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.
Authors
- Chongren Ai
- Xiaochen Wang (ORCID: https://orcid.org/0000-0001-5863-0804)
- Lu Liu (ORCID: https://orcid.org/0000-0001-7712-1765)
Institutions
- Nankai University (CN)
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
Funders
- Tencent
- National Natural Science Foundation of China
- Nankai University
- Natural Science Foundation of Tianjin City
- National Key Research and Development Program of China