A Michael addition of racemic indanone carboxylates to vinyl selenone catalyzed by C6'-hydroxyl cinchona derivatives is the key step of a synthetic sequence for a practical access to highly enantioenriched (up to 98% ee) polycyclic pyrrolidines bearing contiguous tertiary and quaternary stereocenters.

Organocatalytic Michael addition of indanone carboxylates to vinyl selenone for the asymmetric synthesis of polycyclic pyrrolidines

STERNATIVO, Silvia;BATTISTELLI, BENEDETTA;TESTAFERRI, Lorenzo;MARINI, Francesca
2012

Abstract

A Michael addition of racemic indanone carboxylates to vinyl selenone catalyzed by C6'-hydroxyl cinchona derivatives is the key step of a synthetic sequence for a practical access to highly enantioenriched (up to 98% ee) polycyclic pyrrolidines bearing contiguous tertiary and quaternary stereocenters.
2012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/981382
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