选择性保护原叶香素衍生物的制备,用于合成叶香素类似物和新糖缀合物

K. Jatczak, Mariusz M. Gruza, Katarzyna Filip, P. Cmoch, G. Grynkiewicz
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引用次数: 2

摘要

选择七叶树皂苷混合物的主要苷元原叶esenin作为底物,进行选择性保护的化学探索,然后通过丙炔醚形成,随后与叠氮单糖缩合,得到新的三萜三唑缀合物。
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Preparation of selectively protected protoescigenin derivatives for synthesis of escin analogs and neoglycoconjugates
Protoescigenin, the main aglycone of horse chestnut saponin mixture known as escin, was selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene.
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