Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/61725
Type: Artigo de periódico
Title: Diels-Alder reactions of 6-substituted 1-(p-nitrobenzoyl)-5,6-dihydro-2-pyridinones
Author: Dias, LC
Fernandes, AMAP
Zukerman-Schpector, J
Abstract: The first examples of Diels-Alder cycloaddition reactions of 6-substituted 1-(p-nitrobenzoyl)-5,6-dihydro-2-pyridinones are described. This reaction benefits from the fact that the diene adopts an endo orientation trans to the axial substituent at C-6 due to A(1.3) allylic type strain with the N-PNB protecting group.
Subject: heterocycles
cycloadditions
alpha,beta-unsaturated lactams
A(1,3) allylic strain
cis-hydroisoquinotine
Country: Alemanha
Editor: Georg Thieme Verlag Kg
Rights: embargo
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

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