Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/74114
Type: Artigo de periódico
Title: Synthesis of alexine-like compounds from chiral five-membered endocyclic enecarbamates
Author: Valle, MS
Retailleau, P
Correia, CRD
Abstract: Stereoselective syntheses of enantiomerically enriched trihydroxy pyrrolizidine and indolizidines were accomplished from a common chiral endocyclic enecarbamate. The synthetic strategy features an efficient [2+2] cycloaddition of ketenes to the endocyclic enecarbamate and a highly regioselective Baeyer-Villiger oxidation of the intermediate azabicyclic-cyclobutanones. These new heterocycles are compounds structurally related to the alexines. (c) 2008 Elsevier Ltd. All rights reserved.
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.tetlet.2008.01.098
Date Issue: 2008
Appears in Collections:Unicamp - Artigos e Outros Documentos

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