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Conformational isomers and ring inversion of neolinderalactone, a ten-membered-ring furanosesquiterpene
Journal of the Chemical Society D: Chemical Communications Pub Date : , DOI:10.1039/C29700000957
Abstract

The 1H n.m.r. and c.d. spectra of two conformational isomers of neolinderalactone (I) at various temperatures have been examined to determine their conformations, their Gibbs' free energy difference, and the potential barrier to inversion of the ten-membered ring.

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