期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 127, 期 11, 页码 3767-3773出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja045613g
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A novel flexible assembly strategy is described for the modular synthesis of heparin and heparan sulfates. The reported strategy uses monomeric building bocks to construct the oligosaccharide chain to attain a maximum degree of flexibility. In the assembly, 1-hydroxyl glucosazido- and 1-thio uronic acid donors are combined in a sequential glycosylation protocol using sulfonium triflate activator systems. The key 1-thio uronic acids were obtained in an efficient manner from diacetone glucose employing a chemo- and regioselective oxidation of partially protected glucose and idose thioglycosides.
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