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Issue 20, 2005
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One pot synthesis of 3,5-alkylated acetophenone and methyl benzoate derivatives via an anionic domino process

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Abstract

The reaction of primary 1,3-dinitroalkanes with 2-ene-1,4-dione or 2-ene-4-oxo ester derivatives in acetonitrile with DBU as base, allow the one pot synthesis of 3,5-alkylated acetophenones and methyl benzoate derivatives respectively via an anionic domino process.

Graphical abstract: One pot synthesis of 3,5-alkylated acetophenone and methyl benzoate derivatives via an anionic domino process

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Publication details

The article was received on 20 Jan 2005, accepted on 30 Mar 2005 and first published on 12 Apr 2005


Article type: Communication
DOI: 10.1039/B500846H
Citation: Chem. Commun., 2005, 2633-2634
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    One pot synthesis of 3,5-alkylated acetophenone and methyl benzoate derivatives via an anionic domino process

    R. Ballini, L. Barboni, D. Fiorini, G. Giarlo and A. Palmieri, Chem. Commun., 2005, 2633
    DOI: 10.1039/B500846H

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