Issue 15, 1983

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 802-802

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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