Issue 14, 2003
From the journal:

Chemical Communications

A novel route to the fluorinated diimines: carbon monoxide-promoted reductive homocoupling of fluorinated imidoyl iodides in the presence of a palladium catalyst†

Hideki Amii,a   Mitsuhiro Kohda,a   Motoharu Seoa  and  Kenji Uneyama*a  

* Corresponding authors

a Department of Applied Chemistry, Faculty of Engineering, Okayama University, Okayama 700-8530, Japan
E-mail: uneyamak@cc.okayama-u.ac.jp
Fax: +81-86-251-8021
Tel: +81-86-251-8075

Abstract

A new catalytic access to the fluorinated diimines which involves palladium(0)-catalyzed reductive dimerization of the imidoyl iodides is presented.

Graphical abstract: A novel route to the fluorinated diimines: carbon monoxide-promoted reductive homocoupling of fluorinated imidoyl iodides in the presence of a palladium catalyst

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Article information

DOI
https://doi.org/10.1039/B303040G
Article type
Communication
Submitted
19 Mar 2003
Accepted
28 May 2003
First published
18 Jun 2003

Chem. Commun., 2003, 1752-1753

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A novel route to the fluorinated diimines: carbon monoxide-promoted reductive homocoupling of fluorinated imidoyl iodides in the presence of a palladium catalyst

H. Amii, M. Kohda, M. Seo and K. Uneyama, Chem. Commun., 2003, 1752 DOI: 10.1039/B303040G

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