Crystallography Open Database

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4514024 CIFC94 H118 Ge2 N2 O Si2C 1 2/c 124.283; 21.152; 17.759
90; 114.38; 90		8308Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514025 CIFC52 H69 B N O3.5 Si SnP -110.1191; 12.9066; 18.7646
88.763; 86.92; 85.612		2439.63Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514026 CIFC45 H53 N O2 Si SnP -19.99; 11.36; 18.89
86.59; 85.63; 67.69		1976.4Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514027 CIFC15 H23 N3 O3P b c a16.5344; 9.4279; 20.9981
90; 90; 90		3273.3Bai, He-Yuan; Ma, Zhi-Gang; Yi, Min; Lin, Jun-Bing; Zhang, Shu-Yu
Palladium-Catalyzed Direct Intermolecular Amination of Unactivated Methylene C(sp3)‒H Bonds with Azodiformates via Bidentate-Chelation Assistance
ACS Catalysis, 2017, 7, 2042
4514028 CIFC56.25 H50.5 F12 N10 O4.75 P2 Ru2C 1 2/c 123.6464; 24.1857; 24.249
90; 116.899; 90		12367.7Odrobina, Jann; Scholz, Julius; Pannwitz, Andrea; Francàs, Laia; Dechert, Sebastian; Llobet, Antoni; Jooss, Christian; Meyer, Franc
Backbone Immobilization of the Bis(bipyridyl)pyrazolate Diruthenium Catalyst for Electrochemical Water Oxidation
ACS Catalysis, 2017, 7, 2116
4514029 CIFC61 H60 F12 N10 O7 P2 Ru2C 1 2/c 118.7376; 22.1944; 15.7519
90; 90.788; 90		6550.1Odrobina, Jann; Scholz, Julius; Pannwitz, Andrea; Francàs, Laia; Dechert, Sebastian; Llobet, Antoni; Jooss, Christian; Meyer, Franc
Backbone Immobilization of the Bis(bipyridyl)pyrazolate Diruthenium Catalyst for Electrochemical Water Oxidation
ACS Catalysis, 2017, 7, 2116
4514030 CIFC42 H36 F2 Fe Ni P2 SP -111.2326; 11.336; 16.1197
78.107; 72.51; 67.279		1796.3Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514031 CIFC40 H34 Fe I2 Ni P2P -18.9532; 10.0303; 20.4331
91.917; 99.127; 94.971		1802.83Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514037 CIFC54.5 H45 Ag4 Cl5 O10P 1 21/n 111.2473; 18.5148; 26.3786
90; 97.2988; 90		5448.6Zhou, Zhen; He, Cheng; Yang, Lu; Wang, Yefei; Liu, Tao; Duan, Chunying
Alkyne Activation by a Porous Silver Coordination Polymer for Heterogeneous Catalysis of Carbon Dioxide Cycloaddition
ACS Catalysis, 2017, 7, 2248
4514038 CIFC15 H12 Ag2 O6C 1 2/c 126.064; 19.397; 11.0996
90; 97.166; 90		5567.7Zhou, Zhen; He, Cheng; Yang, Lu; Wang, Yefei; Liu, Tao; Duan, Chunying
Alkyne Activation by a Porous Silver Coordination Polymer for Heterogeneous Catalysis of Carbon Dioxide Cycloaddition
ACS Catalysis, 2017, 7, 2248
4514039 CIFC44 H30 F5 N2 PP 1 21 112.3621; 45.6111; 12.6667
90; 97.7659; 90		7076.6Rokade, Balaji V.; Guiry, Patrick J.
Diastereofacial π-Stacking as an Approach To Access an Axially Chiral P,N-Ligand for Asymmetric Catalysis
ACS Catalysis, 2017, 2334
4514040 CIFC24 H18 Cl6 N O5 VP 1 21 17.20833; 12.3392; 14.6278
90; 93.647; 90		1298.44Miceli, Claudia; Rintjema, Jeroen; Martin, Eddy; Escudero-Adán, Eduardo C.; Zonta, Cristiano; Licini, Giulia; Kleij, Arjan W.
Vanadium(V) Catalysts with High Activity for the Coupling of Epoxides and CO2: Characterization of a Putative Catalytic Intermediate
ACS Catalysis, 2017, 7, 2367
4514041 CIFC24 H17 Cl7 N O5 VP 1 21/c 17.1728; 13.0626; 28.541
90; 96.136; 90		2658.8Miceli, Claudia; Rintjema, Jeroen; Martin, Eddy; Escudero-Adán, Eduardo C.; Zonta, Cristiano; Licini, Giulia; Kleij, Arjan W.
Vanadium(V) Catalysts with High Activity for the Coupling of Epoxides and CO2: Characterization of a Putative Catalytic Intermediate
ACS Catalysis, 2017, 7, 2367
4514048 CIFC21 H26 N2 O5C 1 2 122.5768; 8.5784; 12.0175
90; 121.047; 90		1994.04Chen, Xiaohong; Yang, Shujing; Li, Helong; Wang, Bo; Song, Guoyong
Enantioselective C‒H Annulation of Indoles with Diazo Compounds through a Chiral Rh(III) Catalyst
ACS Catalysis, 2017, 2392
4514051 CIFC44 H30 F5 N2 PP 1 21 112.37; 45.6483; 12.6634
90; 97.6938; 90		7086.3Paioti, Paulo H. S.; Abboud, Khalil A.; Aponick, Aaron
Incorporation of Axial Chirality into Phosphino-Imidazoline Ligands for Enantioselective Catalysis
ACS Catalysis, 2017, 7, 2133
4514052 CIFC78 H65 Br0.69 Cl0.31 F6 P5 Pd3 SbP 1 21/c 115.3662; 16.9466; 27.676
90; 92.693; 90		7199Fu, Fangyu; Xiang, Ji; Cheng, Hao; Cheng, Longjiu; Chong, Hanbao; Wang, Shuxin; Li, Peng; Wei, Shiqiang; Zhu, Manzhou; Li, Yadong
A Robust and Efficient Pd3 Cluster Catalyst for the Suzuki Reaction and Its Odd Mechanism
ACS Catalysis, 2017, 7, 1860
4514053 CIFC50 H64 B Ge N O3 SiP -19.93; 14.88; 15.29
91; 91.6; 98.1		2235.3Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514054 CIFC101 H134 Ge2 N2 O2 Si2C 1 2/c 131.052; 19.593; 17.8613
90; 105.933; 90		10449.4Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514055 CIFC38 H36 N2 O5 S2P 21 21 2110.9061; 12.6404; 28.3159
90; 90; 90		3903.6Feng, Jian-Jun; Zhang, Junliang
Rhodium-Catalyzed Stereoselective Intramolecular Tandem Reaction of Vinyloxiranes with Alkynes: Atom- and Step-Economical Synthesis of Multifunctional Mono-, Bi-, and Tricyclic Compounds
ACS Catalysis, 2017, 7, 1533
4514056 CIFC17 H21 N O3 SP 21 21 218.1166; 13.77; 15.4267
90; 90; 90		1724.17Feng, Jian-Jun; Zhang, Junliang
Rhodium-Catalyzed Stereoselective Intramolecular Tandem Reaction of Vinyloxiranes with Alkynes: Atom- and Step-Economical Synthesis of Multifunctional Mono-, Bi-, and Tricyclic Compounds
ACS Catalysis, 2017, 7, 1533
4514057 CIFC25 H44 Mn N O3 P2P n a 2130.3732; 11.6836; 7.6516
90; 90; 90		2715.3Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Paul, Jean-François; Dumeignil, Franck; Gauvin, Régis M.
Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding
ACS Catalysis, 2017, 7, 2022
4514058 CIFC18 H41 B Mn N O2 P2P b c a17.2037; 14.6522; 19.066
90; 90; 90		4806Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Paul, Jean-François; Dumeignil, Franck; Gauvin, Régis M.
Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding
ACS Catalysis, 2017, 7, 2022
4514059 CIFC18 H38 Mn N O2 P2P 1 21/c 110.6335; 14.5777; 13.8441
90; 97.449; 90		2127.9Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Paul, Jean-François; Dumeignil, Franck; Gauvin, Régis M.
Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding
ACS Catalysis, 2017, 7, 2022
4514060 CIFC40 H34 Br Fe Ni P2P -19.6075; 10.9191; 17.624
96.565; 105.405; 103.759		1699.9Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514061 CIFC72 H64 Fe2 I2 Ni2 O P4C 1 2/c 123.6771; 13.9547; 19.1841
90; 90.394; 90		6338.4Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514062 CIFC18 H17 N O2P -17.3719; 8.0356; 12.4786
82.255; 78.93; 86.099		718.16Wu, Xiaowei; Wang, Bao; Zhou, Shengbin; Zhou, Yu; Liu, Hong
Ruthenium-Catalyzed Redox-Neutral [4 + 1] Annulation of Benzamides and Propargyl Alcohols via C‒H Bond Activation
ACS Catalysis, 2017, 7, 2494
4514063 CIFC30 H64 Br2 P2 Pd2P 1 21/c 114.191; 14.4097; 18.8529
90; 90.638; 90		3855Hu, Huaiyuan; Qu, Fengrui; Gerlach, Deidra L.; Shaughnessy, Kevin H.
Mechanistic Study of the Role of Substrate Steric Effects and Aniline Inhibition on the Bis(trineopentylphosphine)palladium(0)-Catalyzed Arylation of Aniline Derivatives
ACS Catalysis, 2017, 7, 2516
4514064 CIFC48 H88 Br2 Cl4 P2 Pd2P -19.5914; 12.2401; 13.6152
114.515; 94.093; 92.143		1446.66Hu, Huaiyuan; Qu, Fengrui; Gerlach, Deidra L.; Shaughnessy, Kevin H.
Mechanistic Study of the Role of Substrate Steric Effects and Aniline Inhibition on the Bis(trineopentylphosphine)palladium(0)-Catalyzed Arylation of Aniline Derivatives
ACS Catalysis, 2017, 7, 2516
4514066 CIFC18 H19 N3 O2P 1 21/n 18.2446; 18.1585; 10.6143
90; 99.541; 90		1567.08Leitch, Jamie A.; McMullin, Claire L.; Mahon, Mary F.; Bhonoah, Yunas; Frost, Christopher G.
Remote C6-Selective Ruthenium-Catalyzed C‒H Alkylation of Indole Derivatives via σ-Activation
ACS Catalysis, 2017, 2616
4514067 CIFC24 H29 N3 O4P -17.2094; 12.0942; 13.0064
106.921; 90.76; 95.278		1079.4Leitch, Jamie A.; McMullin, Claire L.; Mahon, Mary F.; Bhonoah, Yunas; Frost, Christopher G.
Remote C6-Selective Ruthenium-Catalyzed C‒H Alkylation of Indole Derivatives via σ-Activation
ACS Catalysis, 2017, 2616
4514068 CIFC23 H18 N2 O3 SP -18.1462; 9.4252; 13.2617
104.796; 102.654; 103.208		915.85Li, Jun-Ming; Wang, Yong-Heng; Yu, Yang; Wu, Rui-Bo; Weng, Jiang; Lu, Gui
Copper-Catalyzed Remote C‒H Functionalizations of Naphthylamides through a Coordinating Activation Strategy and Single-Electron-Transfer (SET) Mechanism
ACS Catalysis, 2017, 2661
4514069 CIFC49 H40 N2 O4P -111.406; 12.0431; 13.804
89.519; 88.399; 75.619		1836Uraguchi, Daisuke; Torii, Masahiro; Ooi, Takashi
Acridinium Betaine as a Single-Electron-Transfer Catalyst: Design and Application to Dimerization of Oxindoles
ACS Catalysis, 2017
4514070 CIFC38 H29 F3 N OP b c n15.083; 14.7314; 26.284
90; 90; 90		5840.1Uraguchi, Daisuke; Torii, Masahiro; Ooi, Takashi
Acridinium Betaine as a Single-Electron-Transfer Catalyst: Design and Application to Dimerization of Oxindoles
ACS Catalysis, 2017
4514071 CIFC25 H19 Br N2 O2P 21 21 219.5611; 9.7674; 44.019
90; 90; 90		4110.8Wang, Shoulei; Izquierdo, Javier; Rodríguez-Escrich, Carles; Pericàs, Miquel A.
Asymmetric [4 + 2] Annulation Reactions Catalyzed by a Robust, Immobilized Isothiourea
ACS Catalysis, 2017, 7, 2780
4514072 CIFC24 H17 N O2 SP 21 21 216.2831; 10.506; 28.682
90; 90; 90		1893.3Wang, Shoulei; Izquierdo, Javier; Rodríguez-Escrich, Carles; Pericàs, Miquel A.
Asymmetric [4 + 2] Annulation Reactions Catalyzed by a Robust, Immobilized Isothiourea
ACS Catalysis, 2017, 7, 2780
4514073 CIFC38 H27 N5 O2P b c n17.1283; 9.2992; 18.9173
90; 90; 90		3013.1Du, Cong; Li, Peng-Xiang; Zhu, Xinju; Han, Jiao-Na; Niu, Jun-Long; Song, Mao-Ping
Cobalt-Catalyzed Oxidative C-H/N-H Cross-Coupling: Selective and Facile Access to Triarylamines
ACS Catalysis, 2017
4514074 CIFC45 H33 Cl2 Co N6 O2P 1 21/c 112.2327; 13.1901; 24.1763
90; 103.838; 90		3787.6Du, Cong; Li, Peng-Xiang; Zhu, Xinju; Han, Jiao-Na; Niu, Jun-Long; Song, Mao-Ping
Cobalt-Catalyzed Oxidative C-H/N-H Cross-Coupling: Selective and Facile Access to Triarylamines
ACS Catalysis, 2017
4514080 CIFC38 H52 N2 O2 PdP 1 21/c 112.47076; 21.63215; 13.10657
90; 99.47; 90		3487.57Kim, Jaewoon; Hong, Soon Hyeok
Ligand-Promoted Direct C‒H Arylation of Simple Arenes: Evidence for a Cooperative Bimetallic Mechanism
ACS Catalysis, 2017, 7, 3336
4514083 CIFC28 H29 N O3P -16.3295; 12.336; 14.619
90.792; 95.813; 96.114		1128.8Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip
A Bioinspired Catalytic Aerobic Functionalization of Phenols: Regioselective Construction of Aromatic C‒N and C‒O Bonds
ACS Catalysis, 2017, 7, 3477
4514084 CIFC33 H25 N O4P -19.7185; 15.9184; 15.9702
88.541; 87.598; 85.097		2458.84Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip
A Bioinspired Catalytic Aerobic Functionalization of Phenols: Regioselective Construction of Aromatic C‒N and C‒O Bonds
ACS Catalysis, 2017, 7, 3477
4514085 CIFC34 H23 F2 N O5P 1 21 110.0098; 19.235; 13.3175
90; 91.572; 90		2563.2Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip
A Bioinspired Catalytic Aerobic Functionalization of Phenols: Regioselective Construction of Aromatic C‒N and C‒O Bonds
ACS Catalysis, 2017, 7, 3477
4514089 CIFC38 H34 Co N4P b c a19.206; 15.8073; 19.2815
90; 90; 90		5853.8Maher, Andrew G.; Passard, Guillaume; Dogutan, Dilek K.; Halbach, Robert L.; Anderson, Bryce L.; Gagliardi, Christopher J.; Taniguchi, Masahiko; Lindsey, Jonathan S.; Nocera, Daniel G.
Hydrogen Evolution Catalysis by a Sparsely Substituted Cobalt Chlorin
ACS Catalysis, 2017, 3597
4514090 CIFC25 H19 N O2P 1 21/c 14.88608; 39.9585; 9.27521
90; 91.1105; 90		1810.56Herlé, Bart; Holstein, Philipp M.; Echavarren, Antonio M.
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions.
ACS catalysis, 2017, 7, 3668-3675
4514091 CIFC25 H19 N O2P -19.8574; 10.5363; 19.098
83.974; 85.964; 69.875		1850.88Herlé, Bart; Holstein, Philipp M.; Echavarren, Antonio M.
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions.
ACS catalysis, 2017, 7, 3668-3675
4514094 CIFC62 H65 B Co F24 N O2 P2P -113.0174; 14.9485; 17.504
102.352; 98.18; 99.337		3227.4Yuwen, Jing; Chakraborty, Sumit; Brennessel, William W.; Jones, William D.
Additive-Free Cobalt-Catalyzed Hydrogenation of Esters to Alcohols
ACS Catalysis, 2017, 3735
4514095 CIFC74 H75 B Co F24 N O4 P2P -114.722; 16.791; 17.269
99.053; 113.62; 101.693		3692.2Yuwen, Jing; Chakraborty, Sumit; Brennessel, William W.; Jones, William D.
Additive-Free Cobalt-Catalyzed Hydrogenation of Esters to Alcohols
ACS Catalysis, 2017, 3735
4514096 CIFC12 H10 O5P 21 21 215.9658; 6.8587; 26.877
90; 90; 90		1099.74Ji, Jie; Lin, Lili; Tang, Qiong; Kang, Tengfei; Liu, Xiaohua; Feng, Xiaoming
Highly Efficient Asymmetric Synthesis of Chiral γ-Alkenyl Butenolides Catalyzed by Chiral N,N′-Dioxide‒Scandium(III) Complexes
ACS Catalysis, 2017, 7, 3763
4514100 CIFC60 H54 F18 N12 O4 P3 Ru2P -113.578; 13.579; 13.733
91.45; 100.63; 115.95		2222Fan, Ting; Duan, Lele; Huang, Ping; Chen, Hong; Daniel, Quentin; Ahlquist, Mårten S. G.; Sun, Licheng
The Ru-tpc Water Oxidation Catalyst and Beyond: Water Nucleophilic Attack Pathway versus Radical Coupling Pathway
ACS Catalysis, 2017, 7, 2956
4514101 CIFC21 H39 Cl2 Co N P2P -18.2698; 10.9458; 14.8705
98.19; 90.641; 110.333		1246.6Daw, Prosenjit; Chakraborty, Subrata; Leitus, Gregory; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Selective N-Formylation of Amines with H2 and CO2 Catalyzed by Cobalt Pincer Complexes
ACS Catalysis, 2017, 7, 2500
4514102 CIFC21 H39 Cl Co N P2P 1 21/c 114.2619; 8.3444; 19.9331
90; 96.477; 90		2357Daw, Prosenjit; Chakraborty, Subrata; Leitus, Gregory; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Selective N-Formylation of Amines with H2 and CO2 Catalyzed by Cobalt Pincer Complexes
ACS Catalysis, 2017, 7, 2500
4514103 CIFC50 H40 Cl N3 O P2 RuP n m a18.5484; 15.0463; 16.1704
90; 90; 90		4512.9Sarbajna, Abir; Dutta, Indranil; Daw, Prosenjit; Dinda, Shrabani; Rahaman, S. M. Wahidur; Sarkar, Abheek; Bera, Jitendra K.
Catalytic Conversion of Alcohols to Carboxylic Acid Salts and Hydrogen with Alkaline Water
ACS Catalysis, 2017, 7, 2786
4514104 CIFC54 H47 Cl5 N4 O P2 RuP 1 21/c 114.2935; 18.4185; 22.7313
90; 108.44; 90		5677.1Sarbajna, Abir; Dutta, Indranil; Daw, Prosenjit; Dinda, Shrabani; Rahaman, S. M. Wahidur; Sarkar, Abheek; Bera, Jitendra K.
Catalytic Conversion of Alcohols to Carboxylic Acid Salts and Hydrogen with Alkaline Water
ACS Catalysis, 2017, 7, 2786
4514105 CIFC59 H49 Cl5 N4 O2 P2 Ru2P -111.8324; 14.2246; 18.611
86.239; 84.443; 71.637		2956.9Sarbajna, Abir; Dutta, Indranil; Daw, Prosenjit; Dinda, Shrabani; Rahaman, S. M. Wahidur; Sarkar, Abheek; Bera, Jitendra K.
Catalytic Conversion of Alcohols to Carboxylic Acid Salts and Hydrogen with Alkaline Water
ACS Catalysis, 2017, 7, 2786
4514106 CIFC29 H20 F3 N5 O6 Ru SP -18.4166; 11.03; 16.025
84.085; 76.9; 69.246		1354.52Kagalwala, Husain N.; Tong, Lianpeng; Zong, Ruifa; Kohler, Lars; Ahlquist, Mårten S. G.; Fan, Ting; Gagnon, Kevin J.; Thummel, Randolph P.
Evidence for Oxidative Decay of a Ru-Bound Ligand during Catalyzed Water Oxidation
ACS Catalysis, 2017, 7, 2607
4514107 CIFC13 H15 N O4P 21 21 218.8677; 10.0871; 14.1044
90; 90; 90		1261.63Tukhvatshin, Rinat S.; Kucherenko, Alexander S.; Nelyubina, Yulia V.; Zlotin, Sergei G.
Tertiary Amine-Derived Ionic Liquid-Supported Squaramide as a Recyclable Organocatalyst for Noncovalent “On Water” Catalysis
ACS Catalysis, 2017, 7, 2981
4514108 CIFC13 H8 Br Mn N2 O5P b a m17.7576; 12.9229; 12.7518
90; 90; 90		2926.3Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514109 CIFC15 H12 Br Mn N2 O5P 1 21/n 18.1795; 16.3907; 11.9305
90; 90.478; 90		1599.44Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514110 CIFC13 H10 Br Mn N4 O3P 1 21/n 17.5829; 9.6475; 20.0238
90; 93.812; 90		1461.62Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514111 CIFC16 H11 F3 Mn N3 O8 SP -18.9121; 12.7125; 17.6682
84.4838; 86.3815; 83.4002		1976.5Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514112 CIFC18 H15 F3 Mn N3 O8 SP 1 21/c 18.19264; 11.4621; 23.0399
90; 92.2861; 90		2161.84Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514115 CIFC44 H61 N O10 S SiP 1 21 19.04501; 9.77593; 25.19795
90; 92.5278; 90		2225.92Liao, Yuting; Zhou, Baixin; Xia, Yong; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Asymmetric [3 + 2] Cycloaddition of 2,2′-Diester Aziridines To Synthesize Pyrrolidine Derivatives
ACS Catalysis, 2017, 7, 3934
4514116 CIFC24 H24 Cl N O5P 1 21 19.975; 8.9417; 12.2426
90; 101.043; 90		1071.74Mondal, Santigopal; Mukherjee, Subrata; Das, Tamal Kanti; Gonnade, Rajesh; Biju, Akkattu T.
N-Heterocyclic Carbene-Catalyzed Aldol-Lactonization of Ketoacids via Dynamic Kinetic Resolution
ACS Catalysis, 2017, 3995
4514117 CIFC22 H24 N2 O2 SP 1 21 113.226; 6.2835; 13.615
90; 92.018; 90		1130.8Lin, Tao-Yan; Wu, Hai-Hong; Feng, Jian-Jun; Zhang, Junliang
Design and Enantioselective Synthesis of β-Vinyl Tryptamine Building Blocks for Construction of Privileged Chiral Indole Scaffolds
ACS Catalysis, 2017, 4047
4514118 CIFC20 H24 Cl N O2 SP 1 21/c 19.5931; 12.8055; 15.6673
90; 102.15; 90		1881.53Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514119 CIFC19 H22 N2 O4 SP b c n16.4786; 7.779; 28.3488
90; 90; 90		3633.9Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514120 CIFC25 H18P 1 21/c 113.316; 20.47; 6.2779
90; 101.369; 90		1677.6Yu, Liu-Zhu; Wei, Yin; Shi, Min
Synthesis of Polysubstituted Polycyclic Aromatic Hydrocarbons by Gold-Catalyzed Cyclization‒Oxidation of Alkylidenecyclopropane-Containing 1,5-Enynes
ACS Catalysis, 2017, 7, 4242
4514121 CIFC24 H17 Cl OP -19.3854; 9.6615; 11.064
87.814; 68.304; 85.999		929.8Yu, Liu-Zhu; Wei, Yin; Shi, Min
Synthesis of Polysubstituted Polycyclic Aromatic Hydrocarbons by Gold-Catalyzed Cyclization‒Oxidation of Alkylidenecyclopropane-Containing 1,5-Enynes
ACS Catalysis, 2017, 7, 4242
4514122 CIFC22 H16 SP -14.9712; 11.992; 27.578
79.676; 84.855; 78.156		1580.6Yu, Liu-Zhu; Wei, Yin; Shi, Min
Synthesis of Polysubstituted Polycyclic Aromatic Hydrocarbons by Gold-Catalyzed Cyclization‒Oxidation of Alkylidenecyclopropane-Containing 1,5-Enynes
ACS Catalysis, 2017, 7, 4242
4514123 CIFC25 H26 F2 N2 Pt SP -19.0052; 10.3193; 13.9951
90.135; 92.418; 94.402		1295.52Suslick, Benjamin A.; Liberman-Martin, Allegra L.; Wambach, Truman C.; Tilley, T. Don
Olefin Hydroarylation Catalyzed by (pyridyl-indolate)Pt(II) Complexes: Catalytic Efficiencies and Mechanistic Aspects
ACS Catalysis, 2017, 4313
4514124 CIFC25 H24 F4 N2 Pt SP -18.9213; 10.1362; 14.7554
97.236; 90.819; 94.146		1319.84Suslick, Benjamin A.; Liberman-Martin, Allegra L.; Wambach, Truman C.; Tilley, T. Don
Olefin Hydroarylation Catalyzed by (pyridyl-indolate)Pt(II) Complexes: Catalytic Efficiencies and Mechanistic Aspects
ACS Catalysis, 2017, 4313
4514136 CIFC19 H27 Cl N3 O P RuP b c a8.539; 15.0653; 32.9272
90; 90; 90		4235.84Li, Huaifeng; Wang, Yuan; Lai, Zhiping; Huang, Kuo-Wei
Selective Catalytic Hydrogenation of Arenols by a Well-Defined Complex of Ruthenium and Phosphorus‒Nitrogen PN3‒Pincer Ligand Containing a Phenanthroline Backbone
ACS Catalysis, 2017, 7, 4446
4514137 CIFC22 H31 Cl N3 O2 P RuP 1 21/c 18.4904; 16.3262; 17.4261
90; 97.79; 90		2393.24Li, Huaifeng; Wang, Yuan; Lai, Zhiping; Huang, Kuo-Wei
Selective Catalytic Hydrogenation of Arenols by a Well-Defined Complex of Ruthenium and Phosphorus‒Nitrogen PN3‒Pincer Ligand Containing a Phenanthroline Backbone
ACS Catalysis, 2017, 7, 4446
4514138 CIFC46 H40 Br2 N2 O2P -111.3349; 12.8075; 13.5019
76.483; 84.58; 83.915		1890.13Liu, Yi; Tse, Ying-Lung Steve; Kwong, Fuk Yee; Yeung, Ying-Yeung
Accessing Axially Chiral Biaryls via Organocatalytic Enantioselective Dynamic-Kinetic Resolution-Semipinacol Rearrangement
ACS Catalysis, 2017, 4435
4514139 CIFC28 H28 N2 O6 SP 1 21 114.93; 11.5659; 15.258
90; 101.808; 90		2579Claraz, Aurélie; Serpier, Fabien; Darses, Sylvain
Organoboron Initiated Rh-Catalyzed Asymmetric Cascade Reactions: A Subtle Switch in Regioselectivity Leading to Chiral 3-Benzazepine Derivatives
ACS Catalysis, 2017, 7, 3410
4514140 CIFC42 H30 F6 N2 O4P 21 21 218.8643; 17.5771; 22.5359
90; 90; 90		3511.3Yang, Wenjun; Sun, Wei; Zhang, Cheng; Wang, Qijun; Guo, Zhenyan; Mao, Biming; Liao, Jianning; Guo, Hongchao
Lewis-Base-Catalyzed Asymmetric [3 + 3] Annulation Reaction of Morita‒Baylis‒Hillman Carbonates: Enantioselective Synthesis of Spirocyclohexenes
ACS Catalysis, 2017, 7, 3142
4514141 CIFC18 H18P 1 21 19.035; 5.7594; 13.277
90; 100.891; 90		678.4Herlé, Bart; Holstein, Philipp M.; Echavarren, Antonio M.
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions.
ACS catalysis, 2017, 7, 3668-3675
4514142 CIFC21 H27 N O2 SP 1 21/n 111.6983; 13.0767; 13.6557
90; 114.637; 90		1898.82Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514143 CIFC19 H21 N O2 SP 1 21/c 110.2375; 9.4009; 16.6135
90; 98.412; 90		1581.71Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514151 CIFC13 H22 F3 Ir N2 O2 SI 41 c d16.7238; 16.7238; 23.136
90; 90; 90		6470.8Matsunami, Asuka; Kuwata, Shigeki; Kayaki, Yoshihito
A Bifunctional Iridium Catalyst Modified for Persistent Hydrogen Generation from Formic Acid: Understanding Deactivation via Cyclometalation of a 1,2-Diphenylethylenediamine Motif
ACS Catalysis, 2017, 4479
4514152 CIFC25 H28 F3 Ir N2 O2 SC 1 2 120.7776; 14.3517; 18.813
90; 111.073; 90		5234.75Matsunami, Asuka; Kuwata, Shigeki; Kayaki, Yoshihito
A Bifunctional Iridium Catalyst Modified for Persistent Hydrogen Generation from Formic Acid: Understanding Deactivation via Cyclometalation of a 1,2-Diphenylethylenediamine Motif
ACS Catalysis, 2017, 4479
4514153 CIFC14 H23 Cl3 F3 Ir N2 O2 SP 1 21/c 111.168; 11.884; 16.488
90; 104.162; 90		2121.8Matsunami, Asuka; Kuwata, Shigeki; Kayaki, Yoshihito
A Bifunctional Iridium Catalyst Modified for Persistent Hydrogen Generation from Formic Acid: Understanding Deactivation via Cyclometalation of a 1,2-Diphenylethylenediamine Motif
ACS Catalysis, 2017, 4479
4514154 CIFC16 H11 F5 N3 O7 VP -17.8153; 11.0933; 11.0932
78.955; 85.104; 77.783		921.55Gazi, Sarifuddin; Đokić, Miloš; Moeljadi, Adhitya Mangala Putra; Ganguly, Rakesh; Hirao, Hajime; Soo, Han Sen
Kinetics and DFT Studies of Photoredox Carbon‒Carbon Bond Cleavage Reactions by Molecular Vanadium Catalysts under Ambient Conditions
ACS Catalysis, 2017, 7, 4682
4514155 CIFC25 H22 Br2 F N OP 1 21 113.4096; 5.2499; 16.501
90; 106.995; 90		1110.93Arimitsu, Satoru; Yonamine, Tsunaki; Higashi, Masahiro
Cinchona-Based Primary Amine Catalyzed a Proximal Functionalization of Dienamines: Asymmetric α-Fluorination of α-Branched Enals
ACS Catalysis, 2017, 4736
4514158 CIFC14 H13 Cl3 O4P 1 21 17.1346; 14.8376; 15.0064
90; 98.492; 90		1571.17Cruchter, Thomas; Medvedev, Michael G.; Shen, Xiaodong; Mietke, Thomas; Harms, Klaus; Marsch, Michael; Meggers, Eric
Asymmetric Nucleophilic Catalysis with an Octahedral Chiral-at-Metal Iridium(III) Complex
ACS Catalysis, 2017, 7, 5151
4514159 CIFC22 H38 Si2P 1 21/n 18.809; 15.299; 16.461
90; 93.573; 90		2214.1Chen, Jiazhen; Gao, Yanshan; Xiong, Shuoyan; Delferro, Massimiliano; Lohr, Tracy L.; Marks, Tobin J.
Metal and Counteranion Nuclearity Effects in Organoscandium-Catalyzed Isoprene Polymerization and Copolymerization
ACS Catalysis, 2017, 7, 5214
4514160 CIFC48 H100 O2 Sc2 Si6P 1 21/c 114.3075; 24.95; 17.0373
90; 98.009; 90		6022.5Chen, Jiazhen; Gao, Yanshan; Xiong, Shuoyan; Delferro, Massimiliano; Lohr, Tracy L.; Marks, Tobin J.
Metal and Counteranion Nuclearity Effects in Organoscandium-Catalyzed Isoprene Polymerization and Copolymerization
ACS Catalysis, 2017, 7, 5214
4514161 CIFC20 H20 N2 O3R 321.2602; 21.2602; 10.1814
90; 90; 120		3985.41Reay, Alan J.; Hammarback, L. Anders; Bray, Joshua T. W.; Sheridan, Thomas; Turnbull, David; Whitwood, Adrian C.; Fairlamb, Ian J. S.
Mild and Regioselective Pd(OAc)2-Catalyzed C‒H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
ACS Catalysis, 2017, 5174
4514162 CIFC23 H26 N2 O3P 1 21 18.7152; 13.5902; 8.7625
90; 100.507; 90		1020.44Reay, Alan J.; Hammarback, L. Anders; Bray, Joshua T. W.; Sheridan, Thomas; Turnbull, David; Whitwood, Adrian C.; Fairlamb, Ian J. S.
Mild and Regioselective Pd(OAc)2-Catalyzed C‒H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
ACS Catalysis, 2017, 5174
4514163 CIFC20 H19 Cl N2 O3R 320.7806; 20.7806; 11.18107
90; 90; 120		4181.48Reay, Alan J.; Hammarback, L. Anders; Bray, Joshua T. W.; Sheridan, Thomas; Turnbull, David; Whitwood, Adrian C.; Fairlamb, Ian J. S.
Mild and Regioselective Pd(OAc)2-Catalyzed C‒H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
ACS Catalysis, 2017, 5174
4514164 CIFC55 H44 Cl2 N2 O4C 1 2 122.1203; 7.6123; 16.3803
90; 127.077; 90		2200.58He, Congfa; Hou, Mengqing; Zhu, Zixi; Gu, Zhenhua
Enantioselective Synthesis of Indole-Based Biaryl Atropisomers via Palladium-Catalyzed Dynamic Kinetic Intramolecular C‒H Cyclization
ACS Catalysis, 2017, 7, 5316
4514165 CIFC29 H31 B O2P 21 21 216.2288; 12.593; 30.216
90; 90; 90		2370.1Mateos, Jaime; Rivera-Chao, Eva; Fañanás-Mastral, Martín
Synergistic Copper/Palladium Catalysis for the Regio- and Stereoselective Synthesis of Borylated Skipped Dienes
ACS Catalysis, 2017, 5340
4514166 CIFC9 H14 O4P -4 21 c12.8527; 12.8527; 10.7921
90; 90; 90		1782.77Laserna, Victor; Martin, Eddy; Escudero-Adán, Eduardo C.; Kleij, Arjan W.
Substrate-Triggered Stereoselective Preparation of Highly Substituted Organic Carbonates
ACS Catalysis, 2017, 7, 5478
4514167 CIFC7 H10 O4P 1 21/n 16.5169; 11.8049; 9.5214
90; 105.261; 90		706.66Laserna, Victor; Martin, Eddy; Escudero-Adán, Eduardo C.; Kleij, Arjan W.
Substrate-Triggered Stereoselective Preparation of Highly Substituted Organic Carbonates
ACS Catalysis, 2017, 7, 5478
4514168 CIFC7 H10 O4P 1 21/n 18.3814; 7.0296; 12.3499
90; 96.2862; 90		723.26Laserna, Victor; Martin, Eddy; Escudero-Adán, Eduardo C.; Kleij, Arjan W.
Substrate-Triggered Stereoselective Preparation of Highly Substituted Organic Carbonates
ACS Catalysis, 2017, 7, 5478
4514169 CIFC42 H29 Cl F6 N2 O3P 21 21 218.9232; 17.371; 23.537
90; 90; 90		3648.4Yang, Wenjun; Sun, Wei; Zhang, Cheng; Wang, Qijun; Guo, Zhenyan; Mao, Biming; Liao, Jianning; Guo, Hongchao
Lewis-Base-Catalyzed Asymmetric [3 + 3] Annulation Reaction of Morita‒Baylis‒Hillman Carbonates: Enantioselective Synthesis of Spirocyclohexenes
ACS Catalysis, 2017, 7, 3142
4514170 CIFC34 H30 Cl Co N4 O4P b c a17.0978; 15.1411; 22.9374
90; 90; 90		5938Somekh, Miriam; Cohen, Hagai; Diskin-Posner, Yael; Shimon, Linda J. W.; Carmieli, Raanan; Rosenberg, Jeffrey N.; Neumann, Ronny
Formation of Alkanes by Aerobic Carbon‒Carbon Bond Coupling Reactions Catalyzed by a Phosphovanadomolybdic Acid
ACS Catalysis, 2017, 2725
4514172 CIFC22 H24 O4P 21 21 218.4622; 9.685; 22.9564
90; 90; 90		1881.4Chong, Qinglei; Yue, Zhenting; Zhang, Shuoqing; Ji, Chonglei; Cheng, Fengchang; Zhang, Haiyan; Hong, Xin; Meng, Fanke
N-heterocyclic Carbene‒Cu-Catalyzed Enantioselective Conjugate Additions with Alkenylboronic Esters as Nucleophiles
ACS Catalysis, 2017, 5693
4514173 CIFC55.5 H71 O10.5 Rh2P 1 21/n 116.2948; 17.0253; 20.361
90; 103.07; 90		5502.3Chen, Po-An; Setthakarn, Krit; May, Jeremy A.
A Binaphthyl-Based Scaffold for a Chiral Dirhodium(II) Biscarboxylate Ligand with α-Quaternary Carbon Centers
ACS Catalysis, 2017, 7, 6155
4514183 CIFC46 H96 O2 Sc2 Si6P 1 21/n 118.2889; 18.1841; 18.6875
90; 111.842; 90		5768.7Chen, Jiazhen; Gao, Yanshan; Xiong, Shuoyan; Delferro, Massimiliano; Lohr, Tracy L.; Marks, Tobin J.
Metal and Counteranion Nuclearity Effects in Organoscandium-Catalyzed Isoprene Polymerization and Copolymerization
ACS Catalysis, 2017, 7, 5214
4514184 CIFC19 H12 Au Cl0.25 F6 N O4P 1 2/n 129.449; 4.6494; 29.503
90; 103.649; 90		3925.5Holmsen, Marte Sofie Martinsen; Nova, Ainara; Balcells, David; Langseth, Eirin; Øien-Ødegaard, Sigurd; Heyn, Richard H.; Tilset, Mats; Laurenczy, Gábor
trans-Mutation at Gold(III): A Mechanistic Study of a Catalytic Acetylene Functionalization via a Double Insertion Pathway
ACS Catalysis, 2017, 7, 5023
4514185 CIFC25 H21 O PP -19.8901; 10.4204; 12.056
68.572; 85.149; 69.897		1084.9Toda, Yasunori; Sakamoto, Tomoyuki; Komiyama, Yutaka; Kikuchi, Ayaka; Suga, Hiroyuki
A Phosphonium Ylide as an Ionic Nucleophilic Catalyst for Primary Hydroxyl Group Selective Acylation of Diols
ACS Catalysis, 2017, 7, 6150
4514187 CIFC22 H23 N OP b c a15.4176; 11.3505; 20.247
90; 90; 90		3543.2Li, Yang; Hu, Ming; Li, Jin-Heng
Silver-Catalyzed Intermolecular [3 + 2]/[5 + 2] Annulation of N-Arylpropiolamides with Vinyl Acids: Facile Synthesis of Fused 2H-Benzo[b]azepin-2-ones
ACS Catalysis, 2017, 7, 6757
4514188 CIFC18 H20 N2 O2P -16.3768; 10.567; 11.5596
108.484; 92.159; 106.084		703.06Mampuys, Pieter; Neumann, Helfried; Sergeyev, Sergey; Orru, Romano V. A.; Jiao, Haijun; Spannenberg, Anke; Maes, Bert U. W.; Beller, Matthias
Combining Isocyanides with Carbon Dioxide in Palladium-Catalyzed Heterocycle Synthesis: N3-Substituted Quinazoline-2,4(1H,3H)-diones via a Three-Component Reaction
ACS Catalysis, 2017, 7, 5549
4514189 CIFC16 H22 N2 O2P -110.3381; 12.1298; 12.7543
98.7084; 97.6979; 101.969		1523.79Mampuys, Pieter; Neumann, Helfried; Sergeyev, Sergey; Orru, Romano V. A.; Jiao, Haijun; Spannenberg, Anke; Maes, Bert U. W.; Beller, Matthias
Combining Isocyanides with Carbon Dioxide in Palladium-Catalyzed Heterocycle Synthesis: N3-Substituted Quinazoline-2,4(1H,3H)-diones via a Three-Component Reaction
ACS Catalysis, 2017, 7, 5549
4514190 CIFC27 H52 Cl N O P4 WP 1 21/n 113.5317; 16.7932; 14.6934
90; 95.148; 90		3325.5Rudshteyn, Benjamin; Vibbert, Hunter B.; May, Richard; Wasserman, Eric; Warnke, Ingolf; Hopkins, Michael D.; Batista, Victor S.
Thermodynamic and Structural Factors That Influence the Redox Potentials of Tungsten‒Alkylidyne Complexes
ACS Catalysis, 2017, 7, 6134
4514193 CIFC37.21 H40.41 Cl2.41 Cu I N6P 21 21 2116.9652; 19.7318; 24.8974
90; 90; 90		8334.5Wan, Kai Y.; Sung, Molly M. H.; Lough, Alan J.; Morris, Robert H.
Half-Sandwich Ruthenium Catalyst Bearing an Enantiopure Primary Amine Tethered to an N-Heterocyclic Carbene for Ketone Hydrogenation
ACS Catalysis, 2017, 7, 6827
4514194 CIFC43 H43 Cl Ni P2P 1 21/n 112.3832; 17.1052; 17.3844
90; 106.111; 90		3537.7Mifleur, Alexis; Mérel, Delphine S.; Mortreux, André; Suisse, Isabelle; Capet, Frédéric; Trivelli, Xavier; Sauthier, Mathieu; Macgregor, Stuart A.
Deciphering the Mechanism of the Nickel-Catalyzed Hydroalkoxylation Reaction: A Combined Experimental and Computational Study
ACS Catalysis, 2017, 7, 6915
4514195 CIFC32 H35 Cl Ni P2P -110.3622; 11.0841; 13.1883
100.947; 102.623; 105.014		1377.98Mifleur, Alexis; Mérel, Delphine S.; Mortreux, André; Suisse, Isabelle; Capet, Frédéric; Trivelli, Xavier; Sauthier, Mathieu; Macgregor, Stuart A.
Deciphering the Mechanism of the Nickel-Catalyzed Hydroalkoxylation Reaction: A Combined Experimental and Computational Study
ACS Catalysis, 2017, 7, 6915
4514196 CIFC39 H52 Hf N2P -19.1605; 12.4145; 15.8667
91.003; 105.64; 97.611		1719.61Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514197 CIFC28 H36 Hf N2P 1 21/n 110.3324; 14.8323; 16.0844
90; 97.923; 90		2441.5Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514198 CIFC33 H40 Hf N2P -111.0762; 11.953; 12.8362
79.555; 66.82; 67.872		1446.09Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514199 CIFC32 H38 Hf N2P -19.6947; 12.8143; 22.3108
91.516; 95.983; 93.882		2748.7Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514200 CIFC32 H36 Hf N2P -19.3898; 10.7845; 13.8529
87.005; 78.576; 86.78		1371.63Domski, Gregory J.; Eagan, James M.; De Rosa, Claudio; Di Girolamo, Rocco; LaPointe, Anne M.; Lobkovsky, Emil B.; Talarico, Giovanni; Coates, Geoffrey W.
Combined Experimental and Theoretical Approach for Living and Isoselective Propylene Polymerization
ACS Catalysis, 2017, 7, 6930
4514201 CIFC30 H30 Br N3 O4P 21 21 218.2547; 11.7633; 28.9888
90; 90; 90		2814.89Jiang, Fei; Zhao, Dan; Yang, Xue; Yuan, Fu-Ru; Mei, Guang-Jian; Shi, Feng
Catalyst-Controlled Chemoselective and Enantioselective Reactions of Tryptophols with Isatin-Derived Imines
ACS Catalysis, 2017, 7, 6984
4514202 CIFC30 H30 Cl N3 O4P -19.6201; 10.3131; 14.6525
78.547; 72.894; 89.686		1359.6Jiang, Fei; Zhao, Dan; Yang, Xue; Yuan, Fu-Ru; Mei, Guang-Jian; Shi, Feng
Catalyst-Controlled Chemoselective and Enantioselective Reactions of Tryptophols with Isatin-Derived Imines
ACS Catalysis, 2017, 7, 6984
4514205 CIFC31 H32 Fe O3P 21 21 219.6682; 10.6608; 48.1982
90; 90; 90		4967.8Larionov, Evgeny; Mastandrea, Marco M.; Pericàs, Miquel A.
Asymmetric Visible-Light Photoredox Cross-Dehydrogenative Coupling of Aldehydes with Xanthenes
ACS Catalysis, 2017, 7, 7008
4514206 CIFC20.25 H24.25 Cl0.5 O2C 1 2/c 138.935; 8.5678; 28.446
90; 133.9; 90		6837Larionov, Evgeny; Mastandrea, Marco M.; Pericàs, Miquel A.
Asymmetric Visible-Light Photoredox Cross-Dehydrogenative Coupling of Aldehydes with Xanthenes
ACS Catalysis, 2017, 7, 7008
4514207 CIFC21 H26 F6 Ir N3 O8 S2P b c a15.8414; 14.5592; 24.0253
90; 90; 90		5541.15Fujita, Ken-ichi; Tamura, Ryuichi; Tanaka, Yuhi; Yoshida, Masato; Onoda, Mitsuki; Yamaguchi, Ryohei
Dehydrogenative Oxidation of Alcohols in Aqueous Media Catalyzed by a Water-Soluble Dicationic Iridium Complex Bearing a Functional N-Heterocyclic Carbene Ligand without Using Base
ACS Catalysis, 2017, 7, 7226
4514208 CIFC20 H25 F3 Ir N3 O5 SP -19.5878; 10.2028; 11.8401
83.082; 88.989; 83.868		1143.2Fujita, Ken-ichi; Tamura, Ryuichi; Tanaka, Yuhi; Yoshida, Masato; Onoda, Mitsuki; Yamaguchi, Ryohei
Dehydrogenative Oxidation of Alcohols in Aqueous Media Catalyzed by a Water-Soluble Dicationic Iridium Complex Bearing a Functional N-Heterocyclic Carbene Ligand without Using Base
ACS Catalysis, 2017, 7, 7226
4514209 CIFC35 H32 Cl2 N6P -111.9189; 11.9269; 13.6776
89.671; 67.67; 63.388		1575.9Zhou, Xukai; Luo, Yixin; Kong, Lingheng; Xu, Youwei; Zheng, Guangfan; Lan, Yu; Li, Xingwei
Cp*CoIII-Catalyzed Branch-Selective Hydroarylation of Alkynes via C‒H Activation: Efficient Access to α-gem-Vinylindoles
ACS Catalysis, 2017, 7, 7296
4514216 CIFC42 H43 O P SiP 21 21 2110.3642; 10.71104; 30.9626
90; 90; 90		3437.2Grosheva, Daria; Cramer, Nicolai
Ketene Aminal Phosphates: Competent Substrates for Enantioselective Pd(0)-Catalyzed C‒H Functionalizations
ACS Catalysis, 2017, 7, 7417
4514217 CIFC18 H13 Cl2 N OP 21 21 214.7873; 12.3631; 25.26
90; 90; 90		1495.04Grosheva, Daria; Cramer, Nicolai
Ketene Aminal Phosphates: Competent Substrates for Enantioselective Pd(0)-Catalyzed C‒H Functionalizations
ACS Catalysis, 2017, 7, 7417
4514218 CIFC20 H6 F8 S2P b c a7.1369; 13.1737; 35.7724
90; 90; 90		3363.3Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514219 CIFC18 H25 Cl F4 Mg O3P 1 21 18.8663; 12.7576; 9.7375
90; 112.848; 90		1015.01Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514220 CIFC48 H30 F8 Ni O P2P b c n39.6323; 11.1626; 19.9766
90; 90; 90		8837.6Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514221 CIFC17 H10 F4 O2 S2P 1 21/c 17.7206; 10.8574; 19.0756
90; 90.148; 90		1599.02Wang, Junya; Meng, Ge; Xie, Kun; Li, Liting; Sun, Huaming; Huang, Zhiyan
Mild and Efficient Ni-Catalyzed Biaryl Synthesis with Polyfluoroaryl Magnesium Species: Verification of the Arrest State, Uncovering the Hidden Competitive Second Transmetalation and Ligand-Accelerated Highly Selective Monoarylation
ACS Catalysis, 2017, 7, 7421
4514222 CIFC36 H32 N8 O4P 21 21 215.7087; 16.28; 17.073
90; 90; 90		1586.7Liao, Yun; Lu, Qianqian; Chen, Gui; Yu, Yinghua; Li, Chunsen; Huang, Xueliang
Rhodium-Catalyzed Azide‒Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions
ACS Catalysis, 2017, 7, 7529
4514223 CIFC17 H18 N4 O2 SP 1 21/c 111.611; 19.247; 8.0285
90; 107.27; 90		1713.3Liao, Yun; Lu, Qianqian; Chen, Gui; Yu, Yinghua; Li, Chunsen; Huang, Xueliang
Rhodium-Catalyzed Azide‒Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions
ACS Catalysis, 2017, 7, 7529
4514224 CIFC10 H16 O2P 1 21/n 15.9454; 23.5638; 6.5353
90; 104.593; 90		886.03Zhu, Rui; Jiang, Ju-Long; Li, Xing-Long; Deng, Jin; Fu, Yao
A Comprehensive Study on Metal Triflate-Promoted Hydrogenolysis of Lactones to Carboxylic Acids: From Synthetic and Mechanistic Perspectives
ACS Catalysis, 2017, 7, 7520
4514225 CIFC10 H16 O2P 1 21/n 16.0866; 21.259; 7.3676
90; 106.814; 90		912.6Zhu, Rui; Jiang, Ju-Long; Li, Xing-Long; Deng, Jin; Fu, Yao
A Comprehensive Study on Metal Triflate-Promoted Hydrogenolysis of Lactones to Carboxylic Acids: From Synthetic and Mechanistic Perspectives
ACS Catalysis, 2017, 7, 7520
4514226 CIFC49 H59 Cl3 Fe2 N2 PdC 1 2/c 127.734; 9.9782; 18.5024
90; 111.932; 90		4749.7Zhao, Minhui; Chen, Changle
Accessing Multiple Catalytically Active States in Redox-Controlled Olefin Polymerization
ACS Catalysis, 2017, 7, 7490
4514231 CIFC13 H11 Br O2 SP -16.6244; 9.5477; 11.0255
69.728; 77.396; 74.138		623.31Li, Yiming; Wang, Ming; Jiang, Xuefeng
Controllable Sulfoxidation and Sulfenylation with Organic Thiosulfate Salts via Dual Electron- and Energy-Transfer Photocatalysis
ACS Catalysis, 2017, 7, 7587
4514232 CIFC26 H26 O6 SP 21 21 216.2606; 7.9157; 45.636
90; 90; 90		2261.6Wu, Zijun; Wang, Jian
Enantioselective Medium-Ring Lactone Synthesis through an NHC-Catalyzed Intramolecular Desymmetrization of Prochiral 1,3-Diols
ACS Catalysis, 2017, 7, 7647
4514233 CIFC30 H32 Fe N P SI 1 2/c 115.7631; 9.2957; 35.3175
90; 95.742; 90		5149.07Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514234 CIFC28 H32 B Fe P SP 1 21/n 118.433; 8.274; 18.909
90; 117.569; 90		2556.4Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514235 CIFC36 H44 B Fe P SP 1 21/c 112.13; 11.24; 23.29
90; 96.035; 90		3158Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514236 CIFC42 H41 Fe O P SP b c a17.451; 19.304; 20.241
90; 90; 90		6819Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514237 CIFC28 H29 Cl Fe P SP c 21 n10.13; 14.433; 16.554
90; 90; 90		2420.3Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514238 CIFC29 H29 Fe O P SP c 21 n10.1455; 14.4475; 16.7227
90; 90; 90		2451.2Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514239 CIFC20 H25 B O3P 1 21 16.468; 24.149; 12.121
90; 101.11; 90		1857.8Song, Heng; Ye, Ke; Geng, Peiyu; Han, Xiao; Liao, Rongzhen; Tung, Chen-Ho; Wang, Wenguang
Activation of Epoxides by a Cooperative Iron‒Thiolate Catalyst: Intermediacy of Ferrous Alkoxides in Catalytic Hydroboration
ACS Catalysis, 2017, 7, 7709
4514246 CIFC24 H18 O2 SP 21 21 219.5092; 12.3167; 15.9826
90; 90; 90		1871.91Lu, Hong; Zhang, Jia-Lu; Liu, Jin-Yu; Li, Hong-Yu; Xu, Peng-Fei
N-Heterocyclic Carbene-Catalyzed Atom-Economical and Enantioselective Construction of the C‒S Bond: Asymmetric Synthesis of Functionalized Thiochromans
ACS Catalysis, 2017, 7, 7797
4514247 CIFC19 H19 N O3P 1 21/n 19.3432; 12.1755; 14.6611
90; 102.176; 90		1630.3Peng, Xie-Xue; Wei, Dian; Han, Wen-Jun; Chen, Fei; Yu, Wei; Han, Bing
Dioxygen Activation via Cu-Catalyzed Cascade Radical Reaction: An Approach to Isoxazoline/Cyclic Nitrone-Featured α-Ketols
ACS Catalysis, 2017, 7, 7830
4514248 CIFC11 H11 N O2P 1 21/m 16.417; 7.0536; 10.791
90; 93.618; 90		487.46Peng, Xie-Xue; Wei, Dian; Han, Wen-Jun; Chen, Fei; Yu, Wei; Han, Bing
Dioxygen Activation via Cu-Catalyzed Cascade Radical Reaction: An Approach to Isoxazoline/Cyclic Nitrone-Featured α-Ketols
ACS Catalysis, 2017, 7, 7830
4514249 CIFC18 H17 N O3P 3210.8566; 10.8566; 11.4924
90; 90; 120		1173.08Peng, Xie-Xue; Wei, Dian; Han, Wen-Jun; Chen, Fei; Yu, Wei; Han, Bing
Dioxygen Activation via Cu-Catalyzed Cascade Radical Reaction: An Approach to Isoxazoline/Cyclic Nitrone-Featured α-Ketols
ACS Catalysis, 2017, 7, 7830
4514250 CIFC20 H20 O4P 21 21 215.6577; 8.9036; 32.5408
90; 90; 90		1639.21Su, Yong-Liang; Han, Zhi-Yong; Li, Yu-Hui; Gong, Liu-Zhu
Asymmetric Allylation of Furfural Derivatives: Synergistic Effect of Chiral Ligand and Organocatalyst on Stereochemical Control
ACS Catalysis, 2017, 7, 7917
4514251 CIFC44 H37 Cl4 Ir O3 P2P -111.127; 11.586; 16.948
85.617; 75.929; 70.932		2003Cohen, Shirel; Borin, Veniamin; Schapiro, Igor; Musa, Sanaa; De-Botton, Sophie; Belkova, Natalia V.; Gelman, Dmitri
Ir(III)-PC(sp3)P Bifunctional Catalysts for Production of H2 by Dehydrogenation of Formic Acid: Experimental and Theoretical Study
ACS Catalysis, 2017, 7, 8139
4514252 CIFC44 H32 Cl Ir N O7 P2P 1 21/c 113.554; 25.997; 13.478
90; 108.116; 90		4513.7Cohen, Shirel; Borin, Veniamin; Schapiro, Igor; Musa, Sanaa; De-Botton, Sophie; Belkova, Natalia V.; Gelman, Dmitri
Ir(III)-PC(sp3)P Bifunctional Catalysts for Production of H2 by Dehydrogenation of Formic Acid: Experimental and Theoretical Study
ACS Catalysis, 2017, 7, 8139
4514253 CIFC24 H20 N4 O3 PdP -18.323; 11.108; 11.747
95.97; 98.14; 94.164		1065Deb, Arghya; Singh, Sukriti; Seth, Kapileswar; Pimparkar, Sandeep; Bhaskararao, Bangaru; Guin, Srimanta; Sunoj, Raghavan B.; Maiti, Debabrata
Experimental and Computational Studies on Remote γ-C(sp3)‒H Silylation and Germanylation of Aliphatic Carboxamides
ACS Catalysis, 2017, 7, 8171
4514278 CIFCu2 Gd4 H104 O120 W19 Zn3P -116.3885; 16.597; 21.2038
91.749; 101.863; 113.393		5139.8Zhao, Min; Zhang, Xian-Wei; Wu, Chuan-De
Structural Transformation of Porous Polyoxometalate Frameworks and Highly Efficient Biomimetic Aerobic Oxidation of Aliphatic Alcohols
ACS Catalysis, 2017, 7, 6573
4514279 CIFCu2 Gd4 H114 O105 W19 Zn3P -112.3498; 13.2731; 16.0314
68.011; 70.892; 69.811		2226.9Zhao, Min; Zhang, Xian-Wei; Wu, Chuan-De
Structural Transformation of Porous Polyoxometalate Frameworks and Highly Efficient Biomimetic Aerobic Oxidation of Aliphatic Alcohols
ACS Catalysis, 2017, 7, 6573
4514280 CIFC26 H28 N4 O7 Ru SP 1 21/n 111.051; 15.235; 16.459
90; 105.354; 90		2672.2Matheu, Roc; Ertem, Mehmed Z.; Gimbert-Suriñach, Carolina; Benet-Buchholz, Jordi; Sala, Xavier; Llobet, Antoni
Hydrogen Bonding Rescues Overpotential in Seven-Coordinated Ru Water Oxidation Catalysts
ACS Catalysis, 2017, 7, 6525
4514281 CIFC17 H25 Ir N2 O6 SP -19.919; 10.244; 10.412
65.248; 89.25; 80.89		947Kanega, Ryoichi; Onishi, Naoya; Szalda, David J.; Ertem, Mehmed Z.; Muckerman, James T.; Fujita, Etsuko; Himeda, Yuichiro
CO2 Hydrogenation Catalysts with Deprotonated Picolinamide Ligands
ACS Catalysis, 2017, 7, 6426
4514282 CIFC102 H149 Cl In2 N4 O5P 112.1349; 12.2766; 18.6225
85.388; 74.176; 65.392		2425Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514283 CIFC96.95 H139.51 Cl In2 N4 O5P 112.196; 12.295; 18.618
86.04; 73.489; 64.932		2420.3Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514284 CIFC86 H128 In2 N4 O6P 112.0666; 12.3213; 18.3525
74.092; 87.97; 65.236		2372.91Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514285 CIFC72 H104 In2 N4 O6P 1 21/c 117.557; 19.409; 12.845
90; 99.726; 90		4314Ebrahimi, Tannaz; Aluthge, Dinesh C.; Patrick, Brian O.; Hatzikiriakos, Savvas G.; Mehrkhodavandi, Parisa
Air- and Moisture-Stable Indium Salan Catalysts for Living Multiblock PLA Formation in Air
ACS Catalysis, 2017, 7, 6413
4514286 CIFC14 H11 Br N2 OP 21 21 215.1494; 10.5103; 23.635
90; 90; 90		1279.2Hatano, Manabu; Yamakawa, Katsuya; Ishihara, Kazuaki
Enantioselective Conjugate Hydrocyanation of α,β-Unsaturated N-Acylpyrroles Catalyzed by Chiral Lithium(I) Phosphoryl Phenoxide
ACS Catalysis, 2017, 7, 6686
4514289 CIFC23 H19 F3 N4 O2P 1 21/n 18.76727; 24.7029; 9.7159
90; 100.555; 90		2068.63Ye, Jian-Heng; Zhu, Lei; Yan, Si-Shun; Miao, Meng; Zhang, Xin-Chi; Zhou, Wen-Jun; Li, Jing; Lan, Yu; Yu, Da-Gang
Radical Trifluoromethylative Dearomatization of Indoles and Furans with CO2
ACS Catalysis, 2017, 7, 8324
4514290 CIFC20 H20 Cl2 N8 RuP -19.4232; 10.4405; 14.3166
98.121; 99.958; 116.027		1208.5Telleria, Ainara; Vicent, Cristian; San Nacianceno, Virginia; Garralda, María A.; Freixa, Zoraida
Experimental Evidence Supporting Related Mechanisms for Ru(II)-Catalyzed Dehydrocoupling and Hydrolysis of Amine-Boranes
ACS Catalysis, 2017, 7, 8394
4514291 CIFC24 H22 Cl2 N2 O3.95 RuP -16.9529; 11.5712; 16.87
92.79; 99.326; 96.309		1328.14Telleria, Ainara; Vicent, Cristian; San Nacianceno, Virginia; Garralda, María A.; Freixa, Zoraida
Experimental Evidence Supporting Related Mechanisms for Ru(II)-Catalyzed Dehydrocoupling and Hydrolysis of Amine-Boranes
ACS Catalysis, 2017, 7, 8394
4514292 CIFC23 H23 Br Cl11 N5 RuP -110.6051; 10.7857; 16.5095
93.576; 102.19; 107.715		1742Telleria, Ainara; Vicent, Cristian; San Nacianceno, Virginia; Garralda, María A.; Freixa, Zoraida
Experimental Evidence Supporting Related Mechanisms for Ru(II)-Catalyzed Dehydrocoupling and Hydrolysis of Amine-Boranes
ACS Catalysis, 2017, 7, 8394
4514293 CIFC46 H48 N4 ZnP -112.1191; 13.987; 14.338
66.838; 73.267; 64.731		1999.6Lortie, John L.; Dudding, Travis; Gabidullin, Bulat M.; Nikonov, Georgii I.
Zinc-Catalyzed Hydrosilylation and Hydroboration of N-Heterocycles
ACS Catalysis, 2017, 7, 8454
4514298 CIFC34.67 H38.67 Cl0.67 N1.33 Ni0.67 P0.67P 1 21/n 113.1807; 21.777; 15.5892
90; 97.999; 90		4431.1Nazari, S. Hadi; Bourdeau, Jefferson E.; Talley, Michael R.; Valdivia-Berroeta, Gabriel A.; Smith, Stacey J.; Michaelis, David J.
Nickel-Catalyzed Suzuki Cross Couplings with Unprotected Allylic Alcohols Enabled by Bidentate N-Heterocyclic Carbene (NHC)/Phosphine Ligands
ACS Catalysis, 2017, 8, 86
4514299 CIFC18 H18 O2 S2C 1 2/c 118.468; 5.7696; 29.486
90; 91.375; 90		3140.9Lanzi, Matteo; Cañeque, Tatiana; Marchiò, Luciano; Maggi, Raimondo; Bigi, Franca; Malacria, Max; Maestri, Giovanni
Alternative Routes to Tricyclic Cyclohexenes with Trinuclear Palladium Complexes
ACS Catalysis, 2017, 8, 144
4514300 CIFC29 H29 N O3 SC 1 2/c 119.9655; 9.2515; 27.268
90; 104.314; 90		4880.3Lanzi, Matteo; Cañeque, Tatiana; Marchiò, Luciano; Maggi, Raimondo; Bigi, Franca; Malacria, Max; Maestri, Giovanni
Alternative Routes to Tricyclic Cyclohexenes with Trinuclear Palladium Complexes
ACS Catalysis, 2017, 8, 144
4514301 CIFC121 H176 O12 P2 Sc2P 1 21/n 117.6216; 14.3906; 22.3619
90; 91.6518; 90		5668.3Xu, Pengfei; Xu, Xin
Homoleptic Rare-Earth Aryloxide Based Lewis Pairs for Polymerization of Conjugated Polar Alkenes
ACS Catalysis, 2017, 8, 198
4514302 CIFC60 H86 O5 P ScP 1 21/c 113.4046; 15.1609; 28.5176
90; 103.471; 90		5636.1Xu, Pengfei; Xu, Xin
Homoleptic Rare-Earth Aryloxide Based Lewis Pairs for Polymerization of Conjugated Polar Alkenes
ACS Catalysis, 2017, 8, 198
4514315 CIFC30 H28 N2 O2 SP 19.528; 10.803; 12.452
94.682; 100.658; 98.889		1236.4Hatano, Manabu; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki
Enantioselective Aza-Friedel‒Crafts Reaction of Indoles with Ketimines Catalyzed by Chiral Potassium Binaphthyldisulfonates
ACS Catalysis, 2017, 8, 349
4514316 CIFC60 H48 Ca O10 S2P 1 21 115.348; 11.244; 17.721
90; 102.716; 90		2983Hatano, Manabu; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki
Enantioselective Aza-Friedel‒Crafts Reaction of Indoles with Ketimines Catalyzed by Chiral Potassium Binaphthyldisulfonates
ACS Catalysis, 2017, 8, 349
4514318 CIFC92 H76 Cl4 O10 Rh2P 21 21 2115.5416; 22.2438; 23.488
90; 90; 90		8119.9Liao, Kuangbiao; Liu, Wenbin; Niemeyer, Zachary L.; Ren, Zhi; Bacsa, John; Musaev, Djamaladdin G.; Sigman, Mathew S.; Davies, Huw M. L.
Site-Selective Carbene-Induced C‒H Functionalization Catalyzed by Dirhodium Tetrakis(triarylcyclopropanecarboxylate) Complexes
ACS Catalysis, 2017, 8, 678
4514319 CIFC124 H114 O11 Rh2P 1 21 111.764; 17.436; 26.079
90; 91.389; 90		5348Liao, Kuangbiao; Liu, Wenbin; Niemeyer, Zachary L.; Ren, Zhi; Bacsa, John; Musaev, Djamaladdin G.; Sigman, Mathew S.; Davies, Huw M. L.
Site-Selective Carbene-Induced C‒H Functionalization Catalyzed by Dirhodium Tetrakis(triarylcyclopropanecarboxylate) Complexes
ACS Catalysis, 2017, 8, 678
4514320 CIFC18 H43.6 Ca I2 N6 O6.8P 1 21/c 112.5906; 22.4298; 11.671
90; 101.86; 90		3225.58Longwitz, Lars; Steinbauer, Johannes; Spannenberg, Anke; Werner, Thomas
Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions
ACS Catalysis, 2017, 8, 665
4514321 CIFC18 H39 Ca I2 N3 O7P 1 21/n 110.6093; 7.3183; 18.0196
90; 96.6981; 90		1389.53Longwitz, Lars; Steinbauer, Johannes; Spannenberg, Anke; Werner, Thomas
Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions
ACS Catalysis, 2017, 8, 665
4514324 CIFC18 H17 F O2P 1 21 15.7745; 15.6042; 16.0104
90; 94.458; 90		1438.28Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514325 CIFC40 H32 Cl2 F4 Ir2P 21 21 220.627; 10.6003; 14.9178
90; 90; 90		3261.8Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514326 CIFC17 H13 Br F2 O2P 1 21 118.1462; 7.5224; 22.412
90; 92.604; 90		3056.1Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514327 CIFC14 H18 F N O2 SP 1 21 16.1963; 13.8442; 8.5199
90; 101.713; 90		715.64Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514328 CIFC22 H27 F O2P 21 21 215.9526; 9.1966; 33.092
90; 90; 90		1811.6Mixdorf, Jason C.; Sorlin, Alexandre M.; Zhang, Qi; Nguyen, Hien M.
Asymmetric Synthesis of Allylic Fluorides via Fluorination of Racemic Allylic Trichloroacetimidates Catalyzed by a Chiral Diene-Iridium Complex
ACS Catalysis, 2017, 8, 790
4514336 CIFC34 H33 Br N4 O2P -18.4938; 10.8107; 16.6719
104.927; 95.326; 99.344		1445Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514337 CIFC21 H27 N3 OP -110.1934; 10.7135; 17.2661
89.316; 85.141; 82.592		1863.12Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514338 CIFC23 H21 N3 O3P 21 21 216.2748; 13.137; 24.081
90; 90; 90		1985Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514339 CIFC17 H21 N3 OP 1 21/n 110.0808; 9.7488; 15.9224
90; 108.079; 90		1487.53Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514340 CIFC17 H19 N3 O2P 1 21/n 110.0431; 9.7828; 15.4733
90; 99.887; 90		1497.7Korvorapun, Korkit; Kaplaneris, Nikolaos; Rogge, Torben; Warratz, Svenja; Stückl, A. Claudia; Ackermann, Lutz
Sequential meta-/ortho-C‒H Functionalizations by One-Pot Ruthenium(II/III) Catalysis
ACS Catalysis, 2018, 8, 886
4514341 CIFC25 H21 F N2 O7 SeP 1 21 19.722; 6.1683; 19.747
90; 102.561; 90		1155.8See, Jie Yang; Yang, Hui; Zhao, Yu; Wong, Ming Wah; Ke, Zhihai; Yeung, Ying-Yeung
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
ACS Catalysis, 2018, 8, 850
4514342 CIFC27 H39 O4.5 S0.5 SeP 112.1582; 19.1469; 23.6521
80.268; 80.837; 84.148		5341.6See, Jie Yang; Yang, Hui; Zhao, Yu; Wong, Ming Wah; Ke, Zhihai; Yeung, Ying-Yeung
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
ACS Catalysis, 2018, 8, 850
4514343 CIFC18 H18 F2 O4 SeP 1 21 16.7417; 22.7327; 16.9277
90; 101.477; 90		2542.4See, Jie Yang; Yang, Hui; Zhao, Yu; Wong, Ming Wah; Ke, Zhihai; Yeung, Ying-Yeung
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
ACS Catalysis, 2018, 8, 850
4514344 CIFC31 H50 B N2 P RuP -19.9745; 14.6282; 21.2096
103.406; 99.818; 90.008		2963.7Beguerie, Marion; Dinoi, Chiara; del Rosal, Iker; Faradji, Charly; Alcaraz, Gilles; Vendier, Laure; Sabo-Etienne, Sylviane
Mechanistic Studies on the Catalytic Synthesis of BN Heterocycles (1H-2,1-Benzazaboroles) at Ruthenium
ACS Catalysis, 2018, 8, 939
4514345 CIFC59 H96 Mn N O4 P2P 1 21/m 112.513; 17.266; 12.709
90; 107.182; 90		2623.2Kulkarni, Naveen V.; Brennessel, William W.; Jones, William D.
Catalytic Upgrading of Ethanol to n-Butanol via Manganese-Mediated Guerbet Reaction
ACS Catalysis, 2018, 8, 997
4514346 CIFC47.5 H72 Br Cl3 Mn N O2 P2P 1 21 116.074; 19.166; 16.17
90; 113.805; 90		4557.8Kulkarni, Naveen V.; Brennessel, William W.; Jones, William D.
Catalytic Upgrading of Ethanol to n-Butanol via Manganese-Mediated Guerbet Reaction
ACS Catalysis, 2018, 8, 997
4514350 CIFC46 H38 F12 Fe2 N10 O15 S4P -111.9405; 12.2853; 20.3054
103.183; 102.56; 98.477		2769.26Kottrup, Konstantin G.; D'Agostini, Silvia; van Langevelde, Phebe H.; Siegler, Maxime A.; Hetterscheid, Dennis G. H.
Catalytic Activity of an Iron-Based Water Oxidation Catalyst: Substrate Effects of Graphitic Electrodes.
ACS catalysis, 2018, 8, 1052-1061
4514351 CIFC20 H26 O6P 1 21 120.0688; 9.57471; 21.8114
90; 113.315; 90		3848.9Verrier, Charlie; Alandini, Nurtalya; Pezzetta, Cristofer; Moliterno, Mauro; Buzzetti, Luca; Hepburn, Hamish B.; Vega-Peñaloza, Alberto; Silvi, Mattia; Melchiorre, Paolo
Direct Stereoselective Installation of Alkyl Fragments at the β-Carbon of Enals via Excited Iminium Ion Catalysis
ACS Catalysis, 2018, 8, 1062
4514352 CIFC31 H27 Fe N3 O S4P -111.0218; 16.5594; 17.2264
76.1184; 89.3326; 82.0211		3021.9Das, Uttam K.; Higman, Carolyn S.; Gabidullin, Bulat; Hein, Jason E.; Baker, R. Tom
Efficient and Selective Iron-Complex-Catalyzed Hydroboration of Aldehydes
ACS Catalysis, 2018, 8, 1076
4514353 CIFC32 H32 Fe N2 O S4P -110.4477; 12.8949; 13.2739
64.316; 67.177; 79.099		1484.95Das, Uttam K.; Higman, Carolyn S.; Gabidullin, Bulat; Hein, Jason E.; Baker, R. Tom
Efficient and Selective Iron-Complex-Catalyzed Hydroboration of Aldehydes
ACS Catalysis, 2018, 8, 1076
4514354 CIFC33 H36 Fe N3 O3 P S4P n a 2128.2857; 7.9962; 15.1492
90; 90; 90		3426.42Das, Uttam K.; Higman, Carolyn S.; Gabidullin, Bulat; Hein, Jason E.; Baker, R. Tom
Efficient and Selective Iron-Complex-Catalyzed Hydroboration of Aldehydes
ACS Catalysis, 2018, 8, 1076
4514356 CIFC18 H37 Cl4 Cr Li N2 O2 PP 1 21/c 110.0101; 19.2905; 14.2617
90; 110.537; 90		2578.9Kwon, Doo-Hyun; Fuller, Jack T.; Kilgore, Uriah J.; Sydora, Orson L.; Bischof, Steven M.; Ess, Daniel H.
Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization
ACS Catalysis, 2018, 8, 1138
4514357 CIFC30 H27 Br N2 OP b c a9.92477; 18.1707; 27.0531
90; 90; 90		4878.76Arokianathar, Jude N.; Frost, Aileen B.; Slawin, Alexandra M. Z.; Stead, Darren; Smith, Andrew D.
Isothiourea-Catalyzed Enantioselective Addition of 4-Nitrophenyl Esters to Iminium Ions
ACS Catalysis, 2018, 8, 1153
4514358 CIFC30 H27.67 Br N2 O1.33P -114.476; 17.657; 18.147
81.051; 77.873; 82.012		4452.5Arokianathar, Jude N.; Frost, Aileen B.; Slawin, Alexandra M. Z.; Stead, Darren; Smith, Andrew D.
Isothiourea-Catalyzed Enantioselective Addition of 4-Nitrophenyl Esters to Iminium Ions
ACS Catalysis, 2018, 8, 1153
4514359 CIFC94 H68 Br4 Cl4 N4 Ni2P 1 21/n 111.4354; 18.923; 18.566
90; 97.981; 90		3978.6Pei, Lixia; Liu, Fengshou; Liao, Heng; Gao, Jie; Zhong, Liu; Gao, Haiyang; Wu, Qing
Synthesis of Polyethylenes with Controlled Branching with α-Diimine Nickel Catalysts and Revisiting Formation of Long-Chain Branching
ACS Catalysis, 2018, 8, 1104
4514360 CIFC52 H44 Br2 Cl8 N2 NiI b a 224.752; 10.97; 22.093
90; 90; 90		5999Pei, Lixia; Liu, Fengshou; Liao, Heng; Gao, Jie; Zhong, Liu; Gao, Haiyang; Wu, Qing
Synthesis of Polyethylenes with Controlled Branching with α-Diimine Nickel Catalysts and Revisiting Formation of Long-Chain Branching
ACS Catalysis, 2018, 8, 1104
4514361 CIFC38 H36 Br2 N2 NiP 1 21/c 113.579; 14.443; 18.148
90; 109.503; 90		3355Pei, Lixia; Liu, Fengshou; Liao, Heng; Gao, Jie; Zhong, Liu; Gao, Haiyang; Wu, Qing
Synthesis of Polyethylenes with Controlled Branching with α-Diimine Nickel Catalysts and Revisiting Formation of Long-Chain Branching
ACS Catalysis, 2018, 8, 1104
4514363 CIFC23 H47 Fe N2 O3 P2P 1 21/c 116.336; 12.2113; 27.367
90; 91.146; 90		5458.2Jayarathne, Upul; Hazari, Nilay; Bernskoetter, Wesley H.
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
ACS Catalysis, 2018, 8, 1338
4514364 CIFC19 H39 Fe N O2 P2P 1 21/c 119.086; 16.908; 15.109
90; 113.043; 90		4486.7Jayarathne, Upul; Hazari, Nilay; Bernskoetter, Wesley H.
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
ACS Catalysis, 2018, 8, 1338
4514365 CIFC21 H40 F6 Fe Li N O8 P2 S2P 1 21/n 18.6289; 29.4056; 13.2362
90; 108.974; 90		3176Jayarathne, Upul; Hazari, Nilay; Bernskoetter, Wesley H.
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
ACS Catalysis, 2018, 8, 1338
4514366 CIFC78 H94 Ag4 F9 N24 O22 S6P 21 335.2177; 35.2177; 35.2177
90; 90; 90		43680Chang, Zhiduo; Jing, Xu; He, Cheng; Liu, Xin; Duan, Chunying
Silver Clusters as Robust Nodes and π‒Activation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines
ACS Catalysis, 2018, 8, 1384
4514367 CIFC150 H164 Ag8 F9 N53 O25 S12P 21 335.191; 35.191; 35.191
90; 90; 90		43580.8Chang, Zhiduo; Jing, Xu; He, Cheng; Liu, Xin; Duan, Chunying
Silver Clusters as Robust Nodes and π‒Activation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines
ACS Catalysis, 2018, 8, 1384
4514368 CIFC120 H162 Ag8 F0 N60 O18 S13P a -335.835; 35.835; 35.835
90; 90; 90		46017Chang, Zhiduo; Jing, Xu; He, Cheng; Liu, Xin; Duan, Chunying
Silver Clusters as Robust Nodes and π‒Activation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines
ACS Catalysis, 2018, 8, 1384
4514369 CIFC16 H15 Cl O2P 21 21 216.78; 10.4553; 18.9129
90; 90; 90		1340.7Gollapelli, Krishna Kumar; Donikela, Sangeetha; Manjula, Nemali; Chegondi, Rambabu
Rhodium-Catalyzed Highly Regio- and Enantioselective Reductive Cyclization of Alkyne-Tethered Cyclohexadienones
ACS Catalysis, 2018, 8, 1440
4514377 CIFC45 H38 Ni O P2P -19.418; 10.2752; 18.5554
94.536; 92.905; 96.975		1773.5Zhang, Xin; Tutkowski, Brandon; Oliver, Allen; Helquist, Paul; Wiest, Olaf
Mechanistic Study of the Nickel-Catalyzed α,β-Coupling of Saturated Ketones
ACS Catalysis, 2018, 8, 1740
4514378 CIFC9 H7 N O2P 21 21 214.3637; 8.4176; 20.062
90; 90; 90		736.915Zhu, Gongming; Li, Yiping; Bao, Guangjun; Sun, Wangsheng; Huang, Liwu; Hong, Liang; Wang, Rui
Catalytic Kinetic Resolution of Spiro-Epoxyoxindoles with 1-Naphthols: Switchable Asymmetric Tandem Dearomatization/Oxa-Michael Reaction and Friedel–Crafts Alkylation of 1-Naphthols at the C4 Position
ACS Catalysis, 2018, 1810
4514379 CIFC26 H20 Br N O3P 21 21 219.4584; 13.011; 17.4
90; 90; 90		2141.3Zhu, Gongming; Li, Yiping; Bao, Guangjun; Sun, Wangsheng; Huang, Liwu; Hong, Liang; Wang, Rui
Catalytic Kinetic Resolution of Spiro-Epoxyoxindoles with 1-Naphthols: Switchable Asymmetric Tandem Dearomatization/Oxa-Michael Reaction and Friedel‒Crafts Alkylation of 1-Naphthols at the C4 Position
ACS Catalysis, 2018, 1810
4514380 CIFC21 H21 N O3P 1 21/c 113.6373; 15.8546; 8.1178
90; 104.499; 90		1699.28Kuppusamy, Ramajayam; Santhoshkumar, Rajagopal; Boobalan, Ramadoss; Wu, Hsin-Ru; Cheng, Chien-Hong
Synthesis of 1,2-Dihydroquinolines by Co(III)-Catalyzed [3 + 3] Annulation of Anilides with Benzylallenes
ACS Catalysis, 2018, 8, 1880
4514381 CIFC20 H20 Cl N O4P 21 21 219.027; 10.076; 20.28
90; 90; 90		1844.6Esteban, Francisco; Cieślik, Wioleta; Arpa, Enrique M.; Guerrero-Corella, Andrea; Díaz-Tendero, Sergio; Perles, Josefina; Fernández-Salas, José A; Fraile, Alberto; Alemán, José
Intramolecular Hydrogen Bond Activation: Thiourea-Organocatalyzed Enantioselective 1,3-Dipolar Cycloaddition of Salicylaldehyde-Derived Azomethine Ylides with Nitroalkenes.
ACS catalysis, 2018, 8, 1884-1890
4514382 CIFC20 H19 N O4P 1 21 18.8134; 9.1977; 10.6394
90; 94.6009; 90		859.68Esteban, Francisco; Cieślik, Wioleta; Arpa, Enrique M.; Guerrero-Corella, Andrea; Díaz-Tendero, Sergio; Perles, Josefina; Fernández-Salas, José A; Fraile, Alberto; Alemán, José
Intramolecular Hydrogen Bond Activation: Thiourea-Organocatalyzed Enantioselective 1,3-Dipolar Cycloaddition of Salicylaldehyde-Derived Azomethine Ylides with Nitroalkenes.
ACS catalysis, 2018, 8, 1884-1890
4514383 CIFC18 H17 Br N2 O5P 21 21 213.9676; 23.8405; 5.5166
90; 90; 90		1837Esteban, Francisco; Cieślik, Wioleta; Arpa, Enrique M.; Guerrero-Corella, Andrea; Díaz-Tendero, Sergio; Perles, Josefina; Fernández-Salas, José A; Fraile, Alberto; Alemán, José
Intramolecular Hydrogen Bond Activation: Thiourea-Organocatalyzed Enantioselective 1,3-Dipolar Cycloaddition of Salicylaldehyde-Derived Azomethine Ylides with Nitroalkenes.
ACS catalysis, 2018, 8, 1884-1890
4514384 CIFC24 H29 N2 O3 Rh SP 1 21/n 19.8164; 14.358; 17.0526
90; 90.736; 90		2403.26Ran, You; Yang, Yudong; You, Huansha; You, Jingsong
RhCl3-Catalyzed Oxidative C‒H/C‒H Cross-Coupling of (Hetero)aromatic Sulfonamides with (Hetero)arenes
ACS Catalysis, 2018, 8, 1796
4514387 CIFC26 H24 Br N OP 1 21 111.693; 6.314; 15.57
90; 103.875; 90		1116Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4514388 CIFC23 H22 F6 N3 P PdP 1 21/n 111.7229; 13.9765; 13.8227
90; 91.721; 90		2263.8Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4514394 CIFC24 H33 Ir N2 O6P 1 21/n 114.1793; 34.531; 16.0684
90; 113.726; 90		7202.5Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514395 CIFC28 H43 Ir N2 O7P 1 21/c 117.9996; 11.5553; 15.0325
90; 100.311; 90		3076.1Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514396 CIFC34 H39 Ir N2 O7P -110.4412; 11.3139; 13.9001
75.379; 83.373; 84.494		1574.4Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514397 CIFC28 H39 Ir N2 O7P 1 21/c 112.1132; 39.536; 11.7754
90; 94.196; 90		5624.2Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514398 CIFC87 H190 N3 O38 P Si3 Ti W9P b c a20.2301; 28.431; 43.025
90; 90; 90		24746Zhang, Teng; Mazaud, Louis; Chamoreau, Lise-Marie; Paris, Céline; Proust, Anna; Guillemot, Geoffroy
Unveiling the Active Surface Sites in Heterogeneous Titanium-Based Silicalite Epoxidation Catalysts: Input of Silanol-Functionalized Polyoxotungstates as Soluble Analogues
ACS Catalysis, 2018, 8, 2330
4514400 CIFC27 H18 O2P 1 21/c 117.4516; 7.5513; 15.134
90; 107.604; 90		1900.99Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V.
Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes
ACS Catalysis, 2018, 8, 2748
4514401 CIFC61 H51 Cl3 F6 N3 P3 RuP 1 21/c 110.0272; 23.326; 22.7595
90; 95.922; 90		5294.9Paul, Bhaskar; Shee, Sujan; Panja, Dibyajyoti; Chakrabarti, Kaushik; Kundu, Sabuj
Direct Synthesis of N,N-Dimethylated and β-Methyl N,N-Dimethylated Amines from Nitriles Using Methanol: Experimental and Computational Studies
ACS Catalysis, 2018, 8, 2890
4514406 CIFC52 H49 Cl2 I O2 P2 PdP 1 21 111.6182; 17.9333; 12.329
90; 115.788; 90		2312.95Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514407 CIFC37 H36 Cr N O5 PP 21 21 217.15; 19.5691; 24.0399
90; 90; 90		3363.6Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514408 CIFC62 H74.56 Ag O4.78 P2I 1 2 111.7485; 26.0007; 18.5841
90; 106.036; 90		5456Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514409 CIFC31 H31 N O3 SP 1 21/c 16.4182; 21.7785; 19.0994
90; 96.787; 90		2651Li, Man-Bo; Grape, Erik Svensson; Bäckvall, Jan-E.
Palladium-Catalyzed Stereospecific Oxidative Cascade Reaction of Allenes for the Construction of Pyrrole Rings: Control of Reactivity and Selectivity
ACS Catalysis, 2019, 9, 5184
4514412 CIFC20 H26 Cl RhP 1 21/c 17.4511; 12.8249; 18.6937
90; 94.11; 90		1781.8Burman, Jacob S.; Harris, Robert J.; B. Farr, Caitlin M.; Bacsa, John; Blakey, Simon B.
Rh(III) and Ir(III)Cp* Complexes Provide Complementary Regioselectivity Profiles in Intermolecular Allylic C‒H Amidation Reactions
ACS Catalysis, 2019, 9, 5474
4514413 CIFC20 H26 Cl IrP 1 21/c 17.46343; 12.81878; 18.68909
90; 93.9187; 90		1783.84Burman, Jacob S.; Harris, Robert J.; B. Farr, Caitlin M.; Bacsa, John; Blakey, Simon B.
Rh(III) and Ir(III)Cp* Complexes Provide Complementary Regioselectivity Profiles in Intermolecular Allylic C‒H Amidation Reactions
ACS Catalysis, 2019, 9, 5474
4514414 CIFC15 H27 Br2 Co N3P 1 21/c 110.8842; 11.4192; 15.8101
90; 104.557; 90		1901.94Pattanaik, Sandip; Gunanathan, Chidambaram
Cobalt-Catalyzed Selective Synthesis of Disiloxanes and Hydrodisiloxanes
ACS Catalysis, 2019, 9, 5552
4514415 CIFC17 H15 N3 O2P 1 21/c 111.1449; 12.2086; 11.4303
90; 107.468; 90		1483.5Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei
RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters
ACS Catalysis, 2019, 9, 5545
4514416 CIFC22 H25 N3 O4P -18.7858; 9.9521; 13.706
100.933; 94.003; 112.813		1070.9Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei
RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters
ACS Catalysis, 2019, 9, 5545
4514417 CIFC18 H15 N3 O2P b c a15.251; 10.6393; 19.017
90; 90; 90		3085.7Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei
RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters
ACS Catalysis, 2019, 9, 5545
4514418 CIFC15 H11 N3 O2C 1 2/c 119.26; 6.4425; 20.274
90; 100.533; 90		2473.3Zhao, Kang; Du, Rongrong; Wang, Bingyang; Liu, Jianhua; Xia, Chungu; Yang, Lei
RhCl3·3H2O-Catalyzed Regioselective C(sp2)‒H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters
ACS Catalysis, 2019, 9, 5545
4514419 CIFC12 H10 I N OP 1 21/c 116.093; 9.8036; 6.9586
90; 93.02; 90		1096.33Chen, Fumin; He, Dongxu; Chen, Li; Chang, Xiaoyong; Wang, David Zhigang; Xu, Chen; Xing, Xiangyou
Chirality-Economy Catalysis: Asymmetric Transfer Hydrogenation of Ketones by Ru-Catalysts of Minimal Stereogenicity
ACS Catalysis, 2019, 9, 5562
4514420 CIFC59 H60 Cl2 N2 P2 RuP 21 21 2110.9656; 11.9509; 38.4007
90; 90; 90		5032.4Chen, Fumin; He, Dongxu; Chen, Li; Chang, Xiaoyong; Wang, David Zhigang; Xu, Chen; Xing, Xiangyou
Chirality-Economy Catalysis: Asymmetric Transfer Hydrogenation of Ketones by Ru-Catalysts of Minimal Stereogenicity
ACS Catalysis, 2019, 9, 5562
4514434 CIFC14 H14 O3P 21 21 216.44696; 6.98494; 23.6748
90; 90; 90		1066.11Park, Sung Hwan; Wang, Shou-Guo; Cramer, Nicolai
Enantioselective Ruthenium(II)-Catalyzed Access to Benzonorcaradienes by Coupling of Oxabenzonorbornadienes and Alkynes
ACS Catalysis, 2019, 10226
4514435 CIFC24 H19 F O2 SP 21 21 215.101; 15.6195; 23.695
90; 90; 90		1887.9Moku, Balakrishna; Fang, Wan-Yin; Leng, Jing; Kantchev, Eric Assen B.; Qin, Hua-Li
Rh(I)‒Diene-Catalyzed Addition of (Hetero)aryl Functionality to 1,3-Dienylsulfonyl Fluorides Achieving Exclusive Regioselectivity and High Enantioselectivity: Generality and Mechanism
ACS Catalysis, 2019, 10477
4514436 CIFC16 H14 Br F O2 SP 1 21/n 19.7166; 31.009; 16.0484
90; 97.583; 90		4793.1Moku, Balakrishna; Fang, Wan-Yin; Leng, Jing; Kantchev, Eric Assen B.; Qin, Hua-Li
Rh(I)‒Diene-Catalyzed Addition of (Hetero)aryl Functionality to 1,3-Dienylsulfonyl Fluorides Achieving Exclusive Regioselectivity and High Enantioselectivity: Generality and Mechanism
ACS Catalysis, 2019, 10477
4514437 CIFC10 H19 B10 N OP b c a9.4145; 16.7722; 20.1088
90; 90; 90		3175.2Baek, Yonghyeon; Kim, Suhui; Son, Jeong-Yu; Lee, Kooyeon; Kim, Dongwook; Lee, Phil Ho
Rhodium-Catalyzed Amidation of the Cage B(4)‒H Bond in o-Carboranes with Dioxazolones by Carboxylic Acid-Assisted B(4)‒H Bond Activation
ACS Catalysis, 2019, 10418
4514438 CIFC17 H25 N OP 1 21/c 111.5032; 10.3652; 12.7281
90; 102.844; 90		1479.6Lorenc, Chris; Vibbert, Hunter B.; Yao, Chengbo; Norton, Jack R.; Rauch, Michael
H· Transfer-Initiated Synthesis of γ-Lactams: Interpretation of Cycloisomerization and Hydrogenation Ratios
ACS Catalysis, 2019, 10294
4514439 CIFC17 H25 N OP 1 21/c 111.3195; 10.3547; 12.7097
90; 101.868; 90		1457.9Lorenc, Chris; Vibbert, Hunter B.; Yao, Chengbo; Norton, Jack R.; Rauch, Michael
H· Transfer-Initiated Synthesis of γ-Lactams: Interpretation of Cycloisomerization and Hydrogenation Ratios
ACS Catalysis, 2019, 10294
4514611 CIFC29 H33 B O4 SiP 16.264; 9.621; 11.639
91.385; 96.47; 100.453		684.7Zhao, Zhi-Yuan; Nie, Yi-Xue; Tang, Ren-He; Yin, Guan-Wu; Cao, Jian; Xu, Zheng; Cui, Yu-Ming; Zheng, Zhan-Jiang; Xu, Li-Wen
Enantioselective Rhodium-Catalyzed Desymmetric Hydrosilylation of Cyclopropenes
ACS Catalysis, 2019, 9, 9110
4514612 CIFC72 H63 Ir N2 O6 P2P 21 21 2115.155; 17.531; 22.268
90; 90; 90		5916.2Kim, Seung Wook; Meyer, Cole C.; Mai, Binh Khanh; Liu, Peng; Krische, Michael J.
Inversion of Enantioselectivity in Allene Gas versus Allyl Acetate Reductive Aldehyde Allylation Guided by Metal-Centered Stereogenicity: An Experimental and Computational Study
ACS Catalysis, 2019, 9, 9158
4514613 CIFC23 H29 B O3P 21 21 2111.8365; 12.8133; 13.5157
90; 90; 90		2049.85Whyte, Andrew; Mirabi, Bijan; Torelli, Alexa; Prieto, Liher; Bajohr, Jonathan; Lautens, Mark
Asymmetric Synthesis of Boryl-Functionalized Cyclobutanols
ACS Catalysis, 2019, 9, 9253
4514614 CIFC14 H14 Br F2 N OP -19.6165; 11.7307; 12.572
93.33; 100.541; 92.151		1390.3Chen, Yuanjin; Li, Liangkui; He, Xiao; Li, Zhiping
Four-Component Reactions for the Synthesis of Perfluoroalkyl Isoxazoles
ACS Catalysis, 2019, 9, 9098
4514615 CIFC20 H17 N3 O PdP 6522.1057; 22.1057; 6.7305
90; 90; 120		2848.31Agasti, Soumitra; Mondal, Bhaskar; Achar, Tapas Kumar; Sinha, Soumya Kumar; Sarala Suseelan, Anjana; Szabo, Kalman J.; Schoenebeck, Franziska; Maiti, Debabrata
Orthogonal Selectivity in C‒H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution
ACS Catalysis, 2019, 9, 9606
4514616 CIFC23 N3 O PdP -19.6348; 10.7198; 11.5837
105.639; 103.125; 104.695		1056.88Agasti, Soumitra; Mondal, Bhaskar; Achar, Tapas Kumar; Sinha, Soumya Kumar; Sarala Suseelan, Anjana; Szabo, Kalman J.; Schoenebeck, Franziska; Maiti, Debabrata
Orthogonal Selectivity in C‒H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution
ACS Catalysis, 2019, 9, 9606
4514617 CIFC24 H25 N2 O2P -18.8691; 10.1304; 12.2386
105.617; 100.765; 93.916		1032.17Agasti, Soumitra; Mondal, Bhaskar; Achar, Tapas Kumar; Sinha, Soumya Kumar; Sarala Suseelan, Anjana; Szabo, Kalman J.; Schoenebeck, Franziska; Maiti, Debabrata
Orthogonal Selectivity in C‒H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution
ACS Catalysis, 2019, 9, 9606
4514618 CIFC20 H26 I N O2 SP 1 21/c 112.2416; 20.4922; 7.9382
90; 91.862; 90		1990.3Nugent, Jeremy; Arroniz, Carlos; Shire, Bethany R.; Sterling, Alistair J.; Pickford, Helena D.; Wong, Marie L. J.; Mansfield, Steven J.; Caputo, Dimitri F. J.; Owen, Benjamin; Mousseau, James J.; Duarte, Fernanda; Anderson, Edward A.
A General Route to Bicyclo[1.1.1]pentanes through Photoredox Catalysis
ACS Catalysis, 2019, 9, 9568
4514619 CIFC24 H35 I OP 21 21 216.30332; 11.85008; 28.71209
90; 90; 90		2144.65Nugent, Jeremy; Arroniz, Carlos; Shire, Bethany R.; Sterling, Alistair J.; Pickford, Helena D.; Wong, Marie L. J.; Mansfield, Steven J.; Caputo, Dimitri F. J.; Owen, Benjamin; Mousseau, James J.; Duarte, Fernanda; Anderson, Edward A.
A General Route to Bicyclo[1.1.1]pentanes through Photoredox Catalysis
ACS Catalysis, 2019, 9, 9568
4514620 CIFC21 H25 B O2P -110.2291; 13.3412; 13.527
87.464; 88.582; 80.599		1819.14Léonard, Nadia G.; Palmer, W. Neil; Friedfeld, Max R.; Bezdek, Máté J.; Chirik, Paul J.
Remote, Diastereoselective Cobalt-Catalyzed Alkene Isomerization‒Hydroboration: Access to Stereodefined 1,3-Difunctionalized Indanes
ACS Catalysis, 2019, 9, 9034
4514621 CIFC18 H16 N2 O3P 1 c 111.4615; 5.5002; 12.6887
90; 105.131; 90		772.17Yang, Hui; Wei, Guo; Jiang, Zhiyong
Access to Isoxazolidines through Visible-Light-Induced Difunctionalization of Alkenes
ACS Catalysis, 2019, 9, 9599
4514622 CIFC44 H57 F6 N5 O6I 1 2/a 117.95158; 10.14969; 23.05206
90; 98.418; 90		4154.9Zhang, Yunfei; Jermaks, Janis; MacMillan, Samantha N.; Lambert, Tristan H.
Synthesis of 2H-Chromenes via Hydrazine-Catalyzed Ring-Closing Carbonyl-Olefin Metathesis
ACS Catalysis, 2019, 9, 9259
4514623 CIFC28 H46 Cl2 F3 Ir O5 P2 SP n m a15.492; 24.393; 18.535
90; 90; 90		7004Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I.
Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System
ACS Catalysis, 2019, 9, 9317
4514624 CIFC44 H43 F3 O4 P4 Ru SP b c a23.1713; 14.6301; 24.6604
90; 90; 90		8359.8Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I.
Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System
ACS Catalysis, 2019, 9, 9317
4514625 CIFC46 H45 F6 N O6 P4 Ru S2P 1 21/c 117.445; 19.175; 28.449
90; 95.41; 90		9474Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I.
Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System
ACS Catalysis, 2019, 9, 9317
4514626 CIFC27 H46 Cl2 F3 Ir O4 P2 SP 1 21/n 116.5246; 12.6284; 17.54
90; 116.553; 90		3274.16Chu, Wan-Yi; Culakova, Zuzana; Wang, Bernie T.; Goldberg, Karen I.
Acid-Assisted Hydrogenation of CO2 to Methanol in a Homogeneous Catalytic Cascade System
ACS Catalysis, 2019, 9, 9317
4514627 CIFC15 H12 O2 SC 1 2/c 120.5001; 9.8972; 14.0168
90; 114.293; 90		2592.1Liu, Can; Fang, Yi; Wang, Shun-Yi; Ji, Shun-Jun
RhCl3·3H2O-Catalyzed Ligand-Enabled Highly Regioselective Thiolation of Acrylic Acids
ACS Catalysis, 2019, 9, 8910
4514628 CIFC9 H6 F6 O9 S2 UP -18.7768; 9.4553; 11.5011
75.998; 71.713; 79.448		873.34Monsigny, Louis; Thuéry, Pierre; Berthet, Jean-Claude; Cantat, Thibault
Breaking C‒O Bonds with Uranium: Uranyl Complexes as Selective Catalysts in the Hydrosilylation of Aldehydes
ACS Catalysis, 2019, 9, 9025
4514629 CIFC32 H24 F12 O20 S4 U2P -15.6883; 12.7612; 16.5764
102.634; 94.632; 96.374		1160.02Monsigny, Louis; Thuéry, Pierre; Berthet, Jean-Claude; Cantat, Thibault
Breaking C‒O Bonds with Uranium: Uranyl Complexes as Selective Catalysts in the Hydrosilylation of Aldehydes
ACS Catalysis, 2019, 9, 9025
4514630 CIFC29 H33 F6 N3 O11 S2 UP 1 21/c 19.2981; 22.059; 18.3163
90; 102.709; 90		3664.8Monsigny, Louis; Thuéry, Pierre; Berthet, Jean-Claude; Cantat, Thibault
Breaking C‒O Bonds with Uranium: Uranyl Complexes as Selective Catalysts in the Hydrosilylation of Aldehydes
ACS Catalysis, 2019, 9, 9025
4514631 CIFC25 H22 F N OP 21 21 216.9609; 9.0105; 32.0299
90; 90; 90		2008.95Ma, Teng; Chen, Yate; Li, Yuxiu; Ping, Yuanyuan; Kong, Wangqing
Nickel-Catalyzed Enantioselective Reductive Aryl Fluoroalkenylation of Alkenes
ACS Catalysis, 2019, 9, 9127
4514632 CIFC24 H43.5 O4.75P 1 21 112.5451; 25.5594; 15.6511
90; 110.747; 90		4693.02Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V.
Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass
ACS Catalysis, 2019, 9, 9485
4514633 CIFC15 H17 N3 O4 SP 1 21/n 113.3181; 6.9639; 17.0635
90; 90.091; 90		1582.6Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V.
Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass
ACS Catalysis, 2019, 9, 9485
4514634 CIFC21 H17 NC 1 2/c 118.1884; 10.5558; 25.3027
90; 108.216; 90		4614.5Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V.
Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass
ACS Catalysis, 2019, 9, 9485
4514635 CIFC22 H19 NP 1 21/c 18.8592; 22.189; 8.984
90; 114.717; 90		1604.25Nguyen, Vu T.; Nguyen, Viet D.; Haug, Graham C.; Dang, Hang T.; Jin, Shengfei; Li, Zhiliang; Flores-Hansen, Carsten; Benavides, Brenda S.; Arman, Hadi D.; Larionov, Oleg V.
Alkene Synthesis by Photocatalytic Chemoenzymatically Compatible Dehydrodecarboxylation of Carboxylic Acids and Biomass
ACS Catalysis, 2019, 9, 9485
4514636 CIFC51 H57 Cl Ni O2 P2P 1 21/n 113.151; 15.965; 21.319
90; 91.921; 90		4474McGuire, Ryan T.; Paffile, Julia F. J.; Zhou, Yuqiao; Stradiotto, Mark
Nickel-Catalyzed C‒N Cross-Coupling of Ammonia, (Hetero)anilines, and Indoles with Activated (Hetero)aryl Chlorides Enabled by Ligand Design
ACS Catalysis, 2019, 9, 9292
4514637 CIFC159 H188 Cl4 N12 Rh4P 1 21/n 122.2298; 14.0027; 23.0551
90; 102.788; 90		6998.5Azpíroz, Ramón; Di Giuseppe, Andrea; Urriolabeitia, Asier; Passarelli, Vincenzo; Polo, Victor; Pérez-Torrente, Jesús J.; Oro, Luis A.; Castarlenas, Ricardo
Hydride‒Rhodium(III)-N-Heterocyclic Carbene Catalyst for Tandem Alkylation/Alkenylation via C‒H Activation
ACS Catalysis, 2019, 9, 9372
4514638 CIFC34 H36 Fe N O3 P SP 1 21 111.5035; 10.7831; 13.3149
90; 110.777; 90		1544.22Han, Jie; Zhou, Wei; Zhang, Pei-Chao; Wang, Huamin; Zhang, Ronghua; Wu, Hai-Hong; Zhang, Junliang
Design and Synthesis of WJ-Phos, and Application in Cu-Catalyzed Enantioselective Boroacylation of 1,1-Disubstituted Allenes
ACS Catalysis, 2019, 9, 6890
4514639 CIFC24 H29 B O3P 21 21 218.8534; 12.6813; 18.9601
90; 90; 90		2128.7Han, Jie; Zhou, Wei; Zhang, Pei-Chao; Wang, Huamin; Zhang, Ronghua; Wu, Hai-Hong; Zhang, Junliang
Design and Synthesis of WJ-Phos, and Application in Cu-Catalyzed Enantioselective Boroacylation of 1,1-Disubstituted Allenes
ACS Catalysis, 2019, 9, 6890
4514640 CIFC38 H37 Cl3 Fe N O2 P SP 1 21 110.5036; 11.7796; 15.6619
90; 106.748; 90		1855.62Han, Jie; Zhou, Wei; Zhang, Pei-Chao; Wang, Huamin; Zhang, Ronghua; Wu, Hai-Hong; Zhang, Junliang
Design and Synthesis of WJ-Phos, and Application in Cu-Catalyzed Enantioselective Boroacylation of 1,1-Disubstituted Allenes
ACS Catalysis, 2019, 9, 6890
4514641 CIFC50 H60 N4 O4 Rh2P 1 21/c 119.9451; 11.5613; 20.0794
90; 94.241; 90		4617.5Zhu, Weihao; Luo, Zhongwen; Chen, Junqi; Liu, Chang; Yang, Lu; Dickie, Diane A.; Liu, Naiming; Zhang, Sen; Davis, Robert J.; Gunnoe, T. Brent
Mechanistic Studies of Single-Step Styrene Production Catalyzed by Rh Complexes with Diimine Ligands: An Evaluation of the Role of Ligands and Induction Period
ACS Catalysis, 2019, 9, 7457
4514642 CIFC40 H26 F20 N4 O5 Rh2P 1 21/c 123.889; 9.9822; 19.624
90; 110.013; 90		4397.1Zhu, Weihao; Luo, Zhongwen; Chen, Junqi; Liu, Chang; Yang, Lu; Dickie, Diane A.; Liu, Naiming; Zhang, Sen; Davis, Robert J.; Gunnoe, T. Brent
Mechanistic Studies of Single-Step Styrene Production Catalyzed by Rh Complexes with Diimine Ligands: An Evaluation of the Role of Ligands and Induction Period
ACS Catalysis, 2019, 9, 7457
4514643 CIFC103 H224 Ni4 O32 Si8P 1 21/c 124.2076; 27.078; 21.532
90; 106.288; 90		13547.6Moroz, Ilia B.; Lund, Alicia; Kaushik, Monu; Severy, Laurent; Gajan, David; Fedorov, Alexey; Lesage, Anne; Copéret, Christophe
Specific Localization of Aluminum Sites Favors Ethene-to-Propene Conversion on (Al)MCM-41-Supported Ni(II) Single Sites
ACS Catalysis, 2019, 9, 7476
4514644 CIFC48 H60 Co Li N2 OP m n 2117.4715; 10.5472; 10.9763
90; 90; 90		2022.66Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel
Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates
ACS Catalysis, 2019, 9, 7596
4514645 CIFC45 H53 Co N2P -112.3103; 12.6855; 13.5302
69.519; 77.844; 79.251		1920.22Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel
Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates
ACS Catalysis, 2019, 9, 7596
4514646 CIFC36 H40 Br2 Co N2P 1 21/c 127.0266; 12.0329; 22.8033
90; 113.047; 90		6823.9Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel
Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates
ACS Catalysis, 2019, 9, 7596
4514648 CIFC90 H121 Co2 Li N4 O4.5P b c a25.0102; 21.4146; 30.8908
90; 90; 90		16544.6Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel
Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates
ACS Catalysis, 2019, 9, 7596
4514649 CIFC92 H123 Co2 Li N4 O5P 1 21/n 121.4917; 13.0279; 29.987
90; 101.086; 90		8239.4Sandl, Sebastian; Maier, Thomas M.; van Leest, Nicolaas P.; Kröncke, Susanne; Chakraborty, Uttam; Demeshko, Serhiy; Koszinowski, Konrad; de Bruin, Bas; Meyer, Franc; Bodensteiner, Michael; Herrmann, Carmen; Wolf, Robert; Jacobi von Wangelin, Axel
Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates
ACS Catalysis, 2019, 9, 7596
4514650 CIFC48 H44 B Br N2 P4P -110.551; 12.062; 18.905
82.63; 81.72; 66.18		2171.5Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert
Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis
ACS Catalysis, 2019, 9, 7300
4514651 CIFC54.5 H51 B Br Cl5 Fe O2 P4P -111.496; 12.374; 20.858
97.02; 94.81; 111.71		2709Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert
Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis
ACS Catalysis, 2019, 9, 7300
4514652 CIFC18 H44 B Br Fe N2 O2 P4P 1 21/c 112.7253; 10.5434; 21.3482
90; 102.389; 90		2797.5Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert
Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis
ACS Catalysis, 2019, 9, 7300
4514653 CIFC19 H43 B Br Fe N2 O3 P4P n a 2114.623; 15.131; 12.874
90; 90; 90		2848.5Bäcker, Andreas; Li, Yinwu; Fritz, Maximilian; Grätz, Maik; Ke, Zhuofeng; Langer, Robert
Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis
ACS Catalysis, 2019, 9, 7300
4514654 CIFC18 H21 N O5 SP 1 21/n 19.7666; 7.7835; 22.574
90; 94.062; 90		1711.73Zhou, Kehan; Zhu, Yan; Fan, Weitai; Chen, Yujie; Xu, Xu; Zhang, Jingyu; Zhao, Yingsheng
Late-Stage Functionalization of Aromatic Acids with Aliphatic Aziridines: Direct Approach to Form β-Branched Arylethylamine Backbones
ACS Catalysis, 2019, 9, 6738
4514655 CIFC18 H23 N O6 SP 1 21 18.1162; 11.0214; 10.5496
90; 91.17; 90		943.48Zhou, Kehan; Zhu, Yan; Fan, Weitai; Chen, Yujie; Xu, Xu; Zhang, Jingyu; Zhao, Yingsheng
Late-Stage Functionalization of Aromatic Acids with Aliphatic Aziridines: Direct Approach to Form β-Branched Arylethylamine Backbones
ACS Catalysis, 2019, 9, 6738
4514656 CIFC27 H48 Cl N2 P RuP 4113.2477; 13.2477; 32.623
90; 90; 90		5725.4Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B.
Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes
ACS Catalysis, 2019, 9, 7217
4514657 CIFC24 H39 F9 N2 P2 RuP 1 21/c 122.5581; 12.7798; 22.1335
90; 113.18; 90		5865.7Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B.
Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes
ACS Catalysis, 2019, 9, 7217
4514658 CIFC40 H48 Cl4 F12 Ru4P -111.6853; 20.7278; 21.1082
114.576; 96.847; 99.355		4487.1Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B.
Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes
ACS Catalysis, 2019, 9, 7217
4514659 CIFC20 H34 Cl N2 P RuP 1 21/c 113.3641; 15.0206; 10.9602
90; 93.975; 90		2194.82Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B.
Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes
ACS Catalysis, 2019, 9, 7217
4514660 CIFC24 H42 F6 N2 P2 RuP n a 2122.7385; 13.1551; 9.5634
90; 90; 90		2860.67Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B.
Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes
ACS Catalysis, 2019, 9, 7217
4514661 CIFC20 H31 Cl F3 N2 P RuP 1 21/c 113.915; 14.954; 10.922
90; 95.212; 90		2263.3Paulson, Erik R.; Moore, Curtis E.; Rheingold, Arnold L.; Pullman, David P.; Sindewald, Ryan W.; Cooksy, Andrew L.; Grotjahn, Douglas B.
Dynamic π-Bonding of Imidazolyl Substituent in a Formally 16-Electron Cp*Ru(κ2-P,N)+ Catalyst Allows Dramatic Rate Increases in (E)-Selective Monoisomerization of Alkenes
ACS Catalysis, 2019, 9, 7217
4514662 CIFC24.5 H0.5 Cl1.5 N2 O2 S3P 15.7084; 14.6112; 15.7856
72.801; 87.877; 87.344		1256.02Liang, Yaoyu; Zhao, Xiaodan
Enantioselective Construction of Chiral Sulfides via Catalytic Electrophilic Azidothiolation and Oxythiolation of N-Allyl Sulfonamides
ACS Catalysis, 2019, 9, 6896
4514663 CIFC19 H32 Fe N5 O7 S2P 1 21/c 111.986; 9.3819; 21.7658
90; 90; 90		2447.6Warner, Genoa R.; Somasundar, Yogesh; Jansen, Kyle C.; Kaaret, Evan Z.; Weng, Cindy; Burton, Abigail E.; Mills, Matthew R.; Shen, Longzhu Q.; Ryabov, Alexander D.; Pros, Gabrielle; Pintauer, Tomislav; Biswas, Saborni; Hendrich, Michael P.; Taylor, Julia A.; Vom Saal, Frederick S.; Collins, Terrence J.
Bioinspired, Multidisciplinary, Iterative Catalyst Design Creates the Highest Performance Peroxidase Mimics and the Field of Sustainable Ultradilute Oxidation Catalysis (SUDOC)
ACS Catalysis, 2019, 9, 7023
4514664 CIFC20 H21 NP 1 21/c 110.3039; 11.9306; 12.985
90; 90.816; 90		1596.1Ping, Yuanyuan; Wang, Kuai; Pan, Qi; Ding, Zhengtian; Zhou, Zhijun; Guo, Ya; Kong, Wangqing
Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines
ACS Catalysis, 2019, 9, 7335
4514665 CIFC20 H21 NP 1 21/c 110.2763; 11.8965; 12.9403
90; 90.785; 90		1581.83Ping, Yuanyuan; Wang, Kuai; Pan, Qi; Ding, Zhengtian; Zhou, Zhijun; Guo, Ya; Kong, Wangqing
Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines
ACS Catalysis, 2019, 9, 7335
4514666 CIFC108 H92 Cl12 N8 O4C 1 c 116.9269; 16.7619; 8.8583
90; 91.738; 90		2512.18Ping, Yuanyuan; Wang, Kuai; Pan, Qi; Ding, Zhengtian; Zhou, Zhijun; Guo, Ya; Kong, Wangqing
Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines
ACS Catalysis, 2019, 9, 7335
4514667 CIFC18 H14 Br F3 N2 O3P 1 21 19.89; 9.938; 18.564
90; 101.954; 90		1785Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko
Enantioselective Friedel‒Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate
ACS Catalysis, 2019, 9, 6903
4514668 CIFC38 H27 Br3 N2 O3P 21 21 216.8271; 16.06; 29.396
90; 90; 90		3223.1Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko
Enantioselective Friedel‒Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate
ACS Catalysis, 2019, 9, 6903
4514669 CIFC25 H25 Br N2 O2 SP 419.7248; 9.7248; 48.32
90; 90; 90		4569.7Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko
Enantioselective Friedel‒Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate
ACS Catalysis, 2019, 9, 6903
4514670 CIFC22 H20 O2C 1 2/c 115.8408; 13.142; 16.3982
90; 98.987; 90		3371.9Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514671 CIFC25 H19 N O2P 1 21/c 115.6269; 10.8792; 22.0724
90; 100.839; 90		3685.5Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514672 CIFC18 H11 N OP 1 21/c 18.2853; 31.984; 19.542
90; 93.546; 90		5168.7Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514673 CIFC22 H14 N4P 1 21/c 19.9466; 17.8664; 9.4521
90; 100.253; 90		1652.91Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514674 CIFC19 H13 N OP -17.861; 9.282; 9.934
83.675; 72.702; 85.815		687.2Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514675 CIFC30 H22 O3P 1 21/c 124.6109; 12.239; 14.7299
90; 98.22; 90		4391.3Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514676 CIFC54 H55 B F4 N3 O5 P2 RhP -114.1394; 15.0162; 28.9031
77.688; 87.174; 78.469		5874.4Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H.
Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands
ACS Catalysis, 2019, 9, 7535
4514677 CIFC50 H49 B F4 N5 O5 P2 RhP -112.6207; 13.6039; 15.2008
72.598; 83.301; 76.784		2421.15Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H.
Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands
ACS Catalysis, 2019, 9, 7535
4514678 CIFC92 H86 B2 F8 N6 O10 P4 Rh2P 1 21/n 114.1446; 25.4077; 15.6384
90; 94.839; 90		5600.1Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H.
Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands
ACS Catalysis, 2019, 9, 7535
4514679 CIFC17 H21 B Br N O2P 1 21 111.3502; 7.45; 20.6376
90; 91.376; 90		1744.59Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J.
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
ACS Catalysis, 2019, 9, 6744
4514680 CIFC20 H16 Br N O2P 1 21 114.62776; 8.05742; 15.00218
90; 97.0979; 90		1754.64Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J.
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
ACS Catalysis, 2019, 9, 6744
4514681 CIFC11 H10 I0.96 N OP 1 21 19.8268; 5.6439; 9.8652
90; 99.353; 90		539.86Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J.
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
ACS Catalysis, 2019, 9, 6744
4514682 CIFC14 H24 N2 O4 PdP 1 21/c 19.3121; 10.7025; 8.4772
90; 97.201; 90		838.2Feng, Wenhui; Wang, Tianyang; Liu, Dongzhi; Wang, Xiaotai; Dang, Yanfeng
Mechanism of the Palladium-Catalyzed C(sp3)‒H Arylation of Aliphatic Amines: Unraveling the Crucial Role of Silver(I) Additives
ACS Catalysis, 2019, 9, 6672
4514683 CIFC42 H35 F12 N11 P2 Pd2P -112.0088; 12.3492; 17.137
101.431; 106.142; 105.372		2250.17Zhu, Jiancheng; Lindsay, Vincent N. G.
Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions
ACS Catalysis, 2019, 9, 6993
4514684 CIFC25 H20 Cl F6 N4 O P PdP -18.7896; 12.4079; 13.433
108.517; 105.407; 103.424		1256.4Zhu, Jiancheng; Lindsay, Vincent N. G.
Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions
ACS Catalysis, 2019, 9, 6993
4514685 CIFC45 H48 F12 N8 O3 P2 Pd2C 1 2/c 125.202; 8.3844; 24.157
90; 108.454; 90		4842Zhu, Jiancheng; Lindsay, Vincent N. G.
Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions
ACS Catalysis, 2019, 9, 6993
4514686 CIFC12 H11 Br F3 N3 O2P 1 21/c 110.3636; 10.0648; 28.9197
90; 99.7; 90		2973.4Chen, Zhen; Ren, Nan; Ma, Xiaoxiao; Nie, Jing; Zhang, Fa-Guang; Ma, Jun-An
Silver-Catalyzed [3 + 3] Dipolar Cycloaddition of Trifluorodiazoethane and Glycine Imines: Access to Highly Functionalized Trifluoromethyl-Substituted Triazines and Pyridines
ACS Catalysis, 2019, 9, 4600
4514687 CIFC15 H11 Cl F3 N O2P 1 21/n 117.29; 4.519; 20.77
90; 111.24; 90		1513Chen, Zhen; Ren, Nan; Ma, Xiaoxiao; Nie, Jing; Zhang, Fa-Guang; Ma, Jun-An
Silver-Catalyzed [3 + 3] Dipolar Cycloaddition of Trifluorodiazoethane and Glycine Imines: Access to Highly Functionalized Trifluoromethyl-Substituted Triazines and Pyridines
ACS Catalysis, 2019, 9, 4600
4514688 CIFC34 H26 N2P 1 21/n 111.5593; 7.8828; 27.35
90; 98.043; 90		2467.6Noto, Naoki; Koike, Takashi; Akita, Munetaka
Visible-Light-Triggered Monofluoromethylation of Alkenes by Strongly Reducing 1,4-Bis(diphenylamino)naphthalene Photoredox Catalysis
ACS Catalysis, 2019, 9, 4382
4514689 CIFC21 H20 F3 N O5 SP 19.0328; 9.506; 13.9771
90.165; 95.249; 115.51		1077.42He, Xiao-Long; Zhao, Hui-Ru; Song, Xue; Jiang, Bo; Du, Wei; Chen, Ying-Chun
Asymmetric Barton‒Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons
ACS Catalysis, 2019, 9, 4374
4514690 CIFC24 H25 N3 O4P 21 21 219.2464; 10.0773; 23.4808
90; 90; 90		2187.91He, Xiao-Long; Zhao, Hui-Ru; Song, Xue; Jiang, Bo; Du, Wei; Chen, Ying-Chun
Asymmetric Barton‒Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons
ACS Catalysis, 2019, 9, 4374
4514691 CIFC25 H17 N OP 1 21/n 18.618; 11.775; 18.166
90; 103.293; 90		1794Yuan, Hairui; Guo, Lirong; Liu, Fengting; Miao, Zechen; Feng, Lei; Gao, Hongyin
Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles
ACS Catalysis, 2019, 9, 3906
4514692 CIFC31 H21 N OP 21 21 218.1125; 12.1517; 23.1044
90; 90; 90		2277.65Yuan, Hairui; Guo, Lirong; Liu, Fengting; Miao, Zechen; Feng, Lei; Gao, Hongyin
Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles
ACS Catalysis, 2019, 9, 3906
4514693 CIFC24 H46 N6 Ni O6P 21 21 218.7123; 16.0813; 20.4271
90; 90; 90		2861.9Garrido-Barros, Pablo; Grau, Sergi; Drouet, Samuel; Benet-Buchholz, Jordi; Gimbert-Suriñach, Carolina; Llobet, Antoni
Can Ni Complexes Behave as Molecular Water Oxidation Catalysts?
ACS Catalysis, 2019, 9, 3936
4514694 CIFC21 H44 N6 Ni O9C 1 2/c 155.552; 6.2616; 15.8906
90; 100.323; 90		5438Garrido-Barros, Pablo; Grau, Sergi; Drouet, Samuel; Benet-Buchholz, Jordi; Gimbert-Suriñach, Carolina; Llobet, Antoni
Can Ni Complexes Behave as Molecular Water Oxidation Catalysts?
ACS Catalysis, 2019, 9, 3936
4514695 CIFC26 H29 N OP 1 21/c 16.2208; 18.757; 17.484
90; 93.268; 90		2036.8Han, Chunhua; Fu, Zhiyuan; Guo, Songjin; Fang, Xinxin; Lin, Aijun; Yao, Hequan
Palladium-Catalyzed Remote 1,n-Arylamination of Unactivated Terminal Alkenes
ACS Catalysis, 2019, 9, 4196
4514696 CIFC58 H84 F7 N2 O4 P Pd SP 1 21/c 120.138; 13.1828; 24.998
90; 106.912; 90		6349.4Dennis, Joseph M.; White, Nicholas A.; Liu, Richard Y.; Buchwald, Stephen L.
Pd-Catalyzed C‒N Coupling Reactions Facilitated by Organic Bases: Mechanistic Investigation Leads to Enhanced Reactivity in the Arylation of Weakly Binding Amines
ACS Catalysis, 2019, 9, 3822
4514697 CIFC43 H73.5 P2 Ru SP -113.159; 15.396; 21.596
90.092; 92.283; 101.727		4280.3Zhou, Xiaoguang; Malakar, Santanu; Zhou, Tian; Murugesan, Sathiyamoorthy; Huang, Carlos; Emge, Thomas J.; Krogh-Jespersen, Karsten; Goldman, Alan S.
Catalytic Alkane Transfer Dehydrogenation by PSP-Pincer-Ligated Ruthenium. Deactivation of an Extremely Reactive Fragment by Formation of Allyl Hydride Complexes
ACS Catalysis, 2019, 9, 4072
4514698 CIFC38 H62 P2 Ru SP 1 21/c 113.2907; 15.6689; 18.8836
90; 105.176; 90		3795.4Zhou, Xiaoguang; Malakar, Santanu; Zhou, Tian; Murugesan, Sathiyamoorthy; Huang, Carlos; Emge, Thomas J.; Krogh-Jespersen, Karsten; Goldman, Alan S.
Catalytic Alkane Transfer Dehydrogenation by PSP-Pincer-Ligated Ruthenium. Deactivation of an Extremely Reactive Fragment by Formation of Allyl Hydride Complexes
ACS Catalysis, 2019, 9, 4072
4514699 CIFC30 H41 Br1.02 Fe P3P -19.4966; 9.593; 17.63
101.894; 96.481; 102.236		1515.2Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514700 CIFC30 H41 Fe N4 P3P 1 21/c 117.626; 10.7764; 16.1774
90; 98.63; 90		3038Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514701 CIFC129 H106 B2 F48 Fe2 N8 P6P 1 21/n 122.4451; 12.1053; 25.482
90; 101.904; 90		6774.7Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514702 CIFC42 H65 Fe K N2 O6 P3P 1 21/n 110.4864; 23.9154; 17.8619
90; 93.645; 90		4470.5Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514703 CIFC40 H61 Fe K N2 O4 P3P n m a25.9569; 17.0296; 12.1851
90; 90; 90		5386.2Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514704 CIFC84 H130 Fe2 K4 N4 O6 P6P 1 21/n 114.6713; 16.6256; 18.7129
90; 102.506; 90		4456.1Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514705 CIFC33 H50 Fe K N2 P3 SiP 21 21 2110.5863; 16.3326; 20.8095
90; 90; 90		3598Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514706 CIFC28 H26 N4 O2 PdP 1 21/n 18.3908; 20.0893; 14.6398
90; 100.46; 90		2426.75Luo, Yun-Cheng; Yang, Chao; Qiu, Sheng-Qi; Liang, Qiu-Ju; Xu, Yun-He; Loh, Teck-Peng
Palladium(II)-Catalyzed Stereospecific Alkenyl C‒H Bond Alkylation of Allylamines with Alkyl Iodides
ACS Catalysis, 2019, 9, 4271
4514707 CIFC26 H28 Cl2 Co N4 OP 21 21 219.5625; 11.3203; 24.4937
90; 90; 90		2651.5Chen, Xu; Cheng, Zhaoyang; Lu, Zhan
Cobalt-Catalyzed Asymmetric Markovnikov Hydroboration of Styrenes
ACS Catalysis, 2019, 9, 4025
4514708 CIFC63 H73 Ni2 O3 P2P -110.2617; 16.0861; 17.7316
100.697; 90.004; 105.821		2763.17Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514709 CIFC32 H37 Ni O2 P SP -18.6245; 9.0612; 20.838
84.848; 88.901; 62.929		1443.8Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514710 CIFC34 H42 B Ni O3 PP 1 21/c 122.1829; 9.2102; 15.4936
90; 94.271; 90		3156.7Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514711 CIFC36 H44 B Ni O PP 1 21/n 18.8285; 20.3843; 17.3286
90; 95.23; 90		3105.5Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514712 CIFC28 H31 Ni PP -18.8889; 15.1597; 17.8889
91.217; 96.831; 90.693		2392.67Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514713 CIFC28 H30 Br Ni PP n a 2116.7529; 10.1199; 14.6061
90; 90; 90		2476.28Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514714 CIFC21 H31 B2 N O4P 1 21/c 115.588; 10.6978; 14.1186
90; 107.935; 90		2239.97Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514715 CIFC23 H21 Br N2 O3P 329.5332; 9.5332; 19.5349
90; 90; 120		1537.51Das, Tamal Kanti; Ghosh, Avik; Balanna, Kuruva; Behera, Pradipta; Gonnade, Rajesh G.; Marelli, Udaya Kiran; Das, Abhijit Kumar; Biju, Akkattu T.
N-Heterocyclic Carbene-Catalyzed Umpolung of Imines for the Enantioselective Synthesis of Dihydroquinoxalines
ACS Catalysis, 2019, 9, 4065
4514716 CIFC14 H11 N O2 S2P 1 21/n 18.3903; 17.9634; 9.3448
90; 112.656; 90		1299.75Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514717 CIFC18 H10 Br2 N2 O2 SI 1 2/a 117.7962; 4.9199; 19.1526
90; 105.417; 90		1616.57Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514718 CIFC12 H11 N O2 SP 1 21/c 114.2892; 10.414; 7.4904
90; 103.95; 90		1081.76Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514719 CIFC18 H10 Cl2 N2 SI 1 2/c 118.9763; 13.5616; 24.1428
90; 95.348; 90		6186.1Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514720 CIFC10 H8 Cl N O2 SP 1 21/c 114.4698; 5.8318; 11.9918
90; 103.449; 90		984.18Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514721 CIFC17 H15 Cl N2 O4 SP 1 21/n 110.7209; 11.7327; 13.2944
90; 97.17; 90		1659.16Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514722 CIFC16 H13 N O2 SP 1 21/c 18.3782; 8.266; 20.0756
90; 97; 90		1379.96Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514723 CIFC18 H10 Cl2 N2 O2 SP 1 21/c 112.9582; 9.0843; 14.2001
90; 108.155; 90		1588.37Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514724 CIFC14 H13 N O2 SP 21 21 218.9497; 9.3068; 15.389
90; 90; 90		1281.8Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514725 CIFC16 H12 Cl N O2 SP 1 21/c 18.2088; 24.9454; 6.8433
90; 94.558; 90		1396.88Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514726 CIFC18 H12 N2 O2 SP -17.6361; 13.7285; 14.864
69.516; 85.244; 83.871		1449.62Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514727 CIFC17 H14 F N O4 SP -17.5118; 8.3229; 12.1237
84.045; 88.396; 77.487		735.96Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514728 CIFC22 H24 N2 O6 SP -17.8092; 9.7669; 14.5366
104.686; 101.315; 100.756		1018.49Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514729 CIFC22 H22 Cl N O2 SC 1 2/c 115.7798; 11.6418; 22.199
90; 106.677; 90		3906.54Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514730 CIFC18 H20 I2 N4 PdP 1 21/c 18.3065; 16.337; 7.6187
90; 99.14; 90		1020.8Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514731 CIFC26 H36 Br4 Hg2 N4C 1 2/c 118.486; 9.2309; 20.682
90; 106.8; 90		3378.6Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514732 CIFC18 H20 Hg2 I4 N4P 1 21/n 110.648; 20.021; 12.134
90; 95.49; 90		2574.9Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514733 CIFC102.56 H52 F2 O34 Zr6P 6/m m m39.446; 39.446; 16.4166
90; 90; 120		22122Liu, Jian; Li, Zhanyong; Zhang, Xuan; Otake, Ken-ichi; Zhang, Lin; Peters, Aaron W.; Young, Matthias J.; Bedford, Nicholas M.; Letourneau, Steven P.; Mandia, David J.; Elam, Jeffrey W.; Farha, Omar K.; Hupp, Joseph T.
Introducing Nonstructural Ligands to Zirconia-like Metal‒Organic Framework Nodes To Tune the Activity of Node-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2019, 9, 3198
4514734 CIFC51 H53 Ni P2P 1 2/c 122.883; 9.2579; 21.1481
90; 115.533; 90		4042.6Charboneau, David J.; Brudvig, Gary W.; Hazari, Nilay; Lant, Hannah M. C.; Saydjari, Andrew K.
Development of an Improved System for the Carboxylation of Aryl Halides through Mechanistic Studies.
ACS catalysis, 2019, 9, 3228-3241
4514735 CIFC17 H14 Cl N O4P 21 21 217.7672; 8.6398; 22.845
90; 90; 90		1533.1Dai, Yuanwei; Tian, Baotong; Chen, Huan; Zhang, Qiang
Palladium-Catalyzed Stereospecific C-Glycosylation of Glycals with Vinylogous Acceptors
ACS Catalysis, 2019, 9, 2909
4514736 CIFC22 H37 N3 O4 SiP 1 21 19.1154; 9.7854; 14.6304
90; 96.443; 90		1296.76Zhan, Bei-Bei; Fan, Jun; Jin, Liang; Shi, Bing-Feng
Divergent Synthesis of Silicon-Containing Peptides via Pd-Catalyzed Post-Assembly γ-C(sp3)‒H Silylation
ACS Catalysis, 2019, 9, 3298
4514737 CIFC89 H64 Al B2 F36 N O6 P4 Rh2P -114.5138; 18.5644; 21.462
104.385; 102.683; 107.545		5062.15Adams, Gemma M.; Ryan, David E.; Beattie, Nicholas A.; McKay, Alasdair I.; Lloyd-Jones, Guy C; Weller, Andrew S.
Dehydropolymerization of H<sub>3</sub>B·NMeH<sub>2</sub> Using a [Rh(DPEphos)]<sup>+</sup> Catalyst: The Promoting Effect of NMeH<sub>2</sub>.
ACS catalysis, 2019, 9, 3657-3666
4514738 CIFC27 H36 Cl F Ni P2P 1 21/n 111.8371; 14.1571; 16.2044
90; 99.776; 90		2676.1Russell, John E. A.; Entz, Emily D.; Joyce, Ian M.; Neufeldt, Sharon R.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
ACS catalysis, 2019, 9, 3304-3310
4514739 CIFC29 H42 F N Ni O3 P2 SP 1 21/m 18.6752; 12.5702; 14.4059
90; 101.795; 90		1537.78Russell, John E. A.; Entz, Emily D.; Joyce, Ian M.; Neufeldt, Sharon R.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
ACS catalysis, 2019, 9, 3304-3310
4514740 CIFC32 H58 Co I N4 P2 ZrP n m a15.4307; 22.1735; 10.8845
90; 90; 90		3724.2Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514741 CIFC56 H92 Co2 I6 N4 P4 Zr2P -111.4073; 12.4796; 14.109
100.063; 97.493; 112.211		1787.87Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514742 CIFC45 H67 Co I N2 O P3 ZrP -19.9663; 10.4166; 23.1907
81.58; 83.529; 82.278		2349.34Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514743 CIFC35 H65 Co I N2 O P3 ZrC 1 2/c 138.6599; 12.0858; 18.3535
90; 103.833; 90		8326.7Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514744 CIFC45 H69 Co I N2 O P3 ZrP -112.2182; 13.374; 16.9003
70.756; 71.3; 74.862		2432.1Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514745 CIFC46 H64 Co I N2 O P2 ZrP -110.7474; 11.7734; 20.3607
77.69; 79.557; 69.802		2345.95Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514746 CIFC31 H38 B N3 O4P 1 21 16.5323; 24.418; 9.191
90; 104.387; 90		1420.04Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514747 CIFC17 H18 N2 O3 PdP 1 21/n 18.6104; 10.5955; 17.71
90; 99.051; 90		1595.59Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514748 CIFC30 H36 B N3 O3P 1 21 16.3743; 23.6017; 9.0486
90; 101.68; 90		1333.12Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514749 CIFC44 H40 N6 O10 Zn2P -18.7707; 11.7137; 13.5892
82.784; 81.615; 88.403		1370.2Markad, Datta; Mandal, Sanjay K.
Design of a Primary-Amide-Functionalized Highly Efficient and Recyclable Hydrogen-Bond-Donating Heterogeneous Catalyst for the Friedel‒Crafts Alkylation of Indoles with β-Nitrostyrenes
ACS Catalysis, 2019, 9, 3165
4514750 CIFC42 H33 Cl F2 Ni P2C 1 2/c 130.115; 11.645; 20.4586
90; 102.223; 90		7012Stadler, Sonja M.; Göttker-Schnetmann, Inigo; Mecking, Stefan
Incorporation of Radicals during Ni(II)-Catalyzed Ethylene Insertion Polymerization
ACS Catalysis, 2019, 9, 2760
4514751 CIFC51 H58 F2 N Ni O2 PP b c a16.868; 20.0011; 26.7439
90; 90; 90		9022.8Stadler, Sonja M.; Göttker-Schnetmann, Inigo; Mecking, Stefan
Incorporation of Radicals during Ni(II)-Catalyzed Ethylene Insertion Polymerization
ACS Catalysis, 2019, 9, 2760
4514752 CIFC10 H9 Br O3P 1 21 14.7773; 16.685; 6.289
90; 104.66; 90		485Sawano, Takahiro; Yamamoto, Hisashi
Enantioselective Epoxidation of β,γ-Unsaturated Carboxylic Acids by a Cooperative Binuclear Titanium Complex
ACS Catalysis, 2019, 9, 3384
4514753 CIFC22 H19 Br N2 O2P 21 21 217.3331; 9.8564; 25.7259
90; 90; 90		1859.42Yang, Qian-Qian; Yin, Xiang; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric Formal [5 + 3] Cycloadditions with Unmodified Morita‒Baylis‒Hillman Alcohols via Double Activation Catalysis
ACS Catalysis, 2019, 9, 1258
4514754 CIFC36 H32 Cl2 N4 O2P 1 21 111.3963; 10.25731; 13.268
90; 95.0958; 90		1544.84Yang, Qian-Qian; Yin, Xiang; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric Formal [5 + 3] Cycloadditions with Unmodified Morita‒Baylis‒Hillman Alcohols via Double Activation Catalysis
ACS Catalysis, 2019, 9, 1258
4514755 CIFC22 H19 N O3 SP 1 21 117.546; 6.607; 17.993
90; 115.207; 90		1887.2Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514756 CIFC25 H24 N O3 SP 21 21 219.162; 10.694; 22.484
90; 90; 90		2203Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514757 CIFC29 H21 N O3 SP 21 21 216.556; 13.237; 25.625
90; 90; 90		2223.8Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514758 CIFC23 H21 N O5 SP 21 21 218.9405; 10.0639; 23.127
90; 90; 90		2080.9Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514759 CIFC18 H16 Br2 O2P -324.679; 24.679; 9.5417
90; 90; 120		5032.8Trost, Barry M.; Tracy, Jacob S.
Vanadium-Catalyzed Synthesis of Geometrically Defined Acyclic Tri- and Tetrasubstituted Olefins from Propargyl Alcohols
ACS Catalysis, 2019, 9, 1584
4514760 CIFC12.5 H16 Cl2 Co N1.5 OP 18.5586; 8.9303; 9.6822
76.723; 86.703; 85.126		717.08Wen, Huanan; Wang, Kuan; Zhang, Yanlu; Liu, Guixia; Huang, Zheng
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
ACS Catalysis, 2019, 9, 1612
4514761 CIFC16 H18 Cl2 Co N2 OP 1 21 19.7507; 13.413; 12.9181
90; 90.316; 90		1689.48Wen, Huanan; Wang, Kuan; Zhang, Yanlu; Liu, Guixia; Huang, Zheng
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
ACS Catalysis, 2019, 9, 1612
4514762 CIFC29.48 H29.66 Cl1.27 N O3C 1 2 125.1281; 6.268; 15.987
90; 99.524; 90		2483.29Trost, Barry M.; Hung, Chao-I Joey; Gnanamani, Elumalai
Tuning the Reactivity of Ketones through Unsaturation: Construction of Cyclic and Acyclic Quaternary Stereocenters via Zn-ProPhenol Catalyzed Mannich Reactions
ACS Catalysis, 2019, 9, 1549
4514763 CIFC22 H19 O PP 1 21 115.7797; 6.4246; 18.8309
90; 114.711; 90		1734.23Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514764 CIFC27 H26 F2 N O2 PP 1 21 110.6041; 11.5598; 19.577
90; 94.744; 90		2391.6Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514765 CIFC24 H21 O3 PP 21 21 219.561; 9.713; 20.717
90; 90; 90		1923.9Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514766 CIFC20 H27 N O6P 1 21 16.03; 19.3547; 9.0029
90; 102.453; 90		1026Sim, Jaehoon; Campbell, Mark W.; Molander, Gary A.
Synthesis of α-Fluoro-α-Amino Acid Derivatives via Photoredox-Catalyzed Carbofluorination.
ACS catalysis, 2019, 9, 1558-1563
4514767 CIFC15 H16 O2P 21 21 215.6039; 10.7509; 19.196
90; 90; 90		1156.5Zheng, Pengfei; Wang, Chengpeng; Chen, Ying-Chun; Dong, Guangbin
Pd-Catalyzed Intramolecular α-Allylic Alkylation of Ketones with Alkynes: Rapid and Stereodivergent Construction of [3.2.1] Bicycles
ACS Catalysis, 2019, 9, 5515
4514768 CIFC35 H51 F6 N3 O5 S2 ZnP 21 21 2113.6599; 14.2563; 20.5882
90; 90; 90		4009.34Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514769 CIFC37 H47 F6 N3 O4 S2 ZnP 1 21/c 119.3499; 20.6938; 20.4521
90; 105.975; 90		7873.2Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514770 CIFC26.67 H32.67 Cl2 F4 N2 O2.67 S1.33 Zn0.67P -110.0474; 16.5268; 16.5479
117.002; 106.69; 94.539		2273.4Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514771 CIFC47 H56 N2 ZnP 1 21/c 119.3717; 16.9243; 27.5305
90; 101.738; 90		8837.2Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514772 CIFC35 H54 Cl2 N2 O1.5 ZnP 1 21/c 112.9149; 19.5194; 19.2829
90; 133.379; 90		3533.1Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514773 CIFC41 H52 N2 ZnP 1 21/c 120.3293; 9.7719; 18.4536
90; 106.688; 90		3511.5Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514774 CIFC43 H57 F6 N3 O6 S2 ZnP -111.9544; 13.4764; 15.7416
95.505; 100.925; 110.249		2299.96Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514775 CIFC19 H18 O2P 21 21 219.663; 9.7186; 31.0442
90; 90; 90		2915.39Yang, Junfeng; Sekiguchi, Yoshiya; Yoshikai, Naohiko
Cobalt-Catalyzed Enantioselective and Chemodivergent Addition of Cyclopropanols to Oxabicyclic Alkenes
ACS Catalysis, 2019, 9, 5638
4514776 CIFC27 H25 O3 P SP 21 21 213.6131; 35.785; 9.9738
90; 90; 90		4858.7Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514777 CIFC46 H72 Dy F9 N4 O17 S3P 1 21 112.1386; 16.1932; 15.8018
90; 97.546; 90		3079.1Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514778 CIFC51 H84 F9 N4 O18 Pr S3P 1 21 112.1823; 16.5445; 16.408
90; 101.368; 90		3242.2Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514779 CIFC53 H82 F9 N4 O15 S3 TmP 21 21 2115.6161; 19.6361; 21.6999
90; 90; 90		6654Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514780 CIFC44 H40 O P2P 21 21 219.9449; 17.1268; 19.9556
90; 90; 90		3398.92Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514781 CIFC17 H11 Cr F O5P 17.0791; 7.2172; 16.4881
85.775; 87.502; 64.437		757.81Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514782 CIFC43 H32 Cl2 N4 OP -111.209; 13.582; 13.728
60.753; 79.38; 76.89		1769.4Takamatsu, Kazutaka; Hayashi, Yoshihiro; Kawauchi, Susumu; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Regioselective C‒H Amination of Phenol Derivatives with Assistance of Phenanthroline-Based Bidentate Auxiliary
ACS Catalysis, 2019, 9, 5336
4514783 CIFC31 H31 N O2 SP -110.628; 11.4207; 12.9524
65.936; 85.626; 72.954		1370.77Li, Man-Bo; Grape, Erik Svensson; Bäckvall, Jan-E.
Palladium-Catalyzed Stereospecific Oxidative Cascade Reaction of Allenes for the Construction of Pyrrole Rings: Control of Reactivity and Selectivity
ACS Catalysis, 2019, 9, 5184
4514784 CIFC28 H27 N O2 SP 1 21/c 114.0088; 9.652; 19.0811
90; 109.714; 90		2428.79Li, Man-Bo; Grape, Erik Svensson; Bäckvall, Jan-E.
Palladium-Catalyzed Stereospecific Oxidative Cascade Reaction of Allenes for the Construction of Pyrrole Rings: Control of Reactivity and Selectivity
ACS Catalysis, 2019, 9, 5184
4514785 CIFC15 H17 N O4P n a 219.7201; 26.2838; 5.4483
90; 90; 90		1391.94Wu, Wenli; Cui, Enxin; Zhang, Yun; Zhang, Chen; Zhu, Feng; Tung, Chen-Ho; Wang, Yifeng
Involving Single-Atom Silver(0) in Selective Dehalogenation by AgF under Visible-Light Irradiation
ACS Catalysis, 2019, 9, 6335
4514786 CIFC16 H12 N2P n a 217.5559; 13.9087; 11.4271
90; 90; 90		1200.91Wu, Wenli; Cui, Enxin; Zhang, Yun; Zhang, Chen; Zhu, Feng; Tung, Chen-Ho; Wang, Yifeng
Involving Single-Atom Silver(0) in Selective Dehalogenation by AgF under Visible-Light Irradiation
ACS Catalysis, 2019, 9, 6335
4514787 CIFC8 H6 NP 1 21/n 17.8048; 5.9454; 13.2408
90; 92.593; 90		613.78Wu, Wenli; Cui, Enxin; Zhang, Yun; Zhang, Chen; Zhu, Feng; Tung, Chen-Ho; Wang, Yifeng
Involving Single-Atom Silver(0) in Selective Dehalogenation by AgF under Visible-Light Irradiation
ACS Catalysis, 2019, 9, 6335
4514788 CIFC11 H11 F3 O2P 41 21 27.262; 7.262; 41.516
90; 90; 90		2189.41Kerdphon, Sutthichat; Ponra, Sudipta; Yang, Jianping; Wu, Haibo; Eriksson, Lars; Andersson, Pher G.
Diastereo- and Enantioselective Synthesis of Structurally Diverse Succinate, Butyrolactone, and Trifluoromethyl Derivatives by Iridium-Catalyzed Hydrogenation of Tetrasubstituted Olefins
ACS Catalysis, 2019, 9, 6169
4514789 CIFC18 H15 N O2P 21 21 218.98144; 9.10592; 35.9259
90; 90; 90		2938.17Li, Yi-Pan; Li, Zi-Qi; Zhou, Biying; Li, Mao-Lin; Xue, Xiao-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Chiral Spiro Phosphoric Acid-Catalyzed Friedel‒Crafts Conjugate Addition/Enantioselective Protonation Reactions
ACS Catalysis, 2019, 9, 6522
4514790 CIFC19 H17 N OP 1 21 19.3678; 6.9408; 11.2829
90; 93.95; 90		731.872Li, Yi-Pan; Li, Zi-Qi; Zhou, Biying; Li, Mao-Lin; Xue, Xiao-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Chiral Spiro Phosphoric Acid-Catalyzed Friedel‒Crafts Conjugate Addition/Enantioselective Protonation Reactions
ACS Catalysis, 2019, 9, 6522
4514791 CIFC25 H22 I O PP n a 2114.0443; 8.9519; 34.5515
90; 90; 90		4343.92Zhang, Lumin; Si, Xiaojia; Yang, Yangyang; Witzel, Sina; Sekine, Kohei; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Reductive C‒C Coupling by Desulfurizing Gold-Catalyzed Photoreactions
ACS Catalysis, 2019, 9, 6118
4514792 CIFC40 H48 B2 Fe N12C 1 2/c 120.1074; 16.9145; 25.426
90; 108.024; 90		8223.2Isbill, Sara B.; Chandrachud, Preeti P.; Kern, Jesse L.; Jenkins, David M.; Roy, Sharani
Elucidation of the Reaction Mechanism of C<sub>2</sub> + N<sub>1</sub> Aziridination from Tetracarbene Iron Catalysts.
ACS catalysis, 2019, 9, 6223-6233
4514793 CIFC24 H31 Cl Ir N OP 1 21/n 18.81332; 15.7101; 17.1127
90; 102.781; 90		2310.68Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C‒H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514794 CIFC32 H36 Ir N O2P -111.5179; 13.5428; 18.483
76.588; 87.879; 89.094		2802.44Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C‒H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514795 CIFC19 H21 N O SP b c a10.7285; 17.9511; 18.0222
90; 90; 90		3470.87Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C‒H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514796 CIFC22 H21 N O2P 21 21 217.1896; 13.9891; 17.894
90; 90; 90		1799.71Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C‒H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514797 CIFC22 H23 N OP 4310.6545; 10.6545; 15.1128
90; 90; 90		1715.58Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514798 CIFC20 H19 N OP 21 21 215.6073; 16.7309; 16.9207
90; 90; 90		1587.42Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514799 CIFC24 H22 N2 OP b c a10.4266; 18.053; 19.734
90; 90; 90		3714.6Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514800 CIFC26 H24 N2 OP 1 21 18.7098; 8.9173; 13.0467
90; 93.444; 90		1011.48Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514801 CIFC18 H19 N O2P -19.859; 10.008; 15.838
93.054; 90.75; 99.872		1537Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514802 CIFC30 H36 B N3 O3P 1 21 16.5399; 23.9124; 9.103
90; 102.293; 90		1390.93Bai, Zibo; Zheng, Sujuan; Bai, Ziqian; Song, Fangfang; Wang, Hao; Peng, Qian; Chen, Gong; He, Gang
Palladium-Catalyzed Amide-Directed Enantioselective Carboboration of Unactivated Alkenes Using a Chiral Monodentate Oxazoline Ligand
ACS Catalysis, 2019, 9, 6502
4514803 CIFC30 H36 B N3 O3P 41 21 29.0322; 9.0322; 68.9818
90; 90; 90		5627.58Bai, Zibo; Zheng, Sujuan; Bai, Ziqian; Song, Fangfang; Wang, Hao; Peng, Qian; Chen, Gong; He, Gang
Palladium-Catalyzed Amide-Directed Enantioselective Carboboration of Unactivated Alkenes Using a Chiral Monodentate Oxazoline Ligand
ACS Catalysis, 2019, 9, 6502
4514804 CIFC34 H36 O S2P 1 21/c 112.8072; 13.6963; 17.6483
90; 110.451; 90		2900.59Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514805 CIFC19 H14 S2P -17.9503; 8.3038; 12.6012
78.352; 79.15; 72.944		771.51Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514806 CIFC19 H14 O S2C 1 2/c 116.653; 5.92231; 33.4022
90; 104.977; 90		3182.36Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514807 CIFC21 H24 Cl Rh SP 1 21 17.74658; 14.0941; 9.1196
90; 108.015; 90		946.87Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514808 CIFC18 H10 S2P 1 21/c 13.95493; 12.7072; 25.5848
90; 91.496; 90		1285.35Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514809 CIFC42 H78 N6 O Si6 ThP -111.208; 13.909; 19.199
69.17; 83.14; 71.15		2647.3Saha, Sayantani; Eisen, Moris S.
Catalytic Recycling of a Th‒H Bond via Single or Double Hydroboration of Inactivated Imines or Nitriles
ACS Catalysis, 2019, 9, 5947
4514810 CIFC10 H10 F2 O2P 1 21/c 19.946; 9.088; 10.222
90; 102.351; 90		902.6Nakayama, Yoshiki; Ando, Gaku; Abe, Manabu; Koike, Takashi; Akita, Munetaka
Keto-Difluoromethylation of Aromatic Alkenes by Photoredox Catalysis: Step-Economical Synthesis of α-CF2H-Substituted Ketones in Flow
ACS Catalysis, 2019, 9, 6555
4514811 CIFC15 H18 O2P n a 2125.8841; 7.333; 6.343
90; 90; 90		1203.95Luo, Youran; Gutiérrez-Bonet, Álvaro; Matsui, Jennifer K.; Rotella, Madeline E.; Dykstra, Ryan; Gutierrez, Osvaldo; Molander, Gary A.
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
ACS Catalysis, 2019, 9, 8835
4514812 CIFC21 H29 N O2P 1 21 15.5974; 16.9126; 19.3211
90; 90.056; 90		1829.1Luo, Youran; Gutiérrez-Bonet, Álvaro; Matsui, Jennifer K.; Rotella, Madeline E.; Dykstra, Ryan; Gutierrez, Osvaldo; Molander, Gary A.
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
ACS Catalysis, 2019, 9, 8835
4514813 CIFC93 H84 F3 O31 P4 S Yb2P 1 21 117.0655; 17.2352; 23.1949
90; 95.16; 90		6794.6Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir N.; Cundari, Thomas R.; Wang, Hong
Asymmetric Ring-Opening of Donor‒Acceptor Cyclopropanes with Primary Arylamines Catalyzed by a Chiral Heterobimetallic Catalyst
ACS Catalysis, 2019, 9, 8285
4514814 CIFC20 H23 N O5P 21 21 215.78428; 12.07053; 25.84988
90; 90; 90		1804.82Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir N.; Cundari, Thomas R.; Wang, Hong
Asymmetric Ring-Opening of Donor‒Acceptor Cyclopropanes with Primary Arylamines Catalyzed by a Chiral Heterobimetallic Catalyst
ACS Catalysis, 2019, 9, 8285
4514815 CIFC25 H9 B F15 N OP 1 21/c 115.7548; 8.5218; 17.5186
90; 91.195; 90		2351.52Meng, Shan-Shui; Tang, Xiaowen; Luo, Xiang; Wu, Ruibo; Zhao, Jun-Ling; Chan, Albert S. C.
Borane-Catalyzed Chemoselectivity-Controllable N-Alkylation and ortho C-Alkylation of Unprotected Arylamines Using Benzylic Alcohols
ACS Catalysis, 2019, 9, 8397
4514816 CIFC44 H55 Au N O2 PP -111.7663; 12.5195; 15.6679
101.971; 95.869; 117.925		1941.11Verlee, Arno; Heugebaert, Thomas; van der Meer, Tom; Kerchev, Pavel; Van Hecke, Kristof; Van Breusegem, Frank; Stevens, Christian V.
Gold and Palladium Mediated Bimetallic Catalysis: Mechanistic Investigation through the Isolation of the Organogold(I) Intermediates
ACS Catalysis, 2019, 9, 7862
4514817 CIFC30 H25 Au N O2 PP 1 21/c 112.35599; 11.5441; 17.5685
90; 98.0363; 90		2481.34Verlee, Arno; Heugebaert, Thomas; van der Meer, Tom; Kerchev, Pavel; Van Hecke, Kristof; Van Breusegem, Frank; Stevens, Christian V.
Gold and Palladium Mediated Bimetallic Catalysis: Mechanistic Investigation through the Isolation of the Organogold(I) Intermediates
ACS Catalysis, 2019, 9, 7862
4514818 CIFC19 H20 OP 1 21 18.803; 5.4591; 15.567
90; 104.94; 90		722.8Yu, Zhunzhun; Mendoza, Abraham
Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates
ACS Catalysis, 2019, 9, 7870
4514819 CIFC24 H16 Br N O4P 1 21 19.7213; 9.12937; 12.1367
90; 102.827; 90		1050.24Yu, Zhunzhun; Mendoza, Abraham
Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates
ACS Catalysis, 2019, 9, 7870
4514820 CIFC25 H15 N3 OC 1 2/c 139.582; 6.6842; 13.9095
90; 97.656; 90		3647.3Tian, Cong; Dhawa, Uttam; Scheremetjew, Alexej; Ackermann, Lutz
Cupraelectro-Catalyzed Alkyne Annulation: Evidence for Distinct C‒H Alkynylation and Decarboxylative C‒H/C‒C Manifolds
ACS Catalysis, 2019, 9, 7690
4514821 CIFC14 H17 N O2P 1 21/c 110.9605; 9.5967; 11.9487
90; 93.832; 90		1254Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514822 CIFC16 H21 N O2P n a 2123.054; 8.4318; 7.3235
90; 90; 90		1423.6Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514823 CIFC15 H18 O3P 1 21/c 112.827; 20.383; 5.0473
90; 96.027; 90		1312.3Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514824 CIFC16 H20 O3C 1 2/c 131.2814; 6.1424; 15.8248
90; 111.709; 90		2825Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514825 CIFC19 H28 Cl Cu N3 O4P n a 2123.1742; 9.9101; 9.2756
90; 90; 90		2130.22Hunt, Andrew P.; Batka, Allison E.; Hosseinzadeh, Marjan; Gregory, Jordan D.; Haque, Halima K.; Ren, Hang; Meyerhoff, Mark E.; Lehnert, Nicolai
Nitric Oxide Generation On Demand for Biomedical Applications via Electrocatalytic Nitrite Reduction by Copper BMPA- and BEPA-Carboxylate Complexes.
ACS catalysis, 2019, 9, 7746-7758
4514826 CIFC50 H52 Ir N4P 1 21/c 120.5401; 12.5368; 16.2915
90; 100.551; 90		4124.2Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514827 CIFC43 H42 Ir N6P -110.1805; 13.1835; 14.4356
85.2561; 69.5849; 77.2239		1770.8Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514828 CIFC41 H36 Ir N6P 1 21/n 114.476; 14.367; 34.464
90; 101.797; 90		7016.3Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514829 CIFC39 H45 Ir N4P 1 21/c 111.3918; 14.4386; 20.4434
90; 99.64; 90		3315.1Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514830 CIFC49 H55 Ir N6P 1 21/c 117.6455; 12.6291; 20.6034
90; 111.016; 90		4286Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514831 CIFC11 H23 N3 O3 SP 21 21 218.3707; 11.4502; 14.6387
90; 90; 90		1403.06Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514832 CIFC12 H18 N2 O2 SP b c a17.0285; 6.9101; 21.3006
90; 90; 90		2506.41Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514833 CIFC29 H47 N3 O6 SP 17.0841; 14.1779; 15.2277
98.32; 100.672; 103.356		1433.94Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514834 CIFC17 H20 N2 O2 SP 1 21/n 110.2981; 7.0578; 21.651
90; 94.024; 90		1569.8Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514835 CIFC20 H30 Cl N3 O3 SP b c a15.2153; 14.9228; 18.7632
90; 90; 90		4260.3Lam, Ying-Pong; Wang, Xinyan; Tan, Fei; Ng, Wing-Hin; Tse, Ying-Lung Steve; Yeung, Ying-Yeung
Amide/Iminium Zwitterionic Catalysts for (Trans)esterification: Application in Biodiesel Synthesis
ACS Catalysis, 2019, 9, 8083
4514836 CIFC32 H29 N O4 SP 1 21/c 113.6328; 9.7259; 19.2323
90; 94.976; 90		2540.42Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu
Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis
ACS Catalysis, 2019, 9, 8256
4514837 CIFC27 H27 N O4 SP 1 21/c 137.0525; 12.0473; 10.4128
90; 90.415; 90		4647.97Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu
Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis
ACS Catalysis, 2019, 9, 8256
4514838 CIFC25 H23 N O2P 1 21/c 118.0757; 14.6438; 7.2015
90; 101.012; 90		1871.12Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu
Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis
ACS Catalysis, 2019, 9, 8256
4514839 CIFC21 H26 B N O4 SP 21 21 2110.4319; 14.2343; 29.1953
90; 90; 90		4335.2Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan
Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters
ACS Catalysis, 2019, 9, 8503
4514840 CIFC21 H26 B N O5 SP 319.9417; 9.9417; 18.9939
90; 90; 120		1625.8Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan
Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters
ACS Catalysis, 2019, 9, 8503
4514841 CIFC23 H36 B F3 N2 O6 SP 21 21 219.2674; 10.7476; 28.5667
90; 90; 90		2845.3Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan
Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters
ACS Catalysis, 2019, 9, 8503
4514842 CIFC31 H65 K N3 Si6 YP -19.999; 11.964; 19.292
83.01; 85.8; 82.27		2266.1Zhai, Dan-Dan; Du, Hui-Zhen; Zhang, Xiang-Yu; Liu, Yu-Feng; Guan, Bing-Tao
Potassium Yttrium Ate Complexes: Synergistic Effect Enabled Reversible H2 Activation and Catalytic Hydrogenation
ACS Catalysis, 2019, 9, 8766
4514843 CIFC29 H69 K N3 O Si6 YP 1 21/c 111.344; 11.734; 31.997
90; 92.915; 90		4253.6Zhai, Dan-Dan; Du, Hui-Zhen; Zhang, Xiang-Yu; Liu, Yu-Feng; Guan, Bing-Tao
Potassium Yttrium Ate Complexes: Synergistic Effect Enabled Reversible H2 Activation and Catalytic Hydrogenation
ACS Catalysis, 2019, 9, 8766
4514844 CIFC38 H30 F6 N2 O4 Pd S4C 1 2/c 115.336; 10.1947; 24.0955
90; 98.408; 90		3726.7Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514845 CIFC34 H26 Cl2 F6 N2 O4 Pd S4P -19.0381; 10.3207; 10.3832
68.768; 89.673; 88.327		902.4Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514846 CIFC17 H15 N O2 S2C 1 2/c 132.753; 4.888; 23.981
90; 124.967; 90		3146.2Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514847 CIFC22 H23 N O2 S2P -18.6349; 9.3163; 13.5605
70.251; 85.755; 83.165		1018.75Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514848 CIFC22 H24 O6P 1 21/c 119.271; 4.5166; 23.345
90; 107.803; 90		1934.6Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514849 CIFC24 H23 N O4 S2P 1 21/c 115.796; 15.246; 9.849
90; 105.81; 90		2282.17Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514850 CIFC23 H26 O6P -19.7261; 10.89; 11.528
65.75; 69.528; 86.877		1037.3Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514851 CIFC23 H19 N S2P 1 21/n 110.584; 4.346; 40.473
90; 95.273; 90		1853.8Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514852 CIFC20 H18 F N O2 S2P -17.0055; 10.2801; 13.131
79.22; 84.888; 80.238		913.91Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514853 CIFC24 H32 O10P 1 21 111.2; 5.0559; 11.554
90; 115.351; 90		591.25Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514854 CIFC28 H25 N O4 S2P -18.4844; 12.3314; 12.7997
112.337; 94.171; 98.558		1212.59Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514855 CIFC19 H16 Cl N O2 S2P -16.5696; 10.4589; 13.1664
79.911; 84.189; 81.356		877.96Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514856 CIFC23 H19 N O2 S3P 1 21/n 16.9999; 10.6761; 27.063
90; 92.75; 90		2020.1Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514857 CIFC23 H17 Br N2P 1 21 111.03; 5.7133; 14.591
90; 92.925; 90		918.3Hatano, Manabu; Nishio, Kosuke; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki
Highly Active Chiral Dilithium(I) Binaphthyldisulfonate Catalysts for Enantio- and Chemoselective Strecker-Type Reactions
ACS Catalysis, 2019, 9, 8178
4514858 CIFC20 H19 N O3 SP 1 21/c 18.2877; 14.334; 14.903
90; 103.09; 90		1724.4Liu, Jibing; Chakraborty, Pushkin; Zhang, Heng; Zhong, Liang; Wang, Zhi-Xiang; Huang, Xueliang
Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration
ACS Catalysis, 2019, 9, 2610
4514859 CIFC17 H19 N O6 SP 1 21/c 17.5531; 28.802; 8.5314
90; 113.57; 90		1701.1Liu, Jibing; Chakraborty, Pushkin; Zhang, Heng; Zhong, Liang; Wang, Zhi-Xiang; Huang, Xueliang
Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration
ACS Catalysis, 2019, 9, 2610
4514860 CIFC22 H25 I N2 O2 RuP -18.8149; 10.4274; 12.2762
74.663; 83.855; 77.212		1059.8Kumar, Abhishek; Semwal, Shrivats; Choudhury, Joyanta
Catalytic Conversion of CO2 to Formate with Renewable Hydrogen Donors: An Ambient-Pressure and H2-Independent Strategy
ACS Catalysis, 2019, 9, 2164
4514861 CIFC20 H14 Cl N OP 18.6566; 11.3426; 16.584
89.235; 77.991; 89.031		1592.41Fan, Xiaozhong; Zhang, Xue; Li, Chunyu; Gu, Zhenhua
Enantioselective Atropisomeric Anilides Synthesis via Cu-Catalyzed Intramolecular Adjacent C‒N Coupling
ACS Catalysis, 2019, 9, 2286
4514862 CIFC28 H32 N2 O2P 1 21/c 113.969; 27.1371; 6.25424
90; 99.738; 90		2336.69Wu, Xiao; Chen, Chentuo; Guo, Ziyang; North, Michael; Whitwood, Adrian C.
Metal- and Halide-Free Catalyst for the Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide
ACS Catalysis, 2019, 9, 1895
4514863 CIFC13 H12 Br Mn N2 O4P 1 21/c 111.071; 10.4143; 13.4557
90; 105.015; 90		1498.43Steinlechner, Christoph; Roesel, Arend F.; Oberem, Elisabeth; Päpcke, Ayla; Rockstroh, Nils; Gloaguen, Frédéric; Lochbrunner, Stefan; Ludwig, Ralf; Spannenberg, Anke; Junge, Henrik; Francke, Robert; Beller, Matthias
Selective Earth-Abundant System for CO2 Reduction: Comparing Photo- and Electrocatalytic Processes
ACS Catalysis, 2019, 9, 2091
4514864 CIFC15 H10 Br Mn N2 O4P -17.1769; 9.2213; 11.5716
85.6351; 84.0784; 82.509		753.7Steinlechner, Christoph; Roesel, Arend F.; Oberem, Elisabeth; Päpcke, Ayla; Rockstroh, Nils; Gloaguen, Frédéric; Lochbrunner, Stefan; Ludwig, Ralf; Spannenberg, Anke; Junge, Henrik; Francke, Robert; Beller, Matthias
Selective Earth-Abundant System for CO2 Reduction: Comparing Photo- and Electrocatalytic Processes
ACS Catalysis, 2019, 9, 2091
4514865 CIFC17 H13 Br O3P c a 2110.7383; 18.1542; 7.5303
90; 90; 90		1468Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang
Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols
ACS Catalysis, 2019, 9, 2440
4514866 CIFC27 H32 O3P 1 21 19.72; 7.5084; 16.171
90; 94.588; 90		1176.4Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang
Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols
ACS Catalysis, 2019, 9, 2440
4514867 CIFC18 H12 F3 N3 O3P 1 21/c 110.5383; 19.337; 7.9828
90; 92.029; 90		1625.7Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang
Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols
ACS Catalysis, 2019, 9, 2440
4514868 CIFC50 H39 N Ni O P2P -113.3161; 14.0105; 15.2863
72.192; 64.226; 62.74		2262.59Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne
Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization.
ACS catalysis, 2019, 9, 2458-2481

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