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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 9, 1979 - Issue 10
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Original Articles

Enolate Alkylations with Vinylphosphonates

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Pages 915-921 | Received 02 Jul 1979, Published online: 06 Dec 2006
 

Abstract

A remarkable feature of diethyl-1,3-butadiene-phosphonate, unlike the dienephosphonium salts,2,3 is that it undergoes a simple Michael addition with enolates of aldehydes and ketones without the loss of the phosphorus group.4 Whether such a difference in reactivity exists between the two-carbon reagents, vinyltriphenylphosphonium bromide 1 5 and diethyl vinylphosphonate 2 6 is the subject of this investigation.

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