Chiral primary amines derived from cinchona alkaloids represent a well-established class of stereoselective organocatalysts capable of promoting a great number of chemical transformations with excellent levels of enantioselectivity. Their immobilization onto a polymeric support is an attractive procedure to develop an easily recyclable heterogeneous catalytic system. The supported catalyst proved to be very efficient, versatile and well comparable to the corresponding non-supported one. The confinement of supported catalyst into flow reactors represents an intriguing methodology to perform stereoselective reactions in continuo.

Supported chiral organocatalyst for stereoselective reactions under batch and continuous flow conditions / R. Porta, M. Benaglia, A. Puglisi. ((Intervento presentato al convegno E-Wispoc tenutosi a Bressanone nel 2015.

Supported chiral organocatalyst for stereoselective reactions under batch and continuous flow conditions

R. Porta
Primo
;
M. Benaglia
Secondo
;
A. Puglisi
Ultimo
2015

Abstract

Chiral primary amines derived from cinchona alkaloids represent a well-established class of stereoselective organocatalysts capable of promoting a great number of chemical transformations with excellent levels of enantioselectivity. Their immobilization onto a polymeric support is an attractive procedure to develop an easily recyclable heterogeneous catalytic system. The supported catalyst proved to be very efficient, versatile and well comparable to the corresponding non-supported one. The confinement of supported catalyst into flow reactors represents an intriguing methodology to perform stereoselective reactions in continuo.
2015
Settore CHIM/06 - Chimica Organica
Supported chiral organocatalyst for stereoselective reactions under batch and continuous flow conditions / R. Porta, M. Benaglia, A. Puglisi. ((Intervento presentato al convegno E-Wispoc tenutosi a Bressanone nel 2015.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/263398
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