Development and applications of heterogeneous chiral bifunctional alkaloid-thioureas as recyclable organocatalysts

The development of heterogeneous chiral catalysts is a growing research field, offering recyclable alternatives to their homogeneous counterparts. With the aim of identifying a general and reliable methodology to access highly recyclable catalysts, herein, a structure-activity relationship study of chiral base-thiourea bifunctional catalysts is reported. The solid-supported catalysts have been benchmarked using well-known model reactions, allowing recycling of the catalyst up to 15 times without a decrease in the chiral induction properties.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob01582k
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
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article

Development and applications of heterogeneous chiral bifunctional alkaloid-thioureas as recyclable organocatalysts

Javier Vicario, Aitor Maestro, Patrick Y. Toullec, Xabier del Corte et al.
Organic & Biomolecular Chemistry
Asymmetric Hydrogenation and Catalysis
article

Development and applications of heterogeneous chiral bifunctional alkaloid-thioureas as recyclable organocatalysts

Javier Vicario, Aitor Maestro, Patrick Y. Toullec, Xabier del Corte, Ainara Pellicer, Nora Aranburu
article en

Abstract

The development of heterogeneous chiral catalysts is a growing research field, offering recyclable alternatives to their homogeneous counterparts. With the aim of identifying a general and reliable methodology to access highly recyclable catalysts, herein, a structure-activity relationship study of chiral base-thiourea bifunctional catalysts is reported. The solid-supported catalysts have been benchmarked using well-known model reactions, allowing recycling of the catalyst up to 15 times without a decrease in the chiral induction properties.

Organic & Biomolecular ChemistryVol. 23(48)
Centre National de la Recherche Scientifique (FR), Université de Bordeaux (FR), University of the Basque Country (ES), Institut des Sciences Moléculaires (FR), Institut Polytechnique de Bordeaux (FR)
Openalex Percentile: Top 73%
Asymmetric Hydrogenation and Catalysis
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