The facile syntheses of previously unreported 2,3- and 3,4-unsaturated derivatives of N-glycolylneuraminic acid are herein described. The procedure involves a ring-opening of the 4,5-oxazoline of N-acetylneuraminic acid, the acylation of the intermediate free amine, its conversion into the 4,5-oxazoline of N-glycolylneuraminic acid and the subsequent Ferrier reaction or C4 nucleophilic substitution.

Straightforward access to 2,3- and 3,4-unsaturated derivatives of N-glycolylneuraminic acid

Franco, Valentina;
2020-01-01

Abstract

The facile syntheses of previously unreported 2,3- and 3,4-unsaturated derivatives of N-glycolylneuraminic acid are herein described. The procedure involves a ring-opening of the 4,5-oxazoline of N-acetylneuraminic acid, the acylation of the intermediate free amine, its conversion into the 4,5-oxazoline of N-glycolylneuraminic acid and the subsequent Ferrier reaction or C4 nucleophilic substitution.
2020
Esperti anonimi
Inglese
Internazionale
STAMPA
Available online 24 October 2020, 131699
Sialidase inhibitorN-Glycolylneuraminic acidGlycalsOxazoline of sialic acidFerrier reaction
4
info:eu-repo/semantics/article
262
Rota, Paola; La Rocca, Paolo; Franco, Valentina; Allevi, Pietro
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1349442
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