Hydroazidation of trifluoromethyl alkenes with trimethylsilyl azide enabled by organic photoredox catalysis-Reference-Cited by-同舟云学术

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Hydroazidation of trifluoromethyl alkenes with trimethylsilyl azide enabled by organic photoredox catalysis

Published:2024 Issue:60 Volume:60 Page:7741-7744
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Shi Yutao¹,Zhang Yuliang¹,Ji Xiaochen¹²^ORCID,Huang Huawen¹²^ORCID

Affiliation:

1. Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China

2. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, 453007, China

Abstract

A mild hydroazidation of trifluoromethyl alkenes with trimethylsilyl azide through organic photoredox catalysis was developed, delivering a series of valuable β-CF3-azides with exclusive selectivity.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Scientific Research Foundation of Hunan Provincial Education Department

Henan Normal University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC02503B

Reference49 articles.

1. Applications of Fluorine in Medicinal Chemistry

2. Current Contributions of Organofluorine Compounds to the Agrochemical Industry

3. Fluorine and Fluorinated Motifs in the Design and Application of Bioisosteres for Drug Design

4. Fluorine in medicinal chemistry

5. The Many Roles for Fluorine in Medicinal Chemistry

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