{"title":"1,5-氢原子转移介导的交叉脱氢偶联对羟肟酸衍生物的光氧化还原催化γ - C(sp3)−H乙烯化","authors":"Lingli Liu, Yangjian Cheng, Changduo Pan, Jin-Tao Yu","doi":"10.1039/d5qo00747j","DOIUrl":null,"url":null,"abstract":"A visible-light-induced regioselective γ-C(sp3)-H vinylation of hydroxamic acid derivatives with 2-aryl enamides was developed via cross-dehydrogenative coupling (CDC) reactions for the first time. This remote γ-vinylation was realized by the 1,5-hydrogen atom transfer (1,5-HAT) of the amidyl radicals that in situ generated through the potocatalytic N-O bond cleavage of hydroxamic acid derivatives.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":"36 1","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoredox catalytic γ‑C(sp3)−H vinylation of hydroxamic acid derivatives via 1,5-hydrogen-atom-transfer-mediated cross-dehydrogenative coupling\",\"authors\":\"Lingli Liu, Yangjian Cheng, Changduo Pan, Jin-Tao Yu\",\"doi\":\"10.1039/d5qo00747j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A visible-light-induced regioselective γ-C(sp3)-H vinylation of hydroxamic acid derivatives with 2-aryl enamides was developed via cross-dehydrogenative coupling (CDC) reactions for the first time. This remote γ-vinylation was realized by the 1,5-hydrogen atom transfer (1,5-HAT) of the amidyl radicals that in situ generated through the potocatalytic N-O bond cleavage of hydroxamic acid derivatives.\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":\"36 1\",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5qo00747j\",\"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://doi.org/10.1039/d5qo00747j","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Photoredox catalytic γ‑C(sp3)−H vinylation of hydroxamic acid derivatives via 1,5-hydrogen-atom-transfer-mediated cross-dehydrogenative coupling
A visible-light-induced regioselective γ-C(sp3)-H vinylation of hydroxamic acid derivatives with 2-aryl enamides was developed via cross-dehydrogenative coupling (CDC) reactions for the first time. This remote γ-vinylation was realized by the 1,5-hydrogen atom transfer (1,5-HAT) of the amidyl radicals that in situ generated through the potocatalytic N-O bond cleavage of hydroxamic acid derivatives.
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.