Issue 1, 2001
From the journal:

Chemical Communications

Pd-catalysed arylation of propan-1-ol and derivatives: oxidative role of the arylating agent

Laurence Bagnell,a   Ulf Krehera  and  Christopher R. Strauss*a  

* Corresponding authors

a CSIRO Molecular Science, Private Bag 10, Clayton South, Victoria 3169, Australia.
E-mail: chris.strauss@molsci.csiro.au

Abstract

With excess PhI under Pd catalysis, 1-PrOH was converted to a mixture of 3,3-diphenylpropenal and trans-2,3-diphenylpropenal by a concerted, oxidative sequence that involved two arylative couplings and an olefinic aldehyde that was generated in situ.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B005323F
Article type
Communication
Submitted
03 Jul 2000
Accepted
15 Nov 2000
First published
18 Dec 2000

Chem. Commun., 2001, 29-30

Permissions

Request permissions

Pd-catalysed arylation of propan-1-ol and derivatives: oxidative role of the arylating agent

L. Bagnell, U. Kreher and C. R. Strauss, Chem. Commun., 2001, 29 DOI: 10.1039/B005323F

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