Issue 11, 1972

The conformation of the NH-groups in piperazines, hexahydropyrimidines, tetrahydro-1,2- and 1,3-oxazine, and tetrahydro-1,3-thiazine

Abstract

I.r. band shapes and electric dipole moments show that the predominant conformers for tetrahydro-1,3-oxazine, tetrahydro-1,3-thiazine, and 1-t-butylhexahydropyrimidine are those with the NH axial; the predominant conformer for tetrahydro-1,2-oxazine is that with NH equatorial as determined by the same methods.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 673-674

The conformation of the NH-groups in piperazines, hexahydropyrimidines, tetrahydro-1,2- and 1,3-oxazine, and tetrahydro-1,3-thiazine

R. A. Y. Jones, A. R. Katritzky, A. C. Richards, S. Saba, A. J. Sparrow and D. L. Trepanier, J. Chem. Soc., Chem. Commun., 1972, 673 DOI: 10.1039/C39720000673

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