{"title":"协同钯光催化合成芳基自由基引发的z -烯烃","authors":"Peizhi Bai, Yue Hu*, Yanwei Gu, Min-Jie Zhou, Xiangchao Xu and Yinjun Xie*, ","doi":"10.1021/acs.orglett.5c0007310.1021/acs.orglett.5c00073","DOIUrl":null,"url":null,"abstract":"<p >We report a novel photocatalyzed selective functionalization of terminal olefins for the synthesis of <i>Z</i>-olefins and cyclobutanes under mild conditions in excellent yields. A series of <i>Z</i>-cinnamic acid derivatives, enamines, and amide-containing cyclobutanes were efficiently synthesized using this method. Mechanistic studies indicated that the success of this reaction is based on the triple radical relay strategy, anion−π interaction for aryl halide activation and aryl radical generation, palladium for controlling chemoselectivity of the aryl radical, and photocatalyst for controlling stereoselectivity via diradical species, respectively.</p>","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"27 7","pages":"1679–1685 1679–1685"},"PeriodicalIF":5.0000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Aryl-Radical-Initiated Z-Olefin Synthesis via Synergistic Palladium and Photocatalysis\",\"authors\":\"Peizhi Bai, Yue Hu*, Yanwei Gu, Min-Jie Zhou, Xiangchao Xu and Yinjun Xie*, \",\"doi\":\"10.1021/acs.orglett.5c0007310.1021/acs.orglett.5c00073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We report a novel photocatalyzed selective functionalization of terminal olefins for the synthesis of <i>Z</i>-olefins and cyclobutanes under mild conditions in excellent yields. A series of <i>Z</i>-cinnamic acid derivatives, enamines, and amide-containing cyclobutanes were efficiently synthesized using this method. Mechanistic studies indicated that the success of this reaction is based on the triple radical relay strategy, anion−π interaction for aryl halide activation and aryl radical generation, palladium for controlling chemoselectivity of the aryl radical, and photocatalyst for controlling stereoselectivity via diradical species, respectively.</p>\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"27 7\",\"pages\":\"1679–1685 1679–1685\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.orglett.5c00073\",\"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://pubs.acs.org/doi/10.1021/acs.orglett.5c00073","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Aryl-Radical-Initiated Z-Olefin Synthesis via Synergistic Palladium and Photocatalysis
We report a novel photocatalyzed selective functionalization of terminal olefins for the synthesis of Z-olefins and cyclobutanes under mild conditions in excellent yields. A series of Z-cinnamic acid derivatives, enamines, and amide-containing cyclobutanes were efficiently synthesized using this method. Mechanistic studies indicated that the success of this reaction is based on the triple radical relay strategy, anion−π interaction for aryl halide activation and aryl radical generation, palladium for controlling chemoselectivity of the aryl radical, and photocatalyst for controlling stereoselectivity via diradical species, respectively.
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.