A simplified Wittig synthesis using a solid/liquid transfer process. VIII. Specific behaviour of methyltriphenylphosphorane during condensation with phenolic aldehydes

Article abstract of DOI:10.1080/00397919208019250

Vinylphenols are obtained in a single-step reaction using phenolic aldehydes according to easy operating conditions involving high temperature in the reaction medium. Phenolic compounds are separated by ion-exchange resins.

Full text of DOI:10.1080/00397919208019250

This article was downloaded by: [McGill University Library]
On: 17 November 2014, At: 07:00
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
A Simplified Wittig Synthesis
Using a Solid/Liquid
Transfer Process. VIII -
Specific Behaviour of
Methyltriphenylphosphorane
During Condensation with
Phenolic Aldehydes
N. Bettach a , Y. Le Bigot a , Z. Mouloungui a , M.
Delmas a & A. Gaset a
a Laboratoire de Chimie des Agroressources , Institut
National Polytechnique de Toulouse Ecole Nationale
Supérieure de Chimie , 118 route de Narbonne,
310077, Toulouse Cedex, FRANCE
Published online: 24 Sep 2006.
To cite this article: N. Bettach , Y. Le Bigot , Z. Mouloungui , M. Delmas & A.
Gaset (1992) A Simplified Wittig Synthesis Using a Solid/Liquid Transfer Process.
VIII - Specific Behaviour of Methyltriphenylphosphorane During Condensation
with Phenolic Aldehydes, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 22:4, 513-518, DOI:
10.1080/00397919208019250
To link to this article: http://dx.doi.org/10.1080/00397919208019250

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