Ming Hou, Yuanrui Wang, Hefei Yang, Jiajun Zhang, Prof. Dr. Xiao-Feng Wu
{"title":"Photo-Promoted Nitrogen-Centered Radical Mediated Intermolecular Aminative Carbonylation of Tertiary Allyl Alcohols to Access β-Amino Ketones through (Hetero)Aryl Migration","authors":"Ming Hou, Yuanrui Wang, Hefei Yang, Jiajun Zhang, Prof. Dr. Xiao-Feng Wu","doi":"10.1002/ceur.202500001","DOIUrl":null,"url":null,"abstract":"<p>Carbon monoxide, as a crucial C1 synthon, has been widely used in the difunctionalization of alkenes. Additionally, nitrogen-centered radicals (NCRs) are also effective intermediates for constructing C−N bonds. Herein, a nitrogen-centered radical-mediated aminative carbonylation strategy for producing <i>β</i>-amino ketones from tertiary allyl alcohols has been disclosed. Good yields of <i>β</i>-amino ketones with different functional groups were generated effectively under light irradiation.</p>","PeriodicalId":100234,"journal":{"name":"ChemistryEurope","volume":"3 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ceur.202500001","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistryEurope","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ceur.202500001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Carbon monoxide, as a crucial C1 synthon, has been widely used in the difunctionalization of alkenes. Additionally, nitrogen-centered radicals (NCRs) are also effective intermediates for constructing C−N bonds. Herein, a nitrogen-centered radical-mediated aminative carbonylation strategy for producing β-amino ketones from tertiary allyl alcohols has been disclosed. Good yields of β-amino ketones with different functional groups were generated effectively under light irradiation.