作者:Anaïs Prunier、Charlène Calata、Julien Legros、Jacques Maddaluno、Emmanuel Pfund、Thierry Lequeux
DOI:10.1021/jo401356j
日期:2013.8.16
The synthesis of fluoroaminosulfones derived from piperidine and nucleic bases followed by the study of their chemical behavior in the modified Julia reaction are described. The resulting aminosulfones open a straightforward access to a series of new fluorinated biomolecules including a potent DPP-II inhibitor and acyclonucleoside analogues as potential enzyme inhibitors.