Stereoinvertive Cross-Coupling for Trisubstituted Alkenes Enabled by the Sulfoximine Leaving Group

Although stereodivergent synthesis of alkenes is highly valuable in organic synthesis, its scope has been largely confined to disubstituted alkenes, and extension to multisubstituted alkenes remains a formidable challenge. Herein, we report a stereoinvertive cross-coupling enabled by alkenyl sulfoximines with aryl boronic acid in the presence of nickel catalysis, in stark contrast to typical cross-coupling reactions of alkenyl (pseudo)halides, which proceed with retention of stereochemistry of substrates. Given that our previously developed Pd-catalyzed Suzuki–Miyaura cross-coupling of alkenyl sulfoximines proceeds in a stereoretentive fashion, this Ni-catalyzed protocol paves the way for the stereodivergent synthesis of trisubstituted alkenes from a common precursor. Combined experimental and computational studies reveal that the sulfoximine group plays a pivotal role in achieving the stereoinvertive transformation with its coordinating ability.

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Publication Details

Journal
ACS Catalysis
Published
2026-05-19
DOI
https://doi.org/10.1021/acscatal.6c02296
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Stereoinvertive Cross-Coupling for Trisubstituted Alkenes Enabled by the Sulfoximine Leaving Group

ACS Catalysis
Catalytic C–H Functionalization Methods
article

Stereoinvertive Cross-Coupling for Trisubstituted Alkenes Enabled by the Sulfoximine Leaving Group

article en

Abstract

Although stereodivergent synthesis of alkenes is highly valuable in organic synthesis, its scope has been largely confined to disubstituted alkenes, and extension to multisubstituted alkenes remains a formidable challenge. Herein, we report a stereoinvertive cross-coupling enabled by alkenyl sulfoximines with aryl boronic acid in the presence of nickel catalysis, in stark contrast to typical cross-coupling reactions of alkenyl (pseudo)halides, which proceed with retention of stereochemistry of substrates. Given that our previously developed Pd-catalyzed Suzuki–Miyaura cross-coupling of alkenyl sulfoximines proceeds in a stereoretentive fashion, this Ni-catalyzed protocol paves the way for the stereodivergent synthesis of trisubstituted alkenes from a common precursor. Combined experimental and computational studies reveal that the sulfoximine group plays a pivotal role in achieving the stereoinvertive transformation with its coordinating ability.

ACS Catalysis
Okayama University (JP), Innovative Medicines Initiative (BE), Institute for Schools of the Future (US), Graduate School USA (US)
Japan Society for the Promotion of Science
Openalex Percentile: Top 9%
Catalytic C–H Functionalization Methods
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