The conformational equilibrium of the title compound has been determined by correlating its n.m.r. parameters with those of its 2,2,6,6-tetradeuterio derivative and trans- and cis-2-tert-butyl-4,5-epoxytetrahydropyran. The high preference (ΔG ∼ -0.8 kcal/mol) for the half-chair conformation in which the pyranoid oxygen is furthest from the oxirane oxygen atom can be interpreted in terms of electrostatic interactions between the two oxygen atoms.

CONFORMATIONAL-ANALYSIS OF 3,4-EPOXYTETRAHYDROPYRAN BY NMR-SPECTROSCOPY

CATELANI, GIORGIO;
1981

Abstract

The conformational equilibrium of the title compound has been determined by correlating its n.m.r. parameters with those of its 2,2,6,6-tetradeuterio derivative and trans- and cis-2-tert-butyl-4,5-epoxytetrahydropyran. The high preference (ΔG ∼ -0.8 kcal/mol) for the half-chair conformation in which the pyranoid oxygen is furthest from the oxirane oxygen atom can be interpreted in terms of electrostatic interactions between the two oxygen atoms.
Catelani, Giorgio; Monti, L; Tognetti, P.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11568/6307
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