Showing papers on "Wieland–Miescher ketone published in 1993"

TL;DR: The selective protection of the S-(+)-enantiomer of the Wieland Miescher ketone as the tert-butyldimethylsilyl-protected cyanohydrin 7 and the oxidative cleavage of an α-ketol 8 that was derived from 7 provided a model 10 for the A ring of the taxol.