作者: Audrey Hottin , Faustine Dubar , Agata Steenackers , Philippe Delannoy , Christophe Biot
DOI: 10.1039/C2OB25727K
关键词:
摘要: We prepared a series of new iminosugar–ferrocene hybrids displaying potent inhibition fucosidase (bovine kidney) and inactivation MDA-MB-231 breast cancer cells proliferation at low micromolar concentrations. The synthetic route brought to light an unprecedented isomerisation 2-ethanalylpyrrolidine.