Easy and stereoselective synthesis of cyclopropyl-substituted phosphonates via α-chlorophosphonates

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Date
2007-05-16
Authors
Kumara Swamy, K. C.
Pavan Kumar, K. V.P.
Rama Suresh, R.
Satish Kumar, N.
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Abstract
A facile stereoselective synthesis of cyclopropylphosphonates from the reaction of inexpensive α-chlorophosphonates with alkyl acrylates in the presence of sodium hydride is reported. Reaction with dimethyl maleate or fumarate also leads to cyclopropyl-substituted phosphonates. These reactions take place via Michael addition of acrylate, dimethyl maleate, or fumarate to the phosphonate carbanion, followed by expulsion of the chloride ion. © Georg Thieme Verlag Stuttgart.
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Keywords
Acrylates, Cyclopropanes, Diastereomers, Michael addition, Phosphonates
Citation
Synthesis