Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/194504
Type: Artigo de periódico
Title: Electronically Mediated Selectivity In Ring Opening Of 1-azirines. The 3-z Mode: Convenient Route To 2-aza-1,3-dienes.
Author: Barroso, Marcia T.
Kascheres, Albert
Abstract: Reaction of 1-azirine-3-methylacrylates 1a,b with imidazoles and pyrazoles under mild conditions results in the formation of 2-aza-1,3-dienes 2a-g containing a potential leaving group at the 1-position. Simple alcohols (methanol and ethanol) react similarly with 1a,b in the presence of sodium carbonate to afford 2h-j. Utilization of 2 in the hetero Diels-Alder reaction with electron-deficient dienophiles is described.
Rights: fechado
Identifier DOI: 
Address: http://www.ncbi.nlm.nih.gov/pubmed/11674083
Date Issue: 1999
Appears in Collections:Unicamp - Artigos e Outros Documentos

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