http://www.cnr.it/ontology/cnr/individuo/prodotto/ID33532
Pyrrolic tripodal receptors for carbohydrates. Role of functional groups and binding geometry on carbohydrate recognition (Articolo in rivista)
- Type
- Label
- Pyrrolic tripodal receptors for carbohydrates. Role of functional groups and binding geometry on carbohydrate recognition (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/c0ob00651c (literal)
- Alternative label
M. Cacciarini, C. Nativi, M. Norcini, S. Staderini, O. Francesconi, S. Roelens (2011)
Pyrrolic tripodal receptors for carbohydrates. Role of functional groups and binding geometry on carbohydrate recognition
in Organic & biomolecular chemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- M. Cacciarini, C. Nativi, M. Norcini, S. Staderini, O. Francesconi, S. Roelens (literal)
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- Pagina fine
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Chimica, Università di Firenze; Istituto di Metodologie Chimiche (IMC), Consiglio Nazionale delle
Ricerche (CNR). (literal)
- Titolo
- Pyrrolic tripodal receptors for carbohydrates. Role of functional groups and binding geometry on carbohydrate recognition (literal)
- Abstract
- The contribution from several H-bonding groups and the impact of geometric requirements on the binding ability of benzene-based tripodal receptors toward carbohydrates have been investigated by measuring the affinity of a set of structures toward octyl beta-D-glucopyranoside, selected as a representative monosaccharide. The results reported in the present study demonstrate that a judicious choice of correct geometry and appropriate functional groups is critical to achieve the complementary hydrogen bonding interactions required for an effective carbohydrate recognition. (literal)
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