Issue 17, 1975

Stereospecific synthesis from carbohydrate precurors of (R)- and (S)-ethyl isopropyl methyl phosphate and other optically active neutral phosphorus esters

Abstract

Stereospecific syntheses starting from carbo-hydrate precursors of (+)-(R) and (–)-(S)-ethyl iso-propyl methyl phosphates, (+)-(R)-O-ethyl O,S-dimethyl phosphorothioate, and (+)-(R)-ethyl methyl methyl-phosphonate are described; the enantiomeric purity of these compounds was determined by an n.m.r. method involving the use of tris-[3-(heptafluoro-n-propylhydroxy-methylene)-(+)-camphorato]europium(III).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 720-721

Stereospecific synthesis from carbohydrate precurors of (R)- and (S)-ethyl isopropyl methyl phosphate and other optically active neutral phosphorus esters

C. R. Hall, T. D. Inch, G. J. Lewis and R. A. Chittenden, J. Chem. Soc., Chem. Commun., 1975, 720 DOI: 10.1039/C39750000720

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