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.
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