申请人:The Trustees of Princeton University
公开号:US11136349B2
公开(公告)日:2021-10-05
Synthetic methods are described herein operable to efficiently produce a wide variety of molecular species through conjugate additions via decarboxylative mechanisms. For example, methods of functionalization of peptide residues are described, including selective functionalization of peptide C-terminal residues. In one aspect, a method of peptide functionalization comprises providing a reaction mixture including a Michael acceptor and a peptide and coupling the Michael acceptor with the peptide via a mechanism including decarboxylation of a peptide reside.
本文介绍的合成方法可通过脱羧机制进行共轭添加,从而有效地生产多种分子物质。例如,描述了肽残基官能化的方法,包括肽 C 端残基的选择性官能化。在一个方面,肽官能化的方法包括提供包括迈克尔受体和肽的反应混合物,并通过包括肽残基脱羧的机制将迈克尔受体与肽偶联。