Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/196219
Type: Artigo de periódico
Title: A Concise Route To The Azaspirodecane Moiety Of Halichlorine And Structurally Related Alkaloids.
Author: de Sousa, Andrea L
Pilli, Ronaldo A
Abstract: [reaction: see text] A tandem Michael addition-enolate alkylation followed by Dieckmann cyclization and Beckmann rearrangement provided the corresponding [5.4.0] azaspirobicyclodecane, a key intermediate in our synthetic route to the marine alkaloid halichlorine (1).
Subject: Alkaloids
Animals
Molecular Structure
Porifera
Spiro Compounds
Stereoisomerism
Rights: fechado
Identifier DOI: 10.1021/ol050306g
Address: http://www.ncbi.nlm.nih.gov/pubmed/15816766
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
pmed_15816766.pdf68.34 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.