AbstractSeveral 3‐Ω‐amino monosubstituted hydantoins have been obtained in the reaction of isocyanate of glycine ethyl ester with the appropriate aliphatic or aromatic diamine. It was found, that the 3‐(aminoaryl) monosubstituted hydantoins may be diazotized and their diazonium salts may be coupled and hydrolysed without changes in the hydantoin ring.
Mindl, Jaromir; Sterba, Vojeslav, Collection of Czechoslovak Chemical Communications, 1987, vol. 52, # 1, p. 156 - 161
作者:Mindl, Jaromir、Sterba, Vojeslav
DOI:——
日期:——
Synthesis of 3‐Ω‐aminohydantoins
作者:Józef Ryczek
DOI:10.1002/jhet.5570390521
日期:2002.9
AbstractSeveral 3‐Ω‐amino monosubstituted hydantoins have been obtained in the reaction of isocyanate of glycine ethyl ester with the appropriate aliphatic or aromatic diamine. It was found, that the 3‐(aminoaryl) monosubstituted hydantoins may be diazotized and their diazonium salts may be coupled and hydrolysed without changes in the hydantoin ring.