Issue 17, 2024

Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines via rhodium(iii)-catalyzed C–H allylation/intramolecular 1,3-dipolar cycloaddition

Abstract

Herein, we report a new synthetic route to 1,4-epoxy-2-aryltetrahydro-1-benzazepine derivatives with high efficiency, namely the Rh(III)-catalyzed C–H allylation of nitrones with allyl precursors, followed by subsequent intramolecular 1,3-dipolar cycloaddition, to deliver the title compounds. This reaction is regio- and stereo-selective, generating the cis-isomer with a broad substrate scope and good functional group tolerance.

Graphical abstract: Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines via rhodium(iii)-catalyzed C–H allylation/intramolecular 1,3-dipolar cycloaddition

Supplementary files

Article information

Article type
Communication
Submitted
16 Oct 2023
Accepted
18 Jan 2024
First published
25 Jan 2024

Chem. Commun., 2024,60, 2401-2404

Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines via rhodium(III)-catalyzed C–H allylation/intramolecular 1,3-dipolar cycloaddition

X. Wang, J. Li, H. Du, W. Liang, C. Luo, Y. Wu and B. Liu, Chem. Commun., 2024, 60, 2401 DOI: 10.1039/D3CC05082C

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