Issue 44, 2022

Base-promoted [4 + 2] annulation of pyrrole-2-carbaldehyde derivatives with β,γ-unsaturated α-ketoesters: syntheses of 5,6-dihydroindolizines

Abstract

A base-promoted [4 + 2] annulation of pyrrole-2-carbaldehyde derivatives with β,γ-unsaturated α-ketoesters for the syntheses of multisubstituted 5,6-dihydroindolizines was developed. Using DBN as a base, the reaction proceeds smoothly under mild conditions to provide the target products in moderate to high yields, and many useful functional groups can be tolerated.

Graphical abstract: Base-promoted [4 + 2] annulation of pyrrole-2-carbaldehyde derivatives with β,γ-unsaturated α-ketoesters: syntheses of 5,6-dihydroindolizines

Supplementary files

Article information

Article type
Communication
Submitted
18 Oct 2022
Accepted
25 Oct 2022
First published
27 Oct 2022

Org. Biomol. Chem., 2022,20, 8633-8637

Base-promoted [4 + 2] annulation of pyrrole-2-carbaldehyde derivatives with β,γ-unsaturated α-ketoesters: syntheses of 5,6-dihydroindolizines

Y. Zhang, L. Li, A. Ma, W. Wang and J. Peng, Org. Biomol. Chem., 2022, 20, 8633 DOI: 10.1039/D2OB01903E

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