首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Highly enantioselective reduction of achiral ketones with NaBH_4/Me_3SiCl catalyzed by (S)-#alpha#,#alpha#-diphenylpyrrolidinemethanol
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Highly enantioselective reduction of achiral ketones with NaBH_4/Me_3SiCl catalyzed by (S)-#alpha#,#alpha#-diphenylpyrrolidinemethanol

机译:(S)-#alpha#,#alpha#-二苯基吡咯烷甲醇催化的NaBH_4 / Me_3SiCl高度手性还原非手性酮

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摘要

The reducing agent prepared from sodium borohydride, trimethylsilyl chloride and a catalytic amount of (S)-#alpha#,#alpha#-diphenylpyrrolidinemethanol has been successfully applied to the enantioselective reduction of ketones. The opticaly active secondary alcohols were obtained in excellent enantiomeric excess and almost quantitative cheical yield.
机译:由硼氢化钠,三甲基甲硅烷基氯和催化量的(S)-#alpha#,#alpha#-二苯基吡咯烷甲醇制备的还原剂已成功用于酮的对映选择性还原。以优异的对映体过量和几乎定量的化学产率获得旋光性仲醇。

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