Issue 29, 2024

Au(i)/Sc(iii)-co-catalyzed tandem spiroannulation/cycloisomerization of 3-(2-ethynylaryl)-N-tosylaziridines with indoles to access 5H-benzo[b]carbazoles

Abstract

An unusual spiroannulation/cycloisomerization cascade of 3-(2-ethynylaryl)-N-tosylaziridines with indoles enabled by cooperative gold/scandium catalysis is presented, which facilitates the synthesis of 5H-benzo[b]carbazoles in moderate to excellent yields. This protocol features a broad substrate scope and good functional-group compatibility. Additionally, the resulting 5H-benzo[b]carbazoles exhibit good fluorescence properties, demonstrating the synthetic practicality of this method. Moreover, control experiments were performed to illustrate the reaction mechanism.

Graphical abstract: Au(i)/Sc(iii)-co-catalyzed tandem spiroannulation/cycloisomerization of 3-(2-ethynylaryl)-N-tosylaziridines with indoles to access 5H-benzo[b]carbazoles

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Article information

Article type
Paper
Submitted
14 May 2024
Accepted
02 Jul 2024
First published
12 Jul 2024

Org. Biomol. Chem., 2024,22, 5999-6003

Au(I)/Sc(III)-co-catalyzed tandem spiroannulation/cycloisomerization of 3-(2-ethynylaryl)-N-tosylaziridines with indoles to access 5H-benzo[b]carbazoles

W. Wang, L. Zheng, W. Liang, X. Fu, Y. Zhang, R. Meng, H. Zhang, C. Lin, W. Su and J. Xiao, Org. Biomol. Chem., 2024, 22, 5999 DOI: 10.1039/D4OB00782D

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