(Q56532645)

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Novel electronic effects of remote substituents on the oxazaborolidine-catalyzed enantioselective reduction of ketones

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Novel electronic effects of remote substituents on the oxazaborolidine-catalyzed enantioselective reduction of ketones (English)

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E.J. Corey

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Christopher J. Helal

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2

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December 1995

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Tetrahedron Letters

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36

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page(s)

9153-9156

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issue

50

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cites work

New enantioselective routes to biologically interesting compounds

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Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications

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An efficient and catalytically enantioselective route to (S)-(-)-phenyloxirane

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Robert Robinson Lecture. Retrosynthetic thinking—essentials and examples

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Mechanistic studies of epoxide hydrolase utilizing a continuous spectophotometric assay

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

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The structures of ethylene oxide, cyclopropane, and related molecules

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Microwave Spectra, Dipole Moments, and Torsional Potential Constants ofcis‐ andtrans‐Cyclopropanecarboxaldehyde

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11 October 2022

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

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0040-4039(95)01961-G

A new chiral catalyst for the enantioselective synthesis of secondary alcohols and deuterated primary alcohols by carbonyl reduction

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A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids

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11 October 2022

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10.1016/0040-4039(95)01961-G

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(Q56532645)

Novel electronic effects of remote substituents on the oxazaborolidine-catalyzed enantioselective reduction of ketones

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