Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16442
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dc.contributor.authorHossain, M Amzad-
dc.date.accessioned2013-03-23T12:59:28Z-
dc.date.available2013-03-23T12:59:28Z-
dc.date.issued1999-05-
dc.identifier.urihttp://hdl.handle.net/123456789/16442-
dc.description590-592en_US
dc.description.abstract5,7,4'-Trihydroxy-6-C-prenylflavone 6 isolated from the fruits of Maclura pomifera has been synthesized by the following route. Phloroacetophenone 1 on treatment with methoxymethyl chloride afford 2-hydroxy-4,6-di(methoxymethoxy) acetophenone 2 which on nuclear prenylation yield 2-hydroxy-4,6-di(methoxymethoxy)-5-C-prenylacetophenone 3 and several other minor products. The methoxymethylated product 3 on condensation with p-hyd roxybenzaldehyde gives the chalcone 4. DDQ (2,3 –dichloro-5, 6-dicyano-1,4-benzoquinone) treatment of 4 afford the compound 5 which upon demethoxymethylation furnish the title compound 6.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.38B(05) [May 1999]en_US
dc.titleSynthesis of 5,7,4'-trihydroxy-6-C-prenylflavoneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(05) [May 1999]

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