Issue 33, 2009
From the journal:

Chemical Communications

Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazolesvia tandem reactions†‡

Patrick S. Bäuerlein,a   Ismael Arenas Gonzalez,a   Jarno J. M. Weemers,a   Martin Lutz,b   Anthony L. Spek,b   Dieter Vogta  and  Christian Müller*a  

* Corresponding authors

a Schuit Institute of Catalysis, Laboratory for Homogeneous Catalysis, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands
E-mail: c.mueller@tue.nl
Fax: +31 40 2455054
Tel: +31 40 2474679

b Bijvoet Center for Biomolecular Research, Crystal and Structural Chemistry, Utrecht University, 3584 CH Utrecht, The Netherlands

Abstract

8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(β-methallyl)imidazole by a tandem hydroformylation–cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazole derivatives.

Graphical abstract: Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazoles via tandem reactions

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B911612E
Article type
Communication
Submitted
12 ဇွန် 2009
Accepted
07 ဇူ 2009
First published
23 ဇူ 2009

Chem. Commun., 2009, 4944-4946

Permissions

Request permissions

Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazoles via tandem reactions

P. S. Bäuerlein, I. A. Gonzalez, J. J. M. Weemers, M. Lutz, A. L. Spek, D. Vogt and C. Müller, Chem. Commun., 2009, 4944 DOI: 10.1039/B911612E

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