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- W4241817863 abstract "Abstract Small peptides containing combinations of cysteine, tyrosine, histidine, and serine residues react with octafluorocyclopentene (OFCP) to afford atypically structured macrocycles through successive vinylic substitutions. The reactions proceed rapidly in air at 0 °C and are tolerant of spectating tryptophan, asparagine, glutamine, and threonine residues. Hexapeptides of consensus sequence YXCXXC displace four fluorine atoms from OFCP to generate fluorinated macrobicyclic compounds that display dual‐turn surfaces. The method provides facile access to a wide range of previously unknown heterocyclic structures." @default.
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- W4241817863 date "2019-11-20" @default.
- W4241817863 modified "2023-10-02" @default.
- W4241817863 title "Syntheses of Atypically Fluorinated Peptidyl Macrocycles through Sequential Vinylic Substitutions" @default.
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- W4241817863 doi "https://doi.org/10.1002/ange.201910136" @default.
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