Facile Diastereoselective Entry to 4 beta-Acylamidation of Neu5Ac2en Glycals Using Their N-Perfluoroacylated Congeners as Key Tools
Articolo
Data di Pubblicazione:
2012
Citazione:
Facile Diastereoselective Entry to 4 beta-Acylamidation of Neu5Ac2en Glycals Using Their N-Perfluoroacylated Congeners as Key Tools / P. Rota, I. Agnolin, P. Allevi, M. Anastasia. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1434-193X. - 2012:13(2012), pp. 2508-2510. [10.1002/ejoc.201200151]
Abstract:
An efficient protocol for the 4 beta-acylamidation of the N-acylated glycals of Neu5Ac by using the corresponding N-perfluoroacylated congeners as key tools has been developed and applied to the synthesis of glycals combining the features of the molecules with antiviral properties.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
sialic acid ; glycals ; diastereoselectivity ; Fluorine
Elenco autori:
P. Rota, I. Agnolin, P. Allevi, M. Anastasia
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