{"title":"乙烯基硼酯与芳酰氯自由基氢化反应制备β-硼基酮的研究","authors":"Shuai Tang, Shuting Wang, Hua Zhang","doi":"10.1021/acs.orglett.5c00996","DOIUrl":null,"url":null,"abstract":"A visible-light-induced radical hydroaroylation of vinyl boronic ester with aroyl chlorides has been developed, yielding a variety of β-boryl ketones in moderate to good yields with broad functional group tolerance. This metal-free transformation offers a convenient and practical route to access valuable β-boryl ketones from readily available aroyl chlorides and vinyl boronic ester.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"11 1","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible-Light-Induced Radical Hydroaroylation of Vinyl Boronic Ester with Aroyl Chlorides to Access β-Boryl Ketones\",\"authors\":\"Shuai Tang, Shuting Wang, Hua Zhang\",\"doi\":\"10.1021/acs.orglett.5c00996\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A visible-light-induced radical hydroaroylation of vinyl boronic ester with aroyl chlorides has been developed, yielding a variety of β-boryl ketones in moderate to good yields with broad functional group tolerance. This metal-free transformation offers a convenient and practical route to access valuable β-boryl ketones from readily available aroyl chlorides and vinyl boronic ester.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-03-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.orglett.5c00996\",\"RegionNum\":1,\"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 Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c00996","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Visible-Light-Induced Radical Hydroaroylation of Vinyl Boronic Ester with Aroyl Chlorides to Access β-Boryl Ketones
A visible-light-induced radical hydroaroylation of vinyl boronic ester with aroyl chlorides has been developed, yielding a variety of β-boryl ketones in moderate to good yields with broad functional group tolerance. This metal-free transformation offers a convenient and practical route to access valuable β-boryl ketones from readily available aroyl chlorides and vinyl boronic ester.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.