Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16451
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dc.contributor.authorBhatt, Akhil H-
dc.contributor.authorParikh, Khyati A-
dc.contributor.authorParikh, A R-
dc.date.accessioned2013-03-24T12:53:51Z-
dc.date.available2013-03-24T12:53:51Z-
dc.date.issued1999-05-
dc.identifier.urihttp://hdl.handle.net/123456789/16451-
dc.description628-631en_US
dc.description.abstract4-Aminobe nzophenone 1 on condensation with different aralclehydes yield schiff's bases 2a-o which on cyclization with mercapto acetic acid afford the corresponding 4-(5'H-2'aryl-4'thiazolidinon-3'-yl)-benzophenones 3a-o. While cyclocondensation of 1 with various azlactones yield 4-(4'-aryl idene-2'-phenyl- 5'-oxo-imidazolin-1'-yl )benzophenones 4a-m. The structure of the compounds have been confirmed from elemental analysis, IR , 1H NMR and mass spectral data. All the compounds have been evaluated in vitro for antimicrobial and antimycobacterial activities.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 some thiazolidinones and 5-oxoimidazolines as biologically potent agentsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(05) [May 1999]

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