Breipohl G, Knolle J, Stüber W
Hoechst AG, Frankfurt am Main.
Int J Pept Protein Res. 1990 Mar;35(3):281-3. doi: 10.1111/j.1399-3011.1990.tb00949.x.
Attachment of Fmoc-asparagine or glutamine to p-alkoxybenzyl alcohol type resins has always been difficult and not very effective. A very simple and effective method for the preparation of peptides terminating in asparagine or glutamine is described. The method involves quantitative attachment of Fmoc-Asp-OtBu or Fmoc-Glu-OtBu via their side-chain carboxyl group to a resin functionalized with our TMBPA linker for peptide amides. Peptide synthesis is performed using our standard Fmoc chemistry, and treatment with acid, e.g. TFA/DCM/scavenger mixtures, releases the Asn or Gln peptides.
将Fmoc-天冬酰胺或谷氨酰胺连接到对烷氧基苄醇型树脂上一直都很困难且效率不高。本文描述了一种非常简单有效的制备以天冬酰胺或谷氨酰胺结尾的肽的方法。该方法包括通过其侧链羧基将Fmoc-Asp-OtBu或Fmoc-Glu-OtBu定量连接到用我们的用于肽酰胺的TMBPA接头功能化的树脂上。使用我们的标准Fmoc化学方法进行肽合成,并用酸(例如TFA/DCM/清除剂混合物)处理,可释放出Asn或Gln肽。