Crystallography Open Database

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4514669 CIFC25 H25 Br N2 O2 SP 419.7248; 9.7248; 48.32
90; 90; 90		4569.7Ibáñez, Ignacio; Kaneko, Mio; Kamei, Yuto; Tsutsumi, Ryosuke; Yamanaka, Masahiro; Akiyama, Takahiko
Enantioselective Friedel–Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate
ACS Catalysis, 2019, 9, 6903
4514670 CIFC22 H20 O2C 1 2/c 115.8408; 13.142; 16.3982
90; 98.987; 90		3371.9Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514671 CIFC25 H19 N O2P 1 21/c 115.6269; 10.8792; 22.0724
90; 100.839; 90		3685.5Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514672 CIFC18 H11 N OP 1 21/c 18.2853; 31.984; 19.542
90; 93.546; 90		5168.7Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514673 CIFC22 H14 N4P 1 21/c 19.9466; 17.8664; 9.4521
90; 100.253; 90		1652.91Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514674 CIFC19 H13 N OP -17.861; 9.282; 9.934
83.675; 72.702; 85.815		687.2Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514675 CIFC30 H22 O3P 1 21/c 124.6109; 12.239; 14.7299
90; 98.22; 90		4391.3Giri, Sovan Sundar; Liu, Rai-Shung
Copper-Catalyzed [4+2]-Cycloadditions of Isoxazoles with 2-Alkynylbenzaldehydes To Access Distinct α-Carbonylnaphthalene Derivatives: C(3,4)- versus C(4,5)-Regioselectivity at Isoxazoles
ACS Catalysis, 2019, 9, 7328
4514676 CIFC54 H55 B F4 N3 O5 P2 RhP -114.1394; 15.0162; 28.9031
77.688; 87.174; 78.469		5874.4Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H.
Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands
ACS Catalysis, 2019, 9, 7535
4514677 CIFC50 H49 B F4 N5 O5 P2 RhP -112.6207; 13.6039; 15.2008
72.598; 83.301; 76.784		2421.15Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H.
Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands
ACS Catalysis, 2019, 9, 7535
4514678 CIFC92 H86 B2 F8 N6 O10 P4 Rh2P 1 21/n 114.1446; 25.4077; 15.6384
90; 94.839; 90		5600.1Daubignard, Julien; Lutz, Martin; Detz, Remko J.; de Bruin, Bas; Reek, Joost N. H.
Origin of the Selectivity and Activity in the Rhodium-Catalyzed Asymmetric Hydrogenation Using Supramolecular Ligands
ACS Catalysis, 2019, 9, 7535
4514679 CIFC17 H21 B Br N O2P 1 21 111.3502; 7.45; 20.6376
90; 91.376; 90		1744.59Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J.
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
ACS Catalysis, 2019, 9, 6744
4514680 CIFC20 H16 Br N O2P 1 21 114.62776; 8.05742; 15.00218
90; 97.0979; 90		1754.64Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J.
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
ACS Catalysis, 2019, 9, 6744
4514681 CIFC11 H10 I0.96 N OP 1 21 19.8268; 5.6439; 9.8652
90; 99.353; 90		539.86Jia, Tao; Smith, Marshall J.; Pulis, Alexander P.; Perry, Gregory J. P.; Procter, David J.
Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes
ACS Catalysis, 2019, 9, 6744
4514682 CIFC14 H24 N2 O4 PdP 1 21/c 19.3121; 10.7025; 8.4772
90; 97.201; 90		838.2Feng, Wenhui; Wang, Tianyang; Liu, Dongzhi; Wang, Xiaotai; Dang, Yanfeng
Mechanism of the Palladium-Catalyzed C(sp3)–H Arylation of Aliphatic Amines: Unraveling the Crucial Role of Silver(I) Additives
ACS Catalysis, 2019, 9, 6672
4514683 CIFC42 H35 F12 N11 P2 Pd2P -112.0088; 12.3492; 17.137
101.431; 106.142; 105.372		2250.17Zhu, Jiancheng; Lindsay, Vincent N. G.
Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions
ACS Catalysis, 2019, 9, 6993
4514684 CIFC25 H20 Cl F6 N4 O P PdP -18.7896; 12.4079; 13.433
108.517; 105.407; 103.424		1256.4Zhu, Jiancheng; Lindsay, Vincent N. G.
Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions
ACS Catalysis, 2019, 9, 6993
4514685 CIFC45 H48 F12 N8 O3 P2 Pd2C 1 2/c 125.202; 8.3844; 24.157
90; 108.454; 90		4842Zhu, Jiancheng; Lindsay, Vincent N. G.
Benzimidazolyl Palladium Complexes as Highly Active and General Bifunctional Catalysts in Sustainable Cross-Coupling Reactions
ACS Catalysis, 2019, 9, 6993
4514686 CIFC12 H11 Br F3 N3 O2P 1 21/c 110.3636; 10.0648; 28.9197
90; 99.7; 90		2973.4Chen, Zhen; Ren, Nan; Ma, Xiaoxiao; Nie, Jing; Zhang, Fa-Guang; Ma, Jun-An
Silver-Catalyzed [3 + 3] Dipolar Cycloaddition of Trifluorodiazoethane and Glycine Imines: Access to Highly Functionalized Trifluoromethyl-Substituted Triazines and Pyridines
ACS Catalysis, 2019, 9, 4600
4514687 CIFC15 H11 Cl F3 N O2P 1 21/n 117.29; 4.519; 20.77
90; 111.24; 90		1513Chen, Zhen; Ren, Nan; Ma, Xiaoxiao; Nie, Jing; Zhang, Fa-Guang; Ma, Jun-An
Silver-Catalyzed [3 + 3] Dipolar Cycloaddition of Trifluorodiazoethane and Glycine Imines: Access to Highly Functionalized Trifluoromethyl-Substituted Triazines and Pyridines
ACS Catalysis, 2019, 9, 4600
4514688 CIFC34 H26 N2P 1 21/n 111.5593; 7.8828; 27.35
90; 98.043; 90		2467.6Noto, Naoki; Koike, Takashi; Akita, Munetaka
Visible-Light-Triggered Monofluoromethylation of Alkenes by Strongly Reducing 1,4-Bis(diphenylamino)naphthalene Photoredox Catalysis
ACS Catalysis, 2019, 9, 4382
4514689 CIFC21 H20 F3 N O5 SP 19.0328; 9.506; 13.9771
90.165; 95.249; 115.51		1077.42He, Xiao-Long; Zhao, Hui-Ru; Song, Xue; Jiang, Bo; Du, Wei; Chen, Ying-Chun
Asymmetric Barton–Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons
ACS Catalysis, 2019, 9, 4374
4514690 CIFC24 H25 N3 O4P 21 21 219.2464; 10.0773; 23.4808
90; 90; 90		2187.91He, Xiao-Long; Zhao, Hui-Ru; Song, Xue; Jiang, Bo; Du, Wei; Chen, Ying-Chun
Asymmetric Barton–Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons
ACS Catalysis, 2019, 9, 4374
4514691 CIFC25 H17 N OP 1 21/n 18.618; 11.775; 18.166
90; 103.293; 90		1794Yuan, Hairui; Guo, Lirong; Liu, Fengting; Miao, Zechen; Feng, Lei; Gao, Hongyin
Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles
ACS Catalysis, 2019, 9, 3906
4514692 CIFC31 H21 N OP 21 21 218.1125; 12.1517; 23.1044
90; 90; 90		2277.65Yuan, Hairui; Guo, Lirong; Liu, Fengting; Miao, Zechen; Feng, Lei; Gao, Hongyin
Copper-Catalyzed Tandem O-Vinylation of Arylhydroxylamines/[3,3]-Rearrangement/Cyclization: Synthesis of Highly Substituted Indoles and Benzoindoles
ACS Catalysis, 2019, 9, 3906
4514693 CIFC24 H46 N6 Ni O6P 21 21 218.7123; 16.0813; 20.4271
90; 90; 90		2861.9Garrido-Barros, Pablo; Grau, Sergi; Drouet, Samuel; Benet-Buchholz, Jordi; Gimbert-Suriñach, Carolina; Llobet, Antoni
Can Ni Complexes Behave as Molecular Water Oxidation Catalysts?
ACS Catalysis, 2019, 9, 3936
4514694 CIFC21 H44 N6 Ni O9C 1 2/c 155.552; 6.2616; 15.8906
90; 100.323; 90		5438Garrido-Barros, Pablo; Grau, Sergi; Drouet, Samuel; Benet-Buchholz, Jordi; Gimbert-Suriñach, Carolina; Llobet, Antoni
Can Ni Complexes Behave as Molecular Water Oxidation Catalysts?
ACS Catalysis, 2019, 9, 3936
4514695 CIFC26 H29 N OP 1 21/c 16.2208; 18.757; 17.484
90; 93.268; 90		2036.8Han, Chunhua; Fu, Zhiyuan; Guo, Songjin; Fang, Xinxin; Lin, Aijun; Yao, Hequan
Palladium-Catalyzed Remote 1,n-Arylamination of Unactivated Terminal Alkenes
ACS Catalysis, 2019, 9, 4196
4514696 CIFC58 H84 F7 N2 O4 P Pd SP 1 21/c 120.138; 13.1828; 24.998
90; 106.912; 90		6349.4Dennis, Joseph M.; White, Nicholas A.; Liu, Richard Y.; Buchwald, Stephen L.
Pd-Catalyzed C‒N Coupling Reactions Facilitated by Organic Bases: Mechanistic Investigation Leads to Enhanced Reactivity in the Arylation of Weakly Binding Amines
ACS Catalysis, 2019, 9, 3822
4514697 CIFC43 H73.5 P2 Ru SP -113.159; 15.396; 21.596
90.092; 92.283; 101.727		4280.3Zhou, Xiaoguang; Malakar, Santanu; Zhou, Tian; Murugesan, Sathiyamoorthy; Huang, Carlos; Emge, Thomas J.; Krogh-Jespersen, Karsten; Goldman, Alan S.
Catalytic Alkane Transfer Dehydrogenation by PSP-Pincer-Ligated Ruthenium. Deactivation of an Extremely Reactive Fragment by Formation of Allyl Hydride Complexes
ACS Catalysis, 2019, 9, 4072
4514698 CIFC38 H62 P2 Ru SP 1 21/c 113.2907; 15.6689; 18.8836
90; 105.176; 90		3795.4Zhou, Xiaoguang; Malakar, Santanu; Zhou, Tian; Murugesan, Sathiyamoorthy; Huang, Carlos; Emge, Thomas J.; Krogh-Jespersen, Karsten; Goldman, Alan S.
Catalytic Alkane Transfer Dehydrogenation by PSP-Pincer-Ligated Ruthenium. Deactivation of an Extremely Reactive Fragment by Formation of Allyl Hydride Complexes
ACS Catalysis, 2019, 9, 4072
4514699 CIFC30 H41 Br1.02 Fe P3P -19.4966; 9.593; 17.63
101.894; 96.481; 102.236		1515.2Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514700 CIFC30 H41 Fe N4 P3P 1 21/c 117.626; 10.7764; 16.1774
90; 98.63; 90		3038Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514701 CIFC129 H106 B2 F48 Fe2 N8 P6P 1 21/n 122.4451; 12.1053; 25.482
90; 101.904; 90		6774.7Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514702 CIFC42 H65 Fe K N2 O6 P3P 1 21/n 110.4864; 23.9154; 17.8619
90; 93.645; 90		4470.5Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514703 CIFC40 H61 Fe K N2 O4 P3P n m a25.9569; 17.0296; 12.1851
90; 90; 90		5386.2Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514704 CIFC84 H130 Fe2 K4 N4 O6 P6P 1 21/n 114.6713; 16.6256; 18.7129
90; 102.506; 90		4456.1Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514705 CIFC33 H50 Fe K N2 P3 SiP 21 21 2110.5863; 16.3326; 20.8095
90; 90; 90		3598Schild, Dirk J.; Peters, Jonas C.
Light Enhanced Fe-Mediated Nitrogen Fixation: Mechanistic Insights Regarding H<sub>2</sub> Elimination, HER, and NH<sub>3</sub> Generation.
ACS catalysis, 2019, 9, 4286-4295
4514706 CIFC28 H26 N4 O2 PdP 1 21/n 18.3908; 20.0893; 14.6398
90; 100.46; 90		2426.75Luo, Yun-Cheng; Yang, Chao; Qiu, Sheng-Qi; Liang, Qiu-Ju; Xu, Yun-He; Loh, Teck-Peng
Palladium(II)-Catalyzed Stereospecific Alkenyl C‒H Bond Alkylation of Allylamines with Alkyl Iodides
ACS Catalysis, 2019, 9, 4271
4514707 CIFC26 H28 Cl2 Co N4 OP 21 21 219.5625; 11.3203; 24.4937
90; 90; 90		2651.5Chen, Xu; Cheng, Zhaoyang; Lu, Zhan
Cobalt-Catalyzed Asymmetric Markovnikov Hydroboration of Styrenes
ACS Catalysis, 2019, 9, 4025
4514708 CIFC63 H73 Ni2 O3 P2P -110.2617; 16.0861; 17.7316
100.697; 90.004; 105.821		2763.17Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514709 CIFC32 H37 Ni O2 P SP -18.6245; 9.0612; 20.838
84.848; 88.901; 62.929		1443.8Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514710 CIFC34 H42 B Ni O3 PP 1 21/c 122.1829; 9.2102; 15.4936
90; 94.271; 90		3156.7Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514711 CIFC36 H44 B Ni O PP 1 21/n 18.8285; 20.3843; 17.3286
90; 95.23; 90		3105.5Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514712 CIFC28 H31 Ni PP -18.8889; 15.1597; 17.8889
91.217; 96.831; 90.693		2392.67Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514713 CIFC28 H30 Br Ni PP n a 2116.7529; 10.1199; 14.6061
90; 90; 90		2476.28Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni‒O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514714 CIFC21 H31 B2 N O4P 1 21/c 115.588; 10.6978; 14.1186
90; 107.935; 90		2239.97Liu, Jianguo; Chen, Jia-Yi; Jia, Mengjing; Ming, Bangrong; Jia, Jiong; Liao, Rong-Zhen; Tung, Chen-Ho; Wang, Wenguang
Ni–O Cooperation versus Nickel(II) Hydride in Catalytic Hydroboration of N-Heteroarenes
ACS Catalysis, 2019, 9, 3849
4514715 CIFC23 H21 Br N2 O3P 329.5332; 9.5332; 19.5349
90; 90; 120		1537.51Das, Tamal Kanti; Ghosh, Avik; Balanna, Kuruva; Behera, Pradipta; Gonnade, Rajesh G.; Marelli, Udaya Kiran; Das, Abhijit Kumar; Biju, Akkattu T.
N-Heterocyclic Carbene-Catalyzed Umpolung of Imines for the Enantioselective Synthesis of Dihydroquinoxalines
ACS Catalysis, 2019, 9, 4065
4514716 CIFC14 H11 N O2 S2P 1 21/n 18.3903; 17.9634; 9.3448
90; 112.656; 90		1299.75Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514717 CIFC18 H10 Br2 N2 O2 SI 1 2/a 117.7962; 4.9199; 19.1526
90; 105.417; 90		1616.57Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514718 CIFC12 H11 N O2 SP 1 21/c 114.2892; 10.414; 7.4904
90; 103.95; 90		1081.76Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514719 CIFC18 H10 Cl2 N2 SI 1 2/c 118.9763; 13.5616; 24.1428
90; 95.348; 90		6186.1Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514720 CIFC10 H8 Cl N O2 SP 1 21/c 114.4698; 5.8318; 11.9918
90; 103.449; 90		984.18Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514721 CIFC17 H15 Cl N2 O4 SP 1 21/n 110.7209; 11.7327; 13.2944
90; 97.17; 90		1659.16Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514722 CIFC16 H13 N O2 SP 1 21/c 18.3782; 8.266; 20.0756
90; 97; 90		1379.96Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514723 CIFC18 H10 Cl2 N2 O2 SP 1 21/c 112.9582; 9.0843; 14.2001
90; 108.155; 90		1588.37Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514724 CIFC14 H13 N O2 SP 21 21 218.9497; 9.3068; 15.389
90; 90; 90		1281.8Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514725 CIFC16 H12 Cl N O2 SP 1 21/c 18.2088; 24.9454; 6.8433
90; 94.558; 90		1396.88Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514726 CIFC18 H12 N2 O2 SP -17.6361; 13.7285; 14.864
69.516; 85.244; 83.871		1449.62Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514727 CIFC17 H14 F N O4 SP -17.5118; 8.3229; 12.1237
84.045; 88.396; 77.487		735.96Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514728 CIFC22 H24 N2 O6 SP -17.8092; 9.7669; 14.5366
104.686; 101.315; 100.756		1018.49Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514729 CIFC22 H22 Cl N O2 SC 1 2/c 115.7798; 11.6418; 22.199
90; 106.677; 90		3906.54Nguyen, Viet D.; Nguyen, Vu T.; Haug, Graham C.; Dang, Hang T.; Arman, Hadi D.; Ermler, Walter C.; Larionov, Oleg V.
Rapid and Chemodivergent Synthesis of N-Heterocyclic Sulfones and Sulfides: Mechanistic and Computational Details of the Persulfate-Initiated Catalysis
ACS Catalysis, 2019, 9, 4015
4514730 CIFC18 H20 I2 N4 PdP 1 21/c 18.3065; 16.337; 7.6187
90; 99.14; 90		1020.8Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514731 CIFC26 H36 Br4 Hg2 N4C 1 2/c 118.486; 9.2309; 20.682
90; 106.8; 90		3378.6Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514732 CIFC18 H20 Hg2 I4 N4P 1 21/n 110.648; 20.021; 12.134
90; 95.49; 90		2574.9Chernyshev, Victor M.; Astakhov, Alexander V.; Chikunov, Ilya E.; Tyurin, Roman V.; Eremin, Dmitry B.; Ranny, Gleb S.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?
ACS Catalysis, 2019, 9, 2984
4514733 CIFC102.56 H52 F2 O34 Zr6P 6/m m m39.446; 39.446; 16.4166
90; 90; 120		22122Liu, Jian; Li, Zhanyong; Zhang, Xuan; Otake, Ken-ichi; Zhang, Lin; Peters, Aaron W.; Young, Matthias J.; Bedford, Nicholas M.; Letourneau, Steven P.; Mandia, David J.; Elam, Jeffrey W.; Farha, Omar K.; Hupp, Joseph T.
Introducing Nonstructural Ligands to Zirconia-like Metal‒Organic Framework Nodes To Tune the Activity of Node-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2019, 9, 3198
4514734 CIFC51 H53 Ni P2P 1 2/c 122.883; 9.2579; 21.1481
90; 115.533; 90		4042.6Charboneau, David J.; Brudvig, Gary W.; Hazari, Nilay; Lant, Hannah M. C.; Saydjari, Andrew K.
Development of an Improved System for the Carboxylation of Aryl Halides through Mechanistic Studies.
ACS catalysis, 2019, 9, 3228-3241
4514735 CIFC17 H14 Cl N O4P 21 21 217.7672; 8.6398; 22.845
90; 90; 90		1533.1Dai, Yuanwei; Tian, Baotong; Chen, Huan; Zhang, Qiang
Palladium-Catalyzed Stereospecific C-Glycosylation of Glycals with Vinylogous Acceptors
ACS Catalysis, 2019, 9, 2909
4514736 CIFC22 H37 N3 O4 SiP 1 21 19.1154; 9.7854; 14.6304
90; 96.443; 90		1296.76Zhan, Bei-Bei; Fan, Jun; Jin, Liang; Shi, Bing-Feng
Divergent Synthesis of Silicon-Containing Peptides via Pd-Catalyzed Post-Assembly γ-C(sp3)–H Silylation
ACS Catalysis, 2019, 9, 3298
4514737 CIFC89 H64 Al B2 F36 N O6 P4 Rh2P -114.5138; 18.5644; 21.462
104.385; 102.683; 107.545		5062.15Adams, Gemma M.; Ryan, David E.; Beattie, Nicholas A.; McKay, Alasdair I.; Lloyd-Jones, Guy C; Weller, Andrew S.
Dehydropolymerization of H<sub>3</sub>B·NMeH<sub>2</sub> Using a [Rh(DPEphos)]<sup>+</sup> Catalyst: The Promoting Effect of NMeH<sub>2</sub>.
ACS catalysis, 2019, 9, 3657-3666
4514738 CIFC27 H36 Cl F Ni P2P 1 21/n 111.8371; 14.1571; 16.2044
90; 99.776; 90		2676.1Russell, John E. A.; Entz, Emily D.; Joyce, Ian M.; Neufeldt, Sharon R.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
ACS catalysis, 2019, 9, 3304-3310
4514739 CIFC29 H42 F N Ni O3 P2 SP 1 21/m 18.6752; 12.5702; 14.4059
90; 101.795; 90		1537.78Russell, John E. A.; Entz, Emily D.; Joyce, Ian M.; Neufeldt, Sharon R.
Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.
ACS catalysis, 2019, 9, 3304-3310
4514740 CIFC32 H58 Co I N4 P2 ZrP n m a15.4307; 22.1735; 10.8845
90; 90; 90		3724.2Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514741 CIFC56 H92 Co2 I6 N4 P4 Zr2P -111.4073; 12.4796; 14.109
100.063; 97.493; 112.211		1787.87Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514742 CIFC45 H67 Co I N2 O P3 ZrP -19.9663; 10.4166; 23.1907
81.58; 83.529; 82.278		2349.34Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514743 CIFC35 H65 Co I N2 O P3 ZrC 1 2/c 138.6599; 12.0858; 18.3535
90; 103.833; 90		8326.7Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514744 CIFC45 H69 Co I N2 O P3 ZrP -112.2182; 13.374; 16.9003
70.756; 71.3; 74.862		2432.1Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514745 CIFC46 H64 Co I N2 O P2 ZrP -110.7474; 11.7734; 20.3607
77.69; 79.557; 69.802		2345.95Gramigna, Kathryn M.; Dickie, Diane A.; Foxman, Bruce M.; Thomas, Christine M.
Cooperative H2 Activation across a Metal‒Metal Multiple Bond and Hydrogenation Reactions Catalyzed by a Zr/Co Heterobimetallic Complex
ACS Catalysis, 2019, 9, 3153
4514746 CIFC31 H38 B N3 O4P 1 21 16.5323; 24.418; 9.191
90; 104.387; 90		1420.04Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514747 CIFC17 H18 N2 O3 PdP 1 21/n 18.6104; 10.5955; 17.71
90; 99.051; 90		1595.59Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514748 CIFC30 H36 B N3 O3P 1 21 16.3743; 23.6017; 9.0486
90; 101.68; 90		1333.12Liu, Zhen; Li, Xiaohan; Zeng, Tian; Engle, Keary M.
Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds
ACS Catalysis, 2019, 9, 3260
4514749 CIFC44 H40 N6 O10 Zn2P -18.7707; 11.7137; 13.5892
82.784; 81.615; 88.403		1370.2Markad, Datta; Mandal, Sanjay K.
Design of a Primary-Amide-Functionalized Highly Efficient and Recyclable Hydrogen-Bond-Donating Heterogeneous Catalyst for the Friedel‒Crafts Alkylation of Indoles with β-Nitrostyrenes
ACS Catalysis, 2019, 9, 3165
4514750 CIFC42 H33 Cl F2 Ni P2C 1 2/c 130.115; 11.645; 20.4586
90; 102.223; 90		7012Stadler, Sonja M.; Göttker-Schnetmann, Inigo; Mecking, Stefan
Incorporation of Radicals during Ni(II)-Catalyzed Ethylene Insertion Polymerization
ACS Catalysis, 2019, 9, 2760
4514751 CIFC51 H58 F2 N Ni O2 PP b c a16.868; 20.0011; 26.7439
90; 90; 90		9022.8Stadler, Sonja M.; Göttker-Schnetmann, Inigo; Mecking, Stefan
Incorporation of Radicals during Ni(II)-Catalyzed Ethylene Insertion Polymerization
ACS Catalysis, 2019, 9, 2760
4514752 CIFC10 H9 Br O3P 1 21 14.7773; 16.685; 6.289
90; 104.66; 90		485Sawano, Takahiro; Yamamoto, Hisashi
Enantioselective Epoxidation of β,γ-Unsaturated Carboxylic Acids by a Cooperative Binuclear Titanium Complex
ACS Catalysis, 2019, 9, 3384
4514753 CIFC22 H19 Br N2 O2P 21 21 217.3331; 9.8564; 25.7259
90; 90; 90		1859.42Yang, Qian-Qian; Yin, Xiang; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric Formal [5 + 3] Cycloadditions with Unmodified Morita–Baylis–Hillman Alcohols via Double Activation Catalysis
ACS Catalysis, 2019, 9, 1258
4514754 CIFC36 H32 Cl2 N4 O2P 1 21 111.3963; 10.25731; 13.268
90; 95.0958; 90		1544.84Yang, Qian-Qian; Yin, Xiang; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric Formal [5 + 3] Cycloadditions with Unmodified Morita–Baylis–Hillman Alcohols via Double Activation Catalysis
ACS Catalysis, 2019, 9, 1258
4514755 CIFC22 H19 N O3 SP 1 21 117.546; 6.607; 17.993
90; 115.207; 90		1887.2Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C–H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514756 CIFC25 H24 N O3 SP 21 21 219.162; 10.694; 22.484
90; 90; 90		2203Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C‒H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514757 CIFC29 H21 N O3 SP 21 21 216.556; 13.237; 25.625
90; 90; 90		2223.8Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C–H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514758 CIFC23 H21 N O5 SP 21 21 218.9405; 10.0639; 23.127
90; 90; 90		2080.9Bai, Xing-Feng; Mu, Qiu-Chao; Xu, Zheng; Yang, Ke-Fang; Li, Li; Zheng, Zhan-Jiang; Xia, Chun-Gu; Xu, Li-Wen
Catalytic Asymmetric Carbonylation of Prochiral Sulfonamides via C–H Desymmetrization
ACS Catalysis, 2019, 9, 1431
4514759 CIFC18 H16 Br2 O2P -324.679; 24.679; 9.5417
90; 90; 120		5032.8Trost, Barry M.; Tracy, Jacob S.
Vanadium-Catalyzed Synthesis of Geometrically Defined Acyclic Tri- and Tetrasubstituted Olefins from Propargyl Alcohols
ACS Catalysis, 2019, 9, 1584
4514760 CIFC12.5 H16 Cl2 Co N1.5 OP 18.5586; 8.9303; 9.6822
76.723; 86.703; 85.126		717.08Wen, Huanan; Wang, Kuan; Zhang, Yanlu; Liu, Guixia; Huang, Zheng
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
ACS Catalysis, 2019, 9, 1612
4514761 CIFC16 H18 Cl2 Co N2 OP 1 21 19.7507; 13.413; 12.9181
90; 90.316; 90		1689.48Wen, Huanan; Wang, Kuan; Zhang, Yanlu; Liu, Guixia; Huang, Zheng
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
ACS Catalysis, 2019, 9, 1612
4514762 CIFC29.48 H29.66 Cl1.27 N O3C 1 2 125.1281; 6.268; 15.987
90; 99.524; 90		2483.29Trost, Barry M.; Hung, Chao-I Joey; Gnanamani, Elumalai
Tuning the Reactivity of Ketones through Unsaturation: Construction of Cyclic and Acyclic Quaternary Stereocenters via Zn-ProPhenol Catalyzed Mannich Reactions
ACS Catalysis, 2019, 9, 1549
4514763 CIFC22 H19 O PP 1 21 115.7797; 6.4246; 18.8309
90; 114.711; 90		1734.23Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514764 CIFC27 H26 F2 N O2 PP 1 21 110.6041; 11.5598; 19.577
90; 94.744; 90		2391.6Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514765 CIFC24 H21 O3 PP 21 21 219.561; 9.713; 20.717
90; 90; 90		1923.9Lu, Zhiwu; Zhang, Haoyang; Yang, Zhiping; Ding, Ning; Meng, Ling; Wang, Jun
Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis
ACS Catalysis, 2019, 9, 1457
4514766 CIFC20 H27 N O6P 1 21 16.03; 19.3547; 9.0029
90; 102.453; 90		1026Sim, Jaehoon; Campbell, Mark W.; Molander, Gary A.
Synthesis of α-Fluoro-α-Amino Acid Derivatives via Photoredox-Catalyzed Carbofluorination.
ACS catalysis, 2019, 9, 1558-1563
4514767 CIFC15 H16 O2P 21 21 215.6039; 10.7509; 19.196
90; 90; 90		1156.5Zheng, Pengfei; Wang, Chengpeng; Chen, Ying-Chun; Dong, Guangbin
Pd-Catalyzed Intramolecular α-Allylic Alkylation of Ketones with Alkynes: Rapid and Stereodivergent Construction of [3.2.1] Bicycles
ACS Catalysis, 2019, 9, 5515
4514768 CIFC35 H51 F6 N3 O5 S2 ZnP 21 21 2113.6599; 14.2563; 20.5882
90; 90; 90		4009.34Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514769 CIFC37 H47 F6 N3 O4 S2 ZnP 1 21/c 119.3499; 20.6938; 20.4521
90; 105.975; 90		7873.2Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514770 CIFC26.67 H32.67 Cl2 F4 N2 O2.67 S1.33 Zn0.67P -110.0474; 16.5268; 16.5479
117.002; 106.69; 94.539		2273.4Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514771 CIFC47 H56 N2 ZnP 1 21/c 119.3717; 16.9243; 27.5305
90; 101.738; 90		8837.2Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514772 CIFC35 H54 Cl2 N2 O1.5 ZnP 1 21/c 112.9149; 19.5194; 19.2829
90; 133.379; 90		3533.1Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514773 CIFC41 H52 N2 ZnP 1 21/c 120.3293; 9.7719; 18.4536
90; 106.688; 90		3511.5Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514774 CIFC43 H57 F6 N3 O6 S2 ZnP -111.9544; 13.4764; 15.7416
95.505; 100.925; 110.249		2299.96Procter, Richard J.; Uzelac, Marina; Cid, Jessica; Rushworth, Philip J.; Ingleson, Michael J.
Low-Coordinate NHC‒Zinc Hydride Complexes Catalyze Alkyne C‒H Borylation and Hydroboration Using Pinacolborane
ACS Catalysis, 2019, 9, 5760
4514775 CIFC19 H18 O2P 21 21 219.663; 9.7186; 31.0442
90; 90; 90		2915.39Yang, Junfeng; Sekiguchi, Yoshiya; Yoshikai, Naohiko
Cobalt-Catalyzed Enantioselective and Chemodivergent Addition of Cyclopropanols to Oxabicyclic Alkenes
ACS Catalysis, 2019, 9, 5638
4514776 CIFC27 H25 O3 P SP 21 21 213.6131; 35.785; 9.9738
90; 90; 90		4858.7Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514777 CIFC46 H72 Dy F9 N4 O17 S3P 1 21 112.1386; 16.1932; 15.8018
90; 97.546; 90		3079.1Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514778 CIFC51 H84 F9 N4 O18 Pr S3P 1 21 112.1823; 16.5445; 16.408
90; 101.368; 90		3242.2Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514779 CIFC53 H82 F9 N4 O15 S3 TmP 21 21 2115.6161; 19.6361; 21.6999
90; 90; 90		6654Zhang, Yu; Zhang, Fengcai; Chen, Long; Xu, Jian; Liu, Xiaohua; Feng, Xiaoming
Asymmetric Synthesis of P-Stereogenic Compounds via Thulium(III)-Catalyzed Desymmetrization of Dialkynylphosphine Oxides
ACS Catalysis, 2019, 9, 4834
4514780 CIFC44 H40 O P2P 21 21 219.9449; 17.1268; 19.9556
90; 90; 90		3398.92Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514781 CIFC17 H11 Cr F O5P 17.0791; 7.2172; 16.4881
85.775; 87.502; 64.437		757.81Batuecas, María; Luo, Junfei; Gergelitsová, Ivana; Krämer, Katrina; Whitaker, Daniel; Vitorica-Yrezabal, Iñigo J.; Larrosa, Igor
Catalytic Asymmetric C‒H Arylation of (η6-Arene)Chromium Complexes: Facile Access to Planar-Chiral Phosphines
ACS Catalysis, 2019, 9, 5268
4514782 CIFC43 H32 Cl2 N4 OP -111.209; 13.582; 13.728
60.753; 79.38; 76.89		1769.4Takamatsu, Kazutaka; Hayashi, Yoshihiro; Kawauchi, Susumu; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Regioselective C–H Amination of Phenol Derivatives with Assistance of Phenanthroline-Based Bidentate Auxiliary
ACS Catalysis, 2019, 9, 5336
4514783 CIFC31 H31 N O2 SP -110.628; 11.4207; 12.9524
65.936; 85.626; 72.954		1370.77Li, Man-Bo; Grape, Erik Svensson; Bäckvall, Jan-E.
Palladium-Catalyzed Stereospecific Oxidative Cascade Reaction of Allenes for the Construction of Pyrrole Rings: Control of Reactivity and Selectivity
ACS Catalysis, 2019, 9, 5184
4514784 CIFC28 H27 N O2 SP 1 21/c 114.0088; 9.652; 19.0811
90; 109.714; 90		2428.79Li, Man-Bo; Grape, Erik Svensson; Bäckvall, Jan-E.
Palladium-Catalyzed Stereospecific Oxidative Cascade Reaction of Allenes for the Construction of Pyrrole Rings: Control of Reactivity and Selectivity
ACS Catalysis, 2019, 9, 5184
4514785 CIFC15 H17 N O4P n a 219.7201; 26.2838; 5.4483
90; 90; 90		1391.94Wu, Wenli; Cui, Enxin; Zhang, Yun; Zhang, Chen; Zhu, Feng; Tung, Chen-Ho; Wang, Yifeng
Involving Single-Atom Silver(0) in Selective Dehalogenation by AgF under Visible-Light Irradiation
ACS Catalysis, 2019, 9, 6335
4514786 CIFC16 H12 N2P n a 217.5559; 13.9087; 11.4271
90; 90; 90		1200.91Wu, Wenli; Cui, Enxin; Zhang, Yun; Zhang, Chen; Zhu, Feng; Tung, Chen-Ho; Wang, Yifeng
Involving Single-Atom Silver(0) in Selective Dehalogenation by AgF under Visible-Light Irradiation
ACS Catalysis, 2019, 9, 6335
4514787 CIFC8 H6 NP 1 21/n 17.8048; 5.9454; 13.2408
90; 92.593; 90		613.78Wu, Wenli; Cui, Enxin; Zhang, Yun; Zhang, Chen; Zhu, Feng; Tung, Chen-Ho; Wang, Yifeng
Involving Single-Atom Silver(0) in Selective Dehalogenation by AgF under Visible-Light Irradiation
ACS Catalysis, 2019, 9, 6335
4514788 CIFC11 H11 F3 O2P 41 21 27.262; 7.262; 41.516
90; 90; 90		2189.41Kerdphon, Sutthichat; Ponra, Sudipta; Yang, Jianping; Wu, Haibo; Eriksson, Lars; Andersson, Pher G.
Diastereo- and Enantioselective Synthesis of Structurally Diverse Succinate, Butyrolactone, and Trifluoromethyl Derivatives by Iridium-Catalyzed Hydrogenation of Tetrasubstituted Olefins
ACS Catalysis, 2019, 9, 6169
4514789 CIFC18 H15 N O2P 21 21 218.98144; 9.10592; 35.9259
90; 90; 90		2938.17Li, Yi-Pan; Li, Zi-Qi; Zhou, Biying; Li, Mao-Lin; Xue, Xiao-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Chiral Spiro Phosphoric Acid-Catalyzed Friedel–Crafts Conjugate Addition/Enantioselective Protonation Reactions
ACS Catalysis, 2019, 9, 6522
4514790 CIFC19 H17 N OP 1 21 19.3678; 6.9408; 11.2829
90; 93.95; 90		731.872Li, Yi-Pan; Li, Zi-Qi; Zhou, Biying; Li, Mao-Lin; Xue, Xiao-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Chiral Spiro Phosphoric Acid-Catalyzed Friedel–Crafts Conjugate Addition/Enantioselective Protonation Reactions
ACS Catalysis, 2019, 9, 6522
4514791 CIFC25 H22 I O PP n a 2114.0443; 8.9519; 34.5515
90; 90; 90		4343.92Zhang, Lumin; Si, Xiaojia; Yang, Yangyang; Witzel, Sina; Sekine, Kohei; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Reductive C–C Coupling by Desulfurizing Gold-Catalyzed Photoreactions
ACS Catalysis, 2019, 9, 6118
4514792 CIFC40 H48 B2 Fe N12C 1 2/c 120.1074; 16.9145; 25.426
90; 108.024; 90		8223.2Isbill, Sara B.; Chandrachud, Preeti P.; Kern, Jesse L.; Jenkins, David M.; Roy, Sharani
Elucidation of the Reaction Mechanism of C<sub>2</sub> + N<sub>1</sub> Aziridination from Tetracarbene Iron Catalysts.
ACS catalysis, 2019, 9, 6223-6233
4514793 CIFC24 H31 Cl Ir N OP 1 21/n 18.81332; 15.7101; 17.1127
90; 102.781; 90		2310.68Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C‒H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514794 CIFC32 H36 Ir N O2P -111.5179; 13.5428; 18.483
76.588; 87.879; 89.094		2802.44Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C‒H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514795 CIFC19 H21 N O SP b c a10.7285; 17.9511; 18.0222
90; 90; 90		3470.87Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C–H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514796 CIFC22 H21 N O2P 21 21 217.1896; 13.9891; 17.894
90; 90; 90		1799.71Chen, Shuyou; Zhang, Min; Su, Rongchuan; Chen, Xingyu; Feng, Boya; Yang, Yudong; You, Jingsong
C2/C4 Regioselective Heteroarylation of Indoles by Tuning C–H Metalation Modes
ACS Catalysis, 2019, 9, 6372
4514797 CIFC22 H23 N OP 4310.6545; 10.6545; 15.1128
90; 90; 90		1715.58Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514798 CIFC20 H19 N OP 21 21 215.6073; 16.7309; 16.9207
90; 90; 90		1587.42Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514799 CIFC24 H22 N2 OP b c a10.4266; 18.053; 19.734
90; 90; 90		3714.6Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514800 CIFC26 H24 N2 OP 1 21 18.7098; 8.9173; 13.0467
90; 93.444; 90		1011.48Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514801 CIFC18 H19 N O2P -19.859; 10.008; 15.838
93.054; 90.75; 99.872		1537Sahani, Rajkumar Lalji; Liu, Rai-Shung
Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring
ACS Catalysis, 2019, 9, 5890
4514802 CIFC30 H36 B N3 O3P 1 21 16.5399; 23.9124; 9.103
90; 102.293; 90		1390.93Bai, Zibo; Zheng, Sujuan; Bai, Ziqian; Song, Fangfang; Wang, Hao; Peng, Qian; Chen, Gong; He, Gang
Palladium-Catalyzed Amide-Directed Enantioselective Carboboration of Unactivated Alkenes Using a Chiral Monodentate Oxazoline Ligand
ACS Catalysis, 2019, 9, 6502
4514803 CIFC30 H36 B N3 O3P 41 21 29.0322; 9.0322; 68.9818
90; 90; 90		5627.58Bai, Zibo; Zheng, Sujuan; Bai, Ziqian; Song, Fangfang; Wang, Hao; Peng, Qian; Chen, Gong; He, Gang
Palladium-Catalyzed Amide-Directed Enantioselective Carboboration of Unactivated Alkenes Using a Chiral Monodentate Oxazoline Ligand
ACS Catalysis, 2019, 9, 6502
4514804 CIFC34 H36 O S2P 1 21/c 112.8072; 13.6963; 17.6483
90; 110.451; 90		2900.59Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514805 CIFC19 H14 S2P -17.9503; 8.3038; 12.6012
78.352; 79.15; 72.944		771.51Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514806 CIFC19 H14 O S2C 1 2/c 116.653; 5.92231; 33.4022
90; 104.977; 90		3182.36Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514807 CIFC21 H24 Cl Rh SP 1 21 17.74658; 14.0941; 9.1196
90; 108.015; 90		946.87Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514808 CIFC18 H10 S2P 1 21/c 13.95493; 12.7072; 25.5848
90; 91.496; 90		1285.35Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong
Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes
ACS Catalysis, 2019, 9, 6188
4514809 CIFC42 H78 N6 O Si6 ThP -111.208; 13.909; 19.199
69.17; 83.14; 71.15		2647.3Saha, Sayantani; Eisen, Moris S.
Catalytic Recycling of a Th–H Bond via Single or Double Hydroboration of Inactivated Imines or Nitriles
ACS Catalysis, 2019, 9, 5947
4514810 CIFC10 H10 F2 O2P 1 21/c 19.946; 9.088; 10.222
90; 102.351; 90		902.6Nakayama, Yoshiki; Ando, Gaku; Abe, Manabu; Koike, Takashi; Akita, Munetaka
Keto-Difluoromethylation of Aromatic Alkenes by Photoredox Catalysis: Step-Economical Synthesis of α-CF2H-Substituted Ketones in Flow
ACS Catalysis, 2019, 9, 6555
4514811 CIFC15 H18 O2P n a 2125.8841; 7.333; 6.343
90; 90; 90		1203.95Luo, Youran; Gutiérrez-Bonet, Álvaro; Matsui, Jennifer K.; Rotella, Madeline E.; Dykstra, Ryan; Gutierrez, Osvaldo; Molander, Gary A.
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
ACS Catalysis, 2019, 9, 8835
4514812 CIFC21 H29 N O2P 1 21 15.5974; 16.9126; 19.3211
90; 90.056; 90		1829.1Luo, Youran; Gutiérrez-Bonet, Álvaro; Matsui, Jennifer K.; Rotella, Madeline E.; Dykstra, Ryan; Gutierrez, Osvaldo; Molander, Gary A.
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
ACS Catalysis, 2019, 9, 8835
4514813 CIFC93 H84 F3 O31 P4 S Yb2P 1 21 117.0655; 17.2352; 23.1949
90; 95.16; 90		6794.6Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir N.; Cundari, Thomas R.; Wang, Hong
Asymmetric Ring-Opening of Donor‒Acceptor Cyclopropanes with Primary Arylamines Catalyzed by a Chiral Heterobimetallic Catalyst
ACS Catalysis, 2019, 9, 8285
4514814 CIFC20 H23 N O5P 21 21 215.78428; 12.07053; 25.84988
90; 90; 90		1804.82Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir N.; Cundari, Thomas R.; Wang, Hong
Asymmetric Ring-Opening of Donor–Acceptor Cyclopropanes with Primary Arylamines Catalyzed by a Chiral Heterobimetallic Catalyst
ACS Catalysis, 2019, 9, 8285
4514815 CIFC25 H9 B F15 N OP 1 21/c 115.7548; 8.5218; 17.5186
90; 91.195; 90		2351.52Meng, Shan-Shui; Tang, Xiaowen; Luo, Xiang; Wu, Ruibo; Zhao, Jun-Ling; Chan, Albert S. C.
Borane-Catalyzed Chemoselectivity-Controllable N-Alkylation and ortho C-Alkylation of Unprotected Arylamines Using Benzylic Alcohols
ACS Catalysis, 2019, 9, 8397
4514816 CIFC44 H55 Au N O2 PP -111.7663; 12.5195; 15.6679
101.971; 95.869; 117.925		1941.11Verlee, Arno; Heugebaert, Thomas; van der Meer, Tom; Kerchev, Pavel; Van Hecke, Kristof; Van Breusegem, Frank; Stevens, Christian V.
Gold and Palladium Mediated Bimetallic Catalysis: Mechanistic Investigation through the Isolation of the Organogold(I) Intermediates
ACS Catalysis, 2019, 9, 7862
4514817 CIFC30 H25 Au N O2 PP 1 21/c 112.35599; 11.5441; 17.5685
90; 98.0363; 90		2481.34Verlee, Arno; Heugebaert, Thomas; van der Meer, Tom; Kerchev, Pavel; Van Hecke, Kristof; Van Breusegem, Frank; Stevens, Christian V.
Gold and Palladium Mediated Bimetallic Catalysis: Mechanistic Investigation through the Isolation of the Organogold(I) Intermediates
ACS Catalysis, 2019, 9, 7862
4514818 CIFC19 H20 OP 1 21 18.803; 5.4591; 15.567
90; 104.94; 90		722.8Yu, Zhunzhun; Mendoza, Abraham
Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates
ACS Catalysis, 2019, 9, 7870
4514819 CIFC24 H16 Br N O4P 1 21 19.7213; 9.12937; 12.1367
90; 102.827; 90		1050.24Yu, Zhunzhun; Mendoza, Abraham
Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates
ACS Catalysis, 2019, 9, 7870
4514820 CIFC25 H15 N3 OC 1 2/c 139.582; 6.6842; 13.9095
90; 97.656; 90		3647.3Tian, Cong; Dhawa, Uttam; Scheremetjew, Alexej; Ackermann, Lutz
Cupraelectro-Catalyzed Alkyne Annulation: Evidence for Distinct C–H Alkynylation and Decarboxylative C–H/C–C Manifolds
ACS Catalysis, 2019, 9, 7690
4514821 CIFC14 H17 N O2P 1 21/c 110.9605; 9.5967; 11.9487
90; 93.832; 90		1254Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514822 CIFC16 H21 N O2P n a 2123.054; 8.4318; 7.3235
90; 90; 90		1423.6Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514823 CIFC15 H18 O3P 1 21/c 112.827; 20.383; 5.0473
90; 96.027; 90		1312.3Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514824 CIFC16 H20 O3C 1 2/c 131.2814; 6.1424; 15.8248
90; 111.709; 90		2825Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin
Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes
ACS Catalysis, 2019, 9, 8555
4514825 CIFC19 H28 Cl Cu N3 O4P n a 2123.1742; 9.9101; 9.2756
90; 90; 90		2130.22Hunt, Andrew P.; Batka, Allison E.; Hosseinzadeh, Marjan; Gregory, Jordan D.; Haque, Halima K.; Ren, Hang; Meyerhoff, Mark E.; Lehnert, Nicolai
Nitric Oxide Generation On Demand for Biomedical Applications via Electrocatalytic Nitrite Reduction by Copper BMPA- and BEPA-Carboxylate Complexes.
ACS catalysis, 2019, 9, 7746-7758
4514826 CIFC50 H52 Ir N4P 1 21/c 120.5401; 12.5368; 16.2915
90; 100.551; 90		4124.2Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514827 CIFC43 H42 Ir N6P -110.1805; 13.1835; 14.4356
85.2561; 69.5849; 77.2239		1770.8Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514828 CIFC41 H36 Ir N6P 1 21/n 114.476; 14.367; 34.464
90; 101.797; 90		7016.3Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514829 CIFC39 H45 Ir N4P 1 21/c 111.3918; 14.4386; 20.4434
90; 99.64; 90		3315.1Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514830 CIFC49 H55 Ir N6P 1 21/c 117.6455; 12.6291; 20.6034
90; 111.016; 90		4286Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S.
Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination
ACS Catalysis, 2019, 9, 8646
4514831 CIFC11 H23 N3 O3 SP 21 21 218.3707; 11.4502; 14.6387
90; 90; 90		1403.06Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann–Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514832 CIFC12 H18 N2 O2 SP b c a17.0285; 6.9101; 21.3006
90; 90; 90		2506.41Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann–Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514833 CIFC29 H47 N3 O6 SP 17.0841; 14.1779; 15.2277
98.32; 100.672; 103.356		1433.94Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann–Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514834 CIFC17 H20 N2 O2 SP 1 21/n 110.2981; 7.0578; 21.651
90; 94.024; 90		1569.8Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian
1,3-Diamine Formation from an Interrupted Hofmann–Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination
ACS Catalysis, 2019, 9, 7741
4514835 CIFC20 H30 Cl N3 O3 SP b c a15.2153; 14.9228; 18.7632
90; 90; 90		4260.3Lam, Ying-Pong; Wang, Xinyan; Tan, Fei; Ng, Wing-Hin; Tse, Ying-Lung Steve; Yeung, Ying-Yeung
Amide/Iminium Zwitterionic Catalysts for (Trans)esterification: Application in Biodiesel Synthesis
ACS Catalysis, 2019, 9, 8083
4514836 CIFC32 H29 N O4 SP 1 21/c 113.6328; 9.7259; 19.2323
90; 94.976; 90		2540.42Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu
Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis
ACS Catalysis, 2019, 9, 8256
4514837 CIFC27 H27 N O4 SP 1 21/c 137.0525; 12.0473; 10.4128
90; 90.415; 90		4647.97Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu
Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis
ACS Catalysis, 2019, 9, 8256
4514838 CIFC25 H23 N O2P 1 21/c 118.0757; 14.6438; 7.2015
90; 101.012; 90		1871.12Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu
Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis
ACS Catalysis, 2019, 9, 8256
4514839 CIFC21 H26 B N O4 SP 21 21 2110.4319; 14.2343; 29.1953
90; 90; 90		4335.2Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan
Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters
ACS Catalysis, 2019, 9, 8503
4514840 CIFC21 H26 B N O5 SP 319.9417; 9.9417; 18.9939
90; 90; 120		1625.8Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan
Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters
ACS Catalysis, 2019, 9, 8503
4514841 CIFC23 H36 B F3 N2 O6 SP 21 21 219.2674; 10.7476; 28.5667
90; 90; 90		2845.3Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan
Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters
ACS Catalysis, 2019, 9, 8503
4514842 CIFC31 H65 K N3 Si6 YP -19.999; 11.964; 19.292
83.01; 85.8; 82.27		2266.1Zhai, Dan-Dan; Du, Hui-Zhen; Zhang, Xiang-Yu; Liu, Yu-Feng; Guan, Bing-Tao
Potassium Yttrium Ate Complexes: Synergistic Effect Enabled Reversible H2 Activation and Catalytic Hydrogenation
ACS Catalysis, 2019, 9, 8766
4514843 CIFC29 H69 K N3 O Si6 YP 1 21/c 111.344; 11.734; 31.997
90; 92.915; 90		4253.6Zhai, Dan-Dan; Du, Hui-Zhen; Zhang, Xiang-Yu; Liu, Yu-Feng; Guan, Bing-Tao
Potassium Yttrium Ate Complexes: Synergistic Effect Enabled Reversible H2 Activation and Catalytic Hydrogenation
ACS Catalysis, 2019, 9, 8766
4514844 CIFC38 H30 F6 N2 O4 Pd S4C 1 2/c 115.336; 10.1947; 24.0955
90; 98.408; 90		3726.7Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514845 CIFC34 H26 Cl2 F6 N2 O4 Pd S4P -19.0381; 10.3207; 10.3832
68.768; 89.673; 88.327		902.4Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514846 CIFC17 H15 N O2 S2C 1 2/c 132.753; 4.888; 23.981
90; 124.967; 90		3146.2Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514847 CIFC22 H23 N O2 S2P -18.6349; 9.3163; 13.5605
70.251; 85.755; 83.165		1018.75Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514848 CIFC22 H24 O6P 1 21/c 119.271; 4.5166; 23.345
90; 107.803; 90		1934.6Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514849 CIFC24 H23 N O4 S2P 1 21/c 115.796; 15.246; 9.849
90; 105.81; 90		2282.17Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514850 CIFC23 H26 O6P -19.7261; 10.89; 11.528
65.75; 69.528; 86.877		1037.3Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514851 CIFC23 H19 N S2P 1 21/n 110.584; 4.346; 40.473
90; 95.273; 90		1853.8Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514852 CIFC20 H18 F N O2 S2P -17.0055; 10.2801; 13.131
79.22; 84.888; 80.238		913.91Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514853 CIFC24 H32 O10P 1 21 111.2; 5.0559; 11.554
90; 115.351; 90		591.25Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514854 CIFC28 H25 N O4 S2P -18.4844; 12.3314; 12.7997
112.337; 94.171; 98.558		1212.59Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514855 CIFC19 H16 Cl N O2 S2P -16.5696; 10.4589; 13.1664
79.911; 84.189; 81.356		877.96Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514856 CIFC23 H19 N O2 S3P 1 21/n 16.9999; 10.6761; 27.063
90; 92.75; 90		2020.1Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis
ACS Catalysis, 2019, 9, 7626
4514857 CIFC23 H17 Br N2P 1 21 111.03; 5.7133; 14.591
90; 92.925; 90		918.3Hatano, Manabu; Nishio, Kosuke; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki
Highly Active Chiral Dilithium(I) Binaphthyldisulfonate Catalysts for Enantio- and Chemoselective Strecker-Type Reactions
ACS Catalysis, 2019, 9, 8178
4514858 CIFC20 H19 N O3 SP 1 21/c 18.2877; 14.334; 14.903
90; 103.09; 90		1724.4Liu, Jibing; Chakraborty, Pushkin; Zhang, Heng; Zhong, Liang; Wang, Zhi-Xiang; Huang, Xueliang
Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration
ACS Catalysis, 2019, 9, 2610
4514859 CIFC17 H19 N O6 SP 1 21/c 17.5531; 28.802; 8.5314
90; 113.57; 90		1701.1Liu, Jibing; Chakraborty, Pushkin; Zhang, Heng; Zhong, Liang; Wang, Zhi-Xiang; Huang, Xueliang
Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration
ACS Catalysis, 2019, 9, 2610
4514860 CIFC22 H25 I N2 O2 RuP -18.8149; 10.4274; 12.2762
74.663; 83.855; 77.212		1059.8Kumar, Abhishek; Semwal, Shrivats; Choudhury, Joyanta
Catalytic Conversion of CO2 to Formate with Renewable Hydrogen Donors: An Ambient-Pressure and H2-Independent Strategy
ACS Catalysis, 2019, 9, 2164
4514861 CIFC20 H14 Cl N OP 18.6566; 11.3426; 16.584
89.235; 77.991; 89.031		1592.41Fan, Xiaozhong; Zhang, Xue; Li, Chunyu; Gu, Zhenhua
Enantioselective Atropisomeric Anilides Synthesis via Cu-Catalyzed Intramolecular Adjacent C–N Coupling
ACS Catalysis, 2019, 9, 2286
4514862 CIFC28 H32 N2 O2P 1 21/c 113.969; 27.1371; 6.25424
90; 99.738; 90		2336.69Wu, Xiao; Chen, Chentuo; Guo, Ziyang; North, Michael; Whitwood, Adrian C.
Metal- and Halide-Free Catalyst for the Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide
ACS Catalysis, 2019, 9, 1895
4514863 CIFC13 H12 Br Mn N2 O4P 1 21/c 111.071; 10.4143; 13.4557
90; 105.015; 90		1498.43Steinlechner, Christoph; Roesel, Arend F.; Oberem, Elisabeth; Päpcke, Ayla; Rockstroh, Nils; Gloaguen, Frédéric; Lochbrunner, Stefan; Ludwig, Ralf; Spannenberg, Anke; Junge, Henrik; Francke, Robert; Beller, Matthias
Selective Earth-Abundant System for CO2 Reduction: Comparing Photo- and Electrocatalytic Processes
ACS Catalysis, 2019, 9, 2091
4514864 CIFC15 H10 Br Mn N2 O4P -17.1769; 9.2213; 11.5716
85.6351; 84.0784; 82.509		753.7Steinlechner, Christoph; Roesel, Arend F.; Oberem, Elisabeth; Päpcke, Ayla; Rockstroh, Nils; Gloaguen, Frédéric; Lochbrunner, Stefan; Ludwig, Ralf; Spannenberg, Anke; Junge, Henrik; Francke, Robert; Beller, Matthias
Selective Earth-Abundant System for CO2 Reduction: Comparing Photo- and Electrocatalytic Processes
ACS Catalysis, 2019, 9, 2091
4514865 CIFC17 H13 Br O3P c a 2110.7383; 18.1542; 7.5303
90; 90; 90		1468Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang
Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols
ACS Catalysis, 2019, 9, 2440
4514866 CIFC27 H32 O3P 1 21 19.72; 7.5084; 16.171
90; 94.588; 90		1176.4Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang
Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols
ACS Catalysis, 2019, 9, 2440
4514867 CIFC18 H12 F3 N3 O3P 1 21/c 110.5383; 19.337; 7.9828
90; 92.029; 90		1625.7Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang
Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols
ACS Catalysis, 2019, 9, 2440
4514868 CIFC50 H39 N Ni O P2P -113.3161; 14.0105; 15.2863
72.192; 64.226; 62.74		2262.59Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne
Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization.
ACS catalysis, 2019, 9, 2458-2481

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