Fen-Dou Wang , Jin Jiang , Tiantian Xu , Wen-Chao Yang , Shu-Peng Zhang , Min Wang , Pinhua Li
{"title":"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","authors":"Fen-Dou Wang , Jin Jiang , Tiantian Xu , Wen-Chao Yang , Shu-Peng Zhang , Min Wang , Pinhua Li","doi":"10.1016/j.tchem.2025.100119","DOIUrl":null,"url":null,"abstract":"<div><div>An efficient strategy for intramolecular oxidative cyclization of 2-alkynylthioanisoles toward 3-acylbenzo[<em>b</em>]thiophenes by photochemical hydrogen atom transfer catalysis has been developed. 3-Acylbenzo[<em>b</em>]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.</div></div>","PeriodicalId":74918,"journal":{"name":"Tetrahedron chem","volume":"13 ","pages":"Article 100119"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of Acylbenzo[b]thiophenes, benzofurans and indoles via intramolecular oxidative cyclization enabled by photocatalytic hydrogen atom transfer (HAT)\",\"authors\":\"Fen-Dou Wang , Jin Jiang , Tiantian Xu , Wen-Chao Yang , Shu-Peng Zhang , Min Wang , Pinhua Li\",\"doi\":\"10.1016/j.tchem.2025.100119\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>An efficient strategy for intramolecular oxidative cyclization of 2-alkynylthioanisoles toward 3-acylbenzo[<em>b</em>]thiophenes by photochemical hydrogen atom transfer catalysis has been developed. 3-Acylbenzo[<em>b</em>]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.</div></div>\",\"PeriodicalId\":74918,\"journal\":{\"name\":\"Tetrahedron chem\",\"volume\":\"13 \",\"pages\":\"Article 100119\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron chem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666951X25000014\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron chem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666951X25000014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of Acylbenzo[b]thiophenes, benzofurans and indoles via intramolecular oxidative cyclization enabled by photocatalytic hydrogen atom transfer (HAT)
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.