On a safe and practical method for the preparation of β-keto phosphonates

Article abstract of DOI:10.1080/00397919608004568

Acylations of the magnesium enolate derivatives of trimethyl and triethylphosphonoacetates, using a magnesium chloride-triethylamine system, lead to 2-acetylphosphonoacetates which are decarbalkoxylated to give β-keto phosphonates.

Full text of DOI:10.1080/00397919608004568

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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On A Safe and Practical Method
for The Preparation of β-Keto
Phosphonates1
Bernard Corbel a , Isabelle L'Hostis-Kervella a &
Jean-Pierre Haelters a
a Laboratoire de Chimie Hétéro-Organique, U.F.R.
Sciences , B.P. 809, F-29285, Brest Cedex
Published online: 23 Aug 2006.
To cite this article: Bernard Corbel , Isabelle L'Hostis-Kervella & Jean-Pierre Haelters
(1996) On A Safe and Practical Method for The Preparation of β-Keto Phosphonates1
, Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 26:13, 2561-2568, DOI: 10.1080/00397919608004568
To link to this article: http://dx.doi.org/10.1080/00397919608004568
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