Issue 24, 2008

Facile intramolecular C(sp3)–H bond activation with PdII

Abstract

The treatment of bis(4-tert-butylthiazolyl)isoindoline (4-tBuBTI) with palladium acetate results in the exclusive formation of an organometallic PdII compound with C–H activated t-butyl group and a hemilabile S-coordinated thiazole donor in cis-position.

Graphical abstract: Facile intramolecular C(sp3)–H bond activation with PdII

Supplementary files

Article information

Article type
Communication
Submitted
07 Feb 2008
Accepted
06 Mar 2008
First published
08 Apr 2008

Chem. Commun., 2008, 2777-2778

Facile intramolecular C(sp3)–H bond activation with PdII

M. Bröring and C. Kleeberg, Chem. Commun., 2008, 2777 DOI: 10.1039/B802185F

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