A simple route to optically active, functionalized five-, six- and seven-membered carbocyclic derivatives

Article abstract of DOI:10.1016/0040-4020(96)00652-7

The isoxazolidinocarbocyclic derivatives 6, 7 and 13, useful as precursors for unnatural bioactive chiral carbocyclic nucleosides and for glycosidase inhibitors have been synthesized from D-glucose through intramolecular 1,3-dipolar cycloaddition.