Synthesis of a BINOL‐Derived Sulfide Catalyst Bearing a Diphenylmethanol Unit and Its Application in Asymmetric Bromolactonizations

Abstract A BINOL‐derived sulfide catalyst bearing a diphenylmethanol unit was prepared. The catalytic ability of the chiral sulfide with a diphenylmethanol unit was investigated in the desymmetrizing bromolactonization for the asymmetric synthesis of functionalized chiral γ‐butyrolactones. Excellent catalytic performance was observed in the catalytic desymmetrizing bromolactonization. Furthermore, the role of each functional group in the BINOL‐derived sulfide catalyst was clarified in this study.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-05-28
DOI
https://doi.org/10.1002/ajoc.202500249
Primary Topic
Vanadium and Halogenation Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of a BINOL‐Derived Sulfide Catalyst Bearing a Diphenylmethanol Unit and Its Application in Asymmetric Bromolactonizations

Yasuaki Furuya, Seiji Shirakawa, Ryuichi Nishiyori
Asian Journal of Organic Chemistry
Vanadium and Halogenation Chemistry
article

Synthesis of a BINOL‐Derived Sulfide Catalyst Bearing a Diphenylmethanol Unit and Its Application in Asymmetric Bromolactonizations

Yasuaki Furuya, Seiji Shirakawa, Ryuichi Nishiyori
article en

Abstract

Abstract A BINOL‐derived sulfide catalyst bearing a diphenylmethanol unit was prepared. The catalytic ability of the chiral sulfide with a diphenylmethanol unit was investigated in the desymmetrizing bromolactonization for the asymmetric synthesis of functionalized chiral γ‐butyrolactones. Excellent catalytic performance was observed in the catalytic desymmetrizing bromolactonization. Furthermore, the role of each functional group in the BINOL‐derived sulfide catalyst was clarified in this study.

Asian Journal of Organic ChemistryVol. 14(8)
Zero to Three (US), Nagasaki University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 90%
Vanadium and Halogenation Chemistry
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