Tunable stereoselectivity in a wireless electrochemical microreactor using natural chiral ionic liquids

A single drop of a natural chiral ionic liquid (NCIL) serves as a wireless electrochemical microreactor for enantioselective synthesis. This system yields high selectivity (>90% ee) and demonstrates dynamic stereocontrol, where the enantiomeric excess is directly modulated by the external electric field. This catalyst-free strategy introduces a new paradigm for sustainable, tunable asymmetric reactions.

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Publication Details

Journal
Green Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5gc04756k
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tunable stereoselectivity in a wireless electrochemical microreactor using natural chiral ionic liquids

Andrea Mezzetta, Sara Grecchi, Lorenzo Guazzelli, Serena Arnaboldi
Green Chemistry
Radical Photochemical Reactions
article

Tunable stereoselectivity in a wireless electrochemical microreactor using natural chiral ionic liquids

Andrea Mezzetta, Sara Grecchi, Lorenzo Guazzelli, Serena Arnaboldi
article en

Abstract

A single drop of a natural chiral ionic liquid (NCIL) serves as a wireless electrochemical microreactor for enantioselective synthesis. This system yields high selectivity (>90% ee) and demonstrates dynamic stereocontrol, where the enantiomeric excess is directly modulated by the external electric field. This catalyst-free strategy introduces a new paradigm for sustainable, tunable asymmetric reactions.

Green ChemistryVol. 27(46)
University of Pisa (IT), University of Milan (IT)
Horizon 2020 Framework Programme, H2020 European Research Council
Openalex Percentile: Top 76%
Radical Photochemical Reactions
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Tunable stereoselectivity in a wireless electrochemical microreactor using natural chiral ionic liquids — Andrea Mezzetta, Sara Grecchi, et al. · Green Chemistry (2025) | TGRS Research Map | TGRS