Jingwen Peng , Qingfang Chen , Xingqi Wu , Ruishan Zhan , Yanchen Chen , Meihuan Ji , Caicai Lu , Junlei Wang , Fubin Jiang , Binbin Huang
{"title":"丙基羧酸的电化学硒/碲环化。","authors":"Jingwen Peng , Qingfang Chen , Xingqi Wu , Ruishan Zhan , Yanchen Chen , Meihuan Ji , Caicai Lu , Junlei Wang , Fubin Jiang , Binbin Huang","doi":"10.1039/d5cc03741g","DOIUrl":null,"url":null,"abstract":"<div><div>Reported herein is a novel and sustainable electrochemical seleno-/tellurocyclization of propargyl carboxylic acids, affording a diverse range of valuable Se-/Te-incorporated unsaturated γ-lactones under ambient conditions. Preliminary mechanistic studies suggest that this transformation predominantly proceeds <em>via</em> a cationic pathway.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 66","pages":"Pages 12357-12360"},"PeriodicalIF":4.2000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemical seleno-/tellurocyclization of propargyl carboxylic acids†\",\"authors\":\"Jingwen Peng , Qingfang Chen , Xingqi Wu , Ruishan Zhan , Yanchen Chen , Meihuan Ji , Caicai Lu , Junlei Wang , Fubin Jiang , Binbin Huang\",\"doi\":\"10.1039/d5cc03741g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Reported herein is a novel and sustainable electrochemical seleno-/tellurocyclization of propargyl carboxylic acids, affording a diverse range of valuable Se-/Te-incorporated unsaturated γ-lactones under ambient conditions. Preliminary mechanistic studies suggest that this transformation predominantly proceeds <em>via</em> a cationic pathway.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 66\",\"pages\":\"Pages 12357-12360\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-07-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734525015654\",\"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://www.sciencedirect.com/org/science/article/pii/S1359734525015654","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Electrochemical seleno-/tellurocyclization of propargyl carboxylic acids†
Reported herein is a novel and sustainable electrochemical seleno-/tellurocyclization of propargyl carboxylic acids, affording a diverse range of valuable Se-/Te-incorporated unsaturated γ-lactones under ambient conditions. Preliminary mechanistic studies suggest that this transformation predominantly proceeds via a cationic pathway.
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.