Issue 14, 2014
From the journal:

Organic & Biomolecular Chemistry

Metal free oxidative coupling of aryl formamides with alcohols for the synthesis of carbamates†

N. Veera Reddy,a   K. Rajendra Prasad,a   P. Sudhir Reddy,a   M. Lakshmi Kantama  and  K. Rajender Reddy*a  

* Corresponding authors

a Inorganic and Physical Chemistry Division, CSIR–Indian Institute of Chemical Technology, Tarnaka, Hyderabad – 500 607, India
E-mail: rajender@iict.res.in, rajenderkallu@yahoo.com
Fax: (+91) 040-27160921

Abstract

A direct transformation of N-aryl formamides to the corresponding carbamates via the formation of isocyanate intermediates is achieved in good yields using hypervalent iodine as an oxidant.

Graphical abstract: Metal free oxidative coupling of aryl formamides with alcohols for the synthesis of carbamates

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C4OB00066H
Article type
Communication
Submitted
09 Jan 2014
Accepted
13 Feb 2014
First published
13 Feb 2014

Org. Biomol. Chem., 2014,12, 2172-2175

Author version available

Download author version (PDF)

Permissions

Request permissions

Metal free oxidative coupling of aryl formamides with alcohols for the synthesis of carbamates

N. V. Reddy, K. R. Prasad, P. S. Reddy, M. Lakshmi Kantam and K. R. Reddy, Org. Biomol. Chem., 2014, 12, 2172 DOI: 10.1039/C4OB00066H

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