Issue 12, 1986

Conformation and stereodynamics of the oxepine ring system

Abstract

Low temperature n.m.r. studies on 2-cyano- and 2-ethoxycarbonyl-7-ethyloxepine establish a non-planar ring geometry with a ring inversion barrier of 6.5 kcal mol–1(27.2 kJ mol–1), and provide evidence of a rotational isomerism involving the 2-ethoxycarbonyl substituent; an X-ray crystallographic analysis of 2-t-butoxycarbonyloxepine confirms the non-planar boat geometry.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 970-972

Conformation and stereodynamics of the oxepine ring system

W. B. Jennings, M. Rutherford, S. K. Agarwal, D. R. Boyd, J. F. Malone and D. A. Kennedy, J. Chem. Soc., Chem. Commun., 1986, 970 DOI: 10.1039/C39860000970

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