{"title":"1,2-Aminoalkylacylation of styrenes by cooperative NHC/photoredox dual catalysis","authors":"Lili Wu (Formal analysis Investigation Methodology Writing – original draft) , Chengming Wang (Conceptualization Funding acquisition Project administration Supervision Writing – review & editing)","doi":"10.1080/00397911.2025.2486106","DOIUrl":null,"url":null,"abstract":"<div><div>A novel visible-light-mediated 1,2-aminoalkylacylation reaction of styrenes with α-silyl-protected tertiary amines and acyl fluorides has been developed for the efficient construction of γ-aminoketones. This transformation employs a synergistic dual catalyst system, combining the benefits of N-heterocyclic carbene catalysis and photoredox catalysis, enabling the reaction to proceed under mild conditions.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"55 8","pages":"Pages 618-626"},"PeriodicalIF":1.8000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0039791125000311","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
A novel visible-light-mediated 1,2-aminoalkylacylation reaction of styrenes with α-silyl-protected tertiary amines and acyl fluorides has been developed for the efficient construction of γ-aminoketones. This transformation employs a synergistic dual catalyst system, combining the benefits of N-heterocyclic carbene catalysis and photoredox catalysis, enabling the reaction to proceed under mild conditions.
期刊介绍:
Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.