Issue 41, 2022, Issue in Progress

Divergent copper-catalyzed syntheses of 3-carboxylpyrroles and 3-cyanofurans from O-acetyl oximes and β-ketoesters/nitriles

Abstract

The reaction between O-acetyl oximes and β-ketoesters/nitriles catalyzed by copper generated polysubstituted pyrroles and furans, respectively, under redox–neutral reaction conditions. Using this protocol, pyrroles or furans could be obtained simply by choosing an appropriate active methylene compound. Although both transformations occur essentially under the same reaction conditions, control experiments indicated that they follow different mechanistic pathways.

Graphical abstract: Divergent copper-catalyzed syntheses of 3-carboxylpyrroles and 3-cyanofurans from O-acetyl oximes and β-ketoesters/nitriles

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2022
Accepted
13 Sep 2022
First published
21 Sep 2022
This article is Open Access
Creative Commons BY license

RSC Adv., 2022,12, 26673-26679

Divergent copper-catalyzed syntheses of 3-carboxylpyrroles and 3-cyanofurans from O-acetyl oximes and β-ketoesters/nitriles

W. E. Almaraz-Ortiz, A. Ramos Orea, O. Casadiego-Díaz, A. Reyes-Salgado, A. Mejía-Galindo and R. O. Torres-Ochoa, RSC Adv., 2022, 12, 26673 DOI: 10.1039/D2RA04938D

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