{"title":"N-烷基氨基甲酸酯合成不对称脲的改进","authors":"Prachi Ramteke, Dinesh Kumar Tanwar, M. Gill","doi":"10.1055/a-2157-5925","DOIUrl":null,"url":null,"abstract":"An efficient, cost-effective, easy and green method is reported for the preparation of N,N’-alkyl aryl ureas and N,N’-dialkylureas via carbamates. This improved procedure is devoid of any hazardous reagents such as phosgent, isocyanates etc. and has shown a broad substrate scope with good to excellent yields. As compared to literature reports, this procedure is operationally simple, potentially scalable and significantly benign to synthesize these important motifs.","PeriodicalId":22135,"journal":{"name":"SynOpen","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2023-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"IMPROVED SYNTHESIS OF UNSYMMETRICAL UREAS VIA N-ALKYL CARBAMATES\",\"authors\":\"Prachi Ramteke, Dinesh Kumar Tanwar, M. Gill\",\"doi\":\"10.1055/a-2157-5925\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An efficient, cost-effective, easy and green method is reported for the preparation of N,N’-alkyl aryl ureas and N,N’-dialkylureas via carbamates. This improved procedure is devoid of any hazardous reagents such as phosgent, isocyanates etc. and has shown a broad substrate scope with good to excellent yields. As compared to literature reports, this procedure is operationally simple, potentially scalable and significantly benign to synthesize these important motifs.\",\"PeriodicalId\":22135,\"journal\":{\"name\":\"SynOpen\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2023-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"SynOpen\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/a-2157-5925\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"SynOpen","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2157-5925","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
IMPROVED SYNTHESIS OF UNSYMMETRICAL UREAS VIA N-ALKYL CARBAMATES
An efficient, cost-effective, easy and green method is reported for the preparation of N,N’-alkyl aryl ureas and N,N’-dialkylureas via carbamates. This improved procedure is devoid of any hazardous reagents such as phosgent, isocyanates etc. and has shown a broad substrate scope with good to excellent yields. As compared to literature reports, this procedure is operationally simple, potentially scalable and significantly benign to synthesize these important motifs.