A new
method was developed to synthesize polyfunctionalized dihydrofuran
and tetrahydrofuran derivatives from the three-component [2 + 2 +
1] cycloaddition of the diazoesters with aryl/alkenyl aldehydes and
alkyne/olefin dipolarophiles by using a Ag(I) <i>N</i>-heterocyclic
carbene complex as the catalyst. A carbonyl ylide intermediate was
generated, which undertook an <i>endo</i>-type 1,3-dipolar
cycloaddition to provide the desired dihydro-/tetrahydrofurans in
high regio- and diastereoselectivities by using α-aryl or α-alkenyl
diazoesters.