Polymer‐bound alkyltriazenes for mild racemization‐free esterification of amino acid and peptide derivatives

Abstract

A novel tool for polymer-assisted solution phase (PASP) esterification of amino acid and peptide derivatives has been developed. When treated with carboxylic acids, polymer-bound alkyltriazenes react with a loss of nitrogen and transfer of the alkyl moiety to the carboxylate anion to form the corresponding alkyl esters. There are no limitations with regard to either the protecting groups or the nature of the amino acid. Furthermore no racemization occurs at the chiral centers of the amino acids as demonstrated by chiral GC-MS analyses. Alkyltriazene-resins were also applied successfully to the esterification of peptide acids and other peptidic structures, such as tripalmitoyl-S-glyceryl-cysteine (Pam3Cys). The triazene-mediated esterification reaction is exceptionally mild, and there is no need for prior activation of the carboxy groups. This method is therefore particularly suitable for the alkylation of complex peptidomimetic structures prone to racemization and for acid-sensitive structures.

Anti-cancerous/Anti-bacterial Activities of Allicin Generated In situ from Diastereo Pure Alliins by Alliinase

“…(+)-DL-alliin methyl ester was synthesized by mixing (+) alliin with anhydrous methanol in acidic conditions. The (+)-alliin methyl ester produced contains both (+)-L-alliin methyl ester (7) and (+)-D-alliin methyl ester (8) due to racemization [51,52]. Instead of fractional crystallization in 95% ethanol, RP-HPLC is used to purify compounds 6 and (+)-DL-alliin methyl ester.…”