79435-27-1Relevant academic research and scientific papers
ASYMMETRIC REDUCTION OF KETONES USING LiAlH4 MODIFIED WITH CHIRAL 1,2-AMINODIOLS
Morrison, James D.,Grandbois, Edward R.,Howard, Sachiko I.,Weisman, Gary R.
, p. 2619 - 2622 (1981)
Four chiral aminodiols from ring opening of (S)-propylene oxide and ethylene oxide with n-butylamine and (R) or (S)-α-methylbenzylamine were used to modify LiAlH4.Asymmetric reduction of acetophenone and propiophenone gave the highest percent enantiomeric
Catalysis of oxo transfer to prochiral sulfides by oxovanadium(v) compounds that model the active center of haloperoxidases
Santoni, Gabriella,Licini, Giulia,Rehder, Dieter
, p. 4700 - 4708 (2007/10/03)
The catalytic properties of a new class of chiral vanadium compounds-[(S,S,S)-VO(OMe)L1] (5), [(S,S)-VO(OMe)L2] (6), [(S,S)-VO(OMe)L3] (7), and [(R,R,R)-VO(OMe)L4] (8), as well as the system VO(OiPr)3/ (R,R,R)-H2L4 [H 2L1=
