Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9225
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dc.contributor.authorKanwar, Seema-
dc.contributor.authorSharma, S D-
dc.date.accessioned2010-06-01T04:54:51Z-
dc.date.available2010-06-01T04:54:51Z-
dc.date.issued2005-11-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9225-
dc.description2367-2371en_US
dc.description.abstractA Facile and efficient method for the synthesis of 4-hetryl substituted -lactams 1 have been reported from substituted thienopyrimidinone 2b, which in turn was prepared from appropriately substituted 2-amino-3-carboxamido thiophene 10. The structures of newly synthesized compounds have been established through spectral and analytical analysis.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.44B(11) [November 2005]en_US
dc.subjectThienopyrimidinoneen_US
dc.subjectazetidinoneen_US
dc.subject5-HT1Aen_US
dc.subjectβ-lactamen_US
dc.subjecttherapeutic agentsen_US
dc.titleThienopyrimidines as hetryl moiety in 2-azetidinones: Synthesis of 4-hetryl-2-azetidinonesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(11) [November 2005]

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