Issue 5, 2023

Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO3 perovskites

Abstract

Synthesis of imidazole[2,1-b]benzothiazoles often suffers from the use of pre-functionalized substrates and/or homogeneous, non-recyclable catalytic systems. Herein we report a method for direct coupling of acetophenones and 2-aminobenzothiazoles in the presence of reusable perovskites, namely LaMn0.95Ni0.05O3. Imidazole[2,1-b]benzothiazoles were obtained in moderate to good yields and contained an array of useful functionalities. Control experiments indicated that the perovskites played pivotal roles in halogenation and condensation steps.

Graphical abstract: Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO3 perovskites

Supplementary files

Article information

Article type
Paper
Submitted
17 Dec 2022
Accepted
16 Jan 2023
First published
23 Jan 2023
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2023,13, 3341-3345

Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO3 perovskites

P. T. Pham, D. K. Nguyen, N. T. S. Phan, M. Le and T. T. Nguyen, RSC Adv., 2023, 13, 3341 DOI: 10.1039/D2RA08045A

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