Neo-glycoconjugates: stereoselective synthesis of alpha-glycosyl amides via Staudinger ligation reactions

Articolo
Data di Pubblicazione:
2005
Citazione:
Neo-glycoconjugates: stereoselective synthesis of alpha-glycosyl amides via Staudinger ligation reactions / A. Bianchi, A. Russo, A. Bernardi. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 16:2(2005), pp. 381-386. [10.1016/j.tetasy.2004.11.055]
Abstract:
alpha-Glycosyl azides can be transformed in the corresponding alpha-glycosyl amides with good yields and selectivity via reduction-acylation (Staudinger ligation) reactions using funtionalised phosphines la-f. The limits and scope of this approach for the synthesis of alpha-glycosyl amides are reported. (C) 2004 Elsevier Ltd. All rights reserved.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
carbohydrates, glycoconjugates, stereoselective synthesis
Elenco autori:
A. Bianchi, A. Russo, A. Bernardi
Autori di Ateneo:
BERNARDI ANNA ( autore )
Link alla scheda completa:
https://air.unimi.it/handle/2434/16231

Aree Di Ricerca

Settori


Settore CHIM/06 - Chimica Organica