A convenient synthesis of phenyl 1-chloro-1 alkenyl chalcogenides by one-pot Wittig reaction. Synthesis of selenolesters

Article abstract of DOI:10.1080/10426500108046648

The preparation of 1-chloro-1-chalcogeno(sulfur, selenium) alkenes by a Wittig-type reaction in an one pot procedure is described. Chlorochalcogenyl triphenylphosphoranes are formed in situ by the reaction of dichloromethyl phenylchalcogenide, potassium t

Full text of DOI:10.1080/10426500108046648

This article was downloaded by: [University of Connecticut]
On: 10 October 2014, At: 21:49
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
Phosphorus, Sulfur, and Silicon
and the Related Elements
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/gpss20
A Convenient Synthesis of
Phenyl 1-Chloro-1 Alkenyl
Chalcogenides by One-Pot
Wittig Reaction. Synthesis of
Selenolesters
Claudio C. Silveira a , Paula Boeck a , Mauro L.
Begnini a & Antonio L. Braga a
a Departamento de Química , UFSM , 97 105-900,
Santa Maria, RS, Brazil
Published online: 04 Oct 2006.
To cite this article: Claudio C. Silveira , Paula Boeck , Mauro L. Begnini & Antonio L.
Braga (2001) A Convenient Synthesis of Phenyl 1-Chloro-1 Alkenyl Chalcogenides by
One-Pot Wittig Reaction. Synthesis of Selenolesters, Phosphorus, Sulfur, and Silicon
and the Related Elements, 172:1, 173-179, DOI: 10.1080/10426500108046648
To link to this article: http://dx.doi.org/10.1080/10426500108046648
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