Class-II-aldolase-mimicking polyfunctional Lewis acid/azolium–aryloxide catalysts in direct enantioselective nitro-aldol additions

A polyfunctional Co( ii )/azolium–aryloxide catalyst enables direct highly enantioselective Henry reactions. Synergistic Lewis acid, Brønsted base and H-bond activation mimics class-II aldolases, which is supported by DFT and microkinetic modelling.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-12-23
DOI
https://doi.org/10.1039/d5qo01558h
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Class-II-aldolase-mimicking polyfunctional Lewis acid/azolium–aryloxide catalysts in direct enantioselective nitro-aldol additions

Khushbu Jangid, Radhika Kataria, Alexander Allgaier, Johannes Kästner et al.
Organic Chemistry Frontiers
Cyclopropane Reaction Mechanisms
article

Class-II-aldolase-mimicking polyfunctional Lewis acid/azolium–aryloxide catalysts in direct enantioselective nitro-aldol additions

Khushbu Jangid, Radhika Kataria, Alexander Allgaier, Johannes Kästner, René Peters, Justin Herrmann, Daniel M. Wanner, Lisa A. Schmoltzi, Janis Gschwind, Silvio Münch, Joris van Slageren
article en

Abstract

A polyfunctional Co( ii )/azolium–aryloxide catalyst enables direct highly enantioselective Henry reactions. Synergistic Lewis acid, Brønsted base and H-bond activation mimics class-II aldolases, which is supported by DFT and microkinetic modelling.

Organic Chemistry FrontiersVol. 13(3)
University of Stuttgart (DE)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Studienstiftung des Deutschen Volkes
Openalex Percentile: Top 34%
Cyclopropane Reaction Mechanisms
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