{"title":"吡啶与二酰过氧化物和过氧化氢的副选择性自由基烷基化反应","authors":"Zhe Wang, Pengwei Xu and Armido Studer","doi":"10.1039/D4QO00814F","DOIUrl":null,"url":null,"abstract":"<p >Herein, a practical method for the <em>para</em>-selective alkylation of various pyridines using the corresponding oxazino pyridine intermediates and cheap alkyl carboxylic acid-derived diacyl peroxides or peresters as alkyl radical precursors and internal oxidants is reported. The transformation proceeds in the absence of any transition metal catalyst, is easy to scale up and can be used in consecutive radical <em>para</em>,<em>ortho</em>-difunctionalization.</p>","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":" 14","pages":" 3849-3854"},"PeriodicalIF":4.7000,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"para-Selective radical alkylation of pyridines with diacyl peroxides and peresters†\",\"authors\":\"Zhe Wang, Pengwei Xu and Armido Studer\",\"doi\":\"10.1039/D4QO00814F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, a practical method for the <em>para</em>-selective alkylation of various pyridines using the corresponding oxazino pyridine intermediates and cheap alkyl carboxylic acid-derived diacyl peroxides or peresters as alkyl radical precursors and internal oxidants is reported. The transformation proceeds in the absence of any transition metal catalyst, is easy to scale up and can be used in consecutive radical <em>para</em>,<em>ortho</em>-difunctionalization.</p>\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":\" 14\",\"pages\":\" 3849-3854\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/qo/d4qo00814f\",\"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 Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/qo/d4qo00814f","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
para-Selective radical alkylation of pyridines with diacyl peroxides and peresters†
Herein, a practical method for the para-selective alkylation of various pyridines using the corresponding oxazino pyridine intermediates and cheap alkyl carboxylic acid-derived diacyl peroxides or peresters as alkyl radical precursors and internal oxidants is reported. The transformation proceeds in the absence of any transition metal catalyst, is easy to scale up and can be used in consecutive radical para,ortho-difunctionalization.
期刊介绍:
Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.