Issue 12, 2015
From the journal:

Catalysis Science & Technology

Nucleophile-mediated oxa-Michael addition reactions of divinyl sulfone – a thiol-free option for step-growth polymerisations†

Simone Strassera  and  Christian Slugovc*a  

* Corresponding authors

a Institute for Chemistry and Technology of Materials, Graz University of Technology, NAWI Graz, Stremayrgasse 9, A-8010 Graz, Austria
E-mail: slugovc@tugraz.at

Abstract

Triphenylphosphine and 4-dimethylaminopyridine promote the oxa-Michael addition reaction of alcohols and divinyl sulfone. Under solvent-free conditions, the reaction is particularly fast and allows for the preparation of polymers.

Graphical abstract: Nucleophile-mediated oxa-Michael addition reactions of divinyl sulfone – a thiol-free option for step-growth polymerisations

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C5CY01527H
Article type
Communication
Submitted
10 Sep 2015
Accepted
29 Sep 2015
First published
08 Oct 2015
This article is Open Access
Creative Commons BY license

Catal. Sci. Technol., 2015,5, 5091-5094

Permissions

Request permissions

Nucleophile-mediated oxa-Michael addition reactions of divinyl sulfone – a thiol-free option for step-growth polymerisations

S. Strasser and C. Slugovc, Catal. Sci. Technol., 2015, 5, 5091 DOI: 10.1039/C5CY01527H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements