Macrocyclization of Organo-Peptide Hybrids through a Dual Bio-orthogonal Ligation: Insights from Structure-Reactivity Studies
作者:John R. Frost、Francesca Vitali、Nicholas T. Jacob、Micah D. Brown、Rudi Fasan
DOI:10.1002/cbic.201200579
日期:2013.1.2
Hybrid macrocycles: A novel chemo‐biosynthetic strategy for the synthesis of cyclic organo‐peptides was shown to be remarkably tolerant of structural variations in both the genetically encoded (black) and synthetic (blue) precursor molecules, thus allowing the efficient construction of functionally and topologically diverse macrocycles. The mechanism underlying the macrocyclization reaction was also
杂合大环化合物:合成环状有机肽的新型化学生物合成策略显示出对遗传编码的(黑色)和合成的(蓝色)前体分子的结构变异具有显着的耐受性,因此可以有效地构建功能性和拓扑多样化的大环。还阐明了大环化反应的基础机理。