Issue 94, 2012
From the journal:

Chemical Communications

Efficient synthesis of oxazoles by dirhodium(ii)-catalyzed reactions of styryl diazoacetate with oximes†

Xinfang Xu,ab   Peter Y. Zavalij,a   Wenhao Hub  and  Michael P. Doyle*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland, USA
E-mail: mdoyle3@umd.edu

b Shanghai Engineering Research Center for Molecular Therapeutics and Institute of Drug Discovery and Development, East China Normal University, 3663 Zhongshan Bei Road, Shanghai 200062, China

Abstract

An efficient one-step synthesis of multi-functionalized oxazole derivatives is achieved in high yield by dirhodium(II)-catalyzed reactions of styryl diazoacetate with aryl oximes.

Graphical abstract: Efficient synthesis of oxazoles by dirhodium(ii)-catalyzed reactions of styryl diazoacetate with oximes

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C2CC36537E
Article type
Communication
Submitted
07 Sep 2012
Accepted
11 Oct 2012
First published
12 Oct 2012

Chem. Commun., 2012,48, 11522-11524

Permissions

Request permissions

Efficient synthesis of oxazoles by dirhodium(II)-catalyzed reactions of styryl diazoacetate with oximes

X. Xu, P. Y. Zavalij, W. Hu and M. P. Doyle, Chem. Commun., 2012, 48, 11522 DOI: 10.1039/C2CC36537E

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