Photoinduced C–H heteroarylation of enamines via quadruple cleavage of CF2Br2-Reference-Cited by-同舟云学术

Photoinduced C–H heteroarylation of enamines via quadruple cleavage of CF₂Br₂

Published:2023 Issue:24 Volume:10 Page:6112-6116
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zuo Wanqing¹²,Zuo Lingling¹,Geng Xiao¹^ORCID,Li Zhifang²^ORCID,Wang Lei¹²³^ORCID

Affiliation:

1. Advanced Research Institute and School of Pharmaceutical Sciences, Taizhou University, Jiaojiang 318000, Zhejiang, P. R. China

2. College of Material Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, P. R. China

3. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, P. R. China

Abstract

The C–H functionalization of enamines has attracted much attention over the past few years; however, the heteroarylation of enamines still remains rare.

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO01474F

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1. Lobatamide C: Total Synthesis, Stereochemical Assignment, Preparation of Simplified Analogues, and V-ATPase Inhibition Studies

2. Cu-mediated enamide formation in the total synthesis of complex peptide natural products