Asymmetric Induction. Reduction, Nucleophilic Addition to, and Ene Reactions of Chiral α-Ketoesters

DOI: 10.1039/c39830000802

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 802 (1983)

Update date:2022-08-17

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Authors:

Whitesell, James K.

Deyo, Don

Bhattacharya, Apurba

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Article abstract of DOI:10.1039/c39830000802

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

Full text of DOI:10.1039/c39830000802

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