Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16439
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dc.contributor.authorHossain, M Amzad-
dc.contributor.authorSalehuddin, S M-
dc.date.accessioned2013-03-23T12:56:20Z-
dc.date.available2013-03-23T12:56:20Z-
dc.date.issued1999-05-
dc.identifier.urihttp://hdl.handle.net/123456789/16439-
dc.description593-595en_US
dc.description.abstractThe synthesis of flavanone A 8, a constituent of the leaves and bark of Milletia ovalifolia is described. β-Resacetophenone 1 on treatment with methoxymethyl chloride afford 2,4-dimethoxymcthoxyacctophenone 2 which on nuclear prenylation yield 2,4- dimethoxymcthoxy-3 ,5-di-C-prenylacetophenone 5. Alkaline condensation of 5 with benzaldehyde give 2',4'-dimethoxymethox y-3',5' -di-C-prenylchalcone 6. 2',4'-Dihydroxy-3',5'-di–C-prenylchalcone 7 obtained by the demethoxymethylation of 6, on treatment with NaOAc/EtOH furnish 7-hydroxy-6,8-di-C-prenylflavanone (8, flavanone A).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 7-hydroxy-6,8-di-C-prenylflavanoneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(05) [May 1999]

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