Issue 13, 1974

The conformational analysis of saturated heterocycles. Part LXIII. Tetrahydro-1,2-oxazines 2and related acyclic hydroxylamines

Abstract

Infrared intensities show that the proton attached to nitrogen in tetrahydro-1,2-oxazine exists predominantly in the equatorial position. For an N-methyl group, the equatorial position is favoured by ca. 1·9 kcal mol–1, as deduced from electric dipole moments. The conformations of di- and tri-methylhydroxylamines are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1974, 1554-1557

The conformational analysis of saturated heterocycles. Part LXIII. Tetrahydro-1,2-oxazines 2and related acyclic hydroxylamines

R. A. Y. Jones, A. R. Katritzky, S. Saba and A. J. Sparrow, J. Chem. Soc., Perkin Trans. 2, 1974, 1554 DOI: 10.1039/P29740001554

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