Issue 14, 1976

Nuclear magnetic resonance non-equivalence of the enantiomers in optically active samples of phosphinic amides

Abstract

The 1H n.m.r. spectra of optically active (but optically impure) samples of methylphenylphosphinic amide (3) and its N-phenyl (1) and N-p-nitrophenyl (2) analogues exhibit distinct signals for the P-methyl groups in the (R) and (S) enantiomers.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 555-556

Nuclear magnetic resonance non-equivalence of the enantiomers in optically active samples of phosphinic amides

M. J. P. Harger, J. Chem. Soc., Chem. Commun., 1976, 555 DOI: 10.1039/C39760000555

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