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

Access to Document

10.1021/jo070502w

Cite this

@article{fcccfcaaf79646e6b437dde181d5b864,

title = "Synthesis of kaempferitrin",

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.",

author = "Sameer Urgaonkar and Shaw, {Jared T.}",

year = "2007",

month = jun,

day = "8",

doi = "10.1021/jo070502w",

language = "English (US)",

volume = "72",

pages = "4582--4585",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "12",

}

TY - JOUR

T1 - Synthesis of kaempferitrin

AU - Urgaonkar, Sameer

AU - Shaw, Jared T.

PY - 2007/6/8

Y1 - 2007/6/8

N2 - (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.

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.

UR - http://www.scopus.com/inward/record.url?scp=34250176869&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=34250176869&partnerID=8YFLogxK

U2 - 10.1021/jo070502w

DO - 10.1021/jo070502w

M3 - Article

C2 - 17497804

AN - SCOPUS:34250176869

VL - 72

SP - 4582

EP - 4585

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 12

ER -

Synthesis of kaempferitrin

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this