Abstract
A versatile synthetic route to nonsulfated, as well as mono and disulfated glycohexaosyl serines that correspond to the linkage region of proteoglycans is developed by employing a glycotriaosyl donor and a glycotriaosyl acceptor Chemoselective removal of levuloyl groups among other ester groups without causing any acyl migration was carried out and subsequent regiospecific introduction of sulfate groups was achieved successfully. © 1993 IUPAC
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CITATION STYLE
Goto, F., Ogawa, T., & Ogawa, T. (1993). Recent aspects of glycoconjugate synthesis: A synthetic approach to the linkage region of proteoglycans*. Pure and Applied Chemistry, 65(4), 793–801. https://doi.org/10.1351/pac199365040793
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