The invention relates to methods for the preparation of peptides which are a C-terminal amide derivatives by a combination of solid-phase synthesis and post assembly solution phase synthesis. The peptides which are a C-terminal amide derivatives are further converted to peptide acetates. The invention also relates to pure peptide acetates and to protected peptide precursors.
这项发明涉及一种通过固相合成和后组装溶液相合成相结合的方法制备C-末端酰胺衍
生物的肽。这些C-末端酰胺衍
生物的肽进一步转化为肽
醋酸酯。该发明还涉及纯肽
醋酸酯和受保护的肽前体。