Crystallography Open Database

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4513735 CIFC29 H32 N2 O2P 1 21/n 18.6895; 9.8563; 30.266
90; 94.399; 90		2584.5Kuai, Changsheng; Wang, Lianhui; Cui, Haoyi; Shen, Jinhai; Feng, Yadong; Cui, Xiuling
Efficient and Selective Synthesis of (E)-Enamides via Ru(II)-Catalyzed Hydroamidation of Internal Alkynes
ACS Catalysis, 2016, 6, 186
4513736 CIFC23 H20 N2 OP 1 21/n 112.864; 9.812; 13.652
90; 92.938; 90		1720.9Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513737 CIFC18 H11 F5 N2 O2P 1 21/c 111.342; 6.528; 21.294
90; 95.503; 90		1569.4Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513738 CIFC21 H21 N3P -17.784; 10.507; 11.117
106.154; 96.466; 97.82		854.3Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513739 CIFC25 H19 F N2 O2P 1 21/n 112.243; 7.246; 21.867
90; 105.022; 90		1873.6Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513740 CIFC18 H15 Br N2 O2P 1 21/n 110.221; 6.258; 24.249
90; 97.531; 90		1537.7Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513741 CIFC25.57 H21.14 Cl1.13 N2 O2P 1 21 112.2626; 7.2788; 12.3394
90; 104.51; 90		1066.25Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513742 CIFC20 H18 N2 O2P 1 c 15.238; 12.589; 11.597
90; 91.334; 90		764.5Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513743 CIFC18 H14 Br N3P 1 21/c 18.6369; 26.751; 6.9978
90; 106.79; 90		1547.89Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513744 CIFC19 H18 N2 O2P 1 21/c 19.882; 36.918; 8.62
90; 99.99; 90		3097.1Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513745 CIFC26 H22 N2 O3P 1 21/n 112.352; 7.361; 22.122
90; 98.421; 90		1989.7Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513746 CIFC20 H18 N2 O2P 1 21 111.035; 6.9; 11.373
90; 115.012; 90		784.75Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513747 CIFC22 H13 F5 N4 O2P 1 21 17.91984; 7.77745; 16.8551
90; 101.445; 90		1017.57Xu, Yali; Liao, Yuting; Lin, Lili; Zhou, Yuhang; Li, Jun; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Inverse-Electron Demand 1,3-Dipolar Cycloaddition of Isoquinolinium Methylides with Enecarbamates by a ChiralN,N′-Dioxide/Ag(I) Complex
ACS Catalysis, 2016, 6, 589
4513748 CIFC23.73 H18.45 Cl0.7 N O3.12 SP 21 21 29.7227; 23.8357; 8.7364
90; 90; 90		2024.6Izquierdo, Javier; Pericàs, Miquel A.
A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow
ACS Catalysis, 2016, 6, 348
4513749 CIFC30 H25 N O3 SP 1 21 15.9234; 17.5385; 11.7578
90; 95.5438; 90		1215.78Izquierdo, Javier; Pericàs, Miquel A.
A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow
ACS Catalysis, 2016, 6, 348
4513750 CIFC19 H16 N2 O SP 21 21 219.8811; 10.2565; 15.4749
90; 90; 90		1568.31Izquierdo, Javier; Pericàs, Miquel A.
A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow
ACS Catalysis, 2016, 6, 348
4513751 CIFC22 H19 F N2 OP b c a13.5231; 13.1489; 19.3467
90; 90; 90		3440.1Hiramatsu, Kenichi; Honjo, Takashi; Rauniyar, Vivek; Toste, F. Dean
Enantioselective Synthesis of Fluoro-Dihydroquinazolones and -Benzooxazinones by Fluorination-Initiated Asymmetric Cyclization Reactions.
ACS catalysis, 2015, 6, 151-154
4513752 CIFC12 H15 F N2 OP 1 21 17.6084; 6.4312; 11.7689
90; 103.627; 90		559.66Hiramatsu, Kenichi; Honjo, Takashi; Rauniyar, Vivek; Toste, F. Dean
Enantioselective Synthesis of Fluoro-Dihydroquinazolones and -Benzooxazinones by Fluorination-Initiated Asymmetric Cyclization Reactions.
ACS catalysis, 2015, 6, 151-154
4513753 CIFC13 H4 F5 N SP 1 21/c 114.407; 7.3079; 11.1275
90; 109.808; 90		1102.24Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513754 CIFC12 H6 F4P 1 21/c 112.8062; 5.84755; 12.6869
90; 105.223; 90		916.72Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513755 CIFC13 H5 F7P 21 21 215.92801; 7.5738; 23.6364
90; 90; 90		1061.22Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513756 CIFC12 H5 F5C 2 2 215.80768; 20.9642; 7.68611
90; 90; 90		935.81Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513757 CIFC37 H40 Br N O3P 21 21 2110.038; 15.921; 20.131
90; 90; 90		3217.2He, Fu-Sheng; Jin, Jing-Hai; Yang, Zhong-Tao; Yu, Xingxin; Fossey, John S.; Deng, Wei-Ping
Direct Asymmetric Synthesis of β-Bis-Aryl-α-Amino Acid Esters via Enantioselective Copper-Catalyzed Addition ofp-Quinone Methides
ACS Catalysis, 2016, 6, 652
4513758 CIFC22 H20 F3 N OP b c a19.0615; 9.325; 20.7194
90; 90; 90		3682.8Yu, Liu-Zhu; Xu, Qin; Tang, Xiang-Yiang; Shi, Min
Iron- or Copper-Catalyzed Trifluoromethylation of Acrylamide-Tethered Alkylidenecyclopropanes: Facile Synthesis of CF3-Containing Polycyclic Benzazepine Derivatives
ACS Catalysis, 2016, 6, 526
4513759 CIFC36 H44 Er N O Si2P 1 21/c 116.5508; 9.9149; 20.9543
90; 100.391; 90		3382.2Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513760 CIFC36 H44 Gd N O Si2P 1 21/c 116.5847; 9.9933; 21.0068
90; 100.271; 90		3425.8Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513761 CIFC36 H44 N Nd O Si2P 1 21/c 116.5572; 10.0221; 21.0296
90; 100.37; 90		3432.6Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513762 CIFC31 H44 N O Pr Si2P 1 21/c 114.6913; 11.3369; 19.4321
90; 95.729; 90		3220.3Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513779 CIFC18 H22 Cl N3 NiP 1 21/c 117.067; 10.4806; 18.8193
90; 95.005; 90		3353.4Perez Garcia, Pablo M.; Di Franco, Thomas; Epenoy, Alexandre; Scopelliti, Rosario; Hu, Xile
From Dimethylamine to Pyrrolidine: The Development of an Improved Nickel Pincer Complex for Cross-Coupling of Nonactivated Secondary Alkyl Halides
ACS Catalysis, 2016, 6, 258
4513780 CIFC15 H13 Br N2 O3 SP 18.9143; 10.0383; 10.4508
106.994; 96.214; 108.761		825.44Li, Yi; Yu, Yue-Na; Xu, Ming-Hua
Simple Open-Chain Phosphite-Olefin as Ligand for Rh-Catalyzed Asymmetric Arylation of Cyclic Ketimines: Enantioselective Access to gem-Diaryl α-Amino Acid Derivatives
ACS Catalysis, 2016, 6, 661
4513781 CIFC14 H13 N3P b c a6.9469; 15.845; 20.914
90; 90; 90		2302.1Zhou, Xukai; Yu, Songjie; Kong, Lingheng; Li, Xingwei
Rhodium(III)-Catalyzed Coupling of Arenes with Cyclopropanols via C‒H Activation and Ring Opening
ACS Catalysis, 2016, 6, 647
4513782 CIFC46 H45 B Cl F4 Fe N2 O P2P 21 21 218.2664; 21.4148; 10.4443
90; 90; 90		4085.5Zuo, Weiwei; Prokopchuk, Demyan E.; Lough, Alan J.; Morris, Robert H.
Details of the Mechanism of the Asymmetric Transfer Hydrogenation of Acetophenone Using the Amine(imine)diphosphine Iron Precatalyst: The Base Effect and The Enantiodetermining Step
ACS Catalysis, 2016, 6, 301
4513783 CIFC45 H43 Cl Fe N2 O P2P 21 21 2111.0847; 13.0101; 27.0865
90; 90; 90		3906.2Zuo, Weiwei; Prokopchuk, Demyan E.; Lough, Alan J.; Morris, Robert H.
Details of the Mechanism of the Asymmetric Transfer Hydrogenation of Acetophenone Using the Amine(imine)diphosphine Iron Precatalyst: The Base Effect and The Enantiodetermining Step
ACS Catalysis, 2016, 6, 301
4513784 CIFC27 H38 B Br O3P 32 2 113.3911; 13.3911; 26.1903
90; 90; 120		4067.28Jarava-Barrera, Carlos; Parra, Alejandro; López, Aurora; Cruz-Acosta, Fabio; Collado-Sanz, Daniel; Cárdenas, Diego J; Tortosa, Mariola
Copper-Catalyzed Borylative Aromatization of p-Quinone Methides: Enantioselective Synthesis of Dibenzylic Boronates.
ACS catalysis, 2016, 6, 442-446
4513793 CIFC43 H44 O5.5 PP 1 21 115.3957; 31.578; 17.2918
90; 111.265; 90		7834.3Momiyama, Norie; Funayama, Kosuke; Noda, Hirofumi; Yamanaka, Masahiro; Akasaka, Naohiko; Ishida, Shintaro; Iwamoto, Takeaki; Terada, Masahiro
Hydrogen Bonds-Enabled Design of aC1-Symmetric Chiral Brønsted Acid Catalyst
ACS Catalysis, 2016, 6, 949
4513794 CIFC112 H91 F12 N O16 P4P 31 2 124.1287; 24.1287; 33.801
90; 90; 120		17042.3Momiyama, Norie; Funayama, Kosuke; Noda, Hirofumi; Yamanaka, Masahiro; Akasaka, Naohiko; Ishida, Shintaro; Iwamoto, Takeaki; Terada, Masahiro
Hydrogen Bonds-Enabled Design of aC1-Symmetric Chiral Brønsted Acid Catalyst
ACS Catalysis, 2016, 6, 949
4513795 CIFC18 H19 N3 O3P 1 21/n 110.383; 10.981; 14.706
90; 106.941; 90		1604Zeng, Rong; Chen, Peng-Hao; Dong, Guangbin
Efficient Benzimidazolidinone Synthesis via Rhodium-Catalyzed Double-Decarbonylative C-C Activation/Cycloaddition between Isatins and Isocyanates.
ACS catalysis, 2016, 6, 969-973
4513796 CIFC20 H16 F N3 OP 1 21/c 113.206; 7.219; 17.366
90; 102.062; 90		1619Zeng, Rong; Chen, Peng-Hao; Dong, Guangbin
Efficient Benzimidazolidinone Synthesis via Rhodium-Catalyzed Double-Decarbonylative C-C Activation/Cycloaddition between Isatins and Isocyanates.
ACS catalysis, 2016, 6, 969-973
4513797 CIFC24 H34 F6 Mn N4 O8 S2P 1 21/c 118.0992; 9.65395; 19.7948
90; 110.024; 90		3249.64Ottenbacher, Roman V.; Samsonenko, Denis G.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
Enantioselective Epoxidations of Olefins with Various Oxidants on Bioinspired Mn Complexes: Evidence for Different Mechanisms and Chiral Additive Amplification
ACS Catalysis, 2016, 6, 979
4513798 CIFC18 H10 F3 N O2P 1 21/n 17.3858; 11.7473; 16.1486
90; 97.962; 90		1387.6Yao, Ruwei; Rong, Guangwei; Yan, Bin; Qiu, Lihua; Xu, Xinfang
Dual-Functionalization of Alkynes via Copper-Catalyzed Carbene/Alkyne Metathesis: A Direct Access to the 4-Carboxyl Quinolines
ACS Catalysis, 2016, 6, 1024
4513799 CIFC22 H13 N O2P 1 21/c 16.1061; 22.232; 11.7017
90; 95.582; 90		1581Yao, Ruwei; Rong, Guangwei; Yan, Bin; Qiu, Lihua; Xu, Xinfang
Dual-Functionalization of Alkynes via Copper-Catalyzed Carbene/Alkyne Metathesis: A Direct Access to the 4-Carboxyl Quinolines
ACS Catalysis, 2016, 6, 1024
4513801 CIFC23 H21 F2 N OP 1 21 111.6562; 21.5144; 16.1302
90; 102.368; 90		3951.19Momiyama, Norie; Okamoto, Hiroshi; Kikuchi, Jun; Korenaga, Toshinobu; Terada, Masahiro
Perfluorinated Aryls in the Design of Chiral Brønsted Acid Catalysts: Catalysis of Enantioselective [4 + 2] Cycloadditions and Ene Reactions of Imines with Alkenes by Chiral Mono-Phosphoric Acids with Perfluoroaryls
ACS Catalysis, 2016, 6, 1198
4513802 CIFC30 H41 Al Br2 N2 O3P 1 21/n 111.4113; 21.0276; 12.5491
90; 93.583; 90		3005.3Marlier, Elodie E.; Macaranas, Joahanna A.; Marell, Daniel J.; Dunbar, Christine R.; Johnson, Michelle A.; DePorre, Yvonne; Miranda, Maria O.; Neisen, Benjamin D.; Cramer, Christopher J.; Hillmyer, Marc A.; Tolman, William B.
Mechanistic Studies of ε-Caprolactone Polymerization by (salen)AlOR Complexes and a Predictive Model for Cyclic Ester Polymerizations.
ACS catalysis, 2016, 6, 1215-1224
4513803 CIFC42 H40 N2 O P2 RuP 1 21/c 19.894; 19.922; 22.901
90; 103.78; 90		4384.1Pan, Bing; Liu, Bo; Yue, Erlin; Liu, Qingbin; Yang, Xinzheng; Wang, Zheng; Sun, Wen-Hua
A Ruthenium Catalyst with Unprecedented Effectiveness for the Coupling Cyclization of γ-Amino Alcohols and Secondary Alcohols
ACS Catalysis, 2016, 6, 1247
4513804 CIFC10 H15 N OP 21 21 216.8744; 8.6699; 15.729
90; 90; 90		937.5Pan, Bing; Liu, Bo; Yue, Erlin; Liu, Qingbin; Yang, Xinzheng; Wang, Zheng; Sun, Wen-Hua
A Ruthenium Catalyst with Unprecedented Effectiveness for the Coupling Cyclization of γ-Amino Alcohols and Secondary Alcohols
ACS Catalysis, 2016, 6, 1247
4513806 CIFC31 H33 Fe P SP 1 21 18.6051; 8.456; 18.6229
90; 96.947; 90		1345.14Ogasawara, Masamichi; Arae, Sachie; Watanabe, Susumu; Nakajima, Kiyohiko; Takahashi, Tamotsu
Kinetic Resolution of Planar-Chiral Ferrocenylphosphine Derivatives by Molybdenum-Catalyzed Asymmetric Ring-Closing Metathesis and Their Application in Asymmetric Catalysis
ACS Catalysis, 2016, 6, 1308
4513807 CIFC26 H21 NP -18.219; 10.1031; 12.1768
86.213; 78.34; 86.602		987.01Borie, Cyril; Vanthuyne, Nicolas; Bertrand, Michèle P.; Siri, Didier; Nechab, Malek
Palladium Tandem Catalysis in the Atropodiastereoselective Synthesis of Indenes Bearing Central and Axial Chirality
ACS Catalysis, 2016, 6, 1559
4513808 CIFC14 H17 N O3 SP -16.1084; 14.9045; 15.5068
85.229; 81.551; 83.644		1384.7Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513809 CIFC22 H23 N O3 SP 1 21/n 19.51; 13.531; 15.5036
90; 101.853; 90		1952.46Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513810 CIFC12 H13 N O3 SP -17.4674; 8.2917; 10.159
84.506; 89.933; 69.136		584.71Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513811 CIFC22 H17 N O3 SP 1 21/n 110.3225; 20.9863; 16.6431
90; 95.815; 90		3586.9Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513812 CIFC22 H17 N O3 SP -18.5582; 10.1474; 11.3665
114.204; 92.3803; 95.0132		893.63Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513813 CIFC13 H15 N O3 SP 1 21/c 115.7908; 6.1888; 13.6788
90; 106.523; 90		1281.57Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513814 CIFC13 H15 N O3 SP 21 21 216.4715; 12.2935; 16.0625
90; 90; 90		1277.89Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2016, 6, 1565
4513815 CIFC17 H17 N3 OP 1 21 18.6937; 8.2505; 9.8923
90; 96.8229; 90		704.524Singh, Manish K.; Akula, Hari K.; Satishkumar, Sakilam; Stahl, Lothar; Lakshman, Mahesh K.
Ruthenium-Catalyzed C-H Bond Activation Approach to Azolyl Aminals and Hemiaminal Ethers, Mechanistic Evaluations, and Isomer Interconversion.
ACS catalysis, 2016, 6, 1921-1928
4513816 CIFC33 H27 F2 N O4P -17.9794; 12.355; 27.87
83.268; 84.119; 89.549		2714.2Wang, Qiang; Li, Yingzi; Qi, Zisong; Xie, Fang; Lan, Yu; Li, Xingwei
Rhodium(III)-Catalyzed Annulation betweenN-Sulfinyl Ketoimines and Activated Olefins: C‒H Activation Assisted by an Oxidizing N‒S Bond
ACS Catalysis, 2016, 6, 1971
4513817 CIFC63 H53 B Cl N4 O3 P RuP 1 21/c 110.0715; 28.3272; 21.8875
90; 92.226; 90		6239.7Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K.
Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals
ACS Catalysis, 2016, 6, 1981
4513818 CIFC38 H36 Cl F6 N3 O4 P2 RuP 1 21/n 114.0112; 9.7442; 27.2179
90; 94.215; 90		3706Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K.
Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals
ACS Catalysis, 2016, 6, 1981
4513819 CIFC21 H29 Cl F6 N3 O2 P3 RuP 1 21/n 112.1467; 17.3624; 12.8848
90; 90.182; 90		2717.3Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K.
Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals
ACS Catalysis, 2016, 6, 1981
4513820 CIFC33 H26 Cl2 N3 O2 P RuP 1 21/n 111.6136; 17.269; 14.4146
90; 90.128; 90		2890.9Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K.
Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals
ACS Catalysis, 2016, 6, 1981
4513821 CIFC69 H53 N6 O5 P2 Ru2C 1 2/c 138.209; 13.4891; 24.3071
90; 118.199; 90		11041.1Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K.
Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals
ACS Catalysis, 2016, 6, 1981
4513822 CIFC19 H23 F3 Ir N3 O3 SP 1 21/c 114.9292; 12.2212; 12.2965
90; 109.506; 90		2114.8Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J.
A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid
ACS Catalysis, 2016, 6, 2014
4513823 CIFC27 H31 F3 Ir N3 O3 SP 1 21/c 111.0313; 26.4631; 19.9865
90; 98.415; 90		5771.7Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J.
A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid
ACS Catalysis, 2016, 6, 2014
4513824 CIFC2 H5 Na3 O8C 1 2/c 120.3758; 3.4577; 10.3049
90; 106.491; 90		696.15Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J.
A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid
ACS Catalysis, 2016, 6, 2014
4513825 CIFC28 H33 B O2 SiP -19.8337; 11.7927; 12.4336
112.475; 96.966; 104.18		1254Ansell, Melvyn B.; Spencer, John; Navarro, Oscar
(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies
ACS Catalysis, 2016, 6, 2192
4513826 CIFC33 H49 N4 Pd Si2P -111.8802; 12.1897; 13.9679
86.341; 73.708; 63.295		1729.87Ansell, Melvyn B.; Spencer, John; Navarro, Oscar
(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies
ACS Catalysis, 2016, 6, 2192
4513827 CIFC28 H47 B N4 O2 Pd SiP 1 21/n 112.9381; 17.8318; 14.8311
90; 113.454; 90		3138.98Ansell, Melvyn B.; Spencer, John; Navarro, Oscar
(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies
ACS Catalysis, 2016, 6, 2192
4513837 CIFC23 H26 I2 Ir N3P 1 21/c 117.0173; 7.793; 19.3018
90; 103.52; 90		2488.79Semwal, Shrivats; Choudhury, Joyanta
Molecular Coordination-Switch in a New Role: Controlling Highly Selective Catalytic Hydrogenation with Switchability Function
ACS Catalysis, 2016, 6, 2424
4513838 CIFC23 H25 I Ir N3P -19.2675; 10.21; 12.0027
79.971; 78.553; 83.299		1092.13Semwal, Shrivats; Choudhury, Joyanta
Molecular Coordination-Switch in a New Role: Controlling Highly Selective Catalytic Hydrogenation with Switchability Function
ACS Catalysis, 2016, 6, 2424
4513839 CIFC21 H19 N O4P 21 21 217.32516; 13.4286; 19.6168
90; 90; 90		1929.64Wang, Gang; Liu, Xiaohua; Chen, Yushuang; Yang, Jian; Li, Jun; Lin, Lili; Feng, Xiaoming
Diastereoselective and Enantioselective Alleno-aldol Reaction of Allenoates with Isatins to Synthesis of Carbinol Allenoates Catalyzed by Gold
ACS Catalysis, 2016, 6, 2482
4513840 CIFC17 H10 F6 O2P 1 21/c 15.622; 15.483; 18.549
90; 94.841; 90		1608.8Fu, Ming-Chen; Shang, Rui; Cheng, Wan-Min; Fu, Yao
Nickel-Catalyzed Regio- and Stereoselective Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling
ACS Catalysis, 2016, 6, 2501
4513841 CIFC12 H12 O4P 1 21/n 14.5824; 19.9078; 12.0067
90; 94.374; 90		1092.13Fu, Ming-Chen; Shang, Rui; Cheng, Wan-Min; Fu, Yao
Nickel-Catalyzed Regio- and Stereoselective Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling
ACS Catalysis, 2016, 6, 2501
4513842 CIFC67 H16 B2 Cl2 F40 Fe4 O12 S4P c a 2117.7344; 14.2966; 30.6824
90; 90; 90		7779.3Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513843 CIFC36 H5 B F20 Fe2 O6 S2P b c a16.0418; 20.9445; 23.0959
90; 90; 90		7759.9Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513844 CIFC33 H7 B Cl2 F20 Fe2 O6 S2C 1 c 122.9134; 12.3868; 17.2161
90; 124.699; 90		4017.3Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513845 CIFC11 H7 F9 Fe2 O15 S5P 1 21/m 16.4147; 18.5996; 11.5206
90; 104.145; 90		1332.85Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513846 CIFC18 H16 OP 1 21 110.5879; 4.8182; 13.6534
90; 96.876; 90		691.51Rodríguez, Elsa; Grayson, Matthew N.; Asensio, Amparo; Barrio, Pablo; Houk, K. N.; Fustero, Santos
Chiral Brønsted Acid-Catalyzed Asymmetric Allyl(propargyl)boration Reaction ofortho-Alkynyl Benzaldehydes: Synthetic Applications and Factors Governing the Enantioselectivity
ACS Catalysis, 2016, 6, 2506
4513847 CIFC18 H14 OP 1 21 110.5044; 4.7708; 13.7318
90; 97.605; 90		682.11Rodríguez, Elsa; Grayson, Matthew N.; Asensio, Amparo; Barrio, Pablo; Houk, K. N.; Fustero, Santos
Chiral Brønsted Acid-Catalyzed Asymmetric Allyl(propargyl)boration Reaction ofortho-Alkynyl Benzaldehydes: Synthetic Applications and Factors Governing the Enantioselectivity
ACS Catalysis, 2016, 6, 2506
4513848 CIFC23 H33 Co N3 O4P 1 21/c 18.9984; 21.6663; 12.2395
90; 90.0826; 90		2386.24Schuster, Christopher H.; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes
ACS Catalysis, 2016, 6, 2632
4513849 CIFC21 H35 Co N3 O5P 1 21/c 18.9806; 29.3177; 8.8612
90; 97.9533; 90		2310.63Schuster, Christopher H.; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes
ACS Catalysis, 2016, 6, 2632
4513850 CIFC22 H23 Cl Ir N3 O3P 1 21/c 115.229; 8.446; 17.388
90; 108.03; 90		2126.7Ngo, Anh H.; Ibañez, Miguel; Do, Loi H.
Catalytic Hydrogenation of Cytotoxic Aldehydes Using Nicotinamide Adenine Dinucleotide (NADH) in Cell Growth Media
ACS Catalysis, 2016, 6, 2637
4513853 CIFC20 H38 Br Fe N3 O P2P 1 21 111.7189; 12.5863; 16.7721
90; 99.602; 90		2439.2Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity.
ACS catalysis, 2016, 6, 2664-2672
4513854 CIFC20 H39 Fe N3 O P2P 1 21/c 113.7848; 11.7982; 15.4447
90; 113.332; 90		2306.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity.
ACS catalysis, 2016, 6, 2664-2672
4513855 CIFC29 H26 F3 N3 O6 SP 21 21 218.33; 21.758; 15.532
90; 90; 90		2815.08Montesinos-Magraner, Marc; Vila, Carlos; Rendón-Patiño, Alejandra; Blay, Gonzalo; Fernández, Isabel; Muñoz, M. Carmen; Pedro, José R.
Organocatalytic Enantioselective Friedel‒Crafts Aminoalkylation of Indoles in the Carbocyclic Ring
ACS Catalysis, 2016, 6, 2689
4513856 CIFC29 H29 N3 O6 SP 21 21 218.592; 11.328; 27.778
90; 90; 90		2703.64Montesinos-Magraner, Marc; Vila, Carlos; Rendón-Patiño, Alejandra; Blay, Gonzalo; Fernández, Isabel; Muñoz, M. Carmen; Pedro, José R.
Organocatalytic Enantioselective Friedel‒Crafts Aminoalkylation of Indoles in the Carbocyclic Ring
ACS Catalysis, 2016, 6, 2689
4513857 CIFC29 H26 F3 N3 O6 SP -110.512; 10.602; 13.589
104.085; 99.52; 91.757		1444.7Montesinos-Magraner, Marc; Vila, Carlos; Rendón-Patiño, Alejandra; Blay, Gonzalo; Fernández, Isabel; Muñoz, M. Carmen; Pedro, José R.
Organocatalytic Enantioselective Friedel‒Crafts Aminoalkylation of Indoles in the Carbocyclic Ring
ACS Catalysis, 2016, 6, 2689
4513858 CIFC20 H19 N O2P 21 21 217.23695; 9.22435; 23.1301
90; 90; 90		1544.08Ghosh, Avipsa; Walker, James A.; Ellern, Arkady; Stanley, Levi M.
Coupling Catalytic Alkene Hydroacylation and α-Arylation: Enantioselective Synthesis of Heterocyclic Ketones with α-Chiral Quaternary Stereocenters
ACS Catalysis, 2016, 6, 2673
4513863 CIFC33 H38 B Li O2 P2 S2P -19.0615; 10.7999; 17.4441
88.376; 79.606; 82.091		1663.14Lafage, Mathieu; Pujol, Anthony; Saffon-Merceron, Nathalie; Mézailles, Nicolas
BH3Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2Reduction into Methanol Derivatives
ACS Catalysis, 2016, 6, 3030
4513864 CIFC29 H35 B2 Li O P2 S2C 1 2/c 115.4208; 14.8446; 13.1339
90; 92.9702; 90		3002.52Lafage, Mathieu; Pujol, Anthony; Saffon-Merceron, Nathalie; Mézailles, Nicolas
BH3Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2Reduction into Methanol Derivatives
ACS Catalysis, 2016, 6, 3030
4513865 CIFC20 H20 OP 21 21 218.4103; 8.8487; 20.8277
90; 90; 90		1550Casanova, Noelia; Del Rio, Karina P.; García-Fandiño, Rebeca; Mascareñas, José L; Gulías, Moisés
Palladium(II)-Catalyzed Annulation between ortho-Alkenylphenols and Allenes. Key Role of the Metal Geometry in Determining the Reaction Outcome.
ACS catalysis, 2016, 6, 3349-3353
4513866 CIFC36 H32 O2P 1 21/c 19.4194; 7.0858; 19.435
90; 95.373; 90		1291.5Casanova, Noelia; Del Rio, Karina P.; García-Fandiño, Rebeca; Mascareñas, José L; Gulías, Moisés
Palladium(II)-Catalyzed Annulation between ortho-Alkenylphenols and Allenes. Key Role of the Metal Geometry in Determining the Reaction Outcome.
ACS catalysis, 2016, 6, 3349-3353
4513867 CIFC20 H19 F OP 21 21 216.489; 7.157; 32.722
90; 90; 90		1519.7Casanova, Noelia; Del Rio, Karina P.; García-Fandiño, Rebeca; Mascareñas, José L; Gulías, Moisés
Palladium(II)-Catalyzed Annulation between ortho-Alkenylphenols and Allenes. Key Role of the Metal Geometry in Determining the Reaction Outcome.
ACS catalysis, 2016, 6, 3349-3353
4513868 CIFC16 H19.16 N2 O4.58 PdP 1 21/c 114.136; 9.529; 25.085
90; 94.09; 90		3370.4White, Paul B.; Jaworski, Jonathan N.; Zhu, Geyunjian Harry; Stahl, Shannon S.
Diazafluorenone-Promoted Oxidation Catalysis: Insights into the Role of Bidentate Ligands in Pd-Catalyzed Aerobic Aza-Wacker Reactions.
ACS catalysis, 2016, 6, 3340-3348
4513869 CIFC20 H17 N3 O5 PdP 1 21/n 111.06; 10.703; 15.879
90; 102.713; 90		1833.6White, Paul B.; Jaworski, Jonathan N.; Zhu, Geyunjian Harry; Stahl, Shannon S.
Diazafluorenone-Promoted Oxidation Catalysis: Insights into the Role of Bidentate Ligands in Pd-Catalyzed Aerobic Aza-Wacker Reactions.
ACS catalysis, 2016, 6, 3340-3348
4513870 CIFC22 H23 N3 O4 PdP 1 21/c 112.472; 8.829; 19.26
90; 90.22; 90		2120.8White, Paul B.; Jaworski, Jonathan N.; Zhu, Geyunjian Harry; Stahl, Shannon S.
Diazafluorenone-Promoted Oxidation Catalysis: Insights into the Role of Bidentate Ligands in Pd-Catalyzed Aerobic Aza-Wacker Reactions.
ACS catalysis, 2016, 6, 3340-3348
4513871 CIFC19 H26 B N O2P 1 21 19.8601; 17.3729; 10.9482
90; 111.164; 90		1748.92Zhan, Miao; Li, Ren-Zhe; Mou, Ze-Dong; Cao, Chao-Guo; Liu, Jie; Chen, Yuan-Wei; Niu, Dawen
Silver-Assisted, Iridium-Catalyzed Allylation of Bis[(pinacolato)boryl]methane Allows the Synthesis of Enantioenriched Homoallylic Organoboronic Esters
ACS Catalysis, 2016, 6, 3381
4513872 CIFC51 H32 N4 O9 Zn2P 42/m n m36.0683; 36.0683; 27.0566
90; 90; 90		35199Hall, Edward A.; Redfern, Louis R.; Wang, Michael H.; Scheidt, Karl A.
Lewis Acid Activation of a Hydrogen Bond Donor Metal‒Organic Framework for Catalysis
ACS Catalysis, 2016, 6, 3248
4513873 CIFC15 H19 Ir N2 O6 SP 1 21/c 18.7413; 14.2966; 15.2329
90; 98.084; 90		1884.75Koelewijn, Jacobus M.; Lutz, Martin; Dzik, Wojciech I.; Detz, Remko J.; Reek, Joost N. H.
Reaction Progress Kinetic Analysis as a Tool To Reveal Ligand Effects in Ce(IV)-Driven IrCp*-Catalyzed Water Oxidation
ACS Catalysis, 2016, 6, 3418
4513878 CIFC30 H20 N2 OP 21 21 219.0933; 20.0387; 23.2417
90; 90; 90		4235.05Kumar, Dinesh; Vemula, Sandeep R.; Cook, Gregory R.
Merging C‒H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines
ACS Catalysis, 2016, 6, 3531
4513879 CIFC33 H23 F3 N2 O4P 1 21/c 121.6794; 5.8892; 20.8559
90; 98.889; 90		2630.78Kumar, Dinesh; Vemula, Sandeep R.; Cook, Gregory R.
Merging C‒H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines
ACS Catalysis, 2016, 6, 3531
4513880 CIFC26 H20 N2 OP -112.5358; 12.9306; 14.235
66.91; 68.341; 69.341		1913.41Kumar, Dinesh; Vemula, Sandeep R.; Cook, Gregory R.
Merging C‒H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines
ACS Catalysis, 2016, 6, 3531
4513881 CIFC27 H20 Br N O3 SP 1 21/c 112.857; 15.123; 12.073
90; 102.04; 90		2295.79Sun, Jiaqiong; Zheng, Guangfan; Xiong, Tao; Zhang, Qiao; Zhao, Jinbo; Li, Yan; Zhang, Qian
Copper-Catalyzed Hydroxyl-Directed Aminoarylation of Alkynes
ACS Catalysis, 2016, 6, 3674
4513882 CIFC35 H30 Br N3 O2P -110.6203; 11.0296; 13.8669
102.003; 107.216; 99.873		1469.68Wei, Guo; Zhang, Chenhao; Bureš, Filip; Ye, Xinyi; Tan, Choon-Hong; Jiang, Zhiyong
Enantioselective Aerobic Oxidative C(sp3)‒H Olefination of Amines via Cooperative Photoredox and Asymmetric Catalysis
ACS Catalysis, 2016, 6, 3708
4513883 CIFC27 H26 O3P 1 21/c 114.1082; 18.267; 8.1718
90; 96.84; 90		2091Yan, Jianming; Yoshikai, Naohiko
Cobalt-Catalyzed Arylative Cyclization of Acetylenic Esters and Ketones with Arylzinc Reagents through 1,4-Cobalt Migration
ACS Catalysis, 2016, 6, 3738
4513884 CIFC24 H21 N O2P 1 21/c 112.787; 12.7131; 12.427
90; 114.445; 90		1839.1Li, Bin; Xu, Hong; Wang, Huanan; Wang, Baiquan
Rhodium-Catalyzed Annulation of Tertiary AnilineN-Oxides toN-Alkylindoles: Regioselective C‒H Activation, Oxygen-Atom Transfer, andN-Dealkylative Cyclization
ACS Catalysis, 2016, 6, 3856
4513885 CIFC22 H18 Br NP 1 21/n 19.67; 19.62; 9.9545
90; 112.567; 90		1744Li, Bin; Xu, Hong; Wang, Huanan; Wang, Baiquan
Rhodium-Catalyzed Annulation of Tertiary AnilineN-Oxides toN-Alkylindoles: Regioselective C‒H Activation, Oxygen-Atom Transfer, andN-Dealkylative Cyclization
ACS Catalysis, 2016, 6, 3856
4513886 CIFC14 H16 F3 N3 O3P 21 21 214.8832; 15.6825; 19.696
90; 90; 90		1508.34Barron, Benedict J.; Wong, Wing-Tak; Chiu, Pauline; Hii, King Kuok
“Goldilocks Effect” of Water in Lewis-Brønsted Acid and Base Catalysis
ACS Catalysis, 2016, 6, 4189
4513887 CIFC20 H13 N O2P b c n11.5615; 11.966; 21.75
90; 90; 90		3009Abdellaoui, Fatma; Youssef, Chiraz; Ben Ammar, Hamed; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri
Palladium-Catalyzed Regioselective C‒H Bond Arylations of Benzoxazoles and Benzothiazoles at the C7 Position
ACS Catalysis, 2016, 6, 4248
4513895 CIFC20 H24 Cl2 Ir N3P 21 21 219.263; 13.429; 17.935
90; 90; 90		2231Bucci, Alberto; Menendez Rodriguez, Gabriel; Bellachioma, Gianfranco; Zuccaccia, Cristiano; Poater, Albert; Cavallo, Luigi; Macchioni, Alceo
An Alternative Reaction Pathway for Iridium-Catalyzed Water Oxidation Driven by Cerium Ammonium Nitrate (CAN)
ACS Catalysis, 2016, 6, 4559
4513899 CIFC69 H64 Cl2 Co F51 N7 O5P 1 21/c 124.5991; 14.5605; 25.6393
90; 106.121; 90		8822.2Chen, Ba-Tian; Morlanés, Natalia; Adogla, Enoch; Takanabe, Kazuhiro; Rodionov, Valentin O.
An Efficient and Stable Hydrophobic Molecular Cobalt Catalyst for Water Electro-oxidation at Neutral pH
ACS Catalysis, 2016, 6, 4647
4513900 CIFC29 H20 N O3 SP -19.8908; 10.8195; 12.6228
82.7016; 87.4478; 81.7877		1325.65Chen, Zi-Sheng; Huang, Liang-Zhu; Jeon, Hyun Ji; Xuan, Zi; Lee, Sang-gi
Cooperative Pd(0)/Rh(II) Dual Catalysis: Interceptive Capturing of π-Allyl Pd(II) Complexes with α-Imino Rh(II) Carbenoids
ACS Catalysis, 2016, 6, 4914
4513901 CIFC25 H22 N2 O6 SP -16.3051; 8.242; 21.9792
90.797; 96.108; 96.816		1127.27Chen, Zi-Sheng; Huang, Liang-Zhu; Jeon, Hyun Ji; Xuan, Zi; Lee, Sang-gi
Cooperative Pd(0)/Rh(II) Dual Catalysis: Interceptive Capturing of π-Allyl Pd(II) Complexes with α-Imino Rh(II) Carbenoids
ACS Catalysis, 2016, 6, 4914
4513903 CIFC51 H66 Cl2 N2 O2 TiP 1 21/c 113.4223; 15.5169; 23.9951
90; 104.683; 90		4834.3Pletcher, Paul D.; Switzer, Jeffrey M.; Steelman, D. Keith; Medvedev, Grigori A.; Delgass, W. Nicholas; Caruthers, James M.; Abu-Omar, Mahdi M.
Quantitative Comparative Kinetics of 1-Hexene Polymerization across Group IV Bis-Phenolate Catalysts
ACS Catalysis, 2016, 6, 5138
4513904 CIFC20 H24 I Ir N2P 1 21/c 113.683; 8.7527; 16.3494
90; 102.176; 90		1914Thenarukandiyil, Ranjeesh; Gupta, Suraj K.; Choudhury, Joyanta
Unraveling the Competition of Two C‒H and Two M‒C Bonds in Guiding the Mechanism of Rhodium(III)-Catalyzed C‒H Activation‒Annulation
ACS Catalysis, 2016, 6, 5132
4513905 CIFC26 H30 I Ir N2 O4P 1 21/n 110.646; 17.272; 14.564
90; 101.437; 90		2624.8Thenarukandiyil, Ranjeesh; Gupta, Suraj K.; Choudhury, Joyanta
Unraveling the Competition of Two C‒H and Two M‒C Bonds in Guiding the Mechanism of Rhodium(III)-Catalyzed C‒H Activation‒Annulation
ACS Catalysis, 2016, 6, 5132
4513906 CIFC26 H30 I N2 O4 RhP 1 21/n 110.6334; 17.2916; 14.4816
90; 101.307; 90		2611Thenarukandiyil, Ranjeesh; Gupta, Suraj K.; Choudhury, Joyanta
Unraveling the Competition of Two C‒H and Two M‒C Bonds in Guiding the Mechanism of Rhodium(III)-Catalyzed C‒H Activation‒Annulation
ACS Catalysis, 2016, 6, 5132
4513907 CIFC16 H30 Ca O12C 1 2 119.697; 5.855; 9.532
90; 95.8; 90		1093.7Petrus, Rafał; Bykowski, Dominik; Sobota, Piotr
Solvothermal Alcoholysis Routes for Recycling Polylactide Waste as Lactic Acid Esters
ACS Catalysis, 2016, 6, 5222
4513908 CIFC20 H40 Ca Cl2 O12P 18.768; 9.508; 10.629
97.45; 100.88; 117.39		748.4Petrus, Rafał; Bykowski, Dominik; Sobota, Piotr
Solvothermal Alcoholysis Routes for Recycling Polylactide Waste as Lactic Acid Esters
ACS Catalysis, 2016, 6, 5222
4513910 CIFC4 H12 Cl2 O2 Pd S2P 1 21/n 16.266; 9.3515; 9.3563
90; 108.635; 90		519.5Vemula, Sandeep R.; Kumar, Dinesh; Cook, Gregory R.
Palladium-Catalyzed Allylic Amidation with N-Heterocycles via sp3C‒H Oxidation
ACS Catalysis, 2016, 6, 5295
4513911 CIFC18 H15 Cl2 Pd2P 1 21/n 110.1578; 10.4643; 16.6141
90; 90.274; 90		1765.96Vemula, Sandeep R.; Kumar, Dinesh; Cook, Gregory R.
Palladium-Catalyzed Allylic Amidation with N-Heterocycles via sp3C‒H Oxidation
ACS Catalysis, 2016, 6, 5295
4513912 CIFC23 H22 N2 OP 21 21 218.9213; 9.9325; 20.8095
90; 90; 90		1843.95Zhuo, Chun-Xiang; Zhang, Xiao; You, Shu-Li
Enantioselective Synthesis of Pyrrole-Fused Piperazine and Piperazinone Derivatives via Ir-Catalyzed Asymmetric Allylic Amination
ACS Catalysis, 2016, 6, 5307
4513918 CIFC14 H14 Cl4 N8 Pd2P 1 21/n 110.3908; 11.9666; 17.1508
90; 106.646; 90		2043.2Dehury, Niranjan; Maity, Niladri; Tripathy, Suman Kumar; Basset, Jean-Marie; Patra, Srikanta
Dinuclear Tetrapyrazolyl Palladium Complexes Exhibiting Facile Tandem Transfer Hydrogenation/Suzuki Coupling Reaction of Fluoroarylketone
ACS Catalysis, 2016, 6, 5535
4513919 CIFC20 H18 Cl4 N8 Pd2C 1 2/c 113.098; 14.599; 14.668
90; 113.234; 90		2577.3Dehury, Niranjan; Maity, Niladri; Tripathy, Suman Kumar; Basset, Jean-Marie; Patra, Srikanta
Dinuclear Tetrapyrazolyl Palladium Complexes Exhibiting Facile Tandem Transfer Hydrogenation/Suzuki Coupling Reaction of Fluoroarylketone
ACS Catalysis, 2016, 6, 5535
4513920 CIFC20 H18 Cl4 N8 Pd2P -17.602; 8.298; 10.7372
99.281; 104.335; 102.182		624.94Dehury, Niranjan; Maity, Niladri; Tripathy, Suman Kumar; Basset, Jean-Marie; Patra, Srikanta
Dinuclear Tetrapyrazolyl Palladium Complexes Exhibiting Facile Tandem Transfer Hydrogenation/Suzuki Coupling Reaction of Fluoroarylketone
ACS Catalysis, 2016, 6, 5535
4513921 CIFC15 H18 Cl N3 Ni OC 1 2/c 114.6259; 13.2292; 16.0114
90; 101.154; 90		3039.51Soni, Vineeta; Jagtap, Rahul A.; Gonnade, Rajesh G.; Punji, Benudhar
Unified Strategy for Nickel-Catalyzed C-2 Alkylation of Indoles through Chelation Assistance
ACS Catalysis, 2016, 6, 5666
4513922 CIFC17 H22 N3 Ni O3.5P 1 21/c 115.7724; 14.0286; 16.1653
90; 101.236; 90		3508.25Soni, Vineeta; Jagtap, Rahul A.; Gonnade, Rajesh G.; Punji, Benudhar
Unified Strategy for Nickel-Catalyzed C-2 Alkylation of Indoles through Chelation Assistance
ACS Catalysis, 2016, 6, 5666
4513923 CIFC22 H33 B F4 P RhC 1 2/c 126.861; 7.7454; 21.4543
90; 97.763; 90		4422.6Strom, Alexandra E.; Balcells, David; Hartwig, John F.
Synthetic and Computational Studies on the Rhodium-Catalyzed Hydroamination of Aminoalkenes
ACS Catalysis, 2016, 6, 5651
4513924 CIFC26 H35 B F4 P RhP -110.927; 14.743; 15.848
106.91; 90.715; 94.619		2433Strom, Alexandra E.; Balcells, David; Hartwig, John F.
Synthetic and Computational Studies on the Rhodium-Catalyzed Hydroamination of Aminoalkenes
ACS Catalysis, 2016, 6, 5651
4513925 CIFC22 H35 B F4 P RhP -110.1423; 10.3515; 12.0166
91.342; 100.981; 115.42		1110.7Strom, Alexandra E.; Balcells, David; Hartwig, John F.
Synthetic and Computational Studies on the Rhodium-Catalyzed Hydroamination of Aminoalkenes
ACS Catalysis, 2016, 6, 5651
4513926 CIFC21 H20 Cl N3 O4P 1 21 19.48; 5.679; 19.061
90; 100.77; 90		1008.1Yang, Wu-Lin; Li, Chun-Yan; Qin, Wen-Jing; Tang, Fei-Fei; Yu, Xingxin; Deng, Wei-Ping
Cu(I)-Catalyzed Chemoselective and Stereoselective [3 + 3] Cycloaddition of Azomethine Ylides with 2-Indolylnitroethylenes: Facile Access to Highly Substituted Tetrahydro-γ-Carbolines
ACS Catalysis, 2016, 6, 5685
4513927 CIFC21 H20 Cl N3 O4P 21 21 217.1807; 13.199; 19.659
90; 90; 90		1863.2Yang, Wu-Lin; Li, Chun-Yan; Qin, Wen-Jing; Tang, Fei-Fei; Yu, Xingxin; Deng, Wei-Ping
Cu(I)-Catalyzed Chemoselective and Stereoselective [3 + 3] Cycloaddition of Azomethine Ylides with 2-Indolylnitroethylenes: Facile Access to Highly Substituted Tetrahydro-γ-Carbolines
ACS Catalysis, 2016, 6, 5685
4513928 CIFC17 H14 O2P 21 21 218.6908; 10.3574; 13.9701
90; 90; 90		1257.51Janssen-Müller, Daniel; Fleige, Mirco; Schlüns, Danny; Wollenburg, Marco; Daniliuc, Constantin G.; Neugebauer, Johannes; Glorius, Frank
NHC-Catalyzed Enantioselective Dearomatizing Hydroacylation of Benzofurans and Benzothiophenes for the Synthesis of Spirocycles
ACS Catalysis, 2016, 6, 5735
4513930 CIFC39 H70 O2 P2 Pd2P 1 21/c 19.7885; 32.8507; 26.2822
90; 93.385; 90		8436.5Lauer, Matthew G.; Headford, Benjamin R.; Gobble, Olivia M.; Weyhaupt, Michelle B.; Gerlach, Deidra L.; Zeller, Matthias; Shaughnessy, Kevin H.
A Trialkylphosphine-Derived Palladacycle as a Catalyst in the Selective Cross-Dimerization of Terminal Arylacetylenes with Terminal Propargyl Alcohols and Amides
ACS Catalysis, 2016, 6, 5834
4513932 CIFC28 H32 F6 N2 O3 Rh S SbP 1 21/c 113.8177; 16.467; 14.0445
90; 109.613; 90		3010.2Hu, Xu-Hong; Yang, Xiao-Fei; Loh, Teck-Peng
Chelation-Assisted Rhodium-Catalyzed Direct Amidation with Amidobenziodoxolones: C(sp2)‒H, C(sp3)‒H, and Late-Stage Functionalizations
ACS Catalysis, 2016, 6, 5930
4513933 CIFC28 H24 Cl3 N3 O7 SP 19.8739; 10.6233; 13.8412
86.937; 77.911; 89.004		1417.6Hu, Xu-Hong; Yang, Xiao-Fei; Loh, Teck-Peng
Chelation-Assisted Rhodium-Catalyzed Direct Amidation with Amidobenziodoxolones: C(sp2)‒H, C(sp3)‒H, and Late-Stage Functionalizations
ACS Catalysis, 2016, 6, 5930
4513934 CIFC22 H18 N2 O4 S2P 1 21/c 117.653; 12.7; 9.4888
90; 93.31; 90		2123.8Pan, Fei; Li, Xin-Ling; Chen, Xiu-Mei; Shu, Chao; Ruan, Peng-Peng; Shen, Cang-Hai; Lu, Xin; Ye, Long-Wu
Catalytic Ynamide Oxidation Strategy for the Preparation of α-Functionalized Amides
ACS Catalysis, 2016, 6, 6055
4513935 CIFC29 H25 N O5P -19.2103; 9.7574; 14.5275
75.23; 88.275; 69.461		1179.64Jiang, Liqin; Jin, Weifeng; Hu, Wenhao
Double C‒H Functionalization of Indoles via Three-Component Reactions/CuCl2-Catalyzed Aerobic Dehydrogenative Coupling for the Synthesis of Polyfunctional Cyclopenta[b]indoles
ACS Catalysis, 2016, 6, 6146
4513938 CIFC25 H31 Cl O2P 1 21 19.842; 11.556; 9.8592
90; 97.807; 90		1110.9Ma, Chao; Huang, Yuan; Zhao, Yu
Stereoselective 1,6-Conjugate Addition/Annulation ofpara-Quinone Methides with Vinyl Epoxides/Cyclopropanes
ACS Catalysis, 2016, 6, 6408
4513939 CIFC39 H46 B2 F8 Fe N4 P2P 1 21 110.9646; 16.3287; 11.9006
90; 110.493; 90		1995.8Bigler, Raphael; Huber, Raffael; Stöckli, Marco; Mezzetti, Antonio
Iron(II)/(NH)2P2Macrocycles: Modular, Highly Enantioselective Transfer Hydrogenation Catalysts
ACS Catalysis, 2016, 6, 6455
4513940 CIFC59 H74 B2 Cl4 F8 Fe N4 P2P 110.4939; 10.7859; 13.5065
101.154; 92.256; 102.353		1459.9Bigler, Raphael; Huber, Raffael; Stöckli, Marco; Mezzetti, Antonio
Iron(II)/(NH)2P2Macrocycles: Modular, Highly Enantioselective Transfer Hydrogenation Catalysts
ACS Catalysis, 2016, 6, 6455
4513941 CIFC65.5 H33.5 Co F10 N6.5 O1.71P 1 21/c 117.3254; 30.92; 23.005
90; 90.359; 90		12323.6Lei, Haitao; Liu, Chengyu; Wang, Zhaojun; Zhang, Zongyao; Zhang, Meining; Chang, Xingmao; Zhang, Wei; Cao, Rui
Noncovalent Immobilization of a Pyrene-Modified Cobalt Corrole on Carbon Supports for Enhanced Electrocatalytic Oxygen Reduction and Oxygen Evolution in Aqueous Solutions
ACS Catalysis, 2016, 6, 6429
4513942 CIFC22 H32 Au F6 N4 SbP 1 21/c 18.4122; 11.7102; 14.7141
90; 103.893; 90		1407.06Bartolomé, Camino; Ramiro, Zoraida; Peñas-Defrutos, Marconi N.; Espinet, Pablo
Some Singular Features of Gold Catalysis: Protection of Gold(I) Catalysts by Substoichiometric Agents and Associated Phenomena
ACS Catalysis, 2016, 6, 6537
4513943 CIFC55 H51 B2 F20 N O ZrP 1 21/n 110.6797; 38.6444; 25.5186
90; 94.5702; 90		10498.3Metters, Owen J.; Flynn, Stephanie R.; Dowds, Christiana K.; Sparkes, Hazel A.; Manners, Ian; Wass, Duncan F.
Catalytic Dehydrocoupling of Amine‒Boranes using Cationic Zirconium(IV)‒Phosphine Frustrated Lewis Pairs
ACS Catalysis, 2016, 6, 6601
4513944 CIFC62 H61.5 B2 Cl0.5 F20 N O ZrP -110.8416; 16.5385; 18.9008
68.2519; 74.0118; 72.1388		2945.45Metters, Owen J.; Flynn, Stephanie R.; Dowds, Christiana K.; Sparkes, Hazel A.; Manners, Ian; Wass, Duncan F.
Catalytic Dehydrocoupling of Amine‒Boranes using Cationic Zirconium(IV)‒Phosphine Frustrated Lewis Pairs
ACS Catalysis, 2016, 6, 6601
4513945 CIFC60 H51 B F20 N2 O ZrP c a 2117.1305; 10.7085; 29.9187
90; 90; 90		5488.3Metters, Owen J.; Flynn, Stephanie R.; Dowds, Christiana K.; Sparkes, Hazel A.; Manners, Ian; Wass, Duncan F.
Catalytic Dehydrocoupling of Amine‒Boranes using Cationic Zirconium(IV)‒Phosphine Frustrated Lewis Pairs
ACS Catalysis, 2016, 6, 6601
4513946 CIFC20 H25 N O2P 1 21 19.419; 8.8409; 11.6624
90; 112.966; 90		894.18Zhang, Heyi; Lu, Zhan
Dual-Stereocontrol Asymmetric Cobalt-Catalyzed Hydroboration of Sterically Hindered Styrenes
ACS Catalysis, 2016, 6, 6596
4513948 CIFC25 H38 B3 Cl2 I N12 Ni2P -112.3061; 12.6455; 13.1675
78.8847; 71.0045; 87.4156		1900.8Lu, Zhiyao; Williams, Travis J.
Di(carbene)-Supported Nickel Systems for CO2Reduction Under Ambient Conditions
ACS Catalysis, 2016, 6, 6670
4513949 CIFC59 H68 Cl2 N8 Ni3 O4P 1 21/c 122.9867; 8.2956; 32.6131
90; 109.922; 90		5846.8Lu, Zhiyao; Williams, Travis J.
Di(carbene)-Supported Nickel Systems for CO2Reduction Under Ambient Conditions
ACS Catalysis, 2016, 6, 6670
4513950 CIFC24 H30 B I N4P 1 21/m 18.2687; 19.3361; 8.7596
90; 115.029; 90		1269.01Lu, Zhiyao; Williams, Travis J.
Di(carbene)-Supported Nickel Systems for CO2Reduction Under Ambient Conditions
ACS Catalysis, 2016, 6, 6670
4513951 CIFC40 H55 Cl N4 Ni O0P 1 21 19.586; 12.006; 18.204
90; 96.216; 90		2082.8Pu, Xinghui; Hu, Jiefeng; Zhao, Yue; Shi, Zhuangzhi
Nickel-Catalyzed Decarbonylative Borylation and Silylation of Esters
ACS Catalysis, 2016, 6, 6692
4513952 CIFC42 H57 Cl3 N4 Ni OP n a 2112.7494; 28.039; 11.5771
90; 90; 90		4138.6Pu, Xinghui; Hu, Jiefeng; Zhao, Yue; Shi, Zhuangzhi
Nickel-Catalyzed Decarbonylative Borylation and Silylation of Esters
ACS Catalysis, 2016, 6, 6692
4513953 CIFC24 H55 Cl P2 PdC 1 2/c 145.941; 8.7162; 14.6019
90; 102.274; 90		5713.4Hu, Yue; Shen, Zhiqiang; Huang, Hanmin
Palladium-Catalyzed Intramolecular Hydroaminocarbonylation to Lactams: Additive-Free Protocol Initiated by Palladium Hydride
ACS Catalysis, 2016, 6, 6785
4513954 CIFC10 H8 N O2P 1 21/c 14.5967; 12.2704; 15.393
90; 94.473; 90		865.6Hu, Yue; Shen, Zhiqiang; Huang, Hanmin
Palladium-Catalyzed Intramolecular Hydroaminocarbonylation to Lactams: Additive-Free Protocol Initiated by Palladium Hydride
ACS Catalysis, 2016, 6, 6785
4513955 CIFC16 H15 N OP 14.6759; 11.637; 12.148
101.704; 94.481; 97.981		637.1Hu, Yue; Shen, Zhiqiang; Huang, Hanmin
Palladium-Catalyzed Intramolecular Hydroaminocarbonylation to Lactams: Additive-Free Protocol Initiated by Palladium Hydride
ACS Catalysis, 2016, 6, 6785
4513956 CIFC25 H24 Br O2 PP 1 21/n 114.349; 9.776; 16.959
90; 108.332; 90		2258Toda, Yasunori; Komiyama, Yutaka; Kikuchi, Ayaka; Suga, Hiroyuki
Tetraarylphosphonium Salt-Catalyzed Carbon Dioxide Fixation at Atmospheric Pressure for the Synthesis of Cyclic Carbonates
ACS Catalysis, 2016, 6, 6906
4513960 CIFC11 H13 N O3 SP 1 21/c 19.45565; 18.07717; 13.18336
90; 103.903; 90		2187.43Bizet, Vincent; Borrajo-Calleja, Gustavo M.; Besnard, Céline; Mazet, Clément
Direct Access to Furoindolines by Palladium-Catalyzed Intermolecular Carboamination
ACS Catalysis, 2016, 6, 7183
4513961 CIFC17 H18 N2 O4 SP 1 21/c 111.81121; 8.41417; 16.5698
90; 90.8215; 90		1646.56Bizet, Vincent; Borrajo-Calleja, Gustavo M.; Besnard, Céline; Mazet, Clément
Direct Access to Furoindolines by Palladium-Catalyzed Intermolecular Carboamination
ACS Catalysis, 2016, 6, 7183
4513962 CIFC19 H17 N O4 SP 1 21/c 110.28582; 9.52978; 16.564
90; 90.4024; 90		1623.59Bizet, Vincent; Borrajo-Calleja, Gustavo M.; Besnard, Céline; Mazet, Clément
Direct Access to Furoindolines by Palladium-Catalyzed Intermolecular Carboamination
ACS Catalysis, 2016, 6, 7183
4513963 CIFC18 H19 N O4 SP 21 21 215.45149; 15.7094; 38.6948
90; 90; 90		3313.81Bizet, Vincent; Borrajo-Calleja, Gustavo M.; Besnard, Céline; Mazet, Clément
Direct Access to Furoindolines by Palladium-Catalyzed Intermolecular Carboamination
ACS Catalysis, 2016, 6, 7183
4513970 CIFC84 H84 Cd2 N4 O16 V2P 2 2 2134.388; 34.853; 13.3846
90; 90; 90		16041.8Zhu, Chengfeng; Xia, Qingchun; Chen, Xu; Liu, Yan; Du, Xia; Cui, Yong
Chiral Metal‒Organic Framework as a Platform for Cooperative Catalysis in Asymmetric Cyanosilylation of Aldehydes
ACS Catalysis, 2016, 6, 7590
4513971 CIFC84 H84 Cd2 Cu N4 O16 VP 2 2 2133.9506; 35.3214; 13.4377
90; 90; 90		16114.3Zhu, Chengfeng; Xia, Qingchun; Chen, Xu; Liu, Yan; Du, Xia; Cui, Yong
Chiral Metal‒Organic Framework as a Platform for Cooperative Catalysis in Asymmetric Cyanosilylation of Aldehydes
ACS Catalysis, 2016, 6, 7590
4513972 CIFC22 H16 Cl NP 21 21 216.0503; 14.698; 18.444
90; 90; 90		1640.2Kim, Ju Hyun; Greßies, Steffen; Boultadakis-Arapinis, Mélissa; Daniliuc, Constantin; Glorius, Frank
Rh(I)/NHC*-Catalyzed Site- and Enantioselective Functionalization of C(sp3)‒H Bonds Toward Chiral Triarylmethanes
ACS Catalysis, 2016, 6, 7652
4513973 CIFC23 H19 N OP 21 21 215.7336; 16.8181; 17.4381
90; 90; 90		1681.53Kim, Ju Hyun; Greßies, Steffen; Boultadakis-Arapinis, Mélissa; Daniliuc, Constantin; Glorius, Frank
Rh(I)/NHC*-Catalyzed Site- and Enantioselective Functionalization of C(sp3)‒H Bonds Toward Chiral Triarylmethanes
ACS Catalysis, 2016, 6, 7652
4513974 CIFC45 H37 Cl O P2 PdP 1 21/n 111.0213; 23.615; 16.094
90; 105.537; 90		4035.7Chatterjee, Anamitra; Hopen Eliasson, Sondre H.; Törnroos, Karl W.; Jensen, Vidar R.
Palladium Precatalysts for Decarbonylative Dehydration of Fatty Acids to Linear Alpha Olefins
ACS Catalysis, 2016, 6, 7784
4513975 CIFC11 H13 Br O2 SP 1 21 19.6991; 9.587; 13.7942
90; 105.113; 90		1238.29Zhou, Pengfei; Cai, Yunfei; Zhong, Xia; Luo, Weiwei; Kang, Tengfei; Li, Jun; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Catalytic Asymmetric Intra- and Intermolecular Haloetherification of Enones: An Efficient Approach to (−)-Centrolobine
ACS Catalysis, 2016, 6, 7778
4513976 CIFC20 H21 Br O2P 1 21 15.4678; 8.6283; 18.6625
90; 91.41; 90		880.19Zhou, Pengfei; Cai, Yunfei; Zhong, Xia; Luo, Weiwei; Kang, Tengfei; Li, Jun; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Catalytic Asymmetric Intra- and Intermolecular Haloetherification of Enones: An Efficient Approach to (−)-Centrolobine
ACS Catalysis, 2016, 6, 7778
4513977 CIFC16 H15 Br O2P 1 21 18.8973; 6.9477; 12.2822
90; 100.56; 90		746.37Zhou, Pengfei; Cai, Yunfei; Zhong, Xia; Luo, Weiwei; Kang, Tengfei; Li, Jun; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Catalytic Asymmetric Intra- and Intermolecular Haloetherification of Enones: An Efficient Approach to (−)-Centrolobine
ACS Catalysis, 2016, 6, 7778
4513979 CIFC51 H71 Cu Fe N2 O3 Si2P -110.7287; 11.7933; 20.5611
100.143; 97.14; 93.382		2532.29Chakraborty, Arundhoti; Kinney, R. Garrison; Krause, Jeanette A.; Guan, Hairong
Cooperative Iron‒Oxygen‒Copper Catalysis in the Reduction of Benzaldehyde under Water-Gas Shift Reaction Conditions
ACS Catalysis, 2016, 6, 7855
4513980 CIFC52 H63 Cu D6 Fe N2 O3P 1 21/n 111.9549; 10.1772; 40.3744
90; 95.356; 90		4890.8Chakraborty, Arundhoti; Kinney, R. Garrison; Krause, Jeanette A.; Guan, Hairong
Cooperative Iron‒Oxygen‒Copper Catalysis in the Reduction of Benzaldehyde under Water-Gas Shift Reaction Conditions
ACS Catalysis, 2016, 6, 7855
4513981 CIFC34 H51 Fe N2 PC 1 2/c 120.4853; 14.08083; 22.6949
90; 95.5664; 90		6515.47Espinal-Viguri, Maialen; King, Andrew K.; Lowe, John P.; Mahon, Mary F.; Webster, Ruth L.
Hydrophosphination of Unactivated Alkenes and Alkynes Using Iron(II): Catalysis and Mechanistic Insight
ACS Catalysis, 2016, 6, 7892
4513983 CIFC60.38 H57 Cl1.75 N4 O9C 1 2 133.03; 14.5141; 23.743
90; 106.097; 90		10936.1Ma, Chao; Huang, Yuan; Zhao, Yu
Stereoselective 1,6-Conjugate Addition/Annulation ofpara-Quinone Methides with Vinyl Epoxides/Cyclopropanes
ACS Catalysis, 2016, 6, 6408
4513984 CIFC24 H24 Cl N3 O2P 21 21 2110.405; 14.2652; 14.6935
90; 90; 90		2180.95Bertuzzi, Giulio; Sinisi, Alessandro; Caruana, Lorenzo; Mazzanti, Andrea; Fochi, Mariafrancesca; Bernardi, Luca
Catalytic Enantioselective Addition of Indoles to ActivatedN-Benzylpyridinium Salts: Nucleophilic Dearomatization of Pyridines with Unusual C-4 Regioselectivity
ACS Catalysis, 2016, 6, 6473
4513985 CIFC16 H24 I2 N8 NiP -18.3462; 8.4556; 8.796
113.763; 101.75; 91.594		552.02Lu, Zhiyao; Williams, Travis J.
Di(carbene)-Supported Nickel Systems for CO2Reduction Under Ambient Conditions
ACS Catalysis, 2016, 6, 6670
4513986 CIFC16 H24 B2 N8 NiP 1 21/n 16.8569; 16.0355; 8.668
90; 98.926; 90		941.54Lu, Zhiyao; Williams, Travis J.
Di(carbene)-Supported Nickel Systems for CO2Reduction Under Ambient Conditions
ACS Catalysis, 2016, 6, 6670
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

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