Synthesis of prostaglandins III: Efficient and practical synthesis of antisecretory prostaglandin enprostil

Article abstract of DOI:10.1055/s-1994-25576

An efficient and practical 8-step synthesis of enprostil (1) starting from the lactone 2 has been developed. The propargylic acetate 5 was prepared from the lactol 3 by the reaction with ethynylmagnesium bromide followed by acetylation. Propargylic acetate 5 was converted into enprostil (1) via the introduction of an allene moity by reaction with a Grignard reagent in the presence of a CuI · P(OEt)₃ complex.