Enantioselective evans-tishchenko reduction of β-hydroxyketone catalyzed by lithium binaphtholate

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Abstract

Lithium diphenylbinaphtholate catalyzed the enantioselective Evans-Tishchenko reduction of achiral β-hydroxyketones to afford monoacyl-protected 1,3-diols with high stereoselectivities. In the reaction of racemic β-hydroxyketones, kinetic optical resolution occurred in a highly stereoselective manner. © 2011 by the authors; licensee MDPI, Basel, Switzerland.

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Ichibakase, T., Nakatsu, M., & Nakajima, M. (2011). Enantioselective evans-tishchenko reduction of β-hydroxyketone catalyzed by lithium binaphtholate. Molecules, 16(6), 5008–5019. https://doi.org/10.3390/molecules16065008

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