Asymmetric C3-allenylation of carbazoles with α-indolyl propargylic alcohols

Abstract

A chiral phosphoric acid-catalyzed asymmetric mono- and double-allenylation of carbazoles with α-indolyl propargylic alcohols was realized. This highly efficient protocol produces diverse chiral tetrasubstituted allenes in excellent yields with remarkable chemo-, regio- and enantioselectivities under mild conditions. The practicality of this efficient method is further demonstrated by the good anticancer activities of the obtained chiral allenylationalized carbazole derivatives.

Graphical abstract: Asymmetric C3-allenylation of carbazoles with α-indolyl propargylic alcohols

Supplementary files

Article information

Article type
Research Article
Submitted
15 Dec 2025
Accepted
11 Feb 2026
First published
17 Feb 2026

Org. Chem. Front., 2026, Advance Article

Asymmetric C3-allenylation of carbazoles with α-indolyl propargylic alcohols

X. Deng, Y. Li, Z. Xie, W. Zhu, Y. Liu, G. Lu and J. Weng, Org. Chem. Front., 2026, Advance Article , DOI: 10.1039/D5QO01692D

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