Stereochemical Control in the Still-Wittig Rearrangement Synthesis of Cyclohexyl (Z)-Alkene Inhibitors of Pin1
Fig 2
Synthesis of the Ac–L-pSer–Ψ[(Z)CH = C]-D-Pip–NEA inhibitor (2R,5S)-1.
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Synthesis of the Ac–L-pSer–Ψ[(Z)CH = C]-D-Pip–NEA inhibitor (2R,5S)-1.