Abstract
A solid-state method was developed for generating diarylisonaphthofurans from 1,3-diaryl-1,3-dihydronaphthofuranols. The generated reactive molecules were stable in the solid state and could be stored without any precaution. Their X-ray diffraction analysis revealed a typical quinoidal structure. Furthermore, the mechanochemical Diels-Alder reaction of 1,3-diarylisonaphthofurans with epoxynaphthalenes afforded synthetically attractive diepoxypentacenes.
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