he enantio- or diastereoselective oxidation of readily available (methylthio)methylphosphonates produces optically active (methylsulfinyl)methylphosphonates which can be used as direct precursors of chiral nonracemic methyl sulfoxides in a substitution reaction involving a carbanionic leaving group.

Enantio- or diastereoselective oxidation of (methylthio)methylphosphonates as a route to precursor of chiral sulfoxides

FRACCHIOLLA, GIUSEPPE;TORTORELLA, Paolo
1999

Abstract

he enantio- or diastereoselective oxidation of readily available (methylthio)methylphosphonates produces optically active (methylsulfinyl)methylphosphonates which can be used as direct precursors of chiral nonracemic methyl sulfoxides in a substitution reaction involving a carbanionic leaving group.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11586/132838
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