State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 132 Lanhei Road, Kunming, 650201, China.
Department of Chemistry, Kunming University, 2 Puxing Road, Kunming, 650214, China.
Angew Chem Int Ed Engl. 2020 May 4;59(19):7576-7584. doi: 10.1002/anie.202000992. Epub 2020 Mar 17.
The synthesis of long, branched, and complex carbohydrate sequences remains a challenging task in chemical synthesis. Reported here is an efficient and modular one-pot synthesis of a nona-decasaccharide and shorter sequences from Psidium guajava polysaccharides, which have the potent α-glucosidase inhibitory activity. The synthetic strategy features: 1) several one-pot glycosylation reactions on the basis of N-phenyltrifluoroacetimidate (PTFAI) and Yu glycosylation to streamline the chemical synthesis of oligosaccharides, 2) the successful and efficient assembly sequences (first O3', second O5', final O2') toward the challenging 2,3,5-branched Araf motif, 3) the stereoselective 1,2-cis-glucosylation by reagent control, and 4) the convergent [6+6+7] one-pot coupling reaction for the final assembly of the target nona-decasaccharide. This orthogonal one-pot glycosylation strategy can streamline the chemical synthesis of long, branched, and complicated carbohydrate chains.
长链、支链和复杂碳水化合物序列的合成仍然是化学合成中的一项具有挑战性的任务。本文报道了一种从番石榴多糖中高效、模块化一锅法合成九糖和较短序列的方法,这些多糖具有很强的α-葡萄糖苷酶抑制活性。该合成策略的特点是:1)基于 N-苯基亚磺酰基氟代乙酰胺(PTFAI)和 Yu 糖苷化的几种一锅糖苷化反应,以简化寡糖的化学合成,2)成功高效的组装序列(先 O3',后 O5',最后 O2'),用于构建具有挑战性的 2,3,5-三分支阿拉伯糖基序,3)通过试剂控制实现立体选择性 1,2-顺式-葡萄糖基化,以及 4)用于目标九糖最终组装的收敛式 [6+6+7] 一锅偶联反应。这种正交一锅法糖苷化策略可以简化长链、支链和复杂碳水化合物链的化学合成。