Selenium-catalyzed reductive carbonylation of nitrobenzene with amines as coreagents to give unsymmetric phenylureas
| Data(s) |
25/06/1999
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| Resumo |
The reductive carbonylation of nitrobenzene catalyzed by selenium to yield unsymmetric phenylureas has been studied. When secondary amines were used as coreagents, a single product, PhNHCONR2, was formed; when primary amines were chosen as coreagents, mixed products, including RNHCONHR, RNHCONHPh and PhNHCONHPh, were obtained. (C) 1999 Elsevier Science Ltd. All rights reserved. |
| Identificador | |
| Idioma(s) |
英语 |
| Fonte |
杨瑛 陆世维.Selenium-catalyzed Reductive Carbonylation of Nitrobenzene with Amines as Coreagents to Give Unsymmetric Phenylureas,Tetrahedron Letters; 40(1999)4845-4846,1999,():- |
| Palavras-Chave | #selenium #carbonylation #nitrobenzene #amines #unsymmetrical phenylureas |
| Tipo |
期刊论文 |
