4.6 Article

Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction

Journal

RSC ADVANCES
Volume 13, Issue 3, Pages 1580-1586

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra07244k

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Chiral polymeric particles (CPPs) have been extensively studied in recent years for their significance in pharmaceutical applications. In this study, nanosized CPPs were synthesized and applied as catalysts for direct asymmetric aldol reaction. The CPPs, prepared by miniemulsion or inverse miniemulsion methods using various chiral amino acid derivatives, were characterized by dynamic light scattering and scanning electron microscopy. The spherical nanoparticles with sizes between 250 and 400 nm and high chiral surface area served as catalysts in the aldol reaction at room temperature without additional solvent. Among them, l-tryptophan exhibited the highest enantiomeric excess (>86%) with similar catalytic performance for four times.
Chiral polymeric particles (CPPs) were studied extensively in recent years due to their importance in pharmaceutical applications. Here, nanosized CPPs were synthesized and applied as catalysts for direct asymmetric aldol reaction. The CPPs were prepared by miniemulsion or inverse miniemulsion based on various chiral amino acid derivatives and characterized by dynamic light scattering and scanning electron microscopy. The nanoparticles with spherical structure between 250 and 400 nm and high chiral surface area were used as catalysts in the aldol reaction at room temperature without additional solvent. l-tryptophan gave the highest enantiomeric excess, >86% with similar catalytic performance four times.

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