Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: The Total Synthesis Of (-)-cryptocaryol A.
Author: Dias, L C
Kuroishi, P K
de Lucca, E C
Abstract: A stereoselective total synthesis of (-)-cryptocaryol A () is described. Key features of the 17-step route include the use of three boron-mediated aldol reaction-reduction sequences to control all stereocenters and an Ando modification of the Horner-Wadsworth-Emmons olefination that permitted the installation of the Z double bond of the α-pyrone ring.
Rights: aberto
Identifier DOI: 10.1039/c5ob00080g
Date Issue: 2015
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
pmed_25695350.pdf1.21 MBAdobe PDFView/Open

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