Synthesis of Acylbenzo[b]thiophenes, benzofurans and indoles via intramolecular oxidative cyclization enabled by photocatalytic hydrogen atom transfer (HAT)

Fen-Dou Wang , Jin Jiang , Tiantian Xu , Wen-Chao Yang , Shu-Peng Zhang , Min Wang , Pinhua Li
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引用次数: 0

Abstract

An efficient strategy for intramolecular oxidative cyclization of 2-alkynylthioanisoles toward 3-acylbenzo[b]thiophenes by photochemical hydrogen atom transfer catalysis has been developed. 3-Acylbenzo[b]selenophenes, benzofurans and indoles can also be prepared by this protocol. This reaction is convenient to perform at room temperature under simple conditions using air as the oxidant. Mechanistic studies revealed that the formation of α-thioalkyl radicals intermediate is crucial.

Abstract Image

通过光催化氢原子转移 (HAT) 分子内氧化环化合成酰基苯并[b]噻吩、苯并呋喃和吲哚
提出了一种光化学氢原子转移催化2-炔基噻唑分子内氧化环化制备3-酰基苯并[b]噻吩的有效方法。3-酰基苯并[b]硒苯醚、苯并呋喃和吲哚也可通过该工艺制备。该反应以空气为氧化剂,在室温条件下简便易行。机理研究表明α-硫代烷基自由基中间体的形成至关重要。
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来源期刊
Tetrahedron chem
Tetrahedron chem Organic Chemistry
CiteScore
3.60
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审稿时长
27 days
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