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.
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]
Neo-glycoconjugates: stereoselective synthesis of alpha-glycosyl amides via Staudinger ligation reactions
A. BianchiPrimo
;A. BernardiUltimo
2005
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.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
