(Q57405067)

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β-Hydroxysulfoximines in the catalyzed enantioselective reduction of ketones with borane

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β-Hydroxysulfoximines in the catalyzed enantioselective reduction of ketones with borane (English)

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Carsten Bolm

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author name string

Marcel Felder

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2

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publication date

September 1993

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published in

Tetrahedron Letters

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volume

34

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issue

38

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page(s)

6041-6044

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cites work

Asymmetric syntheses with chiral oxazaborolidines

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New enantioselective routes to biologically interesting compounds

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A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses

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7 January 2021

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X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reduction

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An asymmetric synthesis of MK-0417. Observations on oxazaborolidine-catalyzed reductions

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β-Hydroxy sulfoximines as catalysts for the enantioselective alkylation of aldehydes

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A mechanistic insight leads to a greatly improved osmium-catalyzed asymmetric dihydroxylation process

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Structure and electronic nature of the benzaldehyde/boron trifluoride adduct

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Origins of the enantioselectivity observed in oxazaborolidine-catalyzed reductions of ketones

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10.1016/S0040-4039(00)61722-7

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(Q57405067)

β-Hydroxysulfoximines in the catalyzed enantioselective reduction of ketones with borane

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