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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
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Publication date
January 2012
Icon DOI
10.1002/ejoc.201200151
Publisher
Wiley
ISSN
1434-193X
Citation count (estimate)
4

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

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