Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/8966
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dc.contributor.authorVenkati, M-
dc.contributor.authorKrupadanam, G L David-
dc.date.accessioned2010-05-14T11:30:06Z-
dc.date.available2010-05-14T11:30:06Z-
dc.date.issued2005-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8966-
dc.description618-621en_US
dc.description.abstract-Alkyl chalcones 3a-d on acid catalyzed cyclization give a mixture of (±) trans and (±) cis 2-aryl-3-alkylchroman-4-ones. cis 4a-d are converted to trans 5a-d by epimerization with dil. alkali. a-Aryl chalcones 3e-h on acid catalyzed cyclization give (±) trans 2,3-diaryl-chroman-4-ones 5e-h. On NaBH4 reduction 5a-h give (±) 2,3-trans-3,4-trans-2-aryl-3-alkyl/aryl- chroman-4-ols 6a-h.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 311/30en_US
dc.sourceIJC-B Vol.44B(03) [March 2005]en_US
dc.titleSynthesis of 2,3-trans-3,4-trans-2-aryl-3-alkyl/aryl chroman-4-olsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(03) [March 2005]

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