecarboxylate) Complexes
ACS Catalysis, 2017, 8, 678
4514319 CIFC124 H114 O11 Rh2P 1 21 111.764; 17.436; 26.079
90; 91.389; 90
5348Liao, Kuangbiao; Liu, Wenbin; Niemeyer, Zachary L.; Ren, Zhi; Bacsa, John; Musaev, Djamaladdin G.; Sigman, Mathew S.; Davies, Huw M. L.
Site-Selective Carbene-Induced C‒H Functionalization Catalyzed by Dirhodium Tetrakis(triarylcyclopropanecarboxylate) Complexes
ACS Catalysis, 2017, 8, 678
4514320 CIFC18 H43.6 Ca I2 N6 O6.8P 1 21/c 112.5906; 22.4298; 11.671
90; 101.86; 90
3225.58Longwitz, Lars; Steinbauer, Johannes; Spannenberg, Anke; Werner, Thomas
Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions
ACS Catalysis, 2017, 8, 665
4514321 CIFC18 H39 Ca I2 N3 O7P 1 21/n 110.6093; 7.3183; 18.0196
90; 96.6981; 90
1389.53Longwitz, Lars; Steinbauer, Johannes; Spannenberg, Anke; Werner, Thomas
Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions
ACS Catalysis, 2017, 8, 665
4514324 CIFC18 H17 F O2P 1 21 15.7745; 15.6042; 16.0104
90; 94.458; 90
1438.28Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514325 CIFC40 H32 Cl2 F4 Ir2P 21 21 220.627; 10.6003; 14.9178
90; 90; 90
3261.8Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514326 CIFC17 H13 Br F2 O2P 1 21 118.1462; 7.5224; 22.412
90; 92.604; 90
3056.1Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514327 CIFC14 H18 F N O2 SP 1 21 16.1963; 13.8442; 8.5199
90; 101.713; 90
715.64Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514328 CIFC22 H27 F O2P 21 21 215.9526; 9.1966; 33.092
90; 90; 90
1811.6Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514336 CIFC34 H33 Br N4 O2P -18.4938; 10.8107; 16.6719
104.927; 95.326; 99.344
1445Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514337 CIFC21 H27 N3 OP -110.1934; 10.7135; 17.2661
89.316; 85.141; 82.592
1863.12Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514338 CIFC23 H21 N3 O3P 21 21 216.2748; 13.137; 24.081
90; 90; 90
1985Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514339 CIFC17 H21 N3 OP 1 21/n 110.0808; 9.7488; 15.9224
90; 108.079; 90
1487.53Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514340 CIFC17 H19 N3 O2P 1 21/n 110.0431; 9.7828; 15.4733
90; 99.887; 90
1497.7Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514341 CIFC25 H21 F N2 O7 SeP 1 21 19.722; 6.1683; 19.747
90; 102.561; 90
1155.8See, Jie Yang; Yang, Hui; Zhao, Yu; Wong, Ming Wah; Ke, Zhihai; Yeung, Ying-Yeung
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
ACS Catalysis, 2018, 8, 850
4514342 CIFC27 H39 O4.5 S0.5 SeP 112.1582; 19.1469; 23.6521
80.268; 80.837; 84.148
5341.6See, Jie Yang; Yang, Hui; Zhao, Yu; Wong, Ming Wah; Ke, Zhihai; Yeung, Ying-Yeung
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
ACS Catalysis, 2018, 8, 850
4514343 CIFC18 H18 F2 O4 SeP 1 21 16.7417; 22.7327; 16.9277
90; 101.477; 90
2542.4See, Jie Yang; Yang, Hui; Zhao, Yu; Wong, Ming Wah; Ke, Zhihai; Yeung, Ying-Yeung
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
ACS Catalysis, 2018, 8, 850
4514344 CIFC31 H50 B N2 P RuP -19.9745; 14.6282; 21.2096
103.406; 99.818; 90.008
2963.7Beguerie, Marion; Dinoi, Chiara; del Rosal, Iker; Faradji, Charly; Alcaraz, Gilles; Vendier, Laure; Sabo-Etienne, Sylviane
Mechanistic Studies on the Catalytic Synthesis of BN Heterocycles (1H-2,1-Benzazaboroles) at Ruthenium
ACS Catalysis, 2018, 8, 939
4514345 CIFC59 H96 Mn N O4 P2P 1 21/m 112.513; 17.266; 12.709
90; 107.182; 90
2623.2Kulkarni, Naveen V.; Brennessel, William W.; Jones, William D.
Catalytic Upgrading of Ethanol to n-Butanol via Manganese-Mediated Guerbet Reaction
ACS Catalysis, 2018, 8, 997
4514346 CIFC47.5 H72 Br Cl3 Mn N O2 P2P 1 21 116.074; 19.166; 16.17
90; 113.805; 90
4557.8Kulkarni, Naveen V.; Brennessel, William W.; Jones, William D.
Catalytic Upgrading of Ethanol to n-Butanol via Manganese-Mediated Guerbet Reaction
ACS Catalysis, 2018, 8, 997
4514350 CIFC46 H38 F12 Fe2 N10 O15 S4P -111.9405; 12.2853; 20.3054
103.183; 102.56; 98.477
2769.26Kottrup, Konstantin G.; D'Agostini, Silvia; van Langevelde, Phebe H.; Siegler, Maxime A.; Hetterscheid, Dennis G. H.
Catalytic Activity of an Iron-Based Water Oxidation Catalyst: Substrate Effects of Graphitic Electrodes.
ACS catalysis, 2018, 8, 1052-1061
4514351 CIFC20 H26 O6P 1 21 120.0688; 9.57471; 21.8114
90; 113.315; 90
3848.9Verrier, Charlie; Alandini, Nurtalya; Pezzetta, Cristofer; Moliterno, Mauro; Buzzetti, Luca; Hepburn, Hamish B.; Vega-Peñaloza, Alberto; Silvi, Mattia; Melchiorre, Paolo
Direct Stereoselective Installation of Alkyl Fragments at the β-Carbon of Enals via Excited Iminium Ion Catalysis
ACS Catalysis, 2018, 8, 1062
4514352 CIFC31 H27 Fe N3 O S4P -111.0218; 16.5594; 17.2264
76.1184; 89.3326; 82.0211
3021.9Das, Uttam K.; Higman, Carolyn S.; Gabidullin, Bulat; Hein, Jason E.; Baker, R. Tom
Efficient and Selective Iron-Complex-Catalyzed Hydroboration of Aldehydes
ACS Catalysis, 2018, 8, 1076
4514353 CIFC32 H32 Fe N2 O S4P -110.4477; 12.8949; 13.2739
64.316; 67.177; 79.099
1484.95Das, Uttam K.; Higman, Carolyn S.; Gabidullin, Bulat; Hein, Jason E.; Baker, R. Tom
Efficient and Selective Iron-Complex-Catalyzed Hydroboration of Aldehydes
ACS Catalysis, 2018, 8, 1076
4514354 CIFC33 H36 Fe N3 O3 P S4P n a 2128.2857; 7.9962; 15.1492
90; 90; 90
3426.42Das, Uttam K.; Higman, Carolyn S.; Gabidullin, Bulat; Hein, Jason E.; Baker, R. Tom
Efficient and Selective Iron-Complex-Catalyzed Hydroboration of Aldehydes
ACS Catalysis, 2018, 8, 1076
4514356 CIFC18 H37 Cl4 Cr Li N2 O2 PP 1 21/c 110.0101; 19.2905; 14.2617
90; 110.537; 90
2578.9Kwon, Doo-Hyun; Fuller, Jack T.; Kilgore, Uriah J.; Sydora, Orson L.; Bischof, Steven M.; Ess, Daniel H.
Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization
ACS Catalysis, 2018, 8, 1138
4514357 CIFC30 H27 Br N2 OP b c a9.92477; 18.1707; 27.0531
90; 90; 90
4878.76Arokianathar, Jude N.; Frost, Aileen B.; Slawin, Alexandra M. Z.; Stead, Darren; Smith, Andrew D.
Isothiourea-Catalyzed Enantioselective Addition of 4-Nitrophenyl Esters to Iminium Ions
ACS Catalysis, 2018, 8, 1153
4514358 CIFC30 H27.67 Br N2 O1.33P -114.476; 17.657; 18.147
81.051; 77.873; 82.012
4452.5Arokianathar, Jude N.; Frost, Aileen B.; Slawin, Alexandra M. Z.; Stead, Darren; Smith, Andrew D.
Isothiourea-Catalyzed Enantioselective Addition of 4-Nitrophenyl Esters to Iminium Ions
ACS Catalysis, 2018, 8, 1153
4514359 CIFC94 H68 Br4 Cl4 N4 Ni2P 1 21/n 111.4354; 18.923; 18.566
90; 97.981; 90
3978.6Pei, Lixia; Liu, Fengshou; Liao, Heng; Gao, Jie; Zhong, Liu; Gao, Haiyang; Wu, Qing
Synthesis of Polyethylenes with Controlled Branching with α-Diimine Nickel Catalysts and Revisiting Formation of Long-Chain Branching
ACS Catalysis, 2018, 8, 1104
4514360 CIFC52 H44 Br2 Cl8 N2 NiI b a 224.752; 10.97; 22.093
90; 90; 90
5999Pei, Lixia; Liu, Fengshou; Liao, Heng; Gao, Jie; Zhong, Liu; Gao, Haiyang; Wu, Qing
Synthesis of Polyethylenes with Controlled Branching with α-Diimine Nickel Catalysts and Revisiting Formation of Long-Chain Branching
ACS Catalysis, 2018, 8, 1104
4514361 CIFC38 H36 Br2 N2 NiP 1 21/c 113.579; 14.443; 18.148
90; 109.503; 90
3355Pei, Lixia; Liu, Fengshou; Liao, Heng; Gao, Jie; Zhong, Liu; Gao, Haiyang; Wu, Qing
Synthesis of Polyethylenes with Controlled Branching with α-Diimine Nickel Catalysts and Revisiting Formation of Long-Chain Branching
ACS Catalysis, 2018, 8, 1104
4514363 CIFC23 H47 Fe N2 O3 P2P 1 21/c 116.336; 12.2113; 27.367
90; 91.146; 90
5458.2Jayarathne, Upul; Hazari, Nilay; Bernskoetter, Wesley H.
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
ACS Catalysis, 2018, 8, 1338
4514364 CIFC19 H39 Fe N O2 P2P 1 21/c 119.086; 16.908; 15.109
90; 113.043; 90
4486.7Jayarathne, Upul; Hazari, Nilay; Bernskoetter, Wesley H.
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
ACS Catalysis, 2018, 8, 1338
4514365 CIFC21 H40 F6 Fe Li N O8 P2 S2P 1 21/n 18.6289; 29.4056; 13.2362
90; 108.974; 90
3176Jayarathne, Upul; Hazari, Nilay; Bernskoetter, Wesley H.
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
ACS Catalysis, 2018, 8, 1338
4514366 CIFC78 H94 Ag4 F9 N24 O22 S6P 21 335.2177; 35.2177; 35.2177
90; 90; 90
43680Chang, Zhiduo; Jing, Xu; He, Cheng; Liu, Xin; Duan, Chunying
Silver Clusters as Robust Nodes and π‒Activation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines
ACS Catalysis, 2018, 8, 1384
4514367 CIFC150 H164 Ag8 F9 N53 O25 S12P 21 335.191; 35.191; 35.191
90; 90; 90
43580.8Chang, Zhiduo; Jing, Xu; He, Cheng; Liu, Xin; Duan, Chunying
Silver Clusters as Robust Nodes and π‒Activation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines
ACS Catalysis, 2018, 8, 1384
4514368 CIFC120 H162 Ag8 F0 N60 O18 S13P a -335.835; 35.835; 35.835
90; 90; 90
46017Chang, Zhiduo; Jing, Xu; He, Cheng; Liu, Xin; Duan, Chunying
Silver Clusters as Robust Nodes and π‒Activation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines
ACS Catalysis, 2018, 8, 1384
4514369 CIFC16 H15 Cl O2P 21 21 216.78; 10.4553; 18.9129
90; 90; 90
1340.7Gollapelli, Krishna Kumar; Donikela, Sangeetha; Manjula, Nemali; Chegondi, Rambabu
Rhodium-Catalyzed Highly Regio- and Enantioselective Reductive Cyclization of Alkyne-Tethered Cyclohexadienones
ACS Catalysis, 2018, 8, 1440
4514377 CIFC45 H38 Ni O P2P -19.418; 10.2752; 18.5554
94.536; 92.905; 96.975
1773.5Zhang, Xin; Tutkowski, Brandon; Oliver, Allen; Helquist, Paul; Wiest, Olaf
Mechanistic Study of the Nickel-Catalyzed α,β-Coupling of Saturated Ketones
ACS Catalysis, 2018, 8, 1740
4514378 CIFC9 H7 N O2P 21 21 214.3637; 8.4176; 20.062
90; 90; 90
736.915Zhu, Gongming; Li, Yiping; Bao, Guangjun; Sun, Wangsheng; Huang, Liwu; Hong, Liang; Wang, Rui
Catalytic Kinetic Resolution of Spiro-Epoxyoxindoles with 1-Naphthols: Switchable Asymmetric Tandem Dearomatization/Oxa-Michael Reaction and Friedel–Crafts Alkylation of 1-Naphthols at the C4 Position
ACS Catalysis, 2018, 1810
4514379 CIFC26 H20 Br N O3P 21 21 219.4584; 13.011; 17.4
90; 90; 90
2141.3Zhu, Gongming; Li, Yiping; Bao, Guangjun; Sun, Wangsheng; Huang, Liwu; Hong, Liang; Wang, Rui
Catalytic Kinetic Resolution of Spiro-Epoxyoxindoles with 1-Naphthols: Switchable Asymmetric Tandem Dearomatization/Oxa-Michael Reaction and Friedel‒Crafts Alkylation of 1-Naphthols at the C4 Position
ACS Catalysis, 2018, 1810
4514380 CIFC21 H21 N O3P 1 21/c 113.6373; 15.8546; 8.1178
90; 104.499; 90
1699.28Kuppusamy, Ramajayam; Santhoshkumar, Rajagopal; Boobalan, Ramadoss; Wu, Hsin-Ru; Cheng, Chien-Hong
Synthesis of 1,2-Dihydroquinolines by Co(III)-Catalyzed [3 + 3] Annulation of Anilides with Benzylallenes
ACS Catalysis, 2018, 8, 1880
4514381 CIFC20 H20 Cl N O4P 21 21 219.027; 10.076; 20.28
90; 90; 90
1844.6Esteban, Francisco; Cieślik, Wioleta; Arpa, Enrique M.; Guerrero-Corella, Andrea; Díaz-Tendero, Sergio; Perles, Josefina; Fernández-Salas, José A; Fraile, Alberto; Alemán, José
Intramolecular Hydrogen Bond Activation: Thiourea-Organocatalyzed Enantioselective 1,3-Dipolar Cycloaddition of Salicylaldehyde-Derived Azomethine Ylides with Nitroalkenes.
ACS catalysis, 2018, 8, 1884-1890
4514382 CIFC20 H19 N O4P 1 21 18.8134; 9.1977; 10.6394
90; 94.6009; 90
859.68Esteban, Francisco; Cieślik, Wioleta; Arpa, Enrique M.; Guerrero-Corella, Andrea; Díaz-Tendero, Sergio; Perles, Josefina; Fernández-Salas, José A; Fraile, Alberto; Alemán, José
Intramolecular Hydrogen Bond Activation: Thiourea-Organocatalyzed Enantioselective 1,3-Dipolar Cycloaddition of Salicylaldehyde-Derived Azomethine Ylides with Nitroalkenes.
ACS catalysis, 2018, 8, 1884-1890
4514383 CIFC18 H17 Br N2 O5P 21 21 213.9676; 23.8405; 5.5166
90; 90; 90
1837Esteban, Francisco; Cieślik, Wioleta; Arpa, Enrique M.; Guerrero-Corella, Andrea; Díaz-Tendero, Sergio; Perles, Josefina; Fernández-Salas, José A; Fraile, Alberto; Alemán, José
Intramolecular Hydrogen Bond Activation: Thiourea-Organocatalyzed Enantioselective 1,3-Dipolar Cycloaddition of Salicylaldehyde-Derived Azomethine Ylides with Nitroalkenes.
ACS catalysis, 2018, 8, 1884-1890
4514384 CIFC24 H29 N2 O3 Rh SP 1 21/n 19.8164; 14.358; 17.0526
90; 90.736; 90
2403.26Ran, You; Yang, Yudong; You, Huansha; You, Jingsong
RhCl3-Catalyzed Oxidative C‒H/C‒H Cross-Coupling of (Hetero)aromatic Sulfonamides with (Hetero)arenes
ACS Catalysis, 2018, 8, 1796
4514387 CIFC26 H24 Br N OP 1 21 111.693; 6.314; 15.57
90; 103.875; 90
1116Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4514388 CIFC23 H22 F6 N3 P PdP 1 21/n 111.7229; 13.9765; 13.8227
90; 91.721; 90
2263.8Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4514394 CIFC24 H33 Ir N2 O6P 1 21/n 114.1793; 34.531; 16.0684
90; 113.726; 90
7202.5Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514395 CIFC28 H43 Ir N2 O7P 1 21/c 117.9996; 11.5553; 15.0325
90; 100.311; 90
3076.1Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514396 CIFC34 H39 Ir N2 O7P -110.4412; 11.3139; 13.9001
75.379; 83.373; 84.494
1574.4Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514397 CIFC28 H39 Ir N2 O7P 1 21/c 112.1132; 39.536; 11.7754
90; 94.196; 90
5624.2Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514398 CIFC87 H190 N3 O38 P Si3 Ti W9P b c a20.2301; 28.431; 43.025
90; 90; 90
24746Zhang, Teng; Mazaud, Louis; Chamoreau, Lise-Marie; Paris, Céline; Proust, Anna; Guillemot, Geoffroy
Unveiling the Active Surface Sites in Heterogeneous Titanium-Based Silicalite Epoxidation Catalysts: Input of Silanol-Functionalized Polyoxotungstates as Soluble Analogues
ACS Catalysis, 2018, 8, 2330
4514400 CIFC27 H18 O2P 1 21/c 117.4516; 7.5513; 15.134
90; 107.604; 90
1900.99Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V.
Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes
ACS Catalysis, 2018, 8, 2748
4514401 CIFC61 H51 Cl3 F6 N3 P3 RuP 1 21/c 110.0272; 23.326; 22.7595
90; 95.922; 90
5294.9Paul, Bhaskar; Shee, Sujan; Panja, Dibyajyoti; Chakrabarti, Kaushik; Kundu, Sabuj
Direct Synthesis of N,N-Dimethylated and β-Methyl N,N-Dimethylated Amines from Nitriles Using Methanol: Experimental and Computational Studies
ACS Catalysis, 2018, 8, 2890
4514406 CIFC52 H49 Cl2 I O2 P2 PdP 1 21 111.6182; 17.9333; 12.329
90; 115.788; 90
2312.95Batuecas, 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 CIFC37 H36 Cr N O5 PP 21 21 217.15; 19.5691; 24.0399
90; 90; 90
3363.6Batuecas, 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 CIFC62 H74.56 Ag O4.78 P2I 1 2 111.7485; 26.0007; 18.5841
90; 106.036; 90
5456Batuecas, 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 CIFC31 H31 N O3 SP 1 21/c 16.4182; 21.7785; 19.0994
90; 96.787; 90
2651Li, 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 CIFC20 H26 Cl RhP 1 21/c 17.4511; 12.8249; 18.6937
90; 94.11; 90
1781.8Burman, 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 CIFC20 H26 Cl IrP 1 21/c 17.46343; 12.81878; 18.68909
90; 93.9187; 90
1783.84Burman, 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 CIFC15 H27 Br2 Co N3P 1 21/c 110.8842; 11.4192; 15.8101
90; 104.557; 90
1901.94Pattanaik, Sandip; Gunanathan, Chidambaram
Cobalt-Catalyzed Selective Synthesis of Disiloxanes and Hydrodisiloxanes
ACS Catalysis, 2019, 9, 5552
4514415 CIFC17 H15 N3 O2P 1 21/c 111.1449; 12.2086; 11.4303
90; 107.468; 90
1483.5Zhao, 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 CIFC22 H25 N3 O4P -18.7858; 9.9521; 13.706
100.933; 94.003; 112.813
1070.9Zhao, 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 CIFC18 H15 N3 O2P b c a15.251; 10.6393; 19.017
90; 90; 90
3085.7Zhao, 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 CIFC15 H11 N3 O2C 1 2/c 119.26; 6.4425; 20.274
90; 100.533; 90
2473.3Zhao, 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 CIFC12 H10 I N OP 1 21/c 116.093; 9.8036; 6.9586
90; 93.02; 90
1096.33Chen, 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 CIFC59 H60 Cl2 N2 P2 RuP 21 21 2110.9656; 11.9509; 38.4007
90; 90; 90
5032.4Chen, 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
4514434 CIFC14 H14 O3P 21 21 216.44696; 6.98494; 23.6748
90; 90; 90
1066.11Park, Sung Hwan; Wang, Shou-Guo; Cramer, Nicolai
Enantioselective Ruthenium(II)-Catalyzed Access to Benzonorcaradienes by Coupling of Oxabenzonorbornadienes and Alkynes
ACS Catalysis, 2019, 10226
4514435 CIFC24 H19 F O2 SP 21 21 215.101; 15.6195; 23.695
90; 90; 90
1887.9Moku, Balakrishna; Fang, Wan-Yin; Leng, Jing; Kantchev, Eric Assen B.; Qin, Hua-Li
Rh(I)‒Diene-Catalyzed Addition of (Hetero)aryl Functionality to 1,3-Dienylsulfonyl Fluorides Achieving Exclusive Regioselectivity and High Enantioselectivity: Generality and Mechanism
ACS Catalysis, 2019, 10477
4514436 CIFC16 H14 Br F O2 SP 1 21/n 19.7166; 31.009; 16.0484
90; 97.583; 90
4793.1Moku, Balakrishna; Fang, Wan-Yin; Leng, Jing; Kantchev, Eric Assen B.; Qin, Hua-Li
Rh(I)‒Diene-Catalyzed Addition of (Hetero)aryl Functionality to 1,3-Dienylsulfonyl Fluorides Achieving Exclusive Regioselectivity and High Enantioselectivity: Generality and Mechanism
ACS Catalysis, 2019, 10477
4514437 CIFC10 H19 B10 N OP b c a9.4145; 16.7722; 20.1088
90; 90; 90
3175.2Baek, Yonghyeon; Kim, Suhui; Son, Jeong-Yu; Lee, Kooyeon; Kim, Dongwook; Lee, Phil Ho
Rhodium-Catalyzed Amidation of the Cage B(4)‒H Bond in o-Carboranes with Dioxazolones by Carboxylic Acid-Assisted B(4)‒H Bond Activation
ACS Catalysis, 2019, 10418
4514438 CIFC17 H25 N OP 1 21/c 111.5032; 10.3652; 12.7281
90; 102.844; 90
1479.6Lorenc, Chris; Vibbert, Hunter B.; Yao, Chengbo; Norton, Jack R.; Rauch, Michael
H· Transfer-Initiated Synthesis of γ-Lactams: Interpretation of Cycloisomerization and Hydrogenation Ratios
ACS Catalysis, 2019, 10294
4514439 CIFC17 H25 N OP 1 21/c 111.3195; 10.3547; 12.7097
90; 101.868; 90
1457.9Lorenc, Chris; Vibbert, Hunter B.; Yao, Chengbo; Norton, Jack R.; Rauch, Michael
H· Transfer-Initiated Synthesis of γ-Lactams: Interpretation of Cycloisomerization and Hydrogenation Ratios
ACS Catalysis, 2019, 10294
4514611 CIFC29 H33 B O4 SiP 16.264; 9.621; 11.639
91.385; 96.47; 100.453
684.7Zhao, 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 CIFC72 H63 Ir N2 O6 P2P 21 21 2115.155; 17.531; 22.268
90; 90; 90
5916.2Kim, 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 CIFC23 H29 B O3P 21 21 2111.8365; 12.8133; 13.5157
90; 90; 90
2049.85Whyte, Andrew; Mirabi, Bijan; Torelli, Alexa; Prieto, Liher; Bajohr, Jonathan; Lautens, Mark
Asymmetric Synthesis of Boryl-Functionalized Cyclobutanols
ACS Catalysis, 2019, 9, 9253
4514614 CIFC14 H14 Br F2 N OP -19.6165; 11.7307; 12.572
93.33; 100.541; 92.151
1390.3Chen, Yuanjin; Li, Liangkui; He, Xiao; Li, Zhiping
Four-Component Reactions for the Synthesis of Perfluoroalkyl Isoxazoles
ACS Catalysis, 2019, 9, 9098
4514615 CIFC20 H17 N3 O PdP 6522.1057; 22.1057; 6.7305
90; 90; 120
2848.31Agasti, 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 CIFC23 N3 O PdP -19.6348; 10.7198; 11.5837
105.639; 103.125; 104.695
1056.88Agasti, 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 CIFC24 H25 N2 O2P -18.8691; 10.1304; 12.2386
105.617; 100.765; 93.916
1032.17Agasti, 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 CIFC20 H26 I N O2 SP 1 21/c 112.2416; 20.4922; 7.9382
90; 91.862; 90
1990.3Nugent, 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 CIFC24 H35 I OP 21 21 216.30332; 11.85008; 28.71209
90; 90; 90
2144.65Nugent, 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 CIFC21 H25 B O2P -110.2291; 13.3412; 13.527
87.464; 88.582; 80.599
1819.14Léonard, 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 CIFC18 H16 N2 O3P 1 c 111.4615; 5.5002; 12.6887
90; 105.131; 90
772.17Yang, Hui; Wei, Guo; Jiang, Zhiyong
Access to Isoxazolidines through Visible-Light-Induced Difunctionalization of Alkenes
ACS Catalysis, 2019, 9, 9599
4514622 CIFC44 H57 F6 N5 O6I 1 2/a 117.95158; 10.14969; 23.05206
90; 98.418; 90
4154.9Zhang, 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 CIFC28 H46 Cl2 F3 Ir O5 P2 SP n m a15.492; 24.393; 18.535
90; 90; 90
7004Chu, 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 CIFC44 H43 F3 O4 P4 Ru SP b c a23.1713; 14.6301; 24.6604
90; 90; 90
8359.8Chu, 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 CIFC46 H45 F6 N O6 P4 Ru S2P 1 21/c 117.445; 19.175; 28.449
90; 95.41; 90
9474Chu, 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 CIFC27 H46 Cl2 F3 Ir O4 P2 SP 1 21/n 116.5246; 12.6284; 17.54
90; 116.553; 90
3274.16Chu, 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 CIFC15 H12 O2 SC 1 2/c 120.5001; 9.8972; 14.0168
90; 114.293; 90
2592.1Liu, 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 CIFC9 H6 F6 O9 S2 UP -18.7768; 9.4553; 11.5011
75.998; 71.713; 79.448
873.34Monsigny, 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 CIFC32 H24 F12 O20 S4 U2P -15.6883; 12.7612; 16.5764
102.634; 94.632; 96.374
1160.02Monsigny, 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 CIFC29 H33 F6 N3 O11 S2 UP 1 21/c 19.2981; 22.059; 18.3163
90; 102.709; 90
3664.8Monsigny, 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 CIFC25 H22 F N OP 21 21 216.9609; 9.0105; 32.0299
90; 90; 90
2008.95Ma, Teng; Chen, Yate; Li, Yuxiu; Ping, Yuanyuan; Kong, Wangqing
Nickel-Catalyzed Enantioselective Reductive Aryl Fluoroalkenylation of Alkenes
ACS Catalysis, 2019, 9, 9127
4514632 CIFC24 H43.5 O4.75P 1 21 112.5451; 25.5594; 15.6511
90; 110.747; 90
4693.02Nguyen, 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 CIFC15 H17 N3 O4 SP 1 21/n 113.3181; 6.9639; 17.0635
90; 90.091; 90
1582.6Nguyen, 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 CIFC21 H17 NC 1 2/c 118.1884; 10.5558; 25.3027
90; 108.216; 90
4614.5Nguyen, 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 CIFC22 H19 NP 1 21/c 18.8592; 22.189; 8.984
90; 114.717; 90
1604.25Nguyen, 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 CIFC51 H57 Cl Ni O2 P2P 1 21/n 113.151; 15.965; 21.319
90; 91.921; 90
4474McGuire, 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 CIFC159 H188 Cl4 N12 Rh4P 1 21/n 122.2298; 14.0027; 23.0551
90; 102.788; 90
6998.5Azpíroz, 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 CIFC34 H36 Fe N O3 P SP 1 21 111.5035; 10.7831; 13.3149
90; 110.777; 90
1544.22Han, 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 CIFC24 H29 B O3P 21 21 218.8534; 12.6813; 18.9601
90; 90; 90
2128.7Han, 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 CIFC38 H37 Cl3 Fe N O2 P SP 1 21 110.5036; 11.7796; 15.6619
90; 106.748; 90
1855.62Han, 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 CIFC50 H60 N4 O4 Rh2P 1 21/c 119.9451; 11.5613; 20.0794
90; 94.241; 90
4617.5Zhu, 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 CIFC40 H26 F20 N4 O5 Rh2P 1 21/c 123.889; 9.9822; 19.624
90; 110.013; 90
4397.1Zhu, 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 CIFC103 H224 Ni4 O32 Si8P 1 21/c 124.2076; 27.078; 21.532
90; 106.288; 90
13547.6Moroz, 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 CIFC48 H60 Co Li N2 OP m n 2117.4715; 10.5472; 10.9763
90; 90; 90
2022.66Sandl, 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 CIFC45 H53 Co N2P -112.3103; 12.6855; 13.5302
69.519; 77.844; 79.251
1920.22Sandl, 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 CIFC36 H40 Br2 Co N2P 1 21/c 127.0266; 12.0329; 22.8033
90; 113.047; 90
6823.9Sandl, 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 CIFC90 H121 Co2 Li N4 O4.5P b c a25.0102; 21.4146; 30.8908
90; 90; 90
16544.6Sandl, 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 CIFC92 H123 Co2 Li N4 O5P 1 21/n 121.4917; 13.0279; 29.987
90; 101.086; 90
8239.4Sandl, 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 CIFC48 H44 B Br N2 P4P -110.551; 12.062; 18.905
82.63; 81.72; 66.18
2171.5Bäcker, 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 CIFC54.5 H51 B Br Cl5 Fe O2 P4P -111.496; 12.374; 20.858
97.02; 94.81; 111.71
2709Bäcker, 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 CIFC18 H44 B Br Fe N2 O2 P4P 1 21/c 112.7253; 10.5434; 21.3482
90; 102.389; 90
2797.5Bäcker, 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 CIFC19 H43 B Br Fe N2 O3 P4P n a 2114.623; 15.131; 12.874
90; 90; 90
2848.5Bäcker, 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 CIFC18 H21 N O5 SP 1 21/n 19.7666; 7.7835; 22.574
90; 94.062; 90
1711.73Zhou, 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 CIFC18 H23 N O6 SP 1 21 18.1162; 11.0214; 10.5496
90; 91.17; 90
943.48Zhou, 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 CIFC27 H48 Cl N2 P RuP 4113.2477; 13.2477; 32.623
90; 90; 90
5725.4Paulson, 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 CIFC24 H39 F9 N2 P2 RuP 1 21/c 122.5581; 12.7798; 22.1335
90; 113.18; 90
5865.7Paulson, 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 CIFC40 H48 Cl4 F12 Ru4P -111.6853; 20.7278; 21.1082
114.576; 96.847; 99.355
4487.1Paulson, 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 CIFC20 H34 Cl N2 P RuP 1 21/c 113.3641; 15.0206; 10.9602
90; 93.975; 90
2194.82Paulson, 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 CIFC24 H42 F6 N2 P2 RuP n a 2122.7385; 13.1551; 9.5634
90; 90; 90
2860.67Paulson, 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 CIFC20 H31 Cl F3 N2 P RuP 1 21/c 113.915; 14.954; 10.922
90; 95.212; 90
2263.3Paulson, 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 CIFC24.5 H0.5 Cl1.5 N2 O2 S3P 15.7084; 14.6112; 15.7856
72.801; 87.877; 87.344
1256.02Liang, Yaoyu; Zhao, Xiaodan
Enantioselective Construction of Chiral Sulfides via Catalytic Electrophilic Azidothiolation and Oxythiolation of N-Allyl Sulfonamides
ACS Catalysis, 2019, 9, 6896
4514663 CIFC19 H32 Fe N5 O7 S2P 1 21/c 111.986; 9.3819; 21.7658
90; 90; 90
2447.6Warner, 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 CIFC20 H21 NP 1 21/c 110.3039; 11.9306; 12.985
90; 90.816; 90
1596.1Ping, 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 CIFC20 H21 NP 1 21/c 110.2763; 11.8965; 12.9403
90; 90.785; 90
1581.83Ping, 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 CIFC108 H92 Cl12 N8 O4C 1 c 116.9269; 16.7619; 8.8583
90; 91.738; 90
2512.18Ping, 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 CIFC18 H14 Br F3 N2 O3P 1 21 19.89; 9.938; 18.564
90; 101.954; 90
1785Ibáñez, 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 CIFC38 H27 Br3 N2 O3P 21 21 216.8271; 16.06; 29.396
90; 90; 90
3223.1Ibáñez, 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 CIFC25 H25 Br N2 O2 SP 419.7248; 9.7248; 48.32
90; 90; 90
4569.7Ibáñez, 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 CIFC22 H20 O2C 1 2/c 115.8408; 13.142; 16.3982
90; 98.987; 90
3371.9Giri, 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 CIFC25 H19 N O2P 1 21/c 115.6269; 10.8792; 22.0724
90; 100.839; 90
3685.5Giri, 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 CIFC18 H11 N OP 1 21/c 18.2853; 31.984; 19.542
90; 93.546; 90
5168.7Giri, 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 CIFC22 H14 N4P 1 21/c 19.9466; 17.8664; 9.4521
90; 100.253; 90
1652.91Giri, 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 CIFC19 H13 N OP -17.861; 9.282; 9.934
83.675; 72.702; 85.815
687.2Giri, 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 CIFC30 H22 O3P 1 21/c 124.6109; 12.239; 14.7299
90; 98.22; 90
4391.3Giri, 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 CIFC54 H55 B F4 N3 O5 P2 RhP -114.1394; 15.0162; 28.9031
77.688; 87.174; 78.469
5874.4Daubignard, 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 CIFC50 H49 B F4 N5 O5 P2 RhP -112.6207; 13.6039; 15.2008
72.598; 83.301; 76.784
2421.15Daubignard, 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 CIFC92 H86 B2 F8 N6 O10 P4 Rh2P 1 21/n 114.1446; 25.4077; 15.6384
90; 94.839; 90
5600.1Daubignard, 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 CIFC17 H21 B Br N O2P 1 21 111.3502; 7.45; 20.6376
90; 91.376; 90
1744.59Jia, 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 CIFC20 H16 Br N O2P 1 21 114.62776; 8.05742; 15.00218
90; 97.0979; 90
1754.64Jia, 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 CIFC11 H10 I0.96 N OP 1 21 19.8268; 5.6439; 9.8652
90; 99.353; 90
539.86Jia, 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 CIFC14 H24 N2 O4 PdP 1 21/c 19.3121; 10.7025; 8.4772
90; 97.201; 90
838.2Feng, 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 CIFC42 H35 F12 N11 P2 Pd2P -112.0088; 12.3492; 17.137
101.431; 106.142; 105.372
2250.17Zhu, 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 CIFC25 H20 Cl F6 N4 O P PdP -18.7896; 12.4079; 13.433
108.517; 105.407; 103.424
1256.4Zhu, 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 CIFC45 H48 F12 N8 O3 P2 Pd2C 1 2/c 125.202; 8.3844; 24.157
90; 108.454; 90
4842Zhu, 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 CIFC12 H11 Br F3 N3 O2P 1 21/c 110.3636; 10.0648; 28.9197
90; 99.7; 90
2973.4Chen, 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 CIFC15 H11 Cl F3 N O2P 1 21/n 117.29; 4.519; 20.77
90; 111.24; 90
1513Chen, 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 CIFC34 H26 N2P 1 21/n 111.5593; 7.8828; 27.35
90; 98.043; 90
2467.6Noto, 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 CIFC21 H20 F3 N O5 SP 19.0328; 9.506; 13.9771
90.165; 95.249; 115.51
1077.42He, 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 CIFC24 H25 N3 O4P 21 21 219.2464; 10.0773; 23.4808
90; 90; 90
2187.91He, 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 CIFC25 H17 N OP 1 21/n 18.618; 11.775; 18.166
90; 103.293; 90
1794Yuan, 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 CIFC31 H21 N OP 21 21 218.1125; 12.1517; 23.1044
90; 90; 90
2277.65Yuan, 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 CIFC24 H46 N6 Ni O6P 21 21 218.7123; 16.0813; 20.4271
90; 90; 90
2861.9Garrido-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 CIFC21 H44 N6 Ni O9C 1 2/c 155.552; 6.2616; 15.8906
90; 100.323; 90
5438Garrido-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 CIFC26 H29 N OP 1 21/c 16.2208; 18.757; 17.484
90; 93.268; 90
2036.8Han, 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 CIFC58 H84 F7 N2 O4 P Pd SP 1 21/c 120.138; 13.1828; 24.998
90; 106.912; 90
6349.4Dennis, 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 CIFC43 H73.5 P2 Ru SP -113.159; 15.396; 21.596
90.092; 92.283; 101.727
4280.3Zhou, 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 CIFC38 H62 P2 Ru SP 1 21/c 113.2907; 15.6689; 18.8836
90; 105.176; 90
3795.4Zhou, 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
4514699 CIFC30 H41 Br1.02 Fe P3P -19.4966; 9.593; 17.63
101.894; 96.481; 102.236
1515.2Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514700 CIFC30 H41 Fe N4 P3P 1 21/c 117.626; 10.7764; 16.1774
90; 98.63; 90
3038Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514701 CIFC129 H106 B2 F48 Fe2 N8 P6P 1 21/n 122.4451; 12.1053; 25.482
90; 101.904; 90
6774.7Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514702 CIFC42 H65 Fe K N2 O6 P3P 1 21/n 110.4864; 23.9154; 17.8619
90; 93.645; 90
4470.5Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514703 CIFC40 H61 Fe K N2 O4 P3P n m a25.9569; 17.0296; 12.1851
90; 90; 90
5386.2Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514704 CIFC84 H130 Fe2 K4 N4 O6 P6P 1 21/n 114.6713; 16.6256; 18.7129
90; 102.506; 90
4456.1Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514705 CIFC33 H50 Fe K N2 P3 SiP 21 21 2110.5863; 16.3326; 20.8095
90; 90; 90
3598Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514706 CIFC28 H26 N4 O2 PdP 1 21/n 18.3908; 20.0893; 14.6398
90; 100.46; 90
2426.75Luo, Yun-Cheng; Yang, Chao; Qiu, Sheng-Qi; Liang, Qiu-Ju; Xu, Yun-He; Loh, Teck-Peng
Palladium(II)-Catalyzed Stereospecific Alkenyl C‒H Bond Alkylation of Allylamines with Alkyl Iodides
ACS Catalysis, 2019, 9, 4271
4514707 CIFC26 H28 Cl2 Co N4 OP 21 21 219.5625; 11.3203; 24.4937
90; 90; 90
2651.5Chen, Xu; Cheng, Zhaoyang; Lu, Zhan
Cobalt-Catalyzed Asymmetric Markovnikov Hydroboration of Styrenes
ACS Catalysis, 2019, 9, 4025
4514708 CIFC63 H73 Ni2 O3 P2P -110.2617; 16.0861; 17.7316
100.697; 90.004; 105.821
2763.17Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514709 CIFC32 H37 Ni O2 P SP -18.6245; 9.0612; 20.838
84.848; 88.901; 62.929
1443.8Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514710 CIFC34 H42 B Ni O3 PP 1 21/c 122.1829; 9.2102; 15.4936
90; 94.271; 90
3156.7Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514711 CIFC36 H44 B Ni O PP 1 21/n 18.8285; 20.3843; 17.3286
90; 95.23; 90
3105.5Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514712 CIFC28 H31 Ni PP -18.8889; 15.1597; 17.8889
91.217; 96.831; 90.693
2392.67Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514713 CIFC28 H30 Br Ni PP n a 2116.7529; 10.1199; 14.6061
90; 90; 90
2476.28Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514714 CIFC21 H31 B2 N O4P 1 21/c 115.588; 10.6978; 14.1186
90; 107.935; 90
2239.97Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514715 CIFC23 H21 Br N2 O3P 329.5332; 9.5332; 19.5349
90; 90; 120
1537.51Das, Tamal Kanti; Ghosh, Avik; Balanna, Kuruva; Behera, Pradipta; Gonnade, Rajesh G.; Marelli, Udaya Kiran; Das, Abhijit Kumar; Biju, Akkattu T.
N-Heterocyclic Carbene-Catalyzed Umpolung of Imines for the Enantioselective Synthesis of Dihydroquinoxalines
ACS Catalysis, 2019, 9, 4065
4514716 CIFC14 H11 N O2 S2P 1 21/n 18.3903; 17.9634; 9.3448
90; 112.656; 90
1299.75Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514717 CIFC18 H10 Br2 N2 O2 SI 1 2/a 117.7962; 4.9199; 19.1526
90; 105.417; 90
1616.57Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514718 CIFC12 H11 N O2 SP 1 21/c 114.2892; 10.414; 7.4904
90; 103.95; 90
1081.76Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514719 CIFC18 H10 Cl2 N2 SI 1 2/c 118.9763; 13.5616; 24.1428
90; 95.348; 90
6186.1Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514720 CIFC10 H8 Cl N O2 SP 1 21/c 114.4698; 5.8318; 11.9918
90; 103.449; 90
984.18Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514721 CIFC17 H15 Cl N2 O4 SP 1 21/n 110.7209; 11.7327; 13.2944
90; 97.17; 90
1659.16Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514722 CIFC16 H13 N O2 SP 1 21/c 18.3782; 8.266; 20.0756
90; 97; 90
1379.96Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514723 CIFC18 H10 Cl2 N2 O2 SP 1 21/c 112.9582; 9.0843; 14.2001
90; 108.155; 90
1588.37Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514724 CIFC14 H13 N O2 SP 21 21 218.9497; 9.3068; 15.389
90; 90; 90
1281.8Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514725 CIFC16 H12 Cl N O2 SP 1 21/c 18.2088; 24.9454; 6.8433
90; 94.558; 90
1396.88Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514726 CIFC18 H12 N2 O2 SP -17.6361; 13.7285; 14.864
69.516; 85.244; 83.871
1449.62Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514727 CIFC17 H14 F N O4 SP -17.5118; 8.3229; 12.1237
84.045; 88.396; 77.487
735.96Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514728 CIFC22 H24 N2 O6 SP -17.8092; 9.7669; 14.5366
104.686; 101.315; 100.756
1018.49Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514729 CIFC22 H22 Cl N O2 SC 1 2/c 115.7798; 11.6418; 22.199
90; 106.677; 90
3906.54Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514730 CIFC18 H20 I2 N4 PdP 1 21/c 18.3065; 16.337; 7.6187
90; 99.14; 90
1020.8Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514731 CIFC26 H36 Br4 Hg2 N4C 1 2/c 118.486; 9.2309; 20.682
90; 106.8; 90
3378.6Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514732 CIFC18 H20 Hg2 I4 N4P 1 21/n 110.648; 20.021; 12.134
90; 95.49; 90
2574.9Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514733 CIFC102.56 H52 F2 O34 Zr6P 6/m m m39.446; 39.446; 16.4166
90; 90; 120
22122Liu, Jian; Li, Zhanyong; Zhang, Xuan; Otake, Ken-ichi; Zhang, Lin; Peters, Aaron W.; Young, Matthias J.; Bedford, Nicholas M.; Letourneau, Steven P.; Mandia, David J.; Elam, Jeffrey W.; Farha, Omar K.; Hupp, Joseph T.
Introducing Nonstructural Ligands to Zirconia-like Metal‒Organic Framework Nodes To Tune the Activity of Node-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2019, 9, 3198
4514734 CIFC51 H53 Ni P2P 1 2/c 122.883; 9.2579; 21.1481
90; 115.533; 90
4042.6Charboneau, David J.; Brudvig, Gary W.; Hazari, Nilay; Lant, Hannah M. C.; Saydjari, Andrew K.
Development of an Improved System for the Carboxylation of Aryl Halides through Mechanistic Studies.
ACS catalysis, 2019, 9, 3228-3241
4514735 CIFC17 H14 Cl N O4P 21 21 217.7672; 8.6398; 22.845
90; 90; 90
1533.1Dai, Yuanwei; Tian, Baotong; Chen, Huan; Zhang, Qiang
Palladium-Catalyzed Stereospecific C-Glycosylation of Glycals with Vinylogous Acceptors
ACS Catalysis, 2019, 9, 2909
4514736 CIFC22 H37 N3 O4 SiP 1 21 19.1154; 9.7854; 14.6304
90; 96.443; 90
1296.76Zhan, Bei-Bei; Fan, Jun; Jin, Liang; Shi, Bing-Feng
Divergent Synthesis of Silicon-Containing Peptides via Pd-Catalyzed Post-Assembly γ-C(sp3)‒H Silylation
ACS Catalysis, 2019, 9, 3298
4514737 CIFC89 H64 Al B2 F36 N O6 P4 Rh2P -114.5138; 18.5644; 21.462
104.385; 102.683; 107.545
5062.15Adams, Gemma M.; Ryan, David E.; Beattie, Nicholas A.; McKay, Alasdair I.; Lloyd-Jones, Guy C; Weller, Andrew S.
Dehydropolymerization of H<sub>3</sub>B·NMeH<sub>2</sub> Using a [Rh(DPEphos)]<sup>+</sup> Catalyst: The Promoting Effect of NMeH<sub>2</sub>.
ACS catalysis, 2019, 9, 3657-3666
4514738 CIFC27 H36 Cl F Ni P2P 1 21/n 111.8371; 14.1571; 16.2044
90; 99.776; 90
2676.1Russell, John E. A.; Entz, Emily D.; Joyce, Ian M.; Neufeldt, Sharon R.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
ACS catalysis, 2019, 9, 3304-3310
4514739 CIFC29 H42 F N Ni O3 P2 SP 1 21/m 18.6752; 12.5702; 14.4059
90; 101.795; 90
1537.78Russell, John E. A.; Entz, Emily D.; Joyce, Ian M.; Neufeldt, Sharon R.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
ACS catalysis, 2019, 9, 3304-3310
4514740 CIFC32 H58 Co I N4 P2 ZrP n m a15.4307; 22.1735; 10.8845
90; 90; 90
3724.2Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514741 CIFC56 H92 Co2 I6 N4 P4 Zr2P -111.4073; 12.4796; 14.109
100.063; 97.493; 112.211
1787.87Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514742 CIFC45 H67 Co I N2 O P3 ZrP -19.9663; 10.4166; 23.1907
81.58; 83.529; 82.278
2349.34Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514743 CIFC35 H65 Co I N2 O P3 ZrC 1 2/c 138.6599; 12.0858; 18.3535
90; 103.833; 90
8326.7Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514744 CIFC45 H69 Co I N2 O P3 ZrP -112.2182; 13.374; 16.9003
70.756; 71.3; 74.862
2432.1Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514745 CIFC46 H64 Co I N2 O P2 ZrP -110.7474; 11.7734; 20.3607
77.69; 79.557; 69.802
2345.95Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514746 CIFC31 H38 B N3 O4P 1 21 16.5323; 24.418; 9.191
90; 104.387; 90
1420.04Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514747 CIFC17 H18 N2 O3 PdP 1 21/n 18.6104; 10.5955; 17.71
90; 99.051; 90
1595.59Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514748 CIFC30 H36 B N3 O3P 1 21 16.3743; 23.6017; 9.0486
90; 101.68; 90
1333.12Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514749 CIFC44 H40 N6 O10 Zn2P -18.7707; 11.7137; 13.5892
82.784; 81.615; 88.403
1370.2Markad, Datta; Mandal, Sanjay K.
Design of a Primary-Amide-Functionalized Highly Efficient and Recyclable Hydrogen-Bond-Donating Heterogeneous Catalyst for the Friedel‒Crafts Alkylation of Indoles with β-Nitrostyrenes
ACS Catalysis, 2019, 9, 3165
4514750 CIFC42 H33 Cl F2 Ni P2C 1 2/c 130.115; 11.645; 20.4586
90; 102.223; 90
7012Stadler, Sonja M.; Göttker-Schnetmann, Inigo; Mecking, Stefan
Incorporation of Radicals during Ni(II)-Catalyzed Ethylene Insertion Polymerization
ACS Catalysis, 2019, 9, 2760
4514751 CIFC51 H58 F2 N Ni O2 PP b c a16.868; 20.0011; 26.7439
90; 90; 90
9022.8Stadler, Sonja M.; Göttker-Schnetmann, Inigo; Mecking, Stefan
Incorporation of Radicals during Ni(II)-Catalyzed Ethylene Insertion Polymerization
ACS Catalysis, 2019, 9, 2760
4514752 CIFC10 H9 Br O3P 1 21 14.7773; 16.685; 6.289
90; 104.66; 90
485Sawano, Takahiro; Yamamoto, Hisashi
Enantioselective Epoxidation of β,γ-Unsaturated Carboxylic Acids by a Cooperative Binuclear Titanium Complex
ACS Catalysis, 2019, 9, 3384
4514753 CIFC22 H19 Br N2 O2P 21 21 217.3331; 9.8564; 25.7259
90; 90; 90
1859.42Yang, Qian-Qian; Yin, Xiang; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric Formal [5 + 3] Cycloadditions with Unmodified Morita‒Baylis‒Hillman Alcohols via Double Activation Catalysis
ACS Catalysis, 2019, 9, 1258
4514754 CIFC36 H32 Cl2 N4 O2P 1 21 111.3963; 10.25731; 13.268
90; 95.0958; 90
1544.84Yang, Qian-Qian; Yin, Xiang; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric Formal [5 + 3] Cycloadditions with Unmodified Morita‒Baylis‒Hillman Alcohols via Double Activation Catalysis
ACS Catalysis, 2019, 9, 1258
4514755 CIFC22 H19 N O3 SP 1 21 117.546; 6.607; 17.993
90; 115.207; 90
1887.2Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514756 CIFC25 H24 N O3 SP 21 21 219.162; 10.694; 22.484
90; 90; 90
2203Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514757 CIFC29 H21 N O3 SP 21 21 216.556; 13.237; 25.625
90; 90; 90
2223.8Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514758 CIFC23 H21 N O5 SP 21 21 218.9405; 10.0639; 23.127
90; 90; 90
2080.9Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514759 CIFC18 H16 Br2 O2P -324.679; 24.679; 9.5417
90; 90; 120
5032.8Trost, Barry M.; Tracy, Jacob S.
Vanadium-Catalyzed Synthesis of Geometrically Defined Acyclic Tri- and Tetrasubstituted Olefins from Propargyl Alcohols
ACS Catalysis, 2019, 9, 1584
4514760 CIFC12.5 H16 Cl2 Co N1.5 OP 18.5586; 8.9303; 9.6822
76.723; 86.703; 85.126
717.08Wen, Huanan; Wang, Kuan; Zhang, Yanlu; Liu, Guixia; Huang, Zheng
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
ACS Catalysis, 2019, 9, 1612
4514761 CIFC16 H18 Cl2 Co N2 OP 1 21 19.7507; 13.413; 12.9181
90; 90.316; 90
1689.48Wen, Huanan; Wang, Kuan; Zhang, Yanlu; Liu, Guixia; Huang, Zheng
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
ACS Catalysis, 2019, 9, 1612
4514762 CIFC29.48 H29.66 Cl1.27 N O3C 1 2 125.1281; 6.268; 15.987
90; 99.524; 90
2483.29Trost, Barry M.; Hung, Chao-I Joey; Gnanamani, Elumalai
Tuning the Reactivity of Ketones through Unsaturation: Construction of Cyclic and Acyclic Quaternary Stereocenters via Zn-ProPhenol Catalyzed Mannich Reactions
ACS Catalysis, 2019, 9, 1549
4514763 CIFC22 H19 O PP 1 21 115.7797; 6.4246; 18.8309
90; 114.711; 90
1734.23Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514764 CIFC27 H26 F2 N O2 PP 1 21 110.6041; 11.5598; 19.577
90; 94.744; 90
2391.6Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514765 CIFC24 H21 O3 PP 21 21 219.561; 9.713; 20.717
90; 90; 90
1923.9Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514766 CIFC20 H27 N O6P 1 21 16.03; 19.3547; 9.0029
90; 102.453; 90
1026Sim, Jaehoon; Campbell, Mark W.; Molander, Gary A.
Synthesis of α-Fluoro-α-Amino Acid Derivatives via Photoredox-Catalyzed Carbofluorination.
ACS catalysis, 2019, 9, 1558-1563
4514767 CIFC15 H16 O2P 21 21 215.6039; 10.7509; 19.196
90; 90; 90
1156.5Zheng, Pengfei; Wang, Chengpeng; Chen, Ying-Chun; Dong, Guangbin
Pd-Catalyzed Intramolecular α-Allylic Alkylation of Ketones with Alkynes: Rapid and Stereodivergent Construction of [3.2.1] Bicycles
ACS Catalysis, 2019, 9, 5515
4514768 CIFC35 H51 F6 N3 O5 S2 ZnP 21 21 2113.6599; 14.2563; 20.5882
90; 90; 90
4009.34Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760

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