Please use this identifier to cite or link to this item:
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.
Rights: fechado
Identifier DOI: 
Date Issue: 2003
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
2-s2.0-0142167849.pdf123.57 kBAdobe PDFView/Open

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