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Practical and efficient procedure for the in situ preparation of B-alkoxyoxazaborolidines. Enantioselective reduction of prochiral ketones

Molecules (2000) 5(3) 495-496
DOI: 10.3390/50300495
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Abstract

A new method for the in situ elaboration of B-alkoxyoxazaborolidines is presented. Their use in the enantioselective reduction of prochiral aromatic ketones provides excellent chemical and optical yields of chiral alcohols.

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APA

Ponzo, V. L., & Kaufman, T. S. (2000). Practical and efficient procedure for the in situ preparation of B-alkoxyoxazaborolidines. Enantioselective reduction of prochiral ketones. In Molecules (Vol. 5, pp. 495–496). Molecular Diversity Preservation International. https://doi.org/10.3390/50300495

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