Synthesis of C6-amino agarose and evaluation of its antibacterial activity
In this paper, the biologically inert agarose was selectively modified at C6 of β-d-Galp units to produce an amino derivative with antibacterial property. The synthetic route involved the preparation of tosyl and azido agarose intermediates. All the polysaccharide derivatives were characterized by m...
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Veröffentlicht in: | Carbohydrate research 2021-09, Vol.507, p.108387, Article 108387 |
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Sprache: | eng |
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