1383476-01-4Relevant academic research and scientific papers
A divergent synthetic strategy based on the regioselective reductive ring-opening of a cyclic 1,2-p-methoxybenzylidene acetal
Geant, Pierre-Yves,Martinez, Jean,Rocard, Lou,Salom-Roig, Xavier J.
, p. 1247 - 1252 (2012/06/04)
(1S)-N,N-Dibenzyl-1-[(4R)-2-(4-methoxyphenyl)-1,3-dioxolan-4-yl]ethanamine is obtained in five steps from an -bromo - (R)-sulfinyl ketone and is used as a common intermediate for the synthesis of the p-methoxybenzyl-protected primary and secondary alcohol
