About the synthesis of heterocyclic analogues of marginalin and their transformation products

Article abstract of DOI:10.1080/00397919108021591

Pyridine-2 or 4-carboxaldehyde,furan-2-aldehyde, were condensed on 2-coumaranone and on 5-hydroxy 2-coumaranone to give new ene-lactones analogues of the natural marginalin. Only the addition compounds issued from 2-coumaranone could give stilbene methyl esters and no rearrangement into benzo[b]furan carboxylates could be observed. These observations are discussed in relation with previous results in the series.

Full text of DOI:10.1080/00397919108021591

This article was downloaded by: [Duke University Medical Center]
On: 06 October 2014, At: 02:57
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number:
1072954 Registered office: Mortimer House, 37-41 Mortimer Street,
London W1T 3JH, UK
Synthetic Communications:
An International Journal
for Rapid Communication of
Synthetic Organic Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsyc20
About the Synthesis of
Heterocyclic Analogues
of Marginalin and Their
Transformation Products
Michel Barbier a
a Institut de Chimie des Substances Naturelles,
CNRS , Avenue de la Terrasse, 91198, Gif sur
Yvette, Cedex, France
Published online: 23 Sep 2006.
To cite this article: Michel Barbier (1991) About the Synthesis of Heterocyclic
Analogues of Marginalin and Their Transformation Products, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:22, 2317-2327, DOI: 10.1080/00397919108021591
To link to this article: http://dx.doi.org/10.1080/00397919108021591
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all
the information (the “Content”) contained in the publications on our
platform. However, Taylor & Francis, our agents, and our licensors
make no representations or warranties whatsoever as to the accuracy,
completeness, or suitability for any purpose of the Content. Any opinions
and views expressed in this publication are the opinions and views of
the authors, and are not the views of or endorsed by Taylor & Francis.
The accuracy of the Content should not be relied upon and should be

independently verified with primary sources of information. Taylor and
Francis shall not be liable for any losses, actions, claims, proceedings,
demands, costs, expenses, damages, and other liabilities whatsoever
or howsoever caused arising directly or indirectly in connection with, in
relation to or arising out of the use of the Content.
This article may be used for research, teaching, and private study
purposes. Any substantial or systematic reproduction, redistribution,
reselling, loan, sub-licensing, systematic supply, or distribution in any
form to anyone is expressly forbidden. Terms & Conditions of access
and use can be found at http://www.tandfonline.com/page/terms-and-
conditions