A 13C nuclear magnetic resonance study of glycals (1,5-Anhydro-hex-1-enitols)

Abstract
A series of D-allal and D-glucal derivatives were examined by 13C N.M.R. spectroscopy. Assignments of 13C resonances were established by standard chemical shift considerations, lanthanide shift reagent and proton chemical shift correlations. Configuration-induced chemical shift variations are reported between the glucal and allal systems.

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