作者:Qingjie Zhao、Xiang Li、Wenjuan Li、Yan Zou、Honggang Hu、Qiuye Wu
DOI:10.1016/j.tet.2014.12.097
日期:2015.2
An efficient and practical method for macrocyclic lipoglycopeptide synthesis was developed and utilized to synthesize lipoglycosylated derivatives of Tyrocidine A. The method is based on solid-phase peptide synthesis using 2-chlorotrityl resin as the solid-phase support and lipoglycosyl amino acids as building blocks. This synthetic method should be generally applicable to various macrocyclic lipoglycopeptides
开发了一种有效且实用的大环脂糖肽合成方法,并用于合成酪氨酸A的脂糖基化衍生物。该方法基于固相肽合成,使用2-氯三苯甲基树脂作为固相载体,脂糖基氨基酸作为构建基。该合成方法通常应适用于各种大环脂糖肽。