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.

Unplugging Asymmetric Synthesis with a Wireless, Self-Pumping Electrochemical Reactor / S. Grecchi, G. Salinas, M. Niamlaem, A. Kuhn, S. Arnaboldi. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 147:51(2025 Dec 24), pp. 47467-47476. [10.1021/jacs.5c16187]

Unplugging Asymmetric Synthesis with a Wireless, Self-Pumping Electrochemical Reactor

S. Grecchi
Primo
;
S. Arnaboldi
Ultimo
2025

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.
English
Settore CHEM-01/A - Chimica analitica
Articolo
Esperti anonimi
Pubblicazione scientifica
   Cargo-towing Highly enantioselective Electro-pumps: unconventional asymmetrIc Readout and transmission of chiral information (CHEIR)
   CHEIR
   EUROPEAN COMMISSION
   101040798
24-dic-2025
9-dic-2025
American Chemical Society
147
51
47467
47476
10
Pubblicato
Periodico con rilevanza internazionale
COSPECT
crossref
Aderisco
info:eu-repo/semantics/article
Unplugging Asymmetric Synthesis with a Wireless, Self-Pumping Electrochemical Reactor / S. Grecchi, G. Salinas, M. Niamlaem, A. Kuhn, S. Arnaboldi. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 147:51(2025 Dec 24), pp. 47467-47476. [10.1021/jacs.5c16187]
open
Prodotti della ricerca::01 - Articolo su periodico
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262
Article (author)
Periodico con Impact Factor
S. Grecchi, G. Salinas, M. Niamlaem, A. Kuhn, S. Arnaboldi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1232691
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