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Dipartimento di Chimica e Biologia, Università di Salerno, Via Ponte don Melillo, Fisciano, Italy
E-mail: lattanzi@unisa.it
; Fax: +39 089 969603
; Tel: +39 089 969563
Chem. Commun., 2013,49, 3821-3832
DOI:
10.1039/C3CC36928E
Received
24 Sep 2012,
Accepted
13 Mar 2013
First published online
14 Mar 2013
This feature article illustrates progress in asymmetric organocatalysis achieved by using readily available α,α-L-diaryl prolinols from 2009 up to middle 2012. This class of bifunctional organocatalysts has shown the ability to catalyze a variety of reactions such as epoxidation, cyclopropanation, α-sulfenylation of active methines, cross conjugate addition, direct aldol, cycloaddition and desymmetrization reactions. The most striking feature of these promoters is to enable either non-covalent or covalent activation of the reagents, thus distinguishing themselves as a rare example of organic promoters capable of encompassing alternative mechanistic pathways, namely enamine/iminium catalysis and Brønsted acid/base catalysis.
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