The first total synthesis of 7-O-β-d-glucopyranosyl-4′-O-α-l-rhamnopyranosyl apigenin via a hexanoyl ester-based protection strategy

Carbohydrate Research

Volumn 344, Issue 4, 2009, Pages 511-515

  Gao, Qi ^a   Lian, Gaoyan ^b   Lin, Feng ^a  

^a SHANGHAI INSTITUTE OF PHARMACEUTICAL INDUSTRY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Flavonoid glycoside; Glycosylation; Hexanoyl; Total synthesis

Indexed keywords

FLAVONOID; FLAVONOID GLYCOSIDE; FLAVONOIDS; HEPATITIS B VIRUS; HEXANOYL; PROTECTION STRATEGIES; SELECTIVE PROTECTIONS; SYNTHETIC ROUTES; SYNTHETIC STRATEGIES; TOTAL SYNTHESIS;

ESTERS; GLYCOSYLATION; SUGARS;

ESTERIFICATION;

7 O BETA DEXTRO GLUCOPYRANOSYL 4' O ALPHA RHAMNOPYRANOSYL APIGENIN; ANTIVIRUS AGENT; APIGENIN; ESTER; FLAVONOID; UNCLASSIFIED DRUG;

ANTIVIRAL ACTIVITY; ARTICLE; DRUG ACTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; GLYCOSYLATION; PRIORITY JOURNAL;

APIGENIN; FLAVONOIDS; GLYCOSIDES; GLYCOSYLATION; MODELS, CHEMICAL; MOLECULAR STRUCTURE;

HEPATITIS B VIRUS;

EID: 60849097820     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2008.12.016     Document Type: Article

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