1 research outputs found
Toward the Synthesis of Fluorinated Analogues of HCV NS3/4A Serine Protease Inhibitors Using Methyl α‑Amino-β-fluoro-β-vinylcyclopropanecarboxylate as Key Intermediate
Synthesis
of fluorocyclopropyl building blocks, which constitute
the core of various therapeutic agents against the hepatitis C virus,
is described. The relevant methyl α-amino-β-fluoro-β-vinylcyclopropanecarboxylate
has been used as a key intermediate for the total synthesis of a fluorinated
analogue of Simeprevir (TMC 435), a HCV NS3/4A protease inhibitor