Synthesis of an 11-unsubstituted analogue of (±)-huperzine A

Camps, Pelayo, Contreras, Joan, Morral-Cardoner, Jordi, Muñoz-Torrero, Diego, Font-Bardia, Mercè and Solans, Xavier (1999) Synthesis of an 11-unsubstituted analogue of (±)-huperzine A. Tetrahedron, 55 (28). pp. 8481-8496. ISSN 0040-4020

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Abstract

The synthesis of a new analogue of (±)-huperzine A lacking the ethylidene appendage at position 11 has been accomplished. The key steps of the synthesis were: a) the reduction of the keto function of the known methyl 7,7-ethylenedioxy-3-methyl-9-oxobicyclo[3.3.1]non-3-ene-1-carboxylate into a methylene group by reduction to a mixture of stereoisomeric alcohols follwed by alcohol-deoxygenation through a Barton-McCombie proccdure and b) the elaboration of the pyridone ring in a late stage of the synthesis by reaction of a pyrrolidine enamine with propiolamide, which gave a mixture of regioisomeric pyridone derivatives.

Item Type:	Article
Subjects:	Q Science > Q Science (General) Q Science > QD Chemistry
Schools:	School of Applied Sciences
Related URLs:	Author
Depositing User:	Sara Taylor
Date Deposited:	28 Jun 2011 14:52
Last Modified:	06 Apr 2018 12:15
URI:	http://eprints.hud.ac.uk/id/eprint/10812

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