期刊
POLYMER CHEMISTRY
卷 2, 期 4, 页码 805-811出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0py00412j
关键词
-
资金
- CSIR, New Delhi
- CSIR [NWP0051-C]
- DST, New Delhi
The novel synthesis of O-glycosylated lysine-NCA from a stable glycosyl donor and a commercially available protected amino acid in very high yield is reported. These O-glycosylated lysine-NCA monomers underwent ring opening polymerization using simple primary amine initiators to form well defined, high molecular weight homoglycopolypeptides and diblock co-glycopolypeptides. The synthesis of azide labelled end functionalized glycopolypeptides and amphiphilic diblock copolypeptides is also reported. This methodology represents an easy and practical route to the synthesis of O-glycosylated polypeptides with 100% glycosylation.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据