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
Autori di Ateneo:
ROTA PAOLA ( autore )
Link alla scheda completa:
https://air.unimi.it/handle/2434/178019

Aree Di Ricerca

Settori


Settore BIO/10 - Biochimica