Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Heck Reaction on Morita-Baylis-Hillman Adducts: Diastereoselective Synthesis of Pyrrolizidinones and Pyrrolizidines
Author: Freire, KRD
Tormena, CF
Coelho, F
Abstract: An efficient approach to the diastereoselective synthesis of benzylidene-, benzyl-pyrrolizidinones, and pyrrolizidines is described. The sequence is based on a highly stereoselective Heck reaction between a hydroxylated pyrrolizidinone, prepared from a Morita-Baylis-Hillman adduct, and a suitable aryl halide, using Najera's oxime derived palladacycle as catalyst.
Subject: Morita-Baylis-Hillman
Heck reaction
bicyclic compounds
Country: Alemanha
Editor: Georg Thieme Verlag Kg
Citation: Synlett. Georg Thieme Verlag Kg, n. 14, n. 2059, n. 2063, 2011.
Rights: embargo
Identifier DOI: 10.1055/s-0030-1261161
Date Issue: 2011
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000294161400023.pdf141.61 kBAdobe PDFView/Open

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