Visible-Light-Induced Nickel-Catalyzed Radical Cross-Couplings to Access α-Aryl-α-trifluoromethyl Alcohols-Reference-Cited by-同舟云学术

Visible-Light-Induced Nickel-Catalyzed Radical Cross-Couplings to Access α-Aryl-α-trifluoromethyl Alcohols

Published:2022-12-09 Issue:50 Volume:24 Page:9332-9336
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chen Feng¹,Xu Xiu-Hua¹^ORCID,Chu Lingling²^ORCID,Qing Feng-Ling¹^ORCID

Affiliation:

1. Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China

2. College of Chemistry and Chemical Engineering, Donghua University, 2999 North Renmin Lu, Shanghai 201620, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03943

Reference49 articles.

1. Contribution of Organofluorine Compounds to Pharmaceuticals

2. Current Contributions of Organofluorine Compounds to the Agrochemical Industry

3. A Fruitful Decade of Organofluorine Chemistry: New Reagents and Reactions

4. A reversible monoamine oxidase a inhibitor, befloxatone: structural approach of its mechanism of action

5. ortho Substituent effects on the anticonvulsant properties of 4-hydroxy-trifluoroethyl phenols

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