{"title":"In(OTf)3催化的 3-亚苄基吲哚啉-2-硫酮与 2-吲哚甲醇的正规 (4 + 3) 环加成反应。","authors":"Xue-Long Wang, Yi Yang and Yan Jiang","doi":"10.1039/D4OB00897A","DOIUrl":null,"url":null,"abstract":"<p >We report the In(OTf)<small><sub>3</sub></small>-catalyzed formal (4 + 3) cycloaddition of 3-benzylideneindoline-2-thiones with 2-indolylmethanols. This reaction not only broadens the synthetic utility of 3-benzylideneindoline-2-thiones as scarce indole-based sulfur-containing four-atom building blocks, but also provides a rapid and facile access to synthesize diindole-annulated tetrahydrothiepines.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" 29","pages":" 5902-5906"},"PeriodicalIF":2.7000,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In(OTf)3-catalyzed formal (4 + 3) cycloaddition reactions of 3-benzylideneindoline-2-thiones with 2-indolylmethanols†\",\"authors\":\"Xue-Long Wang, Yi Yang and Yan Jiang\",\"doi\":\"10.1039/D4OB00897A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We report the In(OTf)<small><sub>3</sub></small>-catalyzed formal (4 + 3) cycloaddition of 3-benzylideneindoline-2-thiones with 2-indolylmethanols. This reaction not only broadens the synthetic utility of 3-benzylideneindoline-2-thiones as scarce indole-based sulfur-containing four-atom building blocks, but also provides a rapid and facile access to synthesize diindole-annulated tetrahydrothiepines.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" 29\",\"pages\":\" 5902-5906\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ob/d4ob00897a\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ob/d4ob00897a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
In(OTf)3-catalyzed formal (4 + 3) cycloaddition reactions of 3-benzylideneindoline-2-thiones with 2-indolylmethanols†
We report the In(OTf)3-catalyzed formal (4 + 3) cycloaddition of 3-benzylideneindoline-2-thiones with 2-indolylmethanols. This reaction not only broadens the synthetic utility of 3-benzylideneindoline-2-thiones as scarce indole-based sulfur-containing four-atom building blocks, but also provides a rapid and facile access to synthesize diindole-annulated tetrahydrothiepines.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.