Issue 7, 2024

Enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols: access to polycyclic indolo[2,1-b]quinazoline derivatives

Abstract

A highly enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols with chiral phosphoric acid as a catalyst has been established. This method allows access to a series of optically pure dihydronaphthofuran-fused indolo[2,1-b]quinazoline derivatives with excellent yields and enantioselectivities (up to 99% yield and 99% ee). Moreover, the initial biological evaluation of the products in cell-based assays demonstrated their potential antitumor activity against leukemia cells.

Graphical abstract: Enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols: access to polycyclic indolo[2,1-b]quinazoline derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
26 Dec 2023
Accepted
05 Feb 2024
First published
06 Feb 2024

Org. Chem. Front., 2024,11, 2002-2007

Enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols: access to polycyclic indolo[2,1-b]quinazoline derivatives

Y. You, G. Gan, Q. Li, X. Liu, Y. Zhang, Z. Wang, J. Zhao and W. Yuan, Org. Chem. Front., 2024, 11, 2002 DOI: 10.1039/D3QO02125D

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