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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| Main Authors: | , |
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| Format: | Article |
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Elsevier
1996
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| Online Access: | http://umpir.ump.edu.my/id/eprint/4788/ http://dx.doi.org/10.1016/S0040-4039(96)02039-4 |
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