Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/21818
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAhmed, M G-
dc.contributor.authorAhmed, S A-
dc.contributor.authorRomman, U K R-
dc.contributor.authorSultana, T-
dc.contributor.authorHena, M A-
dc.contributor.authorKiyooka, S-
dc.date.accessioned2013-10-10T10:44:27Z-
dc.date.available2013-10-10T10:44:27Z-
dc.date.issued2002-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21818-
dc.description368-371en_US
dc.description.abstractAnhydrous zinc chloride catalysed reactions of arylideneacetophenones 2a-c give 2, 4-diaryl-5-oxo-5, 6, 7, 8-tetrahydro-2-chromens 4a-c with 1, 3-cyclohexanedione. Under similar conditions arylideneacetophenones 2a-b and 2d-f react with 5, 5-dimethyl-1, 3- cyclohexanedione (dimedone) yielding 7, 7-dimethyl- 2, 4-diaryl-5-oxo-5, 6, 7, 8- tetrahydro-2-chromens 4d -h.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.41B(02) [February 2002]en_US
dc.titleA convenient one pot synthesis 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.41B(02) [February 2002]

Files in This Item:
File Description SizeFormat 
IJCB 41B(2) 368-371.pdf789.79 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.