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从沉香中分离得到的沉香苷通过黄烷的5-O-糖基化进行全合成。

Total synthesis of agalloside, isolated from Aquilaria agallocha, by the 5-O-glycosylation of flavan.

作者信息

Arai Midori A, Yamaguchi Yumi, Ishibashi Masami

机构信息

Department of Natural Product Chemistry, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8675, Japan.

出版信息

Org Biomol Chem. 2017 Jun 14;15(23):5025-5032. doi: 10.1039/c7ob01004d.

Abstract

Agalloside (1) is a neural stem cell differentiation activator isolated from Aquilaria agallocha by our group using Hes1 immobilized beads. We conducted the first total synthesis of agalloside (1) via the 5-O-glycosylation of flavan 25 using glycosyl fluoride 20 in the presence of BF·EtO. Subsequent oxidation with DDQ to flavanone 2 and deprotection successively provided agalloside (1). This synthetic strategy holds promise for use in the synthesis of 5-O-glycosylated flavonoids. The synthesized agalloside (1) accelerated neural stem cell differentiation, which is a result comparable to that for the naturally occurring compound 1.

摘要

沉香苷(1)是我们团队利用固定有Hes1的珠子从沉香中分离得到的一种神经干细胞分化激活剂。我们通过在BF·EtO存在下使用糖基氟化物20对黄烷25进行5-O-糖基化反应,首次全合成了沉香苷(1)。随后用DDQ将其氧化为黄烷酮2,并依次进行脱保护反应,从而得到沉香苷(1)。这种合成策略有望用于5-O-糖基化黄酮类化合物的合成。合成得到的沉香苷(1)能加速神经干细胞分化,这一结果与天然化合物1相当。

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