217089-27-5Relevant articles and documents
Synthesis of enantiomerically pure 3-amino-1,2-diols by reductive amination of racemic 2,3-dialkoxyketones
Hutin, Pierre,Petit, Yves,Larcheveque, Marc
, p. 8277 - 8280 (2007/10/03)
The reductive amination of racemic 2,3-dialkoxyketones by tetrabutylammonium triacetoxyborohydride in the presence of (R) or (S)-α- methylbenzylamine allows the stereocontrolled access to 3-amino-1,2-diols in high enantiomerical purity via a partial dynamic resolution.