Nuclear magnetic resonance evidence for stereospecific ground-state interactions between ethylenes and benzene

Abstract
N.m.r. evidence indicates a preferred exo–orientation in liquid mixtures of ethylenes and benzene when the ethylene is an acceptor relative to the benzene, and an endo-orientation when the ethylene is a donor: these orientations match the stereospecificities observed in the corresponding 1,2-photoaddition reactions.

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