Issue 23, 1998

A significant effect of anion binding ureas on the product ratio in the palladium(II)-catalyzed hydrocarbonylation of alkenes

Abstract

Hydrogen bonding of urea derivatives to the anionic ligands X of (dppp)PdX2 catalysts significantly increases the hydroacylation of cyclopentene relative to the hydroformylation, most probably due to a decreased coordination strength of the anionic ligands.

Article information

Article type
Paper

Chem. Commun., 1998, 2613-2614

A significant effect of anion binding ureas on the product ratio in the palladium(II)-catalyzed hydrocarbonylation of alkenes

J. Scheele, P. Timmerman and D. N. Reinhoudt, Chem. Commun., 1998, 2613 DOI: 10.1039/A806722H

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