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.

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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

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article

Iridium-Catalyzed Enantioselective C4-Alkylation of Indoles with α-Olefins and Styrenes

Ze Song, Kai-yuan Tian, K L Wang, Qi‐Lin Zhou et al.
Journal of the American Chemical Society
Asymmetric Hydrogenation and Catalysis
article

Iridium-Catalyzed Enantioselective C4-Alkylation of Indoles with α-Olefins and Styrenes

Ze Song, Kai-yuan Tian, K L Wang, Qi‐Lin Zhou, Chao Fan, Wen-Yao Wang
article en

Abstract

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.

Journal of the American Chemical Society
Nankai University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 17%
Asymmetric Hydrogenation and Catalysis
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