ArticleJournal of the American Chemical Society2025
Unplugging Asymmetric Synthesis with a Wireless, Self-Pumping Electrochemical Reactor.
Article in Journal of the American Chemical Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Upcycling eggshell waste into sustainable and portable chiral membranes for the physical separation and electrocatalytic deracemization of enantiomers.RSC advances · 2026Article
- Tunable stereoselectivity in a wireless electrochemical microreactor using natural chiral ionic liquids.Green chemistry : an international journal and green chemistry resource : GC · 2025Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Herein, we report the first miniaturized, wireless electrochemical flow reactor capable of performing both reactant pumping and asymmetric synthesis within a single, integrated device. The reactor consists of a hollow, conductive polymer tube where the outer polypyrrole (Ppy) shell acts as an electromechanical pump, and the inner layer, constituted of a chiral thiophene-based oligomer, serves as the enantioselective catalyst. This integrated design overcomes mass-transport limitations and eliminates the need for external pumps. By employing an alternating current (AC) protocol, we achieve near-quantitative yield (99%) and exceptional enantioselectivity (>99% ee) for the reduction of acetophenone. The system's utility is showcased across three mechanistically distinct transformations, ketone reduction, sulfide oxidation, and reductive amination, culminating in the direct asymmetric synthesis of Ugi's amine, the chiral probe used in our mechanistic studies, with high stereocontrol (>99.5% ee). This work introduces a new paradigm for reagent-free, pump-free asymmetric synthesis and provides a validated, predictive model for the rational design of smart, automated chemical manufacturing platforms.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.