D-Glucose derivatives bearing an anomeric thiophenyl group and orthogonally protections on secondary hydroxyl groups were linked to solid supports (PS/DV polymer, tentagel resin) through an ester bond on C-6. It was investigated the possibility to remove orthogonally protecting groups and functionalize selectively the free hydroxyls groups and the anomeric carbon of sugars in solid phase

Peri, F., Leslie, C., Micheli, F., Seneci, P., Marchioro, C., Nicotra, F. (2003). D-glucose as a regioselectively addressable scaffold for combinatorial chemistry on solid phase. JOURNAL OF CARBOHYDRATE CHEMISTRY, 22(1), 57-71 [10.1081/CAR-120019014].

D-glucose as a regioselectively addressable scaffold for combinatorial chemistry on solid phase

Peri, F;
2003

Abstract

D-Glucose derivatives bearing an anomeric thiophenyl group and orthogonally protections on secondary hydroxyl groups were linked to solid supports (PS/DV polymer, tentagel resin) through an ester bond on C-6. It was investigated the possibility to remove orthogonally protecting groups and functionalize selectively the free hydroxyls groups and the anomeric carbon of sugars in solid phase
Articolo in rivista - Articolo scientifico
organic synthesis; combinatorial chemistry; solid phase organic chemistry
English
2003
22
1
57
71
none
Peri, F., Leslie, C., Micheli, F., Seneci, P., Marchioro, C., Nicotra, F. (2003). D-glucose as a regioselectively addressable scaffold for combinatorial chemistry on solid phase. JOURNAL OF CARBOHYDRATE CHEMISTRY, 22(1), 57-71 [10.1081/CAR-120019014].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/34271
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