Issue 23, 2005
From the journal:

Chemical Communications

The synthesis of head-to-tail (H–T) dimers of 3-substituted thiophenes by the hypervalent iodine(iii)-induced oxidative biaryl coupling reaction

Toshifumi Dohi,a   Koji Morimoto,a   Yorito Kiyono,a   Akinobu Maruyama,a   Hirofumi Tohmaa  and  Yasuyuki Kita*a  

* Corresponding authors

a Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-oka, Suita, Osaka, Japan
E-mail: kita@phs.osaka-u.ac.jp
Fax: +81-6-6879-8229
Tel: +81-6-6879-8225

Abstract

The head-to-tail (H–T) dimers could be obtained selectively by the oxidative coupling reaction of 3-substituted thiophenes using a combination of hypervalent iodine(III) reagents and trimethylsilyl trifluoromethanesulfonate.

Graphical abstract: The synthesis of head-to-tail (H–T) dimers of 3-substituted thiophenes by the hypervalent iodine(iii)-induced oxidative biaryl coupling reaction

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B503058G
Article type
Communication
Submitted
03 Mar 2005
Accepted
13 Apr 2005
First published
29 Apr 2005

Chem. Commun., 2005, 2930-2932

Permissions

Request permissions

The synthesis of head-to-tail (H–T) dimers of 3-substituted thiophenes by the hypervalent iodine(III)-induced oxidative biaryl coupling reaction

T. Dohi, K. Morimoto, Y. Kiyono, A. Maruyama, H. Tohma and Y. Kita, Chem. Commun., 2005, 2930 DOI: 10.1039/B503058G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements