Department of Chemistry, Graduate School of Science, Osaka University , 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan.
J Org Chem. 2018 Jan 5;83(1):443-451. doi: 10.1021/acs.joc.7b02485. Epub 2017 Dec 26.
Poly-N-acetyllactosamine (poly-LacNAc) structures on glycoproteins play important roles in essential biological events such as cell-cell adhesion. Here, we report a new strategy for the semisynthesis of LacNAc-extended complex-type biantennary oligosaccharides. We found an efficient isopropylidenation reaction that selectively protects the terminal Gal-3,4-OH of a biantennary complex-type nonasaccharide isolated from a natural source. This finding enabled the conversion of the nonasaccharide into the two types of oligosaccharides containing di-LacNAc units at one or two antennae via ten-step chemical sequences.
糖蛋白上的多聚-N-乙酰乳糖胺(poly-LacNAc)结构在细胞-细胞黏附等重要的生物学事件中发挥着重要作用。在这里,我们报告了一种新的合成 LacNAc 延伸的复杂型双天线寡糖的半合成策略。我们发现了一种有效的异丙叉化反应,该反应可以选择性地保护从天然来源分离的双天线复杂型九糖中末端 Gal-3,4-OH。这一发现使我们能够通过十步化学序列将九糖转化为两种含有一个或两个天线中二聚体 LacNAc 单元的寡糖。