Herein we report an easy and fruitful methods to synthesize 3-(2-haloalkyl)-5-aryl isoxazoles starting from β-nitro-β,γ-unsaturated ketones. The reaction was promoted by the presence of tin (II) chloride or bromide and products were obtained in good yields and in short reaction time. Moreover, we extended our methodology to flow chemical conditions, and we also tested the usefulness of halogenated isoxazoles to obtain amino and ether derivatives.
SnX2 PromotedCyclization of β-Nitro-β,γ-unsaturated Ketones Into 3-(2-Haloalkyl)-5-aryl Isoxazoles
Lu WangSecondo
;Marino PetriniPenultimo
;Alessandro Palmieri
Ultimo
2025-01-01
Abstract
Herein we report an easy and fruitful methods to synthesize 3-(2-haloalkyl)-5-aryl isoxazoles starting from β-nitro-β,γ-unsaturated ketones. The reaction was promoted by the presence of tin (II) chloride or bromide and products were obtained in good yields and in short reaction time. Moreover, we extended our methodology to flow chemical conditions, and we also tested the usefulness of halogenated isoxazoles to obtain amino and ether derivatives.File in questo prodotto:
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Asian J. Org. Chem. 2025,14, e202500076.pdf
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