{"title":"光化学烯丙胺的无金属氢氨基化","authors":"Mariusz Zalewski, Sebastian Stecko","doi":"10.1002/adsc.70148","DOIUrl":null,"url":null,"abstract":"Herein, a photoredox‐catalyzed protocol for allylamine hydrocarbamoylation under metal‐free and mild conditions is reported. The proposed method utilizes readily accessible 4‐carboxyamido Hantzsch esters as convenient substrates that deliver carbamoyl radicals upon a visible light‐mediated SET process. Their addition to various allylamines proceeds with good‐to‐excellent efficiency and with high levels of regio‐ and chemoselectivity to provide the corresponding γ‐amino acid amides.","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":"74 1","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photochemical Metal‐Free Hydrocarbamoylation of Allylamines\",\"authors\":\"Mariusz Zalewski, Sebastian Stecko\",\"doi\":\"10.1002/adsc.70148\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, a photoredox‐catalyzed protocol for allylamine hydrocarbamoylation under metal‐free and mild conditions is reported. The proposed method utilizes readily accessible 4‐carboxyamido Hantzsch esters as convenient substrates that deliver carbamoyl radicals upon a visible light‐mediated SET process. Their addition to various allylamines proceeds with good‐to‐excellent efficiency and with high levels of regio‐ and chemoselectivity to provide the corresponding γ‐amino acid amides.\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":\"74 1\",\"pages\":\"\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-10-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Synthesis & Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/adsc.70148\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Synthesis & Catalysis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/adsc.70148","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Photochemical Metal‐Free Hydrocarbamoylation of Allylamines
Herein, a photoredox‐catalyzed protocol for allylamine hydrocarbamoylation under metal‐free and mild conditions is reported. The proposed method utilizes readily accessible 4‐carboxyamido Hantzsch esters as convenient substrates that deliver carbamoyl radicals upon a visible light‐mediated SET process. Their addition to various allylamines proceeds with good‐to‐excellent efficiency and with high levels of regio‐ and chemoselectivity to provide the corresponding γ‐amino acid amides.
期刊介绍:
Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry.
The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.