Bismuth(iii)chloride catalyzed one-pot synthesis of thioenol ethers from 1,3-dicabonyls/2-oxindoles under ultrasonic irradiation

Abstract

An efficient one-pot, three-component strategy has been devised for the facile construction of thioenol ethers related to biologically potent scaffolds. This method employs β-ketoesters or 1,3-diones or 2-oxindole, N,N-dimethylformamide dimethylacetal (DMF-DMA), and thiols under BiCl3-catalyzed, ultrasound-assisted conditions. This methodology's key features include readily accessible building blocks, a cost-effective and environmentally friendly catalytic system, solvent-free reaction conditions, shorter reaction times, broad substrate scope, and good isolated yields.

Graphical abstract: Bismuth(iii)chloride catalyzed one-pot synthesis of thioenol ethers from 1,3-dicabonyls/2-oxindoles under ultrasonic irradiation

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Article information

Article type
Paper
Submitted
12 Feb 2025
Accepted
22 Apr 2025
First published
28 Apr 2025

Org. Biomol. Chem., 2025, Advance Article

Bismuth(III)chloride catalyzed one-pot synthesis of thioenol ethers from 1,3-dicabonyls/2-oxindoles under ultrasonic irradiation

B. Panchal, B. Panchal, M. Talukdar, A. Bhar, T. Naveen and E. Begari, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D5OB00250H

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