Nickel-Catalyzed Enantioselective Hydroboration of Styrenes

Abstract Herein, we established a Ni-catalyzed enantioselective hydroboration process of styrene derivatives using a chiral Box ligand with B2pin2 as the hydroboration reagent. This approach demonstrates the feasibility of stereoselective transmetalation of a benzylic carbon–nickel bond using B2pin2. The sought-after stable borated product can be achieved with elevated regio- and enantioselectivity under mild circumstances.

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Publication Details

Journal
Synlett
Published
2025-05-09
DOI
https://doi.org/10.1055/a-2605-1414
Citations
1
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.54

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article

Nickel-Catalyzed Enantioselective Hydroboration of Styrenes

Y.B. Chen, Chunpeng Yang
1 citations
Synlett
Asymmetric Hydrogenation and Catalysis
0.54
article

Nickel-Catalyzed Enantioselective Hydroboration of Styrenes

Y.B. Chen, Chunpeng Yang
article en
1 citations

Abstract

Abstract Herein, we established a Ni-catalyzed enantioselective hydroboration process of styrene derivatives using a chiral Box ligand with B2pin2 as the hydroboration reagent. This approach demonstrates the feasibility of stereoselective transmetalation of a benzylic carbon–nickel bond using B2pin2. The sought-after stable borated product can be achieved with elevated regio- and enantioselectivity under mild circumstances.

SynlettVol. 36(18)
Zhejiang Sci-Tech University (CN), Tianjin University (CN)
China Postdoctoral Science Foundation, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 36%
Asymmetric Hydrogenation and Catalysis
0.54
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Nickel-Catalyzed Enantioselective Hydroboration of Styrenes — Y.B. Chen, Chunpeng Yang · Synlett (2025) | TGRS Research Map | TGRS