Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine

Rejzek, Martin, Stockman, Robert A. and Hughes, David L. (2005) Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine. Organic & Biomolecular Chemistry, 3 (1). pp. 73-83. ISSN 1477-0520

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Abstract

Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.

Item Type:	Article
Faculty \ School:	Faculty of Science > School of Chemistry
Depositing User:	Pure Connector
Date Deposited:	12 Jan 2016 17:00
Last Modified:	02 Mar 2023 11:30
URI:	https://ueaeprints.uea.ac.uk/id/eprint/56266
DOI:	10.1039/b413052a

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