Please use this identifier to cite or link to this item:
Type: Artigo
Title: Enantioselective Total Synthesis Of The Highly Selective Sphingosine-1-receptor Vpc01091 By The Heck Desymmetrization Of A Non-activated Cyclopentene-fused Spiro-pyrrolidinone
Author: Khan
Ismat Ullah; Kattela
Shivashankar; Hassan
Abbas; Correia
Carlos Roque Duarte
Abstract: A novel, efficient and enantioselective Heck-Matsuda desymmetrization of non-activated cyclopentene-fused spiro-pyrrolidinones was developed. The reaction provided the Heck products in good to excellent yields and selectivities and tolerated a variety of functional groups in arenediazonium tetrafluoroborates (12 examples) with respect to its electronics and substitution patterns. This methodology was successfully applied in the concise enantioselective total synthesis of VPC01091 (2b), a drug candidate for the treatment of multiple sclerosis.
Editor: Royal Soc Chemistry
Rights: fechado
Identifier DOI: 10.1039/c6ob01892k
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
000385594100005.pdf1.16 MBAdobe PDFView/Open

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