Iridium-Catalyzed Enantioselective C4-Alkylation of Indoles with α-Olefins and Styrenes
Indoles bearing a stereogenic center at the C4 position are key motifs in natural products and pharmaceuticals, yet their catalytic enantioselective synthesis remains a formidable challenge. Herein, we report an iridium-catalyzed enantioselective C4-alkylation of indoles with α-olefins and styrenes. The reaction proceeds with exclusive C4 selectivity and excellent enantioselectivity across a broad range of substrates. The C3 N, N -dibenzylamide directing group and the chiral spiro diphosphite ligand are essential for achieving high regio- and enantioselectivity. Density functional theory calculations elucidate the origins of regio- and enantioselectivity. This method provides a general atom- and step-economical route to chiral C4-alkylated indoles.
Authors
- Ze Song (ORCID: https://orcid.org/0000-0001-7327-7180)
- Kai-yuan Tian
- K L Wang
- Qi‐Lin Zhou (ORCID: https://orcid.org/0000-0002-4700-3765)
- Chao Fan (ORCID: https://orcid.org/0000-0002-6981-7292)
- Wen-Yao Wang
Institutions
- Nankai University (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-07-02
- DOI
- https://doi.org/10.1021/jacs.6c10750
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China