Zhenhui Wang , Shiqing Huang , Hao Hou , Wei Liu , Wei Ou
{"title":"在EDA配合物的辅助下,芳基丙烯腈直接氢化成β-酮腈","authors":"Zhenhui Wang , Shiqing Huang , Hao Hou , Wei Liu , Wei Ou","doi":"10.1039/d5cc00867k","DOIUrl":null,"url":null,"abstract":"<div><div>Here, we present a base-mediated direct hydroacylation reaction of arylacrylonitrile. This method provides an efficient approach for highly site-selective synthesis of β-ketonitriles, demonstrating mild, facile and high atom- and step-economical characteristics. The reaction occurs through a free-radical pathway enabled by an EDA complex in the absence of light.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 41","pages":"Pages 7510-7513"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Direct hydroacylation of arylacrylonitriles toward β-ketonitriles assisted by an EDA complex†\",\"authors\":\"Zhenhui Wang , Shiqing Huang , Hao Hou , Wei Liu , Wei Ou\",\"doi\":\"10.1039/d5cc00867k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Here, we present a base-mediated direct hydroacylation reaction of arylacrylonitrile. This method provides an efficient approach for highly site-selective synthesis of β-ketonitriles, demonstrating mild, facile and high atom- and step-economical characteristics. The reaction occurs through a free-radical pathway enabled by an EDA complex in the absence of light.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 41\",\"pages\":\"Pages 7510-7513\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-04-23\",\"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/S1359734525008286\",\"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/S1359734525008286","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Direct hydroacylation of arylacrylonitriles toward β-ketonitriles assisted by an EDA complex†
Here, we present a base-mediated direct hydroacylation reaction of arylacrylonitrile. This method provides an efficient approach for highly site-selective synthesis of β-ketonitriles, demonstrating mild, facile and high atom- and step-economical characteristics. The reaction occurs through a free-radical pathway enabled by an EDA complex in the absence of light.
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.