Highly selective synthesis of β-amino carbonyl compounds over ZSM-5-SO3h under solvent-free conditions

26Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free