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. PortaPrimo
;M. BenagliaSecondo
;A. PuglisiUltimo
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.File | Dimensione | Formato | |
---|---|---|---|
Riccardo Porta - poster_OK.pdf
accesso aperto
Tipologia:
Post-print, accepted manuscript ecc. (versione accettata dall'editore)
Dimensione
1.34 MB
Formato
Adobe PDF
|
1.34 MB | Adobe PDF | Visualizza/Apri |
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.