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dc.contributor.authorMishra, Bijaya K-
dc.contributor.authorPatel, Namita-
dc.contributor.authorHota, (Mrs) Satya P-
dc.contributor.authorBehera, Gopa B-
dc.date.accessioned2014-01-24T09:41:50Z-
dc.date.available2014-01-24T09:41:50Z-
dc.date.issued2000-07-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/26057-
dc.description721-727en_US
dc.description.abstractNucleophilic reaction at azomethine center of 2-/4-hydroxybenzylidene-2-aminobenzothiozole by aniline has been investigated in sodium Iauryl sulphate(NaLS)- isobutanol-chloroform-water microemulsion media. The role of hydroxy group at ortho and para positions in the benzene nucleus on the reaction mechanism has been analyzed. The entrapment of aniline by the reacting substrate gets support from the reaction kinetics.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-A Vol.39A(07) [July 2000]en_US
dc.titleReactivity of schiff base, Part-4 : Reaction of 2-/4-hydroxybenzylidene-2- aminobenzothiazole with aniline in microemulsionen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.39A(07) [July 2000]

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