Asymmetric transfer hydrogenation is a process that allows for the selective reduction of a prochiral compound to form an enantiomerically enriched product using a chiral catalyst. It is commonly used in the synthesis of chiral compounds.
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syn-(1R,3S)-4,4,4-trifluoro-1-phenylbutane-1,3 diol
7b-(4-methoxyphenyl)-1a,2,3,7b-tetrahydro-1-oxacyclopropa[a ]naphthalene
C21H31NO2
(2R)-2-[benzyl{(2-((diphenylphosphanyl)oxy)ethyl)}amino]butyldiphenylphosphinite
SRC 676
(1'S)-N-(1'-benzyl-2'-hydroxyethyl)-8-quinolinecarboxamide
1-phenyl-2-(2-(trifluoromethyl)phenyl)ethane-1,2-dione
ethyl 2,2-difluoro-3-oxo-5-phenylpentanoate
Oxirane, [3-nitro-4-(phenylmethoxy)phenyl]-, (2S)-
