Showing papers on "Wieland–Miescher ketone published in 1989"
TL;DR: In this paper, the Wieland-Miescher ketone was converted to a 4,4a,5,6,7,8-hexahydro-4aβ-methyl-8-methylene-2(3H)-napthalenone.
13 citations
TL;DR: New efficient methods for stereoselective hydroxymethylation, hydroxylation, and thiophenylation at the C-8 position of the Wieland-Miescher ketone derivatives have been developed by diverse modifications from the Kirk-Petrow reaction.
Abstract: New efficient methods for stereoselective hydroxymethylation, hydroxylation, and thiophenylation at the C-8 position of the Wieland-Miescher ketone derivatives (2__--4__-) have been developed by diverse modifications from the Kirk-Petrow reaction, which involve autoxidation for the hydroxylation.
5 citations