Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16673
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSuma, S-
dc.contributor.authorAsokan, C V-
dc.date.accessioned2013-03-30T17:25:50Z-
dc.date.available2013-03-30T17:25:50Z-
dc.date.issued1999-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/16673-
dc.description1338-1341en_US
dc.description.abstractThe reaction of six membered cyclic ketones such as cyclohexanones and tetralones with arylisothiocyanates in the presence of sodium hydride in DMF undergo oxidative cyclisation to give benzothiazole substituted phenols and naphtholsen_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(12) December 1999]en_US
dc.titleOxidative cyclisations of β-oxo-N-arylthioamides to substituted benzothiazolesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(12) December 1999]

Files in This Item:
File Description SizeFormat 
IJCB 38B(12) 1338-1341.pdf834.81 kBAdobe PDFView/Open


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