Recent Developments in C-H functionalisation of Benzofurans and Benzothiophenes

被引:21
作者
Morgan, David [1 ]
Yarwood, Stephen J. [2 ]
Barker, Graeme [1 ]
机构
[1] Heriot Watt Univ, Inst Chem Sci, Edinburgh EH14 4AS, Midlothian, Scotland
[2] Heriot Watt Univ, Inst Biol Chem Biophys & Bioengn, Edinburgh EH14 4AS, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Benzofuran; Benzothiophene; Functionalization; Heterocycles; Synthetic methods; BOND ARYLATIONS; ARENES; HETEROARYLATION; CONSTRUCTION; THIOLATION;
D O I
10.1002/ejoc.202001470
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Benzofurans and benzothiophenes are important pharmaceutical motifs, appearing in a broad range of small molecule therapeutic classes. Often overlooked by synthetic methodologists in favour reactions of the analogous indole bicyclic system, there is nevertheless a plurality of approaches to effecting benzofuran and benzothiophene C-H functionalisations. In this review, we summarise progress in this area over the past five years, including 1) alkylations, 2) arylations and heteroarylations, 3) carboxylations, carbamoylations, and C-heteroatom bond formations and 4) cyclisations.
引用
收藏
页码:1072 / 1102
页数:31
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