Crystallography Open Database

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4514869 CIFC49 H39 N Ni O P2P -19.5744; 11.9148; 18.1503
102.462; 103.789; 97.605		1926.26Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne
Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization.
ACS catalysis, 2019, 9, 2458-2481
4514870 CIFC54 H47 Ni P3P 1 21/c 120.6558; 9.9242; 22.517
90; 109.612; 90		4348Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne
Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization.
ACS catalysis, 2019, 9, 2458-2481
4514871 CIFC54.5 H46 Ni O P2P -110.3659; 14.4217; 16.331
102.781; 99.4257; 110.567		2149.77Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne
Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization.
ACS catalysis, 2019, 9, 2458-2481
4514872 CIFC210 H154 Br2 Cu6 F18 N30 O24P -115.8225; 19.4848; 21.1157
70.092; 81.078; 72.501		5827.6Prakasam, Thirumurugan; Devaraj, Anthonisamy; Saha, Rupak; Lusi, Matteo; Brandel, Jeremy; Esteban-Gómez, David; Platas-Iglesias, Carlos; Olson, Mark Anthony; Mukherjee, Partha Sarathi; Trabolsi, Ali
Metal‒Organic Self-Assembled Trefoil Knots for C—Br Bond Activation
ACS Catalysis, 2019, 9, 1907
4514873 CIFC18 H28 O2P 315.378; 15.378; 5.9449
90; 90; 120		1217.5Yang, Junfeng; Sun, Qiao; Yoshikai, Naohiko
Cobalt-Catalyzed Regio- and Diastereoselective Formal [3 + 2] Cycloaddition between Cyclopropanols and Allenes
ACS Catalysis, 2019, 9, 1973
4514874 CIFC19 H26 OI -4 c 215.4852; 15.4852; 26.1457
90; 90; 90		6269.5Yang, Junfeng; Sun, Qiao; Yoshikai, Naohiko
Cobalt-Catalyzed Regio- and Diastereoselective Formal [3 + 2] Cycloaddition between Cyclopropanols and Allenes
ACS Catalysis, 2019, 9, 1973
4514875 CIFC21 H22 OP 1 21/n 18.787; 11.718; 14.849
90; 95.361; 90		1522.3Yang, Junfeng; Sun, Qiao; Yoshikai, Naohiko
Cobalt-Catalyzed Regio- and Diastereoselective Formal [3 + 2] Cycloaddition between Cyclopropanols and Allenes
ACS Catalysis, 2019, 9, 1973
4514876 CIFC20 H19 N3 O2P 21 21 217.1039; 11.823; 19.698
90; 90; 90		1654.4Zhang, Lin-Bao; Zhu, Ming-Hui; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming
Silver-Mediated Indole (4 + 2) Dearomative Annulation with N-Radicals: A Strategy To Construct Heterocycle-Fused Indolines
ACS Catalysis, 2019, 9, 1680
4514877 CIFC27 H31 O2 SiC 1 2/c 127.6888; 8.415; 21.6977
90; 90.427; 90		5055.5Zhang, Shuo; Yao, Qi-Jun; Liao, Gang; Li, Xin; Li, Han; Chen, Hao-Ming; Hong, Xin; Shi, Bing-Feng
Enantioselective Synthesis of Atropisomers Featuring Pentatomic Heteroaromatics by Pd-Catalyzed C‒H Alkynylation
ACS Catalysis, 2019, 9, 1956
4514878 CIFC30 H32 O S SiP 21 21 2110.8692; 13.9222; 17.5154
90; 90; 90		2650.49Zhang, Shuo; Yao, Qi-Jun; Liao, Gang; Li, Xin; Li, Han; Chen, Hao-Ming; Hong, Xin; Shi, Bing-Feng
Enantioselective Synthesis of Atropisomers Featuring Pentatomic Heteroaromatics by Pd-Catalyzed C‒H Alkynylation
ACS Catalysis, 2019, 9, 1956
4514879 CIFC32 H33 N O SiP 1 21 17.3547; 43.2835; 8.7345
90; 93.821; 90		2774.3Zhang, Shuo; Yao, Qi-Jun; Liao, Gang; Li, Xin; Li, Han; Chen, Hao-Ming; Hong, Xin; Shi, Bing-Feng
Enantioselective Synthesis of Atropisomers Featuring Pentatomic Heteroaromatics by Pd-Catalyzed C‒H Alkynylation
ACS Catalysis, 2019, 9, 1956
4514880 CIFC23 H30 Br Mn N2 O9 P2P -111.5014; 12.237; 12.4559
61.15; 71.428; 73.307		1436.6Woo, Sung-Jun; Choi, Sunghan; Kim, So-Yoen; Kim, Pil Soo; Jo, Ju Hyoung; Kim, Chul Hoon; Son, Ho-Jin; Pac, Chyongjin; Kang, Sang Ook
Highly Selective and Durable Photochemical CO2 Reduction by Molecular Mn(I) Catalyst Fixed on a Particular Dye-Sensitized TiO2 Platform
ACS Catalysis, 2019, 9, 2580
4514881 CIFC17 H16 Br2 O5P 1 21/c 120.647; 10.3884; 17.2385
90; 114.021; 90		3377.26Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514882 CIFC17 H15 Cl O5P 1 21 16.1976; 17.271; 7.158
90; 103.688; 90		744.4Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514883 CIFC30 H25 Br N2 O5P 1 21 111.584; 7.7058; 15.1367
90; 109.376; 90		1274.63Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514884 CIFC11 H12 O5P 21 21 216.0801; 8.1103; 22.242
90; 90; 90		1096.8Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514885 CIFC33 H33 N3 O8 SP 21 21 218.7971; 17.2916; 20.3839
90; 90; 90		3100.7Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514886 CIFC27 H26 Cl N O7P 1 21/c 16.2963; 32.789; 11.523
90; 100.644; 90		2338Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514887 CIFC11 H12 O5C 1 c 16.0855; 12.683; 13.554
90; 93.29; 90		1044.4Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao
Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy
ACS Catalysis, 2019, 9, 1645
4514888 CIFC28 H26 F6 N2 O8P 21 21 2111.7248; 13.6488; 19.0159
90; 90; 90		3043.1Sletten, Eric T.; Tu, Yi-Jung; Schlegel, H. Bernhard; Nguyen, Hien M.
Are Brønsted Acids the True Promoter of Metal-Triflate-Catalyzed Glycosylations? A Mechanistic Probe into 1,2-cis-Aminoglycoside Formation by Nickel Triflate
ACS Catalysis, 2019, 9, 2110
4514889 CIFC16 H12 Cl N SP n a 217.6912; 23.747; 7.518
90; 90; 90		1373.1Wang, Huamin; Li, Yongli; Lu, Qingquan; Yu, Mingming; Bai, Xudong; Wang, Shengchun; Cong, Hengjiang; Zhang, Heng; Lei, Aiwen
Oxidation-Induced β-Selective C‒H Bond Functionalization: Thiolation and Selenation of N-Heterocycles
ACS Catalysis, 2019, 9, 1888
4514890 CIFC20 H39 Mn O3 P2P 1 21/n 111.654; 14.455; 13.866
90; 98.639; 90		2309.3Weber, Stefan; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Rethinking Basic Concepts—Hydrogenation of Alkenes Catalyzed by Bench-Stable Alkyl Mn(I) Complexes
ACS Catalysis, 2019, 9715
4514891 CIFC92 H121.28 F24 Fe4 N24.43 O27 S8P 1 21/n 131.69; 12.063; 34.405
90; 109.475; 90		12400Zott, Michael D.; Garrido-Barros, Pablo; Peters, Jonas C.
Electrocatalytic Ammonia Oxidation Mediated by a Polypyridyl Iron Catalyst
ACS Catalysis, 2019, 10101
4514892 CIFC12 H18 Al Cl9 Ga2 N6P 21 21 2110.0468; 14.4215; 20.9082
90; 90; 90		3029.4Li, Kai; Choudhary, Hemant; Mishra, Manish Kumar; Rogers, Robin D.
Enhanced Acidity and Activity of Aluminum/Gallium-Based Ionic Liquids Resulting from Dynamic Anionic Speciation
ACS Catalysis, 2019, 9789
4514893 CIFC28 H29 N O3P b c a19.6581; 8.4966; 27.1209
90; 90; 90		4529.9Thopate, Satish B.; Jadhav, Sandip B.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
Stereoselective Desymmetrization of Cyclohexadienone-Tethered Enones: Efficient Access to Highly Strained Polycyclic Indoles
ACS Catalysis, 2019, 10012
4514894 CIFC19 H30 O3I 1 2 110.013; 7.4903; 22.9488
90; 98.688; 90		1701.42Li, Junqi; Grosslight, Samantha; Miller, Scott J.; Sigman, Matthew S.; Toste, F. Dean
Site-Selective Acylation of Natural Products with BINOL-Derived Phosphoric Acids
ACS Catalysis, 2019, 9794
4514895 CIFC21 H22 B PP b c a10.8454; 15.0719; 21.848
90; 90; 90		3571.29Jin, Shengfei; Haug, Graham C.; Nguyen, Vu T.; Flores-Hansen, Carsten; Arman, Hadi D.; Larionov, Oleg V.
Decarboxylative Phosphine Synthesis: Insights into the Catalytic, Autocatalytic, and Inhibitory Roles of Additives and Intermediates
ACS Catalysis, 2019, 9764
4514896 CIFC38 H46 Cl2 P2 PdP -19.4779; 9.5662; 11.438
69.891; 65.634; 67.434		850.88Jin, Shengfei; Haug, Graham C.; Nguyen, Vu T.; Flores-Hansen, Carsten; Arman, Hadi D.; Larionov, Oleg V.
Decarboxylative Phosphine Synthesis: Insights into the Catalytic, Autocatalytic, and Inhibitory Roles of Additives and Intermediates
ACS Catalysis, 2019, 9764
4514897 CIFC19 H26 B PP 1 21/n 19.4514; 18.192; 9.7634
90; 90.35; 90		1678.69Jin, Shengfei; Haug, Graham C.; Nguyen, Vu T.; Flores-Hansen, Carsten; Arman, Hadi D.; Larionov, Oleg V.
Decarboxylative Phosphine Synthesis: Insights into the Catalytic, Autocatalytic, and Inhibitory Roles of Additives and Intermediates
ACS Catalysis, 2019, 9764
4514898 CIFC21 H22 B PP 1 21/c 18.0198; 15.1635; 14.6975
90; 95.659; 90		1778.63Jin, Shengfei; Haug, Graham C.; Nguyen, Vu T.; Flores-Hansen, Carsten; Arman, Hadi D.; Larionov, Oleg V.
Decarboxylative Phosphine Synthesis: Insights into the Catalytic, Autocatalytic, and Inhibitory Roles of Additives and Intermediates
ACS Catalysis, 2019, 9764
4514899 CIFC27 H32 N2 O7P 3119.4343; 19.4343; 6.0779
90; 90; 120		1988.03Nanjo, Takeshi; Zhang, Xuan; Tokuhiro, Yusuke; Takemoto, Yoshiji
Divergent and Scalable Synthesis of α-Hydroxy/Keto-β-amino Acid Analogues by the Catalytic Enantioselective Addition of Glyoxylate Cyanohydrin to Imines
ACS Catalysis, 2019, 10087
4514900 CIFC28 H26 I O4 PP 21 21 217.9972; 16.3553; 18.8545
90; 90; 90		2466.1Duan, Longhui; Zhao, Kun; Wang, Zhonggui; Zhang, Feng-Lian; Gu, Zhenhua
Enantioselective Ring-Opening/Oxidative Phosphorylation and P-Transfer Reaction of Cyclic Diaryliodoniums
ACS Catalysis, 2019, 9852
4514901 CIFC28 H27 O2 PP 1 21 19.27489; 7.39505; 16.7947
90; 94.7237; 90		1148.01Duan, Longhui; Zhao, Kun; Wang, Zhonggui; Zhang, Feng-Lian; Gu, Zhenhua
Enantioselective Ring-Opening/Oxidative Phosphorylation and P-Transfer Reaction of Cyclic Diaryliodoniums
ACS Catalysis, 2019, 9852
4514902 CIFC24 H27 O2 PP 21 21 217.18064; 15.0632; 19.4179
90; 90; 90		2100.31Duan, Longhui; Zhao, Kun; Wang, Zhonggui; Zhang, Feng-Lian; Gu, Zhenhua
Enantioselective Ring-Opening/Oxidative Phosphorylation and P-Transfer Reaction of Cyclic Diaryliodoniums
ACS Catalysis, 2019, 9852
4514903 CIFC22 H35 Cl2 Co N6 O7.5P 113.559; 15.38; 15.989
63.668; 88.605; 74.638		2864.8Dolui, Dependu; Khandelwal, Shikha; Shaik, Althaf; Gaat, Deepika; Thiruvenkatam, Vijay; Dutta, Arnab
Enzyme-Inspired Synthetic Proton Relays Generate Fast and Acid-Stable Cobalt-Based H2 Production Electrocatalysts
ACS Catalysis, 2019, 10115
4514904 CIFC21 H33 Cl2 Co N6 O6P 1 21/n 115.4342; 23.908; 16.1767
90; 117.903; 90		5275.2Dolui, Dependu; Khandelwal, Shikha; Shaik, Althaf; Gaat, Deepika; Thiruvenkatam, Vijay; Dutta, Arnab
Enzyme-Inspired Synthetic Proton Relays Generate Fast and Acid-Stable Cobalt-Based H2 Production Electrocatalysts
ACS Catalysis, 2019, 10115
4515230 CIFC18 H22 Co F6 I N3 SbP -18.4596; 11.7043; 11.7936
94.205; 97.688; 101.396		1128.42Dutta, Champak; Rana, Samim Sohel; Choudhury, Joyanta
Leveraging Metallotropism-Enabled Substrate Activation in Cobalt-Catalyzed Annulation Chemistry: Protic NHC Template Is the Key
ACS Catalysis, 2019, 10674
4515231 CIFC20 H25 Co F12 N4 Sb2P 1 21/c 111.2569; 17.2345; 14.4525
90; 102.365; 90		2738.8Dutta, Champak; Rana, Samim Sohel; Choudhury, Joyanta
Leveraging Metallotropism-Enabled Substrate Activation in Cobalt-Catalyzed Annulation Chemistry: Protic NHC Template Is the Key
ACS Catalysis, 2019, 10674
4515232 CIFC23 H16 F3 N3 O3 SP -17.941; 9.4593; 15.292
76.521; 86.356; 65.536		1016.05Dutta, Champak; Rana, Samim Sohel; Choudhury, Joyanta
Leveraging Metallotropism-Enabled Substrate Activation in Cobalt-Catalyzed Annulation Chemistry: Protic NHC Template Is the Key
ACS Catalysis, 2019, 10674
4515233 CIFC19 H24 Cl2 Co I2 N3P 1 21/n 115.637; 8.3901; 17.491
90; 94.402; 90		2288Dutta, Champak; Rana, Samim Sohel; Choudhury, Joyanta
Leveraging Metallotropism-Enabled Substrate Activation in Cobalt-Catalyzed Annulation Chemistry: Protic NHC Template Is the Key
ACS Catalysis, 2019, 10674
4515234 CIFC26 H21 F3 N4 O3 SP 1 21/c 114.118; 8.4571; 21.1896
90; 106.515; 90		2425.6Dutta, Champak; Rana, Samim Sohel; Choudhury, Joyanta
Leveraging Metallotropism-Enabled Substrate Activation in Cobalt-Catalyzed Annulation Chemistry: Protic NHC Template Is the Key
ACS Catalysis, 2019, 10674
4515235 CIFC18 H23 N O3P b c a11.8576; 9.505; 31.686
90; 90; 90		3571.2Dhungana, Roshan K.; KC, Shekhar; Basnet, Prakash; Aryal, Vivek; Chesley, Lucas J.; Giri, Ramesh
Ni(I)-Catalyzed β,δ-Vinylarylation of γ,δ-Alkenyl α-Cyanocarboxylic Esters via Contraction of Transient Nickellacycles
ACS Catalysis, 2019, 10887
4515236 CIFC19 H13 F3 O3P 1 21/n 112.443; 7.738; 16.21
90; 104.113; 90		1513.7Zeng, Qian; Dong, Kuiyong; Pei, Chao; Dong, Shanliang; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Divergent Construction of Macrocyclic Alkynes via Catalytic Metal Carbene C(sp2)‒H Insertion and the Buchner Reaction
ACS Catalysis, 2019, 10773
4515237 CIFC18 H15 N O2P 1 21/c 19.4722; 10.8657; 14.4561
90; 106.803; 90		1424.3Zeng, Qian; Dong, Kuiyong; Pei, Chao; Dong, Shanliang; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Divergent Construction of Macrocyclic Alkynes via Catalytic Metal Carbene C(sp2)‒H Insertion and the Buchner Reaction
ACS Catalysis, 2019, 10773
4515238 CIFC19 H16 Cl N O2P 1 21/n 18.1685; 19.6127; 19.5534
90; 97.271; 90		3107.4Zeng, Qian; Dong, Kuiyong; Pei, Chao; Dong, Shanliang; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Divergent Construction of Macrocyclic Alkynes via Catalytic Metal Carbene C(sp2)‒H Insertion and the Buchner Reaction
ACS Catalysis, 2019, 10773
4515239 CIFC19 H17 N O2P 1 21/c 113.1381; 7.8049; 14.7103
90; 96.826; 90		1497.72Zeng, Qian; Dong, Kuiyong; Pei, Chao; Dong, Shanliang; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Divergent Construction of Macrocyclic Alkynes via Catalytic Metal Carbene C(sp2)‒H Insertion and the Buchner Reaction
ACS Catalysis, 2019, 10773
4515240 CIFC19 H17 N O2P 1 21/c 16.2893; 20.9264; 11.5081
90; 98.463; 90		1498.1Zeng, Qian; Dong, Kuiyong; Pei, Chao; Dong, Shanliang; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Divergent Construction of Macrocyclic Alkynes via Catalytic Metal Carbene C(sp2)‒H Insertion and the Buchner Reaction
ACS Catalysis, 2019, 10773
4515241 CIFC62 H72 Cu N2 O6P -111.687; 13.565; 18.665
102.623; 92.254; 107.835		2731Jangir, Ritambhara; Ansari, Mursaleem; Kaleeswaran, Dhananjayan; Rajaraman, Gopalan; Palaniandavar, Mallayan; Murugavel, Ramaswamy
Unprecedented Copper(II) Complex with a Topoquinone-like Moiety as a Structural and Functional Mimic for Copper Amine Oxidase: Role of Copper(II) in the Genesis and Amine Oxidase Activity
ACS Catalysis, 2019, 10940
4515242 CIFC42 H50 Cu N2 O2F d d d :221.901; 24.944; 29.952
90; 90; 90		16363Jangir, Ritambhara; Ansari, Mursaleem; Kaleeswaran, Dhananjayan; Rajaraman, Gopalan; Palaniandavar, Mallayan; Murugavel, Ramaswamy
Unprecedented Copper(II) Complex with a Topoquinone-like Moiety as a Structural and Functional Mimic for Copper Amine Oxidase: Role of Copper(II) in the Genesis and Amine Oxidase Activity
ACS Catalysis, 2019, 10940
4515252 CIFC24 H16 N2 O3P 1 21 19.2224; 8.97; 11.92
90; 112.477; 90		911.17Yang, Xing; Luo, Guoyong; Zhou, Liejin; Liu, Bin; Zhang, Xiaolei; Gao, Hui; Jin, Zhichao; Chi, Yonggui Robin
Enantioselective Indole N‒H Functionalization Enabled by Addition of Carbene Catalyst to Indole Aldehyde at Remote Site
ACS Catalysis, 2019, 10971
4515253 CIFC18 H12 N2 O5 SP -18.4139; 8.7598; 11.5432
104.951; 108.859; 96.299		760.3Yang, Xing; Luo, Guoyong; Zhou, Liejin; Liu, Bin; Zhang, Xiaolei; Gao, Hui; Jin, Zhichao; Chi, Yonggui Robin
Enantioselective Indole N‒H Functionalization Enabled by Addition of Carbene Catalyst to Indole Aldehyde at Remote Site
ACS Catalysis, 2019, 10971
4515254 CIFC26 H17 F3 N2 O4 SP 1 21 19.9025; 8.5425; 26.6115
90; 97.442; 90		2232.2Yang, Xing; Luo, Guoyong; Zhou, Liejin; Liu, Bin; Zhang, Xiaolei; Gao, Hui; Jin, Zhichao; Chi, Yonggui Robin
Enantioselective Indole N‒H Functionalization Enabled by Addition of Carbene Catalyst to Indole Aldehyde at Remote Site
ACS Catalysis, 2019, 10971
4515255 CIFC45 H31 Cl3 N2 Ni OP 1 21/n 115.6; 15.771; 16.342
90; 99.93; 90		3960Capdevila, Lorena; Meyer, Tjark H.; Roldán-Gómez, Steven; Luis, Josep M.; Ackermann, Lutz; Ribas, Xavi
Chemodivergent Nickel(0)-Catalyzed Arene C‒F Activation with Alkynes: Unprecedented C‒F/C‒H Double Insertion
ACS Catalysis, 2019, 11074
4515457 CIFC27 H25 NP -111.627; 11.659; 15.889
85.73; 77.49; 69.54		1970.1Tian, Jun-Jie; Zeng, Ning-Ning; Liu, Ning; Tu, Xian-Shuang; Wang, Xiao-Chen
Intramolecular Cyclizations of Vinyl-Substituted N,N-Dialkyl Arylamines Enabled by Borane-Assisted Hydride Transfer
ACS Catalysis, 2018, 9, 295
4515458 CIFC25 H19 Br Mn N2 O2 PP 1 21/c 112.9669; 13.874; 12.3572
90; 93.057; 90		2219.93Das, Uttam Kumar; Ben-David, Yehoshoa; Leitus, Gregory; Diskin-Posner, Yael; Milstein, David
Dehydrogenative Cross-Coupling of Primary Alcohols To Form Cross-Esters Catalyzed by a Manganese Pincer Complex
ACS Catalysis, 2018, 9, 479
4515459 CIFC32 H26 Mn N2 O3 PP 1 21/c 19.7663; 16.9042; 16.0896
90; 97.951; 90		2630.72Das, Uttam Kumar; Ben-David, Yehoshoa; Leitus, Gregory; Diskin-Posner, Yael; Milstein, David
Dehydrogenative Cross-Coupling of Primary Alcohols To Form Cross-Esters Catalyzed by a Manganese Pincer Complex
ACS Catalysis, 2018, 9, 479
4515460 CIFC18 H23 N3 O2P 1 21/c 18.3986; 10.167; 18.964
90; 101.38; 90		1587.5van der Puyl, Vincent A.; Derosa, Joseph; Engle, Keary M.
Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds
ACS Catalysis, 2018, 9, 224
4515461 CIFC20 H27 N3 O2P -19.4368; 11.2965; 18.1549
81.081; 81.652; 73.77		1825.2van der Puyl, Vincent A.; Derosa, Joseph; Engle, Keary M.
Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds
ACS Catalysis, 2018, 9, 224
4515462 CIFC22 H33 B F2 O4 SiP 21 21 217.4443; 10.4007; 31.5827
90; 90; 90		2445.32Guo, Wen-Hao; Zhao, Hai-Yang; Luo, Zhi-Ji; Zhang, Shu; Zhang, Xingang
Fluoroalkylation‒Borylation of Alkynes: An Efficient Method To Obtain (Z)-Tri- and Tetrasubstituted Fluoroalkylated Alkenylboronates
ACS Catalysis, 2018, 9, 38
4515463 CIFC28 H47 B O8 P2 PdC 1 2/c 126.0162; 11.1134; 23.2857
90; 108.358; 90		6389.9Espinosa, Matthew R.; Charboneau, David J.; Garcia de Oliveira, André; Hazari, Nilay
Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels
ACS Catalysis, 2018, 9, 301
4515464 CIFC9 H15 B O2I 41/a c d :213.2301; 13.2301; 38.893
90; 90; 90		6807.7Espinosa, Matthew R.; Charboneau, David J.; Garcia de Oliveira, André; Hazari, Nilay
Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels
ACS Catalysis, 2018, 9, 301
4515465 CIFC15 H15 Cl N2P 1 21/n 18.473; 17.4446; 9.0374
90; 94.072; 90		1332.43Fu, Niankai; Shen, Yifan; Allen, Anthony R.; Song, Lu; Ozaki, Atsushi; Lin, Song
Mn-Catalyzed Electrochemical Chloroalkylation of Alkenes.
ACS catalysis, 2019, 9, 746-754
4515466 CIFC18 H14 F3 N O4P 1 21 111.8498; 9.5906; 14.708
90; 96.008; 90		1662.33Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515467 CIFC17 H15 N O4P 1 21 113.5517; 9.2461; 11.8061
90; 106.796; 90		1416.2Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515468 CIFC60 H79 N6 O15 PP 21 21 219.8665; 19.0145; 31.36
90; 90; 90		5883.3Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515469 CIFC17 H14 Br N O4I 1 2 122.7393; 5.2121; 14.2943
90; 93.045; 90		1691.76Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515470 CIFC17 H15 N O4P 1 21 110.8042; 8.4963; 15.825
90; 103.232; 90		1414.1Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515471 CIFC18 H17 N O4P -19.806; 14.9855; 21.2136
89.141; 86.664; 88.303		3110.4Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515472 CIFC36 H57 N7 O7C 1 2 126.466; 17.7566; 22.8328
90; 124.789; 90		8812.3Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515473 CIFC20 H23 N O2P b c a13.76; 7.1297; 34.2631
90; 90; 90		3361.37Ho, Hon Eong; Stephens, Thomas C.; Payne, Thomas J.; O’Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics
ACS Catalysis, 2018, 9, 504
4515474 CIFC45.67 H35.35 Cl3.35 N2 O2I 1 2/a 17.38319; 26.3138; 19.6731
90; 93.6518; 90		3814.33Ho, Hon Eong; Stephens, Thomas C.; Payne, Thomas J.; O’Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics
ACS Catalysis, 2018, 9, 504
4515475 CIFC22 H40 Mn N3 O5 P2 SP b c a11.5; 14.765; 34.41
90; 90; 90		5843Bertini, Federica; Glatz, Mathias; Stöger, Berthold; Peruzzini, Maurizio; Veiros, Luis F.; Kirchner, Karl; Gonsalvi, Luca
Carbon Dioxide Reduction to Methanol Catalyzed by Mn(I) PNP Pincer Complexes under Mild Reaction Conditions
ACS Catalysis, 2018, 9, 632
4515476 CIFC27 H29 NP -18.9763; 10.84; 11.572
109.84; 99.23; 93.29		1037.8Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui
Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation
ACS Catalysis, 2018, 9, 599
4515477 CIFC23 H40 N Sc Si2P -19.616; 10.433; 13.436
100.936; 95.927; 95.808		1306.3Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui
Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation
ACS Catalysis, 2018, 9, 599
4515478 CIFC15 H24 F6 N PC 1 c 119.003; 10.452; 8.8763
90; 96.73; 90		1750.9Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui
Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation
ACS Catalysis, 2018, 9, 599
4515479 CIFC29 H20 B F18 N6 RhP 1 21/c 118.0106; 9.0679; 19.7109
90; 96.859; 90		3196.1Avullala, Thirupataiah; Asgari, Parham; Hua, Yuanda; Bokka, Apparao; Ridlen, Shawn G.; Yum, Kyungsuk; Dias, H. V. Rasika; Jeon, Junha
Umpolung <i>α</i>-Silylation of Cyclopropyl Acetates via Low-Temperature Catalytic C-C Activation.
ACS catalysis, 2019, 9, 402-408
4515480 CIFC36 H48 Cl2 N2 O RuP 1 21/c 119.3364; 10.43031; 16.58648
90; 95.7369; 90		3328.48Małecki, Paweł; Gajda, Katarzyna; Gajda, Roman; Woźniak, Krzysztof; Trzaskowski, Bartosz; Kajetanowicz, Anna; Grela, Karol
Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application
ACS Catalysis, 2018, 9, 587
4515481 CIFC53 H50 Cl2 N2 O RuP 1 21/n 113.16; 10.12687; 37.8176
90; 98.1376; 90		4989.19Małecki, Paweł; Gajda, Katarzyna; Gajda, Roman; Woźniak, Krzysztof; Trzaskowski, Bartosz; Kajetanowicz, Anna; Grela, Karol
Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application
ACS Catalysis, 2018, 9, 587
4515482 CIFC41 H48 Br N3 O7P 21 21 2111.6704; 12.4895; 24.8148
90; 90; 90		3616.94Paria, Suva; Kang, Qi-Kai; Hatanaka, Miho; Maruoka, Keiji
Design of Efficient Chiral Bifunctional Phase-Transfer Catalysts Possessing an Amino Functionality for Asymmetric Aminations
ACS Catalysis, 2018, 9, 78
4515483 CIFC71 H72 N2 NiP 21 21 2114.9159; 18.747; 20.4012
90; 90; 90		5704.8Cai, Yuan; Zhang, Jia-Wen; Li, Feng; Liu, Jia-Ming; Shi, Shi-Liang
Nickel/N-Heterocyclic Carbene Complex-Catalyzed Enantioselective Redox-Neutral Coupling of Benzyl Alcohols and Alkynes to Allylic Alcohols
ACS Catalysis, 2018, 9, 1
4515484 CIFC23 H22 N2 O4 S2P 19.0036; 10.9036; 11.9944
103.063; 98.741; 91.068		1132Yang, Shengbiao; Wang, Lihong; Zhang, Hongwei; Liu, Chunyang; Zhang, Linli; Wang, Xiaomin; Zhang, Ge; Li, Yan; Zhang, Qian
Copper-Catalyzed Asymmetric Aminocyanation of Arylcyclopropanes for Synthesis of γ-Amino Nitriles
ACS Catalysis, 2018, 9, 716
4515485 CIFC37 H31 F2 I P2 PdC 1 2/c 112.09; 15.2246; 20.0614
90; 91.35; 90		3691.6Hori, Kaishi; Motohashi, Hirotaka; Saito, Daichi; Mikami, Koichi
Precatalyst Effects on Pd-Catalyzed Cross-Coupling Difluoromethylation of Aryl Boronic Acids
ACS Catalysis, 2018, 9, 417
4515486 CIFC56 H34 F16 Ir N4 PC 1 2/c 116.49; 22.606; 13.5064
90; 90.007; 90		5034.8Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François
Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
ACS Catalysis, 2018, 9, 1320
4515487 CIFC49 H32 Cl2 F16 Ir N4 PP -111.7565; 12.8586; 18.657
81.314; 80.238; 73.409		2648.1Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François
Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
ACS Catalysis, 2018, 9, 1320
4515488 CIFC56 H34 F16 Ir N4 PR -3 :H26.5472; 26.5472; 38.495
90; 90; 120		23494.8Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François
Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
ACS Catalysis, 2018, 9, 1320
4515489 CIFC27 H43 Al Cl N3 Si3P -19.6279; 10.9013; 17.0857
98.271; 102.568; 108.408		1616.39Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515490 CIFC24 H24 Al N3P 21 21 217.3795; 13.4511; 21.1096
90; 90; 90		2095.39Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515491 CIFC18 H19 Al Cl N3P 1 21/c 18.9033; 22.602; 8.763
90; 100.967; 90		1731.2Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515492 CIFC35 H44 Al N4P -19.0364; 10.9957; 16.5417
91.033; 97.953; 107.345		1550.72Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515493 CIFC29 H33 Al N3P 1 21/n 19.6204; 24.1661; 10.8834
90; 94.131; 90		2523.68Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515494 CIFC33 H48 Al N3 Si3P -19.2076; 12.1268; 16.763
98.513; 98.865; 103.694		1763.3Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515495 CIFC15 H24 Al Cl4 N3 O7P 1 21/n 17.0617; 25.6486; 13.413
90; 105.218; 90		2344.2Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515496 CIFC27 H37 Al Cl N3P 1 21/n 19.2525; 15.9339; 17.4939
90; 95.425; 90		2567.5Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515497 CIFC27 H38 Al N3P -18.9098; 9.0012; 17.5788
89.93; 76.945; 69.158		1278.64Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515498 CIFC33 H42 Al N3P 1 21/c 116.055; 10.4568; 35.146
90; 98.496; 90		5835.7Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515499 CIFC57 H34 B2 F30 Nd Si3C 1 2/c 139.687; 12.1443; 26.344
90; 98.409; 90		12561Schmidt, Bradley M.; Pindwal, Aradhana; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Zwitterionic Trivalent (Alkyl)lanthanide Complexes in Ziegler-Type Butadiene Polymerization
ACS Catalysis, 2018, 9, 827
4515500 CIFC20 H16 O4I 1 a 16.101; 7.1857; 36.046
90; 94.848; 90		1574.6Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515501 CIFC23 H31 Cl Fe N2P 1 2/c 114.4785; 9.0523; 16.7522
90; 92.179; 90		2194Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515502 CIFC29 H35 Cl Fe N2P b c a16.5485; 10.4399; 31.246
90; 90; 90		5398.2Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515503 CIFC26 H38 Cl Fe N3P b c a11.9206; 15.6644; 27.735
90; 90; 90		5178.93Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515504 CIFC37 H40 Fe N2P 1 21/c 112.631; 15.5444; 16.5595
90; 105.365; 90		3135.1Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515505 CIFC25 H35 Cl Fe N2P 1 21/c 117.827; 15.8552; 11.0869
90; 104.133; 90		3038.9Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515506 CIFC24 H20 Fe2P 1 21/n 111.736; 10.478; 14.979
90; 102.775; 90		1796.4Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515507 CIFC28 H41 Cl Fe N2P 21 21 218.6146; 17.039; 19.7629
90; 90; 90		2900.9Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515508 CIFC32 H41 Cl Fe N2P 1 21/c 18.4344; 22.681; 15.3166
90; 90.017; 90		2930.1Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515509 CIFC26 H37 Cl Fe N2P 1 21/c 18.5309; 16.6841; 17.0048
90; 91.196; 90		2419.8Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515510 CIFC19 H13 N O4 SP -17.0423; 9.2936; 12.8025
89.117; 75.476; 77.243		790.39Shu, Chao; Shi, Chong-Yang; Sun, Qing; Zhou, Bo; Li, Tian-You; He, Qiao; Lu, Xin; Liu, Rai-Shung; Ye, Long-Wu
Generation of Endocyclic Vinyl Carbene Complexes via Gold-Catalyzed Oxidative Cyclization of Terminal Diynes: Toward Naphthoquinones and Carbazolequinones
ACS Catalysis, 2018, 9, 1019
4515511 CIFC30 H29 Al N4 OP -19.633; 11.189; 12.051
89.56; 71.1; 83.22		1220Mandal, Mukunda; Luke, Anna M.; Dereli, Büşra; Elwell, Courtney E.; Reineke, Theresa M.; Tolman, William B.; Cramer, Christopher J.
Computational Prediction and Experimental Verification of ε-Caprolactone Ring-Opening Polymerization Activity by an Aluminum Complex of an Indolide/Schiff-Base Ligand
ACS Catalysis, 2018, 9, 885
4515512 CIFC26 H30 N2 O3P 21 21 219.1036; 13.3256; 36.2038
90; 90; 90		4391.92Shen, Hong-Cheng; Zhang, Ling; Chen, Shu-Sen; Feng, Jiajie; Zhang, Bo-Wen; Zhang, Ying; Zhang, Xinhao; Wu, Yun-Dong; Gong, Liu-Zhu
Enantioselective Addition of Cyclic Ketones to Unactivated Alkenes Enabled by Amine/Pd(II) Cooperative Catalysis
ACS Catalysis, 2018, 9, 791
4515513 CIFC25 H27 Br N2 O2P 21 21 219.0909; 13.2501; 36.0908
90; 90; 90		4347.3Shen, Hong-Cheng; Zhang, Ling; Chen, Shu-Sen; Feng, Jiajie; Zhang, Bo-Wen; Zhang, Ying; Zhang, Xinhao; Wu, Yun-Dong; Gong, Liu-Zhu
Enantioselective Addition of Cyclic Ketones to Unactivated Alkenes Enabled by Amine/Pd(II) Cooperative Catalysis
ACS Catalysis, 2018, 9, 791
4515514 CIFC25 H38 B N O6 SP -111.446; 11.5967; 12.3843
112.094; 115.7; 93.978		1318.18Kim-Lee, Shin-Ho; Alonso, Inés; Mauleón, Pablo; Arrayás, Ramón Gómez; Carretero, Juan C.
Rationalizing the Role of NaOtBu in Copper-Catalyzed Carboboration of Alkynes: Assembly of Allylic All-Carbon Quaternary Stereocenters
ACS Catalysis, 2018, 8, 8993
4515515 CIFC21 H22 F N O4P 1 21/c 127.4465; 6.4873; 22.0138
90; 112.954; 90		3609.3Park, Hojoon; Chekshin, Nikita; Shen, Peng-Xiang; Yu, Jin-Quan
Ligand-Enabled, Palladium-Catalyzed β-C(sp<sup>3</sup>)-H Arylation of Weinreb Amides.
ACS catalysis, 2018, 8, 9292-9297
4515516 CIFC41 H51 Co K N6 O11P 21 21 2111.0919; 18.3376; 21.9261
90; 90; 90		4459.7Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515517 CIFC45 H36 K Mn N7 O3P 1 21/n 111.7651; 21.2221; 16.4682
90; 95.468; 90		4093.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515518 CIFC45 H48 N4P -19.1381; 12.0237; 17.8361
96.278; 90.36; 111.214		1813.7Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515519 CIFC50 H55 K Mn N4 O2P 1 21/n 111.527; 13.729; 27.724
90; 92.471; 90		4383.4Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515520 CIFC53 H47.5 F9 K Mn N4.5 O6.5P 1 21/n 112.3883; 18.995; 21.656
90; 101.457; 90		4994.5Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515521 CIFC48 H39 F9 N4 O6P 1 21/c 119.36; 10.0615; 29.486
90; 128.675; 90		4484Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515522 CIFC88 H131 K Mn N4 O7P -113.4244; 15.4608; 21.041
92.203; 93.474; 102.805		4244.6Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515523 CIFC54 H45 F18 K Mn N4 O3P -112.729; 14.584; 16.701
112.045; 92.891; 99.02		2817.9Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515524 CIFC148 H198 Cl0 K4 Mn4 N20 O19P -112.421; 13.222; 24.754
89.65; 77.831; 72.506		3783.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515525 CIFC64.75 H86 K Mn N4 O4P -111.719; 12.417; 21.77
91.221; 100.827; 100.424		3055Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515526 CIFC58 H71 K Mn N4 O4P 1 21/n 112.4818; 21.792; 20.039
90; 105.708; 90		5247.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515527 CIFC32 H29 F9 K Mn N6 O5C 1 c 118.3717; 10.8662; 19.0286
90; 94.307; 90		3788Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515528 CIFC41 H51 Fe K N6 O11P 21 21 2111.1683; 18.406; 21.83
90; 90; 90		4487.5Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515529 CIFC56 H61 Cl6 K Mn N4 O5P 1 21/n 111.391; 20.1796; 24.488
90; 93.742; 90		5617Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515530 CIFC28 H18 Co F9 K N6 O3P 1 21/c 110.696; 18.855; 15.813
90; 101.378; 90		3126.4Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515531 CIFC86 H118 K2 Mn2 N8 O17C 1 2/c 118.8633; 21.7465; 22.5199
90; 102.759; 90		9009.8Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515532 CIFC36 H39 F9 K N7 Ni O6P 1 21/n 19.133; 29.15; 16.125
90; 95.392; 90		4274Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515533 CIFC28 H18 F9 K Mn N6 O3P 1 21/c 110.661; 18.766; 15.752
90; 100.699; 90		3097Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515534 CIFC78 H105 K2 Mn2 N11 O9P -111.759; 13.541; 26.426
86.003; 80.023; 73.719		3977Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515535 CIFC15 H13 N O2P 1 21/c 15.8829; 8.228; 25.846
90; 96.056; 90		1244.08Liu, Chengwei; Li, Guangchen; Shi, Shicheng; Meng, Guangrong; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon‒Nitrogen Bond Cleavage
ACS Catalysis, 2018, 8, 9131
4515536 CIFC30 H27 N2 O4 PP 1 21/c 112.148; 10.6001; 19.4764
90; 96.366; 90		2492.5Meyer, Tjark H.; Oliveira, João C. A.; Sau, Samaresh Chandra; Ang, Nate W. J.; Ackermann, Lutz
Electrooxidative Allene Annulations by Mild Cobalt-Catalyzed C‒H Activation
ACS Catalysis, 2018, 8, 9140
4515537 CIFC25 H20 Cl N O2P 21 21 216.1285; 10.8042; 30.5592
90; 90; 90		2023.43Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang
Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles
ACS Catalysis, 2018, 8, 9543
4515538 CIFC25 H20 Br N O2P 1 21 113.288; 5.6; 14.983
90; 114.29; 90		1016.23Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang
Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles
ACS Catalysis, 2018, 8, 9543
4515539 CIFC88 H44 Mo0.96 O32 S1.92 Zr6P 6/m m m39.254; 39.254; 16.542
90; 90; 120		22074Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T.
Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework
ACS Catalysis, 2018, 8, 9848
4515540 CIFC88 H44 Mo2.24 O36.88 Zr6P 6/m m m39.4657; 39.4657; 16.3953
90; 90; 120		22115.1Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T.
Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework
ACS Catalysis, 2018, 8, 9848
4515541 CIFC28 H26 N4 O7P 21 21 219.0462; 11.8256; 23.9232
90; 90; 90		2559.23Wang, Jilan; Li, Yongjia; Sun, Jun; Wang, Hongling; Jin, Zhichao; Chi, Yonggui Robin
Carbene-Catalyzed Enantioselective Addition of Benzylic Carbon to Unsaturated Acyl Azolium for Rapid Synthesis of Pyrrolo[3,2-c]quinolines
ACS Catalysis, 2018, 8, 9859
4515542 CIFC14 H21 Ge N O3P b c a13.7717; 11.1518; 18.9206
90; 90; 90		2905.81Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin
Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis
ACS Catalysis, 2018, 8, 9287
4515543 CIFC14 H20 Cl Ge N O3P 1 21/n 114.8342; 13.3798; 16.4653
90; 96.777; 90		3245.18Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin
Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis
ACS Catalysis, 2018, 8, 9287
4515544 CIFC54 H60 N2P -18.3369; 9.3962; 14.592
100.111; 103.43; 98.334		1073.8Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka
Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation
ACS Catalysis, 2018, 8, 9408
4515545 CIFC12 H14 F3 N OP c a 218.8458; 14.526; 9.5388
90; 90; 90		1225.7Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka
Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation
ACS Catalysis, 2018, 8, 9408
4515546 CIFC28 H23 N SP 110.1611; 10.3192; 12.2146
73.14; 71.609; 61.296		1051.13Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong
Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction
ACS Catalysis, 2018, 8, 9364
4515547 CIFC28 H23 N SP 110.082; 10.316; 12.247
73.57; 71.546; 61.603		1049.43Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong
Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction
ACS Catalysis, 2018, 8, 9364
4515548 CIFC15 H14 N2 O3P 1 21/c 18.085; 16.9819; 10.0705
90; 110.13; 90		1298.2Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515549 CIFC23 H19 Cl N2 O3 SP 1 21/c 17.0746; 19.195; 15.3264
90; 100.918; 90		2043.6Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515550 CIFC27 H22 N2 O3 SP n a 2133.95; 8.4972; 7.9321
90; 90; 90		2288.3Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515551 CIFC26 H24 N2 O5 SP 1 21/c 112.008; 7.0368; 30.631
90; 92.288; 90		2586.2Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515552 CIFC28 H28 N2 O3 SC 1 2/c 133.457; 7.1395; 20.377
90; 103.524; 90		4732.4Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515553 CIFC24 H22 Cl N3 O2P -19.5004; 11.278; 11.5979
104.256; 109.363; 106.026		1045.71Liu, Bingxian; Li, Jie; Hu, Panjie; Zhou, Xukai; Bai, Dachang; Li, Xingwei
Divergent Annulative C‒C Coupling of Indoles Initiated by Manganese-Catalyzed C‒H Activation
ACS Catalysis, 2018, 8, 9463
4515554 CIFC23 H25 N O2P 1 21 19.356; 10.7541; 9.6715
90; 96.3296; 90		967.17Huang, Liang-Zhu; Xuan, Zi; Jeon, Hyun Ji; Du, Zhen-Ting; Kim, Ju Hyun; Lee, Sang-gi
Asymmetric Rh(II)/Pd(0) Relay Catalysis: Synthesis of α-Quaternary Chiral β-Lactams through Enantioselective C‒H Insertion/Diastereoselective Allylation of Diazoamides
ACS Catalysis, 2018, 8, 7340
4515555 CIFC11 H17 B Cl N OP n a 2119.738; 5.4134; 11.384
90; 90; 90		1216.4Yang, Ji-Min; Zhao, Yu-Tao; Li, Zi-Qi; Gu, Xue-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Gold-Catalyzed Oxidative Coupling of Terminal Alkynes and Borane Adducts: Efficient Synthesis of α-Boryl Ketones
ACS Catalysis, 2018, 8, 7351
4515556 CIFC62 H42 O6 Ru2P -112.7987; 15.0974; 25.8586
104.39; 95.12; 100		4720.16Gusev, Dmitry G.; Spasyuk, Denis M.
Revised Mechanisms for Aldehyde Disproportionation and the Related Reactions of the Shvo Catalyst
ACS Catalysis, 2018, 8, 6851
4515557 CIFC31 H22 O3 RuP 1 21/n 115.7952; 7.4857; 20.8655
90; 100.47; 90		2426.02Gusev, Dmitry G.; Spasyuk, Denis M.
Revised Mechanisms for Aldehyde Disproportionation and the Related Reactions of the Shvo Catalyst
ACS Catalysis, 2018, 8, 6851
4515558 CIFC57 H75 Cl3 Fe3 N6P -112.6922; 13.0313; 16.647
76.0639; 84.1498; 84.0536		2649.46Ferreira, Ricardo B.; Cook, Brian J.; Knight, Brian J.; Catalano, Vincent J.; García-Serres, Ricardo; Murray, Leslie J.
Catalytic Silylation of Dinitrogen by a Family of Triiron Complexes.
ACS catalysis, 2018, 8, 7208-7212
4515559 CIFC21 H18 Mn N5 O4P 1 21/c 113.4325; 11.7346; 13.7646
90; 92.32; 90		2167.87Liu, Tingting; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Manganese-Catalyzed β-Alkylation of Secondary Alcohols with Primary Alcohols under Phosphine-Free Conditions
ACS Catalysis, 2018, 8, 7201
4515560 CIFC21 H26 N2 OP 1 21/c 117.2156; 7.3295; 13.8834
90; 90.807; 90		1751.66Fernández, David F.; Rodrigues, Catarina A. B.; Calvelo, Martín; Gulías, Moisés; Mascareñas, José L.; López, Fernando
Iridium(I)-Catalyzed Intramolecular Cycloisomerization of Enynes: Scope and Mechanistic Course
ACS Catalysis, 2018, 8, 7397
4515561 CIFC22 H23 N O2P 1 21/c 112.2561; 9.8925; 15.8384
90; 110.254; 90		1801.6Fernández, David F.; Rodrigues, Catarina A. B.; Calvelo, Martín; Gulías, Moisés; Mascareñas, José L.; López, Fernando
Iridium(I)-Catalyzed Intramolecular Cycloisomerization of Enynes: Scope and Mechanistic Course
ACS Catalysis, 2018, 8, 7397
4515562 CIFC37 H46 Cu N3P 1 21/n 112.411; 12.765; 21.416
90; 95.043; 90		3379.7Nakamura, Kimiaki; Hara, Reina; Sunada, Yusuke; Nishikata, Takashi
Radical-Organometallic Hybrid Reaction System Enabling Couplings between Tertiary-Alkyl Groups and 1-Alkenyl Groups
ACS Catalysis, 2018, 8, 6791
4515563 CIFC26 H24 Cu N4 O7 S2P b c a17.7588; 13.939; 20.7682
90; 90; 90		5140.96Hardouin Duparc, Valérie; Bano, Guillaume L.; Schaper, Frank
Chan‒Evans‒Lam Couplings with Copper Iminoarylsulfonate Complexes: Scope and Mechanism
ACS Catalysis, 2018, 8, 7308
4515564 CIFC14 H13 Cu F3 N2 O7 S2P -17.9814; 11.0894; 11.102
96.461; 100.176; 110.007		892.77Hardouin Duparc, Valérie; Bano, Guillaume L.; Schaper, Frank
Chan‒Evans‒Lam Couplings with Copper Iminoarylsulfonate Complexes: Scope and Mechanism
ACS Catalysis, 2018, 8, 7308
4515565 CIFC14 H14 O3P c a 2111.7373; 4.431; 21.078
90; 90; 90		1096.2Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515566 CIFC14 H14 O3P c c n6.6399; 17.0733; 19.2759
90; 90; 90		2185.2Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515567 CIFC15 H18 O2P 1 21/c 114.435; 5.4011; 16.2501
90; 104.851; 90		1224.62Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515568 CIFC15 H20 O2P 1 21 19.1834; 5.2643; 13.7823
90; 107.711; 90		634.72Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515569 CIFC42 H70 Ce N7 O8P -110.5305; 11.181; 20.761
101.915; 91.944; 94.462		2381.4Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515570 CIFC32 H51 Ce N6 O8P -111.5006; 17.4646; 20.0865
67.599; 80.635; 78.648		3639.9Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515571 CIFC49 H66 Ce2 N11 O17C 1 2/c 122.935; 19.6202; 13.5095
90; 114.142; 90		5547.4Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515572 CIFC124 H174 Ce4 N21 O32C 1 2/c 115.263; 27.226; 17.096
90; 96.089; 90		7064Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515573 CIFC68 H102 Ce2 N8 O11C 1 2/c 127.711; 19.4594; 15.5984
90; 122.044; 90		7129.7Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515574 CIFC34 H30 N2 O4P 1 21/c 113.746; 11.435; 18.615
90; 110.457; 90		2741.5Usui, Kenji; Haines, Brandon E.; Musaev, Djamaladdin G.; Sarpong, Richmond
Understanding Regiodivergence in a Pd(II)-Mediated Site-Selective C‒H Alkynylation
ACS Catalysis, 2018, 8, 4516
4515575 CIFC25 H25 N3 O PdP 1 21/n 112.551; 9.9456; 17.6307
90; 106.171; 90		2113.72Usui, Kenji; Haines, Brandon E.; Musaev, Djamaladdin G.; Sarpong, Richmond
Understanding Regiodivergence in a Pd(II)-Mediated Site-Selective C‒H Alkynylation
ACS Catalysis, 2018, 8, 4516
4515576 CIFC19 H17 Cl OP 21 21 215.612; 7.5305; 37.033
90; 90; 90		1565.1Teng, Huai-Long; Ma, Yuanhong; Zhan, Gu; Nishiura, Masayoshi; Hou, Zhaomin
Asymmetric C(sp)‒H Addition of Terminal Alkynes to Cyclopropenes by a Chiral Gadolinium Catalyst
ACS Catalysis, 2018, 8, 4705
4515577 CIFC21 H49 N O3 P2 RuP 1 21/n 113.2573; 13.3386; 15.3535
90; 92.948; 90		2711.4Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515578 CIFC51 H125 N3 O10 P6 Ru3P -115.1793; 16.5074; 16.664
88.609; 71.881; 62.825		3496Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515579 CIFC19 H41 N O3 P2 RuP b c a14.17; 15.3918; 21.741
90; 90; 90		4741.8Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515580 CIFC19 H35 Cl2 Mn N P2P 1 21/c 112.4393; 11.9755; 15.9077
90; 91.637; 90		2368.8Brzozowska, Aleksandra; Azofra, Luis Miguel; Zubar, Viktoriia; Atodiresei, Iuliana; Cavallo, Luigi; Rueping, Magnus; El-Sepelgy, Osama
Highly Chemo- and Stereoselective Transfer Semihydrogenation of Alkynes Catalyzed by a Stable, Well-Defined Manganese(II) Complex
ACS Catalysis, 2018, 8, 4103
4515581 CIFC7 H9 Co O5 PP 1 21/n 14.8553; 32.281; 5.6773
90; 91.788; 90		889.39Cai, Zhong-Sheng; Shi, Yi; Bao, Song-Song; Shen, Yang; Xia, Xing-Hua; Zheng, Li-Min
Bioinspired Engineering of Cobalt-Phosphonate Nanosheets for Robust Hydrogen Evolution Reaction
ACS Catalysis, 2018, 8, 3895
4515582 CIFC25 H40 N3 O2 P2 ReP 21 21 2110.1881; 13.7426; 20.6392
90; 90; 90		2889.7Glatz, Mathias; Stöger, Berthold; Himmelbauer, Daniel; Veiros, Luis F.; Kirchner, Karl
Chemoselective Hydrogenation of Aldehydes under Mild, Base-Free Conditions: Manganese Outperforms Rhenium.
ACS catalysis, 2018, 8, 4009-4016
4515583 CIFC72 H87 B N3 O2 YP 1 21/n 112.047; 17.64; 32.956
90; 96.116; 90		6964Yu, Xiaying; You, Qing; Zhou, Xigeng; Zhang, Lixin
Isoprene Regioblock Copolymerization: Switching the Regioselectivity by the in Situ Ancillary Ligand Transmetalation of Active Yttrium Species
ACS Catalysis, 2018, 8, 4465
4515584 CIFC12 H6 In0.54 N O2.25C m m m7.0996; 33.5115; 16.7335
90; 90; 90		3981.2Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515585 CIFC12 H6 In0.75 N O2.73C m m m7.125; 33.622; 16.583
90; 90; 90		3972.57Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515586 CIFC48 H24 In2 N4 Ni O10C m m m7.0725; 33.2883; 16.666
90; 90; 90		3923.7Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515587 CIFC26 H28 F6 Mn N4 O6 S2P 4318.28107; 18.28107; 36.923
90; 90; 90		12339.6Du, Junyi; Miao, Chengxia; Xia, Chungu; Lee, Yong-Min; Nam, Wonwoo; Sun, Wei
Mechanistic Insights into the Enantioselective Epoxidation of Olefins by Bioinspired Manganese Complexes: Role of Carboxylic Acid and Nature of Active Oxidant
ACS Catalysis, 2018, 8, 4528
4515588 CIFC28 H24 B F12 PP -113.414; 13.786; 18.1493
101.69; 106.173; 109.985		2859.7Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515589 CIFC28 H26 B F12 PP 1 21/n 110.6496; 15.3406; 18.042
90; 95.278; 90		2935Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515590 CIFC28 H27 B2 F12 PP -111.7104; 12.4425; 12.4488
71.092; 69.578; 64.329		1499.65Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515591 CIFC72 H94 Co2 N6P 1 21/n 111.1904; 12.5885; 22.6178
90; 99.722; 90		3140.42Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515592 CIFC31 H48 Co N2 O SiP 1 21/n 117.0369; 10.7343; 17.0418
90; 93.483; 90		3110.83Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515593 CIFC31 H45 Cl2 Co Li N2 O2P 41 21 212.0633; 12.0633; 21.8421
90; 90; 90		3178.53Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515594 CIFC39 H49 N3 O Si ZnP 1 21/n 18.8505; 21.914; 19.0059
90; 100.646; 90		3622.7Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515595 CIFC22.5 H38.5 N3 ZnP 1 21/c 114.8856; 21.731; 16.0804
90; 113.482; 90		4770.9Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515596 CIFC22 H35 N3 O2 ZnP 1 21/c 123.041; 10.016; 22.532
90; 117.531; 90		4611Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515597 CIFC50 H86 N6 Zn2C 1 2/c 121.7365; 14.2049; 20.3579
90; 102.81; 90		6129.4Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515598 CIFC55 H93 N6 O4 Zn2P -112.7688; 13.881; 17.4955
76.808; 73.779; 84.324		2896.9Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515599 CIFC51 H86 N6 O2 Zn2P -116.1366; 16.5978; 23.3164
98.9; 90.984; 119.052		5362.53Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515600 CIFC60 H84 N4 O4 Zn2P -113.4707; 14.5272; 16.2991
88.145; 89.86; 65.496		2900.6Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515601 CIFC10 H12 Fe N11 OP 1 21/n 110.82; 12.675; 11.662
90; 106.559; 90		1533Shen, Shou-Jie; Zhu, Cheng-Liang; Lu, Deng-Fu; Xu, Hao
Iron-Catalyzed Direct Olefin Diazidation via Peroxyester Activation Promoted by Nitrogen-Based Ligands.
ACS catalysis, 2018, 8, 4473-4482
4515602 CIFC44 H54 N4 NiP 21 21 2110.1006; 18.0014; 42.163
90; 90; 90		7666.3Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515603 CIFC110 H136 Cl3 N9 Ni3P 1 21/c 126.6781; 16.5463; 22.7174
90; 90.462; 90		10027.7Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515604 CIFC64 H80 Cl2 N6 Ni2P 21 21 2112.855; 21.217; 24.26
90; 90; 90		6617Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515605 CIFC43 H56 Cl N3 NiC 1 2/c 127.4949; 19.0191; 16.9558
90; 108.589; 90		8404.1Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515606 CIFC22 H37 Ir N PP 21 21 2110.5276; 10.7464; 18.567
90; 90; 90		2100.6Cherepakhin, Valeriy; Williams, Travis J.
Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.
ACS catalysis, 2018, 8, 3754-3763
4515607 CIFC29 H48 Ir2 N2 O P2P 1 21/c 114.836; 15.464; 15.385
90; 114.159; 90		3220.5Cherepakhin, Valeriy; Williams, Travis J.
Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.
ACS catalysis, 2018, 8, 3754-3763
4515608 CIFC34 H26 F6 N6 O9 P Ru2P 1 21/c 113.8587; 23.8714; 12.5805
90; 115.201; 90		3765.8Daniel, Quentin; Duan, Lele; Timmer, Brian J. J.; Chen, Hong; Luo, Xiaodan; Ambre, Ram; Wang, Ying; Zhang, Biaobiao; Zhang, Peili; Wang, Lei; Li, Fusheng; Sun, Junliang; Ahlquist, Mårten; Sun, Licheng
Water Oxidation Initiated by In Situ Dimerization of the Molecular Ru(pdc) Catalyst
ACS Catalysis, 2018, 8, 4375
4515609 CIFC21 H23 Br N OP -18.6881; 9.8467; 11.0731
94.586; 91.58; 105.361		909.36Bai, Dachang; Xu, Teng; Ma, Chaorui; Zheng, Xin; Liu, Bingxian; Xie, Fang; Li, Xingwei
Rh(III)-Catalyzed Mild Coupling of Nitrones and Azomethine Imines with Alkylidenecyclopropanes via C‒H Activation: Facile Access to Bridged Cycles
ACS Catalysis, 2018, 8, 4194
4515610 CIFC8 H7 Cl O3P n a 2114.4042; 3.8522; 14.6641
90; 90; 90		813.68Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515611 CIFC25 H25 Cl O4P 1 21 110.936; 6.5014; 14.9916
90; 95.8987; 90		1060.25Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515612 CIFC6 H3 Br Cl I OP 1 21 17.2559; 4.5474; 13.321
90; 100.781; 90		431.77Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515613 CIFC12 H8 Cl2 O2P b c n6.3191; 15.8114; 21.7404
90; 90; 90		2172.17Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515614 CIFC8 H7 Cl O2P 1 21/c 16.7838; 16.4432; 7.2539
90; 108.069; 90		769.25Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515615 CIFC25 H21 Cl O3C 1 2/c 113.6694; 14.6546; 21.7416
90; 104.277; 90		4220.76Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515616 CIFC8 H6 Br Cl O3P 1 21/c 14.1058; 17.9301; 12.4296
90; 93.138; 90		913.66Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515617 CIFC12 H8 F2 O SeP -15.6425; 9.1159; 11.1839
106.666; 102.943; 93.95		531.61Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515618 CIFC7 H4 Br Cl O2P 1 21/n 17.7896; 13.5178; 15.0171
90; 101.499; 90		1549.54Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515619 CIFC19 H17 Cl O3P 1 21 19.6791; 7.1917; 12.2628
90; 107.906; 90		812.26Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515620 CIFC12 H9 Cl OP 1 21/n 15.7829; 20.3532; 8.3091
90; 97.502; 90		969.61Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515621 CIFC12 H16 B Cl O3I -419.7094; 19.7094; 6.8557
90; 90; 90		2663.2Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515622 CIFC6 H4 Br Cl OP 21 21 215.2204; 11.214; 11.717
90; 90; 90		685.9Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515623 CIFC12 H10 Br2 Cl2 O4C 1 2/c 132.7811; 3.926; 21.7084
90; 91.5018; 90		2792.9Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515624 CIFC48 H38 B Cl2 F27 Fe N4 O3 SP -112.695; 13.3351; 17.1823
102.363; 97.011; 92.487		2812.8Postils, Verònica; Rodríguez, Mònica; Sabenya, Gerard; Conde, Ana; Díaz-Requejo, M. Mar; Pérez, Pedro J.; Costas, Miquel; Solà, Miquel; Luis, Josep M.
Mechanism of the Selective Fe-Catalyzed Arene Carbon‒Hydrogen Bond Functionalization
ACS Catalysis, 2018, 8, 4313
4515625 CIFC26 H36 O4 SP 1 21 19.0489; 8.4426; 15.648
90; 94.577; 90		1191.6Yu, Fei-Le; Bai, Da-Chang; Liu, Xiu-Yan; Jiang, Yang-Jie; Ding, Chang-Hua; Hou, Xue-Long
Pd-Catalyzed Allylic Alkylation of gem-Alkyl,Aryl-Disubstituted Allyl Reagents with Ketones: Diastereoselective Construction of Vicinal Tertiary and Quaternary Carbon Centers
ACS Catalysis, 2018, 8, 3317
4515626 CIFC16 H20 OP 1 21/c 18.6633; 8.4114; 17.9313
90; 99.6888; 90		1288Yu, Fei-Le; Bai, Da-Chang; Liu, Xiu-Yan; Jiang, Yang-Jie; Ding, Chang-Hua; Hou, Xue-Long
Pd-Catalyzed Allylic Alkylation of gem-Alkyl,Aryl-Disubstituted Allyl Reagents with Ketones: Diastereoselective Construction of Vicinal Tertiary and Quaternary Carbon Centers
ACS Catalysis, 2018, 8, 3317
4515627 CIFC21 H21 N3 O3 SP -16.3615; 10.4427; 15.1313
85.229; 87.86; 76.106		972.24Guin, Srimanta; Deb, Arghya; Dolui, Pravas; Chakraborty, Souvik; Singh, Vikas Kumar; Maiti, Debabrata
Promoting Highly Diastereoselective γ-C‒H Chalcogenation of α-Amino Acids and Aliphatic Carboxylic Acids
ACS Catalysis, 2018, 8, 2664
4515628 CIFC16 H20 O5P 21 21 218.793; 10.1042; 16.0484
90; 90; 90		1425.8Biosca, Maria; Margalef, Jèssica; Caldentey, Xisco; Besora, Maria; Rodríguez-Escrich, Carles; Saltó, Joan; Cambeiro, Xacobe C.; Maseras, Feliu; Pàmies, Oscar; Diéguez, Montserrat; Pericàs, Miquel A.
Computationally Guided Design of a Readily Assembled Phosphite‒Thioether Ligand for a Broad Range of Pd-Catalyzed Asymmetric Allylic Substitutions
ACS Catalysis, 2018, 8, 3587
4515629 CIFC13 H15 B F3 KP 19.0823; 10.0446; 16.7815
72.627; 75.846; 89.976		1412.38Gao, De-Wei; Xiao, Yiyang; Liu, Mingyu; Liu, Zhen; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Catalytic, Enantioselective Synthesis of Allenyl Boronates.
ACS catalysis, 2018, 8, 3650-3654
4515630 CIFC14 H13 N O4P 21 21 216.6275; 8.0167; 22.6419
90; 90; 90		1202.98Brandenberg, Oliver F.; Prier, Christopher K.; Chen, Kai; Knight, Anders M.; Wu, Zachary; Arnold, Frances H.
Stereoselective Enzymatic Synthesis of Heteroatom-Substituted Cyclopropanes
ACS Catalysis, 2018, 8, 2629
4515631 CIFC70 H110 Cl2 Co2 N4 P4P 1 21/n 110.4784; 22.1575; 15.6461
90; 105.074; 90		3507.6Suzuki, Tatsuya; Fujimoto, Keisuke; Takemoto, Yoshiyuki; Wasada-Tsutsui, Yuko; Ozawa, Tomohiro; Inomata, Tomohiko; Fryzuk, Michael D.; Masuda, Hideki
Efficient Catalytic Conversion of Dinitrogen to N(SiMe3)3 Using a Homogeneous Mononuclear Cobalt Complex
ACS Catalysis, 2018, 8, 3011
4515632 CIFC70 H110 Co2 N4 P4P 1 21/c 110.7673; 29.054; 12.6363
90; 117.372; 90		3510.5Suzuki, Tatsuya; Fujimoto, Keisuke; Takemoto, Yoshiyuki; Wasada-Tsutsui, Yuko; Ozawa, Tomohiro; Inomata, Tomohiko; Fryzuk, Michael D.; Masuda, Hideki
Efficient Catalytic Conversion of Dinitrogen to N(SiMe3)3 Using a Homogeneous Mononuclear Cobalt Complex
ACS Catalysis, 2018, 8, 3011
4515633 CIFC23 H34 N6 O3 SP 1 21 19.2161; 12.7576; 10.9094
90; 95.835; 90		1276.03Nicholls, Rachel L.; McManus, James A.; Rayner, Christopher M.; Morales-Serna, José A.; White, Andrew J. P.; Nguyen, Bao N.
Guanidine-Catalyzed Reductive Amination of Carbon Dioxide with Silanes: Switching between Pathways and Suppressing Catalyst Deactivation
ACS Catalysis, 2018, 8, 3678
4515634 CIFC23 H16 O2C 1 2/c 115.5099; 7.5217; 28.568
90; 99.09; 90		3290.9Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V.
Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes
ACS Catalysis, 2018, 8, 2748
4515635 CIFC15 H22 Br N OP 1 21 17.5964; 16.0907; 12.1098
90; 99.736; 90		1458.88Liu, Ze-Shui; Qian, Guangyin; Gao, Qianwen; Wang, Peng; Cheng, Hong-Gang; Wei, Qiang; Liu, Qi; Zhou, Qianghui
Palladium/Norbornene Cooperative Catalysis To Access Tetrahydronaphthalenes and Indanes with a Quaternary Center
ACS Catalysis, 2018, 8, 4783
4515636 CIFC29 H30 O5P 1 21/n 110.573; 16.555; 14.695
90; 104.784; 90		2487Liu, Ze-Shui; Qian, Guangyin; Gao, Qianwen; Wang, Peng; Cheng, Hong-Gang; Wei, Qiang; Liu, Qi; Zhou, Qianghui
Palladium/Norbornene Cooperative Catalysis To Access Tetrahydronaphthalenes and Indanes with a Quaternary Center
ACS Catalysis, 2018, 8, 4783
4515637 CIFC13 H17 N O5 SP 1 21/n 15.923; 16.864; 14.255
90; 92.357; 90		1422.7Kishi, Kenta; Takizawa, Shinobu; Sasai, Hiroaki
Phosphine-Catalyzed Dual Umpolung Domino Michael Reaction: Facile Synthesis of Hydroindole- and Hydrobenzofuran-2-Carboxylates
ACS Catalysis, 2018, 8, 5228
4515638 CIFC37 H47 Mo N3 OP 1 21/n 115.8128; 13.0267; 16.0929
90; 98.231; 90		3280.8Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515639 CIFC47 H60 Mo N5 OF d d 232.0833; 33.7453; 17.8428
90; 90; 90		19317.7Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515640 CIFC41 H65 Mo N3 Si2P 1 21/c 111.264; 17.5505; 23.2268
90; 115.23; 90		4153.65Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515641 CIFC41 H50 Cl6 N P PdP 21 21 2113.8095; 15.6122; 19.5369
90; 90; 90		4212.1Ding, Linlin; Sui, Xianwei; Gu, Zhenhua
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
ACS Catalysis, 2018, 8, 5630
4515642 CIFC25.5 H15 Cl5 O3P 1 21 111.39996; 31.0942; 19.9369
90; 96.7204; 90		7018.53Ding, Linlin; Sui, Xianwei; Gu, Zhenhua
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
ACS Catalysis, 2018, 8, 5630
4515643 CIFC29 H34 Cl N O5P 1 21 18.4142; 14.046; 11.3304
90; 104.324; 90		1297.5Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515644 CIFC21 H27 N O5P 1 21/c 112.432; 11.174; 14.1728
90; 96.117; 90		1957.6Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515645 CIFC21 H27 N O5P 1 21/c 18.3767; 12.1262; 39.035
90; 93.093; 90		3959.3Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515646 CIFC39 H38 Br N O Si2P 21 21 219.6879; 9.8487; 34.927
90; 90; 90		3332.5Meng, Fei-Fan; Xie, Jia-Hao; Xu, Yun-He; Loh, Teck-Peng
Catalytically Asymmetric Synthesis of 1,3-Bis(silyl)propenes via Copper-Catalyzed Double Proto-Silylations of Polar Enynes
ACS Catalysis, 2018, 8, 5306
4515647 CIFC15 H21 N O2 SP 1 21/c 116.125; 6.8205; 13.1663
90; 96.287; 90		1439.33Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515648 CIFC30 H42 N2 O4 S2P 1 21/n 119.6621; 8.3363; 19.9464
90; 112.146; 90		3028.2Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515649 CIFC30 H42 N2 O4 S2P n a 2132.802; 8.4124; 10.9145
90; 90; 90		3011.8Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515650 CIFC13 H17 N O2 SP 1 21/n 17.851; 10.524; 15.813
90; 98.263; 90		1293Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515651 CIFC16 H25 O2 PP 1 21 18.589; 5.946; 15.333
90; 100.966; 90		768.8Smaligo, Andrew J.; Vardhineedi, Sriramurthy; Kwon, Ohyun
Carvone-Derived P-Stereogenic Phosphines: Design, Synthesis, and Use in Allene-Imine [3 + 2] Annulation.
ACS catalysis, 2018, 8, 5188-5192
4515652 CIFC16 H23 O3 PP 1 21 110.2543; 10.9798; 13.7645
90; 90.59; 90		1549.67Smaligo, Andrew J.; Vardhineedi, Sriramurthy; Kwon, Ohyun
Carvone-Derived P-Stereogenic Phosphines: Design, Synthesis, and Use in Allene-Imine [3 + 2] Annulation.
ACS catalysis, 2018, 8, 5188-5192
4515653 CIFC25 H18 Cl F3 O2 SP 21 21 217.8069; 7.8369; 35.3156
90; 90; 90		2160.68Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L.
Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.
ACS catalysis, 2018, 8, 5443-5447
4515654 CIFC26 H21 F3 O2 SP 1 21 17.7702; 7.7862; 17.9926
90; 100.144; 90		1071.54Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L.
Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.
ACS catalysis, 2018, 8, 5443-5447
4515655 CIFC23.7 H15 Cl2.1 D0.7 F3 O4 SP 21 21 219.3182; 10.5061; 24.8751
90; 90; 90		2435.2Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L.
Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.
ACS catalysis, 2018, 8, 5443-5447
4515656 CIFC21 H20 N2 O3P 1 21/n 113.218; 8.696; 16.546
90; 98.483; 90		1881.1Pang, Shuai; Yang, Xing; Cao, Ze-Hun; Zhang, Yu-Long; Zhao, Yan; Huang, Yi-Yong
Intermolecular [2 + 2] Cycloaddition/Isomerization of Allenyl Imides and Unactivated Imines for the Synthesis of 1-Azadienes Catalyzed by a Ni(ClO4)2·6H2O Lewis Acid
ACS Catalysis, 2018, 8, 5193
4515657 CIFC22 H22 N2 O4P 1 21/n 110.559; 8.848; 20.03
90; 91.424; 90		1870.7Pang, Shuai; Yang, Xing; Cao, Ze-Hun; Zhang, Yu-Long; Zhao, Yan; Huang, Yi-Yong
Intermolecular [2 + 2] Cycloaddition/Isomerization of Allenyl Imides and Unactivated Imines for the Synthesis of 1-Azadienes Catalyzed by a Ni(ClO4)2·6H2O Lewis Acid
ACS Catalysis, 2018, 8, 5193
4515658 CIFC16 H21 Cl2 Fe N9 O2P n a 2113.7551; 18.856; 8.4263
90; 90; 90		2185.5Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515659 CIFC15 H19 F3 N2 O4 SP -17.6537; 10.3038; 11.7
69.471; 74.774; 75.983		822.2Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515660 CIFC18 H22 Cl3 F3 N2 O4 SP 21 21 216.1287; 17.2349; 21.6302
90; 90; 90		2284.74Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515661 CIFC14 H22 F3 N O2P 1 21/c 111.8893; 5.2263; 24.518
90; 96.137; 90		1514.75Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515662 CIFC16 H26 F3 N O2P 21 21 2111.579; 16.9733; 18.2465
90; 90; 90		3586.05Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515663 CIFC19 H25 F3 N2 O4P 1 21/c 114.9198; 13.8571; 9.9498
90; 95.4351; 90		2047.82Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao
Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis.
ACS catalysis, 2018, 8, 5032-5037
4515664 CIFC17 H39 As Co K2 Mo6 N O39.5P -112.0872; 12.5682; 17.2255
76.7; 74.058; 76.399		2407Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515665 CIFC17 H44 As K2 Mo6 N Ni O42P -111.9612; 12.5318; 17.1943
76.499; 74.053; 76.535		2370.12Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515666 CIFC17 H40 As K2 Mo6 N O41 ZnP -112.1425; 12.5739; 17.2226
76.443; 74.062; 76.225		2415.16Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515667 CIFC17 H39 As K2 Mn Mo6 N O40P -112.2865; 12.6065; 17.2145
76.319; 73.933; 76.064		2445.2Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515668 CIFC18 H87 As2 Co0.5 K3 Mo12 N6 Na O77.5P -116.1055; 18.5246; 19.0707
75.701; 65.877; 64.845		4681.8Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515669 CIFC21 H44 As Co0.5 K5 Mo6 O44.5P -112.6575; 12.671; 18.5916
105.723; 91.318; 106.19		2740.7Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen
Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands
ACS Catalysis, 2018, 8, 6062
4515670 CIFC47.5 H70 N2 Ni O8P -111.54858; 30.1957; 32.8403
64.8392; 80.3426; 86.1838		10218.4Nett, Alex J.; Cañellas, Santiago; Higuchi, Yuki; Robo, Michael T.; Kochkodan, Jeanne M.; Haynes, 2nd, M Taylor; Kampf, Jeff W.; Montgomery, John
Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation.
ACS catalysis, 2018, 8, 6606-6611
4515671 CIFC97 H92 N2 Ni O8.5P -114.0561; 14.806; 22.1265
93.854; 102.679; 118.29		3876.59Nett, Alex J.; Cañellas, Santiago; Higuchi, Yuki; Robo, Michael T.; Kochkodan, Jeanne M.; Haynes, 2nd, M Taylor; Kampf, Jeff W.; Montgomery, John
Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation.
ACS catalysis, 2018, 8, 6606-6611
4515672 CIFC27 H22 N2 O3C 1 2/c 114.2005; 10.38306; 28.0529
90; 102.226; 90		4042.44Rej, Supriya; Chatani, Naoto
Rhodium(I)-Catalyzed C8-Alkylation of 1-Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System
ACS Catalysis, 2018, 8, 6699
4515673 CIFC27 H36 I4 N2 SP -110.6361; 16.8158; 19.6467
91.7164; 105.424; 93.774		3375.9Horibe, Takahiro; Tsuji, Yasutaka; Ishihara, Kazuaki
Thiourea‒I2 as Lewis Base‒Lewis Acid Cooperative Catalysts for Iodochlorination of Alkene with In Situ-Generated I‒Cl
ACS Catalysis, 2018, 8, 6362
4515674 CIFC27 H36 Cl I3 N2 SP 1 21/n 110.689; 18.743; 16.225
90; 102.555; 90		3172.9Horibe, Takahiro; Tsuji, Yasutaka; Ishihara, Kazuaki
Thiourea‒I2 as Lewis Base‒Lewis Acid Cooperative Catalysts for Iodochlorination of Alkene with In Situ-Generated I‒Cl
ACS Catalysis, 2018, 8, 6362
4515675 CIFC17 H20 O7P c a 2112.9176; 15.173; 16.7769
90; 90; 90		3288.25Shu, Wei; Merino, Estíbaliz; Nevado, Cristina
Visible Light Mediated, Redox Neutral Remote 1,6-Difunctionalizations of Alkenes
ACS Catalysis, 2018, 8, 6401
4515676 CIFC27 H39 N2 Sc Si2P 1 21/c 116.7493; 17.9477; 9.7237
90; 105.053; 90		2822.8Li, Shihui; Liu, Dongtao; Wang, Zichuan; Cui, Dongmei
Development of Group 3 Catalysts for Alternating Copolymerization of Ethylene and Styrene Derivatives
ACS Catalysis, 2018, 8, 6086
4515677 CIFC33 H41 N3 O3P -111.5304; 11.8994; 12.6132
107.862; 96.62; 114.133		1444.35Li, Zhenghua; Song, Liangliang; Van Meervelt, Luc; Tian, Guilong; Van der Eycken, Erik V.
Cationic Gold(I)-Catalyzed Cascade Bicyclizations for Divergent Synthesis of (Spiro)polyheterocycles
ACS Catalysis, 2018, 8, 6388
4515678 CIFC21 H22 N2 O2 SP 21 21 219.2626; 11.273; 36.0958
90; 90; 90		3769Rigotti, Thomas; Casado-Sánchez, Antonio; Cabrera, Silvia; Pérez-Ruiz, Raúl; Liras, Marta; de la Peña O’Shea, Víctor A.; Alemán, José
A Bifunctional Photoaminocatalyst for the Alkylation of Aldehydes: Design, Analysis, and Mechanistic Studies
ACS Catalysis, 2018, 8, 5928
4515679 CIFC24 H20 N2 O2 SP 1 21 17.3859; 14.0495; 19.8207
90; 95.797; 90		2046.24Rigotti, Thomas; Casado-Sánchez, Antonio; Cabrera, Silvia; Pérez-Ruiz, Raúl; Liras, Marta; de la Peña O’Shea, Víctor A.; Alemán, José
A Bifunctional Photoaminocatalyst for the Alkylation of Aldehydes: Design, Analysis, and Mechanistic Studies
ACS Catalysis, 2018, 8, 5928
4515680 CIFC22 H17 N3 O2P 1 21/c 16.0252; 14.9032; 19.2088
90; 93.713; 90		1721.23Zhai, Shengxian; Qiu, Shuxian; Chen, Xiaoming; Tao, Cheng; Li, Yun; Cheng, Bin; Wang, Huifei; Zhai, Hongbin
Trifunctionalization of Allenes via Cobalt-Catalyzed MHP-Assisted C‒H Bond Functionalization and Molecular Oxygen Activation
ACS Catalysis, 2018, 8, 6645
4515681 CIFC38 H22 Cl2C 1 2/c 115.8675; 11.3225; 16.9255
90; 116.905; 90		2711.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515682 CIFC40 H26 Cl2C 1 2/c 116.6618; 12.3936; 16.076
90; 119.312; 90		2894.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515683 CIFC45 H54 OP -113.048; 15.9745; 20.3351
69.8393; 74.7061; 79.3386		3817.17Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515684 CIFC115 H108 Cl2 F36 N6 O8 P2 Sb2P 4 21 223.156; 23.156; 45.3164
90; 90; 90		24298.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515685 CIFC40 H28C 1 2/c 124.6931; 9.8945; 11.3008
90; 107.002; 90		2640.4Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515686 CIFC57 H53 Au Cl F18 N3 O4 P SbP 21 21 2111.625; 21.7951; 24.924
90; 90; 90		6314.9Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515687 CIFC85 H148 Au4 Cl4 F24 N4 O10 P4 S2 Sb4P -114.1224; 14.3201; 16.3265
111.05; 108.05; 90.835		2900.2Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515688 CIFC42 H50 Cl2 F6 N2 O4 P SbP 21 21 2114.5593; 16.985; 18.089
90; 90; 90		4473.2Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515689 CIFC64 H59 Cl2 F18 N3 O4 P SbP 1 21 111.2724; 25.712; 22.718
90; 98.349; 90		6514.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515690 CIFC28 H18 Br2P 21 21 216.7543; 9.853; 31.4363
90; 90; 90		2092.09Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515691 CIFC63 H59 Au Cl3 F18 N3 O4 P SbP 1 21 111.5608; 22.3675; 14.1582
90; 95.008; 90		3647.1Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515692 CIFC56 H48 Au Cl5 F18 N2 O4 P SbP 21 21 2111.8911; 20.269; 26.818
90; 90; 90		6463.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515693 CIFC40 H25.94 Cl2.06P 1 21/c 117.9011; 8.3634; 19.4197
90; 90.871; 90		2907.1Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515694 CIFC21 H25 N3P -18.0652; 8.3219; 14.129
77.347; 83.454; 80.93		910.59Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515695 CIFC23 H21 N OP -111.8311; 12.7714; 12.7734
69.209; 81.613; 86.471		1785Li, Deng-Yuan; Liu, Shuo; Chen, Shuang; Wang, An; Zhu, Xiao-Ping; Liu, Pei-Nian
Dual Role of Aryl Iodide in Cascade C‒H Arylation/Amination: Arylation Reagent and Cocatalyst for C‒N Formation
ACS Catalysis, 2018, 8, 6407
4515696 CIFC20 H26 N O4 ZnP 1 21/n 110.811; 16.451; 11.445
90; 101.668; 90		1993.5Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515697 CIFC28 H47 Ni O4 PP -110.2938; 16.839; 17.23
73.123; 78.321; 87.036		2798.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515698 CIFC13 H22 B N O2P 1 21/n 17.204; 34.935; 11.091
90; 92.218; 90		2789Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515699 CIFC24 H32 N2 Ni O4P -17.96; 8.085; 9.656
108.25; 93.812; 94.208		585.9Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515700 CIFC25 H41 Ni O4 PP -110.001; 10.415; 13.862
76.659; 77.984; 62.798		1240.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515701 CIFC22 H22 F6 N2 Ni O4P -16.3927; 8.606; 10.965
86.398; 79.115; 86.957		590.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515702 CIFC24 H28 N2 Ni O8P -16.736; 8.129; 11.969
101.952; 99.095; 99.806		619Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515703 CIFC24 H20 N2 O6 PdP -18.78; 10; 13.272
101.969; 98.6857; 103.084		1086.1Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515704 CIFC22 H17 I N2 O4 PdP 1 21/c 17.939; 16.611; 16.219
90; 93.262; 90		2135.4Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515705 CIFC20 H18 O8C 1 2/c 118.828; 8.059; 12.153
90; 91.24; 90		1844Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515706 CIFC21 H18 Br2P 1 21/c 17.258; 18.732; 12.399
90; 93.746; 90		1682.1Su, Xiang; Chen, Bifeng; Wang, Shaohong; Chen, Hui; Chen, Chao
Atom- and Step-Efficient Construction of Five-Membered Carbocycles with Alkenes and Alkynes Catalyzed by AgSbF6
ACS Catalysis, 2018, 8, 7760
4515707 CIFC17 H15 N O5C 1 2 121.4471; 6.4084; 12.069
90; 113.464; 90		1521.62Li, Kaizhi; Jin, Zhichao; Chan, Wai-Lun; Lu, Yixin
Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut‒Currier Reactions Catalyzed by Thiourea-Phosphines
ACS Catalysis, 2018, 8, 8810
4515708 CIFC19 H17 Br O3P 21 21 218.8312; 11.2095; 16.7904
90; 90; 90		1662.14Li, Kaizhi; Jin, Zhichao; Chan, Wai-Lun; Lu, Yixin
Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut‒Currier Reactions Catalyzed by Thiourea-Phosphines
ACS Catalysis, 2018, 8, 8810
4515709 CIFC17 H12 N2 O4P 1 21/c 16.8554; 18.0992; 11.1588
90; 92.472; 90		1383.26Chen, Fei; Lai, Sheng-Qiang; Zhu, Fei-Fei; Meng, Qiang; Jiang, Yu; Yu, Wei; Han, Bing
Cu-Catalyzed Radical Cascade Annulations of Alkyne-Tethered N-Alkoxyamides with Air: Facile Access to Isoxazolidine/1,2-Oxazinane-Fused Isoquinolin-1(2H)-ones
ACS Catalysis, 2018, 8, 8925
4515710 CIFC18 H29 Cl Ir N OP -18.6737; 8.7731; 13.6686
78.458; 75.85; 88.359		987.94Tan, Guangying; You, Qiulin; You, Jingsong
Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates
ACS Catalysis, 2018, 8, 8709
4515711 CIFC32 H38 N2 O2 S2P 1 21/n 112.5365; 14.4554; 17.4788
90; 103.091; 90		3085.19Tan, Guangying; You, Qiulin; You, Jingsong
Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates
ACS Catalysis, 2018, 8, 8709
4515712 CIFC30 H12.5 Al Cl F15.5 NP 1 21/c 110.307; 26.879; 20.89
90; 101.156; 90		5678Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515713 CIFC22 H21 N SiP -19.3329; 10.0874; 11.22
67.672; 88.245; 65.949		882.58Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515714 CIFC27 H14 Al F16 N4P -110.4075; 10.6369; 13.0972
79.781; 79.01; 71.612		1339.9Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515715 CIFC27 H9 Al F15 NP 1 21 17.4782; 17.022; 9.979
90; 107.975; 90		1208.3Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515716 CIFC15 H11 F3 O2 S2P 1 21/c 111.7791; 5.8649; 21.894
90; 92.863; 90		1510.6Li, Haoyu; Cheng, Zengrui; Tung, Chen-Ho; Xu, Zhenghu
Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
ACS Catalysis, 2018, 8, 8237
4515717 CIFC21 H20 F4 O3 S2P 1 21/c 110.219; 20.254; 10.852
90; 107.747; 90		2139Li, Haoyu; Cheng, Zengrui; Tung, Chen-Ho; Xu, Zhenghu
Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
ACS Catalysis, 2018, 8, 8237
4515718 CIFC21 H36 Mn N O2 P2C 1 2/c 118.6272; 10.623; 23.1001
90; 101.192; 90		4484.04Zou, You-Quan; Chakraborty, Subrata; Nerush, Alexander; Oren, Dror; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal-Ligand Cooperation.
ACS catalysis, 2018, 8, 8014-8019
4515719 CIFC42 H68 Mn2 N4 O4 P4P 1 21/c 111.6109; 18.5885; 21.5322
90; 99.218; 90		4587.26Zou, You-Quan; Chakraborty, Subrata; Nerush, Alexander; Oren, Dror; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal-Ligand Cooperation.
ACS catalysis, 2018, 8, 8014-8019
4515720 CIFC29 H55 Fe N3 P2 Si2P 1 21/c 112.7712; 19.068; 15.4049
90; 110.526; 90		3513.3Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515721 CIFC35 H67 Fe N3 P3 Si2P -110.589; 12.811; 15.92
92.93; 104.249; 99.001		2058.3Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515722 CIFC31 H58 Fe N4 P2 Si2P 1 21/c 116.778; 15.4527; 16.706
90; 99.322; 90		4274.1Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515723 CIFC40 H50 Fe N6 P2P 1 21/n 118.6843; 11.1179; 18.9515
90; 110.665; 90		3683.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515724 CIFC39 H58 B Fe N5 O2 P2P 1 21/c 118.764; 11.2867; 20.592
90; 114.08; 90		3981.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515725 CIFC22 H24 Cl N O RuP 1 21/n 111.6782; 8.2226; 20.44
90; 99.939; 90		1933.3Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515726 CIFC23 H24 N2 O2P 1 21/c 18.295; 11.086; 21.615
90; 93.5; 90		1984Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515727 CIFC33 H39 F6 N2 O2 Ru SbP 1 21/c 113.2275; 10.9193; 24.4944
90; 98.3993; 90		3499.9Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515728 CIFC47 H43 Br Mn N O4 P2P -112.0659; 12.6901; 13.3087
94.285; 102.738; 90.704		1981.22Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515729 CIFC39 H31 B Mn N O2 P2P -110.0379; 11.3687; 15.6568
73.97; 77.542; 72.82		1623.02Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515730 CIFC39 H31 Mn N2 O2 P2R -3 :H37.5012; 37.5012; 11.98047
90; 90; 120		14591.3Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515731 CIFC20 H20 Br Cl2 N O PtP 1 21/c 19.7404; 13.3126; 17.0002
90; 104.115; 90		2137.9Shimbayashi, Takuya; Matsushita, Gaku; Nanya, Atsushi; Eguchi, Akira; Okamoto, Kazuhiro; Ohe, Kouichi
Divergent Catalytic Approach from Cyclic Oxime Esters to Nitrogen-Containing Heterocycles with Group 9 Metal Catalysts
ACS Catalysis, 2018, 8, 7773
4515732 CIFC33 H41 Cl2 N Ru SP 4310.0186; 10.0186; 30.9734
90; 90; 90		3108.87Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515733 CIFC28 H36 Cl2 F3 N Ru SP n a 2116.3382; 16.5805; 10.4655
90; 90; 90		2835.1Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515734 CIFC26 H32 Cl2 F3 N Ru SP -111.0669; 14.1689; 17.6536
103.228; 94.276; 100.447		2630.52Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515735 CIFC32 H39 Cl4 N Ru SP c a 2119.868; 9.2131; 17.5258
90; 90; 90		3208Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515736 CIFC43 H60 S Y2P 1 21/n 112.6411; 16.3119; 19.7095
90; 106.372; 90		3899.3Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515737 CIFC25 H33 S YP 1 21/c 116.796; 8.4624; 16.616
90; 102.549; 90		2305.3Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515738 CIFC50 H66 S2 Y2P -110.343; 10.6225; 10.683
94.507; 108.927; 92.924		1103.18Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515739 CIFC20 H20 S SiP 1 21/n 19.7426; 9.7458; 18.818
90; 90.465; 90		1786.7Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515740 CIFC23 H23 N S SiP 1 21/n 110.304; 17.9385; 11.4674
90; 107.757; 90		2018.6Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515741 CIFC21 H25 Cl3 Ir N O3P 21 21 219.6875; 13.7823; 17.6769
90; 90; 90		2360.1Zhou, Gang; Aboo, Ahmed H.; Robertson, Craig M.; Liu, Ruixia; Li, Zhenhua; Luzyanin, Konstantin; Berry, Neil G.; Chen, Weiping; Xiao, Jianliang
N,O- vs N,C-Chelation in Half-Sandwich Iridium Complexes: A Dramatic Effect on Enantioselectivity in Asymmetric Transfer Hydrogenation of Ketones
ACS Catalysis, 2018, 8, 8020
4515742 CIFC21 H25 Cl Ir N O3P 6118.4094; 18.4094; 11.3169
90; 90; 120		3321.5Zhou, Gang; Aboo, Ahmed H.; Robertson, Craig M.; Liu, Ruixia; Li, Zhenhua; Luzyanin, Konstantin; Berry, Neil G.; Chen, Weiping; Xiao, Jianliang
N,O- vs N,C-Chelation in Half-Sandwich Iridium Complexes: A Dramatic Effect on Enantioselectivity in Asymmetric Transfer Hydrogenation of Ketones
ACS Catalysis, 2018, 8, 8020
4515743 CIFC20 H24 Cl N O4P 1 21 17.421; 16.048; 8.176
90; 101.174; 90		955.2Schmid, Steven C.; Guzei, Ilia A.; Fernández, Israel; Schomaker, Jennifer M.
Ring Expansion of Bicyclic Methyleneaziridines via Concerted, Near-Barrierless [2,3]-Stevens Rearrangements of Aziridinium Ylides.
ACS catalysis, 2018, 8, 7907-7914
4515744 CIFC29 H43 F6 N P SbP b c a16.4612; 13.7221; 26.85
90; 90; 90		6064.9Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515745 CIFC30 H21 F18 N P SbC 1 2/c 127.034; 8.1387; 29.826
90; 95.017; 90		6537.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515746 CIFC32 H24 Au Cl F18 N2 P SbP 1 21/n 18.7962; 27.1915; 16.076
90; 103.535; 90		3738.3Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515747 CIFC27 H27 Cl2 F6 N P SbP -18.4844; 13.1717; 13.5679
92.667; 105.963; 100.874		1423.8Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515748 CIFC26 H37 Au Cl F6 N P SbP -110.6409; 16.737; 17.0626
82.428; 84.084; 87.346		2994.6Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515749 CIFC26 H37 F6 N P SbP 1 21/n 113.8885; 13.3919; 15.6069
90; 112.626; 90		2679.4Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515750 CIFC26 H29 Cl F6 Ir N P SbP 1 21/c 111.9033; 8.2433; 28.535
90; 99.672; 90		2760.1Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515751 CIFC26 H25 Au Cl F6 N P SbP -110.004; 10.1489; 15.7193
107.808; 92.182; 112.364		1383.43Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515752 CIFC31.5 H24 Au Cl6 F18 N O2 P SbP -18.9106; 12.9646; 19.744
73.397; 82.399; 85.849		2165.1Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515753 CIFC46 H40 O5P -111.0227; 11.4514; 15.2564
69.58; 76.609; 74.008		1715.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515754 CIFC25 H23 F6 N O2 P SbP -18.3643; 11.8205; 13.1583
91.321; 104.359; 99.991		1238.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515755 CIFC25 H21 N O2 SC 1 2 126.96; 8.264; 9.337
90; 107.363; 90		1985.5Liu, Xihong; Wang, Pengxin; Bai, Lutao; Li, Dan; Wang, Linqing; Yang, Dongxu; Wang, Rui
Construction of Vicinal All-Carbon Quaternary Stereocenters Enabled by a Catalytic Asymmetric Dearomatization Reaction of β-Naphthols with 3-Bromooxindoles
ACS Catalysis, 2018, 8, 10888
4515756 CIFC22 H22 N4 OP 1 21 16.4088; 7.0686; 19.8625
90; 93.865; 90		897.75Marichev, Kostiantyn O.; Adly, Frady G.; Carranco, Alejandra M.; Garcia, Estevan C.; Arman, Hadi; Doyle, Michael P.
Catalyst Choice for Highly Enantioselective [3 + 3]-Cycloaddition of Enoldiazocarbonyl Compounds
ACS Catalysis, 2018, 8, 10392
4515757 CIFC50.31 H48.22 B Cl1.39 F4 Fe N2 Ni O1.31 S2C 1 2/c 125.286; 23.295; 20.693
90; 127.48; 90		9673Brazzolotto, Deborah; Wang, Lianke; Tang, Hao; Gennari, Marcello; Queyriaux, Nicolas; Philouze, Christian; Demeshko, Serhiy; Meyer, Franc; Orio, Maylis; Artero, Vincent; Hall, Michael B.; Duboc, Carole
Tuning Reactivity of Bioinspired [NiFe]-Hydrogenase Models by Ligand Design and Modeling the CO Inhibition Process
ACS Catalysis, 2018, 8, 10658
4515758 CIFC20 H18 N O2 PP 21 21 219.1903; 10.9348; 17.0654
90; 90; 90		1714.97Wang, Huamin; Li, Yongli; Tang, Zilu; Wang, Shengchun; Zhang, Heng; Cong, Hengjiang; Lei, Aiwen
Z-Selective Addition of Diaryl Phosphine Oxides to Alkynes via Photoredox Catalysis
ACS Catalysis, 2018, 8, 10599
4515759 CIFC58 H94 F9 Ho N4 O22 S3P 1 21 112.992; 16.505; 17.872
90; 102.41; 90		3742.8Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515760 CIFC30 H31 N2 O6 SP 1 21 113.9107; 13.9185; 15.4002
90; 109.507; 90		2810.6Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515761 CIFC42 H60 Br2 F9 N4 O16 S3 TmP 1 21 19.458; 25.399; 11.67
90; 93.281; 90		2798.8Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515762 CIFC36 H36 N2 O6 SP 1 21 19.3322; 18.7754; 9.4931
90; 107.649; 90		1585.05Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515763 CIFC27 H28 Cl F N4 O8P 21 21 2112.2999; 14.3668; 15.8349
90; 90; 90		2798.2Guo, Wengang; Li, Lu; Ding, Qian; Lin, Xiangfeng; Liu, Xianghui; Wang, Kai; Liu, Yan; Fan, Hongjun; Li, Can
Synthesis of Chiral Trispirocyclic Oxindoles via Organic-Base/Au(I)-Catalyzed Sequential Reactions
ACS Catalysis, 2018, 8, 10180
4515764 CIFC27 H28 Cl2 N4 O8P 21 21 2112.4437; 15.4069; 15.5019
90; 90; 90		2972Guo, Wengang; Li, Lu; Ding, Qian; Lin, Xiangfeng; Liu, Xianghui; Wang, Kai; Liu, Yan; Fan, Hongjun; Li, Can
Synthesis of Chiral Trispirocyclic Oxindoles via Organic-Base/Au(I)-Catalyzed Sequential Reactions
ACS Catalysis, 2018, 8, 10180
4515765 CIFC30 H31 N5 O7C 2 2 2110.4443; 14.5326; 38.8497
90; 90; 90		5896.7Guo, Wengang; Li, Lu; Ding, Qian; Lin, Xiangfeng; Liu, Xianghui; Wang, Kai; Liu, Yan; Fan, Hongjun; Li, Can
Synthesis of Chiral Trispirocyclic Oxindoles via Organic-Base/Au(I)-Catalyzed Sequential Reactions
ACS Catalysis, 2018, 8, 10180
4515766 CIFC32 H39 N O4 SP 1 21/c 111.7118; 39.9043; 6.266
90; 97.254; 90		2905Jiang, Fei; Yuan, Fu-Ru; Jin, Li-Wen; Mei, Guang-Jian; Shi, Feng
Metal-Catalyzed (4 + 3) Cyclization of Vinyl Aziridines withpara-Quinone Methide Derivatives
ACS Catalysis, 2018, 8, 10234
4515767 CIFC22 H22 N2 O3 PdP -16.7169; 11.3747; 13.8249
67.899; 87.885; 79.889		962.96Maji, Arun; Reddi, Yernaidu; Sunoj, Raghavan B.; Maiti, Debabrata
Mechanistic Insights on Orthogonal Selectivity in Heterocycle Synthesis
ACS Catalysis, 2018, 8, 10111
4515768 CIFC38 H51 Bi O8 P RhP -110.4797; 13.5923; 13.9879
91.294; 92.227; 91.361		1989.86Ren, Zhi; Sunderland, Travis L.; Tortoreto, Cecilia; Yang, Tzuhsiung; Berry, John F.; Musaev, Djamaladdin G.; Davies, Huw M. L.
Comparison of Reactivity and Enantioselectivity between Chiral Bimetallic Catalysts: Bismuth‒Rhodium- and Dirhodium-Catalyzed Carbene Chemistry
ACS Catalysis, 2018, 8, 10676
4515769 CIFC67.84 H95.68 Bi N4 O17.96 Rh S4I 422.2169; 22.2169; 10.9063
90; 90; 90		5383.2Ren, Zhi; Sunderland, Travis L.; Tortoreto, Cecilia; Yang, Tzuhsiung; Berry, John F.; Musaev, Djamaladdin G.; Davies, Huw M. L.
Comparison of Reactivity and Enantioselectivity between Chiral Bimetallic Catalysts: Bismuth‒Rhodium- and Dirhodium-Catalyzed Carbene Chemistry
ACS Catalysis, 2018, 8, 10676
4515770 CIFC14 H28 Cl Ir P2P 1 21/m 17.1256; 13.4641; 8.7896
90; 102.373; 90		823.69Ahn, Seihwan; Sorsche, Dieter; Berritt, Simon; Gau, Michael R.; Mindiola, Daniel J.; Baik, Mu-Hyun
Rational Design of a Catalyst for the Selective Monoborylation of Methane
ACS Catalysis, 2018, 8, 10021
4515771 CIFC18 H26 N2 O3P 1 21/n 19.2992; 15.198; 12.6751
90; 99.38; 90		1767.4Zhang, Bo-Sheng; Li, Yuke; An, Yang; Zhang, Zhe; Liu, Ce; Wang, Xin-Gang; Liang, Yong-Min
Carboxylate Ligand-Exchanged Amination/C(sp3)‒H Arylation Reaction via Pd/Norbornene Cooperative Catalysis
ACS Catalysis, 2018, 8, 11827
4515772 CIFC16 H22 N2 O3P n a 2110.5957; 18.8441; 7.6415
90; 90; 90		1525.8Zhang, Bo-Sheng; Li, Yuke; An, Yang; Zhang, Zhe; Liu, Ce; Wang, Xin-Gang; Liang, Yong-Min
Carboxylate Ligand-Exchanged Amination/C(sp3)‒H Arylation Reaction via Pd/Norbornene Cooperative Catalysis
ACS Catalysis, 2018, 8, 11827
4515773 CIFC30 H28 O4P -19.097; 12.191; 13.111
114.466; 95.343; 108.732		1209.5Zuo, Zhijun; Wang, Hui; Diao, Yunxia; Ge, Yicong; Liu, Jingjing; Luan, Xinjun
Palladium-Catalyzed Aryne Insertion/Arene Dearomatization Domino Reaction: A Highly Chemoselective Route to Spirofluorenes
ACS Catalysis, 2018, 8, 11029
4515774 CIFC26 H20 O2P 1 21/n 112.157; 12.525; 12.945
90; 91.141; 90		1970.7Zuo, Zhijun; Wang, Hui; Diao, Yunxia; Ge, Yicong; Liu, Jingjing; Luan, Xinjun
Palladium-Catalyzed Aryne Insertion/Arene Dearomatization Domino Reaction: A Highly Chemoselective Route to Spirofluorenes
ACS Catalysis, 2018, 8, 11029
4515775 CIFC8 H7 N O2P 1 21/c 111.6456; 5.1414; 13.0095
90; 110.064; 90		731.67Hota, Pradip Kumar; Sau, Samaresh Chandra; Mandal, Swadhin K.
Metal-Free Catalytic Formylation of Amides Using CO2 under Ambient Conditions
ACS Catalysis, 2018, 8, 11999
4515776 CIFC24 H22 Br I N2 O4 SP 21 21 217.4546; 13.367; 24.063
90; 90; 90		2397.8Struble, Thomas J.; Lankswert, Hannah M.; Pink, Maren; Johnston, Jeffrey N.
Enantioselective Organocatalytic Amine-Isocyanate Capture-Cyclization: Regioselective Alkene Iodoamination for the Synthesis of Chiral Cyclic Ureas.
ACS catalysis, 2018, 8, 11926-11931
4515777 CIFC26 H25 I N2 O4 SP 1 21 16.8374; 14.8665; 12.6176
90; 105.716; 90		1234.61Struble, Thomas J.; Lankswert, Hannah M.; Pink, Maren; Johnston, Jeffrey N.
Enantioselective Organocatalytic Amine-Isocyanate Capture-Cyclization: Regioselective Alkene Iodoamination for the Synthesis of Chiral Cyclic Ureas.
ACS catalysis, 2018, 8, 11926-11931
4515778 CIFC26 H18 O3C 1 2/c 124.897; 5.8589; 26.361
90; 100.161; 90		3784.9Lad, Bapurao Sudam; Katukojvala, Sreenivas
Piano-Stool Rhodium Enalcarbenoids: Application to Catalyst-Controlled Metal-Templated Annulations of Diazoenals and 1,3-Dicarbonyls
ACS Catalysis, 2018, 8, 11807
4515779 CIFC12 H14 O5P -15.8118; 7.6603; 13.506
82.491; 89.314; 82.461		590.97Lad, Bapurao Sudam; Katukojvala, Sreenivas
Piano-Stool Rhodium Enalcarbenoids: Application to Catalyst-Controlled Metal-Templated Annulations of Diazoenals and 1,3-Dicarbonyls
ACS Catalysis, 2018, 8, 11807
4515780 CIFC4 H10 Cl8 N2 W2P -17.7134; 7.817; 7.9908
97.754; 108.946; 112.35		402.67Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515781 CIFC26 H20 Cl8 F6 N2 W2P -17.1984; 9.6255; 12.8058
68.524; 86.291; 81.137		815.79Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515782 CIFC24 H34 Cl8 N2 W2P -19.6082; 9.7882; 10.2905
106.301; 106.481; 110.355		788.82Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515783 CIFC30 H34 Cl8 D6 N2 W2P 1 21/n 19.7378; 11.39; 16.7268
90; 93.494; 90		1851.78Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515784 CIFC10 H10 Cl4 F3 N O WP 1 21/c 111.3589; 11.3408; 11.9422
90; 100.845; 90		1510.91Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515785 CIFC16 H25 Cl4 N O WP -18.5798; 14.0708; 17.3875
95.674; 98.423; 97.281		2044.9Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515786 CIFC32 H54 Cl7 N3 W2P c c n9.5696; 10.714; 40.8756
90; 90; 90		4190.9Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515787 CIFC21 H45 Cl N P3 WP n m a15.7347; 13.6973; 12.7686
90; 90; 90		2751.93Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515788 CIFC9 H14 Cl N WP 1 21/m 16.3483; 7.2804; 11.9671
90; 93.604; 90		552Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515789 CIFC15 H26 Al Cl4 N WP 1 21/c 110.0824; 16.3429; 13.3029
90; 96.616; 90		2177.4Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515790 CIFC56 H120 Co2 N7 O34 V W9P 1 21/n 114.4162; 32.8597; 20.2434
90; 109.886; 90		9017.7Sullivan, Kevin P.; Wieliczko, Marika; Kim, Mooeung; Yin, Qiushi; Collins-Wildman, Daniel L.; Mehta, Anil K.; Bacsa, John; Lu, Xinlin; Geletii, Yurii V.; Hill, Craig L.
Speciation and Dynamics in the [Co4V2W18O68]10‒/Co(II)aq/CoOx Catalytic Water Oxidation System
ACS Catalysis, 2018, 8, 11952
4515791 CIFC24 H24 N2 O2 SP 1 21/c 19.9646; 31.521; 6.9339
90; 101.603; 90		2133.4Wang, Huifei; Qiu, Shuxian; Wang, Sasa; Zhai, Hongbin
Pd-Catalyzed Umpolung of π‒Allylpalladium Intermediates: Assembly of All-Carbon α-Vinyl Quaternary Aldehydes through C(sp3)‒C(sp3) Coupling
ACS Catalysis, 2018, 8, 11960
4515792 CIFC60 H42 Br2 Cu F12 N6 O8 Sb2C 1 2/c 111.7665; 26.084; 21.832
90; 92.097; 90		6696.1Ng, Yik Yie; Tan, Lisa Jiaying; Ng, Shue Mei; Chai, Yoke Tin; Ganguly, Rakesh; Du, Yonghua; Yeow, Edwin Kok Lee; Soo, Han Sen
Spectroscopic Characterization and Mechanistic Studies on Visible Light Photoredox Carbon‒Carbon Bond Formation by Bis(arylimino)acenaphthene Copper Photosensitizers
ACS Catalysis, 2018, 8, 11277
4515793 CIFC76 H92 Br2 Cu F6 N12 O15 PC 1 2/c 126.796; 14.7426; 22.903
90; 114.796; 90		8213.5Ng, Yik Yie; Tan, Lisa Jiaying; Ng, Shue Mei; Chai, Yoke Tin; Ganguly, Rakesh; Du, Yonghua; Yeow, Edwin Kok Lee; Soo, Han Sen
Spectroscopic Characterization and Mechanistic Studies on Visible Light Photoredox Carbon‒Carbon Bond Formation by Bis(arylimino)acenaphthene Copper Photosensitizers
ACS Catalysis, 2018, 8, 11277
4515794 CIFC24 H18 Br N2 OP 15.6607; 8.2437; 10.596
96.24; 99.41; 96.49		480.59Tong, Hua-Rong; Zheng, Sujuan; Li, Xinghua; Deng, Zhiqiang; Wang, Hao; He, Gang; Peng, Qian; Chen, Gong
Pd(0)-Catalyzed Bidentate Auxiliary Directed Enantioselective Benzylic C‒H Arylation of 3-Arylpropanamides Using the BINOL Phosphoramidite Ligand
ACS Catalysis, 2018, 8, 11502
4515795 CIFC40 H32 N12 Ni2P 41 21 211.3157; 11.3157; 31.5787
90; 90; 90		4043.5Ghorai, Debasish; Finger, Lars H.; Zanoni, Giuseppe; Ackermann, Lutz
Bimetallic Nickel Complexes for Aniline C–H Alkylations
ACS Catalysis, 2018, 8, 11657
4515796 CIFC14 H14 F N3P 1 21/c 113.3888; 8.0065; 22.9811
90; 95.656; 90		2451.5Ghorai, Debasish; Finger, Lars H.; Zanoni, Giuseppe; Ackermann, Lutz
Bimetallic Nickel Complexes for Aniline C‒H Alkylations
ACS Catalysis, 2018, 8, 11657
4515797 CIFC40 H28 F4 N12 Ni2P c c n9.5253; 16.5175; 22.4483
90; 90; 90		3531.9Ghorai, Debasish; Finger, Lars H.; Zanoni, Giuseppe; Ackermann, Lutz
Bimetallic Nickel Complexes for Aniline C‒H Alkylations
ACS Catalysis, 2018, 8, 11657
4515798 CIFC90 H64 Cu2 F6 P4 S2P -111.1442; 12.9041; 13.9829
101.643; 97.123; 109.481		1816.4He, Jian; Chen, Caiyou; Fu, Gregory C.; Peters, Jonas C.
Visible-Light-Induced, Copper-Catalyzed Three-Component Coupling of Alkyl Halides, Olefins, and Trifluoromethylthiolate to Generate Trifluoromethyl Thioethers.
ACS catalysis, 2018, 8, 11741-11748
4515799 CIFC24 H18 Fe S2P 1 21 110.1167; 9.2912; 10.2864
90; 105.881; 90		930Xu, Bing-Bin; Ye, Jie; Yuan, Yu; Duan, Wei-Liang
Palladium-Catalyzed Asymmetric C‒H Arylation for the Synthesis of Planar Chiral Benzothiophene-Fused Ferrocenes
ACS Catalysis, 2018, 8, 11735
4515800 CIFC45 H51 Cl N4 Ni O PP 1 21/c 117.8919; 12.6768; 19.8115
90; 114.361; 90		4093.4Wang, Ting-Hsuan; Ambre, Ram; Wang, Qing; Lee, Wei-Chih; Wang, Pen-Cheng; Liu, Yuhua; Zhao, Lili; Ong, Tiow-Gan
Nickel-Catalyzed Heteroarenes Cross Coupling via Tandem C‒H/C‒O Activation
ACS Catalysis, 2018, 8, 11368
4515801 CIFC34 H44 Cl2 N4 WP 21 21 219.8622; 17.5716; 19.3465
90; 90; 90		3352.6Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515802 CIFC27 H43 Cl2 N2 P WP 21 21 2110.5486; 16.4202; 17.086
90; 90; 90		2959.5Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515803 CIFC16 H14 Cl2 F6 N2 O2 WP 21 21 2112.0005; 12.4893; 13.5857
90; 90; 90		2036.2Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515804 CIFC52.4 H45 Cl2 N2 O2.2 WR -3 :H32.8492; 32.8492; 20.7376
90; 90; 120		19379.3Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515805 CIFC22 H14 Cl2 F18 N2 O2 WP 1 21/c 112.5254; 27.3985; 9.0867
90; 105.516; 90		3004.7Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515806 CIFC16 H10 Cl2 F10 N2 O2 WP -17.3379; 7.8387; 17.8616
87.953; 81.828; 87.079		1015.22Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515807 CIFC19 H34 Cl2 N2 O2 WP 1 21/n 113.4052; 9.8029; 18.7197
90; 109.016; 90		2325.7Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515808 CIFC20 H36 Cl2 N2 O2 WP -19.8343; 9.9604; 13.7645
70.528; 85.509; 71.846		1207.4Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515809 CIFC27.5 H43.75 Cl2.5 N2 O2 WP -19.0974; 12.8175; 14.1008
112.357; 90.965; 99.035		1496.5Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515810 CIFC28 H35 Cl5 N2 O2 WP 1 21/c 112.1544; 10.4027; 24.447
90; 91.001; 90		3090.6Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515811 CIFC22 H29 Cl2 F3 N2 O2 WP -18.8303; 11.5526; 12.8453
77.061; 85.454; 74.916		1232.81Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515812 CIFC23 H32 Cl4 N4 O6 WP c a 2116.4344; 10.2454; 17.7291
90; 90; 90		2985.17Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515813 CIFC40 H44 Cl2 N2 O2 WP 1 21/n 116.2309; 10.3469; 22.3012
90; 103.618; 90		3640Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515814 CIFC25 H23 N O4P -18.535; 10.595; 11.444
79.5; 87.548; 81.464		1006.1Li, Guo-Xing; Hu, Xiafei; He, Gang; Chen, Gong
Photoredox-Mediated Minisci-type Alkylation of N-Heteroarenes with Alkanes with High Methylene Selectivity
ACS Catalysis, 2018, 8, 11847
4515815 CIFC25 H23 N O4P -19.737; 10.551; 11.09
68.032; 80.699; 75.858		1021.5Li, Guo-Xing; Hu, Xiafei; He, Gang; Chen, Gong
Photoredox-Mediated Minisci-type Alkylation of N-Heteroarenes with Alkanes with High Methylene Selectivity
ACS Catalysis, 2018, 8, 11847
4515816 CIFC27 H33 N O4P 1 21 18.9557; 9.9317; 13.533
90; 104.289; 90		1166.5Li, Guo-Xing; Hu, Xiafei; He, Gang; Chen, Gong
Photoredox-Mediated Minisci-type Alkylation of N-Heteroarenes with Alkanes with High Methylene Selectivity
ACS Catalysis, 2018, 8, 11847
4515817 CIFC28 H44 O3 Os P2P 1 21/c 115.878; 10.9673; 16.462
90; 90.174; 90		2866.7Esteruelas, Miguel A.; García-Yebra, Cristina; Martín, Jaime; Oñate, Enrique
Dehydrogenation of Formic Acid Promoted by a Trihydride-Hydroxo-Osmium(IV) Complex: Kinetics and Mechanism
ACS Catalysis, 2018, 8, 11314
4515818 CIFC23 H21.5 F6 N3.5 P PdP 21 21 2111.993; 17.981; 22.586
90; 90; 90		4871Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4515819 CIFC47 H44 F3 Fe N2 O6 P Pd SP 21 21 2111.4924; 18.4018; 20.7858
90; 90; 90		4395.8Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4515820 CIFC48 H45 Cl3 F3 Fe N2 O6 P Pd SP 21 21 2111.5846; 16.3753; 25.133
90; 90; 90		4767.8Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4515821 CIFC53 H61 Fe Ni O P2P 1 21/c 114.2235; 16.3932; 19.5487
90; 98.023; 90		4513.5Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515822 CIFC43 H39 Fe Ni P2C 1 2/c 123.2567; 16.9768; 21.0881
90; 106.649; 90		7977Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515823 CIFC56 H53 Fe Ni P2I 1 2/a 114.0344; 13.358; 23.5713
90; 95.985; 90		4394.9Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515824 CIFC63 H67 Br Fe Ni P2P -110.4283; 13.6108; 19.5796
77.34; 81.336; 88.445		2680.5Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515825 CIFC31 H24 N6 O4 RuP n a 2117.4154; 17.0027; 9.3236
90; 90; 90		2760.8Matheu, Roc; Ertem, Mehmed Z.; Pipelier, Muriel; Lebreton, Jacques; Dubreuil, Didier; Benet-Buchholz, Jordi; Sala, Xavier; Tessier, Arnaud; Llobet, Antoni
The Role of Seven-Coordination in Ru-Catalyzed Water Oxidation
ACS Catalysis, 2018, 8, 2039
4515826 CIFC28.5 H28 N5 O6.5 RuP 1 21/c 111.7638; 16.7628; 15.8332
90; 107.656; 90		2975.1Matheu, Roc; Ertem, Mehmed Z.; Pipelier, Muriel; Lebreton, Jacques; Dubreuil, Didier; Benet-Buchholz, Jordi; Sala, Xavier; Tessier, Arnaud; Llobet, Antoni
The Role of Seven-Coordination in Ru-Catalyzed Water Oxidation
ACS Catalysis, 2018, 8, 2039
4515827 CIFC55 H48 Ce N15 O26 Ru2P c a 2117.9909; 22.189; 15.3463
90; 90; 90		6126.24Matheu, Roc; Ertem, Mehmed Z.; Pipelier, Muriel; Lebreton, Jacques; Dubreuil, Didier; Benet-Buchholz, Jordi; Sala, Xavier; Tessier, Arnaud; Llobet, Antoni
The Role of Seven-Coordination in Ru-Catalyzed Water Oxidation
ACS Catalysis, 2018, 8, 2039
4515828 CIFC2.778 H2.333 Cu0.111 N0.444 O0.778 S0.222C 1 2/c 122.2892; 22.2235; 15.7911
90; 101.936; 90		7652.9Zhang, Guiyang; Yang, Huimin; Fei, Honghan
Unusual Missing Linkers in an Organosulfonate-Based Primitive‒Cubic (pcu)-Type Metal‒Organic Framework for CO2 Capture and Conversion under Ambient Conditions
ACS Catalysis, 2018, 8, 2519
4516212 CIFC22 H30 B Mo N9 OP 1 21/n 110.6622; 18.8079; 12.1539
90; 94.352; 90		2430.24Dakermanji, Steven J.; Smith, Jacob A.; Westendorff, Karl S.; Pert, Emmit K.; Chung, Andrew D.; Myers, Jeffery T.; Welch, Kevin D.; Dickie, Diane A.; Harman, W. Dean
Electron-Transfer Chain Catalysis of η2-Arene, η2-Alkene, and η2-Ketone Exchange on Molybdenum
ACS Catalysis, 2019, 11274
4516214 CIFC30 H38 Fe2 N2 O4 Pd2P -17.4139; 12.1658; 17.3075
89.281; 88.144; 71.583		1480.3Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516215 CIFC37 H47 Fe2 N4 O6 Pd2P n n a15.4063; 23.1323; 21.3599
90; 90; 90		7612.3Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516216 CIFC18 H24 Fe N2 OP 21 21 219.6729; 10.7575; 16.1377
90; 90; 90		1679.2Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516217 CIFC46 H60 N4 O6 Pd2P 21 21 220.0614; 9.2769; 13.7686
90; 90; 90		2562.4Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516218 CIFC46 H60 N4 O6 Pd2P 21 21 219.4493; 19.4338; 25.5923
90; 90; 90		4699.7Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516219 CIFC34 H38 N2 O4 Pd2P 1 21/n 19.6636; 18.8875; 16.9545
90; 94.675; 90		3084.3Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516220 CIFC20 H26 N2 O2 PdP 21 21 212.4112; 25.3634; 5.907
90; 90; 90		1859.47Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516221 CIFC32 H32 N2 O4 PdP b c a19.9077; 12.8327; 22.0152
90; 90; 90		5624.2Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516222 CIFC25 H33 Fe N2 O5 PdP -19.319; 10.4167; 13.8973
98.151; 97.964; 108.691		1240.4Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516223 CIFC22 H30 N2 O5 PdP 43 21 26.0598; 6.0598; 60.491
90; 90; 90		2221.3Gair, Joseph J.; Haines, Brandon E.; Filatov, Alexander S.; Musaev, Djamaladdin G.; Lewis, Jared C.
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C‒H Functionalization
ACS Catalysis, 2019, 11386
4516226 CIFC16 H12 N2 OP b c a14.3719; 6.4267; 25.3093
90; 90; 90		2337.67Ghosh, Koushik; Nishii, Yuji; Miura, Masahiro
Rhodium-Catalyzed Annulative Coupling Using Vinylene Carbonate as an Oxidizing Acetylene Surrogate
ACS Catalysis, 2019, 11455
4516227 CIFC20 H13 Cl3 N2P 1 21/c 113.0701; 12.556; 10.8819
90; 104.883; 90		1725.9Ghosh, Koushik; Nishii, Yuji; Miura, Masahiro
Rhodium-Catalyzed Annulative Coupling Using Vinylene Carbonate as an Oxidizing Acetylene Surrogate
ACS Catalysis, 2019, 11455
4516228 CIFC18 H20 N2 O5 S2P 21 21 218.8085; 10.3259; 22.243
90; 90; 90		2023.1Zou, Jiaoxia; Chen, Jinhong; Shi, Tao; Hou, Yongsheng; Cao, Fei; Wang, Yongqiang; Wang, Xiaodong; Jia, Zhong; Zhao, Quanyi; Wang, Zhen
Phthalimide-Carried Disulfur Transfer To Synthesize Unsymmetrical Disulfanes via Copper Catalysis
ACS Catalysis, 2019, 11426
4516231 CIFC12 H14 O2P 21 21 216.1055; 7.4185; 22.4266
90; 90; 90		1015.78Griswold, Jessica A.; Johnson, Jeffrey S.
Stereoconvergent Conjugate Addition of Arylboronic Acids to α-Angelica Lactone Derivatives: Synthesis of Stereochemically Complex γ-Butyrolactones
ACS Catalysis, 2019, 11614
4516232 CIFC15 H14 O2P 21 21 216.1306; 7.3825; 25.8514
90; 90; 90		1170.01Griswold, Jessica A.; Johnson, Jeffrey S.
Stereoconvergent Conjugate Addition of Arylboronic Acids to α-Angelica Lactone Derivatives: Synthesis of Stereochemically Complex γ-Butyrolactones
ACS Catalysis, 2019, 11614
4516233 CIFC11 H11 Br O2P 21 21 216.1359; 7.2261; 23.2488
90; 90; 90		1030.82Griswold, Jessica A.; Johnson, Jeffrey S.
Stereoconvergent Conjugate Addition of Arylboronic Acids to α-Angelica Lactone Derivatives: Synthesis of Stereochemically Complex γ-Butyrolactones
ACS Catalysis, 2019, 11614
4516234 CIFC22 H24 O6P 1 21 16.7404; 10.373; 13.488
90; 90.437; 90		943Uyanik, Muhammet; Kato, Takehiro; Sahara, Naoto; Katade, Outa; Ishihara, Kazuaki
High-Performance Ammonium Hypoiodite/Oxone Catalysis for Enantioselective Oxidative Dearomatization of Arenols
ACS Catalysis, 2019, 11619
4516235 CIFC38 H42 O7P 21 21 219.8131; 16.46; 19.469
90; 90; 90		3144.7Uyanik, Muhammet; Kato, Takehiro; Sahara, Naoto; Katade, Outa; Ishihara, Kazuaki
High-Performance Ammonium Hypoiodite/Oxone Catalysis for Enantioselective Oxidative Dearomatization of Arenols
ACS Catalysis, 2019, 11619
4516239 CIFC33.5 H31.5 Cl4.5 N2 O5 S2C 1 2/c 134.081; 10.527; 22.0782
90; 114.326; 90		7217.8Jin, Hongming; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
The Carbocation-Catalyzed Intermolecular Formal [2 + 2 + 1] Cycloaddition of Ynamides with Quinoxaline N-Oxides
ACS Catalysis, 2019, 11663
4516240 CIFC36 H36 N2 O5 S2P 21 21 2110.1824; 12.255; 25.931
90; 90; 90		3235.8Jin, Hongming; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
The Carbocation-Catalyzed Intermolecular Formal [2 + 2 + 1] Cycloaddition of Ynamides with Quinoxaline N-Oxides
ACS Catalysis, 2019, 11663
4516241 CIFC32 H47 O2 PP 1 21/n 112.342; 19.352; 13.4
90; 99.229; 90		3159.1Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516242 CIFC30 H45 PP b c a30.671; 10.2786; 33.812
90; 90; 90		10659Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516243 CIFC31 H47 O0.33 PR -3 :H19.35; 19.35; 38.469
90; 90; 120		12474Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516244 CIFC32 H49 PP 1 21/n 18.6727; 14.184; 23.006
90; 92.223; 90		2827.9Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516245 CIFC34 H51 O4 PP 1 21/n 19.9251; 11.2824; 28.061
90; 96.421; 90		3122.5Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516246 CIFC36 H53 O3 PP -18.568; 9.1013; 23.827
80.649; 86.357; 63.923		1646.6Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516247 CIFC39 H57 O3 PP n a 2128.119; 13.086; 9.328
90; 90; 90		3432.4Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516248 CIFC40.5 H60 Cl O4 PP -111.6617; 12.3698; 14.951
100.424; 92.731; 115.736		1891.2Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516249 CIFC31 H49 O2 PP b c a18.317; 13.782; 22.811
90; 90; 90		5758.5Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516250 CIFC43 H61.12 O2.06 PP -112.838; 16.357; 19.029
97.751; 102.559; 102.096		3744.9Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516251 CIFC42.5 H58 Br Cl3 N O4 P PdP -111.542; 11.548; 17.998
81.507; 77.635; 72.621		2227.2Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516252 CIFC53.5 H69 Br N O3 P PdP b c a17.7459; 19.0935; 53.801
90; 90; 90		18229.5Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516253 CIFC49.5 H69 Br Cl2 N O3 P PdC 1 2/c 127.66; 21.676; 19.545
90; 123.911; 90		9725Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516254 CIFC47 H63 Br N O4 P PdP 1 21/c 113.126; 11.472; 28.93
90; 91.981; 90		4354Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516255 CIFC53 H77 F3 N O7 P Pd SP 1 21 112.4741; 16.7555; 14.1454
90; 115.68; 90		2664.51Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516256 CIFC48 H71 F3 N O6 P Pd SC 1 2/c 128.3488; 18.5998; 19.6316
90; 112.701; 90		9549.5Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516257 CIFC51 H75 F3 N O6 P Pd SP 1 21/n 115.0843; 17.9837; 19.7605
90; 108.121; 90		5094.6Laffoon, Summer D.; Chan, Vincent S.; Fickes, Michael G.; Kotecki, Brian; Ickes, Andrew R.; Henle, Jeremy; Napolitano, José G.; Franczyk, Thaddeus S.; Dunn, Travis B.; Barnes, David M.; Haight, Anthony R.; Henry, Rodger F.; Shekhar, Shashank
Pd-Catalyzed Cross-Coupling Reactions Promoted by Biaryl Phosphorinane Ligands
ACS Catalysis, 2019, 11691
4516258 CIFC25 H24 OP -16.1623; 7.8828; 20.9413
85.746; 88.386; 77.055		988.59Wang, Quannan; Chen, Rongjun; Lou, Jiang; Zhang, Dong H.; Zhou, Yong-Gui; Yu, Zhengkun
Highly Regioselective C‒H Alkylation of Alkenes Through an Aryl to Vinyl 1,4-Palladium Migration/C‒C Cleavage Cascade
ACS Catalysis, 2019, 11669
4516585 CIFC28.5 H39 Br4 Cl N6 Ti2C 1 2/c 124.481; 9.2829; 32.174
90; 103.789; 90		7101Beaumier, Evan P.; McGreal, Meghan E.; Pancoast, Adam R.; Wilson, R. Hunter; Moore, James T.; Graziano, Brendan J.; Goodpaster, Jason D.; Tonks, Ian A.
Carbodiimide Synthesis via Ti-Catalyzed Nitrene Transfer from Diazenes to Isocyanides
ACS Catalysis, 2019, 11753
4516658 CIFC17 H16 OP -110.073; 10.958; 25.373
100.784; 100.991; 90.485		2697.9Qin, Guiping; Chen, Xiangning; Yang, Lei; Huang, Hanmin
Copper-Catalyzed α-Benzylation of Enones via Radical-Triggered Oxidative Coupling of Two C‒H Bonds
ACS Catalysis, 2015, 5, 2882
4516659 CIFC15 H19 F3 N4 O7P 1 21/c 110.6111; 9.3941; 19.1315
90; 91.384; 90		1906.5Huang, Lin; Lin, Jin-Shun; Tan, Bin; Liu, Xin-Yuan
Alkene Trifluoromethylation-Initiated Remote α-Azidation of Carbonyl Compounds toward Trifluoromethyl γ-Lactam and Spirobenzofuranone-Lactam
ACS Catalysis, 2015, 5, 2826
4516660 CIFC17 H15 Cl F3 N O5P n a 2115.896; 8.7193; 25.283
90; 90; 90		3504.3Huang, Lin; Lin, Jin-Shun; Tan, Bin; Liu, Xin-Yuan
Alkene Trifluoromethylation-Initiated Remote α-Azidation of Carbonyl Compounds toward Trifluoromethyl γ-Lactam and Spirobenzofuranone-Lactam
ACS Catalysis, 2015, 5, 2826
4516661 CIFC55 H40 Cl3 O3 P3 Si3P -3 c 115.5297; 15.5297; 24.1564
90; 90; 120		5045.3Iwai, Tomohiro; Konishi, Shota; Miyazaki, Tatsuya; Kawamorita, Soichiro; Yokokawa, Natsumi; Ohmiya, Hirohisa; Sawamura, Masaya
Silica-Supported Triptycene-Type Phosphine. Synthesis, Characterization, and Application to Pd-Catalyzed Suzuki‒Miyaura Cross-Coupling of Chloroarenes
ACS Catalysis, 2015, 5, 7254
4516662 CIFC38 H31 Cl N5 P RuP 1 21/c 133.581; 10.1257; 19.1334
90; 101.527; 90		6374.7Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516663 CIFC44.5 H38 Cl F6 N5 O6 P Ru S2C 1 2/c 131.847; 12.7757; 25.6211
90; 117.055; 90		9283.7Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516664 CIFC40 H33 F3 N5 O P RuP -19.4999; 10.3978; 18.4333
79.884; 84.512; 68.604		1667.97Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516665 CIFC54 H42 Cl N5 P2 RuP 1 21/c 111.5459; 20.4778; 18.8418
90; 104.485; 90		4313.2Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516666 CIFC56 H46 Cl N5 P2 RuP -111.8598; 13.6537; 16.6403
89.614; 87.952; 69.915		2529Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516667 CIFC60 H54 Cl N5 O3.5 P2 RuP 1 21/c 123.8181; 11.25; 20.994
90; 115.986; 90		5056.7Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516668 CIFC57 H49 Cl4 N5 P2 RuP n a 2121.7779; 23.4319; 9.6235
90; 90; 90		4910.8Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516669 CIFC97 H81 N10 P2 Ru2P -113.7897; 15.8415; 19.6154
71.991; 73.73; 81.086		3900.9Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516670 CIFC38 H32 Cl F6 N5 P2 RuP -19.0716; 12.721; 15.6504
93.195; 103.235; 93.102		1751.2Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516671 CIFC34 H25 B Cu F4 N4 O3 PP 1 21/n 112.5021; 13.6073; 19.1227
90; 108.373; 90		3087.32Knorn, Matthias; Rawner, Thomas; Czerwieniec, Rafał; Reiser, Oliver
[Copper(phenanthroline)(bisisonitrile)]±Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
ACS Catalysis, 2015, 5, 5186
4516672 CIFC42 H28 Cl10 N4 O6 P2 Pd2P -110.5194; 11.305; 12.8486
64.026; 86.154; 63.035		1207.7Knorn, Matthias; Rawner, Thomas; Czerwieniec, Rafał; Reiser, Oliver
[Copper(phenanthroline)(bisisonitrile)]±Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
ACS Catalysis, 2015, 5, 5186
4516673 CIFC47 H35 B Cl2 Cu F4 N4 O3 PP b c n30.0446; 11.56203; 24.6258
90; 90; 90		8554.4Knorn, Matthias; Rawner, Thomas; Czerwieniec, Rafał; Reiser, Oliver
[Copper(phenanthroline)(bisisonitrile)]±Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
ACS Catalysis, 2015, 5, 5186
4516674 CIFC44 H56 Fe Li N2 O Si2P 1 21/n 111.3913; 26.6073; 13.8664
90; 103.752; 90		4082.3Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516675 CIFC35 H33 Fe N2 O3 PP 1 21/c 114.14; 13.3999; 16.5218
90; 112.094; 90		2900.6Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516676 CIFC56 H53 Fe N2 PP 1 21/c 116.7305; 14.4122; 17.4229
90; 93.471; 90		4193.4Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516677 CIFC38 H33 Fe N5P n a 2116.9958; 10.2025; 17.6294
90; 90; 90		3056.9Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516678 CIFC368 H416 F24 Fe8 N16 Na4 O28.7 P4P 4/m n c17.2377; 17.2377; 27.3182
90; 90; 90		8117.3Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516679 CIFC32 H24 Cl2 Fe N2P 1 21/c 119.5314; 9.7274; 13.93
90; 99.058; 90		2613.55Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516680 CIFC46 H64 Fe N2 O4 TiP 21 21 2110.8375; 14.8073; 27.377
90; 90; 90		4393.3Brown, Lauren A.; Rhinehart, Jennifer L.; Long, Brian K.
Effects of Ferrocenyl Proximity and Monomer Presence during Oxidation for the Redox-Switchable Polymerization of l-Lactide
ACS Catalysis, 2015, 5, 6057
4516681 CIFC20 H18 F4P 1 21/a 16.1162; 15.02; 17.666
90; 96.537; 90		1612.3Ichitsuka, Tomohiro; Fujita, Takeshi; Ichikawa, Junji
Nickel-Catalyzed Allylic C(sp3)‒F Bond Activation of Trifluoromethyl Groups via β-Fluorine Elimination: Synthesis of Difluoro-1,4-dienes
ACS Catalysis, 2015, 5, 5947
4516682 CIFC35 H30 Cl2 N2 O4 SP 1 21 110.9711; 7.3155; 19.9974
90; 93.418; 90		1602.1Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita‒Baylis‒Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516683 CIFC20 H22 N2 O3 SP 1 21/c 17.7705; 22.437; 11.0377
90; 105.525; 90		1854.2Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita‒Baylis‒Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516684 CIFC35 H28 Cl2 N2 O4 SP -111.9029; 15.3015; 19.0001
85.692; 79.538; 67.684		3148.1Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita‒Baylis‒Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516685 CIFC24 H26 N2 O4 SP -19.3454; 9.7516; 14.35
92.675; 101.306; 115.481		1144.9Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita‒Baylis‒Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516686 CIFC34 H28 Cl2 N2 O4 SP 21 21 2110.3652; 10.371; 28.86
90; 90; 90		3102.4Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita‒Baylis‒Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516687 CIFC25 H23 N O5 SP 21 21 218.8035; 14.912; 17.9438
90; 90; 90		2355.62Liu, Ren-Rong; Wang, Dan-Jie; Wu, Liang; Xiang, Bin; Zhang, Guo-Qi; Gao, Jian-Rong; Jia, Yi-Xia
Nickel-Catalyzed Enantioselective Addition of Styrenes to Cyclic N-Sulfonyl α-Ketiminoesters
ACS Catalysis, 2015, 5, 6524
4516688 CIFC66 H68 N4 Pd2 S4P 1 21/n 115.6832; 11.3541; 16.787
90; 92.189; 90		2987.1Degtyareva, Evgeniya S.; Burykina, Julia V.; Fakhrutdinov, Artem N.; Gordeev, Evgeniy G.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd-NHC Catalytic System for the Efficient Atom-Economic Synthesis of Vinyl Sulfides from Tertiary, Secondary, or Primary Thiols
ACS Catalysis, 2015, 5, 7208
4516689 CIFC22 H15 P SP n a 218.233; 13.912; 15.188
90; 90; 90		1739.6Unoh, Yuto; Satoh, Tetsuya; Hirano, Koji; Miura, Masahiro
Rhodium(III)-Catalyzed Direct Coupling of Arylphosphine Derivatives with Heterobicyclic Alkenes: A Concise Route to Biarylphosphines and Dibenzophosphole Derivatives
ACS Catalysis, 2015, 5, 6634
4516690 CIFC24 H32 F3 I O3 SP 1 21/c 19.6451; 25.6279; 10.7472
90; 102.565; 90		2592.91Berzina, Beatrise; Sokolovs, Igors; Suna, Edgars
Copper-Catalyzed para-Selective C‒H Amination of Electron-Rich Arenes
ACS Catalysis, 2015, 5, 7008
4516691 CIFC50 H32 B F24 N3 Ni O2P -111.4773; 13.0681; 18.2775
70.951; 80.767; 78.887		2528.57Escobar, Manuel A.; Trofymchuk, Oleksandra S.; Rodriguez, Barbara E.; Lopez-Lira, Claudia; Tapia, Ricardo; Daniliuc, Constantin; Berke, Heinz; Nachtigall, Fabiane M.; Santos, Leonardo S.; Rojas, Rene S.
Lewis Acid Enhanced Ethene Dimerization and Alkene Isomerization—ESI-MS Identification of the Catalytically Active Pyridyldimethoxybenzimidazole Nickel(II) Hydride Species
ACS Catalysis, 2015, 5, 7338
4516692 CIFC124 H186 F24 Ir4 N12 O25 S8P 1 21/c 111.1326; 28.0168; 13.6059
90; 96.8149; 90		4213.7Kim, Hyunwoo; Chang, Sukbok
Iridium-Catalyzed Direct C‒H Amination with Alkylamines: Facile Oxidative Insertion of Amino Group into Iridacycle
ACS Catalysis, 2015, 5, 6665

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