Issue 83, 2024

Copper-catalyzed (4+3)-cycloaddition of 4-indolylcarbinols with aziridines: stereoselective synthesis of azepinoindoles

Abstract

Copper(I)-catalyzed (4+3)-cycloaddition of 4-indolylcarbinols with aziridines has been accomplished to furnish azepinoindoles. The chirality transfer, substrate scope, functional group tolerance, natural product modification and tandem C–C/C–N bond formation are the important practical features.

Graphical abstract: Copper-catalyzed (4+3)-cycloaddition of 4-indolylcarbinols with aziridines: stereoselective synthesis of azepinoindoles

Supplementary files

Article information

Article type
Communication
Submitted
16 Jul 2024
Accepted
19 Sep 2024
First published
20 Sep 2024

Chem. Commun., 2024,60, 12008-12011

Copper-catalyzed (4+3)-cycloaddition of 4-indolylcarbinols with aziridines: stereoselective synthesis of azepinoindoles

S. Kar, P. K. Maharana, S. Maity, V. Trivedi and T. Punniyamurthy, Chem. Commun., 2024, 60, 12008 DOI: 10.1039/D4CC03544E

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