Ring-expansion of an Aziridinone to a Hexahydrotriazine Through the Agency of a Novel Rearrangement

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Ring-expansion of an Aziridinone to a Hexahydrotriazine Through the Agency of a Novel Rearrangement

Reaction of 1,3-di-t,'rt-bu~.laziridinonc (la) and similar aziridinones with thiosemicarbazide affords, as one of the products, a compound devoid of sulfur, vie., a substituted N- aminoimidazolidinone (3a) by selective cleavage of the acyl-nitrogcn bond. Compound 3a undergoes a novel, acid-cata...

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Bibliographic Details
Main Authors:	M. M., Yusoff, Talaty, Erach R
Format:	Article
Published:	Elsevier 1996
Subjects:	Q Science (General)
Online Access:	http://umpir.ump.edu.my/id/eprint/4788/

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