Recently developed organocatalytic stereoselective transformations using polymer-based packed bed and catalytic reactors will be presented. Furthermore, the use of different bifunctional chiral metal-free catalysts in micro- and mesofluidic devices will be described. Metal-free stereoselective additions of activated nucleophiles tonitrostyrenes were investigated under continuous-flow conditions in microreactors. The potential of this flow chemistry approach was demonstrated by the successful synthesis of an advanced intermediate for the preparation of the GABAB receptor agonist Baclofen and other Active Pharmaceutical Ingredients (APIs) such as (S)-Pregabalin and (S)-Warfarin.

Flow chemistry, organocatalysis and 3D-printing : valuable tools in the synthesis of chiral compounds / M. Benaglia. ((Intervento presentato al 3. convegno Green and Sustainable Conference on Green Chemistry tenutosi a Berlin nel 2018.

Flow chemistry, organocatalysis and 3D-printing : valuable tools in the synthesis of chiral compounds

M. Benaglia
2018

Abstract

Recently developed organocatalytic stereoselective transformations using polymer-based packed bed and catalytic reactors will be presented. Furthermore, the use of different bifunctional chiral metal-free catalysts in micro- and mesofluidic devices will be described. Metal-free stereoselective additions of activated nucleophiles tonitrostyrenes were investigated under continuous-flow conditions in microreactors. The potential of this flow chemistry approach was demonstrated by the successful synthesis of an advanced intermediate for the preparation of the GABAB receptor agonist Baclofen and other Active Pharmaceutical Ingredients (APIs) such as (S)-Pregabalin and (S)-Warfarin.
mag-2018
Settore CHIM/06 - Chimica Organica
Flow chemistry, organocatalysis and 3D-printing : valuable tools in the synthesis of chiral compounds / M. Benaglia. ((Intervento presentato al 3. convegno Green and Sustainable Conference on Green Chemistry tenutosi a Berlin nel 2018.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/618192
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