Shengxing Xie, Jinxia Yang, Rong Ma, Minghui Liu, Xinyuan Zhang, Neng-Fei Wang, Chengyu Wang, Lingkai Kong
{"title":"不含过渡金属的1,10-邻菲罗啉促进双芳基二胺的均偶联反应","authors":"Shengxing Xie, Jinxia Yang, Rong Ma, Minghui Liu, Xinyuan Zhang, Neng-Fei Wang, Chengyu Wang, Lingkai Kong","doi":"10.1016/j.tet.2025.134562","DOIUrl":null,"url":null,"abstract":"<div><div>An efficient transition-metal-free 1,10-phenanthroline-promoted homocoupling reaction has been developed to construct biaryl diamides from 2-iodobenzamides. Various desired products were smoothly synthesized with readily available starting materials in good to excellent yields under the standard reaction conditions. And this method showed a wide substrate scope and good functional group tolerance.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"176 ","pages":"Article 134562"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A transition-metal-free 1,10-phenanthroline-promoted homocoupling reaction for the construction of biaryl diamides\",\"authors\":\"Shengxing Xie, Jinxia Yang, Rong Ma, Minghui Liu, Xinyuan Zhang, Neng-Fei Wang, Chengyu Wang, Lingkai Kong\",\"doi\":\"10.1016/j.tet.2025.134562\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>An efficient transition-metal-free 1,10-phenanthroline-promoted homocoupling reaction has been developed to construct biaryl diamides from 2-iodobenzamides. Various desired products were smoothly synthesized with readily available starting materials in good to excellent yields under the standard reaction conditions. And this method showed a wide substrate scope and good functional group tolerance.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"176 \",\"pages\":\"Article 134562\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-05-01\",\"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/S0040402025001188\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/25 0:00:00\",\"PubModel\":\"Epub\",\"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/S0040402025001188","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/25 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
A transition-metal-free 1,10-phenanthroline-promoted homocoupling reaction for the construction of biaryl diamides
An efficient transition-metal-free 1,10-phenanthroline-promoted homocoupling reaction has been developed to construct biaryl diamides from 2-iodobenzamides. Various desired products were smoothly synthesized with readily available starting materials in good to excellent yields under the standard reaction conditions. And this method showed a wide substrate scope and good functional group tolerance.
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.
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
