153667-87-9Relevant academic research and scientific papers
Baker's yeast reduction of prochiral γ-nitroketones: Enantioselective synthesis of (S)-4-nitroalcohols
Guarna, Antonio,Occhiato, Ernesto G.,Spinetti, Laura M.,Vallecchi, Maria E.,Scarpi, Dina
, p. 1775 - 1788 (2007/10/02)
The baker's yeast reduction of seven different prochiral nitroketones 1a-g occurred on the re face of the carbonyl group, thus affording the (S)-nitroalcohols 2a-g, with different level of enantioselectivity (e.e. 15-99%). The best results (e.e. = 99%) we
BAKER'S YEAST REDUCTION OF 2-(2-NITROETHYL)-1-CYCLOALKANONES
Felluga, Fulvia,Nitti, Patrizia,Pitacco, Giuliana,Valentin, Ennio
, p. 443 - 448 (2007/10/02)
Baker's yeast reduction of 2-(2-nitroethyl)-1-cycloalkanones gives (1S,2R)- and (1S,2S)-2-(2-nitroethyl)-1-cycloalkanols in good yield and high enantiomeric excess.
