Issue 22, 2002
From the journal:

Chemical Communications

Efficient synthesis of 3,4-ethylenedioxythiophenes (EDOT) by Mitsunobu reaction

Dolores Caras-Quinteroa  and  Peter Bäuerle*a  

* Corresponding authors

a Department Organic Chemistry II (Organic Materials and Combinatorial Chemistry), University of Ulm, Albert-Einstein-Allee 11, D-89081, Ulm, Germany
E-mail: peter.baeuerle@chemie.uni-ulm.de
Fax: +49-731-50-22840
Tel: +49-731-50-22250

Abstract

Using the Mitsunobu reaction as a key step, a general and efficient method for the synthesis of EDOT monomers has been developed. Novel substituted EDOTs and the first chiral derivatives were generated in high yields.

Graphical abstract: Efficient synthesis of 3,4-ethylenedioxythiophenes (EDOT) by Mitsunobu reaction

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Article information

DOI
https://doi.org/10.1039/B207640C
Article type
Communication
Submitted
06 Aug 2002
Accepted
30 Sep 2002
First published
16 Oct 2002

Chem. Commun., 2002, 2690-2691

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Efficient synthesis of 3,4-ethylenedioxythiophenes (EDOT) by Mitsunobu reaction

D. Caras-Quintero and P. Bäuerle, Chem. Commun., 2002, 2690 DOI: 10.1039/B207640C

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