A copy of this work was available on the public web and has been preserved in the Wayback Machine. The capture dates from 2022; you can also visit the original URL.
The file type is
ANGULAR METHYLATION STUDIES ON Δ4(10)-OCTALONE-1
Δ4(10)-Octalone-1(VI) has been obtained by the Birch reduction of 5:6:7:8-tetrahydro-1-naphthyl hydroxyethyl ether (VII:R= CH2CH2OH), followed by mild acid hydrolysis- The ocalone (VI) cannot be methylated in the angular position under the usual conditions. On catalytic hydrogenation in a neutral medium it affords almost quantitatively trans-1-decalone (IX).doi:10.5281/zenodo.6535922 fatcat:hvttrt2gcnblrpelqouerhhpvy