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- W2950647930 abstract "Fluoroolefin dipeptide isosteres were synthesized applying the Peterson reaction as a novel method for fluoroolefination. The dipeptide isosteres were elaborated to provide the conformationally constrained analogs (1-(R), 1-(S) and 2-(R), 2-(S)) of the Suc-Ala-Gly-Pro-Phe-pNA tetrapeptide, a synthetic substate of cyclophilin." @default.
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- W2950647930 date "1994-08-01" @default.
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- W2950647930 title "Fluoroolefin peptide isosteres - tools for controlling peptide conformations" @default.
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- W2950647930 doi "https://doi.org/10.1016/0040-4039(94)88067-0" @default.
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