Journal of the Chemical Society. Perkin transactions I p. 900 - 905 (1981)
Update date:2022-08-28
Topics:
Hirao, Akira
Itsuno, Shinichi
Owa, Masaki
Nagami, Satoru
Mochizuki, Hidenori
et al.
Asymmetric reduction of aromatic ketones with the reagents prepared from sodium borohydride and carboxylic acids in the presence of 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose at 0 deg C gives (R)-alcohols with enantiomeric excesses as high as 83percent
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