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
1999-01-01
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.File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
