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Synthesis of cyclic peptides on solid support
Tetrahedron Letters ( IF 1.5 ) Pub Date : 3 June 1991 , DOI: 10.1016/s0040-4039(00)78806-x Paolo Rovero , Laura Quartara , Gaetano Fabbri
Tetrahedron Letters ( IF 1.5 ) Pub Date : 3 June 1991 , DOI: 10.1016/s0040-4039(00)78806-x Paolo Rovero , Laura Quartara , Gaetano Fabbri
We describe a general method for the solid-phase synthesis of cyclic peptides containing an Asp residue in their sequence. Boc-Asp-OFm is linked to PAM resin through the β-carboxylic function; the linear precursor is then assembled by classical Boc/Benzyl strategy. Cyclization is accomplished by the BOP method; HF deprotection and cleavage afford the cyclic peptide as a single product.
中文翻译:
在固体支持物上合成环肽
我们描述了一种固相合成环肽的常规方法,该环肽在其序列中包含一个Asp残基。Boc-Asp-OFm通过β-羧基官能团连接到PAM树脂上;然后通过经典的Boc / Benzyl策略组装线性前体。环化是通过BOP方法完成的;HF去保护和裂解得到环状肽,为单一产物。
更新日期:2017-01-31
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
在固体支持物上合成环肽
我们描述了一种固相合成环肽的常规方法,该环肽在其序列中包含一个Asp残基。Boc-Asp-OFm通过β-羧基官能团连接到PAM树脂上;然后通过经典的Boc / Benzyl策略组装线性前体。环化是通过BOP方法完成的;HF去保护和裂解得到环状肽,为单一产物。