Borane-Catalyzed Enantioselective α-Alkylation of Unactivated 2-Alkylbenzoxazoles with Electron-Deficient Olefins

Chiral borane-catalyzed reactions have recently emerged as a powerful tool for the enantioselective production of chiral scaffolds. In this study, we demonstrated for the first time that a chiral bisborane catalyst can be used for the α-functionalization of 2-alkylazaarenes; specifically, we accomplished unprecedented highly enantioselective α-alkylation of unactivated 2-alkylbenzoxazoles with electron-deficient olefins. The strong Lewis acidity and the steric bulk of the bisborane catalyst were essential to the observed reactivity and selectivity.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-08-20
DOI
https://doi.org/10.1021/jacs.4c09067
Citations
12
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
3.00

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article

Borane-Catalyzed Enantioselective α-Alkylation of Unactivated 2-Alkylbenzoxazoles with Electron-Deficient Olefins

Chongren Ai, Xiaochen Wang, Lu Liu
12 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
3.00
article

Borane-Catalyzed Enantioselective α-Alkylation of Unactivated 2-Alkylbenzoxazoles with Electron-Deficient Olefins

Chongren Ai, Xiaochen Wang, Lu Liu
article en
12 citations

Abstract

Chiral borane-catalyzed reactions have recently emerged as a powerful tool for the enantioselective production of chiral scaffolds. In this study, we demonstrated for the first time that a chiral bisborane catalyst can be used for the α-functionalization of 2-alkylazaarenes; specifically, we accomplished unprecedented highly enantioselective α-alkylation of unactivated 2-alkylbenzoxazoles with electron-deficient olefins. The strong Lewis acidity and the steric bulk of the bisborane catalyst were essential to the observed reactivity and selectivity.

Journal of the American Chemical SocietyVol. 146(35)
Nankai University (CN)
Tencent, National Natural Science Foundation of China, Nankai University, Natural Science Foundation of Tianjin City, National Key Research and Development Program of China
Openalex Percentile: Top 8%
Organoboron and organosilicon chemistry
3.00
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