Abstract:The efficient conjugate addition of vicinal -OH and -SH acids such as ethylene glycol and 1,2-ethanedithiol to dibenzoylacetylene in the presence of PPh3 leads to different products depending on the reaction conditions. Ab initio calculations at HF/6-31G* level shows that the unsymmetrical envelope conformation of 2,2-disubstituted 1,3-dioxolane 1 is more stable than the half-chair and Cs symmetric envelope forms.
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