Issue 5, 2014

Zinc-mediated addition of diethyl bromomalonate to alkynes for the cascade reaction towards polysubstituted pyranones and tetracarbonyl derivatives

Abstract

The zinc-mediated regioselective addition reactions of diethyl bromomalonate and aromatic and aliphatic alkynes were investigated for the synthesis of vinyl malonates. When the vinyl organo-zinc intermediates were reacted with acid chlorides 2H-pyran-2-ones were obtained while the application of oxalyl chloride and an amine led to tetracarbonyl derivatives in a one-pot multi-step reaction sequence.

Graphical abstract: Zinc-mediated addition of diethyl bromomalonate to alkynes for the cascade reaction towards polysubstituted pyranones and tetracarbonyl derivatives

Supplementary files

Article information

Article type
Communication
Submitted
05 Sep 2013
Accepted
02 Nov 2013
First published
04 Nov 2013

Chem. Commun., 2014,50, 542-544

Zinc-mediated addition of diethyl bromomalonate to alkynes for the cascade reaction towards polysubstituted pyranones and tetracarbonyl derivatives

A. Miersch, K. Harms and G. Hilt, Chem. Commun., 2014, 50, 542 DOI: 10.1039/C3CC46788K

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