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- W4250291473 abstract "A mild, practical, and simple procedure for peptide-bond formation is reported. Instead of activation of the carboxylic acid functionality, the reaction involves an unprecedented use of activated α-aminoesters. The method provides a straightforward entry to dipeptides and was effective when a sensitive cysteine residue was used, as no epimerization was detected in this case. The applicability of this method to iterative peptide synthesis was illustrated by the synthesis of a model tetrapeptide in the challenging reverse N→C direction." @default.
- W4250291473 created "2022-05-12" @default.
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- W4250291473 date "2014-04-24" @default.
- W4250291473 modified "2023-10-18" @default.
- W4250291473 title "Inverse Peptide Synthesis via Activated α-Aminoesters" @default.
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- W4250291473 doi "https://doi.org/10.1002/ange.201402147" @default.
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