Issue 5, 2021

Calcium-catalyzed formal [3 + 2] annulation of C,N-diacyliminium ions with nucleophilic phenols: a diversity oriented synthesis of 3-aminofurans

Abstract

We have developed a one-pot, three-component, and solvent-free reaction for the synthesis of 3-aminofurans using a calcium catalyst. In this cascade reaction, the key intermediate, C,N-diacyliminium ion, is formed in situ from glyoxal and lactam, which further reacted with phenolic nucleophiles to form furan derivatives in good yields with broad substrate diversity. We also present here the preliminary photophysical studies of selected compounds.

Graphical abstract: Calcium-catalyzed formal [3 + 2] annulation of C,N-diacyliminium ions with nucleophilic phenols: a diversity oriented synthesis of 3-aminofurans

Supplementary files

Article information

Article type
Paper
Submitted
16 Nov 2020
Accepted
22 Dec 2020
First published
08 Jan 2021

Org. Biomol. Chem., 2021,19, 1060-1065

Calcium-catalyzed formal [3 + 2] annulation of C,N-diacyliminium ions with nucleophilic phenols: a diversity oriented synthesis of 3-aminofurans

R. P., A. I. Almansour, N. Arumugam and S. Yaragorla, Org. Biomol. Chem., 2021, 19, 1060 DOI: 10.1039/D0OB02276D

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