Smerdka Joachim, Rademann Jörg, Jung Günther
Institute of Organic Chemistry, University of Tübingen, 72076 Tübingen, Germany.
J Pept Sci. 2004 Oct;10(10):603-11. doi: 10.1002/psc.581.
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.
一种用于氨基酸和肽衍生物的聚合物辅助溶液相(PASP)酯化的新型工具已被开发出来。当与羧酸处理时,聚合物结合的烷基三氮烯会发生氮的损失,并将烷基部分转移到羧酸根阴离子上,形成相应的烷基酯。对于保护基团或氨基酸的性质没有限制。此外,如手性气相色谱 - 质谱分析所示,氨基酸的手性中心不会发生外消旋化。烷基三氮烯树脂也成功应用于肽酸和其他肽结构的酯化,如三棕榈酰 - S - 甘油基 - 半胱氨酸(Pam3Cys)。三氮烯介导的酯化反应异常温和,无需预先活化羧基。因此,该方法特别适用于易于外消旋化的复杂拟肽结构的烷基化以及对酸敏感的结构。