Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/101325
Type: Artigo de periódico
Title: First Comprehensive Bakkane Approach: Stereoselective And Efficient Dichloroketene-based Total Syntheses Of (±)- And (-)-9-acetoxyfukinanolide, (±)- And (+)-bakkenolide A, (-)-bakkenolides Iii, B, C, H, L, V, And X, (±)- And (-)-homogynolide A, (±)-homogynolide B, And (±)-palmosalide C
Author: Brocksom T.J.
Coelho F.
Depres J.-P.
Greene A.E.
Freire de Lima M.E.
Hamelin O.
Hartmann B.
Kanazawa A.M.
Wang Y.
Abstract: Cycloaddition of dichloroketene with dimethylcyclohexenes has been used as the key reaction in an efficient, general approach to the bakkanes. New methods and methodologies that have been developed in this work include spiro β-methylene-γ-butyrolactonizations, a vicinal dicarboxylation, an angelic ester preparation, a transesterification, an epoxy ketone double reduction, and a retro aldol-aldol approach to low-energy aldol isomers.
Editor: 
Rights: fechado
Identifier DOI: 10.1021/ja0208456
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0037176279&partnerID=40&md5=eeab53f83d7861bc33f9e5640ebbe190
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

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