{"title":"可见光光氧化还原催化非活化烯烃氢膦化反应","authors":"Ming Qi, An-Wu Xu","doi":"10.1016/j.tet.2025.134712","DOIUrl":null,"url":null,"abstract":"<div><div>We report a visible light-induced hydrophosphinylation of unactivated alkenes catalyzed by a low-concentration photocatalyst (4CzIPN), affording a simple, efficient and environmentally friendly method for constructing C–P bonds. This method exhibits a broad substrate scope and synthetically useful yields, and its practicability is further demonstrated by gram-scale experiments. The mechanism was elucidated through detailed experimental studies and theoretical calculations. By comparing linear alkenes with functionalized alkenes, we gained insights into the radical process, which is beneficial for the development of synthetic strategies for tertiary phosphine oxides.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"183 ","pages":"Article 134712"},"PeriodicalIF":2.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible light photoredox catalyzed hydrophosphinylation of unactivated alkenes\",\"authors\":\"Ming Qi, An-Wu Xu\",\"doi\":\"10.1016/j.tet.2025.134712\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We report a visible light-induced hydrophosphinylation of unactivated alkenes catalyzed by a low-concentration photocatalyst (4CzIPN), affording a simple, efficient and environmentally friendly method for constructing C–P bonds. This method exhibits a broad substrate scope and synthetically useful yields, and its practicability is further demonstrated by gram-scale experiments. The mechanism was elucidated through detailed experimental studies and theoretical calculations. By comparing linear alkenes with functionalized alkenes, we gained insights into the radical process, which is beneficial for the development of synthetic strategies for tertiary phosphine oxides.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"183 \",\"pages\":\"Article 134712\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-05-14\",\"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/S0040402025002686\",\"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/S0040402025002686","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 photoredox catalyzed hydrophosphinylation of unactivated alkenes
We report a visible light-induced hydrophosphinylation of unactivated alkenes catalyzed by a low-concentration photocatalyst (4CzIPN), affording a simple, efficient and environmentally friendly method for constructing C–P bonds. This method exhibits a broad substrate scope and synthetically useful yields, and its practicability is further demonstrated by gram-scale experiments. The mechanism was elucidated through detailed experimental studies and theoretical calculations. By comparing linear alkenes with functionalized alkenes, we gained insights into the radical process, which is beneficial for the development of synthetic strategies for tertiary phosphine oxides.
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.