The use of platinum-catalyzed hydrosilylation chemistry of silicones greatly simplifies the preparation of bis-oxazoline (box) ligands covalently bound to an insoluble polymeric support. The use of such immobilized chiral ligands in different copper-catalyzed asymmetric transformations (carbonyl-ene, Mukaiyama aldol and olefin cyclopropanation reactions) allows the attainment of high levels of enantioselectivity (91-99 % ee).

Remarkable efficiency improvement in the preparation of insoluble polymer-bound (IPB) enantioselective catalytic systems by the use of silicone chemistry

Evangelisti Claudio;
2008

Abstract

The use of platinum-catalyzed hydrosilylation chemistry of silicones greatly simplifies the preparation of bis-oxazoline (box) ligands covalently bound to an insoluble polymeric support. The use of such immobilized chiral ligands in different copper-catalyzed asymmetric transformations (carbonyl-ene, Mukaiyama aldol and olefin cyclopropanation reactions) allows the attainment of high levels of enantioselectivity (91-99 % ee).
2008
asymmetric catalysi
bis-oxazoline
C-C bond formation
silicones
supported catalysts
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/294928
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