{"title":"cucl2介导的C(sp3)- h和C(sp3)- o氧化/醚双吲哚酰化-双吲哚基甲烷衍生物的合成","authors":"Chenglei Yang, Xiaotao Qin, Jinkai Hu, Bosen Wang, Jinhui Yang, Dianjun Li","doi":"10.1016/j.tet.2025.134949","DOIUrl":null,"url":null,"abstract":"<div><div>Under the participation of cheap and readily available CuCl<sub>2</sub>, a visible light-induced tandem C(sp<sup>3</sup>)-H oxidation, C(sp<sup>3</sup>)-O cleavage and Friedel−Crafts alkylation of indoles and aliphatic ethers in the absence of ligand and oxidants is developed, affording synthetically useful 3,3′-bisindolylmethane derivatives in moderate to good yields. This transformation exhibits broad substrate scope and good functional group compatibility.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"188 ","pages":"Article 134949"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible-light-enabled CuCl2-mediated tandem C(sp3)-H and C(sp3)-O oxidant/bisindolylation of ethers – Synthesis of bisindolylmethane derivatives\",\"authors\":\"Chenglei Yang, Xiaotao Qin, Jinkai Hu, Bosen Wang, Jinhui Yang, Dianjun Li\",\"doi\":\"10.1016/j.tet.2025.134949\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Under the participation of cheap and readily available CuCl<sub>2</sub>, a visible light-induced tandem C(sp<sup>3</sup>)-H oxidation, C(sp<sup>3</sup>)-O cleavage and Friedel−Crafts alkylation of indoles and aliphatic ethers in the absence of ligand and oxidants is developed, affording synthetically useful 3,3′-bisindolylmethane derivatives in moderate to good yields. This transformation exhibits broad substrate scope and good functional group compatibility.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"188 \",\"pages\":\"Article 134949\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402025005058\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402025005058","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Visible-light-enabled CuCl2-mediated tandem C(sp3)-H and C(sp3)-O oxidant/bisindolylation of ethers – Synthesis of bisindolylmethane derivatives
Under the participation of cheap and readily available CuCl2, a visible light-induced tandem C(sp3)-H oxidation, C(sp3)-O cleavage and Friedel−Crafts alkylation of indoles and aliphatic ethers in the absence of ligand and oxidants is developed, affording synthetically useful 3,3′-bisindolylmethane derivatives in moderate to good yields. This transformation exhibits broad substrate scope and good functional group compatibility.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.