Enantiocontrolled Reduction of Prochiral Aromatic Ketones with Borane using Diastereoisomeric Secondary Aminoalcohols as Chiral Catalysts

DOI: 10.1039/c39910001311

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1311 - 1312 (1991)

Update date:2022-08-16

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Authors:

Tanaka, Kazuhiko

Matsui, Junichi

Suzuki, Hitomi

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Article abstract of DOI:10.1039/c39910001311

Exo- and endo-2-hydroxy-3-(1-methyl-2-pyrrolyl)methylaminobornanes were found to be efficient catalysts for enantioselective borane reduction of prochiral aromatic ketones with predictable absolute stereochemistry.

Full text of DOI:10.1039/c39910001311

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