Study on the Asymmetric Reduction of Acetophenone in the Presence of Chiral Amino Alcohols

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Study on the Asymmetric Reduction of Acetophenone in the Presence of Chiral Amino Alcohols
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R,2S) 1 Dibutylamino 2 indanol and its enantiomer were synthesized. These chiral amino alcohols were first applied to the asymmetric reduction of acetophenone. Using mild reductant KBH 4, optically active 1 phenylethanol was obtained with en

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Liu Xiang. Study on the Asymmetric Reduction of Acetophenone in the Presence of Chiral Amino Alcohols[J]. Journal of Food Science and Biotechnology,1997,16(3).

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