Toward fully synthetic glycoproteins by ultimately convergent routes: A solution to a long-standing problem

被引:195
作者
Warren, JD
Miller, JS
Keding, SJ
Danishefsky, SJ
机构
[1] Sloan Kettering Inst Canc Res, Bioorgan Chem Lab, New York, NY 10021 USA
[2] Columbia Univ, Dept Chem, New York, NY 10027 USA
关键词
D O I
10.1021/ja0491836
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A method is disclosed for the convergent synthesis of multiply glycosylated peptides. The approach centers on a convergent technique for generating masked, complex glycopeptide-containing C-terminal acyl donors. Activation of the latent donor in situ and use directly in segment coupling with a second peptide bearing a complex carbohydrate produces a completely unprotected, bifunctional glycopeptide. The system demonstrates a minimum level of hydrolysis and epimerization at the C-terminal amino acid residue of the acyl donor during fully convergent segment coupling and is therefore a powerful tool for the synthesis of glycoproteins. Copyright © 2004 American Chemical Society.
引用
收藏
页码:6576 / 6578
页数:3
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