Issue 6, 1994

Stereoselective phosphonylation of aldehydes via chiral phosphordiamaidites. A potentially versatile asymmetric route to organophosphorus biomolecules

Abstract

The novel, chiral phosphordiamidite, {N,O-(1R,2S)-MeNCHMeCHPhO}PN(SiMe3)2 containing deprotonated ephidrine has been shown to phosphonylate aldehydes readily to afford α-functionalised phosphonate esters with diasteroselectivities upto ca. 96%.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 743-744

Stereoselective phosphonylation of aldehydes via chiral phosphordiamaidites. A potentially versatile asymmetric route to organophosphorus biomolecules

V. Sum, T. P. Kee and M. Thornton-Pett, J. Chem. Soc., Chem. Commun., 1994, 743 DOI: 10.1039/C39940000743

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