Issue 22, 2000
From the journal:

Chemical Communications

Novel synthesis of oxindoles from carbamoyl chlorides via palladium catalysed cyclisation–anion capture

Mark R. Fielding,a   Ronald Grigg*a  and  Christopher J. Urchb  

* Corresponding authors

a Department of Chemistry, University of Leeds, Woodhouse Lane, Leeds, UK
E-mail: R.Grigg@chem.leeds.ac.uk

b Zeneca Agrochemicals, Jealott’s Hill Research Station, Bracknell, UK

Abstract

The synthesis of 3,3-disubstituted and 3-methyleneoxindoles by palladium(0) catalysed cyclisation of carbamoyl chlorides onto proximate alkene or alkyne groups has been achieved in good yields.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B006765M
Article type
Communication
Submitted
17 Aug 2000
Accepted
05 Oct 2000
First published
31 Oct 2000

Chem. Commun., 2000, 2239-2240

Permissions

Request permissions

Novel synthesis of oxindoles from carbamoyl chlorides via palladium catalysed cyclisation–anion capture

M. R. Fielding, R. Grigg and C. J. Urch, Chem. Commun., 2000, 2239 DOI: 10.1039/B006765M

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