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J Org Chem ; 89(12): 9098-9102, 2024 Jun 21.
Article in English | MEDLINE | ID: mdl-38861461

ABSTRACT

We report the first total synthesis of scleropentaside D, a unique C-glycosidic ellagitannin, from the ketal derivative of scleropentaside A employing site-selective O4-protection of C-acyl glycoside and copper-catalyzed oxidative coupling reaction of galloyl groups as the key steps. Our study confirms the proposed structure of this natural product, scleropentaside D, and demonstrates its effectiveness as an inhibitor of α-glycosidase.


Subject(s)
Hydrolyzable Tannins , Hydrolyzable Tannins/chemistry , Hydrolyzable Tannins/pharmacology , Hydrolyzable Tannins/chemical synthesis , Molecular Structure , Glycosides/chemistry , Glycosides/chemical synthesis , Glycosides/pharmacology , Glycoside Hydrolases/antagonists & inhibitors , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Enzyme Inhibitors/chemistry , Catalysis
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