Issue 46, 2022

Redox noninnocence of the formazanate ligand applied to catalytic formation of α-ketoamides

Abstract

The formazan ligands have been investigated as redox-noninnocent backbones for a long time. Despite their well-established behaviour as redox reservoirs, the demonstration of catalytic efficiency governed by redox noninnocence remains elusive. We report an iron–formazanate molecule for efficiently preparing α-keto amides, where a crucial reductive cleavage of the substrate molecule is tightly regulated by the electron donation from the formazanate, in a reversible manner.

Graphical abstract: Redox noninnocence of the formazanate ligand applied to catalytic formation of α-ketoamides

Supplementary files

Article information

Article type
Communication
Submitted
11 رمضان 1443
Accepted
03 شوال 1443
First published
03 شوال 1443

Chem. Commun., 2022,58, 6630-6633

Redox noninnocence of the formazanate ligand applied to catalytic formation of α-ketoamides

V. Singh, A. Kundu, K. Singh and D. Adhikari, Chem. Commun., 2022, 58, 6630 DOI: 10.1039/D2CC02089K

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