作者:Kiran Bajaj、Rajeev Sakhuja
DOI:10.1002/asia.201700538
日期:2017.8.4
An efficient approach towards peptide synthesis that allows easy access to variety of small peptides via one-pot aziridine-mediated ligation/desulfurization strategy has been described. The protocol afforded a library of phenylalanine- and tryptophan-containing α-peptides in good yields by regioselective ring-opening of aziridine-3-aryl-2-carboxylates with peptide thioacids, followed by desulfurization
已经描述了一种有效的肽合成方法,该方法允许通过一锅氮丙啶介导的连接/脱硫策略轻松获得各种小肽。该方案通过用肽硫代酸对氮丙啶-3-芳基-2-羧酸酯的区域选择性开环,然后进行脱硫,以高收率提供了含苯丙氨酸和色氨酸的α-肽文库。