Abstract
ZSM-5-SO3H efficiently catalyzed the one-pot three-component Mannich reaction of aldehydes, anilines, and ketones. β-Aminocarbonyl compounds were obtained in reasonable yields and excellent stereoselectivities when the reaction was carried out at room temperature under solvent-free conditions. Simple experimental conditions and product isolation procedure makes this protocol potential for the development of clean and environment-friendly strategy for the synthesis of β-amino-ketones. The catalyst was recovered and reused for subsequent runs.
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Massah, A. R., Kalbasi, R. J., & Neda, S. (2011). Highly selective synthesis of β-amino carbonyl compounds over ZSM-5-SO3h under solvent-free conditions. Bulletin of the Korean Chemical Society, 32(5), 1703–1708. https://doi.org/10.5012/bkcs.2011.32.5.1703
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