Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/10571
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dc.contributor.authorSangeetha, V-
dc.contributor.authorPrasad, K J Rajendra-
dc.date.accessioned2010-11-11T06:10:27Z-
dc.date.available2010-11-11T06:10:27Z-
dc.date.issued2006-04-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/10571-
dc.description1028-1033en_US
dc.description.abstractTr eatment of 2-hydro xyme thylene-1-oxo-1, 2,3, 4- tetrahydrocarbazoles 1a-d with guanidine nitrate affords 2-amino- 4-hydroxy-1,4,5,6-tetrahydropyrimido[4,5- ]carbazoles 2a-d. In anothe r re ac tion, 2-hydro xyme thylene-1-oxo-1, 2,3, 4- tetrahydroc arbazoles 1a-d are treated with diazotized -toluidine under Japp-Klingemann conditions to furnish the respec ve 4'-methyl-1-oxo-2-phenylhydrazono-1,2,3,4-tetrahydrocarbazoles 3a-d, which upon cyclisation using Kent’s reagent (CH3COOH : HCl, 4:1) yield the corresponding 6,12-dihydro-2-methy xobisindolo[ 1,2- :5,4-b' ]cyclohexanones 5a-d.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.45B(04) [April 2006]en_US
dc.subjectTetrahydrocarbazolesen_US
dc.subjectcyclohexanonesen_US
dc.subjectguanidine nitrateen_US
dc.subjectJapp-Klingemann conditionsen_US
dc.subjectcyclisationen_US
dc.subjectKent' s reagenten_US
dc.titleSynthesis of pyrimido annelatedcarbazoles and 2-methyl-6-oxo-bisindolo[1,2-b :5,4-b' ] cyclohexanones using 2-hydroxymethylene-1-oxo-1,2,3,4-tetrahydrocarbazolesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(04) [April 2006]

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