C–H fluorination promoted by pyridine <i>N</i>-oxyl radicals-Reference-Cited by-同舟云学术

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C–H fluorination promoted by pyridine N-oxyl radicals

Published:2024 Issue:15 Volume:26 Page:8701-8705
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zeng Tianyu¹,Huang Chaoqun²,Zhang Yang¹^ORCID,Luo Yunzi²,Niu Dawen¹^ORCID

Affiliation:

1. Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, and School of Chemical Engineering, Sichuan University, Chengdu 610041, China

2. Frontiers Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China

Abstract

Pyridine N-oxyl radicals can be effectively generated under environmentally friendly mild conditions, significantly enhancing the reactivity of direct C–H fluorination.

Funder

West China Hospital, Sichuan University

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/GC/D4GC02247E

Reference65 articles.

1. Fluorine in medicinal chemistry

2. Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II–III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas

3. Recent progress on fluorination in aqueous media

4. Fluorinated Oligomers and Polymers in Photopolymerization

5. Recent progress in synthesis of fluorine containing monomers for polyimides

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