{"title":"烯烃电化学驱动的溴氯化反应","authors":"Chang-Hui Liu, Su-Yang Xu, Xue-Ting Li, Heng Liu, Hao Zheng and Qing-An Chen","doi":"10.1039/D5CC04608D","DOIUrl":null,"url":null,"abstract":"<p >Organic halides are vital in the synthesis of pharmaceuticals, agrochemicals, and materials. While conventional alkene dihalogenation uses active halogen reagents, we developed an electrochemical strategy for selective bromochlorination. This approach enables precise halogenation under mild conditions.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":" 84","pages":" 16456-16459"},"PeriodicalIF":4.2000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/cc/d5cc04608d?page=search","citationCount":"0","resultStr":"{\"title\":\"Electrochemically driven bromochlorination of alkenes\",\"authors\":\"Chang-Hui Liu, Su-Yang Xu, Xue-Ting Li, Heng Liu, Hao Zheng and Qing-An Chen\",\"doi\":\"10.1039/D5CC04608D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Organic halides are vital in the synthesis of pharmaceuticals, agrochemicals, and materials. While conventional alkene dihalogenation uses active halogen reagents, we developed an electrochemical strategy for selective bromochlorination. This approach enables precise halogenation under mild conditions.</p>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\" 84\",\"pages\":\" 16456-16459\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/cc/d5cc04608d?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/cc/d5cc04608d\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/cc/d5cc04608d","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Electrochemically driven bromochlorination of alkenes
Organic halides are vital in the synthesis of pharmaceuticals, agrochemicals, and materials. While conventional alkene dihalogenation uses active halogen reagents, we developed an electrochemical strategy for selective bromochlorination. This approach enables precise halogenation under mild conditions.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.