A simple and efficient bi-directional solid-phase synthesis, based on the use of a Tentagel solid support, functionalized with a suitably protected 2-amino sugar residue, is proposed for the prepn. of a variety of glycoconjugates, including glycopeptides and nucleo-glycopeptides.
A new strategy for the solid phase synthesis of glycoconjugate biomolecules / DI FABIO, Giovanni; A., DE CAPUA; DE NAPOLI, Lorenzo; Montesarchio, Daniela; Piccialli, Gennaro; Rossi, Filomena; E., Benedetti. - In: SYNLETT. - ISSN 0936-5214. - ELETTRONICO. - 3:(2001), pp. 341-344. [10.1055/s-2001-11391]
A new strategy for the solid phase synthesis of glycoconjugate biomolecules
DI FABIO, GIOVANNI;DE NAPOLI, LORENZO;MONTESARCHIO, DANIELA;PICCIALLI, GENNARO;ROSSI, FILOMENA;
2001
Abstract
A simple and efficient bi-directional solid-phase synthesis, based on the use of a Tentagel solid support, functionalized with a suitably protected 2-amino sugar residue, is proposed for the prepn. of a variety of glycoconjugates, including glycopeptides and nucleo-glycopeptides.File in questo prodotto:
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