"""""""A novel asymmetric nucleophilic epoxidation for R-ylideneoxindole esters has been successfully devised, resulting in enantioenriched spiro compounds with two new contiguous stereocenters. The employed (S)-R,R-diphenylprolinol functions as a bifunctional catalyst, creating a complex H-bond network in conjunction with a substrate and an oxidant"""""""

Gasperi, T., Tofani, D., Gambacorta, A., Palumbo, C., Mazzeo, G., Mazziotta, A., et al. (2011). Noncovalent Organocatalysis: A Powerful Tool for the Nucleophilic Epoxidation of α-Ylideneoxindoles. ORGANIC LETTERS, 13(23), 6248-6251 [10.1021/ol202646w].

Noncovalent Organocatalysis: A Powerful Tool for the Nucleophilic Epoxidation of α-Ylideneoxindoles

GASPERI, TECLA;TOFANI, DANIELA;GAMBACORTA, Augusto;
2011-01-01

Abstract

"""""""A novel asymmetric nucleophilic epoxidation for R-ylideneoxindole esters has been successfully devised, resulting in enantioenriched spiro compounds with two new contiguous stereocenters. The employed (S)-R,R-diphenylprolinol functions as a bifunctional catalyst, creating a complex H-bond network in conjunction with a substrate and an oxidant"""""""
Gasperi, T., Tofani, D., Gambacorta, A., Palumbo, C., Mazzeo, G., Mazziotta, A., et al. (2011). Noncovalent Organocatalysis: A Powerful Tool for the Nucleophilic Epoxidation of α-Ylideneoxindoles. ORGANIC LETTERS, 13(23), 6248-6251 [10.1021/ol202646w].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11590/278767
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