Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/8969
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dc.contributor.authorAhmed, M Giasuddin-
dc.contributor.authorAhmed, Syeda Asghari-
dc.contributor.authorRomman, U K R-
dc.contributor.authorTouchy, A Sultana-
dc.contributor.authorBadal, Mizanur Rahman-
dc.contributor.authorHossain, Mohammad Awlad-
dc.contributor.authorUddin, Md Khabir-
dc.date.accessioned2010-05-14T11:31:06Z-
dc.date.available2010-05-14T11:31:06Z-
dc.date.issued2005-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8969-
dc.description622-624en_US
dc.description.abstractAnhydrous zinc chloride catalysed reactions of arylidene­acetophenones 2a and 2c-e give 2, 4-diaryl-5-oxo-5,6,7,8-tetra­hydro-2-chromens 4a-d with 1,3-cyclohexanedione respectively. Under similar conditions arylideneacetophenones 2b, 2d and 2f react with 5,5-dimethyl-1,3-cyclohexanedione (dimedone) to yield 7,7-dimethyl-2,4-diaryl-5-oxo-5,6,7,8-tetrahydro-2-chromens 4e-g.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 311/00en_US
dc.sourceIJC-B Vol.44B(03) [March 2005]en_US
dc.titleSynthesis of substituted and unsubstituted 2,4-diaryl-5-oxo-5,6,7,8-tetrahydro-2-chromensen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(03) [March 2005]

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