Mechanistic Investigations of Chiral Lithium Binaphtholate Catalysis for Asymmetric Aldol–Tishchenko Reaction of α-Fluoroarylketones

In this study, we analyzed the asymmetric aldol-Tishchenko reaction of α-fluoroarylketones with aldehydes in the presence of chiral lithium binaphtholate, which was readily prepared from a chiral BINOL derivative and lithium <i>tert</i>-butoxide. This tandem reaction afforded enantiomerically enriched 2-fluoro-1,3-diols with three contiguous stereogenic centers in high yield and with high diastereo- and enantioselectivities. Moreover, mechanistic investigations of the lithium binaphtholate-catalyzed enantioselective aldol-Tishchenko reaction were performed based on the kinetic isotope effect and computational analyses.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-11-08
DOI
https://doi.org/10.1021/acs.joc.4c01404
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.21

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article

Mechanistic Investigations of Chiral Lithium Binaphtholate Catalysis for Asymmetric Aldol–Tishchenko Reaction of α-Fluoroarylketones

Shunsuke Kotani, Makoto Nakajima, Sachie Arae, Masaharu Sugiura et al.
1 citations
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.21
article

Mechanistic Investigations of Chiral Lithium Binaphtholate Catalysis for Asymmetric Aldol–Tishchenko Reaction of α-Fluoroarylketones

Shunsuke Kotani, Makoto Nakajima, Sachie Arae, Masaharu Sugiura, Toshifumi Asano
article en
1 citations

Abstract

In this study, we analyzed the asymmetric aldol-Tishchenko reaction of α-fluoroarylketones with aldehydes in the presence of chiral lithium binaphtholate, which was readily prepared from a chiral BINOL derivative and lithium <i>tert</i>-butoxide. This tandem reaction afforded enantiomerically enriched 2-fluoro-1,3-diols with three contiguous stereogenic centers in high yield and with high diastereo- and enantioselectivities. Moreover, mechanistic investigations of the lithium binaphtholate-catalyzed enantioselective aldol-Tishchenko reaction were performed based on the kinetic isotope effect and computational analyses.

The Journal of Organic ChemistryVol. 89(23)
Sojo University (JP), Kumamoto University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 49%
Fluorine in Organic Chemistry
0.21
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