Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/99320
Type: Artigo de periódico
Title: Reaction Of Methyl (e)-2-phenyl-1-azirine-3-acrylates With Hydrazines And Amidines. Synthetic And Mechanistic Implications
Author: Kascheres A.
Oliveira C.M.A.
De Azevedo M.B.M.
Nobre C.M.S.
Abstract: 1-Azirines 2a-b react with hydrazine in methanol to produce hexahydropyrrolo[3,2-c]pyrazol-5-ones 3a-b. The process is suggested to involve intramolecular interception of an unstable 4-aminopyrazoline intermediate resulting from C=N bond cleavage. Reaction of 2a with phenylhydrazine similarly affords 3c. In dimethyl sulfoxide, on the other hand, formamidine, guanidine, and hydrazine afford imidazole 4, pyrimidines 5a-b, amino-s-triazine 6, or triazole 9 as a consequence of C-C bond cleavage in aziridine intermediate 8. The intermediacy of tautomers is proposed to account for the diversity of products in this case. © 1991 American Chemical Society.
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Rights: fechado
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Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0002474594&partnerID=40&md5=9ac8cde587212e02ad47592cde6df259
Date Issue: 1991
Appears in Collections:Unicamp - Artigos e Outros Documentos

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