Crystallography Open Database

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4516693 CIFC26 H24 N2 O3P 1 21 19.4911; 9.8015; 12.0673
90; 103.604; 90		1091.09Li, Dan; Wang, Linqing; Yang, Dongxu; Zhang, Bangzhi; Wang, Rui
Catalytic Desymmetrization of meso-Aziridines with Benzofuran-2(3H)-Ones Employing a Simple In Situ-Generated Magnesium Catalyst
ACS Catalysis, 2015, 5, 7432
4516694 CIFC24 H25 N3 O2P 21 21 215.1839; 17.316; 23.0197
90; 90; 90		2066.35Qureshi, Zafar; Kim, Jung Yun; Bruun, Theodora; Lam, Heather; Lautens, Mark
Cu/Pd-Catalyzed Synthesis of Fully Decorated Polycyclic Triazoles: Introducing C‒H Functionalization to Multicomponent Multicatalytic Reactions ((MC)2R)
ACS Catalysis, 2016, 6, 4946
4516695 CIFC62 H81 O5 Si YP -112.0346; 14.3451; 16.9307
101.182; 90.368; 96		2850.61Xu, Tie-Qi; Yang, Guan-Wen; Lu, Xiao-Bing
Highly Isotactic and High-Molecular-Weight Poly(2-vinylpyridine) by Coordination Polymerization with Yttrium Bis(phenolate) Ether Catalysts
ACS Catalysis, 2016, 6, 4907
4516696 CIFC76 H87 Co N6 O2 Si2P 1 21 112.1686; 15.7163; 17.6104
90; 100.762; 90		3308.67Ibrahim, Abdulrahman D.; Entsminger, Steven W.; Zhu, Lingyang; Fout, Alison R.
A Highly Chemoselective Cobalt Catalyst for the Hydrosilylation of Alkenes using Tertiary Silanes and Hydrosiloxanes
ACS Catalysis, 2016, 6, 3589
4516697 CIFC168 H156 Cl4 N20 P4 Ru4P -419.0698; 19.0698; 9.8294
90; 90; 90		3574.5Hale, Lillian V. A.; Malakar, Tanmay; Tseng, Kuei-Nin T.; Zimmerman, Paul M.; Paul, Ankan; Szymczak, Nathaniel K.
The Mechanism of Acceptorless Amine Double Dehydrogenation byN,N,N-Amide Ruthenium(II) Hydrides: A Combined Experimental and Computational Study
ACS Catalysis, 2016, 6, 4799
4516698 CIFC184 H164 N24 P4 Ru4P 1 21/n 112.9692; 16.8857; 17.268
90; 90.769; 90		3781.2Hale, Lillian V. A.; Malakar, Tanmay; Tseng, Kuei-Nin T.; Zimmerman, Paul M.; Paul, Ankan; Szymczak, Nathaniel K.
The Mechanism of Acceptorless Amine Double Dehydrogenation byN,N,N-Amide Ruthenium(II) Hydrides: A Combined Experimental and Computational Study
ACS Catalysis, 2016, 6, 4799
4516699 CIFC23 H21 Cl N O2P 21 21 219.5413; 12.5331; 16.6646
90; 90; 90		1992.8Zhang, Ming; Sun, Wangsheng; Zhu, Gongming; Bao, Guangjun; Zhang, Bangzhi; Hong, Liang; Li, Min; Wang, Rui
Enantioselective Dearomative Arylation of Isoquinolines
ACS Catalysis, 2016, 6, 5290
4516700 CIFC38 H27 N OP -111.23; 12.753; 20.255
85.686; 80.147; 74.114		2747.7Li, Xingwei; Yang, Xifa; Qi, Zisong
Synthesis of Cyclopentadienols by Rhodium-Catalyzed C‒H Activation of 8-Formylquinolines and [2+2+1] Carbocyclization with Alkynes
ACS Catalysis, 2016, 6, 6372
4516701 CIFC26 H35 O5 PP 1 21/n 19.4338; 11.4458; 23.1231
90; 97.4269; 90		2475.83Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516702 CIFC7 H5 O4 PP 1 21/n 14.5729; 14.1363; 11.7191
90; 100.631; 90		744.57Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516703 CIFC48 H53 O12 P2 RhP -110.8599; 15.1287; 15.5406
102.742; 101.78; 100.56		2367.22Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516704 CIFC18 H19 O5 PP 1 21/c 17.9973; 11.7658; 18.4161
90; 93.7246; 90		1729.2Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Börner, Armin
Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzedn-Regioselective Hydroformylation of Olefins
ACS Catalysis, 2016, 6, 7554
4516705 CIFC24 H27 N O4 SP -18.6854; 11.1584; 12.3533
110.734; 96.486; 95.657		1100.08Teske, Johannes; Plietker, Bernd
A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates
ACS Catalysis, 2016, 6, 7148
4516706 CIFC39 H32 B Cl2 F4 Fe N O3 P2P 1 21/n 116.7984; 13.6152; 16.9579
90; 103.928; 90		3764.5Teske, Johannes; Plietker, Bernd
A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates
ACS Catalysis, 2016, 6, 7148
4516707 CIFC40 H34 B Cl3 F4 Fe N2 O2 P2P -112.2695; 12.9467; 14.1404
78.636; 69.027; 83.561		2054.1Teske, Johannes; Plietker, Bernd
A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates
ACS Catalysis, 2016, 6, 7148
4516708 CIFC18 H21 F3 N4 Ni O3 SP 1 21/n 16.9941; 17.4234; 17.1188
90; 98.8919; 90		2061.04Wei, Yingfei; Liu, Shi-Xia; Mueller-Bunz, Helge; Albrecht, Martin
Synthesis of Triazolylidene Nickel Complexes and Their Catalytic Application in Selective Aldehyde Hydrosilylation
ACS Catalysis, 2016, 6, 8192
4516709 CIFC15 H16 I N3 Ni OP 1 21/c 113.4405; 10.5724; 11.268
90; 93.709; 90		1597.81Wei, Yingfei; Liu, Shi-Xia; Mueller-Bunz, Helge; Albrecht, Martin
Synthesis of Triazolylidene Nickel Complexes and Their Catalytic Application in Selective Aldehyde Hydrosilylation
ACS Catalysis, 2016, 6, 8192
4516710 CIFC18 H21 F3 N4 Ni O3 SC 1 2/c 114.416; 11.0236; 25.901
90; 98.801; 90		4067.62Wei, Yingfei; Liu, Shi-Xia; Mueller-Bunz, Helge; Albrecht, Martin
Synthesis of Triazolylidene Nickel Complexes and Their Catalytic Application in Selective Aldehyde Hydrosilylation
ACS Catalysis, 2016, 6, 8192
4516711 CIFC40 H46 Fe N4 O3P b c n24.0256; 13.1262; 22.3213
90; 90; 90		7039.4MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516712 CIFC150 H162 F12 Fe4 N12 O6 P2P 21 21 222.7811; 22.9453; 13.3383
90; 90; 90		6972.2MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516713 CIFC36 H36 Fe N6 O6P 1 21/n 18.0949; 23.7481; 17.1961
90; 97.427; 90		3278.02MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516714 CIFC42 H50 Fe N4 O5P 1 21 115.49431; 16.23501; 15.84297
90; 107.287; 90		3805.28MacNair, Alistair J.; Millet, Clément R. P.; Nichol, Gary S.; Ironmonger, Alan; Thomas, Stephen P.
Markovnikov-Selective, Activator-Free Iron-Catalyzed Vinylarene Hydroboration
ACS Catalysis, 2016, 6, 7217
4516715 CIFC16 H15 N3 O4P 1 21/c 110.2029; 19.4064; 7.7687
90; 91.548; 90		1537.7Prieto, Alexis; Bouyssi, Didier; Monteiro, Nuno
Copper-Catalyzed Double C‒H Alkylation of Aldehyde-Derived N,N-Dialkylhydrazones with Polyhalomethanes: Flexible Access to 4-Functionalized Pyrazoles
ACS Catalysis, 2016, 6, 7197
4516716 CIFC33 H22 Cl3 N4 Ni O2P -19.0058; 9.3091; 17.9195
79.797; 80.388; 89.868		1457.21He, Zhiqi; Huang, Yong
Diverting C‒H Annulation Pathways: Nickel-Catalyzed Dehydrogenative Homologation of Aromatic Amides
ACS Catalysis, 2016, 6, 7814
4516717 CIFC45 H29 F4 N2 O2C 1 2 129.3161; 8.847; 16.2475
90; 122.222; 90		3564.9He, Zhiqi; Huang, Yong
Diverting C‒H Annulation Pathways: Nickel-Catalyzed Dehydrogenative Homologation of Aromatic Amides
ACS Catalysis, 2016, 6, 7814
4516718 CIFC19 H22 O5 SP 21 21 215.6343; 17.0439; 18.3976
90; 90; 90		1766.73Gutiérrez-Bonet, Álvaro; Tellis, John C.; Matsui, Jennifer K.; Vara, Brandon A.; Molander, Gary A.
1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis.
ACS catalysis, 2016, 6, 8004-8008
4516719 CIFC22 H40 Cl2 N2 Ni O5C 1 2/c 113.0843; 30.4; 6.6223
90; 92.47; 90		2631.7Gutiérrez-Bonet, Álvaro; Tellis, John C.; Matsui, Jennifer K.; Vara, Brandon A.; Molander, Gary A.
1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis.
ACS catalysis, 2016, 6, 8004-8008
4516720 CIFC26 H23 Cl Cu N2 O3P b c a13.278; 17.113; 20.133
90; 90; 90		4574.7Bose, Shubhankar Kumar; Brand, Simon; Omoregie, Helen Oluwatola; Haehnel, Martin; Maier, Jonathan; Bringmann, Gerhard; Marder, Todd B.
Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides in Air
ACS Catalysis, 2016, 6, 8332
4516721 CIFC22 H14 Br Cu F3 N2 O2P 1 21/c 112.615; 13.308; 13.396
90; 116.537; 90		2012Bose, Shubhankar Kumar; Brand, Simon; Omoregie, Helen Oluwatola; Haehnel, Martin; Maier, Jonathan; Bringmann, Gerhard; Marder, Todd B.
Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides in Air
ACS Catalysis, 2016, 6, 8332
4516722 CIFC29 H22 Cl Cu N3 O2P 1 21/n 115.5811; 8.8795; 17.1799
90; 96.394; 90		2362.09Bose, Shubhankar Kumar; Brand, Simon; Omoregie, Helen Oluwatola; Haehnel, Martin; Maier, Jonathan; Bringmann, Gerhard; Marder, Todd B.
Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides in Air
ACS Catalysis, 2016, 6, 8332
4516723 CIFC22 H17 Cu N3 O5P 1 21/n 17.3869; 17.69; 14.677
90; 90.094; 90		1917.9Bose, Shubhankar Kumar; Brand, Simon; Omoregie, Helen Oluwatola; Haehnel, Martin; Maier, Jonathan; Bringmann, Gerhard; Marder, Todd B.
Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides in Air
ACS Catalysis, 2016, 6, 8332
4516724 CIFC31 H38 Cu N2 O4P -19.019; 14.953; 20.897
86.86; 85.15; 89.96		2804Bose, Shubhankar Kumar; Brand, Simon; Omoregie, Helen Oluwatola; Haehnel, Martin; Maier, Jonathan; Bringmann, Gerhard; Marder, Todd B.
Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides in Air
ACS Catalysis, 2016, 6, 8332
4516725 CIFC138 H106 B6 O27P -19.5117; 16.2069; 19.2829
95.824; 98.182; 102.531		2845.1Bose, Shubhankar Kumar; Brand, Simon; Omoregie, Helen Oluwatola; Haehnel, Martin; Maier, Jonathan; Bringmann, Gerhard; Marder, Todd B.
Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides in Air
ACS Catalysis, 2016, 6, 8332
4516726 CIFC28 H21 N3 O3P -18.4814; 13.8492; 19.5575
86.4189; 81.6947; 73.8739		2183.1Yamamoto, Yoshihiko; Nishimura, Kei-ichiro; Shibuya, Masatoshi
Ruthenium-Catalyzed Cycloisomerization of 1,6-Diynes with Styryl Terminals Leading to Indenylidene Cycloalkanes
ACS Catalysis, 2017, 7, 1101
4516727 CIFC33 H40 O7P 16.1366; 11.2261; 11.6894
67.3845; 81.2585; 88.6059		734.21Eisink, Niek N. H. M.; Witte, Martin D.; Minnaard, Adriaan J.
Regioselective Carbohydrate Oxidations: A Nuclear Magnetic Resonance (NMR) Study on Selectivity, Rate, and Side-Product Formation.
ACS catalysis, 2017, 7, 1438-1445
4516728 CIFC17 H18 Cl3 F6 N8 P PdP -16.915; 12.31; 14.954
82.822; 83.631; 85.687		1252.7Schroeter, Felix; Soellner, Johannes; Strassner, Thomas
Cross-Coupling Catalysis by an Anionic Palladium Complex
ACS Catalysis, 2017, 7, 3004
4516729 CIFC18 H42 Cl3 N O Pd SP n a 219.133; 21.693; 12.682
90; 90; 90		2512.6Schroeter, Felix; Soellner, Johannes; Strassner, Thomas
Cross-Coupling Catalysis by an Anionic Palladium Complex
ACS Catalysis, 2017, 7, 3004
4516730 CIFC38.5 H40 F9 N6.5 O2.5 SC 2 2 2113.08003; 23.3536; 26.5956
90; 90; 90		8124.05Neuvonen, Antti J.; Földes, Tamás; Madarász, Ádám; Pápai, Imre; Pihko, Petri M.
Organocatalysts Fold To Generate an Active Site Pocket for the Mannich Reaction
ACS Catalysis, 2017, 7, 3284
4516731 CIFC15 H19 N O4 SP 1 21/c 112.6954; 5.5859; 22.534
90; 102.103; 90		1562.5Cao, Tao; Yang, Zheng; Ma, Shengming
Selectivities in Nickel-Catalyzed Hydrocarboxylation of Enynes with Carbon Dioxide
ACS Catalysis, 2017, 7, 4504
4516732 CIFC23.5 H20 Cl2 N5 O2 RuP -19.0731; 10.4974; 12.7753
98.387; 102.017; 101.29		1144.77Ono, Takashi; Qu, Shuanglin; Gimbert-Suriñach, Carolina; Johnson, Michelle A.; Marell, Daniel J.; Benet-Buchholz, Jordi; Cramer, Christopher J.; Llobet, Antoni
Hydrogenative Carbon Dioxide Reduction Catalyzed by Mononuclear Ruthenium Polypyridyl Complexes: Discerning between Electronic and Steric Effects
ACS Catalysis, 2017, 7, 5932
4516733 CIFC31 H26 Cl3 N7 RuP 1 21/c 110.3114; 14.828; 18.855
90; 92.38; 90		2880.4Ono, Takashi; Qu, Shuanglin; Gimbert-Suriñach, Carolina; Johnson, Michelle A.; Marell, Daniel J.; Benet-Buchholz, Jordi; Cramer, Christopher J.; Llobet, Antoni
Hydrogenative Carbon Dioxide Reduction Catalyzed by Mononuclear Ruthenium Polypyridyl Complexes: Discerning between Electronic and Steric Effects
ACS Catalysis, 2017, 7, 5932
4516734 CIFC20 H20 N2 O2 SP -15.3524; 9.849; 16.789
91.22; 96.68; 91.44		878.5Li, Long; Chen, Xiu-Mei; Wang, Ze-Shu; Zhou, Bo; Liu, Xin; Lu, Xin; Ye, Long-Wu
Reversal of Regioselectivity in Catalytic Arene-Ynamide Cyclization: Direct Synthesis of Valuable Azepino[4,5-b]indoles and β-Carbolines and DFT Calculations
ACS Catalysis, 2017, 7, 4004
4516735 CIFC21 H24 N2 O2 SP 1 21 19.6188; 16.8151; 11.4121
90; 92.913; 90		1843.42Li, Long; Chen, Xiu-Mei; Wang, Ze-Shu; Zhou, Bo; Liu, Xin; Lu, Xin; Ye, Long-Wu
Reversal of Regioselectivity in Catalytic Arene-Ynamide Cyclization: Direct Synthesis of Valuable Azepino[4,5-b]indoles and β-Carbolines and DFT Calculations
ACS Catalysis, 2017, 7, 4004
4516736 CIFC31 H62 B Co N O2 P3P -110.8798; 11.5927; 14.6647
84.709; 78.676; 86.719		1804.42Obligacion, Jennifer V.; Chirik, Paul J.
Mechanistic Studies of Cobalt-Catalyzed C(sp<sup>2</sup>)-H Borylation of Five-Membered Heteroarenes with Pinacolborane.
ACS catalysis, 2017, 7, 4366-4371
4516737 CIFC42 H53 B2 N O8P n a 2113.029; 31.24; 9.883
90; 90; 90		4023Chong, Che Chang; Rao, Bin; Kinjo, Rei
Metal-Free Catalytic Reduction of α,β-Unsaturated Esters by 1,3,2-Diazaphospholene and Subsequent C‒C Coupling with Nitriles
ACS Catalysis, 2017, 7, 5814
4516738 CIFC18 H22 O6P -15.9683; 11.8288; 12.2029
94.8482; 101.631; 100.091		824.32Chong, Che Chang; Rao, Bin; Kinjo, Rei
Metal-Free Catalytic Reduction of α,β-Unsaturated Esters by 1,3,2-Diazaphospholene and Subsequent C‒C Coupling with Nitriles
ACS Catalysis, 2017, 7, 5814
4516739 CIFC28 H44 B2 Co F8 N4 P4P -110.0889; 10.4012; 10.9505
114.987; 111.721; 93.719		933.62Jeletic, Matthew S.; Hulley, Elliott B.; Helm, Monte L.; Mock, Michael T.; Appel, Aaron M.; Wiedner, Eric S.; Linehan, John C.
Understanding the Relationship Between Kinetics and Thermodynamics in CO2 Hydrogenation Catalysis
ACS Catalysis, 2017, 7, 6008
4516740 CIFC22 H51 B2 Co F8 N P4P 1 21/n 115.0848; 20.0234; 32.3058
90; 91.503; 90		9754.6Jeletic, Matthew S.; Hulley, Elliott B.; Helm, Monte L.; Mock, Michael T.; Appel, Aaron M.; Wiedner, Eric S.; Linehan, John C.
Understanding the Relationship Between Kinetics and Thermodynamics in CO2 Hydrogenation Catalysis
ACS Catalysis, 2017, 7, 6008
4516741 CIFC20 H32 Co P4A e a 215.7643; 16.3813; 8.9459
90; 90; 90		2310.19Jeletic, Matthew S.; Hulley, Elliott B.; Helm, Monte L.; Mock, Michael T.; Appel, Aaron M.; Wiedner, Eric S.; Linehan, John C.
Understanding the Relationship Between Kinetics and Thermodynamics in CO2 Hydrogenation Catalysis
ACS Catalysis, 2017, 7, 6008
4516742 CIFC78 H60 Cu3 N8 O15R -3 :H15.598; 15.598; 59.01
90; 90; 120		12434Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian
Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction
ACS Catalysis, 2019, 9, 1726
4516743 CIFC78 H66 Co3 N8 O18R -3 :H15.7439; 15.7439; 61.146
90; 90; 120		13125.7Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian
Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction
ACS Catalysis, 2019, 9, 1726
4516744 CIFC468 H450 N48 Ni18 O135R -3 :H15.7128; 15.7128; 60.539
90; 90; 120		12944.1Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian
Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction
ACS Catalysis, 2019, 9, 1726
4517129 CIFC15 H17 N OP 1 21/c 111.0739; 11.3132; 10.2916
90; 93.622; 90		1286.77Zhang, Min; Luo, Anping; Shi, Yang; Su, Rongchuan; Yang, Yudong; You, Jingsong
F+ Reagent-Promoted Pd-Catalyzed C7‒H Arylation of 1-Naphthamides
ACS Catalysis, 2019, 11802
4517130 CIFC23 H25 N OP -17.4537; 10.8662; 12.8697
105.015; 99.127; 100.612		965.9Zhang, Min; Luo, Anping; Shi, Yang; Su, Rongchuan; Yang, Yudong; You, Jingsong
F+ Reagent-Promoted Pd-Catalyzed C7‒H Arylation of 1-Naphthamides
ACS Catalysis, 2019, 11802
4517131 CIFC21 H24 O3P 1 21/c 15.8229; 19.461; 15.4449
90; 91.423; 90		1749.7Chen, Bin; Zhang, Yunxing; Wu, Rui; Fang, Dongmei; Chen, Xiaozhen; Wang, Simin; Zhao, Yuqiong; Hu, Ping; Zhao, Ke-Qing; Wang, Bi-Qin; Cao, Peng
Modular Synthesis of 2,8-Dioxabicyclo[3.2.1]octanes by Sequential Catalysis
ACS Catalysis, 2019, 11788
4517147 CIFC17 H18 N2 O2P 16.326; 10.0783; 12.7658
69.309; 86.674; 77.439		743.01Robinson, Donovan J.; Spurlin, Sean P.; Gorden, John D.; Karimov, Rashad R.
Enantioselective Synthesis of Dihydropyridines Containing Quaternary Stereocenters Through Dearomatization of Pyridinium Salts
ACS Catalysis, 2019, 51
4517148 CIFC17 H21 N O2P 1 21 16.3498; 10.024; 11.8562
90; 98.403; 90		746.55Robinson, Donovan J.; Spurlin, Sean P.; Gorden, John D.; Karimov, Rashad R.
Enantioselective Synthesis of Dihydropyridines Containing Quaternary Stereocenters Through Dearomatization of Pyridinium Salts
ACS Catalysis, 2019, 51
4517149 CIFC36 H58 Cl3 F3 N2 O7 P2 Ru2 SP 1 21/n 117.416; 15.909; 17.479
90; 111.302; 90		4512.1Cherepakhin, Valeriy; Williams, Travis J.
Catalyst Evolution in Ruthenium-Catalyzed Coupling of Amines and Alcohols
ACS Catalysis, 2019, 56
4517150 CIFC44 H71 Cl2 F3 N3 O4 P3 Ru3 SP 1 21/c 113.4; 20.266; 19.218
90; 97.812; 90		5170Cherepakhin, Valeriy; Williams, Travis J.
Catalyst Evolution in Ruthenium-Catalyzed Coupling of Amines and Alcohols
ACS Catalysis, 2019, 56
4517162 CIFC53 H44 Cl Fe N O3 SP 112.2076; 12.7468; 16.7154
75.2715; 69.3507; 63.0204		2155.2Yoshida, Kazuhiro; Liu, Qiang; Yasue, Risa; Wada, Shiro; Kimura, Ryosuke; Konishi, Takuma; Ogasawara, Masamichi
Versatile and Enantioselective Preparation of Planar-Chiral Metallocene-Fused 4-Dialkylaminopyridines and Their Application in Asymmetric Organocatalysis
ACS Catalysis, 2019, 292
4517163 CIFC50 H46 Fe N2P 21 21 2110.9661; 17.5243; 19.8084
90; 90; 90		3806.6Yoshida, Kazuhiro; Liu, Qiang; Yasue, Risa; Wada, Shiro; Kimura, Ryosuke; Konishi, Takuma; Ogasawara, Masamichi
Versatile and Enantioselective Preparation of Planar-Chiral Metallocene-Fused 4-Dialkylaminopyridines and Their Application in Asymmetric Organocatalysis
ACS Catalysis, 2019, 292
4517164 CIFC25 H29 N SP 1 21 113.0414; 5.7208; 14.1145
90; 93.997; 90		1050.48Feng, Sheng; Hao, Hua; Liu, Peng; Buchwald, Stephen L.
Diastereo- and Enantioselective CuH-Catalyzed Hydroamination of Strained Trisubstituted Alkenes
ACS Catalysis, 2019, 282
4517165 CIFC37 H40 Cl Fe N O P SP -19.5205; 13.2892; 14.2405
76.299; 75.44; 73.252		1643.39Song, Heng; Yang, Zhuoyi; Tung, Chen-Ho; Wang, Wenguang
Iron-Catalyzed Reductive Coupling of Nitroarenes with Olefins: Intermediate of Iron‒Nitroso Complex
ACS Catalysis, 2019, 276
4517166 CIFC49 H50 Fe O P2 S2P 1 21/c 115.0306; 14.4302; 20.0912
90; 106.058; 90		4187.6Song, Heng; Yang, Zhuoyi; Tung, Chen-Ho; Wang, Wenguang
Iron-Catalyzed Reductive Coupling of Nitroarenes with Olefins: Intermediate of Iron‒Nitroso Complex
ACS Catalysis, 2019, 276
4517167 CIFC18 H24 N2 OP b c a11.3428; 11.7215; 24.5548
90; 90; 90		3264.67Song, Heng; Yang, Zhuoyi; Tung, Chen-Ho; Wang, Wenguang
Iron-Catalyzed Reductive Coupling of Nitroarenes with Olefins: Intermediate of Iron‒Nitroso Complex
ACS Catalysis, 2019, 276
4517168 CIFC17 H15 NP b c a16.3043; 8.1054; 18.5358
90; 90; 90		2449.56Song, Heng; Yang, Zhuoyi; Tung, Chen-Ho; Wang, Wenguang
Iron-Catalyzed Reductive Coupling of Nitroarenes with Olefins: Intermediate of Iron‒Nitroso Complex
ACS Catalysis, 2019, 276
4517169 CIFC11 H22 O2P b c a9.6851; 7.3807; 31.3965
90; 90; 90		2244.31Wu, Bin; Zhu, Rong
Radical Philicity Inversion in Co- and Fe-Catalyzed Hydrogen-Atom-Transfer-Initiated Cyclizations of Unsaturated Acylsilanes
ACS Catalysis, 2019, 10, 510
4517170 CIFC49 H39 N O3 P2 RuC 1 2/c 119.1587; 20.6734; 20.688
90; 107.466; 90		7816.2Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517171 CIFC21 H19 Cl N4P -18.9649; 9.952; 11.7814
100.554; 105.986; 111.878		888.28Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517172 CIFC18 H15 F N2P 1 21/c 119.3115; 5.8472; 12.709
90; 106.294; 90		1377.44Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517173 CIFC33 H29 N2 O2 P RuP n a 2116.2264; 9.3716; 17.7053
90; 90; 90		2692.4Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517174 CIFC55 H53 N O3.5 P2 RuP 1 21/n 111.9019; 15.2039; 24.7562
90; 93.907; 90		4469.4Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517175 CIFC18 H16 N2 OP b c a18.7085; 6.2302; 24.4878
90; 90; 90		2854.24Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517176 CIFC18 H15 F N2 OP 1 21/c 18.1191; 5.6386; 31.0628
90; 93.276; 90		1419.74Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517177 CIFC21 H19 F N4P 1 21/c 111.2425; 9.3295; 16.3348
90; 94.764; 90		1707.39Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517178 CIFC27 H22 N4 O2P -16.3344; 12.4251; 13.9524
106.848; 91.291; 93.64		1047.9Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517179 CIFC34 H33 B F2 N6P -110.4593; 16.8136; 16.9094
94.418; 94.02; 90.953		2956.8Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517180 CIFC33 H35 N5 O2P 1 21/n 110.1416; 27.4937; 10.2461
90; 101.977; 90		2794.7Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517181 CIFC18 H16 N2P c a 2112.2928; 6.0102; 36.9034
90; 90; 90		2726.5Korvorapun, Korkit; Kuniyil, Rositha; Ackermann, Lutz
Late-Stage Diversification by Selectivity Switch in meta-C‒H Activation: Evidence for Singlet Stabilization
ACS Catalysis, 2019, 435
4517182 CIFC30 H29 Mo O2 P SC 1 2/c 119.389; 15.694; 17.49
90; 101.224; 90		5220Hou, Shu-Fen; Chen, Jia-Yi; Xue, Minghui; Jia, Mengjing; Zhai, Xiaofang; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Cooperative Molybdenum-Thiolate Reactivity for Transfer Hydrogenation of Nitriles
ACS Catalysis, 2019, 380
4517183 CIFC34 H38 B2 F8 Mo N3 P SP -111.1302; 13.2104; 13.9442
75.533; 73.017; 67.252		1786.43Hou, Shu-Fen; Chen, Jia-Yi; Xue, Minghui; Jia, Mengjing; Zhai, Xiaofang; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Cooperative Molybdenum-Thiolate Reactivity for Transfer Hydrogenation of Nitriles
ACS Catalysis, 2019, 380
4517184 CIFC30 H32 Mo N P SP 1 21/n 111.1248; 18.197; 12.9432
90; 90.632; 90		2620.04Hou, Shu-Fen; Chen, Jia-Yi; Xue, Minghui; Jia, Mengjing; Zhai, Xiaofang; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Cooperative Molybdenum-Thiolate Reactivity for Transfer Hydrogenation of Nitriles
ACS Catalysis, 2019, 380
4517185 CIFC28 H32 B Mo P SP 1 21/n 110.8462; 16.9076; 14.8894
90; 105.26; 90		2634.19Hou, Shu-Fen; Chen, Jia-Yi; Xue, Minghui; Jia, Mengjing; Zhai, Xiaofang; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Cooperative Molybdenum-Thiolate Reactivity for Transfer Hydrogenation of Nitriles
ACS Catalysis, 2019, 380
4517213 CIFC58 H52 F6 O4 P4 PdP 1 21/n 111.0969; 18.3586; 12.3866
90; 94.46; 90		2515.8Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517214 CIFC29 H30 Cl2 P2 PdP 1 21/c 111.3082; 17.6113; 13.8182
90; 92.789; 90		2748.7Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517215 CIFC36 H44 Cl4 P2 PdP b c a21.8565; 14.7082; 22.7524
90; 90; 90		7314.2Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517216 CIFC33 H38 Cl2 P2 PdP 1 21/n 111.2984; 20.6157; 14.14
90; 110.081; 90		3093.3Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517217 CIFC63 H56 B8 O16P -15.1932; 15.4161; 18.5227
72.871; 83.638; 89.832		1407.71Michigami, Kenichi; Sakaguchi, Tatsuhiko; Takemoto, Yoshiji
Catalytic Dehydrative Peptide Synthesis with gem-Diboronic Acids
ACS Catalysis, 2019, 10, 683
4517218 CIFC20 H40 O4 S Si4P 1 21/c 122.0893; 9.47947; 14.2315
90; 107.915; 90		2835.51Zhang, Zhikun; Hu, Xile
Arylsilylation of Electron-Deficient Alkenes via Cooperative Photoredox and Nickel Catalysis
ACS Catalysis, 2019, 10, 777
4517264 CIFC29 H26 N2 O3C 1 2/c 128.645; 9.1579; 22.276
90; 126.87; 90		4675Bai, Zibo; Bai, Ziqian; Song, Fangfang; Wang, Hao; Chen, Gong; He, Gang
Palladium-Catalyzed Amide-Directed Hydrocarbofunctionalization of 3-Alkenamides with Alkynes
ACS Catalysis, 2019, 933
4517265 CIFC24 H21 Br N2 OP 1 21/n 17.5427; 6.6034; 39.366
90; 94.005; 90		1955.9Bai, Zibo; Bai, Ziqian; Song, Fangfang; Wang, Hao; Chen, Gong; He, Gang
Palladium-Catalyzed Amide-Directed Hydrocarbofunctionalization of 3-Alkenamides with Alkynes
ACS Catalysis, 2019, 933
4517271 CIFC49 H85 Cl O2.5 P2 PdP -111.8057; 15.6134; 15.6605
116.403; 99.017; 106.38		2343.1Scharf, Lennart T.; Rodstein, Ilja; Schmidt, Michelle; Scherpf, Thorsten; Gessner, Viktoria H.
Unraveling the High Activity of Ylide-Functionalized Phosphines in Palladium-Catalyzed Amination Reactions: A Comparative Study with CyJohnPhos and PtBu3
ACS Catalysis, 2019, 999
4517272 CIFC43 H76 Cl N P2 PdP -111.3247; 12.9036; 15.526
86.814; 87.399; 68.191		2102.4Scharf, Lennart T.; Rodstein, Ilja; Schmidt, Michelle; Scherpf, Thorsten; Gessner, Viktoria H.
Unraveling the High Activity of Ylide-Functionalized Phosphines in Palladium-Catalyzed Amination Reactions: A Comparative Study with CyJohnPhos and PtBu3
ACS Catalysis, 2019, 999
4517273 CIFC64 H116 P4 PdP -111.6891; 12.0707; 23.6505
80.935; 76.32; 70.62		3047.2Scharf, Lennart T.; Rodstein, Ilja; Schmidt, Michelle; Scherpf, Thorsten; Gessner, Viktoria H.
Unraveling the High Activity of Ylide-Functionalized Phosphines in Palladium-Catalyzed Amination Reactions: A Comparative Study with CyJohnPhos and PtBu3
ACS Catalysis, 2019, 999
4517274 CIFC40 H51 Cl Cr N3 O3P -16.7438; 15.597; 19.696
68.339; 81.912; 81.492		1895.8Hooe, Shelby L.; Dressel, Julia M.; Dickie, Diane A.; Machan, Charles W.
Highly Efficient Electrocatalytic Reduction of CO2 to CO by a Molecular Chromium Complex
ACS Catalysis, 2019, 1146
4517285 CIFC19 H23 N OP 1 21 111.2351; 5.6546; 11.98
90; 96.909; 90		755.56Duewel, Sabine; Schmermund, Luca; Faber, Tabea; Harms, Klaus; Srinivasan, Vasundara; Meggers, Eric; Hoebenreich, Sabrina
Directed Evolution of an FeII-Dependent Halogenase for Asymmetric C(sp3)‒H Chlorination
ACS Catalysis, 2019, 1272
4517286 CIFC25 H31 N OP 1 21 113.5174; 6.0844; 24.6942
90; 92.239; 90		2029.4Duewel, Sabine; Schmermund, Luca; Faber, Tabea; Harms, Klaus; Srinivasan, Vasundara; Meggers, Eric; Hoebenreich, Sabrina
Directed Evolution of an FeII-Dependent Halogenase for Asymmetric C(sp3)‒H Chlorination
ACS Catalysis, 2019, 1272
4517287 CIFC25 H31 N OP 21 21 219.9772; 10.027; 21.2241
90; 90; 90		2123.3Duewel, Sabine; Schmermund, Luca; Faber, Tabea; Harms, Klaus; Srinivasan, Vasundara; Meggers, Eric; Hoebenreich, Sabrina
Directed Evolution of an FeII-Dependent Halogenase for Asymmetric C(sp3)‒H Chlorination
ACS Catalysis, 2019, 1272
4517292 CIFC18 H23 N OP 41 21 29.2782; 9.2782; 39.8985
90; 90; 90		3434.66Zhao, Bin; Shang, Rui; Wang, Guang-Zu; Wang, Shaohong; Chen, Hui; Fu, Yao
Palladium-Catalyzed Dual Ligand-Enabled Alkylation of Silyl Enol Ether and Enamide under Irradiation: Scope, Mechanism, and Theoretical Elucidation of Hybrid Alkyl Pd(I)-Radical Species
ACS Catalysis, 2020, 1334
4517293 CIFC20 H23 N OP 1 21/n 15.6249; 8.6932; 34.663
90; 92.653; 90		1693.15Zhao, Bin; Shang, Rui; Wang, Guang-Zu; Wang, Shaohong; Chen, Hui; Fu, Yao
Palladium-Catalyzed Dual Ligand-Enabled Alkylation of Silyl Enol Ether and Enamide under Irradiation: Scope, Mechanism, and Theoretical Elucidation of Hybrid Alkyl Pd(I)-Radical Species
ACS Catalysis, 2020, 1334
4517294 CIFC16 H21 N O3P -16.5339; 8.3328; 15.0376
85.743; 84.357; 77.273		793.58Zhao, Bin; Shang, Rui; Wang, Guang-Zu; Wang, Shaohong; Chen, Hui; Fu, Yao
Palladium-Catalyzed Dual Ligand-Enabled Alkylation of Silyl Enol Ether and Enamide under Irradiation: Scope, Mechanism, and Theoretical Elucidation of Hybrid Alkyl Pd(I)-Radical Species
ACS Catalysis, 2020, 1334
4517295 CIFC16 H23 N O3P 21 21 219.47792; 11.47657; 15.35077
90; 90; 90		1669.76Zhao, Bin; Shang, Rui; Wang, Guang-Zu; Wang, Shaohong; Chen, Hui; Fu, Yao
Palladium-Catalyzed Dual Ligand-Enabled Alkylation of Silyl Enol Ether and Enamide under Irradiation: Scope, Mechanism, and Theoretical Elucidation of Hybrid Alkyl Pd(I)-Radical Species
ACS Catalysis, 2020, 1334
4517296 CIFC20 H23 N O2P 1 21/c 17.638; 11.3062; 20.7899
90; 95.235; 90		1787.86Zhao, Bin; Shang, Rui; Wang, Guang-Zu; Wang, Shaohong; Chen, Hui; Fu, Yao
Palladium-Catalyzed Dual Ligand-Enabled Alkylation of Silyl Enol Ether and Enamide under Irradiation: Scope, Mechanism, and Theoretical Elucidation of Hybrid Alkyl Pd(I)-Radical Species
ACS Catalysis, 2020, 1334
4517302 CIFC69 H61 B F24 N2 PdP -112.7592; 12.8409; 21.6356
85.111; 78.328; 76.463		3372.4Bermesheva, Evgeniya V.; Wozniak, Alyona I.; Andreyanov, Fedor A.; Karpov, Gleb O.; Nechaev, Mikhail S.; Asachenko, Andrey F.; Topchiy, Maxim A.; Melnikova, Elizaveta K.; Nelyubina, Yulia V.; Gribanov, Pavel S.; Bermeshev, Maxim V.
Polymerization of 5-Alkylidene-2-norbornenes with Highly Active Pd‒N-Heterocyclic Carbene Complex Catalysts: Catalyst Structure‒Activity Relationships
ACS Catalysis, 2020, 1663-1678
4517303 CIFC37 H49 F6 N2 Pd SbP 1 21/c 113.8611; 16.2187; 16.4272
90; 95.818; 90		3674Bermesheva, Evgeniya V.; Wozniak, Alyona I.; Andreyanov, Fedor A.; Karpov, Gleb O.; Nechaev, Mikhail S.; Asachenko, Andrey F.; Topchiy, Maxim A.; Melnikova, Elizaveta K.; Nelyubina, Yulia V.; Gribanov, Pavel S.; Bermeshev, Maxim V.
Polymerization of 5-Alkylidene-2-norbornenes with Highly Active Pd‒N-Heterocyclic Carbene Complex Catalysts: Catalyst Structure‒Activity Relationships
ACS Catalysis, 2020, 1663-1678
4517304 CIFC38 H49.88 B Cl3 F4 N2 PdP 1 21/n 112.2879; 12.5324; 25.74
90; 101.171; 90		3888.8Bermesheva, Evgeniya V.; Wozniak, Alyona I.; Andreyanov, Fedor A.; Karpov, Gleb O.; Nechaev, Mikhail S.; Asachenko, Andrey F.; Topchiy, Maxim A.; Melnikova, Elizaveta K.; Nelyubina, Yulia V.; Gribanov, Pavel S.; Bermeshev, Maxim V.
Polymerization of 5-Alkylidene-2-norbornenes with Highly Active Pd‒N-Heterocyclic Carbene Complex Catalysts: Catalyst Structure‒Activity Relationships
ACS Catalysis, 2020, 1663-1678
4517305 CIFC70 H63 B F24 N2 PdP -112.7466; 13.1407; 21.5974
77.667; 83.865; 74.979		3408.2Bermesheva, Evgeniya V.; Wozniak, Alyona I.; Andreyanov, Fedor A.; Karpov, Gleb O.; Nechaev, Mikhail S.; Asachenko, Andrey F.; Topchiy, Maxim A.; Melnikova, Elizaveta K.; Nelyubina, Yulia V.; Gribanov, Pavel S.; Bermeshev, Maxim V.
Polymerization of 5-Alkylidene-2-norbornenes with Highly Active Pd‒N-Heterocyclic Carbene Complex Catalysts: Catalyst Structure‒Activity Relationships
ACS Catalysis, 2020, 1663-1678
4517310 CIFC18 H20 N2P 1 21/c 19.2067; 5.9745; 24.769
90; 91.977; 90		1361.6Padhi, Birakishore; Kang, Geunhee; Kim, Eunmin; Ha, Jeongmin; Kim, Hyun Tae; Lim, Jeewoo; Joo, Jung Min
Pd-Catalyzed C‒H Annulation of Five-Membered Heteroaryl Halides with Norbornene Derivatives
ACS Catalysis, 2020, 1792-1798
4517319 CIFC18 H18 OP 1 21/c 111.5972; 9.6059; 13.0289
90; 107.205; 90		1386.49Jiang, Cheng; Lu, Hong; Xu, Wen-Hua; Wu, Jianing; Yu, Tian-Yang; Xu, Peng-Fei; Wei, Hao
Ni-Catalyzed 1,2-Acyl Migration Reactions Triggered by C‒C Bond Activation of Ketones
ACS Catalysis, 2020, 1947-1953
4517320 CIFC22 H21 N O3P 1 21/c 111.3444; 16.6403; 10.0554
90; 103.695; 90		1844.23Jiang, Cheng; Lu, Hong; Xu, Wen-Hua; Wu, Jianing; Yu, Tian-Yang; Xu, Peng-Fei; Wei, Hao
Ni-Catalyzed 1,2-Acyl Migration Reactions Triggered by C‒C Bond Activation of Ketones
ACS Catalysis, 2020, 1947-1953
4517322 CIFC36 H42 Fe N4 O6P b c a12.5702; 16.2085; 33.5599
90; 90; 90		6837.6Coufourier, Sébastien; Gaignard Gaillard, Quentin; Lohier, Jean-François; Poater, Albert; Gaillard, Sylvain; Renaud, Jean-Luc
Hydrogenation of CO2, Hydrogenocarbonate, and Carbonate to Formate in Water using Phosphine Free Bifunctional Iron Complexes
ACS Catalysis, 2020, 2108-2116
4517323 CIFC34 H38.5 Fe N4 O6.25P b c a12.3781; 16.2241; 31.858
90; 90; 90		6397.8Coufourier, Sébastien; Gaignard Gaillard, Quentin; Lohier, Jean-François; Poater, Albert; Gaillard, Sylvain; Renaud, Jean-Luc
Hydrogenation of CO2, Hydrogenocarbonate, and Carbonate to Formate in Water using Phosphine Free Bifunctional Iron Complexes
ACS Catalysis, 2020, 2108-2116
4517324 CIFC43 H10 F20 N4 Ni O2I -4 2 d15.3766; 15.3766; 15.4761
90; 90; 90		3659.17Wu, Zhuo-Yan; Xue, Haozong; Wang, Teng; Guo, Yanru; Meng, Yin-Shan; Li, Xingguo; Zheng, Jie; Brückner, Christian; Rao, Guodong; Britt, R. David; Zhang, Jun-Long
Mimicking of Tunichlorin: Deciphering the Importance of a β-Hydroxyl Substituent on Boosting the Hydrogen Evolution Reaction
ACS Catalysis, 2020, 2177-2188
4517325 CIFC43 H8 F20 N4 Ni O2I -4 2 d15.4016; 15.4016; 15.4334
90; 90; 90		3660.95Wu, Zhuo-Yan; Xue, Haozong; Wang, Teng; Guo, Yanru; Meng, Yin-Shan; Li, Xingguo; Zheng, Jie; Brückner, Christian; Rao, Guodong; Britt, R. David; Zhang, Jun-Long
Mimicking of Tunichlorin: Deciphering the Importance of a β-Hydroxyl Substituent on Boosting the Hydrogen Evolution Reaction
ACS Catalysis, 2020, 2177-2188
4517326 CIFC16 H18 Br2 N2 Ni O SP -18.379; 9.2459; 12.5657
80.0558; 75.674; 72.1841		893Yanagi, Tomoyuki; Somerville, Rosie J.; Nogi, Keisuke; Martin, Ruben; Yorimitsu, Hideki
Ni-Catalyzed Carboxylation of C(sp2)‒S Bonds with CO2: Evidence for the Multifaceted Role of Zn
ACS Catalysis, 2020, 2117-2123
4517327 CIFC28 H24 Br N4 NiP b c a12.3683; 11.2848; 32.6128
90; 90; 90		4551.9Yanagi, Tomoyuki; Somerville, Rosie J.; Nogi, Keisuke; Martin, Ruben; Yorimitsu, Hideki
Ni-Catalyzed Carboxylation of C(sp2)‒S Bonds with CO2: Evidence for the Multifaceted Role of Zn
ACS Catalysis, 2020, 2117-2123
4517328 CIFC57 H60 B F24 P2 RhC 1 2 118.1357; 18.1424; 17.9779
90; 90.1029; 90		5915.2Martínez-Martínez, Antonio J.; Royle, Cameron G.; Furfari, Samantha K.; Suriye, Kongkiat; Weller, Andrew S.
Solid‒State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization
ACS Catalysis, 2020, 1984-1992
4517329 CIFC56 H56 B F26 P2 RhP c c n35.55; 17.7103; 18.7565
90; 90; 90		11809.1Martínez-Martínez, Antonio J.; Royle, Cameron G.; Furfari, Samantha K.; Suriye, Kongkiat; Weller, Andrew S.
Solid‒State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization
ACS Catalysis, 2020, 1984-1992
4517330 CIFC54 H60 B F24 P2 RhP 1 21/c 113.8945; 17.8193; 23.5243
90; 96.457; 90		5787.44Martínez-Martínez, Antonio J.; Royle, Cameron G.; Furfari, Samantha K.; Suriye, Kongkiat; Weller, Andrew S.
Solid‒State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization
ACS Catalysis, 2020, 1984-1992
4517331 CIFC54 H58 B F24 P2 RhP 1 2/n 117.59335; 18.77356; 35.33268
90; 91.6093; 90		11665.4Martínez-Martínez, Antonio J.; Royle, Cameron G.; Furfari, Samantha K.; Suriye, Kongkiat; Weller, Andrew S.
Solid‒State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization
ACS Catalysis, 2020, 1984-1992
4517332 CIFC101 H106 B2 Cl2 F48 P4 Rh2P 21 21 224.0564; 18.6694; 12.3508
90; 90; 90		5546.97Martínez-Martínez, Antonio J.; Royle, Cameron G.; Furfari, Samantha K.; Suriye, Kongkiat; Weller, Andrew S.
Solid‒State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization
ACS Catalysis, 2020, 1984-1992
4517333 CIFC50 H53.94 B F24 P2 RhP -113.4962; 15.0316; 15.0479
86.52; 82.231; 64.562		2731.48Martínez-Martínez, Antonio J.; Royle, Cameron G.; Furfari, Samantha K.; Suriye, Kongkiat; Weller, Andrew S.
Solid‒State Molecular Organometallic Catalysis in Gas/Solid Flow (Flow-SMOM) as Demonstrated by Efficient Room Temperature and Pressure 1-Butene Isomerization
ACS Catalysis, 2020, 1984-1992
4517334 CIFC44 H71 Cl F2 O P2 PdP -112.0444; 14.0441; 25.7109
93.9; 97.182; 92.677		4298.3Reina, Antonio; Krachko, Tetiana; Onida, Killian; Bouyssi, Didier; Jeanneau, Erwann; Monteiro, Nuno; Amgoune, Abderrahmane
Development and Mechanistic Investigations of a Base-Free Suzuki‒Miyaura Cross-Coupling of α,α-Difluoroacetamides via C‒N Bond Cleavage
ACS Catalysis, 2020, 2189-2197
4517335 CIFC53 H76.5 F4 N0.5 O3 P2 PdP -113.4397; 18.3716; 21.7868
81.169; 89.195; 73.803		5102.3Reina, Antonio; Krachko, Tetiana; Onida, Killian; Bouyssi, Didier; Jeanneau, Erwann; Monteiro, Nuno; Amgoune, Abderrahmane
Development and Mechanistic Investigations of a Base-Free Suzuki‒Miyaura Cross-Coupling of α,α-Difluoroacetamides via C‒N Bond Cleavage
ACS Catalysis, 2020, 2189-2197
4517336 CIFC28 H39 Ag F9 O PP 1 21/c 19.8179; 14.1041; 20.6209
90; 99.978; 90		2812.24Panigrahi, Adyasha; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Ag/Pd Cocatalyzed Direct Arylation of Fluoroarene Derivatives with Aryl Bromides
ACS Catalysis, 2020, 2100-2107
4517337 CIFC104 H172 Ag4 Br4 Cl6 P4C 1 2/c 127.5364; 15.9525; 25.9141
90; 112.975; 90		10480.4Panigrahi, Adyasha; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Ag/Pd Cocatalyzed Direct Arylation of Fluoroarene Derivatives with Aryl Bromides
ACS Catalysis, 2020, 2100-2107
4517338 CIFC53 H54 Cl2 N2 O3 P RuP -19.051; 12.257; 23.016
99.247; 100.894; 94.83		2457Eivgi, Or; Vaisman, Anna; Nechmad, Noy B.; Baranov, Mark; Lemcoff, N. Gabriel
Latent Ruthenium Benzylidene Phosphite Complexes for Visible-Light-Induced Olefin Metathesis
ACS Catalysis, 2020, 2033-2038
4517339 CIFC61 H62 Cl2 N5 O9 P RuP 1 21/c 114.3812; 16.1503; 26.0144
90; 100.411; 90		5942.65Eivgi, Or; Vaisman, Anna; Nechmad, Noy B.; Baranov, Mark; Lemcoff, N. Gabriel
Latent Ruthenium Benzylidene Phosphite Complexes for Visible-Light-Induced Olefin Metathesis
ACS Catalysis, 2020, 2033-2038
4517340 CIFC25 H22 N O7 PP 15.7494; 9.6543; 10.4417
100.704; 91.306; 94.062		567.68Trost, Barry M.; Shinde, Anand H.; Wang, Youliang; Zuo, Zhijun; Min, Chang
Palladium-Catalyzed Regio-, Enantio-, and Diastereoselective Asymmetric [3 + 2] Cycloaddition Reactions: Synthesis of Chiral Cyclopentyl Phosphonates
ACS Catalysis, 2020, 1969-1975
4517359 CIFC12 H12 Cl N O2P 21 21 218.269; 9.9012; 13.5986
90; 90; 90		1113.36Ren, Xinkun; Chandgude, Ajay L.; Fasan, Rudi
Highly Stereoselective Synthesis of Fused Cyclopropane-γ-Lactams via Biocatalytic Iron-Catalyzed Intramolecular Cyclopropanation
ACS Catalysis, 2020, 2308-2313
4517360 CIFC12 H13 N OP 1 21 15.6803; 9.2798; 9.3092
90; 90.739; 90		490.67Ren, Xinkun; Chandgude, Ajay L.; Fasan, Rudi
Highly Stereoselective Synthesis of Fused Cyclopropane-γ-Lactams via Biocatalytic Iron-Catalyzed Intramolecular Cyclopropanation
ACS Catalysis, 2020, 2308-2313
4517361 CIFC30 H35 I N O5 PP 21 21 219.1592; 11.449; 27.96
90; 90; 90		2932Yang, Guo-Hui; Zheng, Hanliang; Li, Xin; Cheng, Jin-Pei
Asymmetric Synthesis of Axially Chiral Phosphamides via Atroposelective N-Allylic Alkylation
ACS Catalysis, 2020, 2324-2333
4517365 CIFC37 H36 Fe N O P SP 1 21 110.9997; 10.5162; 14.1245
90; 106.586; 90		1565.87Ji, Wangqin; Wu, Hai-Hong; Zhang, Junliang
Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki‒Miyaura Cross-coupling
ACS Catalysis, 2020, 10, 1548-1554
4517366 CIFC32 H23 O PP 1 21 19.5052; 11.4481; 11.0312
90; 93.722; 90		1197.84Ji, Wangqin; Wu, Hai-Hong; Zhang, Junliang
Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki‒Miyaura Cross-coupling
ACS Catalysis, 2020, 10, 1548-1554
4517367 CIFC38 H37 Cl3 Fe N O2 P SP 1 21 110.3729; 11.5112; 15.6134
90; 106.888; 90		1783.91Ji, Wangqin; Wu, Hai-Hong; Zhang, Junliang
Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki‒Miyaura Cross-coupling
ACS Catalysis, 2020, 10, 1548-1554
4517368 CIFC27 H24 F3 N O6 SP b c a13.5499; 15.2341; 24.4346
90; 90; 90		5043.8Uno, Hiroto; Imai, Takanori; Harada, Kyosuke; Shibata, Norio
Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
ACS Catalysis, 2020, 10, 1454-1459
4517369 CIFC16 H12 F3 N O4 SP -18.4561; 8.5762; 12.4229
110.047; 111.941; 90.1156		776.24Uno, Hiroto; Imai, Takanori; Harada, Kyosuke; Shibata, Norio
Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
ACS Catalysis, 2020, 10, 1454-1459
4517370 CIFC29 H29 F4 N O6 SP -19.4313; 11.4154; 13.8509
84.332; 74.645; 85.308		1428.55Uno, Hiroto; Imai, Takanori; Harada, Kyosuke; Shibata, Norio
Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
ACS Catalysis, 2020, 10, 1454-1459
4517371 CIFC75 H89.83 Co Ga N7 O0 P5P -112.177; 18.604; 20.729
111.648; 101.917; 95.562		4192.6Vollmer, Matthew V.; Ye, Jingyun; Linehan, John C.; Graziano, Brendan J.; Preston, Andrew; Wiedner, Eric S.; Lu, Connie C.
Cobalt-Group 13 Complexes Catalyze CO2 Hydrogenation via a Co(−I)/Co(I) Redox Cycle
ACS Catalysis, 2020, 2459-2470
4517372 CIFC79 H98 Co In N7 O P5P -112.2163; 18.704; 20.45
112.181; 100.878; 95.913		4170.4Vollmer, Matthew V.; Ye, Jingyun; Linehan, John C.; Graziano, Brendan J.; Preston, Andrew; Wiedner, Eric S.; Lu, Connie C.
Cobalt-Group 13 Complexes Catalyze CO2 Hydrogenation via a Co(−I)/Co(I) Redox Cycle
ACS Catalysis, 2020, 2459-2470
4517373 CIFC42 H64 Al Co N4 P3P 1 21 112.329; 27.522; 12.652
90; 105.97; 90		4127Vollmer, Matthew V.; Ye, Jingyun; Linehan, John C.; Graziano, Brendan J.; Preston, Andrew; Wiedner, Eric S.; Lu, Connie C.
Cobalt-Group 13 Complexes Catalyze CO2 Hydrogenation via a Co(−I)/Co(I) Redox Cycle
ACS Catalysis, 2020, 2459-2470
4517374 CIFC82 H132 Co2 Ga2 N8 O P6P -112.4071; 19.343; 19.588
110.472; 97.544; 101.928		4201.3Vollmer, Matthew V.; Ye, Jingyun; Linehan, John C.; Graziano, Brendan J.; Preston, Andrew; Wiedner, Eric S.; Lu, Connie C.
Cobalt-Group 13 Complexes Catalyze CO2 Hydrogenation via a Co(−I)/Co(I) Redox Cycle
ACS Catalysis, 2020, 2459-2470
4517382 CIFC20 H23 F3 O SiP 1 21/c 113.3534; 19.2873; 14.681
90; 94.714; 90		3768.32Iwamoto, Hiroaki; Hayashi, Yuta; Ozawa, Yu; Ito, Hajime
Silyl-Group-Directed Linear-Selective Allylation of Carbonyl Compounds with Trisubstituted Allylboronates Using a Copper(I) Catalyst
ACS Catalysis, 2020, 2471
4517383 CIFC31 H26 Br2 O4P 21 21 219.6286; 10.7523; 25.4679
90; 90; 90		2636.68Liu, Na; Zhu, Wanjiang; Yao, Jian; Yin, Long; Lu, Tao; Dou, Xiaowei
Catalyst-Controlled Chemodivergent Synthesis of Spirochromans from Diarylideneacetones and Organoboronic Acids
ACS Catalysis, 2020, 10, 2596-2602
4517384 CIFC24 H20 O3P -17.712; 10.915; 12.298
114.959; 99.228; 100.157		891.3Liu, Na; Zhu, Wanjiang; Yao, Jian; Yin, Long; Lu, Tao; Dou, Xiaowei
Catalyst-Controlled Chemodivergent Synthesis of Spirochromans from Diarylideneacetones and Organoboronic Acids
ACS Catalysis, 2020, 10, 2596-2602
4517385 CIFC53 H42 O2 P2P 1 21 18.89; 21.1643; 11.0358
90; 104.694; 90		2008.48Liu, Na; Zhu, Wanjiang; Yao, Jian; Yin, Long; Lu, Tao; Dou, Xiaowei
Catalyst-Controlled Chemodivergent Synthesis of Spirochromans from Diarylideneacetones and Organoboronic Acids
ACS Catalysis, 2020, 10, 2596-2602
4517389 CIFC16 H14 N4 OC 1 2/c 126.451; 7.875; 13.315
90; 94.256; 90		2765.9Ohmatsu, Kohsuke; Suzuki, Ryuhei; Furukawa, Yukino; Sato, Makoto; Ooi, Takashi
Zwitterionic 1,2,3-Triazolium Amidate as a Catalyst for Photoinduced Hydrogen-Atom Transfer Radical Alkylation
ACS Catalysis, 2020, 2627
4517390 CIFC16 H15 Cl N4 OC 1 2/c 112.465; 11.018; 22.209
90; 92.386; 90		3048Ohmatsu, Kohsuke; Suzuki, Ryuhei; Furukawa, Yukino; Sato, Makoto; Ooi, Takashi
Zwitterionic 1,2,3-Triazolium Amidate as a Catalyst for Photoinduced Hydrogen-Atom Transfer Radical Alkylation
ACS Catalysis, 2020, 2627
4517391 CIFC15 H14 Br Mn N2 O3 SP -16.62; 7.8565; 17.0496
83.308; 86.928; 73.022		842.15Jana, Akash; Das, Kuhali; Kundu, Abhishek; Thorve, Pradip Ramdas; Adhikari, Debashis; Maji, Biplab
A Phosphine-Free Manganese Catalyst Enables Stereoselective Synthesis of (1 + n)-Membered Cycloalkanes from Methyl Ketones and 1,n-Diols
ACS Catalysis, 2020, 2615
4517392 CIFC14 H12 Br Mn N2 O3 SP -17.5394; 9.7257; 11.6722
108.97; 99.234; 101.738		768.37Jana, Akash; Das, Kuhali; Kundu, Abhishek; Thorve, Pradip Ramdas; Adhikari, Debashis; Maji, Biplab
A Phosphine-Free Manganese Catalyst Enables Stereoselective Synthesis of (1 + n)-Membered Cycloalkanes from Methyl Ketones and 1,n-Diols
ACS Catalysis, 2020, 2615
4517394 CIFC24 H25 N O3 SP 1 21 114.1788; 8.3217; 17.7545
90; 107.843; 90		1994.1Chin, Kek Foo; Ye, Xinyi; Li, Yongxin; Lee, Richmond; Kabylda, Adil M.; Leow, Dasheng; Zhang, Xin; Xia Ang, Esther Cai; Tan, Choon-Hong
Bisguanidinium-Catalyzed Epoxidation of Allylic and Homoallylic Amines under Phase Transfer Conditions
ACS Catalysis, 2020, 2684
4517395 CIFC100 H138 N8 O13 W2P 110.9657; 14.7551; 16.165
102.59; 97.3713; 101.976		2455.5Chin, Kek Foo; Ye, Xinyi; Li, Yongxin; Lee, Richmond; Kabylda, Adil M.; Leow, Dasheng; Zhang, Xin; Xia Ang, Esther Cai; Tan, Choon-Hong
Bisguanidinium-Catalyzed Epoxidation of Allylic and Homoallylic Amines under Phase Transfer Conditions
ACS Catalysis, 2020, 2684
4517422 CIFC26 H25 F O6P 1 21/n 115.631; 9.89045; 15.9579
90; 113.655; 90		2259.77Liu, Jian; Vasamsetty, Laxmaiah; Anwar, Muhammad; Yang, Shuang; Xu, Weici; Liu, Jinggong; Nagaraju, Sakkani; Fang, Xinqiang
Organocatalyzed Kinetic Resolution of α-Functionalized Ketones: The Malonate Unit Leads the Way
ACS Catalysis, 2020, 2882-2893
4517423 CIFC23 H24 O5P -18.4862; 11.6076; 21.8095
81.344; 79.625; 70.309		1980.25Liu, Jian; Vasamsetty, Laxmaiah; Anwar, Muhammad; Yang, Shuang; Xu, Weici; Liu, Jinggong; Nagaraju, Sakkani; Fang, Xinqiang
Organocatalyzed Kinetic Resolution of α-Functionalized Ketones: The Malonate Unit Leads the Way
ACS Catalysis, 2020, 2882-2893
4517424 CIFC23 H24 O4P 1 21 110.4234; 6.0234; 15.0661
90; 90.369; 90		945.895Liu, Jian; Vasamsetty, Laxmaiah; Anwar, Muhammad; Yang, Shuang; Xu, Weici; Liu, Jinggong; Nagaraju, Sakkani; Fang, Xinqiang
Organocatalyzed Kinetic Resolution of α-Functionalized Ketones: The Malonate Unit Leads the Way
ACS Catalysis, 2020, 2882-2893
4517425 CIFC13 H15 N O2P 43 21 27.97537; 7.97537; 34.7796
90; 90; 90		2212.21Roque, Jose B.; Kuroda, Yusuke; Jurczyk, Justin; Xu, Li-Ping; Ham, Jin Su; Göttemann, Lucas T.; Roberts, Charis A.; Adpressa, Donovon; Saurí, Josep; Joyce, Leo A.; Musaev, Djamaladdin G.; Yeung, Charles S.; Sarpong, Richmond
C‒C Cleavage Approach to C‒H Functionalization of Saturated Aza-Cycles
ACS Catalysis, 2020, 2929-2941
4517426 CIFC13 H15 N O2P 41 21 27.97639; 7.97639; 34.7863
90; 90; 90		2213.2Roque, Jose B.; Kuroda, Yusuke; Jurczyk, Justin; Xu, Li-Ping; Ham, Jin Su; Göttemann, Lucas T.; Roberts, Charis A.; Adpressa, Donovon; Saurí, Josep; Joyce, Leo A.; Musaev, Djamaladdin G.; Yeung, Charles S.; Sarpong, Richmond
C‒C Cleavage Approach to C‒H Functionalization of Saturated Aza-Cycles
ACS Catalysis, 2020, 2929-2941
4517427 CIFC13 H15 N O2P 1 21/c 18.6719; 15.1388; 9.5746
90; 116.469; 90		1125.21Roque, Jose B.; Kuroda, Yusuke; Jurczyk, Justin; Xu, Li-Ping; Ham, Jin Su; Göttemann, Lucas T.; Roberts, Charis A.; Adpressa, Donovon; Saurí, Josep; Joyce, Leo A.; Musaev, Djamaladdin G.; Yeung, Charles S.; Sarpong, Richmond
C‒C Cleavage Approach to C‒H Functionalization of Saturated Aza-Cycles
ACS Catalysis, 2020, 2929-2941
4517428 CIFC105 H64 F45 P5 Ru2P -114.853; 18.958; 22.386
105.048; 92.216; 95.751		6043Estes, Deven P.; Leutzsch, Markus; Schubert, Lukas; Bordet, Alexis; Leitner, Walter
Effect of Ligand Electronics on the Reversible Catalytic Hydrogenation of CO2 to Formic Acid Using Ruthenium Polyhydride Complexes: A Thermodynamic and Kinetic Study
ACS Catalysis, 2020, 2990-2998
4517429 CIFC20 H17 Br N OP 1 21 15.166; 13.624; 24.035
90; 95.88; 90		1682.72Lemay, Jean-Christian; Dong, Yi; Albert, Vincent; Inouye, Monica; Groves, Michael N.; Boukouvalas, John; McBreen, Peter H.
Relative Abundances of Surface Diastereomeric Complexes Formed by Two Chiral Modifiers That Differ by a Methyl Group
ACS Catalysis, 2020, 3034-3041
4517431 CIFC37 H51 Cl F3 N7 O3 S ZnP 1 21/c 112.4934; 24.7612; 13.0442
90; 95.7511; 90		4014.93Drummond, Michael J.; Miller, Tabitha J.; Ford, Courtney L.; Fout, Alison R.
Catalytic Perchlorate Reduction Using Iron: Mechanistic Insights and Improved Catalyst Turnover
ACS Catalysis, 2020, 3175-3182
4517435 CIFC94 H88 B Br2 Co F24 N6 O8 S2P 21 21 2118.4403; 25.068; 25.5947
90; 90; 90		11831.4Kabes, Connor Q.; Maximuck, William J.; Ghosh, Subrata K.; Kumar, Anil; Bhuvanesh, Nattamai; Gladysz, John A.
Chiral Tricationic Tris(1,2-diphenylethylenediamine) Cobalt(III) Hydrogen Bond Donor Catalysts with Defined Carbon/Metal Configurations; Matched/Mismatched Effects upon Enantioselectivities with Enantiomeric Chiral Counter Anions
ACS Catalysis, 2020, 3249-3263
4517436 CIFC18 H23 B F3 N O4P 21 21 216.2697; 10.8812; 27.9823
90; 90; 90		1909Fan, Dongyang; Zhang, Jian; Hu, Yanhua; Zhang, Zhenfeng; Gridnev, Ilya D.; Zhang, Wanbin
Asymmetric Hydrogenation of α-Boryl Enamides Enabled by Nonbonding Interactions
ACS Catalysis, 2020, 3232-3240
4517437 CIFC14 H15 N O SP 1 21 18.3309; 6.6556; 10.916
90; 96.337; 90		601.6Kim, Alexia N.; Ngamnithiporn, Aurapat; Welin, Eric R.; Daiger, Martin T.; Grünanger, Christian U.; Bartberger, Michael D.; Virgil, Scott C.; Stoltz, Brian M.
Iridium-Catalyzed Enantioselective and Diastereoselective Hydrogenation of 1,3-Disubstituted Isoquinolines
ACS Catalysis, 2020, 3241-3248
4517439 CIFC19 H14 O3P 1 21/n 111.3197; 15.6008; 16.353
90; 102.492; 90		2819.51Rajesh, U. Chinna; Losovyj, Yaroslav; Chen, Chun-Hsing; Zaleski, Jeffrey M.
Designing Synergistic Nanocatalysts for Multiple Substrate Activation: Interlattice Ag‒Fe3O4 Hybrid Materials for CO2-Inserted Lactones
ACS Catalysis, 2020, 3349-3359
4517446 CIFC56 H99 B3 Ir N2 O7 Si2P -114.4073; 14.9016; 16.512
104.953; 111.191; 99.539		3058.53Larsen, Matthew A.; Oeschger, Raphael J.; Hartwig, John F.
Effect of Ligand Structure on the Electron Density and Activity of Iridium Catalysts for the Borylation of Alkanes
ACS Catalysis, 2020, 3415-3424
4517447 CIFC43 H48 Cl2 N6 O12 Pd2 S2P -110.69; 11.3617; 11.7062
62.2925; 85.46; 73.2316		1202.7Cendón, Borja; Font, Marc; Mascareñas, José L.; Gul\?ías, Moisés
Palladium-Catalyzed Formal (4+2) Cycloaddition between Alkyl Amides and Dienes Initiated by the Activation of C(sp3)‒H Bonds
ACS Catalysis, 2020, 3425-3430
4517448 CIFC21 H22 N2 O5 SC 1 2/c 122.973; 6.9135; 25.839
90; 106.258; 90		3939.7Cendón, Borja; Font, Marc; Mascareñas, José L.; Gul\?ías, Moisés
Palladium-Catalyzed Formal (4+2) Cycloaddition between Alkyl Amides and Dienes Initiated by the Activation of C(sp3)‒H Bonds
ACS Catalysis, 2020, 3425-3430
4517449 CIFC21 H22 N4 O5 Pd SP -16.5642; 18.183; 18.879
89.513; 86.524; 85.366		2241.8Cendón, Borja; Font, Marc; Mascareñas, José L.; Gul\?ías, Moisés
Palladium-Catalyzed Formal (4+2) Cycloaddition between Alkyl Amides and Dienes Initiated by the Activation of C(sp3)‒H Bonds
ACS Catalysis, 2020, 3425-3430
4517450 CIFC25 H25 Cl2 N3 O PdP -19.0308; 11.8072; 11.9867
97.855; 105.716; 105.33		1156.3Cendón, Borja; Font, Marc; Mascareñas, José L.; Gul\?ías, Moisés
Palladium-Catalyzed Formal (4+2) Cycloaddition between Alkyl Amides and Dienes Initiated by the Activation of C(sp3)‒H Bonds
ACS Catalysis, 2020, 3425-3430
4517455 CIFC15 H15 Br O4P 21 21 2110.2207; 11.4378; 12.3943
90; 90; 90		1448.9Chen, Jun-Bo; Xu, Man; Zhang, Jun-Qi; Sun, Bing-Bing; Hu, Jia-Ming; Yu, Jie-Qiang; Wang, Xing-Wang; Xia, Yuanzhi; Wang, Zheng
Modular Chiral Bisoxalamide‒Copper-Catalyzed Asymmetric Oxo-Diels‒Alder Reaction: Carbonyl Coordination for High Enantio- and Diastereocontrols
ACS Catalysis, 2020, 3556
4517456 CIFC61 H86 Cl2 N8 O8P 1 21 112.5285; 16.597; 14.9439
90; 93.876; 90		3100.26Chen, Jun-Bo; Xu, Man; Zhang, Jun-Qi; Sun, Bing-Bing; Hu, Jia-Ming; Yu, Jie-Qiang; Wang, Xing-Wang; Xia, Yuanzhi; Wang, Zheng
Modular Chiral Bisoxalamide‒Copper-Catalyzed Asymmetric Oxo-Diels‒Alder Reaction: Carbonyl Coordination for High Enantio- and Diastereocontrols
ACS Catalysis, 2020, 3556
4517457 CIFC20 H26P 1 21/c 121.059; 5.9199; 13.2305
90; 99.636; 90		1626.1Mato, Mauro; García-Morales, Cristina; Echavarren, Antonio M.
Synthesis of Trienes by Rhodium-Catalyzed Assembly and Disassembly of Non-Acceptor Cyclopropanes
ACS Catalysis, 2020, 3564
4517458 CIFC24 H25 N O4P 1 21 125.487; 9.845; 26.272
90; 110.11; 90		6190Feng, Jiaxu; Huang, You
Phosphine-Catalyzed Remote 1,7-Addition for Synthesis of Diene Carboxylates
ACS Catalysis, 2020, 3541
4517459 CIFC22 H23 N O5P 1 21/c 113.199; 17.845; 8.5547
90; 98.41; 90		1993.3Feng, Jiaxu; Huang, You
Phosphine-Catalyzed Remote 1,7-Addition for Synthesis of Diene Carboxylates
ACS Catalysis, 2020, 3541
4517461 CIFC24 H17 F2 N O2P -19.3619; 10.2474; 11.0622
73.881; 65.949; 83.137		931Luo, Kaixiu; Mao, Shuai; He, Kun; Yu, Xianglin; Pan, Junhong; Lin, Jun; Shao, Zhihui; Jin, Yi
Highly Regioselective Synthesis of Multisubstituted Pyrroles via Ag-Catalyzed [4+1C]insert Cascade
ACS Catalysis, 2020, 3733
4517462 CIFC24 H21 N O3P 1 21/c 117.623; 8.753; 12.749
90; 99.38; 90		1940.3Luo, Kaixiu; Mao, Shuai; He, Kun; Yu, Xianglin; Pan, Junhong; Lin, Jun; Shao, Zhihui; Jin, Yi
Highly Regioselective Synthesis of Multisubstituted Pyrroles via Ag-Catalyzed [4+1C]insert Cascade
ACS Catalysis, 2020, 3733
4517476 CIFC23 H33 Br OP 1 21/c 115.7036; 13.5822; 9.9735
90; 97.264; 90		2110.2Takahashi, Toshifumi; Kurahashi, Takuya; Matsubara, Seijiro
Nickel-Catalyzed Intermolecular Carbobromination of Alkynes
ACS Catalysis, 2020, 10, 3773-3777
4517477 CIFC20 H21 Br OP -19.0497; 11.0964; 17.4034
80.749; 86.494; 89.645		1721.66Takahashi, Toshifumi; Kurahashi, Takuya; Matsubara, Seijiro
Nickel-Catalyzed Intermolecular Carbobromination of Alkynes
ACS Catalysis, 2020, 10, 3773-3777
4517478 CIFC93 H27 F30 Fe2 N13P -114.7609; 16.1284; 20.1218
73.575; 89.177; 66.103		4173.5Sinha, Woormileela; Mahammed, Atif; Fridman, Natalia; Gross, Zeev
Water Oxidation Catalysis by Mono- and Binuclear Iron Corroles
ACS Catalysis, 2020, 3764
4517479 CIFC51 H27 Co F6 N6C 1 2/c 136.007; 12.107; 18.503
90; 90.893; 90		8065Sinha, Woormileela; Mahammed, Atif; Fridman, Natalia; Gross, Zeev
Water Oxidation Catalysis by Mono- and Binuclear Iron Corroles
ACS Catalysis, 2020, 3764
4517480 CIFC156 H92 Fe4 N16 O2P -115.257; 17.202; 25.355
83.153; 79.357; 71.301		6181.9Sinha, Woormileela; Mahammed, Atif; Fridman, Natalia; Gross, Zeev
Water Oxidation Catalysis by Mono- and Binuclear Iron Corroles
ACS Catalysis, 2020, 3764
4517481 CIFC21 H24 N4 OP -19.6626; 10.1376; 11.1294
97.909; 105.084; 114.113		923.2Tan, Jin-Fay; Bormann, Carl Thomas; Severin, Kay; Cramer, Nicolai
Alkynyl Triazenes as Fluoroalkyne Surrogates: Regioselective Access to 4-Fluoro-2-pyridones by a Rh(III)-Catalyzed C‒H Activation‒Lossen Rearrangement‒Wallach Reaction
ACS Catalysis, 2020, 10, 3790-3796
4517482 CIFC18 H14 F N OP -110.2367; 11.4102; 13.7829
109.851; 92.169; 112.466		1373.04Tan, Jin-Fay; Bormann, Carl Thomas; Severin, Kay; Cramer, Nicolai
Alkynyl Triazenes as Fluoroalkyne Surrogates: Regioselective Access to 4-Fluoro-2-pyridones by a Rh(III)-Catalyzed C‒H Activation‒Lossen Rearrangement‒Wallach Reaction
ACS Catalysis, 2020, 10, 3790-3796
4517483 CIFC61 H58 Co O5 P3P 1 21/n 115.294; 15.9747; 22.8893
90; 109.52; 90		5270.8Chen, Jia-Feng; Li, Changkun
Cobalt-Catalyzed gem-Cross-Dimerization of Terminal Alkynes
ACS Catalysis, 2020, 3881
4517484 CIFC57 H43 Co O6 P3P 21 21 2111.1714; 19.5049; 22.2984
90; 90; 90		4858.8Chen, Jia-Feng; Li, Changkun
Cobalt-Catalyzed gem-Cross-Dimerization of Terminal Alkynes
ACS Catalysis, 2020, 3881
4517495 CIFC27 H34 O3P 21 21 217.447; 14.6245; 19.8929
90; 90; 90		2166.51Zhuo, Junming; Zhang, Yong; Li, Zijian; Li, Chao
Nickel-Catalyzed Direct Acylation of Aryl and Alkyl Bromides with Acylimidazoles
ACS Catalysis, 2020, 10, 3895-3903
4517496 CIFC39 H54 O5C 1 2 112.2802; 7.2838; 37.4807
90; 90.803; 90		3352.2Zhuo, Junming; Zhang, Yong; Li, Zijian; Li, Chao
Nickel-Catalyzed Direct Acylation of Aryl and Alkyl Bromides with Acylimidazoles
ACS Catalysis, 2020, 10, 3895-3903
4517497 CIFC22 H32 O4P 1 21 15.9236; 13.586; 12.496
90; 100.7; 90		988.2Zhuo, Junming; Zhang, Yong; Li, Zijian; Li, Chao
Nickel-Catalyzed Direct Acylation of Aryl and Alkyl Bromides with Acylimidazoles
ACS Catalysis, 2020, 10, 3895-3903
4517502 CIFC20 H37 Cl3 N P PdC 1 2/c 117.846; 15.0741; 18.2288
90; 94.492; 90		4888.71Hu, Huaiyuan; Gilliam, Ashley M.; Qu, Fengrui; Shaughnessy, Kevin H.
Enolizable Ketones as Activators of Palladium(II) Precatalysts in Amine Arylation Reactions
ACS Catalysis, 2020, 10, 4127-4135
4517513 CIFC86 H64 B Co F24 P4P 1 21/c 116.6366; 12.7954; 37.4749
90; 101.172; 90		7826.2Gray, Montgomery; Hines, Michael T.; Parsutkar, Mahesh M.; Wahlstrom, A. J.; Brunelli, Nicholas A.; RajanBabu, T. V.
Mechanism of Cobalt-Catalyzed Heterodimerization of Acrylates and 1,3-Dienes. A Potential Role of Cationic Cobalt(I) Intermediates
ACS Catalysis, 2020, 10, 4337-4348
4517514 CIFC58 H60 Br3 Co O P4 ZnP 1 21/c 114.1589; 17.0352; 24.3773
90; 100.025; 90		5790Gray, Montgomery; Hines, Michael T.; Parsutkar, Mahesh M.; Wahlstrom, A. J.; Brunelli, Nicholas A.; RajanBabu, T. V.
Mechanism of Cobalt-Catalyzed Heterodimerization of Acrylates and 1,3-Dienes. A Potential Role of Cationic Cobalt(I) Intermediates
ACS Catalysis, 2020, 10, 4337-4348
4517519 CIFC21 H18 N2 OP 1 21/c 110.2077; 19.7705; 8.1575
90; 97.395; 90		1632.58Zhu, Cuiju; Kuniyil, Rositha; Jei, Becky B.; Ackermann, Lutz
Domino C‒H Activation/Directing Group Migration/Alkyne Annulation: Unique Selectivity by d6-Cobalt(III) Catalysts
ACS Catalysis, 2020, 10, 4444-4450
4517520 CIFC22 H20 N2 OP -19.0581; 9.9273; 10.2645
105.947; 96.819; 97.151		869.2Zhu, Cuiju; Kuniyil, Rositha; Jei, Becky B.; Ackermann, Lutz
Domino C‒H Activation/Directing Group Migration/Alkyne Annulation: Unique Selectivity by d6-Cobalt(III) Catalysts
ACS Catalysis, 2020, 10, 4444-4450
4517521 CIFC25 H20 N2 OP -18.7963; 10.354; 11.5419
110.43; 100.373; 101.27		930.16Zhu, Cuiju; Kuniyil, Rositha; Jei, Becky B.; Ackermann, Lutz
Domino C‒H Activation/Directing Group Migration/Alkyne Annulation: Unique Selectivity by d6-Cobalt(III) Catalysts
ACS Catalysis, 2020, 10, 4444-4450
4517522 CIFC39 H45 F3 N2 O5 P Rh SP 1 21 110.0207; 19.056; 10.3059
90; 105.173; 90		1899.4Xu, Wen-Bin; Ghorai, Samir; Huang, Wenyu; Li, Changkun
Rh(I)/Bisoxazolinephosphine-Catalyzed Regio- and Enantioselective Allylic Substitutions
ACS Catalysis, 2020, 4491-4496
4517523 CIFC35 H40 Cl F3 N2 O5 P Rh SP 43 21 210.9434; 10.9434; 60.442
90; 90; 90		7238.4Xu, Wen-Bin; Ghorai, Samir; Huang, Wenyu; Li, Changkun
Rh(I)/Bisoxazolinephosphine-Catalyzed Regio- and Enantioselective Allylic Substitutions
ACS Catalysis, 2020, 4491-4496
4517527 CIFC25 H19 F5 N2P 1 21 18.43; 11.6177; 10.918
90; 108.357; 90		1014.87Li, Jiuling; Zhang, Dan; Chen, Jianghui; Ma, Chaoqun; Hu, Wenhao
Enantioselective Synthesis of Fluoroalkyl-Substituted syn-Diamines by the Asymmetric gem-Difunctionalization of 2,2,2-Trifluorodiazoethane
ACS Catalysis, 2020, 4559-4565
4517528 CIFC42 H64 N Ni P2P 1 21/c 111.8848; 19.0951; 17.618
90; 105.834; 90		3846.55Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517529 CIFC40 H64 Ni P2 SP 1 21/n 111.7655; 14.098; 22.4255
90; 93.047; 90		3714.46Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517530 CIFC52 H96 Ni P4P -112.7568; 12.7744; 17.1688
73.619; 89.592; 75.811		2596.58Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517531 CIFC33 H56 Br2 Ni P2P 1 21/c 112.2203; 18.687; 15.2866
90; 99.052; 90		3447.38Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517532 CIFC13 H13 N O2 SP 1 21/n 114.4888; 5.6004; 15.206
90; 109.454; 90		1163.42Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517533 CIFC36 H61 Br Ni O P2P 1 21/n 110.5652; 22.4696; 15.3099
90; 105.292; 90		3505.82Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517534 CIFC14 H19 NP 1 21/c 110.6205; 8.92; 11.9761
90; 97.617; 90		1124.54Bismuto, Alessandro; Delcaillau, Tristan; Müller, Patrick; Morandi, Bill
Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study
ACS Catalysis, 2020, 4630-4639
4517536 CIFC22 H19 Br F3 N2 NiP -19.3825; 10.3799; 11.1183
76.894; 89.918; 73.255		1007.51Rand, Alexander W.; Yin, Hongfei; Xu, Liang; Giacoboni, Jessica; Martin-Montero, Raul; Romano, Ciro; Montgomery, John; Martin, Ruben
Dual Catalytic Platform for Enabling sp3 α C‒H Arylation and Alkylation of Benzamides
ACS Catalysis, 2020, 4671
4517537 CIFC22 H34 B2 O2P 1 21/c 115.0776; 6.6335; 21.5511
90; 102.6; 90		2103.57Docherty, Jamie H.; Nicholson, Kieran; Dominey, Andrew P.; Thomas, Stephen P.
A Boron‒Boron Double Transborylation Strategy for the Synthesis of gem-Diborylalkanes
ACS Catalysis, 2020, 4686
4517546 CIFC84 H184 N3 O37 Sb Si3 Ti W9P 1 21/n 117.7721; 28.9182; 23.5633
90; 90.112; 90		12110Solé-Daura, Albert; Zhang, Teng; Fouilloux, Hugo; Robert, Carine; Thomas, Christophe M.; Chamoreau, Lise-Marie; Carbó, Jorge J.; Proust, Anna; Guillemot, Geoffroy; Poblet, Josep M.
Catalyst Design for Alkene Epoxidation by Molecular Analogues of Heterogeneous Titanium-Silicalite Catalysts
ACS Catalysis, 2020, 4737
4517547 CIFC17 H22 O2P 1 21 115.249; 6.1775; 16.2653
90; 113.939; 90		1400.4Dai, Zhen-Yao; Nong, Zhong-Sheng; Wang, Pu-Sheng
Light-Mediated Asymmetric Aliphatic C‒H Alkylation with Hydrogen Atom Transfer Catalyst and Chiral Phosphoric Acid
ACS Catalysis, 2020, 10, 4786-4790
4517552 CIFC37 H43 Cl4 N3 O Ru SP 1 21/n 110.081; 26.6065; 14.0765
90; 105.018; 90		3646.6Segalovich-Gerendash, Gal; Rozenberg, Illya; Alassad, Nebal; Nechmad, Noy B.; Goldberg, Israel; Kozuch, Sebastian; Lemcoff, N. Gabriel
Imposing Latency in Ruthenium Sulfoxide-Chelated Benzylidenes: Expanding Opportunities for Thermal and Photoactivation in Olefin Metathesis
ACS Catalysis, 2020, 4827
4517553 CIFC42.65 H53 Ag Cl5.29 I N6 O8.35 SP 1 21/n 112.4359; 16.0865; 26.638
90; 98.824; 90		5265.9Elkoush, Tasneem; Mak, Choi L.; Paley, Daniel W.; Campbell, Michael G.
Silver(II) and Silver(III) Intermediates in Alkene Aziridination with a Dinuclear Silver(I) Nitrene Transfer Catalyst
ACS Catalysis, 2020, 4820
4517554 CIFC40 H47 Ag Cl2 N5 O8 S2P c a 2120.4684; 13.4202; 15.4089
90; 90; 90		4232.67Elkoush, Tasneem; Mak, Choi L.; Paley, Daniel W.; Campbell, Michael G.
Silver(II) and Silver(III) Intermediates in Alkene Aziridination with a Dinuclear Silver(I) Nitrene Transfer Catalyst
ACS Catalysis, 2020, 4820
4517568 CIFC17 H14 Cl I N2 O2A e a 231.3169; 13.0613; 7.9634
90; 90; 90		3257.34Sun, Han-Li; Yang, Fan; Ye, Wei-Ting; Wang, Jun-Jie; Zhu, Rong
Dual Cobalt and Photoredox Catalysis Enabled Intermolecular Oxidative Hydrofunctionalization
ACS Catalysis, 2020, 10, 4983-4989
4517571 CIFC22 H26 Cl Ir N2 OP 1 21/n 18.0634; 19.6046; 12.6297
90; 93.722; 90		1992.29Mahato, Sanjit K.; Chatani, Naoto
The Iridium(III)-Catalyzed Direct C(sp2)‒ and C(sp3)‒H Alkynylation of 2-Acylimidazoles with Various Alkynyl Bromides: Understanding the Full Catalytic Cycle
ACS Catalysis, 2020, 10, 5173-5178
4517572 CIFC23 H32 N2 O2 SiP 1 21/c 120.4075; 8.0569; 14.2212
90; 103.892; 90		2269.87Mahato, Sanjit K.; Chatani, Naoto
The Iridium(III)-Catalyzed Direct C(sp2)‒ and C(sp3)‒H Alkynylation of 2-Acylimidazoles with Various Alkynyl Bromides: Understanding the Full Catalytic Cycle
ACS Catalysis, 2020, 10, 5173-5178
4517573 CIFC27 H36 N2 O3 S SiP -18.2563; 8.5661; 19.6108
78.098; 89.653; 71.445		1283.94Mahato, Sanjit K.; Chatani, Naoto
The Iridium(III)-Catalyzed Direct C(sp2)‒ and C(sp3)‒H Alkynylation of 2-Acylimidazoles with Various Alkynyl Bromides: Understanding the Full Catalytic Cycle
ACS Catalysis, 2020, 10, 5173-5178
4517574 CIFC65 H59 B Cl F24 Ir N2 O SiI 1 2/a 143.3006; 12.9147; 24.7725
90; 103.997; 90		13441.8Mahato, Sanjit K.; Chatani, Naoto
The Iridium(III)-Catalyzed Direct C(sp2)‒ and C(sp3)‒H Alkynylation of 2-Acylimidazoles with Various Alkynyl Bromides: Understanding the Full Catalytic Cycle
ACS Catalysis, 2020, 10, 5173-5178
4517575 CIFC23 H28 Cl Ir N2 OP 1 21/c 120.6873; 7.8511; 26.1279
90; 98.161; 90		4200.7Mahato, Sanjit K.; Chatani, Naoto
The Iridium(III)-Catalyzed Direct C(sp2)‒ and C(sp3)‒H Alkynylation of 2-Acylimidazoles with Various Alkynyl Bromides: Understanding the Full Catalytic Cycle
ACS Catalysis, 2020, 10, 5173-5178
4517576 CIFC18 H14 N2 O5P -17.4602; 7.7802; 14.1269
92.011; 102.586; 97.486		791.72Jeong, Jinseong; Heo, Joon; Kim, Dongwook; Chang, Sukbok
NHC-Catalyzed 1,2-Selective Hydroboration of Quinolines
ACS Catalysis, 2020, 10, 5023-5029
4517577 CIFC12 H9 Br Cl3 N O2P 1 21/n 111.9493; 6.9494; 17.493
90; 104.384; 90		1407.1Jeong, Jinseong; Heo, Joon; Kim, Dongwook; Chang, Sukbok
NHC-Catalyzed 1,2-Selective Hydroboration of Quinolines
ACS Catalysis, 2020, 10, 5023-5029
4517578 CIFC17 H14 N2 O3P 1 21/c 17.5628; 16.969; 11.191
90; 105.563; 90		1383.5Jeong, Jinseong; Heo, Joon; Kim, Dongwook; Chang, Sukbok
NHC-Catalyzed 1,2-Selective Hydroboration of Quinolines
ACS Catalysis, 2020, 10, 5023-5029
4517579 CIFC16 H11 Cl N2 O3P 1 21/c 17.4538; 16.3766; 12.0863
90; 106.556; 90		1414.18Jeong, Jinseong; Heo, Joon; Kim, Dongwook; Chang, Sukbok
NHC-Catalyzed 1,2-Selective Hydroboration of Quinolines
ACS Catalysis, 2020, 10, 5023-5029
4517580 CIFC23 H19 Br N2P -18.6223; 10.073; 11.48
85; 71.73; 76.75		921.5Tan, Zhenda; Ci, Chenggang; Yang, Jian; Wu, Yang; Cao, Liang; Jiang, Huanfeng; Zhang, Min
Catalytic Conversion of N-Heteroaromatics to Functionalized Arylamines by Merging Hydrogen Transfer and Selective Coupling
ACS Catalysis, 2020, 5243
4517581 CIFC23 H20 N2P -17.4417; 9.5742; 13.391
74.82; 87.16; 74.55		887.3Tan, Zhenda; Ci, Chenggang; Yang, Jian; Wu, Yang; Cao, Liang; Jiang, Huanfeng; Zhang, Min
Catalytic Conversion of N-Heteroaromatics to Functionalized Arylamines by Merging Hydrogen Transfer and Selective Coupling
ACS Catalysis, 2020, 5243
4517582 CIFC31 H46 Au B F4 N2P 1 21/c 111.029; 13.8947; 23.635
90; 102.05; 90		3542.1Yazdani, Sima; Junor, Glen P.; Peltier, Jesse L.; Gembicky, Milan; Jazzar, Rodolphe; Grotjahn, Douglas B.; Bertrand, Guy
Influence of Carbene and Phosphine Ligands on the Catalytic Activity of Gold Complexes in the Hydroamination and Hydrohydrazination of Alkynes
ACS Catalysis, 2020, 5190
4517583 CIFC16 H18 N2 O2 SP 1 21/n 15.2585; 15.779; 18.526
90; 95.843; 90		1529.2Yazdani, Sima; Junor, Glen P.; Peltier, Jesse L.; Gembicky, Milan; Jazzar, Rodolphe; Grotjahn, Douglas B.; Bertrand, Guy
Influence of Carbene and Phosphine Ligands on the Catalytic Activity of Gold Complexes in the Hydroamination and Hydrohydrazination of Alkynes
ACS Catalysis, 2020, 5190
4517584 CIFC62 H47 Au B F20 NP -115.2805; 18.4692; 20.3195
78.445; 80.937; 82.219		5516.1Yazdani, Sima; Junor, Glen P.; Peltier, Jesse L.; Gembicky, Milan; Jazzar, Rodolphe; Grotjahn, Douglas B.; Bertrand, Guy
Influence of Carbene and Phosphine Ligands on the Catalytic Activity of Gold Complexes in the Hydroamination and Hydrohydrazination of Alkynes
ACS Catalysis, 2020, 5190
4517585 CIFC56 H78 Au B F4 N2C 1 c 117.9392; 18.2892; 17.3878
90; 118.402; 90		5018.1Yazdani, Sima; Junor, Glen P.; Peltier, Jesse L.; Gembicky, Milan; Jazzar, Rodolphe; Grotjahn, Douglas B.; Bertrand, Guy
Influence of Carbene and Phosphine Ligands on the Catalytic Activity of Gold Complexes in the Hydroamination and Hydrohydrazination of Alkynes
ACS Catalysis, 2020, 5190
4517598 CIFC23 H28 N2 O2 SP 17.7639; 9.7745; 16.044
90.123; 96.248; 112.826		1114.2Rigotti, Thomas; Mas-Ballesté, Rubén; Alemán, José
Enantioselective Aminocatalytic [2 + 2] Cycloaddition through Visible Light Excitation
ACS Catalysis, 2020, 10, 5335-5346
4517604 CIFC26 H39 Au Cl PP 1 21/n 110.0412; 15.8623; 15.2487
90; 91.963; 90		2427.33Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517605 CIFC13 H28 F3 O3 P SP 1 21/n 18.8317; 22.6453; 9.2451
90; 106.967; 90		1768.51Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517606 CIFC31 H52 F3 O3 P SP 21 21 217.362; 16.8285; 25.1572
90; 90; 90		3116.76Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517607 CIFC15 H28 F3 O3 P SP 1 21/n 19.5; 10.6274; 18.6029
90; 100.595; 90		1846.13Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517608 CIFC32 H39 Au Cl PP 1 21/c 111.9313; 15.6446; 15.2881
90; 109.268; 90		2693.84Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517609 CIFC34 H39 PP -110.1139; 12.6246; 13.5249
111.882; 109.918; 96.579		1447.74Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517610 CIFC30 H47 Au Cl PP 1 21/c 110.66; 11.355; 23.7632
90; 100.803; 90		2825.42Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517611 CIFC21 H32 F3 O3 P SP 1 21/c 111.1508; 18.5177; 21.1099
90; 100.488; 90		4286.1Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517612 CIFC24 H31.22 Au Cl O0.11 PP 1 21/n 18.7107; 9.9662; 25.5485
90; 96.659; 90		2202.97Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517613 CIFC40.9 H35.8 Cl1.8 F3 O3 P SP 1 21/c 111.5515; 18.5889; 17.7571
90; 99.907; 90		3756.12Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517614 CIFC47 H68 Au2 Cl2 P2P -110.0872; 14.0744; 16.7016
78.85; 81.86; 78.924		2269.59Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517615 CIFC24 H35 Au Cl PP 1 21/n 110.0134; 14.7285; 15.0955
90; 92.029; 90		2224.92Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517616 CIFC11 H24 F3 O3 P SP 1 21/n 117.478; 10.4898; 17.7113
90; 99.9348; 90		3198.51Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517617 CIFC26 H35 Au Cl PP 1 21/n 110.7821; 20.369; 11.1066
90; 106.794; 90		2335.2Barber, Thomas; Argent, Stephen P.; Ball, Liam T.
Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates
ACS Catalysis, 2020, 5454-5461
4517618 CIFC33 H46 N3 O2 P RuP 1 21/n 119.023; 8.5687; 21.327
90; 113.37; 90		3191.2Kar, Sayan; Rauch, Michael; Kumar, Amit; Leitus, Gregory; Ben-David, Yehoshoa; Milstein, David
Selective Room-Temperature Hydrogenation of Amides to Amines and Alcohols Catalyzed by a Ruthenium Pincer Complex and Mechanistic Insight
ACS Catalysis, 2020, 5511-5515
4517624 CIFC19 H17 N O5 SP 1 21 17.9914; 19.2773; 12.1358
90; 90.712; 90		1869.41Zhang, Hongkui; Jiang, Chunhui; Tan, Jian-Ping; Hu, Hui-Lin; Chen, Yayun; Ren, Xiaoyu; Zhang, Hong-Su; Wang, Tianli
Highly Enantioselective Construction of Fully Substituted Stereocenters Enabled by In Situ Phosphonium-Containing Organocatalysis
ACS Catalysis, 2020, 5698-5706
4517639 CIFC20 H32P 21 21 213.5688; 11.1801; 11.1208
90; 90; 90		1687Li, Zhong; Jiang, Yuanyuan; Zhang, Xingwang; Chang, Yimin; Li, Shuai; Zhang, Xiaomin; Zheng, Shanmin; Geng, Ce; Men, Ping; Ma, Li; Yang, Ying; Gao, Zhengquan; Tang, Ya-Jie; Li, Shengying
Fragrant Venezuelaenes A and B with A 5‒5‒6‒7 Tetracyclic Skeleton: Discovery, Biosynthesis, and Mechanisms of Central Catalysts
ACS Catalysis, 2020, 10, 5846-5851
4517640 CIFC19 H18 Br N OP 1 21 16.6642; 7.7286; 15.5866
90; 95.532; 90		799.05Jadhav, Prakash D.; Chen, Jia-Xuan; Liu, Rai-Shung
Gold(I)-Catalyzed Highly Enantioselective [4 + 2]-Annulations of Cyclopentadienes with Nitrosoarenes via Nitroso-Povarov versus Oxidative Nitroso-Povarov Reactions
ACS Catalysis, 2020, 5840
4517641 CIFC19 H16 Br N O2P 1 21 16.4745; 6.9054; 18.0777
90; 99.293; 90		797.63Jadhav, Prakash D.; Chen, Jia-Xuan; Liu, Rai-Shung
Gold(I)-Catalyzed Highly Enantioselective [4 + 2]-Annulations of Cyclopentadienes with Nitrosoarenes via Nitroso-Povarov versus Oxidative Nitroso-Povarov Reactions
ACS Catalysis, 2020, 5840
4517672 CIFC67 H105 Fe2 N5P 1 21/c 113.7862; 21.4855; 21.9569
90; 94.382; 90		6484.7Gasperini, Danila; King, Andrew K.; Coles, Nathan T.; Mahon, Mary F.; Webster, Ruth L.
Seeking Heteroatom-Rich Compounds: Synthetic and Mechanistic Studies into Iron Catalyzed Dehydrocoupling of Silanes
ACS Catalysis, 2020, 6102-6112
4517677 CIFC22 H20 OP 1 21 111.20707; 5.82419; 12.84587
90; 104.996; 90		809.923Lee, Maizie; Ren, Zhi; Musaev, Djamaladdin G.; Davies, Huw M. L.
Rhodium-Stabilized Diarylcarbenes Behaving as Donor/Acceptor Carbenes
ACS Catalysis, 2020, 6240-6247
4517678 CIFC21 H18P 21 21 215.76988; 11.91662; 21.9056
90; 90; 90		1506.17Lee, Maizie; Ren, Zhi; Musaev, Djamaladdin G.; Davies, Huw M. L.
Rhodium-Stabilized Diarylcarbenes Behaving as Donor/Acceptor Carbenes
ACS Catalysis, 2020, 6240-6247
4517689 CIFC66 H50 B F24 Ir P2P -114.47472; 19.26; 23.9417
107.115; 90.4073; 98.3956		6301.75Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517690 CIFC58 H51 B F24 Ir O0.5 P2P 1 21 112.17636; 38.6268; 12.77708
90; 100.256; 90		5913.47Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517691 CIFC88 H78 B F24 Ir P2P -112.9847; 16.3076; 19.9591
95.5387; 104.592; 92.1533		4062.5Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517692 CIFC88 H60 B F42 Ir P2P 1 21/c 113.0737; 23.7759; 28.1916
90; 99.78; 90		8635.7Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517693 CIFC89 H44 B Cl2 F60 Ir P2P 1 21/c 118.33896; 13.16861; 38.4041
90; 91.6412; 90		9270.73Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517694 CIFC25 H44 O2P 21 21 242.4084; 13.6051; 7.6568
90; 90; 90		4417.75Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517695 CIFC42 H64 O3 SiP 1 21 112.55791; 11.2147; 14.01011
90; 107.532; 90		1881.44Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517696 CIFC25 H44 O3P 1 21 112.21766; 7.39922; 12.74257
90; 95.6028; 90		1146.44Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517697 CIFC24 H42 O2I 1 2 17.6128; 9.7121; 87.346
90; 90.272; 90		6458Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517698 CIFC20 H28 O2P 21 21 217.7735; 12.2996; 16.9155
90; 90; 90		1617.31Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517699 CIFC42 H49 Ir P2 SiP 1 21/n 111.88006; 21.74657; 14.12314
90; 97.1277; 90		3620.52Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517700 CIFC48 H23 F36 Ir P2P -112.3828; 15.2107; 16.6665
64.281; 83.752; 70.114		2656.74Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517701 CIFC54 H37 F36 Ir P2 SiP -113.9408; 14.1616; 16.2996
102.527; 94.566; 101.595		3051.57Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517702 CIFC24 H18 F9 PP -19.2013; 11.6473; 12.4438
62.798; 76.382; 76.134		1139.24Fast, Caleb D.; Jones, Caleb A. H.; Schley, Nathan D.
Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage
ACS Catalysis, 2020, 6450-6456
4517706 CIFC31 H61 In N2 O Si2P 1 21/c 114.5173; 22.1551; 11.8658
90; 106.121; 90		3666.4Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa
Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition
ACS Catalysis, 2020, 6488-6496
4517707 CIFC31 H59 In N2 O Si2P 1 21/n 116.279; 23.517; 37.715
90; 97.103; 90		14328Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa
Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition
ACS Catalysis, 2020, 6488-6496
4517708 CIFC111 H120 B2 F40 In2 N4 O3 Si2P -113.921; 16.027; 26.415
91.032; 101.549; 91.773		5769.7Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa
Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition
ACS Catalysis, 2020, 6488-6496
4517709 CIFC31 H60 F6 In N2 O2 P SiP 43 21 214.75; 14.75; 35.67
90; 90; 90		7760Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa
Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition
ACS Catalysis, 2020, 6488-6496
4517710 CIFC62 H64 B F20 In N2 O2 SiP 1 21/c 114.6691; 25.0259; 17.6496
90; 106.494; 90		6212.7Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa
Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition
ACS Catalysis, 2020, 6488-6496
4517711 CIFC23 H42 Cl Ir N P2 SP b c a12.2672; 15.04; 28.7115
90; 90; 90		5297.23Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517712 CIFC21 H36 Ir N O2 P2C 1 2/c 136.27; 7.8548; 36.2929
90; 113.602; 90		9474.7Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517713 CIFC21 H35 Ir O P2P -111.336; 14.13; 14.921
78.309; 82.053; 89.309		2317.6Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517714 CIFC20 H34 Ir N O2 P2P 1 21/c 113.2206; 11.3239; 15.3513
90; 97.378; 90		2279.2Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517715 CIFC23 H43 Cl Ir N O P2C 1 2/c 131.9259; 7.9828; 20.1715
90; 100.614; 90		5052.91Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517716 CIFC26 H45 Ir O2 P2P 1 21/c 18.6225; 18.5843; 17.0349
90; 90.761; 90		2729.48Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517717 CIFC20 H34 Ir N O P2 SP -18.1801; 17.6065; 17.9383
62.959; 83.152; 82.77		2277.2Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517718 CIFC20 H37 Ir O2 P2 S0.99P 1 21/c 119.059; 8.033; 16.181
90; 92.063; 90		2476Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517719 CIFC22 H36 Ir N O2 P2P 1 21/c 113.6088; 11.1953; 15.5695
90; 100.675; 90		2331.03Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517720 CIFC19 H31 Ir O2 P2 SC 1 2/c 129.6785; 8.0786; 18.7571
90; 101.242; 90		4410.93Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517721 CIFC19 H31 Ir O3 P2P -114.2131; 14.3576; 17.1807
108.37; 97.894; 91.083		3288.59Zhang, Xin; Wu, Song-Bai; Leng, Xuebing; Chung, Lung Wa; Liu, Guixia; Huang, Zheng
N-Bridged Pincer Iridium Complexes for Highly Efficient Alkane Dehydrogenation and the Relevant Linker Effects
ACS Catalysis, 2020, 6475-6487
4517731 CIFC32 H37 N O3P 1 21 111.8096; 6.187; 19.7061
90; 105.867; 90		1384.99Wang, Yaxin; Wang, Nengyong; Zhao, Jianyou; Sun, Minzhi; You, Huichao; Fang, Fang; Liu, Zhong-Quan
Visible-Light-Promoted Site-Specific and Diverse Functionalization of a C(sp3)‒C(sp3) Bond Adjacent to an Arene
ACS Catalysis, 2020, 6603-6612
4517732 CIFC21 H14 Au Cl OP -17.9594; 9.7061; 11.5124
72.844; 89.113; 80.497		837.63Zhang, Caiyun; Wang, Gendi; Zhan, Licheng; Yang, Xueyan; Wang, Jiwei; Wei, Yin; Xu, Sheng; Shi, Min; Zhang, Jun
Gold(I) or Gold(III) as Real Intermediate Species in Gold-Catalyzed Cycloaddition Reactions of Enynal/Enynone?
ACS Catalysis, 2020, 6682-6690
4517733 CIFC24 H18 Cl2 OP -111.6275; 12.6651; 15.1706
113.103; 103.226; 99.082		1922.4Zhang, Caiyun; Wang, Gendi; Zhan, Licheng; Yang, Xueyan; Wang, Jiwei; Wei, Yin; Xu, Sheng; Shi, Min; Zhang, Jun
Gold(I) or Gold(III) as Real Intermediate Species in Gold-Catalyzed Cycloaddition Reactions of Enynal/Enynone?
ACS Catalysis, 2020, 6682-6690
4517734 CIFC22.5 H17 Au Cl6 OC 1 2/c 120.839; 14.241; 16.555
90; 98.828; 90		4854.8Zhang, Caiyun; Wang, Gendi; Zhan, Licheng; Yang, Xueyan; Wang, Jiwei; Wei, Yin; Xu, Sheng; Shi, Min; Zhang, Jun
Gold(I) or Gold(III) as Real Intermediate Species in Gold-Catalyzed Cycloaddition Reactions of Enynal/Enynone?
ACS Catalysis, 2020, 6682-6690
4517770 CIFC12 H18 B2 F6 K2 O4P 1 21 19.9422; 6.0314; 15.453
90; 103.236; 90		902.03Wittmann, Bruce J.; Knight, Anders M.; Hofstra, Julie L.; Reisman, Sarah E.; Jennifer Kan, S. B.; Arnold, Frances H.
Diversity-Oriented Enzymatic Synthesis of Cyclopropane Building Blocks
ACS Catalysis, 2020, 10, 7112-7116
4517771 CIFC49 H59 Cl N4 O2 TiP 1 21/n 119.1679; 10.1706; 23.0399
90; 98.625; 90		4440.8Hao, Han; Schafer, Laurel L.
Metal‒Ligand Cooperativity in Titanium-Catalyzed Anti-Markovnikov Hydroamination
ACS Catalysis, 2020, 7100
4517772 CIFC26 H42 Cl4 Ir2P -18.389; 9.214; 9.659
102.796; 99.295; 100.694		699.2Liu, Lei; Song, Hong; Liu, Yan-Hua; Wu, Le-Song; Shi, Bing-Feng
Achiral CpxIr(III)/Chiral Carboxylic Acid Catalyzed Enantioselective C‒H Amidation of Ferrocenes under Mild Conditions
ACS Catalysis, 2020, 10, 7117-7122
4517773 CIFC20 H18 Br2 Fe N2 O2P 43 21 210.5631; 10.5631; 34.9612
90; 90; 90		3900.9Liu, Lei; Song, Hong; Liu, Yan-Hua; Wu, Le-Song; Shi, Bing-Feng
Achiral CpxIr(III)/Chiral Carboxylic Acid Catalyzed Enantioselective C‒H Amidation of Ferrocenes under Mild Conditions
ACS Catalysis, 2020, 10, 7117-7122
4517774 CIFC21 H17 Br2 N O2 SP 15.2215; 7.9597; 23.385
87.72; 86.471; 89.947		969.3Liu, Wentan; Yang, Wu; Zhu, Jiefeng; Guo, Yonghong; Wang, Na; Ke, Jie; Yu, Peiyuan; He, Chuan
Dual-Ligand-Enabled Ir(III)-Catalyzed Enantioselective C‒H Amidation for the Synthesis of Chiral Sulfoxides
ACS Catalysis, 2020, 10, 7207-7215
4517775 CIFC26 H42 Cl4 Ir2P 1 21/c 112.4627; 18.1472; 12.9349
90; 93.987; 90		2918.3Liu, Wentan; Yang, Wu; Zhu, Jiefeng; Guo, Yonghong; Wang, Na; Ke, Jie; Yu, Peiyuan; He, Chuan
Dual-Ligand-Enabled Ir(III)-Catalyzed Enantioselective C‒H Amidation for the Synthesis of Chiral Sulfoxides
ACS Catalysis, 2020, 10, 7207-7215
4517776 CIFC23 H17 F6 N O4 SP 21 21 215.5584; 14.559; 27.412
90; 90; 90		2218.3Liu, Wentan; Yang, Wu; Zhu, Jiefeng; Guo, Yonghong; Wang, Na; Ke, Jie; Yu, Peiyuan; He, Chuan
Dual-Ligand-Enabled Ir(III)-Catalyzed Enantioselective C‒H Amidation for the Synthesis of Chiral Sulfoxides
ACS Catalysis, 2020, 10, 7207-7215
4517777 CIFC24 H27 Ir O SP 1 21/n 110.993; 14.5354; 12.7588
90; 94.905; 90		2031.23Liu, Wentan; Yang, Wu; Zhu, Jiefeng; Guo, Yonghong; Wang, Na; Ke, Jie; Yu, Peiyuan; He, Chuan
Dual-Ligand-Enabled Ir(III)-Catalyzed Enantioselective C‒H Amidation for the Synthesis of Chiral Sulfoxides
ACS Catalysis, 2020, 10, 7207-7215
4517778 CIFC26 H42 Cl4 Ir2P -18.3494; 9.1549; 9.6175
102.865; 98.989; 100.722		689.02Liu, Wentan; Yang, Wu; Zhu, Jiefeng; Guo, Yonghong; Wang, Na; Ke, Jie; Yu, Peiyuan; He, Chuan
Dual-Ligand-Enabled Ir(III)-Catalyzed Enantioselective C‒H Amidation for the Synthesis of Chiral Sulfoxides
ACS Catalysis, 2020, 10, 7207-7215
4517779 CIFC29 H29 N2 O3P -110.548; 11.96; 13.948
94.54; 111.21; 115.903		1415.3Guo, Tao; Ding, Yalan; Zhou, Lili; Xu, Haiyan; Loh, Teck-Peng; Wu, Xiaojin
Palladium-Catalyzed anti-Michael Reductive Heck Reaction of α,β-Unsaturated Esters
ACS Catalysis, 2020, 10, 7262-7268
4517796 CIFC51 H51 F9 N5 O9 P3 Ru S3P 21 21 2112.6221; 20.3106; 22.3941
90; 90; 90		5741Erickson, Jeremy D.; Preston, Andrew Z.; Linehan, John C.; Wiedner, Eric S.
Enhanced Hydrogenation of Carbon Dioxide to Methanol by a Ruthenium Complex with a Charged Outer-Coordination Sphere
ACS Catalysis, 2020, 10, 7419-7423
4517808 CIFC43 H35 O P2 RhP -111.1012; 11.5775; 13.3634
89.848; 77.424; 78.168		1639.11Ryan, David E.; Andrea, Kori A.; Race, James J.; Boyd, Timothy M.; Lloyd-Jones, Guy C.; Weller, Andrew S.
Amine‒Borane Dehydropolymerization Using Rh-Based Precatalysts: Resting State, Chain Control, and Efficient Polymer Synthesis
ACS Catalysis, 2020, 7443-7448
4517809 CIFC51.1 H44.1 O P2 RhP 1 21/c 116.1346; 10.4118; 24.8442
90; 98.216; 90		4130.7Ryan, David E.; Andrea, Kori A.; Race, James J.; Boyd, Timothy M.; Lloyd-Jones, Guy C.; Weller, Andrew S.
Amine‒Borane Dehydropolymerization Using Rh-Based Precatalysts: Resting State, Chain Control, and Efficient Polymer Synthesis
ACS Catalysis, 2020, 7443-7448
4517813 CIFC17 H34 F3 N O3 S SnP 1 21/n 19.7228; 15.7107; 14.334
90; 92.744; 90		2187.04Sapsford, Joshua S.; Csókás, Dániel; Scott, Daniel J.; Turnell-Ritson, Roland C.; Piascik, Adam D.; Pápai, Imre; Ashley, Andrew E.
Establishing the Role of Triflate Anions in H2 Activation by a Cationic Triorganotin(IV) Lewis Acid
ACS Catalysis, 2020, 7573-7583
4517814 CIFC32 H34 Al F36 N O4 SnP 1 21/c 114.8706; 15.2083; 21.9762
90; 104.671; 90		4808Sapsford, Joshua S.; Csókás, Dániel; Scott, Daniel J.; Turnell-Ritson, Roland C.; Piascik, Adam D.; Pápai, Imre; Ashley, Andrew E.
Establishing the Role of Triflate Anions in H2 Activation by a Cationic Triorganotin(IV) Lewis Acid
ACS Catalysis, 2020, 7573-7583
4517828 CIFC10 H20 K12 N10 O0 Ru2 Sn18C 1 2/c 115.327; 31.192; 13.692
90; 94.911; 90		6522Wang, Yanru; Zhang, Chao; Wang, Xiuyi; Guo, Jinqiu; Sun, Zhong-Ming; Zhang, Hongbo
Site-Selective CO2 Reduction over Highly Dispersed Ru-SnOx Sites Derived from a [Ru@Sn9]6‒ Zintl Cluster
ACS Catalysis, 2020, 7808
4517829 CIFC15 H13 N OP 1 21 17.6989; 5.6085; 13.528
90; 92.652; 90		583.5Mao, Ying; Wang, Zehua; Wang, Gang; Zhao, Ran; Kan, Linglong; Pan, Xiaoguang; Liu, Lei
Redox Deracemization of Tertiary Stereocenters Adjacent to an Electron-Withdrawing Group
ACS Catalysis, 2020, 7785-7791
4517830 CIFC72 H88 Fe2 N2 Si2P 1 21/c 114.1589; 20.1568; 10.773
90; 96.224; 90		3056.5Witzke, Ryan J.; Hait, Diptarka; Chakarawet, Khetpakorn; Head-Gordon, Martin; Tilley, T. Don
Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
ACS Catalysis, 2020, 7800
4517831 CIFC62 H82 Fe2 N2 O Si2P -112.131; 12.86; 18.9741
89.775; 87.91; 85.741		2949.9Witzke, Ryan J.; Hait, Diptarka; Chakarawet, Khetpakorn; Head-Gordon, Martin; Tilley, T. Don
Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
ACS Catalysis, 2020, 7800
4517832 CIFC21 H36 Fe N SiP b c n22.1414; 11.2865; 17.5402
90; 90; 90		4383.3Witzke, Ryan J.; Hait, Diptarka; Chakarawet, Khetpakorn; Head-Gordon, Martin; Tilley, T. Don
Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
ACS Catalysis, 2020, 7800
4517836 CIFC15 H20 Ir N3 O5 SP 1 21/c 18.656; 14.5247; 14.4235
90; 95.387; 90		1805.4Tensi, Leonardo; Macchioni, Alceo
Extremely Fast NADH-Regeneration Using Phosphonic Acid as Hydride Source and Iridium-pyridine-2-sulfonamidate Catalysts
ACS Catalysis, 2020, 7945
4517838 CIFC61 H46 O P2 PdP 1 21/n 118.3983; 13.9556; 20.8118
90; 109.351; 90		5041.7Xiong, Wenfang; Shi, Fuxing; Cheng, Ruixiang; Zhu, Baiyao; Wang, Lu; Chen, Pengquan; Lou, Hongming; Wu, Wanqing; Qi, Chaorong; Lei, Ming; Jiang, Huanfeng
Palladium-Catalyzed Highly Regioselective Hydrocarboxylation of Alkynes with Carbon Dioxide
ACS Catalysis, 2020, 7968
4517839 CIFC23 H28 O2P -110.0446; 12.2899; 17.0614
76.398; 74.831; 88.404		1974.5Xiong, Wenfang; Shi, Fuxing; Cheng, Ruixiang; Zhu, Baiyao; Wang, Lu; Chen, Pengquan; Lou, Hongming; Wu, Wanqing; Qi, Chaorong; Lei, Ming; Jiang, Huanfeng
Palladium-Catalyzed Highly Regioselective Hydrocarboxylation of Alkynes with Carbon Dioxide
ACS Catalysis, 2020, 7968
4517848 CIFC25 H24 N2 O2 PdP -19.3968; 9.484; 11.9025
103.496; 93.933; 90.76		1028.55Li, Ya; Zhang, Pan; Liu, Yue-Jin; Yu, Zhi-Xiang; Shi, Bing-Feng
Remote γ-C(sp3)‒H Alkylation of Aliphatic Carboxamides via an Unexpected Regiodetermining Pd Migration Process: Reaction Development and Mechanistic Study
ACS Catalysis, 2020, 8212-8222
4517849 CIFC19 H24 N4 O2 PdP 1 21/n 114.1106; 6.7889; 20.7976
90; 92.295; 90		1990.7Li, Ya; Zhang, Pan; Liu, Yue-Jin; Yu, Zhi-Xiang; Shi, Bing-Feng
Remote γ-C(sp3)‒H Alkylation of Aliphatic Carboxamides via an Unexpected Regiodetermining Pd Migration Process: Reaction Development and Mechanistic Study
ACS Catalysis, 2020, 8212-8222
4517850 CIFC20 H18 O2P 21 21 216.53867; 6.85703; 35.6756
90; 90; 90		1599.55Wang, Shou-Guo; Cramer, Nicolai
Asymmetric CpxRh(III)-Catalyzed Acrylic Acid C‒H Functionalization with Allenes Provides Chiral γ-Lactones
ACS Catalysis, 2020, 8231-8236
4517851 CIFC25 H23 F N2 OP 21 21 219.2261; 9.7377; 22.6198
90; 90; 90		2032.19Shen, Yang; Shen, Meng-Lan; Wang, Pu-Sheng
Light-Mediated Chiral Phosphate Catalysis for Asymmetric Dicarbofunctionalization of Enamides
ACS Catalysis, 2020, 8247-8253
4517857 CIFC26 H20 F N3 O2 SC 1 2/c 119.9143; 10.6749; 20.1936
90; 92.357; 90		4289.2Hu, Xinwei; Shao, Youxiang; Xie, Haisheng; Chen, Xin; Chen, Fengjuan; Ke, Zhuofeng; Jiang, Huanfeng; Zeng, Wei
Direct Carbon‒Carbon σ Bond Amination of Unstrained Arylalkylketones
ACS Catalysis, 2020, 8402-8408
4517858 CIFC26 H21 N3 O2 SC 1 2/c 119.925; 10.806; 20.27
90; 92.45; 90		4360.3Hu, Xinwei; Shao, Youxiang; Xie, Haisheng; Chen, Xin; Chen, Fengjuan; Ke, Zhuofeng; Jiang, Huanfeng; Zeng, Wei
Direct Carbon‒Carbon σ Bond Amination of Unstrained Arylalkylketones
ACS Catalysis, 2020, 8402-8408
4517861 CIFC26 H40 Hf N2P 419.491; 9.491; 27.7364
90; 90; 90		2498.47Wallace, Mark A.; Zavalij, Peter Y.; Sita, Lawrence R.
Enantioselective Living Coordinative Chain Transfer Polymerization: Production of Optically Active End-Group-Functionalized (+)- or (−)-Poly(methylene-1,3-cyclopentane) via a Homochiral C1-Symmetric Caproamidinate Hafnium Initiator
ACS Catalysis, 2020, 8496-8502
4517862 CIFC26 H40 Hf N2P 439.4877; 9.4877; 27.766
90; 90; 90		2499.4Wallace, Mark A.; Zavalij, Peter Y.; Sita, Lawrence R.
Enantioselective Living Coordinative Chain Transfer Polymerization: Production of Optically Active End-Group-Functionalized (+)- or (−)-Poly(methylene-1,3-cyclopentane) via a Homochiral C1-Symmetric Caproamidinate Hafnium Initiator
ACS Catalysis, 2020, 8496-8502
4517870 CIFC20 H24 O4 S2P 1 21/n 119.047; 8.804; 24.664
90; 105.975; 90		3976.2Gadde, Karthik; Mampuys, Pieter; Guidetti, Andrea; Ching, H. Y. Vincent; Herrebout, Wouter A.; Van Doorslaer, Sabine; Abbaspour Tehrani, Kourosch; Maes, Bert U. W.
Thiosulfonylation of Unactivated Alkenes with Visible-Light Organic Photocatalysis
ACS Catalysis, 2020, 8765-8779
4517879 CIFC75 H109.5 Cl Cr2 N5.5 O5P 21 21 2117.0512; 20.0506; 22.7296
90; 90; 90		7770.9Lipinski, Bryce M.; Walker, Katherine L.; Clayman, Naomi E.; Morris, Lilliana S.; Jugovic, Timothy M. E.; Roessler, Allison G.; Getzler, Yutan D. Y. L.; MacMillan, Samantha N.; Zare, Richard N.; Zimmerman, Paul M.; Waymouth, Robert M.; Coates, Geoffrey W.
Mechanistic Study of Isotactic Poly(propylene oxide) Synthesis using a Tethered Bimetallic Chromium Salen Catalyst
ACS Catalysis, 2020, 8960-8967
4517880 CIFC44.33 H22 Ni0.44 O17 Zr3P 6/m m m39.4522; 39.4522; 16.5041
90; 90; 120		22246.7Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517881 CIFC34 H16 Br2 Ni0.4 O17.3 Zr3P 6/m m m39.903; 39.903; 12.022
90; 90; 120		16577Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517882 CIFC10 H7 Ni0.1 O4 Zr0.75P m -3 m28.2651; 28.2651; 28.2651
90; 90; 90		22581.4Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517883 CIFC34.8 H16 Br2 Hf3 Ni0.44 O16P 6/m m m40.4333; 40.4333; 11.4682
90; 90; 120		16236.9Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517884 CIFC11 H6 Hf0.81 Ni0.16 O4P 6/m m m39.601; 39.601; 16.4314
90; 90; 120		22316Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517890 CIFC18 H21 Cl2 N OP 1 21 17.6233; 7.8881; 13.5115
90; 91.9018; 90		812.04Rong, Zi-Qiang; Yu, Zhaoyuan; Weng, Cheng; Yang, Li-Cheng; Lu, Shenci; Lan, Yu; Zhao, Yu
Dynamic Kinetic Asymmetric Amination of Alcohols Assisted by Microwave: Stereoconvergent Access to Tetralin- and Indane-Derived Chiral Amines
ACS Catalysis, 2020, 9464
4517967 CIFC36 H60 B2 Ir N O4 P2P -114.485; 16.26; 17.548
84.689; 89.852; 71.719		3906Foley, Bryan J.; Bhuvanesh, Nattamai; Zhou, Jia; Ozerov, Oleg V.
Combined Experimental and Computational Studies of the Mechanism of Dehydrogenative Borylation of Terminal Alkynes Catalyzed by PNP Complexes of Iridium
ACS Catalysis, 2020, 9824-9836
4517986 CIFC32 H28 Fe2 N4 O5P -110.734; 10.815; 13.738
67.142; 85.858; 73.156		1405.06Provis-Evans, Cei B.; Lau, Samantha; Krewald, Vera; Webster, Ruth L.
Regioselective Alkyne Cyclotrimerization with an In Situ-Generated [Fe(II)H(salen)]·Bpin Catalyst
ACS Catalysis, 2020, 10157-10168
4517987 CIFC17 H17 N O2P 1 21/c 111.2862; 9.2093; 13.1111
90; 109.258; 90		1286.49Zhang, Zhijie; Yi, Dong; Zhang, Min; Wei, Jun; Lu, Ji; Yang, Lin; Wang, Jun; Hao, Na; Pan, Xianchao; Zhang, Shiqi; Wei, Siping; Fu, Qiang
Photocatalytic Intramolecular [2 + 2] Cycloaddition of Indole Derivatives via Energy Transfer: A Method for Late-Stage Skeletal Transformation
ACS Catalysis, 2020, 10149-10156
4517988 CIFC13 H13 N OP 1 21/n 18.31074; 13.9007; 8.8665
90; 96.992; 90		1016.69Zhang, Zhijie; Yi, Dong; Zhang, Min; Wei, Jun; Lu, Ji; Yang, Lin; Wang, Jun; Hao, Na; Pan, Xianchao; Zhang, Shiqi; Wei, Siping; Fu, Qiang
Photocatalytic Intramolecular [2 + 2] Cycloaddition of Indole Derivatives via Energy Transfer: A Method for Late-Stage Skeletal Transformation
ACS Catalysis, 2020, 10149-10156
4517994 CIFC27 H34 Si2C 1 2/c 114.963; 12.0779; 28.792
90; 105.06; 90		5024.6Lv, Weiwei; Liu, Shihan; Chen, Yanhui; Wen, Si; Lan, Yu; Cheng, Guolin
Palladium-Catalyzed Intermolecular Trans-Selective Carbofunctionalization of Internal Alkynes to Highly Functionalized Alkenes
ACS Catalysis, 2020, 10516
4517995 CIFC30 H28 O2P 1 21/n 111.0772; 15.556; 14.641
90; 110.201; 90		2367.7Lv, Weiwei; Liu, Shihan; Chen, Yanhui; Wen, Si; Lan, Yu; Cheng, Guolin
Palladium-Catalyzed Intermolecular Trans-Selective Carbofunctionalization of Internal Alkynes to Highly Functionalized Alkenes
ACS Catalysis, 2020, 10516
4518014 CIFC110 H72 F12 N10 O2 P2 Ru2P -117.1459; 19.6957; 21.0108
93.42; 112.713; 112.979		5837.9Rajabi, Sheida; Ebrahimi, Fatemeh; Lole, Gaurav; Odrobina, Jann; Dechert, Sebastian; Jooss, Christian; Meyer, Franc
Water Oxidizing Diruthenium Electrocatalysts Immobilized on Carbon Nanotubes: Effects of the Number and Positioning of Pyrene Anchors
ACS Catalysis, 2020, 10614
4518015 CIFC70.5 H58 F12 N10 O3 P2 Ru2P -114.2194; 20.0432; 26.3213
83.352; 79.323; 87.701		7320.9Rajabi, Sheida; Ebrahimi, Fatemeh; Lole, Gaurav; Odrobina, Jann; Dechert, Sebastian; Jooss, Christian; Meyer, Franc
Water Oxidizing Diruthenium Electrocatalysts Immobilized on Carbon Nanotubes: Effects of the Number and Positioning of Pyrene Anchors
ACS Catalysis, 2020, 10614
4518016 CIFC32 H32 N2 O4 S2P 1 21/c 110.9602; 14.7542; 18.1626
90; 94.857; 90		2926.5Qian, Xiaolin; Zhou, Hui; Chaminda Lakmal, Hetti Handi; Lucore, James; Wang, Xuesong; Valle, Henry U.; Donnadieu, Bruno; Xu, Xue; Cui, Xin
Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α-Substituted Styrene Derivatives
ACS Catalysis, 2020, 10627
4518017 CIFC26 H28 N2 O4 S2P -19.95; 10.42; 13.328
73.734; 83.867; 67.198		1222.9Qian, Xiaolin; Zhou, Hui; Chaminda Lakmal, Hetti Handi; Lucore, James; Wang, Xuesong; Valle, Henry U.; Donnadieu, Bruno; Xu, Xue; Cui, Xin
Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α-Substituted Styrene Derivatives
ACS Catalysis, 2020, 10627
4518020 CIFC27 H25 Br O2P 19.6954; 10.1078; 22.4793
97.438; 97.121; 90.238		2167.11McLeod, David; Izzo, Joseph A.; Jørgensen, Danny K. B.; Lauridsen, Rune F.; Jørgensen, Karl Anker
Development and Investigation of an Organocatalytic Enantioselective [10 + 2] Cycloaddition
ACS Catalysis, 2020, 10784
4518021 CIFC82 H82 B F24 Li Ni O7 P2P -114.2489; 14.2542; 20.5358
84.356; 86.902; 86.242		4137.1Tran, Thi V.; Karas, Lucas J.; Wu, Judy I.; Do, Loi H.
Elucidating Secondary Metal Cation Effects on Nickel Olefin Polymerization Catalysts
ACS Catalysis, 2020, 10760
4518022 CIFC80.5 H85.6 B F24 K Ni O8 P2P -113.151; 13.356; 24.585
86.239; 81.17; 87.895		4256.3Tran, Thi V.; Karas, Lucas J.; Wu, Judy I.; Do, Loi H.
Elucidating Secondary Metal Cation Effects on Nickel Olefin Polymerization Catalysts
ACS Catalysis, 2020, 10760
4518023 CIFC76 H68 B Cs F24 Ni O7 P2P 1 21/n 117.3656; 23.606; 20.3261
90; 103.682; 90		8095.9Tran, Thi V.; Karas, Lucas J.; Wu, Judy I.; Do, Loi H.
Elucidating Secondary Metal Cation Effects on Nickel Olefin Polymerization Catalysts
ACS Catalysis, 2020, 10760
4518024 CIFC21 H18 N2P -18.9756; 9.0718; 11.0372
84.016; 85.238; 62.683		793.5Wang, Shengdong; Force, Guillaume; Guillot, Régis; Carpentier, Jean-François; Sarazin, Yann; Bour, Christophe; Gandon, Vincent; Lebœuf, David
Lewis Acid/Hexafluoroisopropanol: A Promoter System for Selective ortho-C-Alkylation of Anilines with Deactivated Styrene Derivatives and Unactivated Alkenes
ACS Catalysis, 2020, 10794
4518037 CIFC29 H26 N2 O4 SP 1 21/c 116.6324; 12.5786; 23.5913
90; 90.5504; 90		4935.4De, Nirupam; Ko, Donguk; Baek, Seung-yeol; Oh, Changjin; Kim, Jiyoung; Baik, Mu-Hyun; Yoo, Eun Jeong
Cu(I)-Catalyzed Enantioselective [5 + 1] Cycloaddition of N-Aromatic Compounds and Alkynes via Chelating-Assisted 1,2-Dearomative Addition
ACS Catalysis, 2020, 10905
4518038 CIFC30 H27 Cl N2 O5 SP 1 21/c 19.7732; 22.9861; 12.4889
90; 107.777; 90		2671.64De, Nirupam; Ko, Donguk; Baek, Seung-yeol; Oh, Changjin; Kim, Jiyoung; Baik, Mu-Hyun; Yoo, Eun Jeong
Cu(I)-Catalyzed Enantioselective [5 + 1] Cycloaddition of N-Aromatic Compounds and Alkynes via Chelating-Assisted 1,2-Dearomative Addition
ACS Catalysis, 2020, 10905
4518039 CIFC27 H26 N4 O6P 1 21 17.25553; 7.4022; 47.0222
90; 92.058; 90		2523.79Xue, Zaikun; Li, Yao; Luo, Sanzhong
Chiral Primary Amine-Catalyzed Divergent Coupling of α-Substituted Acrylaldehydes with α-Diazoesters
ACS Catalysis, 2020, 10989
4518040 CIFC1.74 H1.74 O0.35P 21 21 216.4822; 15.0713; 16.8103
90; 90; 90		1642.29Xue, Zaikun; Li, Yao; Luo, Sanzhong
Chiral Primary Amine-Catalyzed Divergent Coupling of α-Substituted Acrylaldehydes with α-Diazoesters
ACS Catalysis, 2020, 10989
4518041 CIFC18 H22 B N2 O3 S SiP -18.5976; 9.2734; 12.5694
104.461; 99.599; 96.061		945.36Desrosiers, Vincent; Garcia, Cecilia Zavaleta; Fontaine, Frédéric-Georges
Boron Recycling in the Metal-Free Transfer C‒H Borylation of Terminal Alkynes and Heteroarenes
ACS Catalysis, 2020, 11046
4518044 CIFC34 H34 Cl N4 O5 PP -110.705; 11.4472; 13.9654
97.31; 112.09; 95.568		1553.18Garrido-González, José J.; Iglesias Aparicio, Ma Mercedes; García, Miguel Martínez; Simón, Luis; Sanz, Francisca; Morán, Joaquín R.; Fuentes de Arriba, Ángel L.
An Enzyme Model Which Mimics Chymotrypsin and N-Terminal Hydrolases
ACS Catalysis, 2020, 11162
4518051 CIFC11 H21 N O3P c a 219.8601; 5.6544; 44.1243
90; 90; 90		2460.06Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518052 CIFC11 H21 N O3P b c a9.2362; 10.9879; 23.7378
90; 90; 90		2409.06Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518053 CIFC12 H16 OP 1 21/c 114.6389; 5.303; 13.1361
90; 106.994; 90		975.23Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518054 CIFC15 H28 O2P 1 21/c 19.1475; 19.6782; 7.9541
90; 92.11; 90		1430.82Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518056 CIFC20 H24 O5 S2P b c a13.1697; 8.5458; 33.8861
90; 90; 90		3813.73Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518057 CIFC128 H210 O13C 1 2 127.5054; 7.159; 28.9864
90; 91.009; 90		5706.86Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518058 CIFC15 H20 O2P 1 21/n 16.46515; 7.56208; 26.4823
90; 93.8866; 90		1291.74Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518059 CIFC20 H30 B N O4P 1 21/c 113.4325; 9.9472; 15.5089
90; 101.16; 90		2033.05Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518060 CIFC20 H22 F2 O4 S2P 1 21/c 111.66361; 15.02503; 11.25687
90; 97.1362; 90		1957.44Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518061 CIFC37 H56 O3 SP 1 21 114.75517; 11.9167; 18.31913
90; 93.7103; 90		3214.35Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518062 CIFC16 H26 O2C 1 2/c 123.988; 6.72515; 18.4587
90; 109.443; 90		2808Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518064 CIFC14 H12 O5P 1 21/c 114.8299; 7.4261; 11.4598
90; 109.078; 90		1192.73Karlinskii, Bogdan Ya.; Kostyukovich, Alexander Yu.; Kucherov, Fedor A.; Galkin, Konstantin I.; Kozlov, Kirill S.; Ananikov, Valentine P.
Directing-Group-Free, Carbonyl Group-Promoted Catalytic C‒H Arylation of Bio-Based Furans
ACS Catalysis, 2020, 10, 11466-11480
4518065 CIFC18 H12 O3C 1 2/c 112.3333; 11.1772; 19.7023
90; 101.316; 90		2663.2Karlinskii, Bogdan Ya.; Kostyukovich, Alexander Yu.; Kucherov, Fedor A.; Galkin, Konstantin I.; Kozlov, Kirill S.; Ananikov, Valentine P.
Directing-Group-Free, Carbonyl Group-Promoted Catalytic C‒H Arylation of Bio-Based Furans
ACS Catalysis, 2020, 10, 11466-11480
4518066 CIFC13 H7 F3 O3P 1 21/c 111.0065; 13.6364; 7.4223
90; 101.195; 90		1092.81Karlinskii, Bogdan Ya.; Kostyukovich, Alexander Yu.; Kucherov, Fedor A.; Galkin, Konstantin I.; Kozlov, Kirill S.; Ananikov, Valentine P.
Directing-Group-Free, Carbonyl Group-Promoted Catalytic C‒H Arylation of Bio-Based Furans
ACS Catalysis, 2020, 10, 11466-11480
4518081 CIFC23 H27.38 Ir N O2.69P -18.2522; 10.6947; 11.645
88.833; 86.13; 88.885		1025Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518082 CIFC30 H36 N4 O SiP -111.2966; 17.3143; 23.2024
101.869; 102.938; 99.047		4228.98Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518083 CIFC32 H44 Ir N SiP 1 21/n 111.3222; 18.4507; 14.6046
90; 103.017; 90		2972.54Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518084 CIFC22 H28 F N O SiP 1 21/c 120.944; 8.1654; 12.3532
90; 97.35; 90		2095.24Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518085 CIFC39 H55.66 Cl2 N2 O2.83 Si2P -17.4568; 20.0275; 27.8489
88.958; 84.338; 80.073		4076.73Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518086 CIFC26 H31 N O SiP c a 2124.9365; 11.3131; 8.3785
90; 90; 90		2363.65Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518087 CIFC33 H48 F N Si2P 1 21 18.0636; 13.035; 15.6853
90; 96.548; 90		1637.91Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518091 CIFC21 H34 Br2 O4 SiP b c a12.8335; 14.5079; 25.395
90; 90; 90		4728.22Schäfers, Felix; Quach, Linda; Schwarz, J. Luca; Saladrigas, Mar; Daniliuc, Constantin G.; Glorius, Frank
Direct Access to Monoprotected Homoallylic 1,2-Diols via Dual Chromium/Photoredox Catalysis
ACS Catalysis, 2020, 11841-11847
4518092 CIFC42 H52 F6 Mn N4 O6 S2P 21 21 2110.8133; 18.3449; 22.899
90; 90; 90		4542.4Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518093 CIFC53 H76 Cl2 F6 Mn N4 O9 S2P 43 21 218.048; 18.048; 18.684
90; 90; 90		6086Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518094 CIFC36 H40 F6 Mn N4 O8 S2P 43 21 215.2678; 15.2678; 17.167
90; 90; 90		4001.7Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518095 CIFC42 H52 F6 Mn N4 O6 S2P 21 21 2110.8038; 18.2978; 22.8902
90; 90; 90		4525.1Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518103 CIFC25 H25 N O5P 1 21 111.568; 14.8438; 12.2105
90; 94.94; 90		2088.91Harada, Shingo; Yanagawa, Mai; Nemoto, Tetsuhiro
Dual-Functional Enone-Directing Group/Electrophile for Sequential C‒C Bond Formation with α-Diazomalonates: A Short Synthesis of Chiral 3,4-Fused Tricyclic Indoles
ACS Catalysis, 2020, 11971-11979
4518108 CIFC14 H18 Br NP 21 21 216.4796; 10.8112; 17.4816
90; 90; 90		1224.63Li, Zhenghua; Zhang, Liang; Nishiura, Masayoshi; Luo, Gen; Luo, Yi; Hou, Zhaomin
Enantioselective Cyanoborylation of Allenes by N-Heterocyclic Carbene-Copper Catalysts
ACS Catalysis, 2020, 11685-11692
4518109 CIFC5 H8 F N OP 1 21/c 110.9416; 5.8946; 8.9783
90; 112.366; 90		535.51Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518110 CIFC5 H8 F N OP 1 21/c 16.8234; 7.0364; 11.2928
90; 93.296; 90		541.29Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518111 CIFC12 H13 F4 NP b c n16.6845; 6.2599; 21.2252
90; 90; 90		2216.83Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518112 CIFC13 H14 F4 N2 OP 1 21/c 112.8484; 8.4676; 11.8938
90; 95.519; 90		1287.99Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518113 CIFC13 H19 F N2 O2P 1 21/n 111.8985; 7.4145; 15.3304
90; 101.584; 90		1324.92Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518114 CIFC7 H11 F N2 OP 1 21/c 14.7931; 12.9627; 12.803
90; 97.469; 90		788.72Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518115 CIFC5 H11 Cl F NP 1 21 16.6025; 7.3672; 7.036
90; 90.746; 90		342.216Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518119 CIFC47 H51 Al Cl4 N5 O4 P2 RhP 1 21/n 115.4262; 17.0323; 19.6403
90; 111.781; 90		4791.96Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518120 CIFC88 H68 Cl14 Ga4 N8 P4 Rh2P -116.4861; 17.1218; 18.1159
102.604; 96.8135; 92.8749		4939.85Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518121 CIFC47 H45 Cl7 In2 N3 O2 P2 RhP -112.4389; 13.5826; 15.0995
83.4699; 80.9723; 86.2699		2500.25Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518122 CIFC126 H110 Cl12 Ga4 N6 O3 P6 Rh2C 1 2/c 137.4179; 14.6854; 22.6886
90; 90.5378; 90		12466.8Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518130 CIFC11 H12 F3 N O2 SP -17.1106; 8.8828; 9.8984
77.175; 89.3; 74.07		585.4Ge, Hangming; Wu, Botao; Liu, Yafei; Wang, Haoyang; Shen, Qilong
Synergistic Lewis Acid and Photoredox-Catalyzed Trifluoromethylative Difunctionalization of Alkenes with Selenium Ylide-Based Trifluoromethylating Reagent
ACS Catalysis, 2020, 12414-12424
4518133 CIFC57 H37 Al Cl10 N2 O2P 1 21/c 112.236; 21.4326; 20.1723
90; 103.841; 90		5136.56Hubbell, Aran K.; Lamb, Jessica R.; Klimovica, Kristine; Mulzer, Michael; Shaffer, Timothy D.; MacMillan, Samantha N.; Coates, Geoffrey W.
Catalyst-Controlled Regioselective Carbonylation of Isobutylene Oxide to Pivalolactone
ACS Catalysis, 2020, 12537-12543
4518134 CIFC96 H86 Al B N2 O7P 1 n 114.16596; 24.26807; 21.69468
90; 95.347; 90		7425.75Hubbell, Aran K.; Lamb, Jessica R.; Klimovica, Kristine; Mulzer, Michael; Shaffer, Timothy D.; MacMillan, Samantha N.; Coates, Geoffrey W.
Catalyst-Controlled Regioselective Carbonylation of Isobutylene Oxide to Pivalolactone
ACS Catalysis, 2020, 12537-12543
4518143 CIFC20 H20 N2 O2P 1 21/c 112.058; 9.432; 14.999
90; 104.566; 90		1651Zhu, Min; Zhang, Xiao; Zheng, Chao; You, Shu-Li
Visible-Light-Induced Dearomatization via [2+2] Cycloaddition or 1,5-Hydrogen Atom Transfer: Divergent Reaction Pathways of Transient Diradicals
ACS Catalysis, 2020, 12618-12626
4518144 CIFC17 H20 N2 O2P 1 21/c 111.248; 13.4191; 9.9224
90; 96.859; 90		1486.95Zhu, Min; Zhang, Xiao; Zheng, Chao; You, Shu-Li
Visible-Light-Induced Dearomatization via [2+2] Cycloaddition or 1,5-Hydrogen Atom Transfer: Divergent Reaction Pathways of Transient Diradicals
ACS Catalysis, 2020, 12618-12626
4518145 CIFC20 H19 Cl N2 O2P 1 21/c 18.425; 13.085; 16.325
90; 104.597; 90		1741.6Zhu, Min; Zhang, Xiao; Zheng, Chao; You, Shu-Li
Visible-Light-Induced Dearomatization via [2+2] Cycloaddition or 1,5-Hydrogen Atom Transfer: Divergent Reaction Pathways of Transient Diradicals
ACS Catalysis, 2020, 12618-12626
4518146 CIFC20 H16 Br2 Co N4P 1 21/c 18.567; 14.5739; 15.62
90; 97.596; 90		1933.1Dorval, Céline; Tricoire, Maxime; Begouin, Jeanne-Marie; Gandon, Vincent; Gosmini, Corinne
Cobalt-Catalyzed C(sp2)‒CN Bond Activation: Cross-Electrophile Coupling for Biaryl Formation and Mechanistic Insight
ACS Catalysis, 2020, 12819-12827
4518147 CIFC120 H96 Br9 Co4 Mn2 N24P 63 2 213.2935; 13.2935; 40.9
90; 90; 120		6259.4Dorval, Céline; Tricoire, Maxime; Begouin, Jeanne-Marie; Gandon, Vincent; Gosmini, Corinne
Cobalt-Catalyzed C(sp2)‒CN Bond Activation: Cross-Electrophile Coupling for Biaryl Formation and Mechanistic Insight
ACS Catalysis, 2020, 12819-12827
4518163 CIFC22 H30 B Fe NP 21 21 219.618; 14.2124; 14.4586
90; 90; 90		1976.42Dong, Wu-Wei; Li, Yi-Nan; Chang, Xin; Shen, Chong; Wang, Chun-Jiang
Chiral Ugi-Type Amines: Practical Synthesis, Ligand Development, and Asymmetric Catalysis
ACS Catalysis, 2020, 12954-12959
4518164 CIFC27 H27 N O5P 1 21/c 113.9717; 22.3087; 15.064
90; 90.591; 90		4695.06Sugawara, Masumi; Ohnishi, Rikako; Ezawa, Tetsuya; Akakabe, Mai; Sawamura, Miki; Hojo, Daiki; Hashizume, Daisuke; Sohtome, Yoshihiro; Sodeoka, Mikiko
Regiodivergent Oxidative Cross-Coupling of Catechols with Persistent tert-Carbon Radicals
ACS Catalysis, 2020, 12770-12782
4518165 CIFC96 H82 B2 F8 O6 P4 Pd2P 21 21 2113.7004; 20.3764; 29.3278
90; 90; 90		8187.3Sugawara, Masumi; Ohnishi, Rikako; Ezawa, Tetsuya; Akakabe, Mai; Sawamura, Miki; Hojo, Daiki; Hashizume, Daisuke; Sohtome, Yoshihiro; Sodeoka, Mikiko
Regiodivergent Oxidative Cross-Coupling of Catechols with Persistent tert-Carbon Radicals
ACS Catalysis, 2020, 12770-12782
4518175 CIFC24 H42 Cl Ir N O6 PP -17.9554; 13.3409; 13.583
108.591; 95.505; 94.138		1352Dodge, Henry M.; Kita, Matthew R.; Chen, Chun-Hsing; Miller, Alexander J. M.
Identifying and Evading Olefin Isomerization Catalyst Deactivation Pathways Resulting from Ion-Tunable Hemilability
ACS Catalysis, 2020, 13019-13030
4518176 CIFC97 H72 B2 F48 Ir Li N O5 PP 112.8158; 12.8715; 17.2525
80.155; 89.504; 66.413		2564.14Dodge, Henry M.; Kita, Matthew R.; Chen, Chun-Hsing; Miller, Alexander J. M.
Identifying and Evading Olefin Isomerization Catalyst Deactivation Pathways Resulting from Ion-Tunable Hemilability
ACS Catalysis, 2020, 13019-13030
4518181 CIFC7 H13 Cl OP 21 21 215.24; 6.2805; 23.9605
90; 90; 90		788.54Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518182 CIFC8 H15 Cl OP 1 21 16.2973; 5.2861; 12.6948
90; 93.567; 90		421.77Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518183 CIFC9 H15 Cl O2P 21 21 217.2887; 9.0165; 15.2516
90; 90; 90		1002.31Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518184 CIFC10 H16 O2P 21 21 216.1266; 8.4858; 18.3913
90; 90; 90		956.15Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518185 CIFC68 H56 Cl2 Cu2 F8 O2 P4P -113.3478; 14.062; 17.8249
90.177; 93.026; 114.592		3036.8Kang, Taeho; Erbay, Tuğçe G.; Xu, Kane L.; Gallego, Gary M.; Burtea, Alexander; Nair, Sajiv K.; Patman, Ryan L.; Zhou, Ru; Sutton, Scott C.; McAlpine, Indrawan J.; Liu, Peng; Engle, Keary M.
Multifaceted Substrate‒Ligand Interactions Promote the Copper-Catalyzed Hydroboration of Benzylidenecyclobutanes and Related Compounds
ACS Catalysis, 2020, 13075-13083
4518186 CIFC80 H64 Cl2 Cu2 F24 O3 P4P -116.4338; 16.5229; 17.2231
69.906; 77.081; 64.824		3958.2Kang, Taeho; Erbay, Tuğçe G.; Xu, Kane L.; Gallego, Gary M.; Burtea, Alexander; Nair, Sajiv K.; Patman, Ryan L.; Zhou, Ru; Sutton, Scott C.; McAlpine, Indrawan J.; Liu, Peng; Engle, Keary M.
Multifaceted Substrate‒Ligand Interactions Promote the Copper-Catalyzed Hydroboration of Benzylidenecyclobutanes and Related Compounds
ACS Catalysis, 2020, 13075-13083
4518195 CIFC20 H19 Br N2 O3P 21 21 2111.3768; 13.3425; 24.5874
90; 90; 90		3732.24Harada, Shingo; Kobayashi, Mayu; Kono, Masato; Nemoto, Tetsuhiro
Site-Selective and Chemoselective C‒H Functionalization for the Synthesis of Spiroaminals via a Silver-Catalyzed Nitrene Transfer Reaction
ACS Catalysis, 2020, 10, 13296-13304
4518198 CIFC20 H24 I N2 RhP 1 21/c 114.0181; 8.46; 16.4369
90; 102.753; 90		1901.2Sánchez-Page, Beatriz; Munarriz, Julen; Jiménez, M. Victoria; Pérez-Torrente, Jesús J.; Blasco, Javier; Subias, Gloria; Passarelli, Vincenzo; Álvarez, Patricia
β-(Z) Selectivity Control by Cyclometalated Rhodium(III)‒Triazolylidene Homogeneous and Heterogeneous Terminal Alkyne Hydrosilylation Catalysts
ACS Catalysis, 2020, 10, 13334-13351
4518199 CIFC26 H28 Cl3 I N3 RhP 1 21/c 117.652; 12.0217; 14.0368
90; 113.194; 90		2738Sánchez-Page, Beatriz; Munarriz, Julen; Jiménez, M. Victoria; Pérez-Torrente, Jesús J.; Blasco, Javier; Subias, Gloria; Passarelli, Vincenzo; Álvarez, Patricia
β-(Z) Selectivity Control by Cyclometalated Rhodium(III)‒Triazolylidene Homogeneous and Heterogeneous Terminal Alkyne Hydrosilylation Catalysts
ACS Catalysis, 2020, 10, 13334-13351
4518200 CIFC30 H31 N5 TiP 43 21 212.9396; 12.9396; 35.996
90; 90; 90		6026.9See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518201 CIFC82.52 H77.04 N10 Ti2P 1 21/n 19.4737; 36.2928; 19.9562
90; 95.112; 90		6834.2See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518202 CIFC80 H78 Cl N2 O3 P3 Ti2P 1 21/c 124.117; 15.0952; 20.943
90; 114.01; 90		6964.6See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518203 CIFC50 H62 Cl4 N6 Ti2P -19.8644; 12.5071; 12.5128
116.587; 93.947; 112.994		1213.89See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518214 CIFC16 H13 Cl2 N SC 1 c 111.7514; 13.3298; 9.6736
90; 95.87; 90		1507.36Su, Yong-Liang; Tram, Linh; Wherritt, Daniel; Arman, Hadi; Griffith, Wendell P.; Doyle, Michael P.
α-Amino Radical-Mediated Diverse Difunctionalization of Alkenes: Construction of C‒C, C‒N, and C‒S Bonds
ACS Catalysis, 2020, 10, 13682-13687
4518215 CIFC14 H11 Cl2 N SP 1 21 17.9208; 5.9641; 13.9611
90; 95.677; 90		656.294Su, Yong-Liang; Tram, Linh; Wherritt, Daniel; Arman, Hadi; Griffith, Wendell P.; Doyle, Michael P.
α-Amino Radical-Mediated Diverse Difunctionalization of Alkenes: Construction of C‒C, C‒N, and C‒S Bonds
ACS Catalysis, 2020, 10, 13682-13687
4518216 CIFC81 H90 Br5 N13 Ni4 O3P 1 21 112.1646; 21.938; 16.962
90; 102.835; 90		4413.5Long, Cheng-Yu; Ni, Shao-Fei; Su, Min-Hui; Wang, Xue-Qiang; Tan, Weihong
Highly Chemoselective Access to 2,2′-Diaminobiaryls via Ni-Catalyzed Protecting-Group-Free Coupling of 2-Haloanilines
ACS Catalysis, 2020, 10, 13641-13649
4518242 CIFC25 H20 F N O5 SP 1 21/c 116.6287; 9.5046; 14.4444
90; 109.835; 90		2147.5Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518243 CIFC26 H22 F N O5 SP -18.0552; 11.7776; 12.3272
105.882; 95.33; 93.032		1116.24Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518244 CIFC26 H22 F3 N O4 SP c c n20.9621; 13.2147; 17.096
90; 90; 90		4735.73Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518245 CIFC27.5 H28 F2 N O6.5 SP 1 21/c 111.9745; 8.5948; 25.5692
90; 103.368; 90		2560.2Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518246 CIFC20 H20 F N O4 SP c a 2120.8044; 9.0158; 10.0248
90; 90; 90		1880.33Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518247 CIFC26 H25 F2 N O4 SP 1 21/c 118.2175; 7.7392; 16.7579
90; 102.923; 90		2302.83Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518248 CIFC19 H17 N O5 SP 1 21/n 18.91; 10.057; 20.0309
90; 102.026; 90		1755.53Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518249 CIFC26 H23 F2 N O5 SP 1 21 19.9672; 13.3088; 17.6941
90; 97.059; 90		2329.36Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518250 CIFC19 H17 F2 N O4 SP 1 21/n 18.8969; 10.1294; 20.1617
90; 101.962; 90		1777.52Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518251 CIFC25 H20 F3 N O4 SP 1 21 19.7433; 7.3884; 15.0351
90; 97.095; 90		1074.05Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518260 CIFC24 H24 F3 N O2 SP 1 21/n 116.6732; 7.8057; 16.9323
90; 103.9; 90		2139.14Apolinar, Omar; Tran, Van T.; Kim, Nana; Schmidt, Michael A.; Derosa, Joseph; Engle, Keary M.
Sulfonamide Directivity Enables Ni-Catalyzed 1,2-Diarylation of Diverse Alkenyl Amines
ACS Catalysis, 2020, 14234-14239
4518266 CIFC12 H15 N O6P 1 21 18.3518; 9.1518; 9.0312
90; 112.947; 90		635.67Niederer, Kyle A.; Gilmartin, Philip H.; Kozlowski, Marisa C.
Oxidative Photocatalytic Homo- and Cross-Coupling of Phenols: Nonenzymatic, Catalytic Method for Coupling Tyrosine
ACS Catalysis, 2020, 14615-14623
4518269 CIFC38 H28 P2P 1 21/c 110.5142; 13.9784; 19.3527
90; 100.698; 90		2794.9Chen, Xiao-Yang; Zhou, Xukai; Wang, Jianchun; Dong, Guangbin
FMPhos: Expanding the Catalytic Capacity of Small-Bite-Angle Bisphosphine Ligands in Regioselective Alkene Hydrofunctionalizations
ACS Catalysis, 2020, 14349-14358
4518270 CIFC43 H45 Cl2 F6 Fe Mo N3 O6 S2P 1 21 111.4984; 18.3575; 12.3063
90; 115.676; 90		2341.1Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518271 CIFC77 H61 B F33 Mo N3 OP -112.9087; 16.1499; 20.173
101.303; 101.414; 103.356		3879.9Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518272 CIFC75 H59 B F33 Mo N3 OP -112.8175; 15.5311; 20.3008
104.613; 96.591; 92.48		3873.7Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518273 CIFC77 H58 B Cl2 F33 Mo N4 OP -112.8554; 16.2503; 19.8326
105.02; 96.524; 96.704		3929.2Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518274 CIFC76 H58.5 B F33 Mo N3.5 OP -112.871; 15.3569; 39.432
83.163; 86.32; 89.432		7722.7Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518275 CIFC26 H21 F18 Mo N O2P 1 21/n 112.4112; 10.6334; 23.3549
90; 103.504; 90		2997Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518276 CIFC8 H8 Cl N OP 1 21/c 16.1585; 4.6786; 26.8306
90; 96.26; 90		768.46Leong, Bi-Xiang; Teo, Yeow-Chuan; Condamines, Cloé; Yang, Ming-Chung; Su, Ming-Der; So, Cheuk-Wai
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
ACS Catalysis, 2020, 14824-14833
4518277 CIFC8 H9 N O2C 1 2/c 114.8957; 12.8359; 8.415
90; 111.928; 90		1492.55Leong, Bi-Xiang; Teo, Yeow-Chuan; Condamines, Cloé; Yang, Ming-Chung; Su, Ming-Der; So, Cheuk-Wai
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
ACS Catalysis, 2020, 14824-14833
4518278 CIFC13 H19 N OP 6116.8594; 16.8594; 8.3896
90; 90; 120		2065.2Leong, Bi-Xiang; Teo, Yeow-Chuan; Condamines, Cloé; Yang, Ming-Chung; Su, Ming-Der; So, Cheuk-Wai
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
ACS Catalysis, 2020, 14824-14833
4518293 CIFC79 H45.5 Br2 F6 I2 O10P 1 21 118.5988; 13.7054; 26.5064
90; 104.133; 90		6552.1Lai, Junshan; Fianchini, Mauro; Pericàs, Miquel A.
Development of Immobilized SPINOL-Derived Chiral Phosphoric Acids for Catalytic Continuous Flow Processes. Use in the Catalytic Desymmetrization of 3,3-Disubstituted Oxetanes
ACS Catalysis, 2020, 14971-14983
4518327 CIFC28 H33 B Br N O4P -110.0807; 11.1859; 12.2258
74.6461; 84.2332; 88.2173		1322.66Nallagonda, Rajender; Karimov, Rashad R.
Copper-Catalyzed Regio- and Diastereoselective Additions of Boron-Stabilized Carbanions to Heteroarenium Salts: Synthesis of Azaheterocycles Containing Contiguous Stereocenters
ACS Catalysis, 2020, 248-254
4518328 CIFC26 H32 B0 N2 O4 SP -19.2929; 11.4055; 12.1564
104.13; 93.917; 90.897		1245.86Nallagonda, Rajender; Karimov, Rashad R.
Copper-Catalyzed Regio- and Diastereoselective Additions of Boron-Stabilized Carbanions to Heteroarenium Salts: Synthesis of Azaheterocycles Containing Contiguous Stereocenters
ACS Catalysis, 2020, 248-254
4518332 CIFC31 H29 N O2 SP b c a13.793; 18.478; 20.113
90; 90; 90		5126.1Zhong, Long-Jin; Li, Yang; An, De-Lie; Li, Jin-Heng
Heteroannulation of N-Fluoro-N-alkylsulfonamides with Terminal Alkynes via Remote C(sp3)‒H Functionalization
ACS Catalysis, 2020, 383-389
4518334 CIFC35 H26 F16 Ir N6 O PP 1 21/n 113.6349; 13.8194; 20.9311
90; 96.357; 90		3919.7He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518335 CIFC37 H20 F16 Ir N6 PP 1 21/c 113.4456; 15.4907; 19.3081
90; 108.084; 90		3822.9He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518336 CIFC32 H16 F10 Ir N5C 1 2/n 119.625; 17.8886; 17.9372
90; 93.187; 90		6287.4He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518337 CIFC18 H15 N O3 S2P 1 21/n 110.5004; 9.9404; 16.6691
90; 106.602; 90		1667.36He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518338 CIFC38 H21 F16 Ir N5 PC 1 2/c 120.2832; 20.7079; 18.8839
90; 107.83; 90		7550.7He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518339 CIFC23 H18 N2 O2P -15.221; 12.037; 14.359
78.97; 84.119; 87.601		880.8He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518340 CIFC38 H21 F16 Ir N5 PC 1 2/c 120.3077; 20.7973; 18.9412
90; 107.616; 90		7624.6He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518341 CIFC12 H14 O2C 1 2/c 115.2075; 6.9155; 20.9784
90; 110.663; 90		2064.3Nguyen, Kevin; Clement, Helen A.; Bernier, Louise; Coe, Jotham W.; Farrell, William; Helal, Christopher J.; Reese, Matthew R.; Sach, Neal W.; Lee, Jack C.; Hall, Dennis G.
Catalytic Enantioselective Synthesis of a cis-β-Boronyl Cyclobutylcarboxyester Scaffold and Its Highly Diastereoselective Nickel/Photoredox Dual-Catalyzed Csp3‒Csp2 Cross-Coupling to Access Elusive trans-β-Aryl/Heteroaryl Cyclobutylcarboxyesters
ACS Catalysis, 2020, 404-413
4518342 CIFC18 H15 B Br2 F3 K O2P 21 21 220.0712; 30.159; 6.8657
90; 90; 90		4156Nguyen, Kevin; Clement, Helen A.; Bernier, Louise; Coe, Jotham W.; Farrell, William; Helal, Christopher J.; Reese, Matthew R.; Sach, Neal W.; Lee, Jack C.; Hall, Dennis G.
Catalytic Enantioselective Synthesis of a cis-β-Boronyl Cyclobutylcarboxyester Scaffold and Its Highly Diastereoselective Nickel/Photoredox Dual-Catalyzed Csp3‒Csp2 Cross-Coupling to Access Elusive trans-β-Aryl/Heteroaryl Cyclobutylcarboxyesters
ACS Catalysis, 2020, 404-413
4518343 CIFC31 H35 B O5P 21 21 219.1022; 11.2466; 27.186
90; 90; 90		2783Nguyen, Kevin; Clement, Helen A.; Bernier, Louise; Coe, Jotham W.; Farrell, William; Helal, Christopher J.; Reese, Matthew R.; Sach, Neal W.; Lee, Jack C.; Hall, Dennis G.
Catalytic Enantioselective Synthesis of a cis-β-Boronyl Cyclobutylcarboxyester Scaffold and Its Highly Diastereoselective Nickel/Photoredox Dual-Catalyzed Csp3‒Csp2 Cross-Coupling to Access Elusive trans-β-Aryl/Heteroaryl Cyclobutylcarboxyesters
ACS Catalysis, 2020, 404-413
4518345 CIFC118 H75 Cl18 F12 N4 O16.5 Rh2 S8C 1 2 130.933; 17.5225; 24.1606
90; 92.0449; 90		13087.3Murai, Takuya; Lu, Wenjie; Kuribayashi, Toshifumi; Morisaki, Kazuhiro; Ueda, Yoshihiro; Hamada, Shohei; Kobayashi, Yusuke; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo; Furuta, Takumi
Conformational Control in Dirhodium(II) Paddlewheel Catalysts Supported by Chalcogen-Bonding Interactions for Stereoselective Intramolecular C‒H Insertion Reactions
ACS Catalysis, 2020, 568-578
4518346 CIFC98 H66 Cl6 F12 N4 O14 Rh2P 21 21 2114.4646; 23.7613; 26.3686
90; 90; 90		9062.8Murai, Takuya; Lu, Wenjie; Kuribayashi, Toshifumi; Morisaki, Kazuhiro; Ueda, Yoshihiro; Hamada, Shohei; Kobayashi, Yusuke; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo; Furuta, Takumi
Conformational Control in Dirhodium(II) Paddlewheel Catalysts Supported by Chalcogen-Bonding Interactions for Stereoselective Intramolecular C‒H Insertion Reactions
ACS Catalysis, 2020, 568-578
4518347 CIFC110 H94 N10 O16 Rh2P 110.4116; 15.2831; 16.3622
71.608; 89.077; 85.189		2461.74Murai, Takuya; Lu, Wenjie; Kuribayashi, Toshifumi; Morisaki, Kazuhiro; Ueda, Yoshihiro; Hamada, Shohei; Kobayashi, Yusuke; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo; Furuta, Takumi
Conformational Control in Dirhodium(II) Paddlewheel Catalysts Supported by Chalcogen-Bonding Interactions for Stereoselective Intramolecular C‒H Insertion Reactions
ACS Catalysis, 2020, 568-578
4518363 CIFC29.5 H23 Cl F12 Fe N6 O P2C 1 2/c 120.0016; 18.5063; 18.5977
90; 105.98; 90		6618Gonell, Sergio; Lloret-Fillol, Julio; Miller, Alexander J. M.
An Iron Pyridyl-Carbene Electrocatalyst for Low Overpotential CO2 Reduction to CO
ACS Catalysis, 2020, 615-626
4518364 CIFC31 H27 Cl2 F12.43 Fe N7 P2P 1 21/n 113.7127; 17.4292; 16.0993
90; 107.938; 90		3660.72Gonell, Sergio; Lloret-Fillol, Julio; Miller, Alexander J. M.
An Iron Pyridyl-Carbene Electrocatalyst for Low Overpotential CO2 Reduction to CO
ACS Catalysis, 2020, 615-626
4518384 CIFC44 H54 Cl2 N O3 P RuC 1 c 116.577; 15.944; 15.596
90; 99.187; 90		4069.2Eivgi, Or; Vaisman, Anna; Lemcoff, N. Gabriel
Latent, Yet Highly Active Photoswitchable Olefin Metathesis Precatalysts Bearing Cyclic Alkyl Amino Carbene (CAAC)/Phosphite Ligands
ACS Catalysis, 2020, 703-709
4518385 CIFC59 H60 Cl2 N O3 P RuP 1 21/n 112.6005; 18.784; 21.757
90; 101.619; 90		5044.1Eivgi, Or; Vaisman, Anna; Lemcoff, N. Gabriel
Latent, Yet Highly Active Photoswitchable Olefin Metathesis Precatalysts Bearing Cyclic Alkyl Amino Carbene (CAAC)/Phosphite Ligands
ACS Catalysis, 2020, 703-709
4518406 CIFC18 H15 N O3P 1 21/c 16.7743; 23.418; 8.802
90; 101.248; 90		1369.5Xin, Luoting; Wan, Wan; Yu, Yinghua; Wan, Qiuling; Ma, Liyao; Huang, Xueliang
Construction of Protoberberine Alkaloid Core through Palladium Carbene Bridging C‒H Bond Functionalization and Pyridine Dearomatization
ACS Catalysis, 2021, 1570-1577
4518407 CIFC25 H25 B0 F0 N O2P 21 21 217.1212; 13.75566; 18.96034
90; 90; 90		1857.29Xin, Luoting; Wan, Wan; Yu, Yinghua; Wan, Qiuling; Ma, Liyao; Huang, Xueliang
Construction of Protoberberine Alkaloid Core through Palladium Carbene Bridging C‒H Bond Functionalization and Pyridine Dearomatization
ACS Catalysis, 2021, 1570-1577
4518411 CIFC27 H30 N2 O5 S2P -19.172; 11.675; 12.09
91.099; 93.667; 105.21		1245.9Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518412 CIFC52 H52 Br2 F2 N4 O8 S4P 1 21 112.9016; 9.0322; 12.9338
90; 105.257; 90		1454.05Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518413 CIFC27 H30 Cl2 N2 O4 S2P 21 21 219.35619; 16.99; 17.21824
90; 90; 90		2737.04Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518414 CIFC22.5 H19 Br Cl N O4 SP -112.185; 12.529; 14.695
82.566; 83.909; 87.659		2211.2Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518420 CIFC25 H30 N2 O9P 21 21 219.9196; 11.7763; 21.4011
90; 90; 90		2499.99Ghouilem, Juba; Tran, Christine; Grimblat, Nicolas; Retailleau, Pascal; Alami, Mouad; Gandon, Vincent; Messaoudi, Samir
Diastereoselective Pd-Catalyzed Anomeric C(sp3)‒H Activation: Synthesis of α-(Hetero)aryl C-Glycosides
ACS Catalysis, 2021, 1818-1826
4518421 CIFC25 H30 N2 O6P 21 21 2110.0246; 11.6273; 21.2713
90; 90; 90		2479.36Ghouilem, Juba; Tran, Christine; Grimblat, Nicolas; Retailleau, Pascal; Alami, Mouad; Gandon, Vincent; Messaoudi, Samir
Diastereoselective Pd-Catalyzed Anomeric C(sp3)‒H Activation: Synthesis of α-(Hetero)aryl C-Glycosides
ACS Catalysis, 2021, 1818-1826
4518422 CIFC19 H19 N O4 SP 21 21 218.4774; 10.9811; 18.1554
90; 90; 90		1690.11Liang, Ren-Xiao; Zhong, Chao; Liu, Zhi-Hong; Yang, Miao; Tang, Heng-Wei; Chen, Jian-Fei; Yang, Yun-Fang; Jia, Yi-Xia
Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives
ACS Catalysis, 2021, 1827-1832
4518423 CIFC23 H27 N O4 SP 659.7067; 9.7067; 39.2119
90; 90; 120		3199.57Liang, Ren-Xiao; Zhong, Chao; Liu, Zhi-Hong; Yang, Miao; Tang, Heng-Wei; Chen, Jian-Fei; Yang, Yun-Fang; Jia, Yi-Xia
Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives
ACS Catalysis, 2021, 1827-1832
4518426 CIFC32 H34 O4 SiP 1 21/c 19.4521; 26.2261; 11.8032
90; 103.62; 90		2843.6Ni, Dongshun; Brown, M. Kevin
Three-Component Ni-Catalyzed Silylacylation of Alkenes
ACS Catalysis, 2021, 1858-1862
4518429 CIFC34 H29 Cl3 O6P 1 21/c 110.1057; 12.677; 24.493
90; 98.332; 90		3104.7Koshikawa, Takumi; Nagashima, Yuki; Tanaka, Ken
Gold-Catalyzed [3 + 2] Annulation, Carbenoid Transfer, and C‒H Insertion Cascade: Elucidation of Annulation Mechanisms via Benzopyrylium Intermediates
ACS Catalysis, 2021, 1932-1937
4518430 CIFC48 H52 Cl4 N2 O Ru SiP n a 2115.2754; 28.119; 10.416
90; 90; 90		4474Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518431 CIFC43 H51 Cl4 N3 O3 Ru SP 1 21/n 113.6581; 10.7783; 30.3452
90; 96.306; 90		4440.1Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518432 CIFC41 H47 Cl4 N3 O2 Ru SP b c a21.747; 16.485; 23.171
90; 90; 90		8307Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518433 CIFC55 H67 Cl2 N3 O6 Ru SP -111.0039; 12.6857; 20.649
101.995; 101.394; 106.335		2603.1Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518434 CIFC42 H44 Cl2 Fe N2 RuP -112.269; 13.206; 13.74
103.978; 96.479; 116.864		1862.7Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518435 CIFC59 H75 Cl4 N3 O7 Ru SP -112.58; 13.814; 19.537
90.61; 105.904; 113.609		2963.8Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518436 CIFC48 H51 Cl2 N4 O4 Ru S2P 1 21/n 111.6701; 29.6716; 13.7738
90; 93.446; 90		4760.8Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518437 CIFC41 H52 Cl2 N2 O RuP -110.2526; 12.923; 14.9304
75.27; 77.074; 87.61		1864.5Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518438 CIFC40 H45 Cl4 N3 O2 Ru SP 1 21/c 18.471; 26.951; 18.341
90; 97.843; 90		4148Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518439 CIFC46 H55 Cl6 N3 O2 Ru SP 1 21/n 115.3127; 13.8064; 22.985
90; 91.3; 90		4858.1Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518440 CIFC43 H51 Cl4 N3 O3 Ru SP 1 21/n 113.3662; 19.3514; 18.2778
90; 107.451; 90		4510Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518441 CIFC75 H78 Cl10 N6 O4 Ru2P 1 21/n 119.5436; 16.2686; 25.2292
90; 92.134; 90		8016Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518442 CIFC38 H46 Cl2 N2 RuP 1 21 111.9816; 10.5576; 13.8098
90; 93.972; 90		1742.7Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518443 CIFC41 H42 Cl2 N3 O3 Ru SP 1 21/c 110.9001; 16.3943; 21.6403
90; 98.664; 90		3823Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518444 CIFC48 H57 Cl2 N3 O3 Ru SP 1 21/c 112.6853; 12.842; 32.754
90; 96.636; 90		5300Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518456 CIFC26 H49 Co P2P -110.482; 11.48; 12.182
109.71; 102.2; 98.68		1308.9Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518457 CIFC29 H53 Co P2P 1 21/n 19.289; 9.1; 16.695
90; 91.33; 90		1410.8Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518458 CIFC52 H49 Co P4P 1 21/n 19.8781; 20.7751; 20.9768
90; 92.271; 90		4301.4Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518459 CIFC26 H48 Co I2 P2P 21 21 219.1792; 13.8808; 23.1857
90; 90; 90		2954.2Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518460 CIFC37 H35 F N2 O7P 21 21 2116.485; 24.296; 24.715
90; 90; 90		9899Tang, Xiaodong; Tan, Chuan Xiang Alvin; Chan, Wai-Lun; Zhang, Fuhao; Zheng, Wenrui; Lu, Yixin
Dielectrophilic Allenic Ketone-Enabled [4 + 2] Annulation with 3,3’-Bisoxindoles: Enantioselective Creation of Two Contiguous Quaternary Stereogenic Centers
ACS Catalysis, 2021, 1361-1367
4518461 CIFC14 H15 N OP 1 21/n 113.9071; 9.5864; 16.966
90; 100.194; 90		2226.2Mo, Jiayu; Messinis, Antonis M.; Oliveira, João C. A.; Demeshko, Serhiy; Meyer, Franc; Ackermann, Lutz
Iron-Catalyzed Triazole-Enabled C‒H Activation with Bicyclopropylidenes
ACS Catalysis, 2021, 1053-1064
4518462 CIFC36 H51 Br O2P 21 21 215.781; 9.7023; 56.176
90; 90; 90		3150.9Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518463 CIFC11 H9 NP 21 21 214.6608; 8.0082; 22.8683
90; 90; 90		853.55Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518464 CIFC15 H11 NP 1 21/n 110.3922; 8.5924; 13.4648
90; 112.087; 90		1114.09Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518465 CIFC13 H10 O2P 1 21/c 111.807; 11.5282; 7.74435
90; 108.688; 90		998.54Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518466 CIFC12 H10 N2P 1 21/c 116.6487; 5.1944; 11.2609
90; 101.125; 90		955.54Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518467 CIFC63 H98 Ag2 O6 P2P b c a16.8262; 19.3356; 41.108
90; 90; 90		13374.3Tlahuext-Aca, Adrian; Hartwig, John F.
Site-Selective Silver-Catalyzed C‒H Bond Deuteration of Five-Membered Aromatic Heterocycles and Pharmaceuticals
ACS Catalysis, 2021, 1119-1127
4518468 CIFC18 H17 N O S2P 1 21/n 15.591; 21.778; 12.608
90; 99.18; 90		1515.5Wang, Rong-Hua; Li, Jiang-Fei; Li, Yue; Qi, Shao-Long; Zhang, Tao; Luan, Yu-Xin; Ye, Mengchun
Selective C(sp3)‒H Cleavage of Enamides for Synthesis of 2-Pyridones via Ligand-Enabled Ni‒Al Bimetallic Catalysis
ACS Catalysis, 2021, 11, 858-864
4518469 CIFC32 H40 I N3 O5 SP 1 21 112.5558; 12.2352; 21.214
90; 91.478; 90		3257.9Zhang, Yueteng; Ji, Peng; Gao, Feng; Huang, He; Zeng, Fanxun; Wang, Wei
Photoredox Asymmetric Nucleophilic Dearomatization of Indoles with Neutral Radicals
ACS Catalysis, 2021, 11, 998-1007
4518470 CIFC27 H28 N2 O5 SC 1 2 122.7379; 7.3689; 14.3911
90; 91.61; 90		2410.3Zhang, Yueteng; Ji, Peng; Gao, Feng; Huang, He; Zeng, Fanxun; Wang, Wei
Photoredox Asymmetric Nucleophilic Dearomatization of Indoles with Neutral Radicals
ACS Catalysis, 2021, 11, 998-1007
4518471 CIFC19 H2 B F13P 1 21/a 19.912; 17.662; 10.435
90; 114.281; 90		1665.2Nakashima, Tomoya; Nakayama, Yuushou; Shiono, Takeshi; Tanaka, Ryo
Neutral, Noncoordinating, and Hydrocarbon-Soluble Protic Cocatalyst for Olefin Polymerization
ACS Catalysis, 2021, 11, 865-870
4518472 CIFC13 H3 B F8 OP 1 21/c 116.0009; 4.7685; 16.6499
90; 116.991; 90		1132.02Nakashima, Tomoya; Nakayama, Yuushou; Shiono, Takeshi; Tanaka, Ryo
Neutral, Noncoordinating, and Hydrocarbon-Soluble Protic Cocatalyst for Olefin Polymerization
ACS Catalysis, 2021, 11, 865-870

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