Copper-catalyzed aerobic annulation of hydrazones with dienones: an efficient route to pyrazole-linked hybrid molecules

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Date

2024

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Royal Society of Chemistry

Abstract

A copper-catalyzed aerobic [3 + 2] annulation reaction to access various pyrazole-bound chalcones starting from readily available and cost-effective hydrazones and dienones is reported. These pyrazole-bound chalcones were further utilized effectively to prepare a series of pyrazole-linked hybrid molecules, such as pyrazole-pyrazoline, pyrazole-aziridine, and pyrazole-pyridine hybrids by efficient simple transformations. Synthetically challenging hybrid molecules were obtained in a simple, two-step process with high atom economy under aerobic copper catalysis. © 2024 The Royal Society of Chemistry.

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Keywords

Copper, Cost effectiveness, Molecules, Annulation reactions, Chalcones, Copper catalyzed, Cost effective, Dienones, Hybrid molecules, Hydrazones, Pyrazoles, Pyrazolines, Simple++, Catalysis, chalcone derivative, copper, hydrazone derivative, pyrazole, pyridine, annulation reaction, article, catalysis, controlled study, drug analysis, drug development, human tissue, hybrid

Citation

Organic and Biomolecular Chemistry, 2024, 22, 32, pp. 6631-6637

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