Issue 20, 2024

K2CO3-mediated annulation of 1,3-acetonedicarboxylates with 2-fluoro-1-nitroarenes: synthesis of indoles

Abstract

The K2CO3-mediated one-pot reaction of 1,3-acetonedicarboxylates with 2 equiv. of substituted 2-fluoro-1-nitrobenzenes has been developed to synthesize various 2,3-dicarboxylate indoles via a tandem annulation pathway. In the effective reaction, one carbon–carbon double bond, one carbon–carbon single bond and one carbon–nitrogen single bond are formed under open-vessel conditions. DFT calculations are used to rationalize the plausible mechanisms.

Graphical abstract: K2CO3-mediated annulation of 1,3-acetonedicarboxylates with 2-fluoro-1-nitroarenes: synthesis of indoles

Supplementary files

Article information

Article type
Paper
Submitted
25 Mar 2024
Accepted
22 Apr 2024
First published
23 Apr 2024

Org. Biomol. Chem., 2024,22, 4108-4122

K2CO3-mediated annulation of 1,3-acetonedicarboxylates with 2-fluoro-1-nitroarenes: synthesis of indoles

M. Chang, C. Ho and H. Chen, Org. Biomol. Chem., 2024, 22, 4108 DOI: 10.1039/D4OB00488D

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