The C-glycosyl heterocycles join their interest as potential antiviral
and antibacterial agents to their nature as C-glycoside precursors th
rough different heterocycle transformations. With respect to C-glycosy
lfurans, the reaction of sugar condensation with furan, produces bette
r results when it is carried out with Dziewszek's method than with Suz
uki's one (n-BuLi in THF) and yields higher quantities of the isomer h
aving the same configuration at the new asymmetric center than that of
the nearest chiral carbon atom.