{"title":"Facile synthesis of propargylamines by metal-free doubly decarboxylative coupling†","authors":"Junduo Hu, Xiaofan Shi, Liliang Huang, Rongkang Zhang and Huangdi Feng","doi":"10.1039/D4SU00258J","DOIUrl":null,"url":null,"abstract":"<p >Doubly decarboxylative coupling between two different carboxylic acids to form a new C–C bond is a powerful tool for the rapid assembly of complex compounds. Herein, we report a metal-free three-component decarboxylative strategy for the construction of diverse propargylamines in good yields with high chemoselectivity. This operationally simple method can be applied to various amino acids, α-keto acids, and terminal alkynes, providing a powerful new protocol for propargylamine synthesis. The reaction without the addition of metal catalysts has the advantages of broad scope and functional group compatibility, and environmental friendliness.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 9","pages":" 2626-2631"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/su/d4su00258j?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC sustainability","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/su/d4su00258j","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
Doubly decarboxylative coupling between two different carboxylic acids to form a new C–C bond is a powerful tool for the rapid assembly of complex compounds. Herein, we report a metal-free three-component decarboxylative strategy for the construction of diverse propargylamines in good yields with high chemoselectivity. This operationally simple method can be applied to various amino acids, α-keto acids, and terminal alkynes, providing a powerful new protocol for propargylamine synthesis. The reaction without the addition of metal catalysts has the advantages of broad scope and functional group compatibility, and environmental friendliness.