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Abstract

Batch and Flow Asymmetric Catalysis for the Synthesis of Chiral Active Pharmaceutical Compounds †

by
Maurizio Benaglia
Dipartimento di Chimica, Università degli Studi di Milano, 20122 Milano, Italy
Presented at Symmetry 2017—The First International Conference on Symmetry, Barcelona, Spain, 16–18 October 2017.
Proceedings 2018, 2(1), 72; https://doi.org/10.3390/proceedings2010072
Published: 3 January 2018
(This article belongs to the Proceedings of The First International Conference on Symmetry)
Continuous-flow systems have emerged as a powerful technology for performing chemical transformations and have recently attracted attention also for the preparation of chiral APIs (active pharmaceutical ingredients).
Recently developed technology-assisted stereoselective reactions will be discussed, including reactions of nitroacrylates under MW irradiation and organocatalyzed reactions in alternative reaction media (Deep Eutectic Solvents). Some stereoselective transformations have been performed in chiral organocatalytic reactors (packed-bed and monolithic) under continuous flow conditions. Recent developments will be presented, also highlighting the possibility to perform organocatalytic reactions in (micro)-mesoreactors and to synthesize in flow-mode chiral intermediates of pharmaceutical interest. Preliminary results of stereoselective catalytic reactions in 3D-printed reactors will also be briefly highlighted.

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MDPI and ACS Style

Benaglia, M. Batch and Flow Asymmetric Catalysis for the Synthesis of Chiral Active Pharmaceutical Compounds. Proceedings 2018, 2, 72. https://doi.org/10.3390/proceedings2010072

AMA Style

Benaglia M. Batch and Flow Asymmetric Catalysis for the Synthesis of Chiral Active Pharmaceutical Compounds. Proceedings. 2018; 2(1):72. https://doi.org/10.3390/proceedings2010072

Chicago/Turabian Style

Benaglia, Maurizio. 2018. "Batch and Flow Asymmetric Catalysis for the Synthesis of Chiral Active Pharmaceutical Compounds" Proceedings 2, no. 1: 72. https://doi.org/10.3390/proceedings2010072

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