Synthesis of kaempferitrin

Sameer Urgaonkar; Jared T. Shaw

doi:10.1021/jo070502w

Synthesis of kaempferitrin

Sameer Urgaonkar, Jared T. Shaw

Chemistry

Research output: Contribution to journal › Article › peer-review

33 Scopus citations

Abstract

(Chemical Equation Presented) 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.

Original language	English (US)
Pages (from-to)	4582-4585
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	72
Issue number	12
DOIs	https://doi.org/10.1021/jo070502w
State	Published - Jun 8 2007

ASJC Scopus subject areas

Organic Chemistry

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abstract = "(Chemical Equation Presented) 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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AB - (Chemical Equation Presented) 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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Synthesis of kaempferitrin

Abstract

ASJC Scopus subject areas

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