Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/8972
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dc.contributor.authorDubey, P K-
dc.contributor.authorNaidu, A-
dc.contributor.authorVijaya, S-
dc.contributor.authorVineel, B George-
dc.date.accessioned2010-05-14T11:34:01Z-
dc.date.available2010-05-14T11:34:01Z-
dc.date.issued2005-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8972-
dc.description573-576en_US
dc.description.abstractReactions of 2,3-dichloroquinoxaline 1 with various acid hydrazides 2 in acetonitrile under PTC conditions give the corresponding oxadiazinoquinoxalines 3, which on reaction with sodium alkoxides in alcohol yielded the respective ring opened products i.e. 2-acylhydrazino-3-alkoxyquioxalines 4. The compound 4 has been also synthesised from 2-acylhydrazino-3-chloroquinoxaline 5, which is obtained by the reaction of 1 with 2 in DMF at room temperature.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 215/00en_US
dc.sourceIJC-B Vol.44B(03) [March 2005]en_US
dc.titleFacile ring opening of 2-aryl[1,3,4]oxadiazino[5,6-b]quinoxalines with sodium alkoxidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(03) [March 2005]

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