Nickel-CatalyzedDynamic Kinetic Asymmetric ReductiveArylation of Aldehydes with Heterobiaryl Triflates

In this context, we report a nickel-catalyzed dynamic kinetic asymmetric reductive arylation of aldehydes with racemic heterobiaryl triflates, offering a series of axially chiral heterobiaryls bearing a centrally chiral secondary alcohol moiety in a highly diastereo- and enantioselective manner. The simultaneous control of both axial and central stereogenic elements of the products lies in the stereoselective nucleophilic addition of the configurationally labile hetereobiaryl nickel complex to the formyl group of aldehydes.

Publication Details

Journal
Figshare
Published
2025-03-15
DOI
https://doi.org/10.1021/acs.orglett.5c00441.s001
Primary Topic
Sociology and Education Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Nickel-CatalyzedDynamic Kinetic Asymmetric ReductiveArylation of Aldehydes with Heterobiaryl Triflates

Figshare
Sociology and Education Studies
article

Nickel-CatalyzedDynamic Kinetic Asymmetric ReductiveArylation of Aldehydes with Heterobiaryl Triflates

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Abstract

In this context, we report a nickel-catalyzed dynamic kinetic asymmetric reductive arylation of aldehydes with racemic heterobiaryl triflates, offering a series of axially chiral heterobiaryls bearing a centrally chiral secondary alcohol moiety in a highly diastereo- and enantioselective manner. The simultaneous control of both axial and central stereogenic elements of the products lies in the stereoselective nucleophilic addition of the configurationally labile hetereobiaryl nickel complex to the formyl group of aldehydes.

Figshare
Openalex Percentile: Top 45%
Sociology and Education Studies
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Nickel-CatalyzedDynamic Kinetic Asymmetric ReductiveArylation of Aldehydes with Heterobiaryl Triflates · Figshare (2025) | TGRS Research Map | TGRS