Issue 12, 2021

Synthesis of benzofuro- and benzothieno[2,3-c]pyridines via copper-catalyzed [4 + 2] annulation of ketoxime acetates with acetoacetanilide

Abstract

An efficient copper-catalyzed annulation of ketoxime acetates with acetoacetanilide has been developed. This strategy provides an alternate route towards the synthesis of benzofuro- and benzothieno[2,3-c]pyridines with good functional group tolerance and operational simplicity. Mechanistic investigation indicates that an ionic pathway rather than a radical pathway was involved in the transformation.

Graphical abstract: Synthesis of benzofuro- and benzothieno[2,3-c]pyridines via copper-catalyzed [4 + 2] annulation of ketoxime acetates with acetoacetanilide

Supplementary files

Article information

Article type
Research Article
Submitted
19 Jan 2021
Accepted
28 Mar 2021
First published
31 Mar 2021

Org. Chem. Front., 2021,8, 2939-2943

Synthesis of benzofuro- and benzothieno[2,3-c]pyridines via copper-catalyzed [4 + 2] annulation of ketoxime acetates with acetoacetanilide

B. Rong, G. Xu, H. Yan, S. Zhang, Q. Wu, N. Zhu, Z. Fang, J. Duan and K. Guo, Org. Chem. Front., 2021, 8, 2939 DOI: 10.1039/D1QO00094B

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