Disclosed are compounds and methods for highly effective chemoselective peptide cyclization and bicyclization directly on unprotected peptides and other compounds as well as the compounds produced by the methods, which have a novel structural motif. The fast reaction rate and operational simplicity render this method to be highly effective to synthesize cyclic structures, i.e. cyclic peptides. The cyclic compounds allow for various functionalities useful in chemical biology study and drug discovery.
揭示了一种化合物和方法,用于在未保护的肽和其他化合物上实现高效的
化学选择性肽环化和双环化,以及通过这些方法产生的化合物,具有新颖的结构基元。快速的反应速率和操作简单性使得这种方法非常有效,可用于合成环结构,即环肽。这些环化合物允许在
化学生物学研究和药物发现中使用各种有用的功能。