Issue 30, 2025, Issue in Progress

Beckmann rearrangement of ketoximes for accessing amides and lactams promoted by a perimidine-2-thione supported Hg(ii) complex: a mechanistic perception

Abstract

In this study, we present a new distorted tetrahedral mononuclear mercury(II) complex mediated by a 1-isopropyl-1H-perimidine-2(3H)-thione ligand, with a molecular formula C28H28Cl2HgN4S2. Several characterization techniques, such as single-crystal X-ray diffraction, NMR, and FT-IR, were employed to analyze the complex. The synthesized complex acted as a metallic Lewis acid catalyst for the conversion of a wide array of ketoximes into amides and lactams, resulting in an expansion of the Beckmann rearrangement. Different types of substrates were successfully converted into corresponding amides under mild reaction conditions.

Graphical abstract: Beckmann rearrangement of ketoximes for accessing amides and lactams promoted by a perimidine-2-thione supported Hg(ii) complex: a mechanistic perception

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Article information

Article type
Paper
Submitted
23 Apr 2025
Accepted
23 Jun 2025
First published
11 Jul 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 24317-24330

Beckmann rearrangement of ketoximes for accessing amides and lactams promoted by a perimidine-2-thione supported Hg(II) complex: a mechanistic perception

P. Velmurugan, P. Kanniyappan and T. Ghatak, RSC Adv., 2025, 15, 24317 DOI: 10.1039/D5RA02843D

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