Crystallography Open Database

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4513766 CIFC20 H26 Cl F6 N3 P RhA e a 228.458; 12.7428; 13.1834
90; 90; 90		4780.8Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513767 CIFC23 H31 Cl N3 RhR -3 :H21.5542; 21.5542; 26.557
90; 90; 120		10685Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513768 CIFC28 H36 Cl F6 N3 P RhP c a 2116.0545; 7.2176; 24.4803
90; 90; 90		2836.65Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513769 CIFC23 H18 F6 N3 PC 1 2/c 115.136; 8.965; 32.085
90; 102; 90		4259Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513770 CIFC19 H18 F6 N3 PP 1 21/c 18.3203; 17.1518; 13.0268
90; 96.731; 90		1846.22Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513771 CIFC28 H28 Cl2 F6 N3 PP 1 21/n 19.3435; 25.7949; 12.1804
90; 95.655; 90		2921.4Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513772 CIFC22 H30 F3 N3 O3 SP 1 21/c 18.7885; 23.335; 11.5049
90; 97.583; 90		2338.8Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513773 CIFC29 H23 F6 N4 PP 1 21/c 112.1221; 9.8286; 21.8422
90; 93.81; 90		2596.6Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513774 CIFC21 H24 F6 N3 PP 1 21/c 18.0991; 11.7222; 22.981
90; 109.173; 90		2060.8Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513775 CIFC22 H24 F6 N3 PP 1 21/c 113.3734; 11.2225; 15.731
90; 114.074; 90		2155.6Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513776 CIFC37 H28 F6 N3 PP b c a19.6256; 13.0146; 25.6519
90; 90; 90		6552Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513777 CIFC27 H24 F6 N3 PP -110.4464; 10.5483; 13.2843
89.215; 69.09; 66.286		1237.45Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513778 CIFC18 H26 F6 N3 PP 1 21/c 18.1489; 17.045; 15.403
90; 101.334; 90		2097.7Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
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
4513805 CIFC11 H11 N OP 1 21/n 17.5306; 6.1547; 20.6613
90; 91.838; 90		957.13Wu, Jin-Ji; Li, Yinwu; Zhou, Hai-Yun; Wen, A-Hao; Lun, Chu-Chu; Yao, Su-Yang; Ke, Zhuofeng; Ye, Bao-Hui
Copper-Catalyzed Carbamoylation of Terminal Alkynes with Formamides via Cross-Dehydrogenative Coupling
ACS Catalysis, 2016, 1263
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
4513862 CIFC21 H39 Fe N3 O3 P2P 1 21/c 115.1403; 23.6; 14.0883
90; 96.634; 90		5000.2Bertini, Federica; Gorgas, Nikolaus; Stöger, Berthold; Peruzzini, Maurizio; Veiros, Luis F.; Kirchner, Karl; Gonsalvi, Luca
Efficient and Mild Carbon Dioxide Hydrogenation to Formate Catalyzed by Fe(II) Hydrido Carbonyl Complexes Bearing 2,6-(Diaminopyridyl)diphosphine Pincer Ligands
ACS Catalysis, 2016, 2889
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
4513888 CIFC9 H18 Cl N3 SiP 1 21/n 17.3619; 15.6139; 10.5158
90; 95.783; 90		1202.62von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
4513889 CIFC13 H26 Cl N3 SiP 1 21/n 19.2603; 12.2644; 14.0949
90; 101.148; 90		1570.58von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
4513890 CIFC70 H44 B2 F40 N6 O2 Si2C 1 2/c 110.4208; 32.2781; 20.9281
90; 91.711; 90		7036.3von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
4513891 CIFC22 H36 F12 N8 O8 S4 Si2P b c a17.0441; 17.1344; 26.8405
90; 90; 90		7838.5von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
4513892 CIFC12.5 H20.5 Cl N3.5 O2 SiP 1 21 18.6635; 9.8107; 9.9624
90; 92.613; 90		845.87von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
4513893 CIFC34 H18 B F20 N3 O2 SiP -17.9383; 13.9155; 16.4838
75.2; 84.476; 76.031		1707.3von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
4513894 CIFC19 H23 N3 SiP 1 21 18.5953; 8.5523; 11.7943
90; 92.704; 90		866.03von Wolff, N.; Lefèvre, G.; Berthet, J.-C.; Thuéry, P.; Cantat, T.
Implications of CO2Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+Frustrated Lewis Pairs
ACS Catalysis, 2016, 4526
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
4513902 CIFC32 H48.9 Cl3 Co2 N8 O16.71P 1 21/c 118.2143; 12.64794; 19.337
90; 111.871; 90		4134.1Wang, Jia-Wei; Sahoo, Pathik; Lu, Tong-Bu
Reinvestigation of Water Oxidation Catalyzed by a Dinuclear Cobalt Polypyridine Complex: Identification of CoOxas a Real Heterogeneous Catalyst
ACS Catalysis, 2016, 5062
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
4513917 CIFC29 H22 N2 OP 1 21/n 113.936; 8.669; 18.401
90; 104.393; 90		2153Maity, Soham; Kancherla, Rajesh; Dhawa, Uttam; Hoque, Ehtasimul; Pimparkar, Sandeep; Maiti, Debabrata
Switch to Allylic Selectivity in Cobalt-Catalyzed Dehydrogenative Heck Reactions with Unbiased Aliphatic Olefins
ACS Catalysis, 2016, 5493
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
4513931 CIFC13 H24 N2 O3C 1 c 117.0431; 25.6881; 10.2924
90; 90.01; 90		4506.1Kim, Hyunwoo; Park, Gyeongtae; Park, Juhyeon; Chang, Sukbok
A Facile Access to Primary Alkylamines and Anilines via Ir(III)-Catalyzed C‒H Amidation Using Azidoformates
ACS Catalysis, 2016, 5922
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
4513936 CIFC20 H20 I2 N2P 21 21 218.0059; 12.7607; 18.742
90; 90; 90		1914.7Yu, Xiao-Long; Kuang, Liping; Chen, Su; Zhu, Xiao-Long; Li, Zhong-Liang; Tan, Bin; Liu, Xin-Yuan
Counteranion-Controlled Unprecedented Diastereo- and Enantioselective Tandem Formal Povarov Reaction for Construction of Bioactive Octahydro-Dipyrroloquinolines
ACS Catalysis, 2016, 6182
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
4513958 CIFC16 H15 Br O4 SP 1 21 18.8773; 7.1193; 14.0576
90; 103.929; 90		862.32Tan, Fei; Liu, Xiaohua; Hao, Xiaoyu; Tang, Yu; Lin, Lili; Feng, Xiaoming
Asymmetric Catalytic Insertion of α-Diazo Carbonyl Compounds into O‒H Bonds of Carboxylic Acids
ACS Catalysis, 2016, 6930
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
4513967 CIFC61.75 H82.75 Au3 B Cl5.25 F4 O P3P n a 2125.4511; 14.4307; 18.9787
90; 90; 90		6970.4Zhu, Yuyang; Zhou, Wentong; Petryna, Ellen M.; Rogers, Brock R.; Day, Cynthia S.; Jones, Amanda C.
Insights into Alkene Activation by Gold: Nucleophile Activation with Base as a Trigger for Generation of Lewis Acidic Gold
ACS Catalysis, 2016, 7357
4513968 CIFC45 H55 Au Cl2 N2 OP -19.1823; 9.5417; 26.1911
90.453; 90.84; 114.659		2084.99Zhu, Yuyang; Zhou, Wentong; Petryna, Ellen M.; Rogers, Brock R.; Day, Cynthia S.; Jones, Amanda C.
Insights into Alkene Activation by Gold: Nucleophile Activation with Base as a Trigger for Generation of Lewis Acidic Gold
ACS Catalysis, 2016, 7357
4513969 CIFC35 H32 Au O PP 1 21/c 116.333; 8.8197; 19.533
90; 90.342; 90		2813.7Zhu, Yuyang; Zhou, Wentong; Petryna, Ellen M.; Rogers, Brock R.; Day, Cynthia S.; Jones, Amanda C.
Insights into Alkene Activation by Gold: Nucleophile Activation with Base as a Trigger for Generation of Lewis Acidic Gold
ACS Catalysis, 2016, 7357
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
4513978 CIFC14 H16 Cl3 Ir N2 O5P -19.1361; 10.454; 10.987
109.018; 100.334; 109.417		885.6Abril, Paula; del R\?ío, M. Pilar; Tejel, Cristina; Verhoeven, Tiny W. G. M.; Niemantsverdriet, J. W. Hans; Van der Ham, Cornelis J. M.; Kottrup, Konstantin G.; Hetterscheid, Dennis G. H.
Detangling Catalyst Modification Reactions from the Oxygen Evolution Reaction by Online Mass Spectrometry
ACS Catalysis, 2016, 7872
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
4513982 CIFC34 H36 Cl2 N P TiP b c a8.463; 20.965; 35.984
90; 90; 90		6385Ehm, Christian; Cipullo, Roberta; Passaro, Miriana; Zaccaria, Francesco; Budzelaar, Peter H. M.; Busico, Vincenzo
Chain Transfer to Solvent in Propene Polymerization with Ti Cp-phosphinimide Catalysts: Evidence for Chain Termination via Ti‒C Bond Homolysis
ACS Catalysis, 2016, 7989
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
4513987 CIFC22 H24 O6P 1 21/c 112.7894; 10.6893; 14.2151
90; 99.57; 90		1916.3Liu, Yuliang; Zhang, Mingfu; Tung, Chen-Ho; Wang, Yifeng
TiO2 Photocatalytic Cyclization Reactions for the Syntheses of Aryltetralones
ACS Catalysis, 2016, 8389
4513988 CIFC18 H18 O3P 1 21/c 112.469; 13.936; 8.2701
90; 96.849; 90		1426.8Liu, Yuliang; Zhang, Mingfu; Tung, Chen-Ho; Wang, Yifeng
TiO2 Photocatalytic Cyclization Reactions for the Syntheses of Aryltetralones
ACS Catalysis, 2016, 8389
4513990 CIFC30 H30 O4 P2P 1 21/c 124.0185; 5.3968; 20.965
90; 94.688; 90		2708.46Ilies, Laurean; Itabashi, Yuki; Shang, Rui; Nakamura, Eiichi
Iron/Zinc-Co-catalyzed Directed Arylation and Alkenylation of C(sp3)‒H Bonds with Organoborates
ACS Catalysis, 2016, 89
4513993 CIFC30 H30 Ni O2 P2I 1 2/a 118.9022; 9.9937; 43.3265
90; 91.431; 90		8181.9Dey, Aniruddha; Sasmal, Sheuli; Seth, Kapileswar; Lahiri, Goutam Kumar; Maiti, Debabrata
Nickel-Catalyzed Deamidative Step-Down Reduction of Amides to Aromatic Hydrocarbons
ACS Catalysis, 2016, 433
4513994 CIFC46 H52 Cu2 N10P 21 21 2115.431; 16.964; 23.348
90; 90; 90		6112Trose, Michael; Lazreg, Faïma; Chang, Tao; Nahra, Fady; Cordes, David B.; Slawin, Alexandra M. Z.; Cazin, Catherine S. J.
Neutral Dinuclear Copper(I)-NHC Complexes: Synthesis and Application in the Hydrosilylation of Ketones
ACS Catalysis, 2017, 7, 238
4513995 CIFC18 H20 Br Cl O4P -18.6779; 9.0204; 12.802
92.405; 96.467; 113.588		908.37Gao, Yuzhen; Zhang, Pengbo; Ji, Zhe; Tang, Guo; Zhao, Yufen
Copper-Catalyzed Cascade Radical Addition‒Cyclization Halogen Atom Transfer between Alkynes and Unsaturated α-Halogenocarbonyls
ACS Catalysis, 2016, 186
4513996 CIFC16 H17 Br O5P 21 21 219.4351; 12.256; 13.14
90; 90; 90		1519.5Uyanik, Muhammet; Sasakura, Niiha; Mizuno, Masahiro; Ishihara, Kazuaki
Enantioselective Synthesis of Masked Benzoquinones Using Designer Chiral Hypervalent Organoiodine(III) Catalysis
ACS Catalysis, 2016, 872
4513997 CIFC15 H13 N OP b c a10.2112; 7.7666; 27.5135
90; 90; 90		2182Potter, Tyler J.; Kamber, David N.; Mercado, Brandon Q.; Ellman, Jonathan A.
Rh(III)-Catalyzed Aryl and Alkenyl C‒H Bond Addition to Diverse Nitroalkenes
ACS Catalysis, 2016, 150
4513998 CIFC31 H36 B N O4 SP -110.9835; 12.2187; 13.4045
62.987; 70.987; 71.821		1486.2Xi, Tuo; Lu, Zhan
Cobalt-Catalyzed Ligand-Controlled Regioselective Hydroboration/Cyclization of 1,6-Enynes
ACS Catalysis, 2017, 1181
4513999 CIFC25 H39 Cl F3 Ir N O3 P SP 1 21/c 18.1455; 16.5588; 20.962
90; 94.132; 90		2820Celaje, Jeff Joseph A.; Zhang, Xingyue; Zhang, Forrest; Kam, Lisa; Herron, Jessica R.; Williams, Travis J.
A Base and Solvent-Free Ruthenium-Catalyzed Alkylation of Amines
ACS Catalysis, 2017, 7, 1136
4514003 CIFC53 H50 Ni O5 P2 S SiP -112.3423; 19.324; 21.3802
88.813; 82.852; 76.64		4922.5Chen, Min; Chen, Changle
Rational Design of High-Performance Phosphine Sulfonate Nickel Catalysts for Ethylene Polymerization and Copolymerization with Polar Monomers
ACS Catalysis, 2017, 1308
4514007 CIFC15 H32 N2 O3P 21 21 219.6788; 11.2486; 16.793
90; 90; 90		1828.3Cañellas, Santiago; Ayats, Carles; Henseler, Andrea H.; Pericàs, Miquel A.
A Highly Active Polymer-Supported Catalyst for Asymmetric Robinson Annulations in Continuous Flow
ACS Catalysis, 2017
4514008 CIFC17 H24 N O3 SP 1 21 19.0973; 8.2011; 22.9008
90; 99.357; 90		1685.85Feng, Jian-Jun; Zhang, Junliang
Rhodium-Catalyzed Stereoselective Intramolecular Tandem Reaction of Vinyloxiranes with Alkynes: Atom- and Step-Economical Synthesis of Multifunctional Mono-, Bi-, and Tricyclic Compounds
ACS Catalysis, 2017, 7, 1533
4514010 CIFC54 H46 Al F15 N3 O ReP -112.546; 14.078; 17.037
67.591; 72.379; 69.555		2556.2Lambic, Nikola S.; Sommer, Roger D.; Ison, Elon A.
Tuning Catalytic Activity in the Hydrogenation of Unactivated Olefins with Transition-Metal Oxos as the Lewis Base Component of Frustrated Lewis Pairs
ACS Catalysis, 2017, 7, 1170
4514011 CIFC37.5 H47 Cl N3 O ReP 1 21/n 115.6648; 13.4862; 17.082
90; 105.914; 90		3470.4Lambic, Nikola S.; Sommer, Roger D.; Ison, Elon A.
Tuning Catalytic Activity in the Hydrogenation of Unactivated Olefins with Transition-Metal Oxos as the Lewis Base Component of Frustrated Lewis Pairs
ACS Catalysis, 2017, 7, 1170
4514012 CIFC28 H27 N3 O8 S2C 1 c 116.946; 13.855; 12.2464
90; 100.543; 90		2826.8Rivinoja, Daniel J.; Gee, Yi Sing; Gardiner, Michael G.; Ryan, John H.; Hyland, Christopher J. T.
The Diastereoselective Synthesis of Pyrroloindolines by Pd-Catalyzed Dearomative Cycloaddition of 1-Tosyl-2-vinylaziridine to 3-Nitroindoles
ACS Catalysis, 2017, 7, 1053
4514013 CIFC25 H24 O3P 21 21 216.72474; 16.401; 17.4977
90; 90; 90		1929.86James, Jinju; Guiry, Patrick J.
Highly Enantioselective Construction of Sterically Hindered α-Allyl-α-Aryl Lactones via Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation
ACS Catalysis, 2017, 7, 1397
4514014 CIFC16 H13 Au Cl5 N O2P -18.2785; 8.9703; 14.5673
76.336; 87.282; 65.557		955.4Tomás-Mendivil, Eder; Heinrich, Clément F.; Ortuno, Jean-Claude; Starck, Jérôme; Michelet, Véronique
Gold-Catalyzed Access to 1H-Isochromenes: Reaction Development and Mechanistic Insight
ACS Catalysis, 2017, 7, 380
4514015 CIFC17 H19 F3 I N O3C 1 2/c 147.1143; 4.86847; 16.0241
90; 97.7446; 90		3641.99Shen, Yangyang; Cornella, Josep; Juliá-Hernández, Francisco; Martin, Ruben
Visible-Light-Promoted Atom Transfer Radical Cyclization of Unactivated Alkyl Iodides
ACS Catalysis, 2017, 7, 409
4514016 CIFC46 H56 Cu2 N10P 1 21/c 111.3017; 13.5088; 14.966
90; 108.686; 90		2164.5Trose, Michael; Lazreg, Faïma; Chang, Tao; Nahra, Fady; Cordes, David B.; Slawin, Alexandra M. Z.; Cazin, Catherine S. J.
Neutral Dinuclear Copper(I)-NHC Complexes: Synthesis and Application in the Hydrosilylation of Ketones
ACS Catalysis, 2017, 7, 238
4514017 CIFC35 H54 Cl2 Cu2 N10I 41/a20.4817; 20.4817; 21.6349
90; 90; 90		9075.8Trose, Michael; Lazreg, Faïma; Chang, Tao; Nahra, Fady; Cordes, David B.; Slawin, Alexandra M. Z.; Cazin, Catherine S. J.
Neutral Dinuclear Copper(I)-NHC Complexes: Synthesis and Application in the Hydrosilylation of Ketones
ACS Catalysis, 2017, 7, 238
4514023 CIFC78 H65 Cl F6 P5 Pd3 SbP 1 21/c 115.3747; 16.9302; 27.578
90; 93.07; 90		7168.2Fu, Fangyu; Xiang, Ji; Cheng, Hao; Cheng, Longjiu; Chong, Hanbao; Wang, Shuxin; Li, Peng; Wei, Shiqiang; Zhu, Manzhou; Li, Yadong
A Robust and Efficient Pd3 Cluster Catalyst for the Suzuki Reaction and Its Odd Mechanism
ACS Catalysis, 2017, 7, 1860
4514024 CIFC94 H118 Ge2 N2 O Si2C 1 2/c 124.283; 21.152; 17.759
90; 114.38; 90		8308Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514025 CIFC52 H69 B N O3.5 Si SnP -110.1191; 12.9066; 18.7646
88.763; 86.92; 85.612		2439.63Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514026 CIFC45 H53 N O2 Si SnP -19.99; 11.36; 18.89
86.59; 85.63; 67.69		1976.4Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514027 CIFC15 H23 N3 O3P b c a16.5344; 9.4279; 20.9981
90; 90; 90		3273.3Bai, He-Yuan; Ma, Zhi-Gang; Yi, Min; Lin, Jun-Bing; Zhang, Shu-Yu
Palladium-Catalyzed Direct Intermolecular Amination of Unactivated Methylene C(sp3)‒H Bonds with Azodiformates via Bidentate-Chelation Assistance
ACS Catalysis, 2017, 7, 2042
4514028 CIFC56.25 H50.5 F12 N10 O4.75 P2 Ru2C 1 2/c 123.6464; 24.1857; 24.249
90; 116.899; 90		12367.7Odrobina, Jann; Scholz, Julius; Pannwitz, Andrea; Francàs, Laia; Dechert, Sebastian; Llobet, Antoni; Jooss, Christian; Meyer, Franc
Backbone Immobilization of the Bis(bipyridyl)pyrazolate Diruthenium Catalyst for Electrochemical Water Oxidation
ACS Catalysis, 2017, 7, 2116
4514029 CIFC61 H60 F12 N10 O7 P2 Ru2C 1 2/c 118.7376; 22.1944; 15.7519
90; 90.788; 90		6550.1Odrobina, Jann; Scholz, Julius; Pannwitz, Andrea; Francàs, Laia; Dechert, Sebastian; Llobet, Antoni; Jooss, Christian; Meyer, Franc
Backbone Immobilization of the Bis(bipyridyl)pyrazolate Diruthenium Catalyst for Electrochemical Water Oxidation
ACS Catalysis, 2017, 7, 2116
4514030 CIFC42 H36 F2 Fe Ni P2 SP -111.2326; 11.336; 16.1197
78.107; 72.51; 67.279		1796.3Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514031 CIFC40 H34 Fe I2 Ni P2P -18.9532; 10.0303; 20.4331
91.917; 99.127; 94.971		1802.83Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514037 CIFC54.5 H45 Ag4 Cl5 O10P 1 21/n 111.2473; 18.5148; 26.3786
90; 97.2988; 90		5448.6Zhou, Zhen; He, Cheng; Yang, Lu; Wang, Yefei; Liu, Tao; Duan, Chunying
Alkyne Activation by a Porous Silver Coordination Polymer for Heterogeneous Catalysis of Carbon Dioxide Cycloaddition
ACS Catalysis, 2017, 7, 2248
4514038 CIFC15 H12 Ag2 O6C 1 2/c 126.064; 19.397; 11.0996
90; 97.166; 90		5567.7Zhou, Zhen; He, Cheng; Yang, Lu; Wang, Yefei; Liu, Tao; Duan, Chunying
Alkyne Activation by a Porous Silver Coordination Polymer for Heterogeneous Catalysis of Carbon Dioxide Cycloaddition
ACS Catalysis, 2017, 7, 2248
4514039 CIFC44 H30 F5 N2 PP 1 21 112.3621; 45.6111; 12.6667
90; 97.7659; 90		7076.6Rokade, Balaji V.; Guiry, Patrick J.
Diastereofacial π-Stacking as an Approach To Access an Axially Chiral P,N-Ligand for Asymmetric Catalysis
ACS Catalysis, 2017, 2334
4514040 CIFC24 H18 Cl6 N O5 VP 1 21 17.20833; 12.3392; 14.6278
90; 93.647; 90		1298.44Miceli, Claudia; Rintjema, Jeroen; Martin, Eddy; Escudero-Adán, Eduardo C.; Zonta, Cristiano; Licini, Giulia; Kleij, Arjan W.
Vanadium(V) Catalysts with High Activity for the Coupling of Epoxides and CO2: Characterization of a Putative Catalytic Intermediate
ACS Catalysis, 2017, 7, 2367
4514041 CIFC24 H17 Cl7 N O5 VP 1 21/c 17.1728; 13.0626; 28.541
90; 96.136; 90		2658.8Miceli, Claudia; Rintjema, Jeroen; Martin, Eddy; Escudero-Adán, Eduardo C.; Zonta, Cristiano; Licini, Giulia; Kleij, Arjan W.
Vanadium(V) Catalysts with High Activity for the Coupling of Epoxides and CO2: Characterization of a Putative Catalytic Intermediate
ACS Catalysis, 2017, 7, 2367
4514048 CIFC21 H26 N2 O5C 1 2 122.5768; 8.5784; 12.0175
90; 121.047; 90		1994.04Chen, Xiaohong; Yang, Shujing; Li, Helong; Wang, Bo; Song, Guoyong
Enantioselective C‒H Annulation of Indoles with Diazo Compounds through a Chiral Rh(III) Catalyst
ACS Catalysis, 2017, 2392
4514051 CIFC44 H30 F5 N2 PP 1 21 112.37; 45.6483; 12.6634
90; 97.6938; 90		7086.3Paioti, Paulo H. S.; Abboud, Khalil A.; Aponick, Aaron
Incorporation of Axial Chirality into Phosphino-Imidazoline Ligands for Enantioselective Catalysis
ACS Catalysis, 2017, 7, 2133
4514052 CIFC78 H65 Br0.69 Cl0.31 F6 P5 Pd3 SbP 1 21/c 115.3662; 16.9466; 27.676
90; 92.693; 90		7199Fu, Fangyu; Xiang, Ji; Cheng, Hao; Cheng, Longjiu; Chong, Hanbao; Wang, Shuxin; Li, Peng; Wei, Shiqiang; Zhu, Manzhou; Li, Yadong
A Robust and Efficient Pd3 Cluster Catalyst for the Suzuki Reaction and Its Odd Mechanism
ACS Catalysis, 2017, 7, 1860
4514053 CIFC50 H64 B Ge N O3 SiP -19.93; 14.88; 15.29
91; 91.6; 98.1		2235.3Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514054 CIFC101 H134 Ge2 N2 O2 Si2C 1 2/c 131.052; 19.593; 17.8613
90; 105.933; 90		10449.4Hadlington, Terrance J.; Kefalidis, Christos E.; Maron, Laurent; Jones, Cameron
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido‒Germanium(II) and −Tin(II) Hydride Complexes
ACS Catalysis, 2017, 7, 1853
4514055 CIFC38 H36 N2 O5 S2P 21 21 2110.9061; 12.6404; 28.3159
90; 90; 90		3903.6Feng, Jian-Jun; Zhang, Junliang
Rhodium-Catalyzed Stereoselective Intramolecular Tandem Reaction of Vinyloxiranes with Alkynes: Atom- and Step-Economical Synthesis of Multifunctional Mono-, Bi-, and Tricyclic Compounds
ACS Catalysis, 2017, 7, 1533
4514056 CIFC17 H21 N O3 SP 21 21 218.1166; 13.77; 15.4267
90; 90; 90		1724.17Feng, Jian-Jun; Zhang, Junliang
Rhodium-Catalyzed Stereoselective Intramolecular Tandem Reaction of Vinyloxiranes with Alkynes: Atom- and Step-Economical Synthesis of Multifunctional Mono-, Bi-, and Tricyclic Compounds
ACS Catalysis, 2017, 7, 1533
4514057 CIFC25 H44 Mn N O3 P2P n a 2130.3732; 11.6836; 7.6516
90; 90; 90		2715.3Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Paul, Jean-François; Dumeignil, Franck; Gauvin, Régis M.
Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding
ACS Catalysis, 2017, 7, 2022
4514058 CIFC18 H41 B Mn N O2 P2P b c a17.2037; 14.6522; 19.066
90; 90; 90		4806Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Paul, Jean-François; Dumeignil, Franck; Gauvin, Régis M.
Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding
ACS Catalysis, 2017, 7, 2022
4514059 CIFC18 H38 Mn N O2 P2P 1 21/c 110.6335; 14.5777; 13.8441
90; 97.449; 90		2127.9Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Paul, Jean-François; Dumeignil, Franck; Gauvin, Régis M.
Manganese Pincer Complexes for the Base-Free, Acceptorless Dehydrogenative Coupling of Alcohols to Esters: Development, Scope, and Understanding
ACS Catalysis, 2017, 7, 2022
4514060 CIFC40 H34 Br Fe Ni P2P -19.6075; 10.9191; 17.624
96.565; 105.405; 103.759		1699.9Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514061 CIFC72 H64 Fe2 I2 Ni2 O P4C 1 2/c 123.6771; 13.9547; 19.1841
90; 90.394; 90		6338.4Kalvet, Indrek; Guo, Qianqian; Tizzard, Graham J.; Schoenebeck, Franziska
When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.
ACS catalysis, 2017, 7, 2126-2132
4514062 CIFC18 H17 N O2P -17.3719; 8.0356; 12.4786
82.255; 78.93; 86.099		718.16Wu, Xiaowei; Wang, Bao; Zhou, Shengbin; Zhou, Yu; Liu, Hong
Ruthenium-Catalyzed Redox-Neutral [4 + 1] Annulation of Benzamides and Propargyl Alcohols via C‒H Bond Activation
ACS Catalysis, 2017, 7, 2494
4514063 CIFC30 H64 Br2 P2 Pd2P 1 21/c 114.191; 14.4097; 18.8529
90; 90.638; 90		3855Hu, Huaiyuan; Qu, Fengrui; Gerlach, Deidra L.; Shaughnessy, Kevin H.
Mechanistic Study of the Role of Substrate Steric Effects and Aniline Inhibition on the Bis(trineopentylphosphine)palladium(0)-Catalyzed Arylation of Aniline Derivatives
ACS Catalysis, 2017, 7, 2516
4514064 CIFC48 H88 Br2 Cl4 P2 Pd2P -19.5914; 12.2401; 13.6152
114.515; 94.093; 92.143		1446.66Hu, Huaiyuan; Qu, Fengrui; Gerlach, Deidra L.; Shaughnessy, Kevin H.
Mechanistic Study of the Role of Substrate Steric Effects and Aniline Inhibition on the Bis(trineopentylphosphine)palladium(0)-Catalyzed Arylation of Aniline Derivatives
ACS Catalysis, 2017, 7, 2516
4514066 CIFC18 H19 N3 O2P 1 21/n 18.2446; 18.1585; 10.6143
90; 99.541; 90		1567.08Leitch, Jamie A.; McMullin, Claire L.; Mahon, Mary F.; Bhonoah, Yunas; Frost, Christopher G.
Remote C6-Selective Ruthenium-Catalyzed C‒H Alkylation of Indole Derivatives via σ-Activation
ACS Catalysis, 2017, 2616
4514067 CIFC24 H29 N3 O4P -17.2094; 12.0942; 13.0064
106.921; 90.76; 95.278		1079.4Leitch, Jamie A.; McMullin, Claire L.; Mahon, Mary F.; Bhonoah, Yunas; Frost, Christopher G.
Remote C6-Selective Ruthenium-Catalyzed C‒H Alkylation of Indole Derivatives via σ-Activation
ACS Catalysis, 2017, 2616
4514068 CIFC23 H18 N2 O3 SP -18.1462; 9.4252; 13.2617
104.796; 102.654; 103.208		915.85Li, Jun-Ming; Wang, Yong-Heng; Yu, Yang; Wu, Rui-Bo; Weng, Jiang; Lu, Gui
Copper-Catalyzed Remote C‒H Functionalizations of Naphthylamides through a Coordinating Activation Strategy and Single-Electron-Transfer (SET) Mechanism
ACS Catalysis, 2017, 2661
4514069 CIFC49 H40 N2 O4P -111.406; 12.0431; 13.804
89.519; 88.399; 75.619		1836Uraguchi, Daisuke; Torii, Masahiro; Ooi, Takashi
Acridinium Betaine as a Single-Electron-Transfer Catalyst: Design and Application to Dimerization of Oxindoles
ACS Catalysis, 2017
4514070 CIFC38 H29 F3 N OP b c n15.083; 14.7314; 26.284
90; 90; 90		5840.1Uraguchi, Daisuke; Torii, Masahiro; Ooi, Takashi
Acridinium Betaine as a Single-Electron-Transfer Catalyst: Design and Application to Dimerization of Oxindoles
ACS Catalysis, 2017
4514071 CIFC25 H19 Br N2 O2P 21 21 219.5611; 9.7674; 44.019
90; 90; 90		4110.8Wang, Shoulei; Izquierdo, Javier; Rodríguez-Escrich, Carles; Pericàs, Miquel A.
Asymmetric [4 + 2] Annulation Reactions Catalyzed by a Robust, Immobilized Isothiourea
ACS Catalysis, 2017, 7, 2780
4514072 CIFC24 H17 N O2 SP 21 21 216.2831; 10.506; 28.682
90; 90; 90		1893.3Wang, Shoulei; Izquierdo, Javier; Rodríguez-Escrich, Carles; Pericàs, Miquel A.
Asymmetric [4 + 2] Annulation Reactions Catalyzed by a Robust, Immobilized Isothiourea
ACS Catalysis, 2017, 7, 2780
4514073 CIFC38 H27 N5 O2P b c n17.1283; 9.2992; 18.9173
90; 90; 90		3013.1Du, Cong; Li, Peng-Xiang; Zhu, Xinju; Han, Jiao-Na; Niu, Jun-Long; Song, Mao-Ping
Cobalt-Catalyzed Oxidative C-H/N-H Cross-Coupling: Selective and Facile Access to Triarylamines
ACS Catalysis, 2017
4514074 CIFC45 H33 Cl2 Co N6 O2P 1 21/c 112.2327; 13.1901; 24.1763
90; 103.838; 90		3787.6Du, Cong; Li, Peng-Xiang; Zhu, Xinju; Han, Jiao-Na; Niu, Jun-Long; Song, Mao-Ping
Cobalt-Catalyzed Oxidative C-H/N-H Cross-Coupling: Selective and Facile Access to Triarylamines
ACS Catalysis, 2017
4514080 CIFC38 H52 N2 O2 PdP 1 21/c 112.47076; 21.63215; 13.10657
90; 99.47; 90		3487.57Kim, Jaewoon; Hong, Soon Hyeok
Ligand-Promoted Direct C‒H Arylation of Simple Arenes: Evidence for a Cooperative Bimetallic Mechanism
ACS Catalysis, 2017, 7, 3336
4514083 CIFC28 H29 N O3P -16.3295; 12.336; 14.619
90.792; 95.813; 96.114		1128.8Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip
A Bioinspired Catalytic Aerobic Functionalization of Phenols: Regioselective Construction of Aromatic C‒N and C‒O Bonds
ACS Catalysis, 2017, 7, 3477
4514084 CIFC33 H25 N O4P -19.7185; 15.9184; 15.9702
88.541; 87.598; 85.097		2458.84Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip
A Bioinspired Catalytic Aerobic Functionalization of Phenols: Regioselective Construction of Aromatic C‒N and C‒O Bonds
ACS Catalysis, 2017, 7, 3477
4514085 CIFC34 H23 F2 N O5P 1 21 110.0098; 19.235; 13.3175
90; 91.572; 90		2563.2Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip
A Bioinspired Catalytic Aerobic Functionalization of Phenols: Regioselective Construction of Aromatic C‒N and C‒O Bonds
ACS Catalysis, 2017, 7, 3477
4514089 CIFC38 H34 Co N4P b c a19.206; 15.8073; 19.2815
90; 90; 90		5853.8Maher, Andrew G.; Passard, Guillaume; Dogutan, Dilek K.; Halbach, Robert L.; Anderson, Bryce L.; Gagliardi, Christopher J.; Taniguchi, Masahiko; Lindsey, Jonathan S.; Nocera, Daniel G.
Hydrogen Evolution Catalysis by a Sparsely Substituted Cobalt Chlorin
ACS Catalysis, 2017, 3597
4514090 CIFC25 H19 N O2P 1 21/c 14.88608; 39.9585; 9.27521
90; 91.1105; 90		1810.56Herlé, Bart; Holstein, Philipp M.; Echavarren, Antonio M.
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions.
ACS catalysis, 2017, 7, 3668-3675
4514091 CIFC25 H19 N O2P -19.8574; 10.5363; 19.098
83.974; 85.964; 69.875		1850.88Herlé, Bart; Holstein, Philipp M.; Echavarren, Antonio M.
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions.
ACS catalysis, 2017, 7, 3668-3675
4514094 CIFC62 H65 B Co F24 N O2 P2P -113.0174; 14.9485; 17.504
102.352; 98.18; 99.337		3227.4Yuwen, Jing; Chakraborty, Sumit; Brennessel, William W.; Jones, William D.
Additive-Free Cobalt-Catalyzed Hydrogenation of Esters to Alcohols
ACS Catalysis, 2017, 3735
4514095 CIFC74 H75 B Co F24 N O4 P2P -114.722; 16.791; 17.269
99.053; 113.62; 101.693		3692.2Yuwen, Jing; Chakraborty, Sumit; Brennessel, William W.; Jones, William D.
Additive-Free Cobalt-Catalyzed Hydrogenation of Esters to Alcohols
ACS Catalysis, 2017, 3735
4514096 CIFC12 H10 O5P 21 21 215.9658; 6.8587; 26.877
90; 90; 90		1099.74Ji, Jie; Lin, Lili; Tang, Qiong; Kang, Tengfei; Liu, Xiaohua; Feng, Xiaoming
Highly Efficient Asymmetric Synthesis of Chiral γ-Alkenyl Butenolides Catalyzed by Chiral N,N′-Dioxide‒Scandium(III) Complexes
ACS Catalysis, 2017, 7, 3763
4514100 CIFC60 H54 F18 N12 O4 P3 Ru2P -113.578; 13.579; 13.733
91.45; 100.63; 115.95		2222Fan, Ting; Duan, Lele; Huang, Ping; Chen, Hong; Daniel, Quentin; Ahlquist, Mårten S. G.; Sun, Licheng
The Ru-tpc Water Oxidation Catalyst and Beyond: Water Nucleophilic Attack Pathway versus Radical Coupling Pathway
ACS Catalysis, 2017, 7, 2956
4514101 CIFC21 H39 Cl2 Co N P2P -18.2698; 10.9458; 14.8705
98.19; 90.641; 110.333		1246.6Daw, Prosenjit; Chakraborty, Subrata; Leitus, Gregory; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Selective N-Formylation of Amines with H2 and CO2 Catalyzed by Cobalt Pincer Complexes
ACS Catalysis, 2017, 7, 2500
4514102 CIFC21 H39 Cl Co N P2P 1 21/c 114.2619; 8.3444; 19.9331
90; 96.477; 90		2357Daw, Prosenjit; Chakraborty, Subrata; Leitus, Gregory; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Selective N-Formylation of Amines with H2 and CO2 Catalyzed by Cobalt Pincer Complexes
ACS Catalysis, 2017, 7, 2500
4514103 CIFC50 H40 Cl N3 O P2 RuP n m a18.5484; 15.0463; 16.1704
90; 90; 90		4512.9Sarbajna, Abir; Dutta, Indranil; Daw, Prosenjit; Dinda, Shrabani; Rahaman, S. M. Wahidur; Sarkar, Abheek; Bera, Jitendra K.
Catalytic Conversion of Alcohols to Carboxylic Acid Salts and Hydrogen with Alkaline Water
ACS Catalysis, 2017, 7, 2786
4514104 CIFC54 H47 Cl5 N4 O P2 RuP 1 21/c 114.2935; 18.4185; 22.7313
90; 108.44; 90		5677.1Sarbajna, Abir; Dutta, Indranil; Daw, Prosenjit; Dinda, Shrabani; Rahaman, S. M. Wahidur; Sarkar, Abheek; Bera, Jitendra K.
Catalytic Conversion of Alcohols to Carboxylic Acid Salts and Hydrogen with Alkaline Water
ACS Catalysis, 2017, 7, 2786
4514105 CIFC59 H49 Cl5 N4 O2 P2 Ru2P -111.8324; 14.2246; 18.611
86.239; 84.443; 71.637		2956.9Sarbajna, Abir; Dutta, Indranil; Daw, Prosenjit; Dinda, Shrabani; Rahaman, S. M. Wahidur; Sarkar, Abheek; Bera, Jitendra K.
Catalytic Conversion of Alcohols to Carboxylic Acid Salts and Hydrogen with Alkaline Water
ACS Catalysis, 2017, 7, 2786
4514106 CIFC29 H20 F3 N5 O6 Ru SP -18.4166; 11.03; 16.025
84.085; 76.9; 69.246		1354.52Kagalwala, Husain N.; Tong, Lianpeng; Zong, Ruifa; Kohler, Lars; Ahlquist, Mårten S. G.; Fan, Ting; Gagnon, Kevin J.; Thummel, Randolph P.
Evidence for Oxidative Decay of a Ru-Bound Ligand during Catalyzed Water Oxidation
ACS Catalysis, 2017, 7, 2607
4514107 CIFC13 H15 N O4P 21 21 218.8677; 10.0871; 14.1044
90; 90; 90		1261.63Tukhvatshin, Rinat S.; Kucherenko, Alexander S.; Nelyubina, Yulia V.; Zlotin, Sergei G.
Tertiary Amine-Derived Ionic Liquid-Supported Squaramide as a Recyclable Organocatalyst for Noncovalent “On Water” Catalysis
ACS Catalysis, 2017, 7, 2981
4514108 CIFC13 H8 Br Mn N2 O5P b a m17.7576; 12.9229; 12.7518
90; 90; 90		2926.3Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514109 CIFC15 H12 Br Mn N2 O5P 1 21/n 18.1795; 16.3907; 11.9305
90; 90.478; 90		1599.44Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514110 CIFC13 H10 Br Mn N4 O3P 1 21/n 17.5829; 9.6475; 20.0238
90; 93.812; 90		1461.62Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514111 CIFC16 H11 F3 Mn N3 O8 SP -18.9121; 12.7125; 17.6682
84.4838; 86.3815; 83.4002		1976.5Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514112 CIFC18 H15 F3 Mn N3 O8 SP 1 21/c 18.19264; 11.4621; 23.0399
90; 92.2861; 90		2161.84Dubey, Abhishek; Nencini, Luca; Fayzullin, Robert R.; Nervi, Carlo; Khusnutdinova, Julia R.
Bio-Inspired Mn(I) Complexes for the Hydrogenation of CO2 to Formate and Formamide
ACS Catalysis, 2017, 7, 3864
4514115 CIFC44 H61 N O10 S SiP 1 21 19.04501; 9.77593; 25.19795
90; 92.5278; 90		2225.92Liao, Yuting; Zhou, Baixin; Xia, Yong; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Asymmetric [3 + 2] Cycloaddition of 2,2′-Diester Aziridines To Synthesize Pyrrolidine Derivatives
ACS Catalysis, 2017, 7, 3934
4514116 CIFC24 H24 Cl N O5P 1 21 19.975; 8.9417; 12.2426
90; 101.043; 90		1071.74Mondal, Santigopal; Mukherjee, Subrata; Das, Tamal Kanti; Gonnade, Rajesh; Biju, Akkattu T.
N-Heterocyclic Carbene-Catalyzed Aldol-Lactonization of Ketoacids via Dynamic Kinetic Resolution
ACS Catalysis, 2017, 3995
4514117 CIFC22 H24 N2 O2 SP 1 21 113.226; 6.2835; 13.615
90; 92.018; 90		1130.8Lin, Tao-Yan; Wu, Hai-Hong; Feng, Jian-Jun; Zhang, Junliang
Design and Enantioselective Synthesis of β-Vinyl Tryptamine Building Blocks for Construction of Privileged Chiral Indole Scaffolds
ACS Catalysis, 2017, 4047
4514118 CIFC20 H24 Cl N O2 SP 1 21/c 19.5931; 12.8055; 15.6673
90; 102.15; 90		1881.53Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514119 CIFC19 H22 N2 O4 SP b c n16.4786; 7.779; 28.3488
90; 90; 90		3633.9Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514120 CIFC25 H18P 1 21/c 113.316; 20.47; 6.2779
90; 101.369; 90		1677.6Yu, Liu-Zhu; Wei, Yin; Shi, Min
Synthesis of Polysubstituted Polycyclic Aromatic Hydrocarbons by Gold-Catalyzed Cyclization‒Oxidation of Alkylidenecyclopropane-Containing 1,5-Enynes
ACS Catalysis, 2017, 7, 4242
4514121 CIFC24 H17 Cl OP -19.3854; 9.6615; 11.064
87.814; 68.304; 85.999		929.8Yu, Liu-Zhu; Wei, Yin; Shi, Min
Synthesis of Polysubstituted Polycyclic Aromatic Hydrocarbons by Gold-Catalyzed Cyclization‒Oxidation of Alkylidenecyclopropane-Containing 1,5-Enynes
ACS Catalysis, 2017, 7, 4242
4514122 CIFC22 H16 SP -14.9712; 11.992; 27.578
79.676; 84.855; 78.156		1580.6Yu, Liu-Zhu; Wei, Yin; Shi, Min
Synthesis of Polysubstituted Polycyclic Aromatic Hydrocarbons by Gold-Catalyzed Cyclization‒Oxidation of Alkylidenecyclopropane-Containing 1,5-Enynes
ACS Catalysis, 2017, 7, 4242
4514123 CIFC25 H26 F2 N2 Pt SP -19.0052; 10.3193; 13.9951
90.135; 92.418; 94.402		1295.52Suslick, Benjamin A.; Liberman-Martin, Allegra L.; Wambach, Truman C.; Tilley, T. Don
Olefin Hydroarylation Catalyzed by (pyridyl-indolate)Pt(II) Complexes: Catalytic Efficiencies and Mechanistic Aspects
ACS Catalysis, 2017, 4313
4514124 CIFC25 H24 F4 N2 Pt SP -18.9213; 10.1362; 14.7554
97.236; 90.819; 94.146		1319.84Suslick, Benjamin A.; Liberman-Martin, Allegra L.; Wambach, Truman C.; Tilley, T. Don
Olefin Hydroarylation Catalyzed by (pyridyl-indolate)Pt(II) Complexes: Catalytic Efficiencies and Mechanistic Aspects
ACS Catalysis, 2017, 4313
4514136 CIFC19 H27 Cl N3 O P RuP b c a8.539; 15.0653; 32.9272
90; 90; 90		4235.84Li, Huaifeng; Wang, Yuan; Lai, Zhiping; Huang, Kuo-Wei
Selective Catalytic Hydrogenation of Arenols by a Well-Defined Complex of Ruthenium and Phosphorus‒Nitrogen PN3‒Pincer Ligand Containing a Phenanthroline Backbone
ACS Catalysis, 2017, 7, 4446
4514137 CIFC22 H31 Cl N3 O2 P RuP 1 21/c 18.4904; 16.3262; 17.4261
90; 97.79; 90		2393.24Li, Huaifeng; Wang, Yuan; Lai, Zhiping; Huang, Kuo-Wei
Selective Catalytic Hydrogenation of Arenols by a Well-Defined Complex of Ruthenium and Phosphorus‒Nitrogen PN3‒Pincer Ligand Containing a Phenanthroline Backbone
ACS Catalysis, 2017, 7, 4446
4514138 CIFC46 H40 Br2 N2 O2P -111.3349; 12.8075; 13.5019
76.483; 84.58; 83.915		1890.13Liu, Yi; Tse, Ying-Lung Steve; Kwong, Fuk Yee; Yeung, Ying-Yeung
Accessing Axially Chiral Biaryls via Organocatalytic Enantioselective Dynamic-Kinetic Resolution-Semipinacol Rearrangement
ACS Catalysis, 2017, 4435
4514139 CIFC28 H28 N2 O6 SP 1 21 114.93; 11.5659; 15.258
90; 101.808; 90		2579Claraz, Aurélie; Serpier, Fabien; Darses, Sylvain
Organoboron Initiated Rh-Catalyzed Asymmetric Cascade Reactions: A Subtle Switch in Regioselectivity Leading to Chiral 3-Benzazepine Derivatives
ACS Catalysis, 2017, 7, 3410
4514140 CIFC42 H30 F6 N2 O4P 21 21 218.8643; 17.5771; 22.5359
90; 90; 90		3511.3Yang, Wenjun; Sun, Wei; Zhang, Cheng; Wang, Qijun; Guo, Zhenyan; Mao, Biming; Liao, Jianning; Guo, Hongchao
Lewis-Base-Catalyzed Asymmetric [3 + 3] Annulation Reaction of Morita‒Baylis‒Hillman Carbonates: Enantioselective Synthesis of Spirocyclohexenes
ACS Catalysis, 2017, 7, 3142
4514141 CIFC18 H18P 1 21 19.035; 5.7594; 13.277
90; 100.891; 90		678.4Herlé, Bart; Holstein, Philipp M.; Echavarren, Antonio M.
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions.
ACS catalysis, 2017, 7, 3668-3675
4514142 CIFC21 H27 N O2 SP 1 21/n 111.6983; 13.0767; 13.6557
90; 114.637; 90		1898.82Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514143 CIFC19 H21 N O2 SP 1 21/c 110.2375; 9.4009; 16.6135
90; 98.412; 90		1581.71Zhang, Hongwei; Muñiz, Kilian
Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3‒H Amination under Visible Light
ACS Catalysis, 2017, 7, 4122
4514151 CIFC13 H22 F3 Ir N2 O2 SI 41 c d16.7238; 16.7238; 23.136
90; 90; 90		6470.8Matsunami, Asuka; Kuwata, Shigeki; Kayaki, Yoshihito
A Bifunctional Iridium Catalyst Modified for Persistent Hydrogen Generation from Formic Acid: Understanding Deactivation via Cyclometalation of a 1,2-Diphenylethylenediamine Motif
ACS Catalysis, 2017, 4479
4514152 CIFC25 H28 F3 Ir N2 O2 SC 1 2 120.7776; 14.3517; 18.813
90; 111.073; 90		5234.75Matsunami, Asuka; Kuwata, Shigeki; Kayaki, Yoshihito
A Bifunctional Iridium Catalyst Modified for Persistent Hydrogen Generation from Formic Acid: Understanding Deactivation via Cyclometalation of a 1,2-Diphenylethylenediamine Motif
ACS Catalysis, 2017, 4479
4514153 CIFC14 H23 Cl3 F3 Ir N2 O2 SP 1 21/c 111.168; 11.884; 16.488
90; 104.162; 90		2121.8Matsunami, Asuka; Kuwata, Shigeki; Kayaki, Yoshihito
A Bifunctional Iridium Catalyst Modified for Persistent Hydrogen Generation from Formic Acid: Understanding Deactivation via Cyclometalation of a 1,2-Diphenylethylenediamine Motif
ACS Catalysis, 2017, 4479
4514154 CIFC16 H11 F5 N3 O7 VP -17.8153; 11.0933; 11.0932
78.955; 85.104; 77.783		921.55Gazi, Sarifuddin; Đokić, Miloš; Moeljadi, Adhitya Mangala Putra; Ganguly, Rakesh; Hirao, Hajime; Soo, Han Sen
Kinetics and DFT Studies of Photoredox Carbon‒Carbon Bond Cleavage Reactions by Molecular Vanadium Catalysts under Ambient Conditions
ACS Catalysis, 2017, 7, 4682
4514155 CIFC25 H22 Br2 F N OP 1 21 113.4096; 5.2499; 16.501
90; 106.995; 90		1110.93Arimitsu, Satoru; Yonamine, Tsunaki; Higashi, Masahiro
Cinchona-Based Primary Amine Catalyzed a Proximal Functionalization of Dienamines: Asymmetric α-Fluorination of α-Branched Enals
ACS Catalysis, 2017, 4736
4514158 CIFC14 H13 Cl3 O4P 1 21 17.1346; 14.8376; 15.0064
90; 98.492; 90		1571.17Cruchter, Thomas; Medvedev, Michael G.; Shen, Xiaodong; Mietke, Thomas; Harms, Klaus; Marsch, Michael; Meggers, Eric
Asymmetric Nucleophilic Catalysis with an Octahedral Chiral-at-Metal Iridium(III) Complex
ACS Catalysis, 2017, 7, 5151
4514159 CIFC22 H38 Si2P 1 21/n 18.809; 15.299; 16.461
90; 93.573; 90		2214.1Chen, Jiazhen; Gao, Yanshan; Xiong, Shuoyan; Delferro, Massimiliano; Lohr, Tracy L.; Marks, Tobin J.
Metal and Counteranion Nuclearity Effects in Organoscandium-Catalyzed Isoprene Polymerization and Copolymerization
ACS Catalysis, 2017, 7, 5214
4514160 CIFC48 H100 O2 Sc2 Si6P 1 21/c 114.3075; 24.95; 17.0373
90; 98.009; 90		6022.5Chen, Jiazhen; Gao, Yanshan; Xiong, Shuoyan; Delferro, Massimiliano; Lohr, Tracy L.; Marks, Tobin J.
Metal and Counteranion Nuclearity Effects in Organoscandium-Catalyzed Isoprene Polymerization and Copolymerization
ACS Catalysis, 2017, 7, 5214
4514161 CIFC20 H20 N2 O3R 321.2602; 21.2602; 10.1814
90; 90; 120		3985.41Reay, Alan J.; Hammarback, L. Anders; Bray, Joshua T. W.; Sheridan, Thomas; Turnbull, David; Whitwood, Adrian C.; Fairlamb, Ian J. S.
Mild and Regioselective Pd(OAc)2-Catalyzed C‒H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
ACS Catalysis, 2017, 5174
4514162 CIFC23 H26 N2 O3P 1 21 18.7152; 13.5902; 8.7625
90; 100.507; 90		1020.44Reay, Alan J.; Hammarback, L. Anders; Bray, Joshua T. W.; Sheridan, Thomas; Turnbull, David; Whitwood, Adrian C.; Fairlamb, Ian J. S.
Mild and Regioselective Pd(OAc)2-Catalyzed C‒H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
ACS Catalysis, 2017, 5174
4514163 CIFC20 H19 Cl N2 O3R 320.7806; 20.7806; 11.18107
90; 90; 120		4181.48Reay, Alan J.; Hammarback, L. Anders; Bray, Joshua T. W.; Sheridan, Thomas; Turnbull, David; Whitwood, Adrian C.; Fairlamb, Ian J. S.
Mild and Regioselective Pd(OAc)2-Catalyzed C‒H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
ACS Catalysis, 2017, 5174
4514164 CIFC55 H44 Cl2 N2 O4C 1 2 122.1203; 7.6123; 16.3803
90; 127.077; 90		2200.58He, Congfa; Hou, Mengqing; Zhu, Zixi; Gu, Zhenhua
Enantioselective Synthesis of Indole-Based Biaryl Atropisomers via Palladium-Catalyzed Dynamic Kinetic Intramolecular C‒H Cyclization
ACS Catalysis, 2017, 7, 5316
4514165 CIFC29 H31 B O2P 21 21 216.2288; 12.593; 30.216
90; 90; 90		2370.1Mateos, Jaime; Rivera-Chao, Eva; Fañanás-Mastral, Martín
Synergistic Copper/Palladium Catalysis for the Regio- and Stereoselective Synthesis of Borylated Skipped Dienes
ACS Catalysis, 2017, 5340
4514166 CIFC9 H14 O4P -4 21 c12.8527; 12.8527; 10.7921
90; 90; 90		1782.77Laserna, Victor; Martin, Eddy; Escudero-Adán, Eduardo C.; Kleij, Arjan W.
Substrate-Triggered Stereoselective Preparation of Highly Substituted Organic Carbonates
ACS Catalysis, 2017, 7, 5478
4514167 CIFC7 H10 O4P 1 21/n 16.5169; 11.8049; 9.5214
90; 105.261; 90		706.66Laserna, Victor; Martin, Eddy; Escudero-Adán, Eduardo C.; Kleij, Arjan W.
Substrate-Triggered Stereoselective Preparation of Highly Substituted Organic Carbonates
ACS Catalysis, 2017, 7, 5478
4514168 CIFC7 H10 O4P 1 21/n 18.3814; 7.0296; 12.3499
90; 96.2862; 90		723.26Laserna, Victor; Martin, Eddy; Escudero-Adán, Eduardo C.; Kleij, Arjan W.
Substrate-Triggered Stereoselective Preparation of Highly Substituted Organic Carbonates
ACS Catalysis, 2017, 7, 5478
4514169 CIFC42 H29 Cl F6 N2 O3P 21 21 218.9232; 17.371; 23.537
90; 90; 90		3648.4Yang, Wenjun; Sun, Wei; Zhang, Cheng; Wang, Qijun; Guo, Zhenyan; Mao, Biming; Liao, Jianning; Guo, Hongchao
Lewis-Base-Catalyzed Asymmetric [3 + 3] Annulation Reaction of Morita‒Baylis‒Hillman Carbonates: Enantioselective Synthesis of Spirocyclohexenes
ACS Catalysis, 2017, 7, 3142
4514170 CIFC34 H30 Cl Co N4 O4P b c a17.0978; 15.1411; 22.9374
90; 90; 90		5938Somekh, Miriam; Cohen, Hagai; Diskin-Posner, Yael; Shimon, Linda J. W.; Carmieli, Raanan; Rosenberg, Jeffrey N.; Neumann, Ronny
Formation of Alkanes by Aerobic Carbon‒Carbon Bond Coupling Reactions Catalyzed by a Phosphovanadomolybdic Acid
ACS Catalysis, 2017, 2725
4514172 CIFC22 H24 O4P 21 21 218.4622; 9.685; 22.9564
90; 90; 90		1881.4Chong, Qinglei; Yue, Zhenting; Zhang, Shuoqing; Ji, Chonglei; Cheng, Fengchang; Zhang, Haiyan; Hong, Xin; Meng, Fanke
N-heterocyclic Carbene‒Cu-Catalyzed Enantioselective Conjugate Additions with Alkenylboronic Esters as Nucleophiles
ACS Catalysis, 2017, 5693
4514173 CIFC55.5 H71 O10.5 Rh2P 1 21/n 116.2948; 17.0253; 20.361
90; 103.07; 90		5502.3Chen, Po-An; Setthakarn, Krit; May, Jeremy A.
A Binaphthyl-Based Scaffold for a Chiral Dirhodium(II) Biscarboxylate Ligand with α-Quaternary Carbon Centers
ACS Catalysis, 2017, 7, 6155
4514183 CIFC46 H96 O2 Sc2 Si6P 1 21/n 118.2889; 18.1841; 18.6875
90; 111.842; 90		5768.7Chen, Jiazhen; Gao, Yanshan; Xiong, Shuoyan; Delferro, Massimiliano; Lohr, Tracy L.; Marks, Tobin J.
Metal and Counteranion Nuclearity Effects in Organoscandium-Catalyzed Isoprene Polymerization and Copolymerization
ACS Catalysis, 2017, 7, 5214
4514184 CIFC19 H12 Au Cl0.25 F6 N O4P 1 2/n 129.449; 4.6494; 29.503
90; 103.649; 90		3925.5Holmsen, Marte Sofie Martinsen; Nova, Ainara; Balcells, David; Langseth, Eirin; Øien-Ødegaard, Sigurd; Heyn, Richard H.; Tilset, Mats; Laurenczy, Gábor
trans-Mutation at Gold(III): A Mechanistic Study of a Catalytic Acetylene Functionalization via a Double Insertion Pathway
ACS Catalysis, 2017, 7, 5023

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