Issue 3, 2024

Electrochemical oxidative dehydrogenative annulation of 1-(2-aminophenyl)pyrroles with cleavage of ethers to synthesize pyrrolo[1,2-a]quinoxaline derivatives

Abstract

An array of pyrrolo[1,2-a]quinoxaline derivatives were achieved with moderate to good yields via the electrochemical redox reaction, which includes the functionalization of C(sp3)–H bonds and the construction of C–C and C–N bonds. In this atom economic reaction, THF was used as both a reactant and a solvent, and H2 was the sole by-product.

Graphical abstract: Electrochemical oxidative dehydrogenative annulation of 1-(2-aminophenyl)pyrroles with cleavage of ethers to synthesize pyrrolo[1,2-a]quinoxaline derivatives

Supplementary files

Article information

Article type
Communication
Submitted
16 Nov 2023
Accepted
07 Dec 2023
First published
07 Dec 2023

Org. Biomol. Chem., 2024,22, 472-476

Electrochemical oxidative dehydrogenative annulation of 1-(2-aminophenyl)pyrroles with cleavage of ethers to synthesize pyrrolo[1,2-a]quinoxaline derivatives

F. Sun, M. Miao, W. Li, X. Lan, J. Yu, J. Zhang and Z. An, Org. Biomol. Chem., 2024, 22, 472 DOI: 10.1039/D3OB01867A

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