Issue 15, 2003
From the journal:

Chemical Communications

A very efficient, copper-free palladiumcatalyst for the Sonogashira reaction with aryl halides

Denise Méry,a   Karine Heuzéa  and  Didier Astruca  

a Groupe Nanosciences Moléculaires et Catalyse, LCOO, UMR N° 5802, Université Bordeaux 1, 351 Cours de la Libération, 33405 Talence Cedex, France

Abstract

The new complex [Pd{t-Bu2PCH2N(CH2Ph)CH2Pt-Bu2}(OAc)2] is a very efficient catalyst for the Sonogashira cross-coupling reaction of aryl halides with acetylenes at room temperature, without co-catalyst.

Graphical abstract: A very efficient, copper-free palladium catalyst for the Sonogashira reaction with aryl halides

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B305391C
Article type
Communication
Submitted
13 May 2003
Accepted
16 Jun 2003
First published
01 Jul 2003

Chem. Commun., 2003, 1934-1935

Permissions

Request permissions

A very efficient, copper-free palladium catalyst for the Sonogashira reaction with aryl halides

D. Méry, K. Heuzé and D. Astruc, Chem. Commun., 2003, 1934 DOI: 10.1039/B305391C

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