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For: Onyeagusi CI, Malcolmson SJ. Strategies for the Catalytic Enantioselective Synthesis of α-Trifluoromethyl Amines. ACS Catal 2020;10:12507-36. [PMID: 34306806 DOI: 10.1021/acscatal.0c03569] [Cited by in Crossref: 18] [Cited by in F6Publishing: 11] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 Wan LQ, Cao JG, Niu D, Zhang X. Cobalt-Catalyzed Umpolung Alkylation of Imines To Generate α-Branched Aliphatic Amines. Org Lett 2021;23:3818-22. [PMID: 33974795 DOI: 10.1021/acs.orglett.1c00835] [Reference Citation Analysis]
2 Ye ZP, Gao J, Duan XY, Guan JP, Liu F, Chen K, Xiao JA, Xiang HY, Yang H. Electrochemical heterodifunctionalization of α-CF3 alkenes to access α-trifluoromethyl-β-sulfonyl tertiary alcohols. Chem Commun (Camb) 2021;57:8969-72. [PMID: 34486594 DOI: 10.1039/d1cc03288g] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Wu J, Wu H, Li X, Liu X, Zhao Q, Huang G, Zhang C. Copper-Catalyzed Highly Selective Protoboration of CF3 -Containing 1,3-Dienes. Angew Chem Int Ed Engl 2021;60:20376-82. [PMID: 34146388 DOI: 10.1002/anie.202105896] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Ramirez NP, Pisella G, Waser J. Cu(I)-Catalyzed gem-Aminoalkynylation of Diazo Compounds: Synthesis of Fluorinated Propargylic Amines. J Org Chem 2021;86:10928-38. [PMID: 34260244 DOI: 10.1021/acs.joc.1c01423] [Reference Citation Analysis]
5 Nam D, Tinoco A, Shen Z, Adukure RD, Sreenilayam G, Khare SD, Fasan R. Enantioselective Synthesis of α-Trifluoromethyl Amines via Biocatalytic N-H Bond Insertion with Acceptor-Acceptor Carbene Donors. J Am Chem Soc 2022. [PMID: 35107997 DOI: 10.1021/jacs.1c10750] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
6 Hsu C, Gonçalves CR, Tona V, Pons A, Kaiser M, Maulide N. Nutzung von elektronenarmen Iminiumintermediaten zur Synthese von wertvollen Aminen. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202115435] [Reference Citation Analysis]
7 Uchikura T, Aruga K, Suzuki R, Akiyama T. Enantioselective Friedel-Crafts Alkylation Reaction of Pyrroles with N-Unprotected Alkynyl Trifluoromethyl Ketimines. Org Lett 2022;24:4699-703. [PMID: 35728276 DOI: 10.1021/acs.orglett.2c01972] [Reference Citation Analysis]
8 Hu M, Tan BB, Ge S. Enantioselective Cobalt-Catalyzed Hydroboration of Fluoroalkyl-Substituted Alkenes to Access Chiral Fluoroalkylboronates. J Am Chem Soc 2022. [PMID: 35953077 DOI: 10.1021/jacs.2c06488] [Reference Citation Analysis]
9 Zhao Y, Wang X, Yao R, Li C, Xu Z, Zhang L, Han G, Hou J, Liu Y, Song Y. Iron‐Catalyzed Alkene Trifluoromethylation in Tandem with Phenol Dearomatizing Spirocyclization: Regioselective Construction of Trifluoromethylated Spirocarbocycles. Adv Synth Catal 2022;364:637-42. [DOI: 10.1002/adsc.202101201] [Reference Citation Analysis]
10 Huang S, Tong FF, Bai DC, Zhang GP, Jiang YJ, Zhang B, Leng X, Guo YL, Wan XL, Zhang X, Ding CH, Hou XL. Regio- and enantioselective umpolung gem-difluoroallylation of hydrazones via palladium catalysis enabled by N-heterocyclic carbene ligand. Nat Commun 2021;12:6551. [PMID: 34772944 DOI: 10.1038/s41467-021-26667-0] [Reference Citation Analysis]
11 Reshi NUD, Saptal VB, Beller M, Bera JK. Recent Progress in Transition-Metal-Catalyzed Asymmetric Reductive Amination. ACS Catal 2021;11:13809-37. [DOI: 10.1021/acscatal.1c04208] [Cited by in Crossref: 14] [Cited by in F6Publishing: 6] [Article Influence: 14.0] [Reference Citation Analysis]
12 Kojima Y, Miura M, Hirano K. Copper-Catalyzed Regio- and Enantioselective Hydroallylation of 1-Trifluoromethylalkenes: Effect of Crown Ether. ACS Catal 2021;11:11663-70. [DOI: 10.1021/acscatal.1c02947] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
13 Zhu C, Zhang H, Liu Q, Chen K, Liu Z, Feng C. Nickel-Catalyzed anti-Markovnikov Hydroalkylation of Trifluoromethylalkenes. ACS Catal . [DOI: 10.1021/acscatal.2c02052] [Reference Citation Analysis]
14 Wu X, Ren J, Shao Z, Yang X, Qian D. Transition-Metal-Catalyzed Asymmetric Couplings of α-Aminoalkyl Fragments to Access Chiral Alkylamines. ACS Catal 2021;11:6560-77. [DOI: 10.1021/acscatal.1c01545] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
15 Liu YL, Wang XP, Wei J, Li Y. Synthesis of oxindoles bearing a stereogenic 3-fluorinated carbon center from 3-fluorooxindoles. Org Biomol Chem 2021. [PMID: 34935824 DOI: 10.1039/d1ob01964c] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Verma S, Choudhary RN, Kanadje AP, Banerjee UC. Diversifying Arena of Drug Synthesis: In the Realm of Lipase Mediated Waves of Biocatalysis. Catalysts 2021;11:1328. [DOI: 10.3390/catal11111328] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Xing SN, Hua YZ, Yang XC, Du SS, Jia SK, Mei GJ, Wang MC. Catalytic Asymmetric Umpolung Tandem Reactions of Hemiacetals via Dinuclear Zinc Cooperative Catalysis. Org Lett 2022. [PMID: 35467355 DOI: 10.1021/acs.orglett.2c00913] [Reference Citation Analysis]