Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5588
Title: An improved synthesis of α,β-unsaturated nitrones relevant to the stephacidins and analogs thereof
Authors: Hafensteiner, B. D.
Escribano, M.
Petricci, Elena 
Baran, P. S.
Keywords: Click-chemistry; Methodology; Oxidations; Synthesis; Antineoplastic Agents; Indole Alkaloids; Indoles; Nitrogen Oxides; Oxidation-Reduction; Biochemistry; Clinical Biochemistry; Molecular Biology; Molecular Medicine; Organic Chemistry; Drug Discovery3003 Pharmaceutical Science; 3003
Issue Date: 2009
Project: None 
Journal: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Abstract: 
A new method is reported for the synthesis of the α,β-unsaturated nitrone moiety characteristic of the stephacidin/avrainvillamide family of bioactive prenylated indole alkaloids. Application to the synthesis of stephacidin analogs and a potential biological probe are showcased.
Description: 
6932
URI: http://hdl.handle.net/20.500.12779/5588
ISSN: 0960-894X
DOI: 10.1016/j.bmcl.2009.04.045
Appears in Collections:Publications

Show full item record

Google ScholarTM

Check

Altmetric


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