Crystallography Open Database

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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
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
4515514 CIFC25 H38 B N O6 SP -111.446; 11.5967; 12.3843
112.094; 115.7; 93.978		1318.18Kim-Lee, Shin-Ho; Alonso, Inés; Mauleón, Pablo; Arrayás, Ramón Gómez; Carretero, Juan C.
Rationalizing the Role of NaOtBu in Copper-Catalyzed Carboboration of Alkynes: Assembly of Allylic All-Carbon Quaternary Stereocenters
ACS Catalysis, 2018, 8, 8993
4515515 CIFC21 H22 F N O4P 1 21/c 127.4465; 6.4873; 22.0138
90; 112.954; 90		3609.3Park, Hojoon; Chekshin, Nikita; Shen, Peng-Xiang; Yu, Jin-Quan
Ligand-Enabled, Palladium-Catalyzed β-C(sp<sup>3</sup>)-H Arylation of Weinreb Amides.
ACS catalysis, 2018, 8, 9292-9297
4515516 CIFC41 H51 Co K N6 O11P 21 21 2111.0919; 18.3376; 21.9261
90; 90; 90		4459.7Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515517 CIFC45 H36 K Mn N7 O3P 1 21/n 111.7651; 21.2221; 16.4682
90; 95.468; 90		4093.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515518 CIFC45 H48 N4P -19.1381; 12.0237; 17.8361
96.278; 90.36; 111.214		1813.7Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515519 CIFC50 H55 K Mn N4 O2P 1 21/n 111.527; 13.729; 27.724
90; 92.471; 90		4383.4Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515520 CIFC53 H47.5 F9 K Mn N4.5 O6.5P 1 21/n 112.3883; 18.995; 21.656
90; 101.457; 90		4994.5Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515521 CIFC48 H39 F9 N4 O6P 1 21/c 119.36; 10.0615; 29.486
90; 128.675; 90		4484Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515522 CIFC88 H131 K Mn N4 O7P -113.4244; 15.4608; 21.041
92.203; 93.474; 102.805		4244.6Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515523 CIFC54 H45 F18 K Mn N4 O3P -112.729; 14.584; 16.701
112.045; 92.891; 99.02		2817.9Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515524 CIFC148 H198 Cl0 K4 Mn4 N20 O19P -112.421; 13.222; 24.754
89.65; 77.831; 72.506		3783.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515525 CIFC64.75 H86 K Mn N4 O4P -111.719; 12.417; 21.77
91.221; 100.827; 100.424		3055Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515526 CIFC58 H71 K Mn N4 O4P 1 21/n 112.4818; 21.792; 20.039
90; 105.708; 90		5247.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515527 CIFC32 H29 F9 K Mn N6 O5C 1 c 118.3717; 10.8662; 19.0286
90; 94.307; 90		3788Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515528 CIFC41 H51 Fe K N6 O11P 21 21 2111.1683; 18.406; 21.83
90; 90; 90		4487.5Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515529 CIFC56 H61 Cl6 K Mn N4 O5P 1 21/n 111.391; 20.1796; 24.488
90; 93.742; 90		5617Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515530 CIFC28 H18 Co F9 K N6 O3P 1 21/c 110.696; 18.855; 15.813
90; 101.378; 90		3126.4Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515531 CIFC86 H118 K2 Mn2 N8 O17C 1 2/c 118.8633; 21.7465; 22.5199
90; 102.759; 90		9009.8Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515532 CIFC36 H39 F9 K N7 Ni O6P 1 21/n 19.133; 29.15; 16.125
90; 95.392; 90		4274Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515533 CIFC28 H18 F9 K Mn N6 O3P 1 21/c 110.661; 18.766; 15.752
90; 100.699; 90		3097Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515534 CIFC78 H105 K2 Mn2 N11 O9P -111.759; 13.541; 26.426
86.003; 80.023; 73.719		3977Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515535 CIFC15 H13 N O2P 1 21/c 15.8829; 8.228; 25.846
90; 96.056; 90		1244.08Liu, Chengwei; Li, Guangchen; Shi, Shicheng; Meng, Guangrong; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon‒Nitrogen Bond Cleavage
ACS Catalysis, 2018, 8, 9131
4515536 CIFC30 H27 N2 O4 PP 1 21/c 112.148; 10.6001; 19.4764
90; 96.366; 90		2492.5Meyer, Tjark H.; Oliveira, João C. A.; Sau, Samaresh Chandra; Ang, Nate W. J.; Ackermann, Lutz
Electrooxidative Allene Annulations by Mild Cobalt-Catalyzed C‒H Activation
ACS Catalysis, 2018, 8, 9140
4515537 CIFC25 H20 Cl N O2P 21 21 216.1285; 10.8042; 30.5592
90; 90; 90		2023.43Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang
Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles
ACS Catalysis, 2018, 8, 9543
4515538 CIFC25 H20 Br N O2P 1 21 113.288; 5.6; 14.983
90; 114.29; 90		1016.23Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang
Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles
ACS Catalysis, 2018, 8, 9543
4515539 CIFC88 H44 Mo0.96 O32 S1.92 Zr6P 6/m m m39.254; 39.254; 16.542
90; 90; 120		22074Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T.
Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework
ACS Catalysis, 2018, 8, 9848
4515540 CIFC88 H44 Mo2.24 O36.88 Zr6P 6/m m m39.4657; 39.4657; 16.3953
90; 90; 120		22115.1Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T.
Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework
ACS Catalysis, 2018, 8, 9848
4515541 CIFC28 H26 N4 O7P 21 21 219.0462; 11.8256; 23.9232
90; 90; 90		2559.23Wang, Jilan; Li, Yongjia; Sun, Jun; Wang, Hongling; Jin, Zhichao; Chi, Yonggui Robin
Carbene-Catalyzed Enantioselective Addition of Benzylic Carbon to Unsaturated Acyl Azolium for Rapid Synthesis of Pyrrolo[3,2-c]quinolines
ACS Catalysis, 2018, 8, 9859
4515542 CIFC14 H21 Ge N O3P b c a13.7717; 11.1518; 18.9206
90; 90; 90		2905.81Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin
Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis
ACS Catalysis, 2018, 8, 9287
4515543 CIFC14 H20 Cl Ge N O3P 1 21/n 114.8342; 13.3798; 16.4653
90; 96.777; 90		3245.18Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin
Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis
ACS Catalysis, 2018, 8, 9287
4515544 CIFC54 H60 N2P -18.3369; 9.3962; 14.592
100.111; 103.43; 98.334		1073.8Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka
Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation
ACS Catalysis, 2018, 8, 9408
4515545 CIFC12 H14 F3 N OP c a 218.8458; 14.526; 9.5388
90; 90; 90		1225.7Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka
Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation
ACS Catalysis, 2018, 8, 9408
4515546 CIFC28 H23 N SP 110.1611; 10.3192; 12.2146
73.14; 71.609; 61.296		1051.13Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong
Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction
ACS Catalysis, 2018, 8, 9364
4515547 CIFC28 H23 N SP 110.082; 10.316; 12.247
73.57; 71.546; 61.603		1049.43Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong
Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction
ACS Catalysis, 2018, 8, 9364
4515548 CIFC15 H14 N2 O3P 1 21/c 18.085; 16.9819; 10.0705
90; 110.13; 90		1298.2Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515549 CIFC23 H19 Cl N2 O3 SP 1 21/c 17.0746; 19.195; 15.3264
90; 100.918; 90		2043.6Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515550 CIFC27 H22 N2 O3 SP n a 2133.95; 8.4972; 7.9321
90; 90; 90		2288.3Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515551 CIFC26 H24 N2 O5 SP 1 21/c 112.008; 7.0368; 30.631
90; 92.288; 90		2586.2Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515552 CIFC28 H28 N2 O3 SC 1 2/c 133.457; 7.1395; 20.377
90; 103.524; 90		4732.4Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515553 CIFC24 H22 Cl N3 O2P -19.5004; 11.278; 11.5979
104.256; 109.363; 106.026		1045.71Liu, Bingxian; Li, Jie; Hu, Panjie; Zhou, Xukai; Bai, Dachang; Li, Xingwei
Divergent Annulative C‒C Coupling of Indoles Initiated by Manganese-Catalyzed C‒H Activation
ACS Catalysis, 2018, 8, 9463
4515554 CIFC23 H25 N O2P 1 21 19.356; 10.7541; 9.6715
90; 96.3296; 90		967.17Huang, Liang-Zhu; Xuan, Zi; Jeon, Hyun Ji; Du, Zhen-Ting; Kim, Ju Hyun; Lee, Sang-gi
Asymmetric Rh(II)/Pd(0) Relay Catalysis: Synthesis of α-Quaternary Chiral β-Lactams through Enantioselective C‒H Insertion/Diastereoselective Allylation of Diazoamides
ACS Catalysis, 2018, 8, 7340
4515555 CIFC11 H17 B Cl N OP n a 2119.738; 5.4134; 11.384
90; 90; 90		1216.4Yang, Ji-Min; Zhao, Yu-Tao; Li, Zi-Qi; Gu, Xue-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Gold-Catalyzed Oxidative Coupling of Terminal Alkynes and Borane Adducts: Efficient Synthesis of α-Boryl Ketones
ACS Catalysis, 2018, 8, 7351
4515556 CIFC62 H42 O6 Ru2P -112.7987; 15.0974; 25.8586
104.39; 95.12; 100		4720.16Gusev, Dmitry G.; Spasyuk, Denis M.
Revised Mechanisms for Aldehyde Disproportionation and the Related Reactions of the Shvo Catalyst
ACS Catalysis, 2018, 8, 6851
4515557 CIFC31 H22 O3 RuP 1 21/n 115.7952; 7.4857; 20.8655
90; 100.47; 90		2426.02Gusev, Dmitry G.; Spasyuk, Denis M.
Revised Mechanisms for Aldehyde Disproportionation and the Related Reactions of the Shvo Catalyst
ACS Catalysis, 2018, 8, 6851
4515558 CIFC57 H75 Cl3 Fe3 N6P -112.6922; 13.0313; 16.647
76.0639; 84.1498; 84.0536		2649.46Ferreira, Ricardo B.; Cook, Brian J.; Knight, Brian J.; Catalano, Vincent J.; García-Serres, Ricardo; Murray, Leslie J.
Catalytic Silylation of Dinitrogen by a Family of Triiron Complexes.
ACS catalysis, 2018, 8, 7208-7212
4515559 CIFC21 H18 Mn N5 O4P 1 21/c 113.4325; 11.7346; 13.7646
90; 92.32; 90		2167.87Liu, Tingting; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Manganese-Catalyzed β-Alkylation of Secondary Alcohols with Primary Alcohols under Phosphine-Free Conditions
ACS Catalysis, 2018, 8, 7201
4515560 CIFC21 H26 N2 OP 1 21/c 117.2156; 7.3295; 13.8834
90; 90.807; 90		1751.66Fernández, David F.; Rodrigues, Catarina A. B.; Calvelo, Martín; Gulías, Moisés; Mascareñas, José L.; López, Fernando
Iridium(I)-Catalyzed Intramolecular Cycloisomerization of Enynes: Scope and Mechanistic Course
ACS Catalysis, 2018, 8, 7397
4515561 CIFC22 H23 N O2P 1 21/c 112.2561; 9.8925; 15.8384
90; 110.254; 90		1801.6Fernández, David F.; Rodrigues, Catarina A. B.; Calvelo, Martín; Gulías, Moisés; Mascareñas, José L.; López, Fernando
Iridium(I)-Catalyzed Intramolecular Cycloisomerization of Enynes: Scope and Mechanistic Course
ACS Catalysis, 2018, 8, 7397
4515562 CIFC37 H46 Cu N3P 1 21/n 112.411; 12.765; 21.416
90; 95.043; 90		3379.7Nakamura, Kimiaki; Hara, Reina; Sunada, Yusuke; Nishikata, Takashi
Radical-Organometallic Hybrid Reaction System Enabling Couplings between Tertiary-Alkyl Groups and 1-Alkenyl Groups
ACS Catalysis, 2018, 8, 6791
4515563 CIFC26 H24 Cu N4 O7 S2P b c a17.7588; 13.939; 20.7682
90; 90; 90		5140.96Hardouin Duparc, Valérie; Bano, Guillaume L.; Schaper, Frank
Chan‒Evans‒Lam Couplings with Copper Iminoarylsulfonate Complexes: Scope and Mechanism
ACS Catalysis, 2018, 8, 7308
4515564 CIFC14 H13 Cu F3 N2 O7 S2P -17.9814; 11.0894; 11.102
96.461; 100.176; 110.007		892.77Hardouin Duparc, Valérie; Bano, Guillaume L.; Schaper, Frank
Chan‒Evans‒Lam Couplings with Copper Iminoarylsulfonate Complexes: Scope and Mechanism
ACS Catalysis, 2018, 8, 7308
4515565 CIFC14 H14 O3P c a 2111.7373; 4.431; 21.078
90; 90; 90		1096.2Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515566 CIFC14 H14 O3P c c n6.6399; 17.0733; 19.2759
90; 90; 90		2185.2Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515567 CIFC15 H18 O2P 1 21/c 114.435; 5.4011; 16.2501
90; 104.851; 90		1224.62Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515568 CIFC15 H20 O2P 1 21 19.1834; 5.2643; 13.7823
90; 107.711; 90		634.72Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515569 CIFC42 H70 Ce N7 O8P -110.5305; 11.181; 20.761
101.915; 91.944; 94.462		2381.4Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515570 CIFC32 H51 Ce N6 O8P -111.5006; 17.4646; 20.0865
67.599; 80.635; 78.648		3639.9Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515571 CIFC49 H66 Ce2 N11 O17C 1 2/c 122.935; 19.6202; 13.5095
90; 114.142; 90		5547.4Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515572 CIFC124 H174 Ce4 N21 O32C 1 2/c 115.263; 27.226; 17.096
90; 96.089; 90		7064Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515573 CIFC68 H102 Ce2 N8 O11C 1 2/c 127.711; 19.4594; 15.5984
90; 122.044; 90		7129.7Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515574 CIFC34 H30 N2 O4P 1 21/c 113.746; 11.435; 18.615
90; 110.457; 90		2741.5Usui, Kenji; Haines, Brandon E.; Musaev, Djamaladdin G.; Sarpong, Richmond
Understanding Regiodivergence in a Pd(II)-Mediated Site-Selective C‒H Alkynylation
ACS Catalysis, 2018, 8, 4516
4515575 CIFC25 H25 N3 O PdP 1 21/n 112.551; 9.9456; 17.6307
90; 106.171; 90		2113.72Usui, Kenji; Haines, Brandon E.; Musaev, Djamaladdin G.; Sarpong, Richmond
Understanding Regiodivergence in a Pd(II)-Mediated Site-Selective C‒H Alkynylation
ACS Catalysis, 2018, 8, 4516
4515576 CIFC19 H17 Cl OP 21 21 215.612; 7.5305; 37.033
90; 90; 90		1565.1Teng, Huai-Long; Ma, Yuanhong; Zhan, Gu; Nishiura, Masayoshi; Hou, Zhaomin
Asymmetric C(sp)‒H Addition of Terminal Alkynes to Cyclopropenes by a Chiral Gadolinium Catalyst
ACS Catalysis, 2018, 8, 4705
4515577 CIFC21 H49 N O3 P2 RuP 1 21/n 113.2573; 13.3386; 15.3535
90; 92.948; 90		2711.4Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515578 CIFC51 H125 N3 O10 P6 Ru3P -115.1793; 16.5074; 16.664
88.609; 71.881; 62.825		3496Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515579 CIFC19 H41 N O3 P2 RuP b c a14.17; 15.3918; 21.741
90; 90; 90		4741.8Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515580 CIFC19 H35 Cl2 Mn N P2P 1 21/c 112.4393; 11.9755; 15.9077
90; 91.637; 90		2368.8Brzozowska, Aleksandra; Azofra, Luis Miguel; Zubar, Viktoriia; Atodiresei, Iuliana; Cavallo, Luigi; Rueping, Magnus; El-Sepelgy, Osama
Highly Chemo- and Stereoselective Transfer Semihydrogenation of Alkynes Catalyzed by a Stable, Well-Defined Manganese(II) Complex
ACS Catalysis, 2018, 8, 4103
4515581 CIFC7 H9 Co O5 PP 1 21/n 14.8553; 32.281; 5.6773
90; 91.788; 90		889.39Cai, Zhong-Sheng; Shi, Yi; Bao, Song-Song; Shen, Yang; Xia, Xing-Hua; Zheng, Li-Min
Bioinspired Engineering of Cobalt-Phosphonate Nanosheets for Robust Hydrogen Evolution Reaction
ACS Catalysis, 2018, 8, 3895
4515582 CIFC25 H40 N3 O2 P2 ReP 21 21 2110.1881; 13.7426; 20.6392
90; 90; 90		2889.7Glatz, Mathias; Stöger, Berthold; Himmelbauer, Daniel; Veiros, Luis F.; Kirchner, Karl
Chemoselective Hydrogenation of Aldehydes under Mild, Base-Free Conditions: Manganese Outperforms Rhenium.
ACS catalysis, 2018, 8, 4009-4016
4515583 CIFC72 H87 B N3 O2 YP 1 21/n 112.047; 17.64; 32.956
90; 96.116; 90		6964Yu, Xiaying; You, Qing; Zhou, Xigeng; Zhang, Lixin
Isoprene Regioblock Copolymerization: Switching the Regioselectivity by the in Situ Ancillary Ligand Transmetalation of Active Yttrium Species
ACS Catalysis, 2018, 8, 4465
4515584 CIFC12 H6 In0.54 N O2.25C m m m7.0996; 33.5115; 16.7335
90; 90; 90		3981.2Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515585 CIFC12 H6 In0.75 N O2.73C m m m7.125; 33.622; 16.583
90; 90; 90		3972.57Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515586 CIFC48 H24 In2 N4 Ni O10C m m m7.0725; 33.2883; 16.666
90; 90; 90		3923.7Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515587 CIFC26 H28 F6 Mn N4 O6 S2P 4318.28107; 18.28107; 36.923
90; 90; 90		12339.6Du, Junyi; Miao, Chengxia; Xia, Chungu; Lee, Yong-Min; Nam, Wonwoo; Sun, Wei
Mechanistic Insights into the Enantioselective Epoxidation of Olefins by Bioinspired Manganese Complexes: Role of Carboxylic Acid and Nature of Active Oxidant
ACS Catalysis, 2018, 8, 4528
4515588 CIFC28 H24 B F12 PP -113.414; 13.786; 18.1493
101.69; 106.173; 109.985		2859.7Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515589 CIFC28 H26 B F12 PP 1 21/n 110.6496; 15.3406; 18.042
90; 95.278; 90		2935Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515590 CIFC28 H27 B2 F12 PP -111.7104; 12.4425; 12.4488
71.092; 69.578; 64.329		1499.65Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515591 CIFC72 H94 Co2 N6P 1 21/n 111.1904; 12.5885; 22.6178
90; 99.722; 90		3140.42Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515592 CIFC31 H48 Co N2 O SiP 1 21/n 117.0369; 10.7343; 17.0418
90; 93.483; 90		3110.83Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515593 CIFC31 H45 Cl2 Co Li N2 O2P 41 21 212.0633; 12.0633; 21.8421
90; 90; 90		3178.53Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515594 CIFC39 H49 N3 O Si ZnP 1 21/n 18.8505; 21.914; 19.0059
90; 100.646; 90		3622.7Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515595 CIFC22.5 H38.5 N3 ZnP 1 21/c 114.8856; 21.731; 16.0804
90; 113.482; 90		4770.9Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515596 CIFC22 H35 N3 O2 ZnP 1 21/c 123.041; 10.016; 22.532
90; 117.531; 90		4611Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515597 CIFC50 H86 N6 Zn2C 1 2/c 121.7365; 14.2049; 20.3579
90; 102.81; 90		6129.4Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515598 CIFC55 H93 N6 O4 Zn2P -112.7688; 13.881; 17.4955
76.808; 73.779; 84.324		2896.9Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515599 CIFC51 H86 N6 O2 Zn2P -116.1366; 16.5978; 23.3164
98.9; 90.984; 119.052		5362.53Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515600 CIFC60 H84 N4 O4 Zn2P -113.4707; 14.5272; 16.2991
88.145; 89.86; 65.496		2900.6Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515601 CIFC10 H12 Fe N11 OP 1 21/n 110.82; 12.675; 11.662
90; 106.559; 90		1533Shen, Shou-Jie; Zhu, Cheng-Liang; Lu, Deng-Fu; Xu, Hao
Iron-Catalyzed Direct Olefin Diazidation via Peroxyester Activation Promoted by Nitrogen-Based Ligands.
ACS catalysis, 2018, 8, 4473-4482
4515602 CIFC44 H54 N4 NiP 21 21 2110.1006; 18.0014; 42.163
90; 90; 90		7666.3Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515603 CIFC110 H136 Cl3 N9 Ni3P 1 21/c 126.6781; 16.5463; 22.7174
90; 90.462; 90		10027.7Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515604 CIFC64 H80 Cl2 N6 Ni2P 21 21 2112.855; 21.217; 24.26
90; 90; 90		6617Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515605 CIFC43 H56 Cl N3 NiC 1 2/c 127.4949; 19.0191; 16.9558
90; 108.589; 90		8404.1Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515606 CIFC22 H37 Ir N PP 21 21 2110.5276; 10.7464; 18.567
90; 90; 90		2100.6Cherepakhin, Valeriy; Williams, Travis J.
Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.
ACS catalysis, 2018, 8, 3754-3763
4515607 CIFC29 H48 Ir2 N2 O P2P 1 21/c 114.836; 15.464; 15.385
90; 114.159; 90		3220.5Cherepakhin, Valeriy; Williams, Travis J.
Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.
ACS catalysis, 2018, 8, 3754-3763
4515608 CIFC34 H26 F6 N6 O9 P Ru2P 1 21/c 113.8587; 23.8714; 12.5805
90; 115.201; 90		3765.8Daniel, Quentin; Duan, Lele; Timmer, Brian J. J.; Chen, Hong; Luo, Xiaodan; Ambre, Ram; Wang, Ying; Zhang, Biaobiao; Zhang, Peili; Wang, Lei; Li, Fusheng; Sun, Junliang; Ahlquist, Mårten; Sun, Licheng
Water Oxidation Initiated by In Situ Dimerization of the Molecular Ru(pdc) Catalyst
ACS Catalysis, 2018, 8, 4375
4515609 CIFC21 H23 Br N OP -18.6881; 9.8467; 11.0731
94.586; 91.58; 105.361		909.36Bai, Dachang; Xu, Teng; Ma, Chaorui; Zheng, Xin; Liu, Bingxian; Xie, Fang; Li, Xingwei
Rh(III)-Catalyzed Mild Coupling of Nitrones and Azomethine Imines with Alkylidenecyclopropanes via C‒H Activation: Facile Access to Bridged Cycles
ACS Catalysis, 2018, 8, 4194
4515610 CIFC8 H7 Cl O3P n a 2114.4042; 3.8522; 14.6641
90; 90; 90		813.68Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515611 CIFC25 H25 Cl O4P 1 21 110.936; 6.5014; 14.9916
90; 95.8987; 90		1060.25Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515612 CIFC6 H3 Br Cl I OP 1 21 17.2559; 4.5474; 13.321
90; 100.781; 90		431.77Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515613 CIFC12 H8 Cl2 O2P b c n6.3191; 15.8114; 21.7404
90; 90; 90		2172.17Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515614 CIFC8 H7 Cl O2P 1 21/c 16.7838; 16.4432; 7.2539
90; 108.069; 90		769.25Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515615 CIFC25 H21 Cl O3C 1 2/c 113.6694; 14.6546; 21.7416
90; 104.277; 90		4220.76Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515616 CIFC8 H6 Br Cl O3P 1 21/c 14.1058; 17.9301; 12.4296
90; 93.138; 90		913.66Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515617 CIFC12 H8 F2 O SeP -15.6425; 9.1159; 11.1839
106.666; 102.943; 93.95		531.61Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515618 CIFC7 H4 Br Cl O2P 1 21/n 17.7896; 13.5178; 15.0171
90; 101.499; 90		1549.54Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515619 CIFC19 H17 Cl O3P 1 21 19.6791; 7.1917; 12.2628
90; 107.906; 90		812.26Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515620 CIFC12 H9 Cl OP 1 21/n 15.7829; 20.3532; 8.3091
90; 97.502; 90		969.61Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515621 CIFC12 H16 B Cl O3I -419.7094; 19.7094; 6.8557
90; 90; 90		2663.2Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515622 CIFC6 H4 Br Cl OP 21 21 215.2204; 11.214; 11.717
90; 90; 90		685.9Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515623 CIFC12 H10 Br2 Cl2 O4C 1 2/c 132.7811; 3.926; 21.7084
90; 91.5018; 90		2792.9Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515624 CIFC48 H38 B Cl2 F27 Fe N4 O3 SP -112.695; 13.3351; 17.1823
102.363; 97.011; 92.487		2812.8Postils, Verònica; Rodríguez, Mònica; Sabenya, Gerard; Conde, Ana; Díaz-Requejo, M. Mar; Pérez, Pedro J.; Costas, Miquel; Solà, Miquel; Luis, Josep M.
Mechanism of the Selective Fe-Catalyzed Arene Carbon‒Hydrogen Bond Functionalization
ACS Catalysis, 2018, 8, 4313
4515625 CIFC26 H36 O4 SP 1 21 19.0489; 8.4426; 15.648
90; 94.577; 90		1191.6Yu, Fei-Le; Bai, Da-Chang; Liu, Xiu-Yan; Jiang, Yang-Jie; Ding, Chang-Hua; Hou, Xue-Long
Pd-Catalyzed Allylic Alkylation of gem-Alkyl,Aryl-Disubstituted Allyl Reagents with Ketones: Diastereoselective Construction of Vicinal Tertiary and Quaternary Carbon Centers
ACS Catalysis, 2018, 8, 3317
4515626 CIFC16 H20 OP 1 21/c 18.6633; 8.4114; 17.9313
90; 99.6888; 90		1288Yu, Fei-Le; Bai, Da-Chang; Liu, Xiu-Yan; Jiang, Yang-Jie; Ding, Chang-Hua; Hou, Xue-Long
Pd-Catalyzed Allylic Alkylation of gem-Alkyl,Aryl-Disubstituted Allyl Reagents with Ketones: Diastereoselective Construction of Vicinal Tertiary and Quaternary Carbon Centers
ACS Catalysis, 2018, 8, 3317
4515627 CIFC21 H21 N3 O3 SP -16.3615; 10.4427; 15.1313
85.229; 87.86; 76.106		972.24Guin, Srimanta; Deb, Arghya; Dolui, Pravas; Chakraborty, Souvik; Singh, Vikas Kumar; Maiti, Debabrata
Promoting Highly Diastereoselective γ-C‒H Chalcogenation of α-Amino Acids and Aliphatic Carboxylic Acids
ACS Catalysis, 2018, 8, 2664
4515628 CIFC16 H20 O5P 21 21 218.793; 10.1042; 16.0484
90; 90; 90		1425.8Biosca, Maria; Margalef, Jèssica; Caldentey, Xisco; Besora, Maria; Rodríguez-Escrich, Carles; Saltó, Joan; Cambeiro, Xacobe C.; Maseras, Feliu; Pàmies, Oscar; Diéguez, Montserrat; Pericàs, Miquel A.
Computationally Guided Design of a Readily Assembled Phosphite‒Thioether Ligand for a Broad Range of Pd-Catalyzed Asymmetric Allylic Substitutions
ACS Catalysis, 2018, 8, 3587
4515629 CIFC13 H15 B F3 KP 19.0823; 10.0446; 16.7815
72.627; 75.846; 89.976		1412.38Gao, De-Wei; Xiao, Yiyang; Liu, Mingyu; Liu, Zhen; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Catalytic, Enantioselective Synthesis of Allenyl Boronates.
ACS catalysis, 2018, 8, 3650-3654
4515630 CIFC14 H13 N O4P 21 21 216.6275; 8.0167; 22.6419
90; 90; 90		1202.98Brandenberg, Oliver F.; Prier, Christopher K.; Chen, Kai; Knight, Anders M.; Wu, Zachary; Arnold, Frances H.
Stereoselective Enzymatic Synthesis of Heteroatom-Substituted Cyclopropanes
ACS Catalysis, 2018, 8, 2629
4515631 CIFC70 H110 Cl2 Co2 N4 P4P 1 21/n 110.4784; 22.1575; 15.6461
90; 105.074; 90		3507.6Suzuki, Tatsuya; Fujimoto, Keisuke; Takemoto, Yoshiyuki; Wasada-Tsutsui, Yuko; Ozawa, Tomohiro; Inomata, Tomohiko; Fryzuk, Michael D.; Masuda, Hideki
Efficient Catalytic Conversion of Dinitrogen to N(SiMe3)3 Using a Homogeneous Mononuclear Cobalt Complex
ACS Catalysis, 2018, 8, 3011
4515632 CIFC70 H110 Co2 N4 P4P 1 21/c 110.7673; 29.054; 12.6363
90; 117.372; 90		3510.5Suzuki, Tatsuya; Fujimoto, Keisuke; Takemoto, Yoshiyuki; Wasada-Tsutsui, Yuko; Ozawa, Tomohiro; Inomata, Tomohiko; Fryzuk, Michael D.; Masuda, Hideki
Efficient Catalytic Conversion of Dinitrogen to N(SiMe3)3 Using a Homogeneous Mononuclear Cobalt Complex
ACS Catalysis, 2018, 8, 3011
4515633 CIFC23 H34 N6 O3 SP 1 21 19.2161; 12.7576; 10.9094
90; 95.835; 90		1276.03Nicholls, Rachel L.; McManus, James A.; Rayner, Christopher M.; Morales-Serna, José A.; White, Andrew J. P.; Nguyen, Bao N.
Guanidine-Catalyzed Reductive Amination of Carbon Dioxide with Silanes: Switching between Pathways and Suppressing Catalyst Deactivation
ACS Catalysis, 2018, 8, 3678
4515634 CIFC23 H16 O2C 1 2/c 115.5099; 7.5217; 28.568
90; 99.09; 90		3290.9Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V.
Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes
ACS Catalysis, 2018, 8, 2748
4515635 CIFC15 H22 Br N OP 1 21 17.5964; 16.0907; 12.1098
90; 99.736; 90		1458.88Liu, Ze-Shui; Qian, Guangyin; Gao, Qianwen; Wang, Peng; Cheng, Hong-Gang; Wei, Qiang; Liu, Qi; Zhou, Qianghui
Palladium/Norbornene Cooperative Catalysis To Access Tetrahydronaphthalenes and Indanes with a Quaternary Center
ACS Catalysis, 2018, 8, 4783
4515636 CIFC29 H30 O5P 1 21/n 110.573; 16.555; 14.695
90; 104.784; 90		2487Liu, Ze-Shui; Qian, Guangyin; Gao, Qianwen; Wang, Peng; Cheng, Hong-Gang; Wei, Qiang; Liu, Qi; Zhou, Qianghui
Palladium/Norbornene Cooperative Catalysis To Access Tetrahydronaphthalenes and Indanes with a Quaternary Center
ACS Catalysis, 2018, 8, 4783
4515637 CIFC13 H17 N O5 SP 1 21/n 15.923; 16.864; 14.255
90; 92.357; 90		1422.7Kishi, Kenta; Takizawa, Shinobu; Sasai, Hiroaki
Phosphine-Catalyzed Dual Umpolung Domino Michael Reaction: Facile Synthesis of Hydroindole- and Hydrobenzofuran-2-Carboxylates
ACS Catalysis, 2018, 8, 5228
4515638 CIFC37 H47 Mo N3 OP 1 21/n 115.8128; 13.0267; 16.0929
90; 98.231; 90		3280.8Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515639 CIFC47 H60 Mo N5 OF d d 232.0833; 33.7453; 17.8428
90; 90; 90		19317.7Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515640 CIFC41 H65 Mo N3 Si2P 1 21/c 111.264; 17.5505; 23.2268
90; 115.23; 90		4153.65Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515641 CIFC41 H50 Cl6 N P PdP 21 21 2113.8095; 15.6122; 19.5369
90; 90; 90		4212.1Ding, Linlin; Sui, Xianwei; Gu, Zhenhua
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
ACS Catalysis, 2018, 8, 5630
4515642 CIFC25.5 H15 Cl5 O3P 1 21 111.39996; 31.0942; 19.9369
90; 96.7204; 90		7018.53Ding, Linlin; Sui, Xianwei; Gu, Zhenhua
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
ACS Catalysis, 2018, 8, 5630
4515643 CIFC29 H34 Cl N O5P 1 21 18.4142; 14.046; 11.3304
90; 104.324; 90		1297.5Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515644 CIFC21 H27 N O5P 1 21/c 112.432; 11.174; 14.1728
90; 96.117; 90		1957.6Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515645 CIFC21 H27 N O5P 1 21/c 18.3767; 12.1262; 39.035
90; 93.093; 90		3959.3Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515646 CIFC39 H38 Br N O Si2P 21 21 219.6879; 9.8487; 34.927
90; 90; 90		3332.5Meng, Fei-Fan; Xie, Jia-Hao; Xu, Yun-He; Loh, Teck-Peng
Catalytically Asymmetric Synthesis of 1,3-Bis(silyl)propenes via Copper-Catalyzed Double Proto-Silylations of Polar Enynes
ACS Catalysis, 2018, 8, 5306
4515647 CIFC15 H21 N O2 SP 1 21/c 116.125; 6.8205; 13.1663
90; 96.287; 90		1439.33Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515648 CIFC30 H42 N2 O4 S2P 1 21/n 119.6621; 8.3363; 19.9464
90; 112.146; 90		3028.2Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515649 CIFC30 H42 N2 O4 S2P n a 2132.802; 8.4124; 10.9145
90; 90; 90		3011.8Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515650 CIFC13 H17 N O2 SP 1 21/n 17.851; 10.524; 15.813
90; 98.263; 90		1293Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515651 CIFC16 H25 O2 PP 1 21 18.589; 5.946; 15.333
90; 100.966; 90		768.8Smaligo, Andrew J.; Vardhineedi, Sriramurthy; Kwon, Ohyun
Carvone-Derived P-Stereogenic Phosphines: Design, Synthesis, and Use in Allene-Imine [3 + 2] Annulation.
ACS catalysis, 2018, 8, 5188-5192
4515652 CIFC16 H23 O3 PP 1 21 110.2543; 10.9798; 13.7645
90; 90.59; 90		1549.67Smaligo, Andrew J.; Vardhineedi, Sriramurthy; Kwon, Ohyun
Carvone-Derived P-Stereogenic Phosphines: Design, Synthesis, and Use in Allene-Imine [3 + 2] Annulation.
ACS catalysis, 2018, 8, 5188-5192
4515653 CIFC25 H18 Cl F3 O2 SP 21 21 217.8069; 7.8369; 35.3156
90; 90; 90		2160.68Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L.
Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.
ACS catalysis, 2018, 8, 5443-5447
4515654 CIFC26 H21 F3 O2 SP 1 21 17.7702; 7.7862; 17.9926
90; 100.144; 90		1071.54Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L.
Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.
ACS catalysis, 2018, 8, 5443-5447
4515655 CIFC23.7 H15 Cl2.1 D0.7 F3 O4 SP 21 21 219.3182; 10.5061; 24.8751
90; 90; 90		2435.2Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L.
Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.
ACS catalysis, 2018, 8, 5443-5447
4515656 CIFC21 H20 N2 O3P 1 21/n 113.218; 8.696; 16.546
90; 98.483; 90		1881.1Pang, Shuai; Yang, Xing; Cao, Ze-Hun; Zhang, Yu-Long; Zhao, Yan; Huang, Yi-Yong
Intermolecular [2 + 2] Cycloaddition/Isomerization of Allenyl Imides and Unactivated Imines for the Synthesis of 1-Azadienes Catalyzed by a Ni(ClO4)2·6H2O Lewis Acid
ACS Catalysis, 2018, 8, 5193
4515657 CIFC22 H22 N2 O4P 1 21/n 110.559; 8.848; 20.03
90; 91.424; 90		1870.7Pang, Shuai; Yang, Xing; Cao, Ze-Hun; Zhang, Yu-Long; Zhao, Yan; Huang, Yi-Yong
Intermolecular [2 + 2] Cycloaddition/Isomerization of Allenyl Imides and Unactivated Imines for the Synthesis of 1-Azadienes Catalyzed by a Ni(ClO4)2·6H2O Lewis Acid
ACS Catalysis, 2018, 8, 5193
4515658 CIFC16 H21 Cl2 Fe N9 O2P n a 2113.7551; 18.856; 8.4263
90; 90; 90		2185.5Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515659 CIFC15 H19 F3 N2 O4 SP -17.6537; 10.3038; 11.7
69.471; 74.774; 75.983		822.2Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515660 CIFC18 H22 Cl3 F3 N2 O4 SP 21 21 216.1287; 17.2349; 21.6302
90; 90; 90		2284.74Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515661 CIFC14 H22 F3 N O2P 1 21/c 111.8893; 5.2263; 24.518
90; 96.137; 90		1514.75Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515662 CIFC16 H26 F3 N O2P 21 21 2111.579; 16.9733; 18.2465
90; 90; 90		3586.05Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515663 CIFC19 H25 F3 N2 O4P 1 21/c 114.9198; 13.8571; 9.9498
90; 95.4351; 90		2047.82Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515664 CIFC17 H39 As Co K2 Mo6 N O39.5P -112.0872; 12.5682; 17.2255
76.7; 74.058; 76.399		2407Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515665 CIFC17 H44 As K2 Mo6 N Ni O42P -111.9612; 12.5318; 17.1943
76.499; 74.053; 76.535		2370.12Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515666 CIFC17 H40 As K2 Mo6 N O41 ZnP -112.1425; 12.5739; 17.2226
76.443; 74.062; 76.225		2415.16Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515667 CIFC17 H39 As K2 Mn Mo6 N O40P -112.2865; 12.6065; 17.2145
76.319; 73.933; 76.064		2445.2Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515668 CIFC18 H87 As2 Co0.5 K3 Mo12 N6 Na O77.5P -116.1055; 18.5246; 19.0707
75.701; 65.877; 64.845		4681.8Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515669 CIFC21 H44 As Co0.5 K5 Mo6 O44.5P -112.6575; 12.671; 18.5916
105.723; 91.318; 106.19		2740.7Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515670 CIFC47.5 H70 N2 Ni O8P -111.54858; 30.1957; 32.8403
64.8392; 80.3426; 86.1838		10218.4Nett, Alex J.; Cañellas, Santiago; Higuchi, Yuki; Robo, Michael T.; Kochkodan, Jeanne M.; Haynes, 2nd, M Taylor; Kampf, Jeff W.; Montgomery, John
Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation.
ACS catalysis, 2018, 8, 6606-6611
4515671 CIFC97 H92 N2 Ni O8.5P -114.0561; 14.806; 22.1265
93.854; 102.679; 118.29		3876.59Nett, Alex J.; Cañellas, Santiago; Higuchi, Yuki; Robo, Michael T.; Kochkodan, Jeanne M.; Haynes, 2nd, M Taylor; Kampf, Jeff W.; Montgomery, John
Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation.
ACS catalysis, 2018, 8, 6606-6611
4515672 CIFC27 H22 N2 O3C 1 2/c 114.2005; 10.38306; 28.0529
90; 102.226; 90		4042.44Rej, Supriya; Chatani, Naoto
Rhodium(I)-Catalyzed C8-Alkylation of 1-Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System
ACS Catalysis, 2018, 8, 6699
4515673 CIFC27 H36 I4 N2 SP -110.6361; 16.8158; 19.6467
91.7164; 105.424; 93.774		3375.9Horibe, Takahiro; Tsuji, Yasutaka; Ishihara, Kazuaki
Thiourea‒I2 as Lewis Base‒Lewis Acid Cooperative Catalysts for Iodochlorination of Alkene with In Situ-Generated I‒Cl
ACS Catalysis, 2018, 8, 6362
4515674 CIFC27 H36 Cl I3 N2 SP 1 21/n 110.689; 18.743; 16.225
90; 102.555; 90		3172.9Horibe, Takahiro; Tsuji, Yasutaka; Ishihara, Kazuaki
Thiourea‒I2 as Lewis Base‒Lewis Acid Cooperative Catalysts for Iodochlorination of Alkene with In Situ-Generated I‒Cl
ACS Catalysis, 2018, 8, 6362
4515675 CIFC17 H20 O7P c a 2112.9176; 15.173; 16.7769
90; 90; 90		3288.25Shu, Wei; Merino, Estíbaliz; Nevado, Cristina
Visible Light Mediated, Redox Neutral Remote 1,6-Difunctionalizations of Alkenes
ACS Catalysis, 2018, 8, 6401
4515676 CIFC27 H39 N2 Sc Si2P 1 21/c 116.7493; 17.9477; 9.7237
90; 105.053; 90		2822.8Li, Shihui; Liu, Dongtao; Wang, Zichuan; Cui, Dongmei
Development of Group 3 Catalysts for Alternating Copolymerization of Ethylene and Styrene Derivatives
ACS Catalysis, 2018, 8, 6086
4515677 CIFC33 H41 N3 O3P -111.5304; 11.8994; 12.6132
107.862; 96.62; 114.133		1444.35Li, Zhenghua; Song, Liangliang; Van Meervelt, Luc; Tian, Guilong; Van der Eycken, Erik V.
Cationic Gold(I)-Catalyzed Cascade Bicyclizations for Divergent Synthesis of (Spiro)polyheterocycles
ACS Catalysis, 2018, 8, 6388
4515678 CIFC21 H22 N2 O2 SP 21 21 219.2626; 11.273; 36.0958
90; 90; 90		3769Rigotti, Thomas; Casado-Sánchez, Antonio; Cabrera, Silvia; Pérez-Ruiz, Raúl; Liras, Marta; de la Peña O’Shea, Víctor A.; Alemán, José
A Bifunctional Photoaminocatalyst for the Alkylation of Aldehydes: Design, Analysis, and Mechanistic Studies
ACS Catalysis, 2018, 8, 5928
4515679 CIFC24 H20 N2 O2 SP 1 21 17.3859; 14.0495; 19.8207
90; 95.797; 90		2046.24Rigotti, Thomas; Casado-Sánchez, Antonio; Cabrera, Silvia; Pérez-Ruiz, Raúl; Liras, Marta; de la Peña O’Shea, Víctor A.; Alemán, José
A Bifunctional Photoaminocatalyst for the Alkylation of Aldehydes: Design, Analysis, and Mechanistic Studies
ACS Catalysis, 2018, 8, 5928
4515680 CIFC22 H17 N3 O2P 1 21/c 16.0252; 14.9032; 19.2088
90; 93.713; 90		1721.23Zhai, Shengxian; Qiu, Shuxian; Chen, Xiaoming; Tao, Cheng; Li, Yun; Cheng, Bin; Wang, Huifei; Zhai, Hongbin
Trifunctionalization of Allenes via Cobalt-Catalyzed MHP-Assisted C‒H Bond Functionalization and Molecular Oxygen Activation
ACS Catalysis, 2018, 8, 6645
4515681 CIFC38 H22 Cl2C 1 2/c 115.8675; 11.3225; 16.9255
90; 116.905; 90		2711.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515682 CIFC40 H26 Cl2C 1 2/c 116.6618; 12.3936; 16.076
90; 119.312; 90		2894.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515683 CIFC45 H54 OP -113.048; 15.9745; 20.3351
69.8393; 74.7061; 79.3386		3817.17Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515684 CIFC115 H108 Cl2 F36 N6 O8 P2 Sb2P 4 21 223.156; 23.156; 45.3164
90; 90; 90		24298.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515685 CIFC40 H28C 1 2/c 124.6931; 9.8945; 11.3008
90; 107.002; 90		2640.4Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515686 CIFC57 H53 Au Cl F18 N3 O4 P SbP 21 21 2111.625; 21.7951; 24.924
90; 90; 90		6314.9Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515687 CIFC85 H148 Au4 Cl4 F24 N4 O10 P4 S2 Sb4P -114.1224; 14.3201; 16.3265
111.05; 108.05; 90.835		2900.2Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515688 CIFC42 H50 Cl2 F6 N2 O4 P SbP 21 21 2114.5593; 16.985; 18.089
90; 90; 90		4473.2Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515689 CIFC64 H59 Cl2 F18 N3 O4 P SbP 1 21 111.2724; 25.712; 22.718
90; 98.349; 90		6514.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515690 CIFC28 H18 Br2P 21 21 216.7543; 9.853; 31.4363
90; 90; 90		2092.09Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515691 CIFC63 H59 Au Cl3 F18 N3 O4 P SbP 1 21 111.5608; 22.3675; 14.1582
90; 95.008; 90		3647.1Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515692 CIFC56 H48 Au Cl5 F18 N2 O4 P SbP 21 21 2111.8911; 20.269; 26.818
90; 90; 90		6463.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515693 CIFC40 H25.94 Cl2.06P 1 21/c 117.9011; 8.3634; 19.4197
90; 90.871; 90		2907.1Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515694 CIFC21 H25 N3P -18.0652; 8.3219; 14.129
77.347; 83.454; 80.93		910.59Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515695 CIFC23 H21 N OP -111.8311; 12.7714; 12.7734
69.209; 81.613; 86.471		1785Li, Deng-Yuan; Liu, Shuo; Chen, Shuang; Wang, An; Zhu, Xiao-Ping; Liu, Pei-Nian
Dual Role of Aryl Iodide in Cascade C‒H Arylation/Amination: Arylation Reagent and Cocatalyst for C‒N Formation
ACS Catalysis, 2018, 8, 6407
4515696 CIFC20 H26 N O4 ZnP 1 21/n 110.811; 16.451; 11.445
90; 101.668; 90		1993.5Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515697 CIFC28 H47 Ni O4 PP -110.2938; 16.839; 17.23
73.123; 78.321; 87.036		2798.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515698 CIFC13 H22 B N O2P 1 21/n 17.204; 34.935; 11.091
90; 92.218; 90		2789Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515699 CIFC24 H32 N2 Ni O4P -17.96; 8.085; 9.656
108.25; 93.812; 94.208		585.9Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515700 CIFC25 H41 Ni O4 PP -110.001; 10.415; 13.862
76.659; 77.984; 62.798		1240.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515701 CIFC22 H22 F6 N2 Ni O4P -16.3927; 8.606; 10.965
86.398; 79.115; 86.957		590.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515702 CIFC24 H28 N2 Ni O8P -16.736; 8.129; 11.969
101.952; 99.095; 99.806		619Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515703 CIFC24 H20 N2 O6 PdP -18.78; 10; 13.272
101.969; 98.6857; 103.084		1086.1Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515704 CIFC22 H17 I N2 O4 PdP 1 21/c 17.939; 16.611; 16.219
90; 93.262; 90		2135.4Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515705 CIFC20 H18 O8C 1 2/c 118.828; 8.059; 12.153
90; 91.24; 90		1844Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515706 CIFC21 H18 Br2P 1 21/c 17.258; 18.732; 12.399
90; 93.746; 90		1682.1Su, Xiang; Chen, Bifeng; Wang, Shaohong; Chen, Hui; Chen, Chao
Atom- and Step-Efficient Construction of Five-Membered Carbocycles with Alkenes and Alkynes Catalyzed by AgSbF6
ACS Catalysis, 2018, 8, 7760
4515707 CIFC17 H15 N O5C 1 2 121.4471; 6.4084; 12.069
90; 113.464; 90		1521.62Li, Kaizhi; Jin, Zhichao; Chan, Wai-Lun; Lu, Yixin
Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut‒Currier Reactions Catalyzed by Thiourea-Phosphines
ACS Catalysis, 2018, 8, 8810
4515708 CIFC19 H17 Br O3P 21 21 218.8312; 11.2095; 16.7904
90; 90; 90		1662.14Li, Kaizhi; Jin, Zhichao; Chan, Wai-Lun; Lu, Yixin
Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut‒Currier Reactions Catalyzed by Thiourea-Phosphines
ACS Catalysis, 2018, 8, 8810
4515709 CIFC17 H12 N2 O4P 1 21/c 16.8554; 18.0992; 11.1588
90; 92.472; 90		1383.26Chen, Fei; Lai, Sheng-Qiang; Zhu, Fei-Fei; Meng, Qiang; Jiang, Yu; Yu, Wei; Han, Bing
Cu-Catalyzed Radical Cascade Annulations of Alkyne-Tethered N-Alkoxyamides with Air: Facile Access to Isoxazolidine/1,2-Oxazinane-Fused Isoquinolin-1(2H)-ones
ACS Catalysis, 2018, 8, 8925
4515710 CIFC18 H29 Cl Ir N OP -18.6737; 8.7731; 13.6686
78.458; 75.85; 88.359		987.94Tan, Guangying; You, Qiulin; You, Jingsong
Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates
ACS Catalysis, 2018, 8, 8709
4515711 CIFC32 H38 N2 O2 S2P 1 21/n 112.5365; 14.4554; 17.4788
90; 103.091; 90		3085.19Tan, Guangying; You, Qiulin; You, Jingsong
Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates
ACS Catalysis, 2018, 8, 8709
4515712 CIFC30 H12.5 Al Cl F15.5 NP 1 21/c 110.307; 26.879; 20.89
90; 101.156; 90		5678Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515713 CIFC22 H21 N SiP -19.3329; 10.0874; 11.22
67.672; 88.245; 65.949		882.58Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515714 CIFC27 H14 Al F16 N4P -110.4075; 10.6369; 13.0972
79.781; 79.01; 71.612		1339.9Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515715 CIFC27 H9 Al F15 NP 1 21 17.4782; 17.022; 9.979
90; 107.975; 90		1208.3Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515716 CIFC15 H11 F3 O2 S2P 1 21/c 111.7791; 5.8649; 21.894
90; 92.863; 90		1510.6Li, Haoyu; Cheng, Zengrui; Tung, Chen-Ho; Xu, Zhenghu
Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
ACS Catalysis, 2018, 8, 8237
4515717 CIFC21 H20 F4 O3 S2P 1 21/c 110.219; 20.254; 10.852
90; 107.747; 90		2139Li, Haoyu; Cheng, Zengrui; Tung, Chen-Ho; Xu, Zhenghu
Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
ACS Catalysis, 2018, 8, 8237
4515718 CIFC21 H36 Mn N O2 P2C 1 2/c 118.6272; 10.623; 23.1001
90; 101.192; 90		4484.04Zou, You-Quan; Chakraborty, Subrata; Nerush, Alexander; Oren, Dror; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal-Ligand Cooperation.
ACS catalysis, 2018, 8, 8014-8019
4515719 CIFC42 H68 Mn2 N4 O4 P4P 1 21/c 111.6109; 18.5885; 21.5322
90; 99.218; 90		4587.26Zou, You-Quan; Chakraborty, Subrata; Nerush, Alexander; Oren, Dror; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal-Ligand Cooperation.
ACS catalysis, 2018, 8, 8014-8019
4515720 CIFC29 H55 Fe N3 P2 Si2P 1 21/c 112.7712; 19.068; 15.4049
90; 110.526; 90		3513.3Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515721 CIFC35 H67 Fe N3 P3 Si2P -110.589; 12.811; 15.92
92.93; 104.249; 99.001		2058.3Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515722 CIFC31 H58 Fe N4 P2 Si2P 1 21/c 116.778; 15.4527; 16.706
90; 99.322; 90		4274.1Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515723 CIFC40 H50 Fe N6 P2P 1 21/n 118.6843; 11.1179; 18.9515
90; 110.665; 90		3683.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515724 CIFC39 H58 B Fe N5 O2 P2P 1 21/c 118.764; 11.2867; 20.592
90; 114.08; 90		3981.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515725 CIFC22 H24 Cl N O RuP 1 21/n 111.6782; 8.2226; 20.44
90; 99.939; 90		1933.3Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515726 CIFC23 H24 N2 O2P 1 21/c 18.295; 11.086; 21.615
90; 93.5; 90		1984Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515727 CIFC33 H39 F6 N2 O2 Ru SbP 1 21/c 113.2275; 10.9193; 24.4944
90; 98.3993; 90		3499.9Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515728 CIFC47 H43 Br Mn N O4 P2P -112.0659; 12.6901; 13.3087
94.285; 102.738; 90.704		1981.22Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515729 CIFC39 H31 B Mn N O2 P2P -110.0379; 11.3687; 15.6568
73.97; 77.542; 72.82		1623.02Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515730 CIFC39 H31 Mn N2 O2 P2R -3 :H37.5012; 37.5012; 11.98047
90; 90; 120		14591.3Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515731 CIFC20 H20 Br Cl2 N O PtP 1 21/c 19.7404; 13.3126; 17.0002
90; 104.115; 90		2137.9Shimbayashi, Takuya; Matsushita, Gaku; Nanya, Atsushi; Eguchi, Akira; Okamoto, Kazuhiro; Ohe, Kouichi
Divergent Catalytic Approach from Cyclic Oxime Esters to Nitrogen-Containing Heterocycles with Group 9 Metal Catalysts
ACS Catalysis, 2018, 8, 7773
4515732 CIFC33 H41 Cl2 N Ru SP 4310.0186; 10.0186; 30.9734
90; 90; 90		3108.87Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515733 CIFC28 H36 Cl2 F3 N Ru SP n a 2116.3382; 16.5805; 10.4655
90; 90; 90		2835.1Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515734 CIFC26 H32 Cl2 F3 N Ru SP -111.0669; 14.1689; 17.6536
103.228; 94.276; 100.447		2630.52Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515735 CIFC32 H39 Cl4 N Ru SP c a 2119.868; 9.2131; 17.5258
90; 90; 90		3208Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515736 CIFC43 H60 S Y2P 1 21/n 112.6411; 16.3119; 19.7095
90; 106.372; 90		3899.3Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515737 CIFC25 H33 S YP 1 21/c 116.796; 8.4624; 16.616
90; 102.549; 90		2305.3Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515738 CIFC50 H66 S2 Y2P -110.343; 10.6225; 10.683
94.507; 108.927; 92.924		1103.18Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515739 CIFC20 H20 S SiP 1 21/n 19.7426; 9.7458; 18.818
90; 90.465; 90		1786.7Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515740 CIFC23 H23 N S SiP 1 21/n 110.304; 17.9385; 11.4674
90; 107.757; 90		2018.6Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515741 CIFC21 H25 Cl3 Ir N O3P 21 21 219.6875; 13.7823; 17.6769
90; 90; 90		2360.1Zhou, Gang; Aboo, Ahmed H.; Robertson, Craig M.; Liu, Ruixia; Li, Zhenhua; Luzyanin, Konstantin; Berry, Neil G.; Chen, Weiping; Xiao, Jianliang
N,O- vs N,C-Chelation in Half-Sandwich Iridium Complexes: A Dramatic Effect on Enantioselectivity in Asymmetric Transfer Hydrogenation of Ketones
ACS Catalysis, 2018, 8, 8020
4515742 CIFC21 H25 Cl Ir N O3P 6118.4094; 18.4094; 11.3169
90; 90; 120		3321.5Zhou, Gang; Aboo, Ahmed H.; Robertson, Craig M.; Liu, Ruixia; Li, Zhenhua; Luzyanin, Konstantin; Berry, Neil G.; Chen, Weiping; Xiao, Jianliang
N,O- vs N,C-Chelation in Half-Sandwich Iridium Complexes: A Dramatic Effect on Enantioselectivity in Asymmetric Transfer Hydrogenation of Ketones
ACS Catalysis, 2018, 8, 8020
4515743 CIFC20 H24 Cl N O4P 1 21 17.421; 16.048; 8.176
90; 101.174; 90		955.2Schmid, Steven C.; Guzei, Ilia A.; Fernández, Israel; Schomaker, Jennifer M.
Ring Expansion of Bicyclic Methyleneaziridines via Concerted, Near-Barrierless [2,3]-Stevens Rearrangements of Aziridinium Ylides.
ACS catalysis, 2018, 8, 7907-7914
4515744 CIFC29 H43 F6 N P SbP b c a16.4612; 13.7221; 26.85
90; 90; 90		6064.9Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515745 CIFC30 H21 F18 N P SbC 1 2/c 127.034; 8.1387; 29.826
90; 95.017; 90		6537.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515746 CIFC32 H24 Au Cl F18 N2 P SbP 1 21/n 18.7962; 27.1915; 16.076
90; 103.535; 90		3738.3Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515747 CIFC27 H27 Cl2 F6 N P SbP -18.4844; 13.1717; 13.5679
92.667; 105.963; 100.874		1423.8Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515748 CIFC26 H37 Au Cl F6 N P SbP -110.6409; 16.737; 17.0626
82.428; 84.084; 87.346		2994.6Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515749 CIFC26 H37 F6 N P SbP 1 21/n 113.8885; 13.3919; 15.6069
90; 112.626; 90		2679.4Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515750 CIFC26 H29 Cl F6 Ir N P SbP 1 21/c 111.9033; 8.2433; 28.535
90; 99.672; 90		2760.1Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515751 CIFC26 H25 Au Cl F6 N P SbP -110.004; 10.1489; 15.7193
107.808; 92.182; 112.364		1383.43Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515752 CIFC31.5 H24 Au Cl6 F18 N O2 P SbP -18.9106; 12.9646; 19.744
73.397; 82.399; 85.849		2165.1Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515753 CIFC46 H40 O5P -111.0227; 11.4514; 15.2564
69.58; 76.609; 74.008		1715.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457

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