A new method for the synthesis of 2,3-dihydrofurans from readily available starting
enones and pyridinium salts has been developed. This protocol can provide a novel
and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective
fashion. To increase the efficiency of this reaction the one-pot process was also
developed, in which the pyridinium salts were generated in situ from corresponding
halides.
pyridinium ylide - 2,3-dihydrofuran - conjugate addition - O-cyclization - one-pot
process