Synthesizing Chiral Vicinal Bisphosphine Derivatives through Hydrophosphinylation and Asymmetric Protonation of Secondary Phosphine Sulfides with Vinylphosphine Oxides

Herein, we report bifunctional iminophosphorane-catalyzed hydrophosphinylation and asymmetric protonation of secondary phosphine sulfides with vinylphosphine oxides. This reaction efficiently afforded chiral vicinal bisphosphine derivatives in high yields with excellent enantioselectivities (up to 99% yield and 95% ee). Furthermore, the produced chiral vicinal bisphosphine derivatives could be readily transformed into vicinal bisphosphines and vicinal bisphosphine monosulfides. This study presents the first methodology for using secondary phosphine sulfides as pronucleophiles in asymmetric protonation reactions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-01
DOI
https://doi.org/10.1021/acs.joc.5c00414
Citations
5
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
2.69

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article

Synthesizing Chiral Vicinal Bisphosphine Derivatives through Hydrophosphinylation and Asymmetric Protonation of Secondary Phosphine Sulfides with Vinylphosphine Oxides

E. Hirota, Kosuke Nakashima, Tsuyoshi Miura, Shin‐ichi Hirashima et al.
5 citations
The Journal of Organic Chemistry
Asymmetric Hydrogenation and Catalysis
2.69
article

Synthesizing Chiral Vicinal Bisphosphine Derivatives through Hydrophosphinylation and Asymmetric Protonation of Secondary Phosphine Sulfides with Vinylphosphine Oxides

E. Hirota, Kosuke Nakashima, Tsuyoshi Miura, Shin‐ichi Hirashima, Yasuyuki Matsushima, Akira Suzuki, Chika Tadasue
article en
5 citations

Abstract

Herein, we report bifunctional iminophosphorane-catalyzed hydrophosphinylation and asymmetric protonation of secondary phosphine sulfides with vinylphosphine oxides. This reaction efficiently afforded chiral vicinal bisphosphine derivatives in high yields with excellent enantioselectivities (up to 99% yield and 95% ee). Furthermore, the produced chiral vicinal bisphosphine derivatives could be readily transformed into vicinal bisphosphines and vicinal bisphosphine monosulfides. This study presents the first methodology for using secondary phosphine sulfides as pronucleophiles in asymmetric protonation reactions.

The Journal of Organic ChemistryVol. 90(14)
Tokyo University of Pharmacy and Life Sciences (JP)
Japan Society for the Promotion of Science
Clean water and sanitation
Openalex Percentile: Top 10%
Asymmetric Hydrogenation and Catalysis
2.69
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