Synthesis and evaluation of a bicyclic deo×ymannojirimycin derivative as a potential glycosidase inhibitor
摘要:
A bicyclo[2.2.2] analogue of the glycosidase inhibitor 1-deoxynojirimycin, 2,6-anhydro-l-deoxymannojirimycin (6), has been synthesized in nine steps from I,5-anhydro-D-glucitol. This conformationally restricted aza-sugar has been shown to inhibit, albeit weakly, several glycosidase enzymes.