Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/102392
Type: Artigo de periódico
Title: Enantioselective Approach To The Asymmetric Synthesis Of(6r)-hydroxymethyl-5,6-dihydro-2h-pyran-2-one. A Formal Synthesis Of(r)-argentilactone And Total Synthesis Of (r)-goniothalamin
Author: De Fatima A.
Pilli R.A.
Abstract: The asymmetric synthesis of the (6R)-hydroxymethyl-5,6-dihydro-2H-pyran-2- one, a key intermediate in the formal synthesis of (R)-argentilactone, and the total synthesis of (R)-goniothalamin are described. Our aproach involved the Lemieux-Johnson oxidative cleavage, enantioselective Keck allylation, ring-closing metathesis and Wittig olefination.
Editor: 
Rights: fechado
Identifier DOI: 
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0142167849&partnerID=40&md5=3e3f421b26036f3ac17449b67aea4565
Date Issue: 2003
Appears in Collections:Unicamp - Artigos e Outros Documentos

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