R-O-Linked glycohomoglutamates are obtained as diastereomerically pure compounds by chemo-, regio-, and stereoselective cycloadditions between glycals and aspartic acid derivatives. The latter constitute orthogonally functionalized scaffolds for glycopeptide mimetics.

A new scaffold for the stereoselective synthesis of a-O-linked glycopeptide mimetics / F. VENTURI; C. VENTURI; F. LIGUORI; M. CACCIARINI; M. MONTALBANO; C. NATIVI. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 69:(2004), pp. 6153-6155. [10.1021/jo049441h]

A new scaffold for the stereoselective synthesis of a-O-linked glycopeptide mimetics

CACCIARINI, MARTINA;NATIVI, CRISTINA
2004

Abstract

R-O-Linked glycohomoglutamates are obtained as diastereomerically pure compounds by chemo-, regio-, and stereoselective cycloadditions between glycals and aspartic acid derivatives. The latter constitute orthogonally functionalized scaffolds for glycopeptide mimetics.
2004
69
6153
6155
F. VENTURI; C. VENTURI; F. LIGUORI; M. CACCIARINI; M. MONTALBANO; C. NATIVI
File in questo prodotto:
File Dimensione Formato  
JOC_2004.pdf

Accesso chiuso

Tipologia: Versione finale referata (Postprint, Accepted manuscript)
Licenza: Tutti i diritti riservati
Dimensione 100.61 kB
Formato Adobe PDF
100.61 kB Adobe PDF   Richiedi una copia

I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/334657
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 21
  • ???jsp.display-item.citation.isi??? 20
social impact