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通过分子内糖苷配基传递合成蔗糖模拟二糖。

Synthesis of Sucrose-Mimicking Disaccharide by Intramolecular Aglycone Delivery.

作者信息

Sano Kanae, Ishiwata Akihiro, Takamori Hiroto, Kikuma Takashi, Tanaka Katsunori, Ito Yukishige, Takeda Yoichi

机构信息

Department of Biotechnology, College of Life Sciences, Ritsumeikan University, Kusatsu 525-8577, Japan.

RIKEN Cluster for Pioneering Research, Wako 351-0198, Japan.

出版信息

Molecules. 2024 Apr 13;29(8):1771. doi: 10.3390/molecules29081771.

Abstract

Rare sugars are known for their ability to suppress postprandial blood glucose levels. Therefore, oligosaccharides and disaccharides derived from rare sugars could potentially serve as functional sweeteners. A disaccharide [α-d-allopyranosyl-(1→2)-β-d-psicofuranoside] mimicking sucrose was synthesized from rare monosaccharides D-allose and D-psicose. Glycosylation using the intermolecular aglycon delivery (IAD) method was employed to selectively form 1,2- α-glycosidic linkages of the allopyranose residues. Moreover, β-selective psicofuranosylation was performed using a psicofuranosyl acceptor with 1,3,4,6-tetra--benzoyl groups. This is the first report on the synthesis of non-reducing disaccharides comprising only rare d-sugars by IAD using protected ketose as a unique acceptor; additionally, this approach is expected to be applicable to the synthesis of functional sweeteners.

摘要

稀有糖以其抑制餐后血糖水平的能力而闻名。因此,源自稀有糖的寡糖和二糖有可能用作功能性甜味剂。由稀有单糖D-阿洛糖和D-阿洛酮糖合成了一种模拟蔗糖的二糖[α-D-阿洛吡喃糖基-(1→2)-β-D-阿洛呋喃糖苷]。采用分子间苷元传递(IAD)方法进行糖基化,以选择性地形成阿洛吡喃糖残基的1,2-α-糖苷键。此外,使用具有1,3,4,6-四苯甲酰基的阿洛呋喃糖受体进行β-选择性阿洛呋喃糖基化。这是关于使用受保护的酮糖作为唯一受体通过IAD合成仅包含稀有D-糖的非还原性二糖的首次报道;此外,该方法有望应用于功能性甜味剂的合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f753/11051705/c3c6bc5b04a7/molecules-29-01771-g001.jpg

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