Issue 92, 2012
From the journal:

Chemical Communications

A versatile and green mechanochemical route for aldehyde–oxime conversions†‡

Christer B. Aakeröy,*a   Abhijeet S. Sinha,a   Kanishka N. Epa,a   Christine L. Spartza  and  John Despera  

* Corresponding authors

a Department of Chemistry, Kansas State University, Manhattan, USA
E-mail: aakeröy@ksu.edu

Abstract

A robust, facile and solvent-free mechanochemical path for aldehyde–oxime transformations using hydroxylamine and NaOH is explored; the method is suitable for aromatic and aliphatic aldehydes decorated with a range of substituents.

Graphical abstract: A versatile and green mechanochemical route for aldehyde–oxime conversions

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C2CC36315A
Article type
Communication
Submitted
30 Aug 2012
Accepted
21 Sep 2012
First published
05 Oct 2012

Chem. Commun., 2012,48, 11289-11291

Permissions

Request permissions

A versatile and green mechanochemical route for aldehyde–oxime conversions

C. B. Aakeröy, A. S. Sinha, K. N. Epa, C. L. Spartz and J. Desper, Chem. Commun., 2012, 48, 11289 DOI: 10.1039/C2CC36315A

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