期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 72, 期 12, 页码 4582-4585出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo070502w
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资金
- NIAID NIH HHS [R03 AI062905-01] Funding Source: Medline
- NIGMS NIH HHS [P50 GM069721] Funding Source: Medline
A short synthesis of Kaempferitrin (1), a 3,7-diglycosylflavone, is reported. Key features include the synthesis of a protected form of kaempferol in which all four hydroxy groups are differentiated and the first bis-glycosylation of a dihydroxyflavone. This synthesis will allow the preparation of derivatives for further explorations into the origins of this compound's biological activity.
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