Published in
Oxford University Press, Journal of Pharmacy and Pharmacology, 7(53), p. 955-958, 2001
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Studies on the reactivity of a tertiary allylic alcohol in an acetophenonic series, a model for natural products synthesis
Journal article published in 2001 by
J. J. Hélesbeux 
,
D. Séraphin,
O. Duval,
P. Richomme,
J. Bruneton
,
D. Séraphin,
O. Duval,
P. Richomme,
J. Bruneton
This paper is made freely available by the publisher.
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Abstract
Abstract The synthesis of benzopyranic simplified analogues of dibenzopyranic natural compounds is described, together with the access to a precursor of a new furobenzopyranic natural product. These natural products have anti-cancer activity. The 1,3-diacetoxy-2-acetyl-4-(3-hydroxy-3-methylbut-1-enyl)benzene synthone is used as a common precursor to these structures.