作者:Delphine Valognes、Philippe Belmont、Ning Xi、Marco A Ciufolini
DOI:10.1016/s0040-4039(01)00080-6
日期:2001.3
The synthesis of luzopeptin C has been accomplished by self-assembly of the macrocycle via activation of a pentapeptide monomer. The present work underscores the generality of the spontaneous macrocyclization approach to the peptins, a strategy introduced by us in connection with the synthesis of luzopeptin E2.
Luzopeptin C的合成已通过五肽单体的活化通过大环的自组装完成。目前的工作强调了自发性大环肽化方法对肽类的普遍性,这是我们在合成luzopeptin E2时引入的一种策略。