762266-65-9Relevant academic research and scientific papers
Enantioselective [1,2]-Stevens rearrangement using sugar-derived alkoxides as chiral promoters
Tomooka, Katsuhiko,Sakamaki, Junichiro,Harada, Manabu,Wada, Ryoji
, p. 683 - 686 (2008/12/20)
The first example of enantioselective base-induced [1,2]-Stevens rearrangement was achieved by using the newly developed D-glucose-derived lithium alkoxide as a chiral promoter. This rearrangement provides an α-amino ketone having a pseudoquaternary chira
