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dc.contributor.authorLang'at-Thoruwa, C.
dc.contributor.authorSong, T.T.
dc.contributor.authorHu, J.
dc.contributor.authorSimon, A.L.
dc.contributor.authorMurphy, P.A.
dc.date.accessioned2016-02-16T08:48:41Z
dc.date.available2016-02-16T08:48:41Z
dc.date.issued2003
dc.identifier.citationJ Nat Prod. 2003 Jan;66(1):149-51en_US
dc.identifier.issn0974-5211
dc.identifier.urihttp://ir-library.ku.ac.ke/handle/123456789/14187
dc.descriptionResearch Articleen_US
dc.description.abstract4-Methoxyresorcinol (3) was synthesized as the precursor for glycitein (6) synthesis by the oxidation of 3-hydroxy-4-methoxybenzaldehyde (1) to the aryl formate with H2O2 and a catalytic amount of SeO2. Glycitein (6) was synthesized by cyclization of 2,4,4'-trihydroxy-5-methoxydeoxybenzoin (5) with N,N-dimethylformamide, boron trifluoride diethyl ether, and methanesulfonyl chloride in a microwave oven.en_US
dc.language.isoenen_US
dc.publisherJournal of Natural Productsen_US
dc.titleA simple synthesis of 7,4'-dihydroxy-6-methoxyisoflavone, glycitein, the third soybean isoflavone.en_US
dc.typeArticleen_US


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