Easy and stereoselective synthesis of cyclopropyl-substituted phosphonates via α-chlorophosphonates
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.
Description
Keywords
Acrylates,
Cyclopropanes,
Diastereomers,
Michael addition,
Phosphonates
Citation
Synthesis