Journal of the Chemical Society. Chemical communications p. 1018 - 1019 (1986)
Update date:2022-08-16
Topics:
Soai, Kenso
Niwa, Seiji
Yamanoi, Takashi
Hikima, Hitoshi
Ishizaki, Miyuki
Optically active 2-aryl substituted oxetanes are synthesised in high enantiomeric excesses (up to 89percent e.e.) via enantioselective reduction of β-halogenoketones with lithium borohydride using (R,R')-N,N'-dibenzoylcystine and t-butyl alcohols as ligands.
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Doi:10.1021/jo01050a043
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