Issue 39, 2012
From the journal:

Chemical Communications

Iridium catalysed chemoselective alkylation of 2′-aminoacetophenone with primary benzyl type alcohols under microwave conditions†

Shailen Bhata  and  Visuvanathar Sridharan*a  

* Corresponding authors

a School of Chemistry, University of Leeds, Leeds, UK
E-mail: v.sridharan@leeds.ac.uk
Tel: +44-(0)113-3436520

Abstract

2′-Aminoacetophenone was chemoselectively alkylated with a range of substituted benzyl, heteroaryl alcohols to afford either the corresponding C- or N- alkylated products in good yield.

Graphical abstract: Iridium catalysed chemoselective alkylation of 2′-aminoacetophenone with primary benzyl type alcohols under microwave conditions

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Article information

DOI
https://doi.org/10.1039/C2CC31055D
Article type
Communication
Submitted
13 Feb 2012
Accepted
19 Mar 2012
First published
20 Mar 2012

Chem. Commun., 2012,48, 4701-4703

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Iridium catalysed chemoselective alkylation of 2′-aminoacetophenone with primary benzyl type alcohols under microwave conditions

S. Bhat and V. Sridharan, Chem. Commun., 2012, 48, 4701 DOI: 10.1039/C2CC31055D

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