Crystallography Open Database

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4512489 CIFC20 H16 Br Fe N5C 1 2/c 116.847; 13.0275; 16.3223
90; 96.25; 90		3561Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Regulation of Iron-Catalyzed Olefin Hydroboration by Ligand Modifications at a Remote Site
ACS Catalysis, 2015, 5, 411
4512490 CIFC25 H24 F3 Fe N5 O4 SP 18.4756; 8.8071; 18.6806
99.732; 90.796; 112.598		1264.06Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Regulation of Iron-Catalyzed Olefin Hydroboration by Ligand Modifications at a Remote Site
ACS Catalysis, 2015, 5, 411
4512491 CIFC23 H19 F6 Fe N5 O6 S2P -110.7036; 12.1278; 12.2733
66.351; 73.133; 69.747		1347.8Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Regulation of Iron-Catalyzed Olefin Hydroboration by Ligand Modifications at a Remote Site
ACS Catalysis, 2015, 5, 411
4512510 CIFC40 H36 Cl2 F3 N3 O7 P Re SP 1 21/n 112.089; 9.0476; 36.982
90; 91.534; 90		4043.5Liu, Jinyong; Choe, Jong Kwon; Wang, Yin; Shapley, John R.; Werth, Charles J.; Strathmann, Timothy J.
Bioinspired Complex-Nanoparticle Hybrid Catalyst System for Aqueous Perchlorate Reduction: Rhenium Speciation and Its Influence on Catalyst Activity
ACS Catalysis, 2015, 5, 511
4512511 CIFC55 H46 F3 N2 O7 P2 Re SP 21 21 2111.209; 11.6194; 37.5809
90; 90; 90		4894.6Liu, Jinyong; Choe, Jong Kwon; Wang, Yin; Shapley, John R.; Werth, Charles J.; Strathmann, Timothy J.
Bioinspired Complex-Nanoparticle Hybrid Catalyst System for Aqueous Perchlorate Reduction: Rhenium Speciation and Its Influence on Catalyst Activity
ACS Catalysis, 2015, 5, 511
4512512 CIFC37 H56 Co N3 SiP 1 21/n 117.8016; 12.0498; 18.7953
90; 117.63; 90		3571.93Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512513 CIFC31 H45 Co N2C 1 2/c 116.1764; 9.2233; 18.8751
90; 92.623; 90		2813.2Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512514 CIFC38 H57 Co N2C 1 2/c 138.978; 10.046; 18.259
90; 104.3; 90		6928Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512515 CIFC19 H22 Co N3 SiP 1 21/n 111.086; 19.096; 16.774
90; 94.52; 90		3540Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512516 CIFC14 H21 Cl Co N2 SiR -3 :H31.103; 31.103; 9.4729
90; 90; 120		7936.3Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512529 CIFC45 H40 F4 N3 O P RuP 21 21 2113.869; 16.834; 16.985
90; 90; 90		3965.5McKay, David; Riddlestone, Ian M.; Macgregor, Stuart A.; Mahon, Mary F.; Whittlesey, Michael K.
Mechanistic Study of Ru-NHC-Catalyzed Hydrodefluorination of Fluoropyridines: The Influence of the NHC on the Regioselectivity of C‒F Activation and Chemoselectivity of C‒F versus C‒H Bond Cleavage
ACS Catalysis, 2015, 5, 776
4512584 CIFC12 H20 Cl N3 NiP c a 2116.1973; 9.2551; 18.251
90; 90; 90		2736Pérez García, Pablo M.; Ren, Peng; Scopelliti, Rosario; Hu, Xile
Nickel-Catalyzed Direct Alkylation of Terminal Alkynes at Room Temperature: A Hemilabile Pincer Ligand Enhances Catalytic Activity
ACS Catalysis, 2015, 5, 1164
4512585 CIFC20 H25 N3 NiP 1 21/n 19.7694; 14.6639; 12.8939
90; 100.806; 90		1814.4Pérez García, Pablo M.; Ren, Peng; Scopelliti, Rosario; Hu, Xile
Nickel-Catalyzed Direct Alkylation of Terminal Alkynes at Room Temperature: A Hemilabile Pincer Ligand Enhances Catalytic Activity
ACS Catalysis, 2015, 5, 1164
4512586 CIFC144 H154 B2 Fe3 O13 P8P -114.7034; 15.3502; 30.5317
81.607; 77.192; 79.041		6558.1Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512587 CIFC42 H44 Fe P4P -111.3961; 11.8042; 14.9611
88.014; 81.462; 63.904		1786.33Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512588 CIFC49 H58 B F4 Fe N P4P -111.6311; 12.2422; 18.0737
104.224; 98.681; 106.392		2325.12Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512589 CIFC66 H63 B Fe P4P -112.4918; 13.5351; 19.2058
92.091; 105.612; 94.273		3113.4Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512590 CIFC103 H117 B4 F16 Fe2 N7 P8C 1 2/c 133.6116; 14.8734; 20.7957
90; 105.833; 90		10001.7Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512815 CIFC58 H58 B2 F8 N2 Ni P4P 1 21/n 19.2602; 20.7179; 14.2353
90; 97.2; 90		2709.5Brown, Houston J. S.; Wiese, Stefan; Roberts, John A. S.; Bullock, R. Morris; Helm, Monte L.
Electrocatalytic Hydrogen Production by [Ni(7PPh2NH)2]2+: Removing the Distinction Between Endo- and Exo-Protonation Sites
ACS Catalysis, 2015, 5, 2116
4512816 CIFC38 H44 B2 Cl4 F14 N2 Ni O4 P4P -110.3197; 13.2465; 19.7249
94.91; 101.046; 109.554		2460.92Brown, Houston J. S.; Wiese, Stefan; Roberts, John A. S.; Bullock, R. Morris; Helm, Monte L.
Electrocatalytic Hydrogen Production by [Ni(7PPh2NH)2]2+: Removing the Distinction Between Endo- and Exo-Protonation Sites
ACS Catalysis, 2015, 5, 2116
4512822 CIFC31 H32 B2 N2 O2P -19.5673; 12.0514; 12.4802
85.896; 77.575; 73.572		1347.8Guo, Xi; Nelson, Amanda K.; Slebodnick, Carla; Santos, Webster L.
Regio- and Chemoselective Diboration of Allenes with Unsymmetrical Diboron: Formation of Vinyl and Allyl Boronic Acid Derivatives
ACS Catalysis, 2015, 2172
4512852 CIFC58 H81 F12 Fe2 N9 O18 S4P 21 21 2116.9742; 17.1155; 50.282
90; 90; 90		14608Lyakin, Oleg Y.; Zima, Alexandra M.; Samsonenko, Denis G.; Bryliakov, Konstantin P.; Talsi, Evgenii P.
EPR Spectroscopic Detection of the Elusive FeV═O Intermediates in Selective Catalytic Oxofunctionalizations of Hydrocarbons Mediated by Biomimetic Ferric Complexes
ACS Catalysis, 2015, 5, 2702
4512854 CIFC31 H27 F3 N2 O4 SP -19.4555; 12.671; 13.141
89.372; 83.024; 70.301		1470.6Ghorai, Debasish; Choudhury, Joyanta
Rhodium(III)‒N-Heterocyclic Carbene-Driven Cascade C‒H Activation Catalysis
ACS Catalysis, 2015, 5, 2692
4512855 CIFC45 H31 F3 N2 O3 SP -110.6172; 12.7911; 14.6372
102.793; 106.868; 96.17		1823.39Ghorai, Debasish; Choudhury, Joyanta
Rhodium(III)‒N-Heterocyclic Carbene-Driven Cascade C‒H Activation Catalysis
ACS Catalysis, 2015, 5, 2692
4512856 CIFC12 H10 N2 Ni S2P 1 21/c 112.301; 5.883; 8.098
90; 95.547; 90		583.3Das, Amit; Han, Zhiji; Brennessel, William W.; Holland, Patrick L.; Eisenberg, Richard
Nickel Complexes for Robust Light-Driven and Electrocatalytic Hydrogen Production from Water
ACS Catalysis, 2015, 5, 1397
4512857 CIFC20 H36 N2 Ni O4 S6P -18.3237; 11.0567; 15.928
92.197; 99.883; 94.145		1438.4Das, Amit; Han, Zhiji; Brennessel, William W.; Holland, Patrick L.; Eisenberg, Richard
Nickel Complexes for Robust Light-Driven and Electrocatalytic Hydrogen Production from Water
ACS Catalysis, 2015, 5, 1397
4512930 CIFC10 H17 N O3P 21 21 219.8502; 13.6853; 16.4912
90; 90; 90		2223.1Bae, Han Yong; Song, Choong Eui
Unprecedented Hydrophobic Amplification in Noncovalent Organocatalysis “on Water”: Hydrophobic Chiral Squaramide Catalyzed Michael Addition of Malonates to Nitroalkenes
ACS Catalysis, 2015, 5, 3613
4512945 CIFC36 H52 Br Co N2 O2P 110.795; 12.6416; 14.6957
65.979; 89.9734; 71.994		1723.83North, Michael; Quek, Sophie C. Z.; Pridmore, Natalie E.; Whitwood, Adrian C.; Wu, Xiao
Aluminum(salen) Complexes as Catalysts for the Kinetic Resolution of Terminal Epoxides via CO2Coupling
ACS Catalysis, 2015, 5, 3398
4512946 CIFC16 H12 F3 N O2P -18.167; 8.306; 10.825
91.64; 99.308; 92.741		723.3Albaladejo, María José; Alonso, Francisco; González-Soria, María José
Synthetic and Mechanistic Studies on the Solvent-Dependent Copper-Catalyzed Formation of Indolizines and Chalcones
ACS Catalysis, 2015, 5, 3446
4512947 CIFBi4 Na20.72 O213.36 W36 Zn8P 1 21/n 113.234; 17.661; 20.966
90; 93.12; 90		4893Amanchi, Srinivasa Rao; Khenkin, Alexander M.; Diskin-Posner, Yael; Neumann, Ronny
Bismuth-Substituted “Sandwich” Type Polyoxometalate Catalyst for Activation of Peroxide: Umpolung of the Peroxo Intermediate and Change of Chemoselectivity
ACS Catalysis, 2015, 5, 3336
4512948 CIFBi2 Na4 O98.55 W18 Zn6P n n m16.187; 19.43; 14.641
90; 90; 90		4604.8Amanchi, Srinivasa Rao; Khenkin, Alexander M.; Diskin-Posner, Yael; Neumann, Ronny
Bismuth-Substituted “Sandwich” Type Polyoxometalate Catalyst for Activation of Peroxide: Umpolung of the Peroxo Intermediate and Change of Chemoselectivity
ACS Catalysis, 2015, 5, 3336
4513027 CIFC23 H24 Br N OP 21 21 217.2425; 15.4541; 17.01
90; 90; 90		1903.9Hu, Haoxiang; Meng, Chunna; Dong, Yun; Li, Xin; Ye, Jinxing
Catalytic Asymmetric Formal Aza-Diels‒Alder Reactions of α,β-Unsaturated Ketones and 3H-Indoles
ACS Catalysis, 2015, 5, 3700
4513028 CIFC15 H B Br3 F18 N6 TlP -19.4814; 10.765; 13.9827
111.406; 92.343; 99.301		1303.49Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C‒H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513029 CIFC17 H4 B Br3 Cu F18 N7C 1 2/c 121.9569; 16.6067; 17.0174
90; 105.863; 90		5968.8Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C‒H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513030 CIFC19 H9 Ag B Br3 F18 N6 OP -19.5396; 12.6988; 12.9452
100.867; 94.371; 98.592		1514Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C‒H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513043 CIFC24 H20 N4 O5 Ru SP -18.7507; 10.3497; 14.1618
79.212; 73.228; 77.234		1187.17Wang, Ying; Duan, Lele; Wang, Lei; Chen, Hong; Sun, Junliang; Sun, Licheng; Ahlquist, Mårten S. G.
Alkene Epoxidation Catalysts [Ru(pdc)(tpy)] and [Ru(pdc)(pybox)] Revisited: Revealing a Unique RuIV═O Structure from a Dimethyl Sulfoxide Coordinating Complex
ACS Catalysis, 2015, 5, 3966
4513044 CIFC45 H57 Cl F N2 O3 P RuP -19.25; 10.543; 21.668
84.919; 89.766; 81.66		2082.5Guidone, Stefano; Songis, Olivier; Falivene, Laura; Nahra, Fady; Slawin, Alexandra M. Z.; Jacobsen, Heiko; Cavallo, Luigi; Cazin, Catherine S. J.
Ruthenium Olefin Metathesis Catalysts Containing Fluoride
ACS Catalysis, 2015, 5, 3932
4513045 CIFC45 H57 F2 N2 O3 P RuP -19.123; 10.569; 21.751
94.901; 90.209; 99.166		2062.6Guidone, Stefano; Songis, Olivier; Falivene, Laura; Nahra, Fady; Slawin, Alexandra M. Z.; Jacobsen, Heiko; Cavallo, Luigi; Cazin, Catherine S. J.
Ruthenium Olefin Metathesis Catalysts Containing Fluoride
ACS Catalysis, 2015, 5, 3932
4513186 CIFC49 H47 Cl F6 N2 P2 RuP -111.185; 12.2337; 15.712
87.763; 85.343; 75.988		2078.7Xie, Xiaoke; Huynh, Han Vinh
Tunable Dehydrogenative Amidation versus Amination Using a Single Ruthenium-NHC Catalyst
ACS Catalysis, 2015, 5, 4143
4513187 CIFC45 H47 Cl F6 N2 P2 RuC 1 c 118.524; 15.304; 14.862
90; 98.269; 90		4169.4Xie, Xiaoke; Huynh, Han Vinh
Tunable Dehydrogenative Amidation versus Amination Using a Single Ruthenium-NHC Catalyst
ACS Catalysis, 2015, 5, 4143
4513215 CIFC32 H28 B Fe PP 21 21 217.8373; 11.1807; 28.7574
90; 90; 90		2519.91Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513216 CIFC20 H25 NP 1 21 18.4925; 18.0565; 21.7726
90; 92.034; 90		3336.61Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513217 CIFC18 H21 NP -17.6079; 9.9255; 10.7036
113.746; 100.964; 95.416		713.05Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513218 CIFC25 H29 Fe N OP 21 21 2110.843; 12.6988; 15.1797
90; 90; 90		2090.14Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513219 CIFC43 H38 N O3.5 P Pd SP 41 21 214.5165; 14.5165; 37.1387
90; 90; 90		7826.2Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513383 CIFC72 H78 N4 O11 Ti2P 43 21 212.3687; 12.3687; 44.436
90; 90; 90		6798Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513384 CIFC76 H78 N4 O11 Ti2P 31 2 119.0457; 19.0457; 41.0671
90; 90; 120		12900.9Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513385 CIFC65 H61 Cl3 N4 O6 Ti2P 1 21 111.5315; 19.176; 13.4627
90; 98.481; 90		2944.4Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513386 CIFC68 H66 Br4 N4 O7 Ti2P 43 21 212.2324; 12.2324; 45.9762
90; 90; 90		6879.5Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513387 CIFC64 H56 Br4 N4 O6 Ti2P 113.8302; 15.4438; 16.7517
108.353; 90.647; 116.089		3002.56Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513439 CIFC54 H47 N4 O7P 21 21 2112.3766; 16.424; 28.578
90; 90; 90		5809.1Alcaide, Benito; Almendros, Pedro; Fernández, Israel; Martín-Montero, Raúl; Martínez-Peña, Francisco; Ruiz, M. Pilar; Torres, M. Rosario
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
ACS Catalysis, 2015, 5, 4842
4513440 CIFC22 H22 N2 O3P 1 21 110.202; 7.487; 11.933
90; 100.922; 90		895Alcaide, Benito; Almendros, Pedro; Fernández, Israel; Martín-Montero, Raúl; Martínez-Peña, Francisco; Ruiz, M. Pilar; Torres, M. Rosario
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
ACS Catalysis, 2015, 5, 4842
4513441 CIFC22 H16 F3 N O3 SC 1 2/c 140.887; 9.2404; 27.6197
90; 131.709; 90		7790.1Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)‒H and C(sp2)‒H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513442 CIFC21 H16 B F4 NP 21 21 216.1068; 15.2343; 18.4646
90; 90; 90		1717.81Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)‒H and C(sp2)‒H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513443 CIFC21 H16 F6 N SbC 1 2/c 113.0833; 9.1095; 33.015
90; 91.371; 90		3933.7Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)‒H and C(sp2)‒H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513454 CIFC15 H13 Br N2P 4115.9607; 15.9607; 5.4313
90; 90; 90		1383.59Zhang, De-Yang; Shao, Long; Xu, Jie; Hu, Xiang-Ping
Copper-Catalyzed Asymmetric Formal [3 + 2] Cycloaddition of Propargylic Acetates with Hydrazines: Enantioselective Synthesis of Optically Active 2-Pyrazolines
ACS Catalysis, 2015, 5, 5026
4513487 CIFC38 H46 Au N3 O2P 1 21/n 19.1636; 36.3601; 21.4472
90; 97.684; 90		7081.8Hase, Shun; Kayaki, Yoshihito; Ikariya, Takao
Mechanistic Aspects of the Carboxylative Cyclization of Propargylamines and Carbon Dioxide Catalyzed by Gold(I) Complexes Bearing anN-Heterocyclic Carbene Ligand
ACS Catalysis, 2015, 5, 5135
4513497 CIFC39 H14 Cl6 Cu F10 N5 O2P -110.2256; 13.2327; 15.2136
75.791; 82.911; 77.348		1941.9Lei, Haitao; Fang, Huayi; Han, Yongzhen; Lai, Wenzhen; Fu, Xuefeng; Cao, Rui
Reactivity and Mechanism Studies of Hydrogen Evolution Catalyzed by Copper Corroles
ACS Catalysis, 2015, 5, 5145
4513498 CIFC39 H12 Cl4 Cu F15 N4P 1 21/c 113.6323; 13.187; 21.0645
90; 105.96; 90		3640.78Lei, Haitao; Fang, Huayi; Han, Yongzhen; Lai, Wenzhen; Fu, Xuefeng; Cao, Rui
Reactivity and Mechanism Studies of Hydrogen Evolution Catalyzed by Copper Corroles
ACS Catalysis, 2015, 5, 5145
4513610 CIFC20 H20 Cl N O4P 21 21 218.1602; 11.357; 20.59
90; 90; 90		1908.2Bai, Xing-Feng; Xu, Zheng; Xia, Chun-Gu; Zheng, Zhan-Jiang; Xu, Li-Wen
Aromatic-Amide-Derived Nonbiaryl Atropisomer as Highly Efficient Ligand for Asymmetric Silver-Catalyzed [3 + 2] Cycloaddition
ACS Catalysis, 2015, 5, 6016
4513611 CIFC25 H23 N O3P 1 21 16.0364; 17.033; 10.4225
90; 102.271; 90		1047.1Bai, Xing-Feng; Xu, Zheng; Xia, Chun-Gu; Zheng, Zhan-Jiang; Xu, Li-Wen
Aromatic-Amide-Derived Nonbiaryl Atropisomer as Highly Efficient Ligand for Asymmetric Silver-Catalyzed [3 + 2] Cycloaddition
ACS Catalysis, 2015, 5, 6016
4513656 CIFC29 H27 N O6 SC 1 2 127.301; 8.7461; 10.8469
90; 96.239; 90		2574.7Hao, Xiaoyu; Lin, Lili; Tan, Fei; Yin, Chengkai; Liu, Xiaohua; Feng, Xiaoming
Ligand Control of Diastereodivergency in Asymmetric Inverse Electron Demand Diels‒Alder Reaction
ACS Catalysis, 2015, 5, 6052
4513657 CIFC29 H27 N O6 SP 21 21 2112.1813; 12.9222; 16.9425
90; 90; 90		2666.9Hao, Xiaoyu; Lin, Lili; Tan, Fei; Yin, Chengkai; Liu, Xiaohua; Feng, Xiaoming
Ligand Control of Diastereodivergency in Asymmetric Inverse Electron Demand Diels‒Alder Reaction
ACS Catalysis, 2015, 5, 6052
4513663 CIFC32 H42 Ag N2C 1 2/c 116.043; 6.7774; 27.121
90; 94.443; 90		2940Liu, Qilun; Yuan, Zheliang; Wang, Hao-yang; Li, Yang; Wu, Yichen; Xu, Tao; Leng, Xuebing; Chen, Pinhong; Guo, Yin-long; Lin, Zhenyang; Liu, Guosheng
Abnormal Mesoionic Carbene Silver Complex: Synthesis, Reactivity, and Mechanistic Insight on Oxidative Fluorination
ACS Catalysis, 2015, 5, 6732
4513664 CIFC32 H40 Ag F2 N3 O3C 1 2/c 130.342; 14.1754; 27.882
90; 98.13; 90		11872Liu, Qilun; Yuan, Zheliang; Wang, Hao-yang; Li, Yang; Wu, Yichen; Xu, Tao; Leng, Xuebing; Chen, Pinhong; Guo, Yin-long; Lin, Zhenyang; Liu, Guosheng
Abnormal Mesoionic Carbene Silver Complex: Synthesis, Reactivity, and Mechanistic Insight on Oxidative Fluorination
ACS Catalysis, 2015, 5, 6732
4513677 CIFC25 H28 Cr N O4 PP 21 21 2110.0194; 14.8755; 33.308
90; 90; 90		4964.3Radcliffe, James E.; Batsanov, Andrei S.; Smith, David M.; Scott, John A.; Dyer, Philip W.; Hanton, Martin J.
Phosphanyl Methanimine (PCN) Ligands for the Selective Trimerization/Tetramerization of Ethylene with Chromium
ACS Catalysis, 2015, 5, 7095
4513678 CIFC29 H36 Cr N O4 PP 1 21/n 111.79138; 14.69577; 16.3394
90; 94.4771; 90		2822.71Radcliffe, James E.; Batsanov, Andrei S.; Smith, David M.; Scott, John A.; Dyer, Philip W.; Hanton, Martin J.
Phosphanyl Methanimine (PCN) Ligands for the Selective Trimerization/Tetramerization of Ethylene with Chromium
ACS Catalysis, 2015, 5, 7095
4513679 CIFC32 H38 Cl3 N P2 Pd SP b c a11.77; 16.605; 35.069
90; 90; 90		6854Sui, Xuelin; Dai, Shengyu; Chen, Changle
Ethylene Polymerization and Copolymerization with Polar Monomers by Cationic Phosphine Phosphonic Amide Palladium Complexes
ACS Catalysis, 2015, 5, 5932
4513680 CIFC31 H36 Cl N O P2 PdC 1 c 112.1032; 15.8942; 16.1513
90; 106.192; 90		2983.8Sui, Xuelin; Dai, Shengyu; Chen, Changle
Ethylene Polymerization and Copolymerization with Polar Monomers by Cationic Phosphine Phosphonic Amide Palladium Complexes
ACS Catalysis, 2015, 5, 5932
4513735 CIFC29 H32 N2 O2P 1 21/n 18.6895; 9.8563; 30.266
90; 94.399; 90		2584.5Kuai, Changsheng; Wang, Lianhui; Cui, Haoyi; Shen, Jinhai; Feng, Yadong; Cui, Xiuling
Efficient and Selective Synthesis of (E)-Enamides via Ru(II)-Catalyzed Hydroamidation of Internal Alkynes
ACS Catalysis, 2016, 6, 186
4513736 CIFC23 H20 N2 OP 1 21/n 112.864; 9.812; 13.652
90; 92.938; 90		1720.9Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513737 CIFC18 H11 F5 N2 O2P 1 21/c 111.342; 6.528; 21.294
90; 95.503; 90		1569.4Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513738 CIFC21 H21 N3P -17.784; 10.507; 11.117
106.154; 96.466; 97.82		854.3Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513739 CIFC25 H19 F N2 O2P 1 21/n 112.243; 7.246; 21.867
90; 105.022; 90		1873.6Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513740 CIFC18 H15 Br N2 O2P 1 21/n 110.221; 6.258; 24.249
90; 97.531; 90		1537.7Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513741 CIFC25.57 H21.14 Cl1.13 N2 O2P 1 21 112.2626; 7.2788; 12.3394
90; 104.51; 90		1066.25Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513742 CIFC20 H18 N2 O2P 1 c 15.238; 12.589; 11.597
90; 91.334; 90		764.5Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513743 CIFC18 H14 Br N3P 1 21/c 18.6369; 26.751; 6.9978
90; 106.79; 90		1547.89Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513744 CIFC19 H18 N2 O2P 1 21/c 19.882; 36.918; 8.62
90; 99.99; 90		3097.1Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513745 CIFC26 H22 N2 O3P 1 21/n 112.352; 7.361; 22.122
90; 98.421; 90		1989.7Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513746 CIFC20 H18 N2 O2P 1 21 111.035; 6.9; 11.373
90; 115.012; 90		784.75Nicholls, Thomas P.; Constable, Grace E.; Robertson, Johnathon C.; Gardiner, Michael G.; Bissember, Alex C.
Brønsted Acid Cocatalysis in Copper(I)-Photocatalyzed α-Amino C‒H Bond Functionalization
ACS Catalysis, 2016, 6, 451
4513747 CIFC22 H13 F5 N4 O2P 1 21 17.91984; 7.77745; 16.8551
90; 101.445; 90		1017.57Xu, Yali; Liao, Yuting; Lin, Lili; Zhou, Yuhang; Li, Jun; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Inverse-Electron Demand 1,3-Dipolar Cycloaddition of Isoquinolinium Methylides with Enecarbamates by a ChiralN,N′-Dioxide/Ag(I) Complex
ACS Catalysis, 2016, 6, 589
4513748 CIFC23.73 H18.45 Cl0.7 N O3.12 SP 21 21 29.7227; 23.8357; 8.7364
90; 90; 90		2024.6Izquierdo, Javier; Pericàs, Miquel A.
A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow
ACS Catalysis, 2016, 6, 348
4513749 CIFC30 H25 N O3 SP 1 21 15.9234; 17.5385; 11.7578
90; 95.5438; 90		1215.78Izquierdo, Javier; Pericàs, Miquel A.
A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow
ACS Catalysis, 2016, 6, 348
4513750 CIFC19 H16 N2 O SP 21 21 219.8811; 10.2565; 15.4749
90; 90; 90		1568.31Izquierdo, Javier; Pericàs, Miquel A.
A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow
ACS Catalysis, 2016, 6, 348
4513751 CIFC22 H19 F N2 OP b c a13.5231; 13.1489; 19.3467
90; 90; 90		3440.1Hiramatsu, Kenichi; Honjo, Takashi; Rauniyar, Vivek; Toste, F. Dean
Enantioselective Synthesis of Fluoro-Dihydroquinazolones and -Benzooxazinones by Fluorination-Initiated Asymmetric Cyclization Reactions.
ACS catalysis, 2015, 6, 151-154
4513752 CIFC12 H15 F N2 OP 1 21 17.6084; 6.4312; 11.7689
90; 103.627; 90		559.66Hiramatsu, Kenichi; Honjo, Takashi; Rauniyar, Vivek; Toste, F. Dean
Enantioselective Synthesis of Fluoro-Dihydroquinazolones and -Benzooxazinones by Fluorination-Initiated Asymmetric Cyclization Reactions.
ACS catalysis, 2015, 6, 151-154
4513753 CIFC13 H4 F5 N SP 1 21/c 114.407; 7.3079; 11.1275
90; 109.808; 90		1102.24Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513754 CIFC12 H6 F4P 1 21/c 112.8062; 5.84755; 12.6869
90; 105.223; 90		916.72Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513755 CIFC13 H5 F7P 21 21 215.92801; 7.5738; 23.6364
90; 90; 90		1061.22Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513756 CIFC12 H5 F5C 2 2 215.80768; 20.9642; 7.68611
90; 90; 90		935.81Meyer, Andreas U.; Slanina, Tomáš; Yao, Chang-Jiang; König, Burkhard
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
ACS Catalysis, 2016, 6, 369
4513757 CIFC37 H40 Br N O3P 21 21 2110.038; 15.921; 20.131
90; 90; 90		3217.2He, Fu-Sheng; Jin, Jing-Hai; Yang, Zhong-Tao; Yu, Xingxin; Fossey, John S.; Deng, Wei-Ping
Direct Asymmetric Synthesis of β-Bis-Aryl-α-Amino Acid Esters via Enantioselective Copper-Catalyzed Addition ofp-Quinone Methides
ACS Catalysis, 2016, 6, 652
4513758 CIFC22 H20 F3 N OP b c a19.0615; 9.325; 20.7194
90; 90; 90		3682.8Yu, Liu-Zhu; Xu, Qin; Tang, Xiang-Yiang; Shi, Min
Iron- or Copper-Catalyzed Trifluoromethylation of Acrylamide-Tethered Alkylidenecyclopropanes: Facile Synthesis of CF3-Containing Polycyclic Benzazepine Derivatives
ACS Catalysis, 2016, 6, 526
4513759 CIFC36 H44 Er N O Si2P 1 21/c 116.5508; 9.9149; 20.9543
90; 100.391; 90		3382.2Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513760 CIFC36 H44 Gd N O Si2P 1 21/c 116.5847; 9.9933; 21.0068
90; 100.271; 90		3425.8Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513761 CIFC36 H44 N Nd O Si2P 1 21/c 116.5572; 10.0221; 21.0296
90; 100.37; 90		3432.6Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513762 CIFC31 H44 N O Pr Si2P 1 21/c 114.6913; 11.3369; 19.4321
90; 95.729; 90		3220.3Lin, Fei; Wang, Xingbao; Pan, Yupeng; Wang, Meiyan; Liu, Bo; Luo, Yi; Cui, Dongmei
Nature of the Entire Range of Rare Earth Metal-Based Cationic Catalysts for Highly Active and Syndioselective Styrene Polymerization
ACS Catalysis, 2016, 6, 176
4513763 CIFC19 H24 Cl F6 N3 P RhP -17.8557; 11.6834; 13.6223
103.37; 94.785; 101.888		1178.97Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513764 CIFC20 H26 Cl F6 N3 O P RhP c a 2115.666; 7.2906; 21.328
90; 90; 90		2436Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
4513765 CIFC25 H29 Cl F6 N4 P RhC 1 2/c 130.566; 8.1625; 22.272
90; 98.215; 90		5499.7Ghorai, Debasish; Dutta, Champak; Choudhury, Joyanta
Switching of “Rollover Pathway” in Rhodium(III)-Catalyzed C‒H Activation of Chelating Molecules
ACS Catalysis, 2015, 709
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

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