Issue 4, 2012
From the journal:

Organic & Biomolecular Chemistry

N-Heterocyclic carbene catalysed aerobic oxidation of aromatic aldehydes to aryl esters using boronic acids†

Panjab Arde,a   B. T. Ramanjaneyulu,a   Virsinha Reddy,a   Apurv Saxenaa  and  R. Vijaya Anand*a  

* Corresponding authors

a Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, SAS Nagar, Manuali, Punjab, India
E-mail: rvijayan@iisermohali.ac.in
Fax: +91-172-2240266

Abstract

The organocatalytic behavior of N-heterocyclic carbenes in the aerobic oxidation of aromatic aldehydes to esters with boronic acids has been explored. This transition metal-free protocol allows access to a wide variety of aromatic esters in good to excellent yields under mild reaction conditions.

Graphical abstract: N-Heterocyclic carbene catalysed aerobic oxidation of aromatic aldehydes to aryl esters using boronic acids

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1OB06566A
Article type
Paper
Submitted
13 Sep 2011
Accepted
19 Oct 2011
First published
01 Dec 2011

Org. Biomol. Chem., 2012,10, 848-851

Permissions

Request permissions

N-Heterocyclic carbene catalysed aerobic oxidation of aromatic aldehydes to aryl esters using boronic acids

P. Arde, B. T. Ramanjaneyulu, V. Reddy, A. Saxena and R. V. Anand, Org. Biomol. Chem., 2012, 10, 848 DOI: 10.1039/C1OB06566A

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