Highly efficient synthesis of ureas and carbamates from amides by iodosylbenzene-induced hofmann rearrangement
A simple and efficient method for the synthesis of 1,3-disubstituted ureas and carbamates from amides by using iodosylbenzene as the oxidant is described. Symmetric and asymmetric ureas and carbamates can be prepared by this procedure in up to 98 % yield. Ureidopeptides can also be prepared in good yield by this method. A simple and efficient method for the synthesis of 1,3-disubstituted ureas and carbamates from amides by using iodosylbenzene as the oxidant is described. By using this method, heterocyclic products can be easily obtained in excellent yield. Ureidopeptides can also be prepared in good yield by this procedure. Copyright
Liu, Peng,Wang, Zhiming,Hu, Xianming
experimental part
p. 1994 - 2000
(2012/05/05)
Diiodosilane: A Reagent for Mild, Efficient Conversion of Carbamates to Ureas via Isocyanates
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Gastaldi, Stephane,Weinreb, Steven M.,Stien, Didier
p. 3239 - 3240
(2007/10/03)
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