{"title":"钯催化硫醚-环丙烯硫羰基化制备羰基化双官能化环丙烯的高收敛模块化途径。","authors":"Xuening Li,Suliang Wang,Jian Song,Xianjie Fang","doi":"10.1021/acs.orglett.5c01709","DOIUrl":null,"url":null,"abstract":"A novel and efficient synthesis of carbonylative difunctionalized cyclopropanes was disclosed by the palladium-catalyzed thioether-thiocarbonylation of cyclopropenes with organic disulfides. Preliminary studies show that the electron-rich unit in organic disulfide was more conducive to the production of the thioesters. This process is applicable to a series of cyclopropane derivatives and employs commercially available diaryl disulfides as the partners. Notably, the gram-scale reaction and further transformations demonstrate the practicality and application potential of this approach for organic synthesis.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"15 1","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly Convergent Modular Access to Carbonylative Difunctionalized Cyclopropanes via Palladium-Catalyzed Thioether-Thiocarbonylation of Cyclopropenes.\",\"authors\":\"Xuening Li,Suliang Wang,Jian Song,Xianjie Fang\",\"doi\":\"10.1021/acs.orglett.5c01709\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A novel and efficient synthesis of carbonylative difunctionalized cyclopropanes was disclosed by the palladium-catalyzed thioether-thiocarbonylation of cyclopropenes with organic disulfides. Preliminary studies show that the electron-rich unit in organic disulfide was more conducive to the production of the thioesters. This process is applicable to a series of cyclopropane derivatives and employs commercially available diaryl disulfides as the partners. Notably, the gram-scale reaction and further transformations demonstrate the practicality and application potential of this approach for organic synthesis.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-05-16\",\"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.5c01709\",\"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.5c01709","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Highly Convergent Modular Access to Carbonylative Difunctionalized Cyclopropanes via Palladium-Catalyzed Thioether-Thiocarbonylation of Cyclopropenes.
A novel and efficient synthesis of carbonylative difunctionalized cyclopropanes was disclosed by the palladium-catalyzed thioether-thiocarbonylation of cyclopropenes with organic disulfides. Preliminary studies show that the electron-rich unit in organic disulfide was more conducive to the production of the thioesters. This process is applicable to a series of cyclopropane derivatives and employs commercially available diaryl disulfides as the partners. Notably, the gram-scale reaction and further transformations demonstrate the practicality and application potential of this approach for organic synthesis.
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.