Novel nojirimycin-derived bicyclic structures, containing cyclic carbamate, urea and guanidine moieties have been synthesised starting from suitably protected a-C-vinylnojirimycin and a-C-allylnojirimycin, respectively, and their biological activity against different glycosidases and as antibacterial agents tested

Cipolla, L., Reis Fernandes, M., Gregori, M., Airoldi, C., Nicotra, F. (2007). Synthesis and biological evaluation of a small library of nojirimycin derived bicyclic iminosugars. CARBOHYDRATE RESEARCH, 342(12-13), 1813-1830 [10.1016/j.carres.2007.04.002].

Synthesis and biological evaluation of a small library of nojirimycin derived bicyclic iminosugars

CIPOLLA, LAURA FRANCESCA;GREGORI, MARIA;AIROLDI, CRISTINA;NICOTRA, FRANCESCO
2007

Abstract

Novel nojirimycin-derived bicyclic structures, containing cyclic carbamate, urea and guanidine moieties have been synthesised starting from suitably protected a-C-vinylnojirimycin and a-C-allylnojirimycin, respectively, and their biological activity against different glycosidases and as antibacterial agents tested
Articolo in rivista - Articolo scientifico
Iminosugars; Nojirimycin; Glycosidases; Enzyme inhibitors; Glucuronidase; Antibacterial
English
18-apr-2007
342
12-13
1813
1830
none
Cipolla, L., Reis Fernandes, M., Gregori, M., Airoldi, C., Nicotra, F. (2007). Synthesis and biological evaluation of a small library of nojirimycin derived bicyclic iminosugars. CARBOHYDRATE RESEARCH, 342(12-13), 1813-1830 [10.1016/j.carres.2007.04.002].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/8234
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