Journal of the Chemical Society. Chemical communications p. 138 - 139 (1985)
Update date:2022-08-24
Topics:
Soai, Kenso
Yamanoi, Takashi
Hikima, Hitoshi
Oyamada, Hidekazu
Optically active 3-aryl-3-hydroxyesters of high enantiomeric excess (80-92percent e.e.) are obtained by the reduction of 3-aryl-3-oxoesters with lithium borohydride which has been chirally modified with N,N'-dibenzoylcystine and t-butyl alcohol.
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