Radical trifluoromethylation-Reference-Cited by-同舟云学术

Radical trifluoromethylation

Published:2021 Issue:11 Volume:50 Page:6308-6319
ISSN:0306-0012
Container-title:Chemical Society Reviews
language:en
Short-container-title:Chem. Soc. Rev.

Author:

Xiao Haiwen¹²³,Zhang Zhenzhen⁴⁵⁶⁷⁸,Fang Yewen¹²³^ORCID,Zhu Lin⁴⁵⁶⁷⁸,Li Chaozhong¹²³⁴⁵^ORCID

Affiliation:

1. School of Materials and Chemical Engineering, Ningbo University of Technology

2. Ningbo 315211

3. China

4. Key Laboratory of Organofluorine Chemistry

5. Center for Excellence in Molecular Synthesis

6. Shanghai Institute of Organic Chemistry

7. Chinese Academy of Sciences

8. Shanghai 200032

Abstract

Radical trifluoromethylation has been emerging as a versatile tool for the synthesis of trifluoromethylated compounds that play increasingly important roles in pharmaceuticals, agrochemicals and materials science.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CS/D1CS00200G

Reference48 articles.

1. Carbon Trifluoromethylation Reactions of Hydrocarbon Derivatives and Heteroarenes

2. Shelf-stable electrophilic trifluoromethylating reagents: A brief historical perspective

3. Trifluoromethylation of Alkyl Radicals: Breakthrough and Challenges †

4. A “Renaissance” in Radical Trifluoromethylation

5. Electrochemical Oxidation of Trifluoroacetic Acid in an Organic Substrate. III. In the Presence of Substituted Malonic Acid Half Esters and Unsaturated Carboxylic Acid Esters

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