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Synfacts 2009(11): 1283-1283
DOI: 10.1055/s-0029-1218112
DOI: 10.1055/s-0029-1218112
Organo- and Biocatalysis
© Georg Thieme Verlag
Stuttgart ˙ New York
Aminocatalysis Cascades of Enones
L.-Y. Wu, G. Bencivenni, M. Mancinelli, A. Mazzanti, G. Bartoli, P. Melchiorre*
Università di Bologna, Italy
Further Information
Publication History
Publication Date:
22 October 2009 (online)

Significance
The authors identified the cinchona alkaloid derived primary amine 1 in combination with acid 2 as a powerful catalyst system for organocatalytic cascade reactions of enones. Employing nitroalkenes as reaction partners, the corresponding cyclohexanones were obtained in high optical purity and in favor of the trans isomer (see A). Depending on the reaction partner, also cyclohexanones containing all-carbon quaternary centers (see B) as well as bicyclic scaffolds (see C) can be constructed with high efficiency.