{"title":"Palladium-catalyzed decarboxylation [2 + 2 + 2] annulation approach to chromone-containing polycyclic compounds†","authors":"Yu-Chen Fang , Jia-He Chen , Ren-Feng Xiu , Li-Ren Zhang , Fang-Hua Zheng , Yong-Zheng Chen , Zi-Wei Gao , Wen-Yong Han","doi":"10.1039/d3qo00764b","DOIUrl":null,"url":null,"abstract":"<div><p>We present herein a palladium-catalyzed decarboxylation [2 + 2 + 2] annulation with 3-iodochromones, bridged olefins, and <em>o</em>-bromobenzoic acids to give various <em>exo</em>-chromone-containing polycyclic compounds (49 examples, up to 92% yield), in which <em>o</em>-bromobenzoic acids were employed as the electrophilic aryl units. Gram-scale experiments, late-stage modification of estrone, and further transformations of products show a great potential of this palladium-catalyzed Heck coupling/C(sp<sup>2</sup>)–H activation/decarboxylation cascade for drug discovery and development.</p></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"10 15","pages":"Pages 3752-3759"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052411023009367","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We present herein a palladium-catalyzed decarboxylation [2 + 2 + 2] annulation with 3-iodochromones, bridged olefins, and o-bromobenzoic acids to give various exo-chromone-containing polycyclic compounds (49 examples, up to 92% yield), in which o-bromobenzoic acids were employed as the electrophilic aryl units. Gram-scale experiments, late-stage modification of estrone, and further transformations of products show a great potential of this palladium-catalyzed Heck coupling/C(sp2)–H activation/decarboxylation cascade for drug discovery and development.