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Issue 10, 1994
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(E/Z) stereoisomer assignment by 13C NMR in trifunctional phosphonate α-oximes and α-arylhdrazones

Abstract

13 NMR 1JPC coupling constants have predictive value in determining (E)vs.(Z) isomerism in oxophosphonoacetate α-oximes and α-hydrazones, and in distinguishing syn from anti phosphorus atoms in carbonyldiphosphonate α-hydrazones.

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Article information


J. Chem. Soc., Chem. Commun., 1994, 1211-1212
Article type
Paper

(E/Z) stereoisomer assignment by 13C NMR in trifunctional phosphonate α-oximes and α-arylhdrazones

C. E. McKenna, B. A. Kashemirov and J. Ju, J. Chem. Soc., Chem. Commun., 1994, 1211
DOI: 10.1039/C39940001211

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