Issue 13, 1986

Asymmetric synthesis of 2-aryl substituted oxetanes by enantioselective reduction of β-halogenoketones using lithium borohydride modified with N,N′-dibenzoylcystine

Abstract

Optically active 2-aryl substituted oxetanes are synthesised in high enantiomeric excesses (up to 89% e.e.)via enantioselective reduction of β-halogenoketones with lithium borohydride using (R,R′)-N,N′-dibenzoylcystine and t-butyl alcohol as ligands.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1018-1019

Asymmetric synthesis of 2-aryl substituted oxetanes by enantioselective reduction of β-halogenoketones using lithium borohydride modified with N,N′-dibenzoylcystine

K. Soai, S. Niwa, T. Yamanoi, H. Hikima and M. Ishizaki, J. Chem. Soc., Chem. Commun., 1986, 1018 DOI: 10.1039/C39860001018

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