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Abstract
Room temperature 60 MHz NMR data of α,β-diarylacrylonitriles were interpreted in a search for a method for routine stereochemical assignments and to establish the conformational preferences of the β-heterocyclic ring. The conformation of the α-phenyl group differs from that of diaryl ethylenes previously investigated. Solvent effect on the conformations is observed only for pyrrole derivatives.
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