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Issue 15, 1983
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Asymmetric induction. Reduction, nucleophilic addition to, and ene reactions of chiral α-ketoesters

Abstract

Ketoesters of 8-phenylmenthol undergo reduction with potassium tri-isopropoxyborohydride, addition of Grignard reagents, and ene reactions with asymmetric induction levels of 90% and above.

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Article type: Paper
DOI: 10.1039/C39830000802
Citation: J. Chem. Soc., Chem. Commun., 1983, 802-802
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    Asymmetric induction. Reduction, nucleophilic addition to, and ene reactions of chiral α-ketoesters

    J. K. Whitesell, D. Deyo and A. Bhattacharya, J. Chem. Soc., Chem. Commun., 1983, 802
    DOI: 10.1039/C39830000802

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