Synthesis and Structural Characterization of 1‑(E‑1-Arylpropenon-3-yl)-3,4,6-tri‑O‑benzyl‑d‑glucals and Their Transformation into Pentasubstituted (2R,3S,4R)‑Chromanes via Pd-Catalyzed Cross Dehydrogenative Coupling Reaction

We have developed an efficient methodology for the synthesis of (2R,3S,4R)-2-hydroxymethyl-3,4-dihydroxy-6-aryl-7-aroylchromanes in which the chirality at the C-2, C-3, and C-4 positions is being drawn from C-glucopyranosyl aldehyde, which in turn can be efficiently synthesized from d-glucose. Thus, the synthesis starts with the transformation of sugar aldehyde into 1-(E-1-arylpropenon-3-yl)-3,4,6-tri-O-benzyl-d-glucals using Claisen–Schmidt type condensation reaction with different acetophenones and then to 1,2-disubstituted glucals via Pd­(II)-catalyzed cross dehydrogenative coupling reaction, which in turn has been efficiently converted into (2R,3S,4R)-chromanes via 6π-electrocyclization and in situ dehydrogenative aromatization.