Design and Development of a Common Synthetic Strategy for a Variety of 1-N-Iminosugars
摘要:
[GRAPHICS]A new synthetic strategy has been developed for a general approach toward the synthesis of a variety of 1-N-iminosugar-type glycosidase inhibitors utilizing precursors developed by the PET-mediated cyclization of alpha-trimethylsilylmethylamine radical cation to a tethered pi-functionality.