Sano Kanae, Ishiwata Akihiro, Takamori Hiroto, Kikuma Takashi, Tanaka Katsunori, Ito Yukishige, Takeda Yoichi
Department of Biotechnology, College of Life Sciences, Ritsumeikan University, Kusatsu 525-8577, Japan.
RIKEN Cluster for Pioneering Research, Wako 351-0198, Japan.
Molecules. 2024 Apr 13;29(8):1771. doi: 10.3390/molecules29081771.
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.
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。