Issue 14, 2002
From the journal:

Chemical Communications

Synthesis of epoxides from aldehydes and tosylhydrazone salts catalysed by triphenylarsine: complete trans selectivity for all combinations of coupling partners†

Varinder K. Aggarwal,*a   Mamta Patela  and  John Studleya  

* Corresponding authors

a School of Chemistry, Bristol University, Cantock′s Close, Bristol, UK
E-mail: V.aggarwal@bristol.ac.uk
Fax: (+44) 117-929861
Tel: (+44) 117-99546315

Abstract

Triphenylarsine catalyses the formation of epoxides from carbonyl compounds and tosylhydrazone salts. This convergent synthesis gives complete trans selectivity for all aldehyde and tosylhydrazone salt coupling partners.

Graphical abstract: Synthesis of epoxides from aldehydes and tosylhydrazone salts catalysed by triphenylarsine: complete trans selectivity for all combinations of coupling partners

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B204252E
Article type
Communication
Submitted
03 May 2002
Accepted
27 May 2002
First published
19 Jun 2002

Chem. Commun., 2002, 1514-1515

Permissions

Request permissions

Synthesis of epoxides from aldehydes and tosylhydrazone salts catalysed by triphenylarsine: complete trans selectivity for all combinations of coupling partners

V. K. Aggarwal, M. Patel and J. Studley, Chem. Commun., 2002, 1514 DOI: 10.1039/B204252E

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