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Sequential native chemical ligation utilizing peptide thioacids derived from newly developed Fmoc-based synthetic method

机译:利用新开发的基于Fmoc的合成方法衍生的肽硫代酸进行顺序天然化学连接

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摘要

The first facile Fmoc-based synthetic procedure for peptide thioacids was developed. Successful application of the resulting thioacids to sequential native chemical ligation (NCL) in the N to C direction was achieved. Conversion of the peptide thioacids to the corresponding thioesters with Ellman’s reagent followed by NCL in the presence of tris(2-carboxyethyl)phosphine (TCEP) and thiophenol was accomplished in a one-pot manner
机译:开发了第一个简便的基于Fmoc的肽硫代酸合成方法。成功地将所得的硫代酸成功应用于从N到C的顺序自然化学连接(NCL)。在三(2-羧乙基)膦(TCEP)和苯硫酚的存在下,使用Ellman试剂和NCL将肽硫酸酸转化为相应的硫酯,以一锅法完成

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