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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
Molecular Structure
Spiro Compounds
Rights: fechado
Identifier DOI: 10.1021/ol050306g
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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