Issue 20, 2005

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

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

Article information

Article type
Communication
Submitted
20 Jan 2005
Accepted
30 Mar 2005
First published
12 Apr 2005

Chem. Commun., 2005, 2633-2634

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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