Arginine thioacid in synthesis of arginine conjugates and peptides

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    6 Scopus citations

    Abstract

    Protected arginine thioacid enables convenient N-acylation with no detectable racemization. We report efficient syntheses of potentially biologically active arginine conjugates and novel arginine-containing di-, tri- and tetrapeptides in good yields without loss of chiral integrity. This journal is

    Original languageEnglish (US)
    Pages (from-to)55210-55216
    Number of pages7
    JournalRSC Advances
    Volume4
    Issue number98
    DOIs
    StatePublished - 2014

    ASJC Scopus subject areas

    • General Chemical Engineering
    • General Chemistry

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