Downey A Michael, Hocek Michal
Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Flemingovo nam. 2, 16610 Prague 6, Czech Republic.
Department of Organic Chemistry, Faculty of Science, Charles University in Prague, 12843 Prague 2, Czech Republic.
Beilstein J Org Chem. 2017 Jun 27;13:1239-1279. doi: 10.3762/bjoc.13.123. eCollection 2017.
Glycosylation is an immensely important biological process and one that is highly controlled and very efficient in nature. However, in a chemical laboratory the process is much more challenging and usually requires the extensive use of protecting groups to squelch reactivity at undesired reactive moieties. Nonetheless, by taking advantage of the differential reactivity of the anomeric center, a selective activation at this position is possible. As a result, protecting group-free strategies to effect glycosylations are available thanks to the tremendous efforts of many research groups. In this review, we showcase the methods available for the selective activation of the anomeric center on the glycosyl donor and the mechanisms by which the glycosylation reactions take place to illustrate the power these techniques.
糖基化是一个极其重要的生物过程,在自然界中受到高度控制且效率极高。然而,在化学实验室中,这个过程更具挑战性,通常需要大量使用保护基团来抑制不期望的反应性部分的反应活性。尽管如此,通过利用异头中心的差异反应性,在该位置进行选择性活化是可能的。因此,由于许多研究小组的巨大努力,现在有了无需保护基团的糖基化策略。在这篇综述中,我们展示了用于糖基供体上异头中心选择性活化的可用方法以及糖基化反应发生的机制,以说明这些技术的强大之处。