Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/21302
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dc.contributor.authorPandey, V K-
dc.contributor.authorSaxena, S K-
dc.contributor.authorJoshi, M N-
dc.contributor.authorBajpai, S K-
dc.date.accessioned2013-09-23T05:00:17Z-
dc.date.available2013-09-23T05:00:17Z-
dc.date.issued2004-05-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21302-
dc.description1015-1017en_US
dc.description.abstractHydroquinone on reaction with amido alcohols 1 in the presence of conc. H2SO4 gives 2-arylamidolimidoalkyl-1,4-dihydroxybenzenes 2 which undergo cyclization with aromatic primary amine and sulphur in the presence of iodine to yield 2-arylamidoli midoalkyl-10H-phenothiazin-3-ols 3. Compounds 3 are further substituted to 2-arylamido/imidoalkyl-10-[(4-methoxyphenyl/phenyl) phenylamino-methyl]-10H-phenothiazin-3-ols 4.Compounds 4 have been screened for their antiviral activity against Japanese encephalitis virus (JEV) and Herpes simplex virus type-I (HSV-I).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D279/00 en_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.43B(05) [May 2004]en_US
dc.titleSynthesis and antiviral activity of some novel substituted phenothiazinesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.43B(05) [May 2004]

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