Crystallography Open Database

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4517828 CIFC10 H20 K12 N10 O0 Ru2 Sn18C 1 2/c 115.327; 31.192; 13.692
90; 94.911; 90
6522Wang, Yanru; Zhang, Chao; Wang, Xiuyi; Guo, Jinqiu; Sun, Zhong-Ming; Zhang, Hongbo
Site-Selective CO2 Reduction over Highly Dispersed Ru-SnOx Sites Derived from a [Ru@Sn9]6‒ Zintl Cluster
ACS Catalysis, 2020, 7808
4517829 CIFC15 H13 N OP 1 21 17.6989; 5.6085; 13.528
90; 92.652; 90
583.5Mao, Ying; Wang, Zehua; Wang, Gang; Zhao, Ran; Kan, Linglong; Pan, Xiaoguang; Liu, Lei
Redox Deracemization of Tertiary Stereocenters Adjacent to an Electron-Withdrawing Group
ACS Catalysis, 2020, 7785-7791
4517830 CIFC72 H88 Fe2 N2 Si2P 1 21/c 114.1589; 20.1568; 10.773
90; 96.224; 90
3056.5Witzke, Ryan J.; Hait, Diptarka; Chakarawet, Khetpakorn; Head-Gordon, Martin; Tilley, T. Don
Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
ACS Catalysis, 2020, 7800
4517831 CIFC62 H82 Fe2 N2 O Si2P -112.131; 12.86; 18.9741
89.775; 87.91; 85.741
2949.9Witzke, Ryan J.; Hait, Diptarka; Chakarawet, Khetpakorn; Head-Gordon, Martin; Tilley, T. Don
Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
ACS Catalysis, 2020, 7800
4517832 CIFC21 H36 Fe N SiP b c n22.1414; 11.2865; 17.5402
90; 90; 90
4383.3Witzke, Ryan J.; Hait, Diptarka; Chakarawet, Khetpakorn; Head-Gordon, Martin; Tilley, T. Don
Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
ACS Catalysis, 2020, 7800
4517836 CIFC15 H20 Ir N3 O5 SP 1 21/c 18.656; 14.5247; 14.4235
90; 95.387; 90
1805.4Tensi, Leonardo; Macchioni, Alceo
Extremely Fast NADH-Regeneration Using Phosphonic Acid as Hydride Source and Iridium-pyridine-2-sulfonamidate Catalysts
ACS Catalysis, 2020, 7945
4517838 CIFC61 H46 O P2 PdP 1 21/n 118.3983; 13.9556; 20.8118
90; 109.351; 90
5041.7Xiong, Wenfang; Shi, Fuxing; Cheng, Ruixiang; Zhu, Baiyao; Wang, Lu; Chen, Pengquan; Lou, Hongming; Wu, Wanqing; Qi, Chaorong; Lei, Ming; Jiang, Huanfeng
Palladium-Catalyzed Highly Regioselective Hydrocarboxylation of Alkynes with Carbon Dioxide
ACS Catalysis, 2020, 7968
4517839 CIFC23 H28 O2P -110.0446; 12.2899; 17.0614
76.398; 74.831; 88.404
1974.5Xiong, Wenfang; Shi, Fuxing; Cheng, Ruixiang; Zhu, Baiyao; Wang, Lu; Chen, Pengquan; Lou, Hongming; Wu, Wanqing; Qi, Chaorong; Lei, Ming; Jiang, Huanfeng
Palladium-Catalyzed Highly Regioselective Hydrocarboxylation of Alkynes with Carbon Dioxide
ACS Catalysis, 2020, 7968
4517848 CIFC25 H24 N2 O2 PdP -19.3968; 9.484; 11.9025
103.496; 93.933; 90.76
1028.55Li, Ya; Zhang, Pan; Liu, Yue-Jin; Yu, Zhi-Xiang; Shi, Bing-Feng
Remote γ-C(sp3)‒H Alkylation of Aliphatic Carboxamides via an Unexpected Regiodetermining Pd Migration Process: Reaction Development and Mechanistic Study
ACS Catalysis, 2020, 8212-8222
4517849 CIFC19 H24 N4 O2 PdP 1 21/n 114.1106; 6.7889; 20.7976
90; 92.295; 90
1990.7Li, Ya; Zhang, Pan; Liu, Yue-Jin; Yu, Zhi-Xiang; Shi, Bing-Feng
Remote γ-C(sp3)‒H Alkylation of Aliphatic Carboxamides via an Unexpected Regiodetermining Pd Migration Process: Reaction Development and Mechanistic Study
ACS Catalysis, 2020, 8212-8222
4517850 CIFC20 H18 O2P 21 21 216.53867; 6.85703; 35.6756
90; 90; 90
1599.55Wang, Shou-Guo; Cramer, Nicolai
Asymmetric CpxRh(III)-Catalyzed Acrylic Acid C‒H Functionalization with Allenes Provides Chiral γ-Lactones
ACS Catalysis, 2020, 8231-8236
4517851 CIFC25 H23 F N2 OP 21 21 219.2261; 9.7377; 22.6198
90; 90; 90
2032.19Shen, Yang; Shen, Meng-Lan; Wang, Pu-Sheng
Light-Mediated Chiral Phosphate Catalysis for Asymmetric Dicarbofunctionalization of Enamides
ACS Catalysis, 2020, 8247-8253
4517857 CIFC26 H20 F N3 O2 SC 1 2/c 119.9143; 10.6749; 20.1936
90; 92.357; 90
4289.2Hu, Xinwei; Shao, Youxiang; Xie, Haisheng; Chen, Xin; Chen, Fengjuan; Ke, Zhuofeng; Jiang, Huanfeng; Zeng, Wei
Direct Carbon‒Carbon σ Bond Amination of Unstrained Arylalkylketones
ACS Catalysis, 2020, 8402-8408
4517858 CIFC26 H21 N3 O2 SC 1 2/c 119.925; 10.806; 20.27
90; 92.45; 90
4360.3Hu, Xinwei; Shao, Youxiang; Xie, Haisheng; Chen, Xin; Chen, Fengjuan; Ke, Zhuofeng; Jiang, Huanfeng; Zeng, Wei
Direct Carbon‒Carbon σ Bond Amination of Unstrained Arylalkylketones
ACS Catalysis, 2020, 8402-8408
4517861 CIFC26 H40 Hf N2P 419.491; 9.491; 27.7364
90; 90; 90
2498.47Wallace, Mark A.; Zavalij, Peter Y.; Sita, Lawrence R.
Enantioselective Living Coordinative Chain Transfer Polymerization: Production of Optically Active End-Group-Functionalized (+)- or (−)-Poly(methylene-1,3-cyclopentane) via a Homochiral C1-Symmetric Caproamidinate Hafnium Initiator
ACS Catalysis, 2020, 8496-8502
4517862 CIFC26 H40 Hf N2P 439.4877; 9.4877; 27.766
90; 90; 90
2499.4Wallace, Mark A.; Zavalij, Peter Y.; Sita, Lawrence R.
Enantioselective Living Coordinative Chain Transfer Polymerization: Production of Optically Active End-Group-Functionalized (+)- or (−)-Poly(methylene-1,3-cyclopentane) via a Homochiral C1-Symmetric Caproamidinate Hafnium Initiator
ACS Catalysis, 2020, 8496-8502
4517870 CIFC20 H24 O4 S2P 1 21/n 119.047; 8.804; 24.664
90; 105.975; 90
3976.2Gadde, Karthik; Mampuys, Pieter; Guidetti, Andrea; Ching, H. Y. Vincent; Herrebout, Wouter A.; Van Doorslaer, Sabine; Abbaspour Tehrani, Kourosch; Maes, Bert U. W.
Thiosulfonylation of Unactivated Alkenes with Visible-Light Organic Photocatalysis
ACS Catalysis, 2020, 8765-8779
4517879 CIFC75 H109.5 Cl Cr2 N5.5 O5P 21 21 2117.0512; 20.0506; 22.7296
90; 90; 90
7770.9Lipinski, Bryce M.; Walker, Katherine L.; Clayman, Naomi E.; Morris, Lilliana S.; Jugovic, Timothy M. E.; Roessler, Allison G.; Getzler, Yutan D. Y. L.; MacMillan, Samantha N.; Zare, Richard N.; Zimmerman, Paul M.; Waymouth, Robert M.; Coates, Geoffrey W.
Mechanistic Study of Isotactic Poly(propylene oxide) Synthesis using a Tethered Bimetallic Chromium Salen Catalyst
ACS Catalysis, 2020, 8960-8967
4517880 CIFC44.33 H22 Ni0.44 O17 Zr3P 6/m m m39.4522; 39.4522; 16.5041
90; 90; 120
22246.7Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517881 CIFC34 H16 Br2 Ni0.4 O17.3 Zr3P 6/m m m39.903; 39.903; 12.022
90; 90; 120
16577Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517882 CIFC10 H7 Ni0.1 O4 Zr0.75P m -3 m28.2651; 28.2651; 28.2651
90; 90; 90
22581.4Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517883 CIFC34.8 H16 Br2 Hf3 Ni0.44 O16P 6/m m m40.4333; 40.4333; 11.4682
90; 90; 120
16236.9Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517884 CIFC11 H6 Hf0.81 Ni0.16 O4P 6/m m m39.601; 39.601; 16.4314
90; 90; 120
22316Wang, Xingjie; Zhang, Xuan; Pandharkar, Riddhish; Lyu, Jiafei; Ray, Debmalya; Yang, Ying; Kato, Satoshi; Liu, Jian; Wasson, Megan C.; Islamoglu, Timur; Li, Zhong; Hupp, Joseph T.; Cramer, Christopher J.; Gagliardi, Laura; Farha, Omar K.
Insights into the Structure‒Activity Relationships in Metal‒Organic Framework-Supported Nickel Catalysts for Ethylene Hydrogenation
ACS Catalysis, 2020, 8995-9005
4517890 CIFC18 H21 Cl2 N OP 1 21 17.6233; 7.8881; 13.5115
90; 91.9018; 90
812.04Rong, Zi-Qiang; Yu, Zhaoyuan; Weng, Cheng; Yang, Li-Cheng; Lu, Shenci; Lan, Yu; Zhao, Yu
Dynamic Kinetic Asymmetric Amination of Alcohols Assisted by Microwave: Stereoconvergent Access to Tetralin- and Indane-Derived Chiral Amines
ACS Catalysis, 2020, 9464
4517967 CIFC36 H60 B2 Ir N O4 P2P -114.485; 16.26; 17.548
84.689; 89.852; 71.719
3906Foley, Bryan J.; Bhuvanesh, Nattamai; Zhou, Jia; Ozerov, Oleg V.
Combined Experimental and Computational Studies of the Mechanism of Dehydrogenative Borylation of Terminal Alkynes Catalyzed by PNP Complexes of Iridium
ACS Catalysis, 2020, 9824-9836
4517986 CIFC32 H28 Fe2 N4 O5P -110.734; 10.815; 13.738
67.142; 85.858; 73.156
1405.06Provis-Evans, Cei B.; Lau, Samantha; Krewald, Vera; Webster, Ruth L.
Regioselective Alkyne Cyclotrimerization with an In Situ-Generated [Fe(II)H(salen)]·Bpin Catalyst
ACS Catalysis, 2020, 10157-10168
4517987 CIFC17 H17 N O2P 1 21/c 111.2862; 9.2093; 13.1111
90; 109.258; 90
1286.49Zhang, Zhijie; Yi, Dong; Zhang, Min; Wei, Jun; Lu, Ji; Yang, Lin; Wang, Jun; Hao, Na; Pan, Xianchao; Zhang, Shiqi; Wei, Siping; Fu, Qiang
Photocatalytic Intramolecular [2 + 2] Cycloaddition of Indole Derivatives via Energy Transfer: A Method for Late-Stage Skeletal Transformation
ACS Catalysis, 2020, 10149-10156
4517988 CIFC13 H13 N OP 1 21/n 18.31074; 13.9007; 8.8665
90; 96.992; 90
1016.69Zhang, Zhijie; Yi, Dong; Zhang, Min; Wei, Jun; Lu, Ji; Yang, Lin; Wang, Jun; Hao, Na; Pan, Xianchao; Zhang, Shiqi; Wei, Siping; Fu, Qiang
Photocatalytic Intramolecular [2 + 2] Cycloaddition of Indole Derivatives via Energy Transfer: A Method for Late-Stage Skeletal Transformation
ACS Catalysis, 2020, 10149-10156
4517994 CIFC27 H34 Si2C 1 2/c 114.963; 12.0779; 28.792
90; 105.06; 90
5024.6Lv, Weiwei; Liu, Shihan; Chen, Yanhui; Wen, Si; Lan, Yu; Cheng, Guolin
Palladium-Catalyzed Intermolecular Trans-Selective Carbofunctionalization of Internal Alkynes to Highly Functionalized Alkenes
ACS Catalysis, 2020, 10516
4517995 CIFC30 H28 O2P 1 21/n 111.0772; 15.556; 14.641
90; 110.201; 90
2367.7Lv, Weiwei; Liu, Shihan; Chen, Yanhui; Wen, Si; Lan, Yu; Cheng, Guolin
Palladium-Catalyzed Intermolecular Trans-Selective Carbofunctionalization of Internal Alkynes to Highly Functionalized Alkenes
ACS Catalysis, 2020, 10516
4518014 CIFC110 H72 F12 N10 O2 P2 Ru2P -117.1459; 19.6957; 21.0108
93.42; 112.713; 112.979
5837.9Rajabi, Sheida; Ebrahimi, Fatemeh; Lole, Gaurav; Odrobina, Jann; Dechert, Sebastian; Jooss, Christian; Meyer, Franc
Water Oxidizing Diruthenium Electrocatalysts Immobilized on Carbon Nanotubes: Effects of the Number and Positioning of Pyrene Anchors
ACS Catalysis, 2020, 10614
4518015 CIFC70.5 H58 F12 N10 O3 P2 Ru2P -114.2194; 20.0432; 26.3213
83.352; 79.323; 87.701
7320.9Rajabi, Sheida; Ebrahimi, Fatemeh; Lole, Gaurav; Odrobina, Jann; Dechert, Sebastian; Jooss, Christian; Meyer, Franc
Water Oxidizing Diruthenium Electrocatalysts Immobilized on Carbon Nanotubes: Effects of the Number and Positioning of Pyrene Anchors
ACS Catalysis, 2020, 10614
4518016 CIFC32 H32 N2 O4 S2P 1 21/c 110.9602; 14.7542; 18.1626
90; 94.857; 90
2926.5Qian, Xiaolin; Zhou, Hui; Chaminda Lakmal, Hetti Handi; Lucore, James; Wang, Xuesong; Valle, Henry U.; Donnadieu, Bruno; Xu, Xue; Cui, Xin
Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α-Substituted Styrene Derivatives
ACS Catalysis, 2020, 10627
4518017 CIFC26 H28 N2 O4 S2P -19.95; 10.42; 13.328
73.734; 83.867; 67.198
1222.9Qian, Xiaolin; Zhou, Hui; Chaminda Lakmal, Hetti Handi; Lucore, James; Wang, Xuesong; Valle, Henry U.; Donnadieu, Bruno; Xu, Xue; Cui, Xin
Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α-Substituted Styrene Derivatives
ACS Catalysis, 2020, 10627
4518020 CIFC27 H25 Br O2P 19.6954; 10.1078; 22.4793
97.438; 97.121; 90.238
2167.11McLeod, David; Izzo, Joseph A.; Jørgensen, Danny K. B.; Lauridsen, Rune F.; Jørgensen, Karl Anker
Development and Investigation of an Organocatalytic Enantioselective [10 + 2] Cycloaddition
ACS Catalysis, 2020, 10784
4518021 CIFC82 H82 B F24 Li Ni O7 P2P -114.2489; 14.2542; 20.5358
84.356; 86.902; 86.242
4137.1Tran, Thi V.; Karas, Lucas J.; Wu, Judy I.; Do, Loi H.
Elucidating Secondary Metal Cation Effects on Nickel Olefin Polymerization Catalysts
ACS Catalysis, 2020, 10760
4518022 CIFC80.5 H85.6 B F24 K Ni O8 P2P -113.151; 13.356; 24.585
86.239; 81.17; 87.895
4256.3Tran, Thi V.; Karas, Lucas J.; Wu, Judy I.; Do, Loi H.
Elucidating Secondary Metal Cation Effects on Nickel Olefin Polymerization Catalysts
ACS Catalysis, 2020, 10760
4518023 CIFC76 H68 B Cs F24 Ni O7 P2P 1 21/n 117.3656; 23.606; 20.3261
90; 103.682; 90
8095.9Tran, Thi V.; Karas, Lucas J.; Wu, Judy I.; Do, Loi H.
Elucidating Secondary Metal Cation Effects on Nickel Olefin Polymerization Catalysts
ACS Catalysis, 2020, 10760
4518024 CIFC21 H18 N2P -18.9756; 9.0718; 11.0372
84.016; 85.238; 62.683
793.5Wang, Shengdong; Force, Guillaume; Guillot, Régis; Carpentier, Jean-François; Sarazin, Yann; Bour, Christophe; Gandon, Vincent; Lebœuf, David
Lewis Acid/Hexafluoroisopropanol: A Promoter System for Selective ortho-C-Alkylation of Anilines with Deactivated Styrene Derivatives and Unactivated Alkenes
ACS Catalysis, 2020, 10794
4518037 CIFC29 H26 N2 O4 SP 1 21/c 116.6324; 12.5786; 23.5913
90; 90.5504; 90
4935.4De, Nirupam; Ko, Donguk; Baek, Seung-yeol; Oh, Changjin; Kim, Jiyoung; Baik, Mu-Hyun; Yoo, Eun Jeong
Cu(I)-Catalyzed Enantioselective [5 + 1] Cycloaddition of N-Aromatic Compounds and Alkynes via Chelating-Assisted 1,2-Dearomative Addition
ACS Catalysis, 2020, 10905
4518038 CIFC30 H27 Cl N2 O5 SP 1 21/c 19.7732; 22.9861; 12.4889
90; 107.777; 90
2671.64De, Nirupam; Ko, Donguk; Baek, Seung-yeol; Oh, Changjin; Kim, Jiyoung; Baik, Mu-Hyun; Yoo, Eun Jeong
Cu(I)-Catalyzed Enantioselective [5 + 1] Cycloaddition of N-Aromatic Compounds and Alkynes via Chelating-Assisted 1,2-Dearomative Addition
ACS Catalysis, 2020, 10905
4518039 CIFC27 H26 N4 O6P 1 21 17.25553; 7.4022; 47.0222
90; 92.058; 90
2523.79Xue, Zaikun; Li, Yao; Luo, Sanzhong
Chiral Primary Amine-Catalyzed Divergent Coupling of α-Substituted Acrylaldehydes with α-Diazoesters
ACS Catalysis, 2020, 10989
4518040 CIFC1.74 H1.74 O0.35P 21 21 216.4822; 15.0713; 16.8103
90; 90; 90
1642.29Xue, Zaikun; Li, Yao; Luo, Sanzhong
Chiral Primary Amine-Catalyzed Divergent Coupling of α-Substituted Acrylaldehydes with α-Diazoesters
ACS Catalysis, 2020, 10989
4518041 CIFC18 H22 B N2 O3 S SiP -18.5976; 9.2734; 12.5694
104.461; 99.599; 96.061
945.36Desrosiers, Vincent; Garcia, Cecilia Zavaleta; Fontaine, Frédéric-Georges
Boron Recycling in the Metal-Free Transfer C‒H Borylation of Terminal Alkynes and Heteroarenes
ACS Catalysis, 2020, 11046
4518044 CIFC34 H34 Cl N4 O5 PP -110.705; 11.4472; 13.9654
97.31; 112.09; 95.568
1553.18Garrido-González, José J.; Iglesias Aparicio, Ma Mercedes; García, Miguel Martínez; Simón, Luis; Sanz, Francisca; Morán, Joaquín R.; Fuentes de Arriba, Ángel L.
An Enzyme Model Which Mimics Chymotrypsin and N-Terminal Hydrolases
ACS Catalysis, 2020, 11162
4518051 CIFC11 H21 N O3P c a 219.8601; 5.6544; 44.1243
90; 90; 90
2460.06Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518052 CIFC11 H21 N O3P b c a9.2362; 10.9879; 23.7378
90; 90; 90
2409.06Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518053 CIFC12 H16 OP 1 21/c 114.6389; 5.303; 13.1361
90; 106.994; 90
975.23Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518054 CIFC15 H28 O2P 1 21/c 19.1475; 19.6782; 7.9541
90; 92.11; 90
1430.82Wollenburg, Marco; Heusler, Arne; Bergander, Klaus; Glorius, Frank
trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives
ACS Catalysis, 2020, 10, 11365-11370
4518056 CIFC20 H24 O5 S2P b c a13.1697; 8.5458; 33.8861
90; 90; 90
3813.73Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518057 CIFC128 H210 O13C 1 2 127.5054; 7.159; 28.9864
90; 91.009; 90
5706.86Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518058 CIFC15 H20 O2P 1 21/n 16.46515; 7.56208; 26.4823
90; 93.8866; 90
1291.74Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518059 CIFC20 H30 B N O4P 1 21/c 113.4325; 9.9472; 15.5089
90; 101.16; 90
2033.05Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518060 CIFC20 H22 F2 O4 S2P 1 21/c 111.66361; 15.02503; 11.25687
90; 97.1362; 90
1957.44Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518061 CIFC37 H56 O3 SP 1 21 114.75517; 11.9167; 18.31913
90; 93.7103; 90
3214.35Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518062 CIFC16 H26 O2C 1 2/c 123.988; 6.72515; 18.4587
90; 109.443; 90
2808Dang, Hang T.; Haug, Graham C.; Nguyen, Vu T.; Vuong, Ngan T. H.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V.
Acridine Photocatalysis: Insights into the Mechanism and Development of a Dual-Catalytic Direct Decarboxylative Conjugate Addition
ACS Catalysis, 2020, 10, 11448-11457
4518064 CIFC14 H12 O5P 1 21/c 114.8299; 7.4261; 11.4598
90; 109.078; 90
1192.73Karlinskii, Bogdan Ya.; Kostyukovich, Alexander Yu.; Kucherov, Fedor A.; Galkin, Konstantin I.; Kozlov, Kirill S.; Ananikov, Valentine P.
Directing-Group-Free, Carbonyl Group-Promoted Catalytic C‒H Arylation of Bio-Based Furans
ACS Catalysis, 2020, 10, 11466-11480
4518065 CIFC18 H12 O3C 1 2/c 112.3333; 11.1772; 19.7023
90; 101.316; 90
2663.2Karlinskii, Bogdan Ya.; Kostyukovich, Alexander Yu.; Kucherov, Fedor A.; Galkin, Konstantin I.; Kozlov, Kirill S.; Ananikov, Valentine P.
Directing-Group-Free, Carbonyl Group-Promoted Catalytic C‒H Arylation of Bio-Based Furans
ACS Catalysis, 2020, 10, 11466-11480
4518066 CIFC13 H7 F3 O3P 1 21/c 111.0065; 13.6364; 7.4223
90; 101.195; 90
1092.81Karlinskii, Bogdan Ya.; Kostyukovich, Alexander Yu.; Kucherov, Fedor A.; Galkin, Konstantin I.; Kozlov, Kirill S.; Ananikov, Valentine P.
Directing-Group-Free, Carbonyl Group-Promoted Catalytic C‒H Arylation of Bio-Based Furans
ACS Catalysis, 2020, 10, 11466-11480
4518081 CIFC23 H27.38 Ir N O2.69P -18.2522; 10.6947; 11.645
88.833; 86.13; 88.885
1025Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518082 CIFC30 H36 N4 O SiP -111.2966; 17.3143; 23.2024
101.869; 102.938; 99.047
4228.98Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518083 CIFC32 H44 Ir N SiP 1 21/n 111.3222; 18.4507; 14.6046
90; 103.017; 90
2972.54Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518084 CIFC22 H28 F N O SiP 1 21/c 120.944; 8.1654; 12.3532
90; 97.35; 90
2095.24Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518085 CIFC39 H55.66 Cl2 N2 O2.83 Si2P -17.4568; 20.0275; 27.8489
88.958; 84.338; 80.073
4076.73Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518086 CIFC26 H31 N O SiP c a 2124.9365; 11.3131; 8.3785
90; 90; 90
2363.65Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518087 CIFC33 H48 F N Si2P 1 21 18.0636; 13.035; 15.6853
90; 96.548; 90
1637.91Ye, Xiaohan; Wang, Chenhuan; Zhang, Shuyao; Wei, Jingwen; Shan, Chuan; Wojtas, Lukasz; Xie, Yan; Shi, Xiaodong
Facilitating Ir-Catalyzed C‒H Alkynylation with Electrochemistry: Anodic Oxidation-Induced Reductive Elimination
ACS Catalysis, 2020, 11693-11699
4518091 CIFC21 H34 Br2 O4 SiP b c a12.8335; 14.5079; 25.395
90; 90; 90
4728.22Schäfers, Felix; Quach, Linda; Schwarz, J. Luca; Saladrigas, Mar; Daniliuc, Constantin G.; Glorius, Frank
Direct Access to Monoprotected Homoallylic 1,2-Diols via Dual Chromium/Photoredox Catalysis
ACS Catalysis, 2020, 11841-11847
4518092 CIFC42 H52 F6 Mn N4 O6 S2P 21 21 2110.8133; 18.3449; 22.899
90; 90; 90
4542.4Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518093 CIFC53 H76 Cl2 F6 Mn N4 O9 S2P 43 21 218.048; 18.048; 18.684
90; 90; 90
6086Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518094 CIFC36 H40 F6 Mn N4 O8 S2P 43 21 215.2678; 15.2678; 17.167
90; 90; 90
4001.7Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518095 CIFC42 H52 F6 Mn N4 O6 S2P 21 21 2110.8038; 18.2978; 22.8902
90; 90; 90
4525.1Lin, Jin; Miao, Chengxia; Wang, Fang; Yang, Peiju; Sun, Qiangsheng; Sun, Wei
Effect of Ligand Topology on the Reactivity of Chiral Tetradentate Aminopyridine Manganese Complexes
ACS Catalysis, 2020, 11857-11863
4518103 CIFC25 H25 N O5P 1 21 111.568; 14.8438; 12.2105
90; 94.94; 90
2088.91Harada, Shingo; Yanagawa, Mai; Nemoto, Tetsuhiro
Dual-Functional Enone-Directing Group/Electrophile for Sequential C‒C Bond Formation with α-Diazomalonates: A Short Synthesis of Chiral 3,4-Fused Tricyclic Indoles
ACS Catalysis, 2020, 11971-11979
4518108 CIFC14 H18 Br NP 21 21 216.4796; 10.8112; 17.4816
90; 90; 90
1224.63Li, Zhenghua; Zhang, Liang; Nishiura, Masayoshi; Luo, Gen; Luo, Yi; Hou, Zhaomin
Enantioselective Cyanoborylation of Allenes by N-Heterocyclic Carbene-Copper Catalysts
ACS Catalysis, 2020, 11685-11692
4518109 CIFC5 H8 F N OP 1 21/c 110.9416; 5.8946; 8.9783
90; 112.366; 90
535.51Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518110 CIFC5 H8 F N OP 1 21/c 16.8234; 7.0364; 11.2928
90; 93.296; 90
541.29Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518111 CIFC12 H13 F4 NP b c n16.6845; 6.2599; 21.2252
90; 90; 90
2216.83Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518112 CIFC13 H14 F4 N2 OP 1 21/c 112.8484; 8.4676; 11.8938
90; 95.519; 90
1287.99Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518113 CIFC13 H19 F N2 O2P 1 21/n 111.8985; 7.4145; 15.3304
90; 101.584; 90
1324.92Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518114 CIFC7 H11 F N2 OP 1 21/c 14.7931; 12.9627; 12.803
90; 97.469; 90
788.72Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518115 CIFC5 H11 Cl F NP 1 21 16.6025; 7.3672; 7.036
90; 90.746; 90
342.216Wagener, Tobias; Heusler, Arne; Nairoukh, Zackaria; Bergander, Klaus; Daniliuc, Constantin G.; Glorius, Frank
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation
ACS Catalysis, 2020, 12052-12057
4518119 CIFC47 H51 Al Cl4 N5 O4 P2 RhP 1 21/n 115.4262; 17.0323; 19.6403
90; 111.781; 90
4791.96Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518120 CIFC88 H68 Cl14 Ga4 N8 P4 Rh2P -116.4861; 17.1218; 18.1159
102.604; 96.8135; 92.8749
4939.85Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518121 CIFC47 H45 Cl7 In2 N3 O2 P2 RhP -112.4389; 13.5826; 15.0995
83.4699; 80.9723; 86.2699
2500.25Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518122 CIFC126 H110 Cl12 Ga4 N6 O3 P6 Rh2C 1 2/c 137.4179; 14.6854; 22.6886
90; 90.5378; 90
12466.8Takaya, Jun; Ogawa, Koki; Nakaya, Ryota; Iwasawa, Nobuharu
Rhodium-Catalyzed Chemoselective Hydrosilylation of Nitriles to an Imine Oxidation Level Enabled by a Pincer-type Group 13 Metallylene Ligand
ACS Catalysis, 2020, 10, 12223-12228
4518130 CIFC11 H12 F3 N O2 SP -17.1106; 8.8828; 9.8984
77.175; 89.3; 74.07
585.4Ge, Hangming; Wu, Botao; Liu, Yafei; Wang, Haoyang; Shen, Qilong
Synergistic Lewis Acid and Photoredox-Catalyzed Trifluoromethylative Difunctionalization of Alkenes with Selenium Ylide-Based Trifluoromethylating Reagent
ACS Catalysis, 2020, 12414-12424
4518133 CIFC57 H37 Al Cl10 N2 O2P 1 21/c 112.236; 21.4326; 20.1723
90; 103.841; 90
5136.56Hubbell, Aran K.; Lamb, Jessica R.; Klimovica, Kristine; Mulzer, Michael; Shaffer, Timothy D.; MacMillan, Samantha N.; Coates, Geoffrey W.
Catalyst-Controlled Regioselective Carbonylation of Isobutylene Oxide to Pivalolactone
ACS Catalysis, 2020, 12537-12543
4518134 CIFC96 H86 Al B N2 O7P 1 n 114.16596; 24.26807; 21.69468
90; 95.347; 90
7425.75Hubbell, Aran K.; Lamb, Jessica R.; Klimovica, Kristine; Mulzer, Michael; Shaffer, Timothy D.; MacMillan, Samantha N.; Coates, Geoffrey W.
Catalyst-Controlled Regioselective Carbonylation of Isobutylene Oxide to Pivalolactone
ACS Catalysis, 2020, 12537-12543
4518143 CIFC20 H20 N2 O2P 1 21/c 112.058; 9.432; 14.999
90; 104.566; 90
1651Zhu, Min; Zhang, Xiao; Zheng, Chao; You, Shu-Li
Visible-Light-Induced Dearomatization via [2+2] Cycloaddition or 1,5-Hydrogen Atom Transfer: Divergent Reaction Pathways of Transient Diradicals
ACS Catalysis, 2020, 12618-12626
4518144 CIFC17 H20 N2 O2P 1 21/c 111.248; 13.4191; 9.9224
90; 96.859; 90
1486.95Zhu, Min; Zhang, Xiao; Zheng, Chao; You, Shu-Li
Visible-Light-Induced Dearomatization via [2+2] Cycloaddition or 1,5-Hydrogen Atom Transfer: Divergent Reaction Pathways of Transient Diradicals
ACS Catalysis, 2020, 12618-12626
4518145 CIFC20 H19 Cl N2 O2P 1 21/c 18.425; 13.085; 16.325
90; 104.597; 90
1741.6Zhu, Min; Zhang, Xiao; Zheng, Chao; You, Shu-Li
Visible-Light-Induced Dearomatization via [2+2] Cycloaddition or 1,5-Hydrogen Atom Transfer: Divergent Reaction Pathways of Transient Diradicals
ACS Catalysis, 2020, 12618-12626
4518146 CIFC20 H16 Br2 Co N4P 1 21/c 18.567; 14.5739; 15.62
90; 97.596; 90
1933.1Dorval, Céline; Tricoire, Maxime; Begouin, Jeanne-Marie; Gandon, Vincent; Gosmini, Corinne
Cobalt-Catalyzed C(sp2)‒CN Bond Activation: Cross-Electrophile Coupling for Biaryl Formation and Mechanistic Insight
ACS Catalysis, 2020, 12819-12827
4518147 CIFC120 H96 Br9 Co4 Mn2 N24P 63 2 213.2935; 13.2935; 40.9
90; 90; 120
6259.4Dorval, Céline; Tricoire, Maxime; Begouin, Jeanne-Marie; Gandon, Vincent; Gosmini, Corinne
Cobalt-Catalyzed C(sp2)‒CN Bond Activation: Cross-Electrophile Coupling for Biaryl Formation and Mechanistic Insight
ACS Catalysis, 2020, 12819-12827
4518163 CIFC22 H30 B Fe NP 21 21 219.618; 14.2124; 14.4586
90; 90; 90
1976.42Dong, Wu-Wei; Li, Yi-Nan; Chang, Xin; Shen, Chong; Wang, Chun-Jiang
Chiral Ugi-Type Amines: Practical Synthesis, Ligand Development, and Asymmetric Catalysis
ACS Catalysis, 2020, 12954-12959
4518164 CIFC27 H27 N O5P 1 21/c 113.9717; 22.3087; 15.064
90; 90.591; 90
4695.06Sugawara, Masumi; Ohnishi, Rikako; Ezawa, Tetsuya; Akakabe, Mai; Sawamura, Miki; Hojo, Daiki; Hashizume, Daisuke; Sohtome, Yoshihiro; Sodeoka, Mikiko
Regiodivergent Oxidative Cross-Coupling of Catechols with Persistent tert-Carbon Radicals
ACS Catalysis, 2020, 12770-12782
4518165 CIFC96 H82 B2 F8 O6 P4 Pd2P 21 21 2113.7004; 20.3764; 29.3278
90; 90; 90
8187.3Sugawara, Masumi; Ohnishi, Rikako; Ezawa, Tetsuya; Akakabe, Mai; Sawamura, Miki; Hojo, Daiki; Hashizume, Daisuke; Sohtome, Yoshihiro; Sodeoka, Mikiko
Regiodivergent Oxidative Cross-Coupling of Catechols with Persistent tert-Carbon Radicals
ACS Catalysis, 2020, 12770-12782
4518175 CIFC24 H42 Cl Ir N O6 PP -17.9554; 13.3409; 13.583
108.591; 95.505; 94.138
1352Dodge, Henry M.; Kita, Matthew R.; Chen, Chun-Hsing; Miller, Alexander J. M.
Identifying and Evading Olefin Isomerization Catalyst Deactivation Pathways Resulting from Ion-Tunable Hemilability
ACS Catalysis, 2020, 13019-13030
4518176 CIFC97 H72 B2 F48 Ir Li N O5 PP 112.8158; 12.8715; 17.2525
80.155; 89.504; 66.413
2564.14Dodge, Henry M.; Kita, Matthew R.; Chen, Chun-Hsing; Miller, Alexander J. M.
Identifying and Evading Olefin Isomerization Catalyst Deactivation Pathways Resulting from Ion-Tunable Hemilability
ACS Catalysis, 2020, 13019-13030
4518181 CIFC7 H13 Cl OP 21 21 215.24; 6.2805; 23.9605
90; 90; 90
788.54Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518182 CIFC8 H15 Cl OP 1 21 16.2973; 5.2861; 12.6948
90; 93.567; 90
421.77Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518183 CIFC9 H15 Cl O2P 21 21 217.2887; 9.0165; 15.2516
90; 90; 90
1002.31Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518184 CIFC10 H16 O2P 21 21 216.1266; 8.4858; 18.3913
90; 90; 90
956.15Venturi, Silvia; Brenna, Elisabetta; Colombo, Danilo; Fraaije, Marco W.; Gatti, Francesco G.; Macchi, Piero; Monti, Daniela; Trajkovic, Milos; Zamboni, Emilio
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers
ACS Catalysis, 2020, 13050-13057
4518185 CIFC68 H56 Cl2 Cu2 F8 O2 P4P -113.3478; 14.062; 17.8249
90.177; 93.026; 114.592
3036.8Kang, Taeho; Erbay, Tuğçe G.; Xu, Kane L.; Gallego, Gary M.; Burtea, Alexander; Nair, Sajiv K.; Patman, Ryan L.; Zhou, Ru; Sutton, Scott C.; McAlpine, Indrawan J.; Liu, Peng; Engle, Keary M.
Multifaceted Substrate‒Ligand Interactions Promote the Copper-Catalyzed Hydroboration of Benzylidenecyclobutanes and Related Compounds
ACS Catalysis, 2020, 13075-13083
4518186 CIFC80 H64 Cl2 Cu2 F24 O3 P4P -116.4338; 16.5229; 17.2231
69.906; 77.081; 64.824
3958.2Kang, Taeho; Erbay, Tuğçe G.; Xu, Kane L.; Gallego, Gary M.; Burtea, Alexander; Nair, Sajiv K.; Patman, Ryan L.; Zhou, Ru; Sutton, Scott C.; McAlpine, Indrawan J.; Liu, Peng; Engle, Keary M.
Multifaceted Substrate‒Ligand Interactions Promote the Copper-Catalyzed Hydroboration of Benzylidenecyclobutanes and Related Compounds
ACS Catalysis, 2020, 13075-13083
4518195 CIFC20 H19 Br N2 O3P 21 21 2111.3768; 13.3425; 24.5874
90; 90; 90
3732.24Harada, Shingo; Kobayashi, Mayu; Kono, Masato; Nemoto, Tetsuhiro
Site-Selective and Chemoselective C‒H Functionalization for the Synthesis of Spiroaminals via a Silver-Catalyzed Nitrene Transfer Reaction
ACS Catalysis, 2020, 10, 13296-13304
4518198 CIFC20 H24 I N2 RhP 1 21/c 114.0181; 8.46; 16.4369
90; 102.753; 90
1901.2Sánchez-Page, Beatriz; Munarriz, Julen; Jiménez, M. Victoria; Pérez-Torrente, Jesús J.; Blasco, Javier; Subias, Gloria; Passarelli, Vincenzo; Álvarez, Patricia
β-(Z) Selectivity Control by Cyclometalated Rhodium(III)‒Triazolylidene Homogeneous and Heterogeneous Terminal Alkyne Hydrosilylation Catalysts
ACS Catalysis, 2020, 10, 13334-13351
4518199 CIFC26 H28 Cl3 I N3 RhP 1 21/c 117.652; 12.0217; 14.0368
90; 113.194; 90
2738Sánchez-Page, Beatriz; Munarriz, Julen; Jiménez, M. Victoria; Pérez-Torrente, Jesús J.; Blasco, Javier; Subias, Gloria; Passarelli, Vincenzo; Álvarez, Patricia
β-(Z) Selectivity Control by Cyclometalated Rhodium(III)‒Triazolylidene Homogeneous and Heterogeneous Terminal Alkyne Hydrosilylation Catalysts
ACS Catalysis, 2020, 10, 13334-13351
4518200 CIFC30 H31 N5 TiP 43 21 212.9396; 12.9396; 35.996
90; 90; 90
6026.9See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518201 CIFC82.52 H77.04 N10 Ti2P 1 21/n 19.4737; 36.2928; 19.9562
90; 95.112; 90
6834.2See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518202 CIFC80 H78 Cl N2 O3 P3 Ti2P 1 21/c 124.117; 15.0952; 20.943
90; 114.01; 90
6964.6See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518203 CIFC50 H62 Cl4 N6 Ti2P -19.8644; 12.5071; 12.5128
116.587; 93.947; 112.994
1213.89See, Xin Yi; Wen, Xuelan; Wheeler, T. Alexander; Klein, Channing K.; Goodpaster, Jason D.; Reiner, Benjamin R.; Tonks, Ian A.
Iterative Supervised Principal Component Analysis Driven Ligand Design for Regioselective Ti-Catalyzed Pyrrole Synthesis
ACS Catalysis, 2020, 10, 13504-13517
4518214 CIFC16 H13 Cl2 N SC 1 c 111.7514; 13.3298; 9.6736
90; 95.87; 90
1507.36Su, Yong-Liang; Tram, Linh; Wherritt, Daniel; Arman, Hadi; Griffith, Wendell P.; Doyle, Michael P.
α-Amino Radical-Mediated Diverse Difunctionalization of Alkenes: Construction of C‒C, C‒N, and C‒S Bonds
ACS Catalysis, 2020, 10, 13682-13687
4518215 CIFC14 H11 Cl2 N SP 1 21 17.9208; 5.9641; 13.9611
90; 95.677; 90
656.294Su, Yong-Liang; Tram, Linh; Wherritt, Daniel; Arman, Hadi; Griffith, Wendell P.; Doyle, Michael P.
α-Amino Radical-Mediated Diverse Difunctionalization of Alkenes: Construction of C‒C, C‒N, and C‒S Bonds
ACS Catalysis, 2020, 10, 13682-13687
4518216 CIFC81 H90 Br5 N13 Ni4 O3P 1 21 112.1646; 21.938; 16.962
90; 102.835; 90
4413.5Long, Cheng-Yu; Ni, Shao-Fei; Su, Min-Hui; Wang, Xue-Qiang; Tan, Weihong
Highly Chemoselective Access to 2,2′-Diaminobiaryls via Ni-Catalyzed Protecting-Group-Free Coupling of 2-Haloanilines
ACS Catalysis, 2020, 10, 13641-13649
4518242 CIFC25 H20 F N O5 SP 1 21/c 116.6287; 9.5046; 14.4444
90; 109.835; 90
2147.5Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518243 CIFC26 H22 F N O5 SP -18.0552; 11.7776; 12.3272
105.882; 95.33; 93.032
1116.24Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518244 CIFC26 H22 F3 N O4 SP c c n20.9621; 13.2147; 17.096
90; 90; 90
4735.73Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518245 CIFC27.5 H28 F2 N O6.5 SP 1 21/c 111.9745; 8.5948; 25.5692
90; 103.368; 90
2560.2Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518246 CIFC20 H20 F N O4 SP c a 2120.8044; 9.0158; 10.0248
90; 90; 90
1880.33Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518247 CIFC26 H25 F2 N O4 SP 1 21/c 118.2175; 7.7392; 16.7579
90; 102.923; 90
2302.83Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518248 CIFC19 H17 N O5 SP 1 21/n 18.91; 10.057; 20.0309
90; 102.026; 90
1755.53Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518249 CIFC26 H23 F2 N O5 SP 1 21 19.9672; 13.3088; 17.6941
90; 97.059; 90
2329.36Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518250 CIFC19 H17 F2 N O4 SP 1 21/n 18.8969; 10.1294; 20.1617
90; 101.962; 90
1777.52Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518251 CIFC25 H20 F3 N O4 SP 1 21 19.7433; 7.3884; 15.0351
90; 97.095; 90
1074.05Uno, Hiroto; Kawai, Koki; Shiro, Motoo; Shibata, Norio
Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
ACS Catalysis, 2020, 14117-14126
4518260 CIFC24 H24 F3 N O2 SP 1 21/n 116.6732; 7.8057; 16.9323
90; 103.9; 90
2139.14Apolinar, Omar; Tran, Van T.; Kim, Nana; Schmidt, Michael A.; Derosa, Joseph; Engle, Keary M.
Sulfonamide Directivity Enables Ni-Catalyzed 1,2-Diarylation of Diverse Alkenyl Amines
ACS Catalysis, 2020, 14234-14239
4518266 CIFC12 H15 N O6P 1 21 18.3518; 9.1518; 9.0312
90; 112.947; 90
635.67Niederer, Kyle A.; Gilmartin, Philip H.; Kozlowski, Marisa C.
Oxidative Photocatalytic Homo- and Cross-Coupling of Phenols: Nonenzymatic, Catalytic Method for Coupling Tyrosine
ACS Catalysis, 2020, 14615-14623
4518269 CIFC38 H28 P2P 1 21/c 110.5142; 13.9784; 19.3527
90; 100.698; 90
2794.9Chen, Xiao-Yang; Zhou, Xukai; Wang, Jianchun; Dong, Guangbin
FMPhos: Expanding the Catalytic Capacity of Small-Bite-Angle Bisphosphine Ligands in Regioselective Alkene Hydrofunctionalizations
ACS Catalysis, 2020, 14349-14358
4518270 CIFC43 H45 Cl2 F6 Fe Mo N3 O6 S2P 1 21 111.4984; 18.3575; 12.3063
90; 115.676; 90
2341.1Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518271 CIFC77 H61 B F33 Mo N3 OP -112.9087; 16.1499; 20.173
101.303; 101.414; 103.356
3879.9Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518272 CIFC75 H59 B F33 Mo N3 OP -112.8175; 15.5311; 20.3008
104.613; 96.591; 92.48
3873.7Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518273 CIFC77 H58 B Cl2 F33 Mo N4 OP -112.8554; 16.2503; 19.8326
105.02; 96.524; 96.704
3929.2Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518274 CIFC76 H58.5 B F33 Mo N3.5 OP -112.871; 15.3569; 39.432
83.163; 86.32; 89.432
7722.7Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518275 CIFC26 H21 F18 Mo N O2P 1 21/n 112.4112; 10.6334; 23.3549
90; 103.504; 90
2997Benedikter, Mathis; Musso, Janis; Kesharwani, Manoj K.; Sterz, K. Leonard; Elser, Iris; Ziegler, Felix; Fischer, Felix; Plietker, Bernd; Frey, Wolfgang; Kästner, Johannes; Winkler, Mario; van Slageren, Joris; Nowakowski, Michal; Bauer, Matthias; Buchmeiser, Michael R.
Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
ACS Catalysis, 2020, 14810-14823
4518276 CIFC8 H8 Cl N OP 1 21/c 16.1585; 4.6786; 26.8306
90; 96.26; 90
768.46Leong, Bi-Xiang; Teo, Yeow-Chuan; Condamines, Cloé; Yang, Ming-Chung; Su, Ming-Der; So, Cheuk-Wai
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
ACS Catalysis, 2020, 14824-14833
4518277 CIFC8 H9 N O2C 1 2/c 114.8957; 12.8359; 8.415
90; 111.928; 90
1492.55Leong, Bi-Xiang; Teo, Yeow-Chuan; Condamines, Cloé; Yang, Ming-Chung; Su, Ming-Der; So, Cheuk-Wai
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
ACS Catalysis, 2020, 14824-14833
4518278 CIFC13 H19 N OP 6116.8594; 16.8594; 8.3896
90; 90; 120
2065.2Leong, Bi-Xiang; Teo, Yeow-Chuan; Condamines, Cloé; Yang, Ming-Chung; Su, Ming-Der; So, Cheuk-Wai
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
ACS Catalysis, 2020, 14824-14833
4518293 CIFC79 H45.5 Br2 F6 I2 O10P 1 21 118.5988; 13.7054; 26.5064
90; 104.133; 90
6552.1Lai, Junshan; Fianchini, Mauro; Pericàs, Miquel A.
Development of Immobilized SPINOL-Derived Chiral Phosphoric Acids for Catalytic Continuous Flow Processes. Use in the Catalytic Desymmetrization of 3,3-Disubstituted Oxetanes
ACS Catalysis, 2020, 14971-14983
4518327 CIFC28 H33 B Br N O4P -110.0807; 11.1859; 12.2258
74.6461; 84.2332; 88.2173
1322.66Nallagonda, Rajender; Karimov, Rashad R.
Copper-Catalyzed Regio- and Diastereoselective Additions of Boron-Stabilized Carbanions to Heteroarenium Salts: Synthesis of Azaheterocycles Containing Contiguous Stereocenters
ACS Catalysis, 2020, 248-254
4518328 CIFC26 H32 B0 N2 O4 SP -19.2929; 11.4055; 12.1564
104.13; 93.917; 90.897
1245.86Nallagonda, Rajender; Karimov, Rashad R.
Copper-Catalyzed Regio- and Diastereoselective Additions of Boron-Stabilized Carbanions to Heteroarenium Salts: Synthesis of Azaheterocycles Containing Contiguous Stereocenters
ACS Catalysis, 2020, 248-254
4518332 CIFC31 H29 N O2 SP b c a13.793; 18.478; 20.113
90; 90; 90
5126.1Zhong, Long-Jin; Li, Yang; An, De-Lie; Li, Jin-Heng
Heteroannulation of N-Fluoro-N-alkylsulfonamides with Terminal Alkynes via Remote C(sp3)‒H Functionalization
ACS Catalysis, 2020, 383-389
4518334 CIFC35 H26 F16 Ir N6 O PP 1 21/n 113.6349; 13.8194; 20.9311
90; 96.357; 90
3919.7He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518335 CIFC37 H20 F16 Ir N6 PP 1 21/c 113.4456; 15.4907; 19.3081
90; 108.084; 90
3822.9He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518336 CIFC32 H16 F10 Ir N5C 1 2/n 119.625; 17.8886; 17.9372
90; 93.187; 90
6287.4He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518337 CIFC18 H15 N O3 S2P 1 21/n 110.5004; 9.9404; 16.6691
90; 106.602; 90
1667.36He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518338 CIFC38 H21 F16 Ir N5 PC 1 2/c 120.2832; 20.7079; 18.8839
90; 107.83; 90
7550.7He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518339 CIFC23 H18 N2 O2P -15.221; 12.037; 14.359
78.97; 84.119; 87.601
880.8He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518340 CIFC38 H21 F16 Ir N5 PC 1 2/c 120.3077; 20.7973; 18.9412
90; 107.616; 90
7624.6He, Jian; Bai, Zhi-Qin; Yuan, Pan-Feng; Wu, Li-Zhu; Liu, Qiang
Highly Efficient Iridium-Based Photosensitizers for Thia-Paternò‒Büchi Reaction and Aza-Photocyclization
ACS Catalysis, 2020, 446-455
4518341 CIFC12 H14 O2C 1 2/c 115.2075; 6.9155; 20.9784
90; 110.663; 90
2064.3Nguyen, Kevin; Clement, Helen A.; Bernier, Louise; Coe, Jotham W.; Farrell, William; Helal, Christopher J.; Reese, Matthew R.; Sach, Neal W.; Lee, Jack C.; Hall, Dennis G.
Catalytic Enantioselective Synthesis of a cis-β-Boronyl Cyclobutylcarboxyester Scaffold and Its Highly Diastereoselective Nickel/Photoredox Dual-Catalyzed Csp3‒Csp2 Cross-Coupling to Access Elusive trans-β-Aryl/Heteroaryl Cyclobutylcarboxyesters
ACS Catalysis, 2020, 404-413
4518342 CIFC18 H15 B Br2 F3 K O2P 21 21 220.0712; 30.159; 6.8657
90; 90; 90
4156Nguyen, Kevin; Clement, Helen A.; Bernier, Louise; Coe, Jotham W.; Farrell, William; Helal, Christopher J.; Reese, Matthew R.; Sach, Neal W.; Lee, Jack C.; Hall, Dennis G.
Catalytic Enantioselective Synthesis of a cis-β-Boronyl Cyclobutylcarboxyester Scaffold and Its Highly Diastereoselective Nickel/Photoredox Dual-Catalyzed Csp3‒Csp2 Cross-Coupling to Access Elusive trans-β-Aryl/Heteroaryl Cyclobutylcarboxyesters
ACS Catalysis, 2020, 404-413
4518343 CIFC31 H35 B O5P 21 21 219.1022; 11.2466; 27.186
90; 90; 90
2783Nguyen, Kevin; Clement, Helen A.; Bernier, Louise; Coe, Jotham W.; Farrell, William; Helal, Christopher J.; Reese, Matthew R.; Sach, Neal W.; Lee, Jack C.; Hall, Dennis G.
Catalytic Enantioselective Synthesis of a cis-β-Boronyl Cyclobutylcarboxyester Scaffold and Its Highly Diastereoselective Nickel/Photoredox Dual-Catalyzed Csp3‒Csp2 Cross-Coupling to Access Elusive trans-β-Aryl/Heteroaryl Cyclobutylcarboxyesters
ACS Catalysis, 2020, 404-413
4518345 CIFC118 H75 Cl18 F12 N4 O16.5 Rh2 S8C 1 2 130.933; 17.5225; 24.1606
90; 92.0449; 90
13087.3Murai, Takuya; Lu, Wenjie; Kuribayashi, Toshifumi; Morisaki, Kazuhiro; Ueda, Yoshihiro; Hamada, Shohei; Kobayashi, Yusuke; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo; Furuta, Takumi
Conformational Control in Dirhodium(II) Paddlewheel Catalysts Supported by Chalcogen-Bonding Interactions for Stereoselective Intramolecular C‒H Insertion Reactions
ACS Catalysis, 2020, 568-578
4518346 CIFC98 H66 Cl6 F12 N4 O14 Rh2P 21 21 2114.4646; 23.7613; 26.3686
90; 90; 90
9062.8Murai, Takuya; Lu, Wenjie; Kuribayashi, Toshifumi; Morisaki, Kazuhiro; Ueda, Yoshihiro; Hamada, Shohei; Kobayashi, Yusuke; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo; Furuta, Takumi
Conformational Control in Dirhodium(II) Paddlewheel Catalysts Supported by Chalcogen-Bonding Interactions for Stereoselective Intramolecular C‒H Insertion Reactions
ACS Catalysis, 2020, 568-578
4518347 CIFC110 H94 N10 O16 Rh2P 110.4116; 15.2831; 16.3622
71.608; 89.077; 85.189
2461.74Murai, Takuya; Lu, Wenjie; Kuribayashi, Toshifumi; Morisaki, Kazuhiro; Ueda, Yoshihiro; Hamada, Shohei; Kobayashi, Yusuke; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo; Furuta, Takumi
Conformational Control in Dirhodium(II) Paddlewheel Catalysts Supported by Chalcogen-Bonding Interactions for Stereoselective Intramolecular C‒H Insertion Reactions
ACS Catalysis, 2020, 568-578
4518363 CIFC29.5 H23 Cl F12 Fe N6 O P2C 1 2/c 120.0016; 18.5063; 18.5977
90; 105.98; 90
6618Gonell, Sergio; Lloret-Fillol, Julio; Miller, Alexander J. M.
An Iron Pyridyl-Carbene Electrocatalyst for Low Overpotential CO2 Reduction to CO
ACS Catalysis, 2020, 615-626
4518364 CIFC31 H27 Cl2 F12.43 Fe N7 P2P 1 21/n 113.7127; 17.4292; 16.0993
90; 107.938; 90
3660.72Gonell, Sergio; Lloret-Fillol, Julio; Miller, Alexander J. M.
An Iron Pyridyl-Carbene Electrocatalyst for Low Overpotential CO2 Reduction to CO
ACS Catalysis, 2020, 615-626
4518384 CIFC44 H54 Cl2 N O3 P RuC 1 c 116.577; 15.944; 15.596
90; 99.187; 90
4069.2Eivgi, Or; Vaisman, Anna; Lemcoff, N. Gabriel
Latent, Yet Highly Active Photoswitchable Olefin Metathesis Precatalysts Bearing Cyclic Alkyl Amino Carbene (CAAC)/Phosphite Ligands
ACS Catalysis, 2020, 703-709
4518385 CIFC59 H60 Cl2 N O3 P RuP 1 21/n 112.6005; 18.784; 21.757
90; 101.619; 90
5044.1Eivgi, Or; Vaisman, Anna; Lemcoff, N. Gabriel
Latent, Yet Highly Active Photoswitchable Olefin Metathesis Precatalysts Bearing Cyclic Alkyl Amino Carbene (CAAC)/Phosphite Ligands
ACS Catalysis, 2020, 703-709
4518406 CIFC18 H15 N O3P 1 21/c 16.7743; 23.418; 8.802
90; 101.248; 90
1369.5Xin, Luoting; Wan, Wan; Yu, Yinghua; Wan, Qiuling; Ma, Liyao; Huang, Xueliang
Construction of Protoberberine Alkaloid Core through Palladium Carbene Bridging C‒H Bond Functionalization and Pyridine Dearomatization
ACS Catalysis, 2021, 1570-1577
4518407 CIFC25 H25 B0 F0 N O2P 21 21 217.1212; 13.75566; 18.96034
90; 90; 90
1857.29Xin, Luoting; Wan, Wan; Yu, Yinghua; Wan, Qiuling; Ma, Liyao; Huang, Xueliang
Construction of Protoberberine Alkaloid Core through Palladium Carbene Bridging C‒H Bond Functionalization and Pyridine Dearomatization
ACS Catalysis, 2021, 1570-1577
4518411 CIFC27 H30 N2 O5 S2P -19.172; 11.675; 12.09
91.099; 93.667; 105.21
1245.9Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518412 CIFC52 H52 Br2 F2 N4 O8 S4P 1 21 112.9016; 9.0322; 12.9338
90; 105.257; 90
1454.05Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518413 CIFC27 H30 Cl2 N2 O4 S2P 21 21 219.35619; 16.99; 17.21824
90; 90; 90
2737.04Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518414 CIFC22.5 H19 Br Cl N O4 SP -112.185; 12.529; 14.695
82.566; 83.909; 87.659
2211.2Zhu, Bo-Han; Zhang, Ying-Qi; Xu, Hao-Jin; Li, Long; Deng, Guo-Cheng; Qian, Peng-Cheng; Deng, Chao; Ye, Long-Wu
Regio- and Stereoselective Synthesis of Diverse 3,4-Dihydro-2-quinolones through Catalytic Hydrative Cyclization of Imine- and Carbonyl-Ynamides with Water
ACS Catalysis, 2021, 1706-1713
4518420 CIFC25 H30 N2 O9P 21 21 219.9196; 11.7763; 21.4011
90; 90; 90
2499.99Ghouilem, Juba; Tran, Christine; Grimblat, Nicolas; Retailleau, Pascal; Alami, Mouad; Gandon, Vincent; Messaoudi, Samir
Diastereoselective Pd-Catalyzed Anomeric C(sp3)‒H Activation: Synthesis of α-(Hetero)aryl C-Glycosides
ACS Catalysis, 2021, 1818-1826
4518421 CIFC25 H30 N2 O6P 21 21 2110.0246; 11.6273; 21.2713
90; 90; 90
2479.36Ghouilem, Juba; Tran, Christine; Grimblat, Nicolas; Retailleau, Pascal; Alami, Mouad; Gandon, Vincent; Messaoudi, Samir
Diastereoselective Pd-Catalyzed Anomeric C(sp3)‒H Activation: Synthesis of α-(Hetero)aryl C-Glycosides
ACS Catalysis, 2021, 1818-1826
4518422 CIFC19 H19 N O4 SP 21 21 218.4774; 10.9811; 18.1554
90; 90; 90
1690.11Liang, Ren-Xiao; Zhong, Chao; Liu, Zhi-Hong; Yang, Miao; Tang, Heng-Wei; Chen, Jian-Fei; Yang, Yun-Fang; Jia, Yi-Xia
Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives
ACS Catalysis, 2021, 1827-1832
4518423 CIFC23 H27 N O4 SP 659.7067; 9.7067; 39.2119
90; 90; 120
3199.57Liang, Ren-Xiao; Zhong, Chao; Liu, Zhi-Hong; Yang, Miao; Tang, Heng-Wei; Chen, Jian-Fei; Yang, Yun-Fang; Jia, Yi-Xia
Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives
ACS Catalysis, 2021, 1827-1832
4518426 CIFC32 H34 O4 SiP 1 21/c 19.4521; 26.2261; 11.8032
90; 103.62; 90
2843.6Ni, Dongshun; Brown, M. Kevin
Three-Component Ni-Catalyzed Silylacylation of Alkenes
ACS Catalysis, 2021, 1858-1862
4518429 CIFC34 H29 Cl3 O6P 1 21/c 110.1057; 12.677; 24.493
90; 98.332; 90
3104.7Koshikawa, Takumi; Nagashima, Yuki; Tanaka, Ken
Gold-Catalyzed [3 + 2] Annulation, Carbenoid Transfer, and C‒H Insertion Cascade: Elucidation of Annulation Mechanisms via Benzopyrylium Intermediates
ACS Catalysis, 2021, 1932-1937
4518430 CIFC48 H52 Cl4 N2 O Ru SiP n a 2115.2754; 28.119; 10.416
90; 90; 90
4474Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518431 CIFC43 H51 Cl4 N3 O3 Ru SP 1 21/n 113.6581; 10.7783; 30.3452
90; 96.306; 90
4440.1Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518432 CIFC41 H47 Cl4 N3 O2 Ru SP b c a21.747; 16.485; 23.171
90; 90; 90
8307Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518433 CIFC55 H67 Cl2 N3 O6 Ru SP -111.0039; 12.6857; 20.649
101.995; 101.394; 106.335
2603.1Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518434 CIFC42 H44 Cl2 Fe N2 RuP -112.269; 13.206; 13.74
103.978; 96.479; 116.864
1862.7Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518435 CIFC59 H75 Cl4 N3 O7 Ru SP -112.58; 13.814; 19.537
90.61; 105.904; 113.609
2963.8Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518436 CIFC48 H51 Cl2 N4 O4 Ru S2P 1 21/n 111.6701; 29.6716; 13.7738
90; 93.446; 90
4760.8Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518437 CIFC41 H52 Cl2 N2 O RuP -110.2526; 12.923; 14.9304
75.27; 77.074; 87.61
1864.5Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518438 CIFC40 H45 Cl4 N3 O2 Ru SP 1 21/c 18.471; 26.951; 18.341
90; 97.843; 90
4148Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518439 CIFC46 H55 Cl6 N3 O2 Ru SP 1 21/n 115.3127; 13.8064; 22.985
90; 91.3; 90
4858.1Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518440 CIFC43 H51 Cl4 N3 O3 Ru SP 1 21/n 113.3662; 19.3514; 18.2778
90; 107.451; 90
4510Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518441 CIFC75 H78 Cl10 N6 O4 Ru2P 1 21/n 119.5436; 16.2686; 25.2292
90; 92.134; 90
8016Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518442 CIFC38 H46 Cl2 N2 RuP 1 21 111.9816; 10.5576; 13.8098
90; 93.972; 90
1742.7Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518443 CIFC41 H42 Cl2 N3 O3 Ru SP 1 21/c 110.9001; 16.3943; 21.6403
90; 98.664; 90
3823Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518444 CIFC48 H57 Cl2 N3 O3 Ru SP 1 21/c 112.6853; 12.842; 32.754
90; 96.636; 90
5300Gupta, Saswata; Sabbasani, Venkata R.; Su, Siyuan; Wink, Donald J.; Lee, Daesung
Alkene-Chelated Ruthenium Alkylidenes: A Missing Link to New Catalysts
ACS Catalysis, 2021, 11, 1977-1987
4518456 CIFC26 H49 Co P2P -110.482; 11.48; 12.182
109.71; 102.2; 98.68
1308.9Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518457 CIFC29 H53 Co P2P 1 21/n 19.289; 9.1; 16.695
90; 91.33; 90
1410.8Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518458 CIFC52 H49 Co P4P 1 21/n 19.8781; 20.7751; 20.9768
90; 92.271; 90
4301.4Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518459 CIFC26 H48 Co I2 P2P 21 21 219.1792; 13.8808; 23.1857
90; 90; 90
2954.2Kim, Yeong Bum; Kim, Dongwook; Dighe, Shashikant U.; Chang, Sukbok; Park, Jung-Woo
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying π-Bond Migration
ACS Catalysis, 2021, 1548-1553
4518460 CIFC37 H35 F N2 O7P 21 21 2116.485; 24.296; 24.715
90; 90; 90
9899Tang, Xiaodong; Tan, Chuan Xiang Alvin; Chan, Wai-Lun; Zhang, Fuhao; Zheng, Wenrui; Lu, Yixin
Dielectrophilic Allenic Ketone-Enabled [4 + 2] Annulation with 3,3’-Bisoxindoles: Enantioselective Creation of Two Contiguous Quaternary Stereogenic Centers
ACS Catalysis, 2021, 1361-1367
4518461 CIFC14 H15 N OP 1 21/n 113.9071; 9.5864; 16.966
90; 100.194; 90
2226.2Mo, Jiayu; Messinis, Antonis M.; Oliveira, João C. A.; Demeshko, Serhiy; Meyer, Franc; Ackermann, Lutz
Iron-Catalyzed Triazole-Enabled C‒H Activation with Bicyclopropylidenes
ACS Catalysis, 2021, 1053-1064
4518462 CIFC36 H51 Br O2P 21 21 215.781; 9.7023; 56.176
90; 90; 90
3150.9Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518463 CIFC11 H9 NP 21 21 214.6608; 8.0082; 22.8683
90; 90; 90
853.55Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518464 CIFC15 H11 NP 1 21/n 110.3922; 8.5924; 13.4648
90; 112.087; 90
1114.09Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518465 CIFC13 H10 O2P 1 21/c 111.807; 11.5282; 7.74435
90; 108.688; 90
998.54Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518466 CIFC12 H10 N2P 1 21/c 116.6487; 5.1944; 11.2609
90; 101.125; 90
955.54Dang, Hang T.; Nguyen, Viet D.; Haug, Graham C.; Vuong, Ngan T. H.; Arman, Hadi D.; Larionov, Oleg V.
Z-Selective Dienylation Enables Stereodivergent Construction of Dienes and Unravels a Ligand-Driven Mechanistic Dichotomy
ACS Catalysis, 2021, 1042-1052
4518467 CIFC63 H98 Ag2 O6 P2P b c a16.8262; 19.3356; 41.108
90; 90; 90
13374.3Tlahuext-Aca, Adrian; Hartwig, John F.
Site-Selective Silver-Catalyzed C‒H Bond Deuteration of Five-Membered Aromatic Heterocycles and Pharmaceuticals
ACS Catalysis, 2021, 1119-1127
4518468 CIFC18 H17 N O S2P 1 21/n 15.591; 21.778; 12.608
90; 99.18; 90
1515.5Wang, Rong-Hua; Li, Jiang-Fei; Li, Yue; Qi, Shao-Long; Zhang, Tao; Luan, Yu-Xin; Ye, Mengchun
Selective C(sp3)‒H Cleavage of Enamides for Synthesis of 2-Pyridones via Ligand-Enabled Ni‒Al Bimetallic Catalysis
ACS Catalysis, 2021, 11, 858-864
4518469 CIFC32 H40 I N3 O5 SP 1 21 112.5558; 12.2352; 21.214
90; 91.478; 90
3257.9Zhang, Yueteng; Ji, Peng; Gao, Feng; Huang, He; Zeng, Fanxun; Wang, Wei
Photoredox Asymmetric Nucleophilic Dearomatization of Indoles with Neutral Radicals
ACS Catalysis, 2021, 11, 998-1007
4518470 CIFC27 H28 N2 O5 SC 1 2 122.7379; 7.3689; 14.3911
90; 91.61; 90
2410.3Zhang, Yueteng; Ji, Peng; Gao, Feng; Huang, He; Zeng, Fanxun; Wang, Wei
Photoredox Asymmetric Nucleophilic Dearomatization of Indoles with Neutral Radicals
ACS Catalysis, 2021, 11, 998-1007
4518471 CIFC19 H2 B F13P 1 21/a 19.912; 17.662; 10.435
90; 114.281; 90
1665.2Nakashima, Tomoya; Nakayama, Yuushou; Shiono, Takeshi; Tanaka, Ryo
Neutral, Noncoordinating, and Hydrocarbon-Soluble Protic Cocatalyst for Olefin Polymerization
ACS Catalysis, 2021, 11, 865-870
4518472 CIFC13 H3 B F8 OP 1 21/c 116.0009; 4.7685; 16.6499
90; 116.991; 90
1132.02Nakashima, Tomoya; Nakayama, Yuushou; Shiono, Takeshi; Tanaka, Ryo
Neutral, Noncoordinating, and Hydrocarbon-Soluble Protic Cocatalyst for Olefin Polymerization
ACS Catalysis, 2021, 11, 865-870

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