Photoinduced C–H heteroarylation of enamines via quadruple cleavage of CF2Br2
文献信息
发布日期
2023-10-20
DOI
10.1039/D3QO01474F
影响因子
5.281
作者
Lingling Zuo, Xiao Geng, Zhifang Li
查看原文
摘要
The C–H functionalization of enamines has attracted much attention over the past few years; however, the heteroarylation of enamines still remains rare. Herein, we wish to report a photoinduced three-component coupling/cyclization reaction for the de novo synthesis of 1,3,4-oxdiazole- or benzothiazole-functionalized enamines via quadruple cleavage of CF2Br2. Notably, the reaction provides an efficient and general approach for the C–H heteroarylation of enamines and exploits a new reactivity of CF2Br2, as the C1 source.
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来源期刊
Organic Chemistry Frontiers
CiteScore:
7.8
自引率:
8.7%
年发文量:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
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