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Issue 39, 2012
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Iridium catalysed chemoselective alkylation of 2′-aminoacetophenone with primary benzyl type alcohols under microwave conditions

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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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Publication details

The article was received on 13 Feb 2012, accepted on 19 Mar 2012 and first published on 20 Mar 2012


Article type: Communication
DOI: 10.1039/C2CC31055D
Citation: 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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