Crystallography Open Database

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4501447 CIFC39 H42 Cl4 N2 O2 TiP 1 21/c 116.8818; 10.7967; 20.6102
90; 99.5901; 90		3704.08Terao, Hiroshi; Iwashita, Akihiko; Matsukawa, Naoto; Ishii, Seiichi; Mitani, Makoto; Tanaka, Hidetsugu; Nakano, Takashi; Fujita, Terunori
Ethylene and Ethylene/α-Olefin (Co)Polymerization Behavior of Bis(phenoxy−imine)Ti Catalysts: Significant Substituent Effects on Activity and Comonomer Incorporation
ACS Catalysis, 2011, 1, 254
4501448 CIFC47 H59 Cl2 N2 O2 TiP 1 21/a 115.976; 25.591; 10.943
90; 102.3; 90		4371Terao, Hiroshi; Iwashita, Akihiko; Matsukawa, Naoto; Ishii, Seiichi; Mitani, Makoto; Tanaka, Hidetsugu; Nakano, Takashi; Fujita, Terunori
Ethylene and Ethylene/α-Olefin (Co)Polymerization Behavior of Bis(phenoxy−imine)Ti Catalysts: Significant Substituent Effects on Activity and Comonomer Incorporation
ACS Catalysis, 2011, 1, 254
4501449 CIFC20 H19 Br N4 O5P 1 21 17.8416; 13.964; 9.5724
90; 106.198; 90		1006.6Hua, Qiu-Lin; Li, Chao; Wang, Xu-Fan; Lu, Liang-Qiu; Chen, Jia-Rong; Xiao, Wen-Jing
Enantioselective Synthesis of Chromans with a Quaternary Stereogenic Centre through Catalytic Asymmetric Cascade Reactions
ACS Catalysis, 2011, 1, 221
4501450 CIFC22 H32 B N3 O3 ZnP 1 21/c 110.8363; 13.4156; 16.1656
90; 96.788; 90		2333.61Mukherjee, Debabrata; Thompson, Richard R.; Ellern, Arkady; Sadow, Aaron D.
Coordinatively Saturated Tris(oxazolinyl)borato Zinc Hydride-Catalyzed Cross Dehydrocoupling of Silanes and Alcohols
ACS Catalysis, 2011, 1, 698
4501451 CIFC31 H42 B N3 O4.5 ZnP 1 21/c 121.569; 9.896; 15.813
90; 106.292; 90		3240Mukherjee, Debabrata; Thompson, Richard R.; Ellern, Arkady; Sadow, Aaron D.
Coordinatively Saturated Tris(oxazolinyl)borato Zinc Hydride-Catalyzed Cross Dehydrocoupling of Silanes and Alcohols
ACS Catalysis, 2011, 1, 698
4501452 CIFC17 H20 O2 SiP -17.821; 8.589; 13.088
84.193; 86.915; 63.19		780.6Mukherjee, Debabrata; Thompson, Richard R.; Ellern, Arkady; Sadow, Aaron D.
Coordinatively Saturated Tris(oxazolinyl)borato Zinc Hydride-Catalyzed Cross Dehydrocoupling of Silanes and Alcohols
ACS Catalysis, 2011, 1, 698
4501453 CIFC13 H20 O2 SiP 1 21/c 17.7423; 12.8158; 13.6032
90; 97.565; 90		1338.01Mukherjee, Debabrata; Thompson, Richard R.; Ellern, Arkady; Sadow, Aaron D.
Coordinatively Saturated Tris(oxazolinyl)borato Zinc Hydride-Catalyzed Cross Dehydrocoupling of Silanes and Alcohols
ACS Catalysis, 2011, 1, 698
4501454 CIFC53.33 H52 Co F6 N4 O6.67 S2.67 SbP -115.694; 16.579; 17.451
87.054; 88.06; 62.315		4015.2Venkatasubbaiah, Krishnan; Zhu, Xunjin; Kays, Elizabeth; Hardcastle, Kenneth I.; Jones, Christopher W.
Co(III)-Porphyrin-Mediated Highly Regioselective Ring-Opening of Terminal Epoxides with Alcohols and Phenols
ACS Catalysis, 2011, 489
4501455 CIFC41 H55 Hf N5 SP 1 21/c 117.633; 10.0494; 22.504
90; 97.714; 90		3951.6Diamond, Gary M.; Hall, Keith A.; LaPointe, Anne M.; Leclerc, Margarete K.; Longmire, James; Shoemaker, James A. W.; Sun, Pu
High-Throughput Discovery and Optimization of Hafnium Heteroaryl-amido Catalysts for the Isospecific Polymerization of Propylene
ACS Catalysis, 2011, 1, 887
4501456 CIFC38 H46 Hf N2 SP -111.2458; 13.4734; 13.5863
67.489; 81.795; 88.766		1881Diamond, Gary M.; Hall, Keith A.; LaPointe, Anne M.; Leclerc, Margarete K.; Longmire, James; Shoemaker, James A. W.; Sun, Pu
High-Throughput Discovery and Optimization of Hafnium Heteroaryl-amido Catalysts for the Isospecific Polymerization of Propylene
ACS Catalysis, 2011, 1, 887
4501457 CIFC35 H46 Hf N4 O SP 1 21/c 114.4153; 14.2346; 16.653
90; 98.959; 90		3375.4Diamond, Gary M.; Hall, Keith A.; LaPointe, Anne M.; Leclerc, Margarete K.; Longmire, James; Shoemaker, James A. W.; Sun, Pu
High-Throughput Discovery and Optimization of Hafnium Heteroaryl-amido Catalysts for the Isospecific Polymerization of Propylene
ACS Catalysis, 2011, 1, 887
4501458 CIFC48 H72 Hf N6 OP 1 21/n 121.626; 19.173; 25.68
90; 108.965; 90		10070Diamond, Gary M.; Hall, Keith A.; LaPointe, Anne M.; Leclerc, Margarete K.; Longmire, James; Shoemaker, James A. W.; Sun, Pu
High-Throughput Discovery and Optimization of Hafnium Heteroaryl-amido Catalysts for the Isospecific Polymerization of Propylene
ACS Catalysis, 2011, 1, 887
4501459 CIFC33 H49 Cl N O P RuP -18.972; 9.6985; 18.4616
100.458; 94.892; 90.021		1573.79Schachner, Jörg A.; Cabrera, José; Padilla, Robin; Fischer, Christoph; van der Schaaf, Paul A.; Pretot, Roger; Rominger, Frank; Limbach, Michael
A Set of Olefin Metathesis Catalysts with Extraordinary Stickiness to Silica
ACS Catalysis, 2011, 1, 872
4501460 CIFC43 H50 Cl N3 O RuP 1 21/c 116.7458; 16.9502; 14.9589
90; 109.887; 90		3992.8Schachner, Jörg A.; Cabrera, José; Padilla, Robin; Fischer, Christoph; van der Schaaf, Paul A.; Pretot, Roger; Rominger, Frank; Limbach, Michael
A Set of Olefin Metathesis Catalysts with Extraordinary Stickiness to Silica
ACS Catalysis, 2011, 1, 872
4501461 CIFC18 H36 F5 N4 O4 ZnP -17.944; 8.854; 16.032
79.805; 81.63; 80.763		1087.4Maegawa, Yusuke; Ohshima, Takashi; Hayashi, Yukiko; Agura, Kazushi; Iwasaki, Takanori; Mashima, Kazushi
Additive Effect ofN-Heteroaromatics on Transesterification Catalyzed by Tetranuclear Zinc Cluster
ACS Catalysis, 2011, 1, 1178
4501462 CIFC42 H78 N2 O8 Pd Si2P 1 21/n 113.76; 24.958; 14.913
90; 101.799; 90		5013Choi, Yeon S.; Moschetta, Eric G.; Miller, Jeffrey T.; Fasulo, Meg; McMurdo, Meredith J.; Rioux, Robert M.; Tilley, T. Don
Highly Dispersed Pd-SBA15 Materials from Tris(tert-butoxy)siloxy Complexes of Pd(II)
ACS Catalysis, 2011, 1, 1166
4501463 CIFC31 H54 N2 O4 Pd SiC 1 2/c 133.989; 9.3744; 28.483
90; 121.11; 90		7770.2Choi, Yeon S.; Moschetta, Eric G.; Miller, Jeffrey T.; Fasulo, Meg; McMurdo, Meredith J.; Rioux, Robert M.; Tilley, T. Don
Highly Dispersed Pd-SBA15 Materials from Tris(tert-butoxy)siloxy Complexes of Pd(II)
ACS Catalysis, 2011, 1, 1166
4501464 CIFC16 H30 F6 Fe N4 O6 S2F d d 28.8289; 32.679; 16.3726
90; 90; 90		4723.8Feng, Yan; England, Jason; Que, Lawrence
Iron-Catalyzed Olefin Epoxidation and cis-Dihydroxylation by Tetraalkylcyclam Complexes: the Importance of cis-Labile Sites
ACS Catalysis, 2011, 1, 1035
4501465 CIFC20 H23 Cl4 N3 Ni O2P -17.7306; 10.879; 13.935
87.26; 78.61; 82.14		1137.8Zhang, Liping; Hao, Xiang; Sun, Wen-Hua; Redshaw, Carl
Synthesis, Characterization, and Ethylene Polymerization Behavior of 8-(Nitroarylamino)-5,6,7-trihydroquinolylnickel Dichlorides: Influence of the Nitro Group and Impurities on Catalytic Activity
ACS Catalysis, 2011, 1, 1213
4501466 CIFC21 H25 Cl2 N3 Ni O2P 1 21/n 19.1206; 28.489; 9.4194
90; 116.45; 90		2191.3Zhang, Liping; Hao, Xiang; Sun, Wen-Hua; Redshaw, Carl
Synthesis, Characterization, and Ethylene Polymerization Behavior of 8-(Nitroarylamino)-5,6,7-trihydroquinolylnickel Dichlorides: Influence of the Nitro Group and Impurities on Catalytic Activity
ACS Catalysis, 2011, 1, 1213
4501467 CIFC21 H25 Cl2 N3 Ni O2P -18.4918; 11.126; 14.794
107.41; 103.11; 96.34		1274.8Zhang, Liping; Hao, Xiang; Sun, Wen-Hua; Redshaw, Carl
Synthesis, Characterization, and Ethylene Polymerization Behavior of 8-(Nitroarylamino)-5,6,7-trihydroquinolylnickel Dichlorides: Influence of the Nitro Group and Impurities on Catalytic Activity
ACS Catalysis, 2011, 1, 1213
4501468 CIFC20 H23 Cl3 N3 Ni0.5 O2P -19.1269; 10.212; 12.557
112.06; 96.8; 98.4		1053.7Zhang, Liping; Hao, Xiang; Sun, Wen-Hua; Redshaw, Carl
Synthesis, Characterization, and Ethylene Polymerization Behavior of 8-(Nitroarylamino)-5,6,7-trihydroquinolylnickel Dichlorides: Influence of the Nitro Group and Impurities on Catalytic Activity
ACS Catalysis, 2011, 1, 1213
4505631 CIFC48 H56 Br4 N4 Ni2P 1 21/n 114.0495; 9.9391; 17.681
90; 110.777; 90		2308.4Zai, Shaobo; Gao, Haiyang; Huang, Zengfang; Hu, Haibin; Wu, Han; Wu, Qing
Substituent Effects of Pyridine-amine Nickel Catalyst Precursors on Ethylene Polymerization
ACS Catalysis, 2012, 2, 433
4505632 CIFC27 H35 Br2 Cl4 N2 Ni OP 1 21/c 118.146; 12.048; 18.386
90; 119.14; 90		3510.9Zai, Shaobo; Gao, Haiyang; Huang, Zengfang; Hu, Haibin; Wu, Han; Wu, Qing
Substituent Effects of Pyridine-amine Nickel Catalyst Precursors on Ethylene Polymerization
ACS Catalysis, 2012, 2, 433
4505633 CIFC38 H52 Br2 N4 NiP 1 21/c 111.7518; 10.9119; 18.5929
90; 128.486; 90		1866.3Zai, Shaobo; Gao, Haiyang; Huang, Zengfang; Hu, Haibin; Wu, Han; Wu, Qing
Substituent Effects of Pyridine-amine Nickel Catalyst Precursors on Ethylene Polymerization
ACS Catalysis, 2012, 2, 433
4505634 CIFC18 H20 I N O5 SP 1 21/n 19.806; 12.76; 15.657
90; 102.62; 90		1911.7Guilbault, Audrey-Anne; Legault, Claude Y.
Drastic Enhancement of Activity in Iodane-Based α-Tosyloxylation of Ketones: Iodine(III) Does the Hypervalent Twist
ACS Catalysis, 2012, 2, 219
4505635 CIFC19 H22 I N O5 SP 1 21/c 17.172; 7.921; 33.699
90; 93.67; 90		1910.5Guilbault, Audrey-Anne; Legault, Claude Y.
Drastic Enhancement of Activity in Iodane-Based α-Tosyloxylation of Ketones: Iodine(III) Does the Hypervalent Twist
ACS Catalysis, 2012, 2, 219
4506119 CIFC50 H58 Cl4 O6 P2 Pd2 S2C 1 2/c 120.009; 13.184; 19.278
90; 95.989; 90		5058Cai, Zhengguo; Shen, Zhongliang; Zhou, Xiaoyuan; Jordan, Richard F.
Enhancement of Chain Growth and Chain Transfer Rates in Ethylene Polymerization by (Phosphine-sulfonate)PdMe Catalysts by Binding of B(C6F5)3to the Sulfonate Group
ACS Catalysis, 2012, 2, 1187
4506120 CIFC72 H102 O6 P2 Pd2 S2P 1 21/c 117.934; 10.371; 25.392
90; 131.536; 90		3535.2Cai, Zhengguo; Shen, Zhongliang; Zhou, Xiaoyuan; Jordan, Richard F.
Enhancement of Chain Growth and Chain Transfer Rates in Ethylene Polymerization by (Phosphine-sulfonate)PdMe Catalysts by Binding of B(C6F5)3to the Sulfonate Group
ACS Catalysis, 2012, 2, 1187
4506121 CIFC58 H61 B F15 O4 P Pd SC 1 2/c 136.529; 13.21; 24.939
90; 100.456; 90		11834Cai, Zhengguo; Shen, Zhongliang; Zhou, Xiaoyuan; Jordan, Richard F.
Enhancement of Chain Growth and Chain Transfer Rates in Ethylene Polymerization by (Phosphine-sulfonate)PdMe Catalysts by Binding of B(C6F5)3to the Sulfonate Group
ACS Catalysis, 2012, 2, 1187
4506122 CIFC56 H48 Cl12 N4 O18 Rh2I 2 337.1893; 37.1893; 37.1893
90; 90; 90		51434.4Lindsay, Vincent N. G.; Charette, André B.
Design and Synthesis of Chiral Heteroleptic Rhodium(II) Carboxylate Catalysts: Experimental Investigation of Halogen Bond Rigidification Effects in Asymmetric Cyclopropanation
ACS Catalysis, 2012, 2, 1221
4506582 CIFC21 H27 N O3 SiP 1 21 111.7148; 6.9828; 13.444
90; 114.935; 90		997.24Min, Taewoo; Fettinger, James C.; Franz, Annaliese K.
Enantiocontrol with a Hydrogen-bond Directing Pyrrolidinylsilanol Catalyst
ACS Catalysis, 2012, 2, 1661
4506583 CIFC23 H32 F3 N O4 S SiP 21 21 218.52; 8.5557; 33.4637
90; 90; 90		2439.32Min, Taewoo; Fettinger, James C.; Franz, Annaliese K.
Enantiocontrol with a Hydrogen-bond Directing Pyrrolidinylsilanol Catalyst
ACS Catalysis, 2012, 2, 1661
4506584 CIFC27 H39 N O3 SiP 21 21 2112.6433; 13.8501; 14.684
90; 90; 90		2571.33Min, Taewoo; Fettinger, James C.; Franz, Annaliese K.
Enantiocontrol with a Hydrogen-bond Directing Pyrrolidinylsilanol Catalyst
ACS Catalysis, 2012, 2, 1661
4506585 CIFC16 H20 Cl N O SiP 21 21 217.5343; 8.5707; 25.2748
90; 90; 90		1632.1Min, Taewoo; Fettinger, James C.; Franz, Annaliese K.
Enantiocontrol with a Hydrogen-bond Directing Pyrrolidinylsilanol Catalyst
ACS Catalysis, 2012, 2, 1661
4506586 CIFC11 H8 Br N3 O3P 1 21 19.4259; 5.1093; 12.799
90; 110.279; 90		578.19Li, Wenjun; Liu, Hui; Jiang, Xuefeng; Wang, Jian
Enantioselective Organocatalytic Conjugate Addition of Nitroalkanes to Electrophilic 2-Iminochromenes
ACS Catalysis, 2012, 2, 1535
4506587 CIFC62 H70 Fe2 N16 O2C 1 2/c 131.222; 17.025; 23.69
90; 101.133; 90		12356Yu, Renyuan Pony; Darmon, Jonathan M.; Hoyt, Jordan M.; Margulieux, Grant W.; Turner, Zoë R.; Chirik, Paul J.
High-Activity Iron Catalysts for the Hydrogenation of Hindered, Unfunctionalized Alkenes
ACS Catalysis, 2012, 2, 1760
4506588 CIFC29 H29 Fe N9P 1 21/c 115.7139; 10.318; 17.0218
90; 98.758; 90		2727.7Yu, Renyuan Pony; Darmon, Jonathan M.; Hoyt, Jordan M.; Margulieux, Grant W.; Turner, Zoë R.; Chirik, Paul J.
High-Activity Iron Catalysts for the Hydrogenation of Hindered, Unfunctionalized Alkenes
ACS Catalysis, 2012, 2, 1760
4507135 CIFC39 H21 Ag3 F18 N6P -19.7393; 13.5428; 16.9533
94.039; 104.186; 109.322		2017.54Flores, Jaime A.; Komine, Nobuyuki; Pal, Kuntal; Pinter, Balazs; Pink, Maren; Chen, Chun-Hsing; Caulton, Kenneth G.; Mindiola, Daniel J.
Silver(I)-Catalyzed Insertion of Carbene into Alkane C‒H Bonds and the Origin of the Special Challenge of Methane Activation Using DFT as a Mechanistic Probe
ACS Catalysis, 2012, 2, 2066
4507136 CIFC31 H31 Cl3 Cr N4 PP b c a11.2332; 16.7375; 33.095
90; 90; 90		6222.4Sydora, Orson L.; Jones, Thomas C.; Small, Brooke L.; Nett, Alex J.; Fischer, Anne A.; Carney, Michael J.
Selective Ethylene Tri-/Tetramerization Catalysts
ACS Catalysis, 2012, 2, 2452
4507137 CIFC23 H26 Cl3 Cr N3 PP n a 2111.5487; 14.419; 15.38
90; 90; 90		2561.1Sydora, Orson L.; Jones, Thomas C.; Small, Brooke L.; Nett, Alex J.; Fischer, Anne A.; Carney, Michael J.
Selective Ethylene Tri-/Tetramerization Catalysts
ACS Catalysis, 2012, 2, 2452
4507138 CIFC33 H40 Cl3 F3 N2 O3 Ru SP -110.788; 12.131; 16.206
89.72; 71.49; 64.83		1799.1Schreiber, Dominique F.; O’Connor, Crystal; Grave, Christian; Ortin, Yannick; Müller-Bunz, Helge; Phillips, Andrew D.
Application of β-Diketiminato Arene-Substituted Ru(II) Complexes in Highly Efficient H2Dehydrocoupling of Amine Boranes
ACS Catalysis, 2012, 2, 2505
4507139 CIFC35 H44 Cl3 F3 N2 O3 Ru SP 1 21/c 113.3963; 12.4531; 23.0725
90; 106.164; 90		3696.92Schreiber, Dominique F.; O’Connor, Crystal; Grave, Christian; Ortin, Yannick; Müller-Bunz, Helge; Phillips, Andrew D.
Application of β-Diketiminato Arene-Substituted Ru(II) Complexes in Highly Efficient H2Dehydrocoupling of Amine Boranes
ACS Catalysis, 2012, 2, 2505
4507140 CIFC29.91 H29 Cl0.09 F2.73 N2 O2.73 Ru S0.91P -113.411; 14.9649; 18.0317
98.982; 96.074; 108.632		3340Schreiber, Dominique F.; O’Connor, Crystal; Grave, Christian; Ortin, Yannick; Müller-Bunz, Helge; Phillips, Andrew D.
Application of β-Diketiminato Arene-Substituted Ru(II) Complexes in Highly Efficient H2Dehydrocoupling of Amine Boranes
ACS Catalysis, 2012, 2, 2505
4507141 CIFC28 H34 N2 RuP 1 21 17.7447; 12.5622; 12.1814
90; 94.917; 90		1180.77Schreiber, Dominique F.; O’Connor, Crystal; Grave, Christian; Ortin, Yannick; Müller-Bunz, Helge; Phillips, Andrew D.
Application of β-Diketiminato Arene-Substituted Ru(II) Complexes in Highly Efficient H2Dehydrocoupling of Amine Boranes
ACS Catalysis, 2012, 2, 2505
4507142 CIFC51 H48 B F25 N P2 RhP 1 21/c 117.2281; 17.5318; 18.888
90; 104.533; 90		5522.39Pernik, Indrek; Hooper, Joel F.; Chaplin, Adrian B.; Weller, Andrew S.; Willis, Michael C.
Exploring Small Bite-Angle Ligands for the Rhodium-Catalyzed Intermolecular Hydroacylation of β-S-Substituted Aldehydes with 1-Octene and 1-Octyne
ACS Catalysis, 2012, 2, 2779
4507143 CIFC53 H51 B F24 N O P2 Rh SP -112.2384; 15.4948; 17.5543
103.603; 109.864; 98.834		2942.02Pernik, Indrek; Hooper, Joel F.; Chaplin, Adrian B.; Weller, Andrew S.; Willis, Michael C.
Exploring Small Bite-Angle Ligands for the Rhodium-Catalyzed Intermolecular Hydroacylation of β-S-Substituted Aldehydes with 1-Octene and 1-Octyne
ACS Catalysis, 2012, 2, 2779
4507144 CIFC57 H52 B F26 P2 RhP 4313.1403; 13.1403; 34.4622
90; 90; 90		5950.5Pernik, Indrek; Hooper, Joel F.; Chaplin, Adrian B.; Weller, Andrew S.; Willis, Michael C.
Exploring Small Bite-Angle Ligands for the Rhodium-Catalyzed Intermolecular Hydroacylation of β-S-Substituted Aldehydes with 1-Octene and 1-Octyne
ACS Catalysis, 2012, 2, 2779
4507145 CIFC52 H49 B F25 P2 RhP 1 21/c 117.7994; 17.3901; 19.0524
90; 109.328; 90		5564.97Pernik, Indrek; Hooper, Joel F.; Chaplin, Adrian B.; Weller, Andrew S.; Willis, Michael C.
Exploring Small Bite-Angle Ligands for the Rhodium-Catalyzed Intermolecular Hydroacylation of β-S-Substituted Aldehydes with 1-Octene and 1-Octyne
ACS Catalysis, 2012, 2, 2779
4507146 CIFC59 H56 B F26 P2 RhP -112.6572; 13.247; 19.6804
104.275; 106.494; 91.3854		3050.53Pernik, Indrek; Hooper, Joel F.; Chaplin, Adrian B.; Weller, Andrew S.; Willis, Michael C.
Exploring Small Bite-Angle Ligands for the Rhodium-Catalyzed Intermolecular Hydroacylation of β-S-Substituted Aldehydes with 1-Octene and 1-Octyne
ACS Catalysis, 2012, 2, 2779
4507147 CIFC63 H64 B F25 N P2 RhP 1 21/c 113.8162; 18.0951; 26.4511
90; 92.0377; 90		6608.74Pernik, Indrek; Hooper, Joel F.; Chaplin, Adrian B.; Weller, Andrew S.; Willis, Michael C.
Exploring Small Bite-Angle Ligands for the Rhodium-Catalyzed Intermolecular Hydroacylation of β-S-Substituted Aldehydes with 1-Octene and 1-Octyne
ACS Catalysis, 2012, 2, 2779
4507148 CIFC39 H51 Cu N2 OP 1 21/n 112.747; 14.427; 19.799
90; 96.74; 90		3615.9Pouy, Mark J.; Delp, Samuel A.; Uddin, Jamal; Ramdeen, Vijay M.; Cochrane, Nikki A.; Fortman, George C.; Gunnoe, T. Brent; Cundari, Thomas R.; Sabat, Michal; Myers, William H.
Intramolecular Hydroalkoxylation and Hydroamination of Alkynes Catalyzed by Cu(I) Complexes Supported byN-Heterocyclic Carbene Ligands
ACS Catalysis, 2012, 2, 2182
4507149 CIFC19 H18 Co O4 PP n a 2114.5719; 17.2445; 7.3877
90; 90; 90		1856.4Birbeck, James M.; Haynes, Anthony; Adams, Harry; Damoense, Llewellyn; Otto, Stefanus
Ligand Effects on Reactivity of Cobalt Acyl Complexes
ACS Catalysis, 2012, 2, 2512
4507150 CIFC16 H25 Co O3 PP -19.0646; 9.2649; 11.4599
94.012; 108.645; 109.326		843.74Birbeck, James M.; Haynes, Anthony; Adams, Harry; Damoense, Llewellyn; Otto, Stefanus
Ligand Effects on Reactivity of Cobalt Acyl Complexes
ACS Catalysis, 2012, 2, 2512
4507151 CIFC32 H50 Co2 O6 P2P 1 21/n 112.6461; 9.7325; 14.7834
90; 110.949; 90		1699.24Birbeck, James M.; Haynes, Anthony; Adams, Harry; Damoense, Llewellyn; Otto, Stefanus
Ligand Effects on Reactivity of Cobalt Acyl Complexes
ACS Catalysis, 2012, 2, 2512
4507431 CIFC192 H144 Cu4 N28 O12A b a 226.531; 29.2825; 21.2848
90; 90; 90		16536He, Qi-Ting; Li, Xiang-Ping; Chen, Lian-Fen; Zhang, Li; Wang, Wei; Su, Cheng-Yong
Nanosized Coordination Cages Incorporating Multiple Cu(I) Reactive Sites: Host‒Guest Modulated Catalytic Activity
ACS Catalysis, 2013, 3, 1
4507432 CIFC100 H80 Cu4 N20 O22P -113.373; 13.767; 14.926
104.973; 103.729; 109.545		2338.2He, Qi-Ting; Li, Xiang-Ping; Chen, Lian-Fen; Zhang, Li; Wang, Wei; Su, Cheng-Yong
Nanosized Coordination Cages Incorporating Multiple Cu(I) Reactive Sites: Host‒Guest Modulated Catalytic Activity
ACS Catalysis, 2013, 3, 1
4507433 CIFC46 H50 Cl2 F5 N3 O3 RuP 1 21/n 124.2414; 12.5158; 30.0577
90; 106.816; 90		8729.6Nelson, David J.; Queval, Pierre; Rouen, Mathieu; Magrez, Magaly; Toupet, Loïc; Caijo, Frédéric; Borré, Etienne; Laurent, Isabelle; Crévisy, Christophe; Baslé, Olivier; Mauduit, Marc; Percy, Jonathan M.
Synergic Effects Between N-Heterocyclic Carbene and Chelating Benzylidene‒Ether Ligands Toward the Initiation Step of Hoveyda‒Grubbs Type Ru Complexes
ACS Catalysis, 2013, 3, 259-264
4507438 CIFC14 H8 Br Fe2 N O6 S2P -17.6922; 10.824; 11.227
74.383; 86.307; 80.513		887.7Dey, Subal; Rana, Atanu; Dey, Somdatta Ghosh; Dey, Abhishek
Electrochemical Hydrogen Production in Acidic Water by an Azadithiolate Bridged Synthetic Hydrogenese Mimic: Role of Aqueous Solvation in Lowering Overpotential
ACS Catalysis, 2013, 3, 429
4507767 CIFC20 H18 N2 O3P 1 21/n 110.5224; 8.7192; 20.0164
90; 102.322; 90		1794.1Zhang, Xiao-Nan; Shi, Min
Phosphine-Catalyzed [3 + 2] Cycloaddition of 4,4-Dicyano-2-methylenebut-3-enoates with Benzyl Buta-2,3-dienoate and Penta-3,4-dien-2-one
ACS Catalysis, 2013, 3, 507
4507768 CIFC11 H13 F3 N2 O7P 21 21 216.0338; 7.3229; 32.512
90; 90; 90		1436.5Wen, Lele; Yin, Liang; Shen, Qilong; Lu, Long
Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to β-Trifluoromethylated Acrylamides
ACS Catalysis, 2013, 3, 502
4507769 CIFC10 H11 F3 O4P 1 21 15.2612; 8.0356; 26.8522
90; 90.009; 90		1135.23Wen, Lele; Yin, Liang; Shen, Qilong; Lu, Long
Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to β-Trifluoromethylated Acrylamides
ACS Catalysis, 2013, 3, 502
4507770 CIFC7 H10 F3 N O3P 43 21 27.0694; 7.0694; 35.24
90; 90; 90		1761.2Wen, Lele; Yin, Liang; Shen, Qilong; Lu, Long
Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to β-Trifluoromethylated Acrylamides
ACS Catalysis, 2013, 3, 502
4507771 CIFC8 H12 F3 N O3P 21 21 216.4729; 7.3947; 21.763
90; 90; 90		1041.7Wen, Lele; Yin, Liang; Shen, Qilong; Lu, Long
Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to β-Trifluoromethylated Acrylamides
ACS Catalysis, 2013, 3, 502
4507772 CIFC12 H12 F3 N O3 SP 15.1139; 6.3453; 11.289
82.575; 79.056; 68.124		333.07Wen, Lele; Yin, Liang; Shen, Qilong; Lu, Long
Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to β-Trifluoromethylated Acrylamides
ACS Catalysis, 2013, 3, 502
4507773 CIFC19 H19 Cl2 N O2 SP -17.077; 7.792; 17.241
83.163; 83.039; 75.993		911.7Cheng, Jiajia; Tang, Xinjun; Ma, Shengming
Highly Selective FeCl3-Catalyzed Cyclization of β-Sulfonamidoallenes or β-Allenols and Aldehydes
ACS Catalysis, 2013, 3, 663
4507774 CIFC16 H22 Cl N O2 SP b c a14.8823; 15.0709; 15.0819
90; 90; 90		3382.7Cheng, Jiajia; Tang, Xinjun; Ma, Shengming
Highly Selective FeCl3-Catalyzed Cyclization of β-Sulfonamidoallenes or β-Allenols and Aldehydes
ACS Catalysis, 2013, 3, 663
4507775 CIFC22 H18 Br N O4 SP 21 21 218.6638; 10.6945; 21.769
90; 90; 90		2017Jia, Min-Qiang; You, Shu-Li
N-Heterocyclic Carbene-Catalyzed Enantioselective Intramolecular N-Tethered Aldehyde‒Ketone Benzoin Reactions
ACS Catalysis, 2013, 3, 622
4507776 CIFC13 H15 N O2P -16.5346; 8.803; 10.4461
85.089; 75.857; 68.462		542Baronsky, Thilo; Beattie, Christopher; Harrington, Ross W.; Irfan, Reyhan; North, Michael; Osende, Javier G.; Young, Carl
Bimetallic Aluminum(salen) Catalyzed Synthesis of Oxazolidinones from Epoxides and Isocyanates
ACS Catalysis, 2013, 3, 790
4507881 CIFC60 H52 Cl2 F12 N10 O4 P2 Ru2C 1 2/c 119.5432; 27.2305; 23.3159
90; 99.748; 90		12228.9Aiki, Shota; Kijima, Yuhei; Kuwabara, Junpei; Taketoshi, Ayako; Koizumi, Take-aki; Akine, Shigehisa; Kanbara, Takaki
Ligand Modification of Cyclometalated Ruthenium Complexes in the Aerobic Oxidative Dehydrogenation of Imidazolines
ACS Catalysis, 2013, 3, 812
4507882 CIFC30 H27 Cl F6 N4 O2 P RuP 1 21/n 111.4748; 22.961; 11.4873
90; 95.161; 90		3014.3Aiki, Shota; Kijima, Yuhei; Kuwabara, Junpei; Taketoshi, Ayako; Koizumi, Take-aki; Akine, Shigehisa; Kanbara, Takaki
Ligand Modification of Cyclometalated Ruthenium Complexes in the Aerobic Oxidative Dehydrogenation of Imidazolines
ACS Catalysis, 2013, 3, 812
4507883 CIFC29 H34 Cl F9 N5 P RuP 1 21/n 18.6237; 30.965; 11.965
90; 109.38; 90		3014Aiki, Shota; Kijima, Yuhei; Kuwabara, Junpei; Taketoshi, Ayako; Koizumi, Take-aki; Akine, Shigehisa; Kanbara, Takaki
Ligand Modification of Cyclometalated Ruthenium Complexes in the Aerobic Oxidative Dehydrogenation of Imidazolines
ACS Catalysis, 2013, 3, 812
4508109 CIFC25 H20 Br N6 O4 ReP 1 21/n 111.6786; 19.4125; 11.7398
90; 104.932; 90		2571.7Andrade, Gabriel A.; Pistner, Allen J.; Yap, Glenn P. A.; Lutterman, Daniel A.; Rosenthal, Joel
Photocatalytic Conversion of CO2to CO Using Rhenium Bipyridine Platforms Containing Ancillary Phenyl or BODIPY Moieties
ACS Catalysis, 2013, 3, 1685
4508110 CIFC44 H72 O4 S2 VP 1 21/c 114.843; 16.907; 17.478
90; 93.767; 90		4376.6Toda, Tomoyuki; Nakata, Norio; Matsuo, Tsukasa; Ishii, Akihiko
Synthesis, Structure, and 1-Hexene Polymerization Catalytic Ability of Group 5 Metal Complexes Incorporating an [OSSO]-Type Ligand
ACS Catalysis, 2013, 3, 1764
4508111 CIFC56 H70 Cl3 Nb O2 S2P 1 21/c 117.747; 15.722; 19.957
90; 103.391; 90		5417Toda, Tomoyuki; Nakata, Norio; Matsuo, Tsukasa; Ishii, Akihiko
Synthesis, Structure, and 1-Hexene Polymerization Catalytic Ability of Group 5 Metal Complexes Incorporating an [OSSO]-Type Ligand
ACS Catalysis, 2013, 3, 1764
4508112 CIFC44 H64 Cl3 O2 S2 TaP 1 21 114.0634; 11.496; 14.0371
90; 101.661; 90		2222.6Toda, Tomoyuki; Nakata, Norio; Matsuo, Tsukasa; Ishii, Akihiko
Synthesis, Structure, and 1-Hexene Polymerization Catalytic Ability of Group 5 Metal Complexes Incorporating an [OSSO]-Type Ligand
ACS Catalysis, 2013, 3, 1764
4508355 CIFC44 H70 Cl5 Co N4 O2C 1 2/c 139.868; 11.8049; 19.788
90; 93.947; 90		9290.9Belokon, Yuri N.; Maleev, Victor I.; North, Michael; Larionov, Vladimir A.; Savel’yeva, Tat’yana F.; Nijland, Aike; Nelyubina, Yuliya V.
Chiral Octahedral Complexes of CoIIIAs a Family of Asymmetric Catalysts Operating under Phase Transfer Conditions
ACS Catalysis, 2013, 1951
4508356 CIFC25 H25 Cl1.25 Co1.25 N5 O2.5P 21 21 2134.074; 10.4676; 13.8502
90; 90; 90		4940Belokon, Yuri N.; Maleev, Victor I.; North, Michael; Larionov, Vladimir A.; Savel’yeva, Tat’yana F.; Nijland, Aike; Nelyubina, Yuliya V.
Chiral Octahedral Complexes of CoIIIAs a Family of Asymmetric Catalysts Operating under Phase Transfer Conditions
ACS Catalysis, 2013, 1951
4508362 CIFC18 H28 Cl2 F6 Ir N2 O2 PP 1 21/c 112.129; 11.4374; 17.545
90; 95.165; 90		2424Lehman, Matthew C.; Gary, J. Brannon; Boyle, Paul D.; Sanford, Melanie S.; Ison, Elon A.
Effect of Solvent and Ancillary Ligands on the Catalytic H/D Exchange Reactivity of Cp*IrIII(L) Complexes
ACS Catalysis, 2013, 3, 2304
4508363 CIFC32 H50 F6 Ir2 N4 O7 S2P -110.982; 13.584; 15.035
95.693; 108.315; 110.76		1934.2Lehman, Matthew C.; Gary, J. Brannon; Boyle, Paul D.; Sanford, Melanie S.; Ison, Elon A.
Effect of Solvent and Ancillary Ligands on the Catalytic H/D Exchange Reactivity of Cp*IrIII(L) Complexes
ACS Catalysis, 2013, 3, 2304
4508364 CIFC49 H45 Cl3 Mo N4 O2 P2 ZnP 1 21/c 120.0576; 14.3652; 17.229
90; 95.415; 90		4942.06Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz
Highly Efficient Large Bite Angle Diphosphine Substituted Molybdenum Catalyst for Hydrosilylation
ACS Catalysis, 2013, 3, 2208
4508365 CIFC153 H110 B2 F48 Mo2 N8 O4 P4P -112.4979; 15.4233; 19.774
88.382; 81.163; 87.527		3761.96Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz
Highly Efficient Large Bite Angle Diphosphine Substituted Molybdenum Catalyst for Hydrosilylation
ACS Catalysis, 2013, 3, 2208
4508366 CIFC151 H103 B2 Cl3 F48 Mo2 N4 O4 P4P -116.0776; 17.0716; 18.0135
105.257; 115.011; 98.938		4116.7Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz
Highly Efficient Large Bite Angle Diphosphine Substituted Molybdenum Catalyst for Hydrosilylation
ACS Catalysis, 2013, 3, 2208
4508367 CIFC45 H36 Cl Mo N O4 P2P 1 21/c 111.5883; 13.8586; 24.9475
90; 101.155; 90		3930.82Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz
Highly Efficient Large Bite Angle Diphosphine Substituted Molybdenum Catalyst for Hydrosilylation
ACS Catalysis, 2013, 3, 2208
4508368 CIFC82 H84 Cl2 Mo2 N2 O5 P6P 1 21/n 110.2639; 21.2569; 18.332
90; 105.192; 90		3859.88Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz
Highly Efficient Large Bite Angle Diphosphine Substituted Molybdenum Catalyst for Hydrosilylation
ACS Catalysis, 2013, 3, 2208
4508369 CIFC54 H43 Cl Mo N O2 P3P 1 21/n 119.3956; 12.6738; 20.4746
90; 114.639; 90		4574.74Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz
Highly Efficient Large Bite Angle Diphosphine Substituted Molybdenum Catalyst for Hydrosilylation
ACS Catalysis, 2013, 3, 2208
4508370 CIFC23 H39 Ir O3 P2P -18.288; 11.99; 13.424
100.742; 95.96; 103.708		1257.9Lao, David B.; Owens, Alisa C. E.; Heinekey, D. Michael; Goldberg, Karen I.
Partial Deoxygenation of Glycerol Catalyzed by Iridium Pincer Complexes
ACS Catalysis, 2013, 3, 2391
4508371 CIFC55 H52 B F24 Ir O3 P2C 1 2/c 116.707; 18.088; 39.933
90; 96.48; 90		11991Lao, David B.; Owens, Alisa C. E.; Heinekey, D. Michael; Goldberg, Karen I.
Partial Deoxygenation of Glycerol Catalyzed by Iridium Pincer Complexes
ACS Catalysis, 2013, 3, 2391
4508372 CIFC36 H47 N3 ZnP 1 21/n 112.4548; 12.8516; 20.4735
90; 93.992; 90		3269.12Boone, Courtney; Korobkov, Ilia; Nikonov, Georgii I.
Unexpected Role of Zinc Hydride in Catalytic Hydrosilylation of Ketones and Nitriles
ACS Catalysis, 2013, 3, 2336
4508373 CIFC24 H40 N2 O3 P RuC 1 2/c 132.0382; 11.1091; 16.1622
90; 118.402; 90		5060Huff, Chelsea A.; Sanford, Melanie S.
Catalytic CO2Hydrogenation to Formate by a Ruthenium Pincer Complex
ACS Catalysis, 2013, 3, 2412
4508374 CIFC34 H30 Cr O4 P2P b c a18.625; 20.786; 32.239
90; 90; 90		12481Zhang, Jun; Wang, Xiao; Zhang, Xuejun; Wu, Weijie; Zhang, Gengtao; Xu, Sheng; Shi, Min
Switchable Ethylene Tri-/Tetramerization with High Activity: Subtle Effect Presented by Backbone-Substituent of Carbon-Bridged Diphosphine Ligands
ACS Catalysis, 2013, 3, 2311
4508375 CIFC16 H27 Ir O5 SP b c a9.218; 16.424; 24.589
90; 90; 90		3722.7Frasco, Daniel A.; Lilly, Cassandra P.; Boyle, Paul D.; Ison, Elon A.
Cp*IrIII-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes
ACS Catalysis, 2013, 3, 2421
4508376 CIFC16 H21 F6 Ir O5 SP 21 21 219.08; 14.954; 15.588
90; 90; 90		2116.6Frasco, Daniel A.; Lilly, Cassandra P.; Boyle, Paul D.; Ison, Elon A.
Cp*IrIII-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes
ACS Catalysis, 2013, 3, 2421
4508377 CIFC19 H24 Ir N O5 SP 1 21/c 18.2462; 14.311; 16.825
90; 103.277; 90		1932.5Frasco, Daniel A.; Lilly, Cassandra P.; Boyle, Paul D.; Ison, Elon A.
Cp*IrIII-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes
ACS Catalysis, 2013, 3, 2421
4508378 CIFC19 H24 Cl Ir O3 SP 1 21/c 119.779; 8.4715; 30.216
90; 128.931; 90		3938.5Frasco, Daniel A.; Lilly, Cassandra P.; Boyle, Paul D.; Ison, Elon A.
Cp*IrIII-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes
ACS Catalysis, 2013, 3, 2421
4508379 CIFC44 H36 Cu4 F12 N8 O16 S4P 1 21/c 125.452; 13.8983; 15.856
90; 104.624; 90		5427.2Hoover, Jessica M.; Ryland, Bradford L.; Stahl, Shannon S.
Copper/TEMPO-Catalyzed Aerobic Alcohol Oxidation: Mechanistic Assessment of Different Catalyst Systems
ACS Catalysis, 2013, 3, 2599
4508380 CIFC32 H28 N2 O5P -19.231; 10.439; 15.222
92.356; 94.503; 113.508		1336.7Hao, Wen-Juan; Wang, Shun-Yi; Ji, Shun-Jun
Iodine-Catalyzed Cascade Formal [3 + 3] Cycloaddition Reaction of Indolyl Alcohol Derivatives with Enaminones: Constructions of Functionalized Spirodihydrocarbolines
ACS Catalysis, 2013, 3, 2501
4508381 CIFC31 H24 N3 O5.5C 1 2/c 115.715; 22.582; 16.682
90; 102.4; 90		5781.9Hao, Wen-Juan; Wang, Shun-Yi; Ji, Shun-Jun
Iodine-Catalyzed Cascade Formal [3 + 3] Cycloaddition Reaction of Indolyl Alcohol Derivatives with Enaminones: Constructions of Functionalized Spirodihydrocarbolines
ACS Catalysis, 2013, 3, 2501
4508603 CIFC15 H10 Cl N O2P 1 21/n 13.9967; 25.9143; 12.3646
90; 95.947; 90		1273.73Han, Runfeng; Qi, Jing; Gu, Jixiang; Ma, Donghui; Xie, Xingang; She, Xuegong
N-Heterocyclic Carbene-Catalyzed Formal [3+2] Annulation of Alkynyl Aldehydes with Nitrosobenzenes: A Highly Regioselective Umpolung Strategy
ACS Catalysis, 2013, 3, 2705
4508604 CIFC70 H102 N4 O2 Rh2P -111.021; 11.519; 14.052
68.604; 73.514; 74.287		1564.5Palacios, Laura; Artigas, Maria Jose; Polo, Victor; Lahoz, Fernando J.; Castarlenas, Ricardo; Pérez-Torrente, Jesús J.; Oro, Luis A.
Hydroxo‒Rhodium‒N-Heterocyclic Carbene Complexes as Efficient Catalyst Precursors for Alkyne Hydrothiolation
ACS Catalysis, 2013, 3, 2910
4508605 CIFC18 H21 N O2C 1 2 122.6541; 8.25169; 17.39574
90; 107.371; 90		3103.55Goubert, Guillaume; Demers-Carpentier, Vincent; Loach, Richard P.; Lafleur-Lambert, Raphaél; Lemay, Jean-Christian; Boukouvalas, John; McBreen, Peter H.
Aminolactone Chiral Modifiers for Heterogeneous Asymmetric Hydrogenation: Corrected Structure of Pantoyl-Naphthylethylamine, In-Situ Hydrogenolysis, and Scanning Tunneling Microscopy Observation of Supramolecular Aminolactone/Substrate Assemblies on Pt(111)
ACS Catalysis, 2013, 3, 2677
4508606 CIFC13 H21 Au Cl N3 O5 SC 1 2/c 128.7265; 8.8069; 14.8574
90; 95.337; 90		3742.5Tomás-Mendivil, Eder; Toullec, Patrick Y.; Borge, Javier; Conejero, Salvador; Michelet, Véronique; Cadierno, Victorio
Water-Soluble Gold(I) and Gold(III) Complexes with SulfonatedN-Heterocyclic Carbene Ligands: Synthesis, Characterization, and Application in the Catalytic Cycloisomerization of γ-Alkynoic Acids into Enol-Lactones
ACS Catalysis, 2013, 3, 3086
4508607 CIFC14 H21 Au Cl3 N3 O4 S2C 1 2/c 125.769; 11.48; 18.59
90; 107.214; 90		5253Tomás-Mendivil, Eder; Toullec, Patrick Y.; Borge, Javier; Conejero, Salvador; Michelet, Véronique; Cadierno, Victorio
Water-Soluble Gold(I) and Gold(III) Complexes with SulfonatedN-Heterocyclic Carbene Ligands: Synthesis, Characterization, and Application in the Catalytic Cycloisomerization of γ-Alkynoic Acids into Enol-Lactones
ACS Catalysis, 2013, 3, 3086
4508608 CIFC14.5 H20 Au Cl3 N3 O3.5 SP 1 2/c 124.0394; 8.8925; 21.0847
90; 116.022; 90		4050.36Tomás-Mendivil, Eder; Toullec, Patrick Y.; Borge, Javier; Conejero, Salvador; Michelet, Véronique; Cadierno, Victorio
Water-Soluble Gold(I) and Gold(III) Complexes with SulfonatedN-Heterocyclic Carbene Ligands: Synthesis, Characterization, and Application in the Catalytic Cycloisomerization of γ-Alkynoic Acids into Enol-Lactones
ACS Catalysis, 2013, 3, 3086
4508609 CIFC12 H14 Au Cl2 N3 O3 SP 1 21/n 19.717; 12.6841; 13.5632
90; 108.02; 90		1589.68Tomás-Mendivil, Eder; Toullec, Patrick Y.; Borge, Javier; Conejero, Salvador; Michelet, Véronique; Cadierno, Victorio
Water-Soluble Gold(I) and Gold(III) Complexes with SulfonatedN-Heterocyclic Carbene Ligands: Synthesis, Characterization, and Application in the Catalytic Cycloisomerization of γ-Alkynoic Acids into Enol-Lactones
ACS Catalysis, 2013, 3, 3086
4509833 CIFC22 H24 N2 O6P 659.8241; 9.8241; 37.0024
90; 90; 120		3092.76Barber, David M.; Duriš, Andrej; Thompson, Amber L.; Sanganee, Hitesh J.; Dixon, Darren J.
One-Pot Asymmetric Nitro-Mannich/Hydroamination Cascades for the Synthesis of Pyrrolidine Derivatives: Combining Organocatalysis and Gold Catalysis.
ACS catalysis, 2014, 4, 634-638
4509834 CIFC34 H30 Cl N O4 SP 1 21/c 113.489; 19.154; 12.366
90; 116.81; 90		2851.5Li, Erqing; Jia, Penghao; Liang, Ling; Huang, You
Phosphine-Catalyzed Sequential [2 +3] and [3 + 2] Annulation Domino Reaction of γ-Benzyl-Substituted Allenoates with α,β-Unsaturated Ketimines To Construct aza-Bicyclo[3,3,0]octane Derivatives
ACS Catalysis, 2014, 4, 600
4509835 CIFC15.5 H19 I Ir N O2P 1 21/c 19.0412; 31.3975; 12.3426
90; 96.356; 90		3482.2Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509836 CIFC14 H23 Cl Ir N O2P -19.1576; 11.2916; 16.2687
99.653; 91.159; 91.704		1657.2Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509837 CIFC42 H63 F9 Ir3 N3 O16 S3P 21 21 2112.8738; 16.382; 26.73
90; 90; 90		5637.3Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509838 CIFC15 H22 F3 Ir N2 O5 SC 1 2/c 126.456; 8.5874; 21.4517
90; 121.888; 90		4138.1Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509839 CIFC14 H26 Cl Ir N2 O2P -18.9727; 10.0097; 10.1814
75.441; 78.89; 68.698		819.37Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509840 CIFC10.5 H26 Cl2 Ir N3 O0.5P 1 21/c 110.3281; 13.3359; 24.1586
90; 94.1269; 90		3318.8Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509841 CIFC6 H13 N O2P 1 21/n 18.3622; 9.0389; 9.9889
90; 105.24; 90		728.5Wöckel, Simone; Plessow, Philipp; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Alcohol Amination with Aminoacidato Cp*Ir(III)-Complexes as Catalysts: Dissociation of the Chelating Ligand during Initiation
ACS Catalysis, 2014, 4, 152
4509842 CIFC42 H34 Cl6 O6 P2 RuP -19.915; 11.919; 20.194
97.563; 91.49; 112.378		2180Czaun, Miklos; Goeppert, Alain; Kothandaraman, Jotheeswari; May, Robert B.; Haiges, Ralf; Prakash, G. K. Surya; Olah, George A.
Formic Acid As a Hydrogen Storage Medium: Ruthenium-Catalyzed Generation of Hydrogen from Formic Acid in Emulsions
ACS Catalysis, 2014, 4, 311
4509843 CIFC76 H64 Na O30 P3 Ru6P -116.3958; 17.5531; 17.6055
101.46; 113.756; 107.585		4111.9Czaun, Miklos; Goeppert, Alain; Kothandaraman, Jotheeswari; May, Robert B.; Haiges, Ralf; Prakash, G. K. Surya; Olah, George A.
Formic Acid As a Hydrogen Storage Medium: Ruthenium-Catalyzed Generation of Hydrogen from Formic Acid in Emulsions
ACS Catalysis, 2014, 4, 311
4509844 CIFC42.2 H34 Cl0.3 O2.71 P2 RuP 1 21/c 117.7301; 12.3659; 18.3431
90; 102.999; 90		3918.6Czaun, Miklos; Goeppert, Alain; Kothandaraman, Jotheeswari; May, Robert B.; Haiges, Ralf; Prakash, G. K. Surya; Olah, George A.
Formic Acid As a Hydrogen Storage Medium: Ruthenium-Catalyzed Generation of Hydrogen from Formic Acid in Emulsions
ACS Catalysis, 2014, 4, 311
4509845 CIFC39 H32 O6 P2 RuP b c n19.0814; 10.8848; 15.6495
90; 90; 90		3250.4Czaun, Miklos; Goeppert, Alain; Kothandaraman, Jotheeswari; May, Robert B.; Haiges, Ralf; Prakash, G. K. Surya; Olah, George A.
Formic Acid As a Hydrogen Storage Medium: Ruthenium-Catalyzed Generation of Hydrogen from Formic Acid in Emulsions
ACS Catalysis, 2014, 4, 311
4509846 CIFC42 H32 O8 P2 Ru2P 1 21/n 113.2898; 19.8988; 14.5203
90; 94.197; 90		3829.6Czaun, Miklos; Goeppert, Alain; Kothandaraman, Jotheeswari; May, Robert B.; Haiges, Ralf; Prakash, G. K. Surya; Olah, George A.
Formic Acid As a Hydrogen Storage Medium: Ruthenium-Catalyzed Generation of Hydrogen from Formic Acid in Emulsions
ACS Catalysis, 2014, 4, 311
4509847 CIFC19 H22 Cl F N2 OP -19.508; 9.679; 10.314
82.54; 74.65; 73.17		874.7Gu, Zheng-Yang; Zhu, Tong-Hao; Cao, Jia-Jia; Xu, Xiao-Ping; Wang, Shun-Yi; Ji, Shun-Jun
Palladium-Catalyzed Cascade Reactions of Isocyanides with Enaminones: Synthesis of 4-Aminoquinoline Derivatives
ACS Catalysis, 2014, 4, 49
4510029 CIFC19 H44 B2 F8 Ir N4 O2 P3P 21 21 2112.4567; 14.2413; 18.0693
90; 90; 90		3205.5Campos, Jesús; Hintermair, Ulrich; Brewster, Timothy P.; Takase, Michael K.; Crabtree, Robert H.
Catalyst Activation by Loss of Cyclopentadienyl Ligands in Hydrogen Transfer Catalysis with Cp*IrIIIComplexes
ACS Catalysis, 2014, 4, 973
4510030 CIFC15 H21 B Cl F4 Ir N4P 1 21 18.4218; 10.3619; 10.7421
90; 102.256; 90		916.05Campos, Jesús; Hintermair, Ulrich; Brewster, Timothy P.; Takase, Michael K.; Crabtree, Robert H.
Catalyst Activation by Loss of Cyclopentadienyl Ligands in Hydrogen Transfer Catalysis with Cp*IrIIIComplexes
ACS Catalysis, 2014, 4, 973
4510031 CIFC36 H63 B Cl F4 Ir N4 OP 1 21/c 113.9451; 22.7483; 13.5566
90; 112.44; 90		3974.9Campos, Jesús; Hintermair, Ulrich; Brewster, Timothy P.; Takase, Michael K.; Crabtree, Robert H.
Catalyst Activation by Loss of Cyclopentadienyl Ligands in Hydrogen Transfer Catalysis with Cp*IrIIIComplexes
ACS Catalysis, 2014, 4, 973
4510032 CIFC27 H53 B2 F8 Ir N4 O3 P2P 21 21 2110.2065; 11.645; 30.295
90; 90; 90		3600.7Campos, Jesús; Hintermair, Ulrich; Brewster, Timothy P.; Takase, Michael K.; Crabtree, Robert H.
Catalyst Activation by Loss of Cyclopentadienyl Ligands in Hydrogen Transfer Catalysis with Cp*IrIIIComplexes
ACS Catalysis, 2014, 4, 973
4510033 CIFC24 H44 B2 F8 Ir N4 O PP 1 21/c 110.6139; 10.4084; 27.7107
90; 96.783; 90		3039.9Campos, Jesús; Hintermair, Ulrich; Brewster, Timothy P.; Takase, Michael K.; Crabtree, Robert H.
Catalyst Activation by Loss of Cyclopentadienyl Ligands in Hydrogen Transfer Catalysis with Cp*IrIIIComplexes
ACS Catalysis, 2014, 4, 973
4510034 CIFC20 H45 B2 F8 Ir N4 P4P 1 21/c 115.4119; 10.641; 20.2231
90; 102.973; 90		3231.9Campos, Jesús; Hintermair, Ulrich; Brewster, Timothy P.; Takase, Michael K.; Crabtree, Robert H.
Catalyst Activation by Loss of Cyclopentadienyl Ligands in Hydrogen Transfer Catalysis with Cp*IrIIIComplexes
ACS Catalysis, 2014, 4, 973
4510035 CIFC28 H36 N Ni O PP 1 21/c 110.6892; 27.0455; 9.0785
90; 108.475; 90		2489.28Stephenson, Casey J.; McInnis, Jennifer P.; Chen, Changle; Weberski, Michael P.; Motta, Alessandro; Delferro, Massimiliano; Marks, Tobin J.
Ni(II) Phenoxyiminato Olefin Polymerization Catalysis: Striking Coordinative Modulation of Hyperbranched Polymer Microstructure and Stability by a Proximate Sulfonyl Group
ACS Catalysis, 2014, 4, 999
4510036 CIFC53 H52 N2 Ni O6 S2C 1 c 116.4657; 18.901; 16.0566
90; 112.481; 90		4617.4Stephenson, Casey J.; McInnis, Jennifer P.; Chen, Changle; Weberski, Michael P.; Motta, Alessandro; Delferro, Massimiliano; Marks, Tobin J.
Ni(II) Phenoxyiminato Olefin Polymerization Catalysis: Striking Coordinative Modulation of Hyperbranched Polymer Microstructure and Stability by a Proximate Sulfonyl Group
ACS Catalysis, 2014, 4, 999
4510037 CIFC22 H32 N Ni O3 P SP -110.1443; 10.6795; 11.1867
89.583; 69.987; 83.908		1131.76Stephenson, Casey J.; McInnis, Jennifer P.; Chen, Changle; Weberski, Michael P.; Motta, Alessandro; Delferro, Massimiliano; Marks, Tobin J.
Ni(II) Phenoxyiminato Olefin Polymerization Catalysis: Striking Coordinative Modulation of Hyperbranched Polymer Microstructure and Stability by a Proximate Sulfonyl Group
ACS Catalysis, 2014, 4, 999
4510383 CIFC19 H17 O4 PP 1 21 18.8426; 7.5945; 12.9242
90; 90.186; 90		867.92Zhou, Yougui; Zhang, Xuepeng; Liang, Huiyi; Cao, Zhenkun; Zhao, Xiaoyu; He, Yuwei; Wang, Shouliang; Pang, Jiyan; Zhou, Zhongyuan; Ke, Zhuofeng; Qiu, Liqin
Enantioselective Synthesis of Axially Chiral Biaryl Monophosphine Oxides via Direct Asymmetric Suzuki Coupling and DFT Investigations of the Enantioselectivity
ACS Catalysis, 2014, 4, 1390
4510384 CIFC29 H21 O2 PP 21 21 2110.228; 20.6215; 21.8081
90; 90; 90		4599.69Zhou, Yougui; Zhang, Xuepeng; Liang, Huiyi; Cao, Zhenkun; Zhao, Xiaoyu; He, Yuwei; Wang, Shouliang; Pang, Jiyan; Zhou, Zhongyuan; Ke, Zhuofeng; Qiu, Liqin
Enantioselective Synthesis of Axially Chiral Biaryl Monophosphine Oxides via Direct Asymmetric Suzuki Coupling and DFT Investigations of the Enantioselectivity
ACS Catalysis, 2014, 4, 1390
4510477 CIFC36 H39 F6 Mn N4 O6.5 S2P 1 21 110.6617; 24.3076; 15.0889
90; 90.1235; 90		3910.44Ottenbacher, Roman V.; Samsonenko, Denis G.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
Highly Enantioselective Bioinspired Epoxidation of Electron-Deficient Olefins with H2O2on Aminopyridine Mn Catalysts
ACS Catalysis, 2014, 4, 1599
4510478 CIFC30 H30 F6 Mn N4 O6 S2P 1 21 19.6677; 15.7748; 11.2312
90; 105.41; 90		1651.25Ottenbacher, Roman V.; Samsonenko, Denis G.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
Highly Enantioselective Bioinspired Epoxidation of Electron-Deficient Olefins with H2O2on Aminopyridine Mn Catalysts
ACS Catalysis, 2014, 4, 1599
4510479 CIFC28 H38 F6 Mn N4 O8 S2P 21 21 217.4006; 17.4254; 11.0395
90; 90; 90		3347.3Ottenbacher, Roman V.; Samsonenko, Denis G.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
Highly Enantioselective Bioinspired Epoxidation of Electron-Deficient Olefins with H2O2on Aminopyridine Mn Catalysts
ACS Catalysis, 2014, 4, 1599
4510480 CIFC26 H36 F6 Mn N6 O6 S2I 2 332.4626; 32.4626; 32.4626
90; 90; 90		34210Ottenbacher, Roman V.; Samsonenko, Denis G.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
Highly Enantioselective Bioinspired Epoxidation of Electron-Deficient Olefins with H2O2on Aminopyridine Mn Catalysts
ACS Catalysis, 2014, 4, 1599
4510481 CIFC30 H44 F6 Mn N6 O6 S2P 1 21 18.6096; 19.9107; 11.0566
90; 110.506; 90		1775.26Ottenbacher, Roman V.; Samsonenko, Denis G.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
Highly Enantioselective Bioinspired Epoxidation of Electron-Deficient Olefins with H2O2on Aminopyridine Mn Catalysts
ACS Catalysis, 2014, 4, 1599
4510813 CIFC115 H96 Cl25 N8 O8 Pd4 Ru2 S4P 1 21 115.433; 29.985; 15.798
90; 119.094; 90		6388.2Hellmuth, Tina; Rieckhoff, Stefan; Weiss, Marcel; Dorst, Konstantin; Frey, Wolfgang; Peters, René
Cooperative Bimetallic Asymmetric Catalysis: Comparison of a Planar Chiral Ruthenocene Bis-Palladacycle to the Corresponding Ferrocene
ACS Catalysis, 2014, 4, 1850
4510814 CIFC65 H56 Cl4 N4 O4 Pd2 Ru2 S2P 21 21 2111.5116; 13.6607; 39.4718
90; 90; 90		6207.2Hellmuth, Tina; Rieckhoff, Stefan; Weiss, Marcel; Dorst, Konstantin; Frey, Wolfgang; Peters, René
Cooperative Bimetallic Asymmetric Catalysis: Comparison of a Planar Chiral Ruthenocene Bis-Palladacycle to the Corresponding Ferrocene
ACS Catalysis, 2014, 4, 1850
4510835 CIFC11 H18 N O2 RhP 21 21 2110.3322; 10.5059; 10.5715
90; 90; 90		1147.53Walters, Annemarie J. C.; Jellema, Erica; Finger, Markus; Aarnoutse, Petra; Smits, Jan M. M.; Reek, Joost N. H.; de Bruin, Bas
Rh-Mediated Carbene Polymerization: from Multistep Catalyst Activation to Alcohol-Mediated Chain-Transfer
ACS Catalysis, 2012, 2, 246
4510836 CIFC35 H38 P RhC 1 2/c 132.151; 9.3724; 19.869
90; 107.394; 90		5713.4Walters, Annemarie J. C.; Jellema, Erica; Finger, Markus; Aarnoutse, Petra; Smits, Jan M. M.; Reek, Joost N. H.; de Bruin, Bas
Rh-Mediated Carbene Polymerization: from Multistep Catalyst Activation to Alcohol-Mediated Chain-Transfer
ACS Catalysis, 2012, 2, 246
4510837 CIFC14 H22 Cl2 N2 RuP 1 21/c 116.9808; 8.2512; 27.3173
90; 122.317; 90		3234.62Díez, Josefina; Gimeno, José; Lledós, Agustí; Suárez, Francisco J.; Vicent, Cristian
Imidazole Based Ruthenium(IV) Complexes as Highly Efficient Bifunctional Catalysts for the Redox Isomerization of Allylic Alcohols in Aqueous Medium: Water as Cooperating Ligand
ACS Catalysis, 2012, 2, 2087
4510838 CIFC17 H22 Cl2 N2 RuP b c a14.9645; 14.1657; 15.9196
90; 90; 90		3374.68Díez, Josefina; Gimeno, José; Lledós, Agustí; Suárez, Francisco J.; Vicent, Cristian
Imidazole Based Ruthenium(IV) Complexes as Highly Efficient Bifunctional Catalysts for the Redox Isomerization of Allylic Alcohols in Aqueous Medium: Water as Cooperating Ligand
ACS Catalysis, 2012, 2, 2087
4510839 CIFC13 H20 Cl2 N2 RuC 1 c 112.1026; 11.1887; 11.2215
90; 93.417; 90		1516.83Díez, Josefina; Gimeno, José; Lledós, Agustí; Suárez, Francisco J.; Vicent, Cristian
Imidazole Based Ruthenium(IV) Complexes as Highly Efficient Bifunctional Catalysts for the Redox Isomerization of Allylic Alcohols in Aqueous Medium: Water as Cooperating Ligand
ACS Catalysis, 2012, 2, 2087
4510942 CIFC30 H28 Br N3 PdC 1 2/c 135.108; 12.2811; 18.782
90; 140.71; 90		5128Sabater, Sara; Mata, Jose A.; Peris, Eduardo
Catalyst Enhancement and Recyclability by Immobilization of Metal Complexes onto Graphene Surface by Noncovalent Interactions
ACS Catalysis, 2014, 4, 2038
4511609 CIFC32 H34 Br0.56 Cl0.44 N5 O RuC 1 c 114.6916; 19.3357; 12.8728
90; 111.282; 90		3407.43Filonenko, Georgy A.; Cosimi, Elena; Lefort, Laurent; Conley, Matthew P.; Copéret, Christophe; Lutz, Martin; Hensen, Emiel J. M.; Pidko, Evgeny A.
Lutidine-Derived Ru-CNC Hydrogenation Pincer Catalysts with Versatile Coordination Properties
ACS Catalysis, 2014, 4, 2667
4511610 CIFC34 H37 B F4 N6 O RuP -110.2126; 12.2383; 16.6522
96.359; 100.516; 101.949		1977.96Filonenko, Georgy A.; Cosimi, Elena; Lefort, Laurent; Conley, Matthew P.; Copéret, Christophe; Lutz, Martin; Hensen, Emiel J. M.; Pidko, Evgeny A.
Lutidine-Derived Ru-CNC Hydrogenation Pincer Catalysts with Versatile Coordination Properties
ACS Catalysis, 2014, 4, 2667
4511611 CIFC35 H41 Br N6 O2 RuC 1 2/c 121.7318; 11.4791; 30.4353
90; 107.522; 90		7240.2Filonenko, Georgy A.; Cosimi, Elena; Lefort, Laurent; Conley, Matthew P.; Copéret, Christophe; Lutz, Martin; Hensen, Emiel J. M.; Pidko, Evgeny A.
Lutidine-Derived Ru-CNC Hydrogenation Pincer Catalysts with Versatile Coordination Properties
ACS Catalysis, 2014, 4, 2667
4511612 CIFC40 H49 Br N6 O RuP 1 21/n 113.7607; 17.3199; 18.3721
90; 108.243; 90		4158.6Filonenko, Georgy A.; Cosimi, Elena; Lefort, Laurent; Conley, Matthew P.; Copéret, Christophe; Lutz, Martin; Hensen, Emiel J. M.; Pidko, Evgeny A.
Lutidine-Derived Ru-CNC Hydrogenation Pincer Catalysts with Versatile Coordination Properties
ACS Catalysis, 2014, 4, 2667
4511613 CIFC40 H43 Br N6 O2 RuP 1 21/c 118.358; 14.6031; 14.0683
90; 93.583; 90		3764.1Filonenko, Georgy A.; Cosimi, Elena; Lefort, Laurent; Conley, Matthew P.; Copéret, Christophe; Lutz, Martin; Hensen, Emiel J. M.; Pidko, Evgeny A.
Lutidine-Derived Ru-CNC Hydrogenation Pincer Catalysts with Versatile Coordination Properties
ACS Catalysis, 2014, 4, 2667
4511614 CIFC60 H67 Br0.65 Cl0.35 N7 O P RuP -110.6089; 15.4581; 18.9255
70.365; 88.255; 84.453		2909.49Filonenko, Georgy A.; Cosimi, Elena; Lefort, Laurent; Conley, Matthew P.; Copéret, Christophe; Lutz, Martin; Hensen, Emiel J. M.; Pidko, Evgeny A.
Lutidine-Derived Ru-CNC Hydrogenation Pincer Catalysts with Versatile Coordination Properties
ACS Catalysis, 2014, 4, 2667
4511615 CIFC21 H29 N2 O3 P RuP -18.6291; 15.0143; 16.9802
88.131; 88.041; 86.19		2192.79Hu, Peng; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Reusable Homogeneous Catalytic System for Hydrogen Production from Methanol and Water
ACS Catalysis, 2014, 4, 2649
4511628 CIFC31 H34 N O6 P Pd SP 1 21/c 115.784; 10.3015; 19.7923
90; 90.938; 90		3217.8Wucher, Philipp; Schwaderer, Judith B.; Mecking, Stefan
Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization
ACS Catalysis, 2014, 4, 2672
4511629 CIFC26 H26 N O5 P Pd SP 1 21/c 19.5988; 8.6559; 29.9833
90; 106.094; 90		2393.6Wucher, Philipp; Schwaderer, Judith B.; Mecking, Stefan
Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization
ACS Catalysis, 2014, 4, 2672
4511630 CIFC48 H54 Cl2 Li2 O12 P2 Pd2 S2P -19.6353; 10.7338; 13.7048
103.819; 93.508; 106.9		1303.85Wucher, Philipp; Schwaderer, Judith B.; Mecking, Stefan
Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization
ACS Catalysis, 2014, 4, 2672
4511631 CIFC27 H28 N O6 P Pd SP 1 21/c 113.7944; 9.9669; 22.1792
90; 120.694; 90		2622.2Wucher, Philipp; Schwaderer, Judith B.; Mecking, Stefan
Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization
ACS Catalysis, 2014, 4, 2672
4511643 CIFC13 H10 Br F3 O2P 21 21 216.384; 11.747; 17.072
90; 90; 90		1280.3Davies, Alyn T.; Pickett, Philip M.; Slawin, Alexandra M. Z.; Smith, Andrew D.
Asymmetric Synthesis of Tri- and Tetrasubstituted Trifluoromethyl Dihydropyranones from α-Aroyloxyaldehydes via NHC Redox Catalysis
ACS Catalysis, 2014, 4, 2696
4511644 CIFC14 H12 Br F3 O2P 1 21 18.1604; 9.5399; 9.6845
90; 109.041; 90		712.7Davies, Alyn T.; Pickett, Philip M.; Slawin, Alexandra M. Z.; Smith, Andrew D.
Asymmetric Synthesis of Tri- and Tetrasubstituted Trifluoromethyl Dihydropyranones from α-Aroyloxyaldehydes via NHC Redox Catalysis
ACS Catalysis, 2014, 4, 2696
4511645 CIFC13 H14 Br F3 O2P 21 21 216.043; 7.8416; 29.273
90; 90; 90		1387.2Davies, Alyn T.; Pickett, Philip M.; Slawin, Alexandra M. Z.; Smith, Andrew D.
Asymmetric Synthesis of Tri- and Tetrasubstituted Trifluoromethyl Dihydropyranones from α-Aroyloxyaldehydes via NHC Redox Catalysis
ACS Catalysis, 2014, 4, 2696
4511667 CIFC19 H12 I N OP 1 21 18.2619; 7.6594; 12.583
90; 99.974; 90		784.2Gao, De-Wei; Gu, Qing; You, Shu-Li
Pd(II)-Catalyzed Intermolecular Direct C‒H Bond Iodination: An Efficient Approach toward the Synthesis of Axially Chiral Compounds via Kinetic Resolution
ACS Catalysis, 2014, 4, 2741
4511670 CIFC56 H70 Cl10 N4 Ru2C 1 2/c 123.4392; 12.8809; 20.9819
90; 108.654; 90		6002Gonell, Sergio; Peris, Eduardo
Pyrene-Based Mono- and Di-N-Heterocyclic Carbene Ligand Complexes of Ruthenium for the Preparation of Mixed Arylated/Alkylated Arylpyridines
ACS Catalysis, 2014, 4, 2811
4511774 CIFC22 H42 Cl N Ni P2P 21 21 2111.354; 14.53; 14.976
90; 90; 90		2470.6Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511775 CIFC36 H56 N2 Ni P2P 42 b c18.924; 18.924; 19.322
90; 90; 90		6919.6Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511776 CIFC36 H55 N Ni O P2P 42 b c18.927; 18.927; 19.275
90; 90; 90		6904.9Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511777 CIFC36 H31 N Ni O P2P 1 n 114.1636; 11.3071; 18.0536
90; 90.216; 90		2891.2Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511778 CIFC42 H61 N Ni P2 SP 1 21/n 111.218; 17.049; 20.543
90; 103.831; 90		3815Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511779 CIFC36 H31 N Ni P2 SP c a 2110.107; 17.521; 17.023
90; 90; 90		3015Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511780 CIFC30 H46.8 Cl0.2 N Ni O0.8 P2P 1 21/c 110.3866; 18.0201; 15.5109
90; 92.576; 90		2900.2Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511781 CIFC30 H51 N Ni P2 SP 1 21/c 110.2239; 18.5337; 15.7104
90; 91.024; 90		2976.4Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J.
Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands
ACS Catalysis, 2014, 4, 2941
4511782 CIFC32 H57 B2 F8 N3 Ni P2P 1 21/c 112.2559; 15.9677; 19.9262
90; 102.37; 90		3809Weiss, Charles J.; Das, Parthapratim; Miller, Deanna L.; Helm, Monte L.; Appel, Aaron M.
Catalytic Oxidation of Alcohol via Nickel Phosphine Complexes with Pendant Amines
ACS Catalysis, 2014, 4, 2951
4511783 CIFC26 H53 B2 F8 N5 Ni P2P 1 21 110.6454; 10.5867; 17.3734
90; 90.393; 90		1957.9Weiss, Charles J.; Das, Parthapratim; Miller, Deanna L.; Helm, Monte L.; Appel, Aaron M.
Catalytic Oxidation of Alcohol via Nickel Phosphine Complexes with Pendant Amines
ACS Catalysis, 2014, 4, 2951
4511784 CIFC148 H222 B3 F12 N14 Ni3 P12P 1 2/n 114.8297; 11.6379; 43.244
90; 92.88; 90		7453.9Weiss, Charles J.; Das, Parthapratim; Miller, Deanna L.; Helm, Monte L.; Appel, Aaron M.
Catalytic Oxidation of Alcohol via Nickel Phosphine Complexes with Pendant Amines
ACS Catalysis, 2014, 4, 2951
4511901 CIFC32 H40 Cl Ir P2P n a 2115.2261; 11.1905; 17.3055
90; 90; 90		2948.64Bézier, David; Brookhart, Maurice
Applications of PC(sp3)P Iridium Complexes in Transfer Dehydrogenation of Alkanes
ACS Catalysis, 2014, 4, 3411
4511978 CIFC46 H74 O P4 Pd2 S4P 1 21/c 118.0562; 14.0451; 22.0832
90; 113.61; 90		5131.5Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2014, 4, 3605
4511979 CIFC75 H138 Cl4 N2 P4 Pd2 S4P -110.2156; 16.2747; 26.6821
91.603; 90.239; 103.725		4307.4Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier
Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams
ACS Catalysis, 2014, 4, 3605
4511980 CIFC18 H16 O6P -110.209; 11.5382; 15.259
72.37; 89.09; 66.272		1556.57Mbofana, Curren T.; Miller, Scott J.
Phosphine-Catalyzed Annulation Reactions of 2-Butynoate and α-Keto Esters: Synthesis of Cyclopentene Derivatives
ACS Catalysis, 2014, 4, 3671
4511983 CIFC59 H60 F3 O4 P4 Rh SP 1 21/n 112.7463; 15.5086; 13.5727
90; 109.429; 90		2530.23Bays, John Timothy; Priyadarshani, Nilusha; Jeletic, Matthew S.; Hulley, Elliot B.; Miller, Deanna L.; Linehan, John C.; Shaw, Wendy J.
The Influence of the Second and Outer Coordination Spheres on Rh(diphosphine)2 CO2 Hydrogenation Catalysts
ACS Catalysis, 2014, 140903144432009
4511984 CIFC65.5 H70.875 F3 N2 O9.125 P4 Rh SP 1 21/c 112.4663; 47.636; 42.394
90; 91.499; 90		25167Bays, John Timothy; Priyadarshani, Nilusha; Jeletic, Matthew S.; Hulley, Elliot B.; Miller, Deanna L.; Linehan, John C.; Shaw, Wendy J.
The Influence of the Second and Outer Coordination Spheres on Rh(diphosphine)2 CO2 Hydrogenation Catalysts
ACS Catalysis, 2014, 140903144432009
4511985 CIFC55 H54 F3 N2 O3 P4 Rh SP -111.1175; 13.2349; 18.044
93.743; 95.848; 109.218		2480.1Bays, John Timothy; Priyadarshani, Nilusha; Jeletic, Matthew S.; Hulley, Elliot B.; Miller, Deanna L.; Linehan, John C.; Shaw, Wendy J.
The Influence of the Second and Outer Coordination Spheres on Rh(diphosphine)2 CO2 Hydrogenation Catalysts
ACS Catalysis, 2014, 140903144432009
4511995 CIFC16 H39 N4 O5 PP -18.8946; 9.599; 14.595
105.46; 94.446; 114.78		1064.6Jeletic, Matthew S.; Helm, Monte L.; Hulley, Elliott B.; Mock, Michael T.; Appel, Aaron M.; Linehan, John C.
A Cobalt Hydride Catalyst for the Hydrogenation of CO2: Pathways for Catalysis and Deactivation
ACS Catalysis, 2014, 4, 3755
4511996 CIFC16 H35 N4 O2 PP -19.492; 10.0652; 11.6878
72.135; 84.493; 64.509		958.49Jeletic, Matthew S.; Helm, Monte L.; Hulley, Elliott B.; Mock, Michael T.; Appel, Aaron M.; Linehan, John C.
A Cobalt Hydride Catalyst for the Hydrogenation of CO2: Pathways for Catalysis and Deactivation
ACS Catalysis, 2014, 4, 3755
4512057 CIFC16 H22 O6P 1 21 19.64383; 5.51183; 14.44803
90; 95.6537; 90		764.251Kim, Junghwa; Lee, Dong-Hwan; Kalutharage, Nishantha; Yi, Chae S.
Selective Catalytic Synthesis of Unsymmetrical Ethers from the Dehydrative Etherification of Two Different Alcohols
ACS Catalysis, 2014, 4, 3881
4512058 CIFC35 H54 O2P 1 21 112.0622; 9.18339; 13.6306
90; 94.3; 90		1505.64Kim, Junghwa; Lee, Dong-Hwan; Kalutharage, Nishantha; Yi, Chae S.
Selective Catalytic Synthesis of Unsymmetrical Ethers from the Dehydrative Etherification of Two Different Alcohols
ACS Catalysis, 2014, 4, 3881
4512105 CIFC44 H31 Cl Ir N2 O2 PP -111.7801; 14.2655; 17.1787
88.278; 80.64; 69.608		2668.8Wang, Dawei; Zhao, Keyan; Xu, Chongying; Miao, Hongyan; Ding, Yuqiang
Synthesis, Structures of Benzoxazolyl Iridium(III) Complexes, and Applications on C‒C and C‒N Bond Formation Reactions under Solvent-Free Conditions: Catalytic Activity Enhanced by Noncoordinating Anion without Silver Effect
ACS Catalysis, 2014, 4, 3910
4512106 CIFC38 H43 Cl Ir N2 O2 PP 1 21/c 19.2237; 23.848; 16.3363
90; 103.348; 90		3496.4Wang, Dawei; Zhao, Keyan; Xu, Chongying; Miao, Hongyan; Ding, Yuqiang
Synthesis, Structures of Benzoxazolyl Iridium(III) Complexes, and Applications on C‒C and C‒N Bond Formation Reactions under Solvent-Free Conditions: Catalytic Activity Enhanced by Noncoordinating Anion without Silver Effect
ACS Catalysis, 2014, 4, 3910
4512210 CIFC46 H51 B Cl6 Cu N7 OP -111.8005; 12.088; 18.1433
101.21; 93.076; 105.213		2434.7Corro, Macarena; Besora, Maria; Maya, Celia; Álvarez, Eleuterio; Urbano, Juan; Fructos, Manuel R.; Maseras, Feliu; Pérez, Pedro J.
Catalytic Copper-Mediated Ring Opening and Functionalization of Benzoxazoles
ACS Catalysis, 2014, 4, 4215
4512211 CIFC16.5 H7 B Br9 Cl Cu N7 SP -111.1605; 13.8447; 19.6313
83.707; 80.497; 79.114		2928.2Corro, Macarena; Besora, Maria; Maya, Celia; Álvarez, Eleuterio; Urbano, Juan; Fructos, Manuel R.; Maseras, Feliu; Pérez, Pedro J.
Catalytic Copper-Mediated Ring Opening and Functionalization of Benzoxazoles
ACS Catalysis, 2014, 4, 4215
4512212 CIFC17 H17 N O4P -17.9337; 8.6976; 11.8982
110.549; 102.752; 93.549		741.04Corro, Macarena; Besora, Maria; Maya, Celia; Álvarez, Eleuterio; Urbano, Juan; Fructos, Manuel R.; Maseras, Feliu; Pérez, Pedro J.
Catalytic Copper-Mediated Ring Opening and Functionalization of Benzoxazoles
ACS Catalysis, 2014, 4, 4215
4512224 CIFC34 H46 Cl N4 RhP 1 21/c 124.481; 13.201; 20.184
90; 93.847; 90		6508.2Azpíroz, Ramón; Rubio-Pérez, Laura; Di Giuseppe, Andrea; Passarelli, Vincenzo; Lahoz, Fernando J.; Castarlenas, Ricardo; Pérez-Torrente, Jesús J.; Oro, Luis A.
Rhodium(I)-N-Heterocyclic Carbene Catalyst for Selective Coupling ofN-Vinylpyrazoles with Alkynes via C‒H Activation
ACS Catalysis, 2014, 4, 4244
4512225 CIFC39 H51 Cl N5 RhP 1 21/n 115.579; 13.803; 18.6728
90; 112.173; 90		3718.4Azpíroz, Ramón; Rubio-Pérez, Laura; Di Giuseppe, Andrea; Passarelli, Vincenzo; Lahoz, Fernando J.; Castarlenas, Ricardo; Pérez-Torrente, Jesús J.; Oro, Luis A.
Rhodium(I)-N-Heterocyclic Carbene Catalyst for Selective Coupling ofN-Vinylpyrazoles with Alkynes via C‒H Activation
ACS Catalysis, 2014, 4, 4244
4512242 CIFC26 H26 N3 O7 S2P 1 21 110.08; 20.648; 13.183
90; 107.503; 90		2616.8Ohmatsu, Kohsuke; Kawai, Shinya; Imagawa, Naomichi; Ooi, Takashi
Palladium-Catalyzed Asymmetric [3 + 2] Cycloaddition of 5-Vinyloxazolidinones with Imines Using Chiral Ammonium-Phosphine Hybrid Ligand
ACS Catalysis, 2014, 4, 4304
4512275 CIFC15 H11 Cl OP 1 21/c 15.8543; 22.954; 8.9509
90; 96.206; 90		1195.8Gandeepan, Parthasarathy; Rajamalli, P.; Cheng, Chien-Hong
Palladium-Catalyzed Dehydrogenative β-Arylation of Simple Saturated Carbonyls by Aryl Halides
ACS Catalysis, 2014, 4, 4485
4512276 CIFC22 H18 OP 1 21/n 15.8215; 8.3087; 33.2148
90; 94.567; 90		1601.47Gandeepan, Parthasarathy; Rajamalli, P.; Cheng, Chien-Hong
Palladium-Catalyzed Dehydrogenative β-Arylation of Simple Saturated Carbonyls by Aryl Halides
ACS Catalysis, 2014, 4, 4485
4512277 CIFC17 H16 OP 1 21/c 112.7973; 6.1187; 16.9311
90; 101.782; 90		1297.82Gandeepan, Parthasarathy; Rajamalli, P.; Cheng, Chien-Hong
Palladium-Catalyzed Dehydrogenative β-Arylation of Simple Saturated Carbonyls by Aryl Halides
ACS Catalysis, 2014, 4, 4485
4512454 CIFC17 H26 O4P 1 21/c 15.4051; 35.529; 16.8799
90; 99.541; 90		3196.7Weiss, Marcel; Peters, René
Catalytic Direct Dehydrogenative Cross-Couplings of C‒H (Pro)Nucleophiles and Allylic Alcohols without an Additional Oxidant
ACS Catalysis, 2015, 5, 310
4512455 CIFC23 H27 N OP 1 21 15.1067; 11.928; 15.558
90; 96.711; 90		941.19Weiss, Marcel; Peters, René
Catalytic Direct Dehydrogenative Cross-Couplings of C‒H (Pro)Nucleophiles and Allylic Alcohols without an Additional Oxidant
ACS Catalysis, 2015, 5, 310
4512456 CIFC22 H19 F4 N O4P 21 21 2112.878; 15.68; 19.97
90; 90; 90		4032Avidan-Shlomovich, Shlomit; Ghosh, Harisadhan; Szpilman, Alex M.
Synthetic and Mechanistic Study of the Catalytic Enantioselective Preparation of Primary β-Amino Ketones from Enones and a Fluorinated Gabriel Reagent
ACS Catalysis, 2015, 5, 336
4512457 CIFC22 H27.5 Cl2 N3.5 Ni O8 PC 1 2/c 128.443; 8.4569; 22.9631
90; 107.39; 90		5271.1Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512458 CIFC15 H25 Cl2 N3 Ni O8 SP -18.7289; 8.7999; 13.9708
93.47; 106.608; 93.681		1022.76Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512459 CIFC30 H42 Cl4 N6 Ni2 O8 S2P -18.0156; 12.2115; 19.7215
91.373; 99.117; 93.388		1901.6Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512460 CIFC24 H36 Cl2 N3 Ni O9 PP -19.3883; 13.0308; 13.093
79.943; 89.364; 73.953		1514.52Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
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

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