Copper catalyzed synthesis of thiazole derivatives from enaminones, amines and CS₂
Синтез производных тиазола из енаминонов, аминов и CS₂ с использованием меди в качестве катализатора
2026-02-16
SCID: 54.1/hfmr29he
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aminescarbon disulfide (CS₂)copper-catalyzed synthesisenaminonesthiazole derivatives
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Abstract (AI)
An efficient copper-catalyzed method for the synthesis of thiazoles from enaminones, amines, and carbon disulfide (CS₂) is described. This one-pot, ligand- and additive-free protocol proceeds under relatively simple reaction conditions, affording thiazole derivatives in good to excellent yields. Notably, CS₂ serves as a combined sulfur and carbon source, contributing to the synthetic practicality of the transformation. The method demonstrates good functional-group tolerance and provides a straightforward approach to biologically relevant thiazole scaffolds.
Key Findings
1
A copper-catalyzed one-pot method synthesizes thiazoles from enaminones, amines, and CS₂
2
CS₂ acts as both the sulfur and carbon source in the transformation
3
The method affords thiazole derivatives in good to excellent yields
4
The protocol is ligand- and additive-free and operates under relatively simple reaction conditions
5
The reaction shows good functional-group tolerance and provides access to biologically relevant thiazole scaffolds
Research Object
Copper-catalyzed one-pot synthesis of thiazole derivatives from enaminones, amines, and carbon disulfide (CS₂)
Research Subject
Development and evaluation of a ligand- and additive-free copper-catalyzed protocol (reaction conditions, yield, functional-group tolerance) that uses CS₂ as combined sulfur and carbon source to form thiazole scaffolds
Publication Details
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2026-02-16
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