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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4938
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dc.contributor.authorManjunath, SY
dc.contributor.authorBiradar, JS
dc.contributor.authorBasawaraj, R
dc.date.accessioned2020-06-12T15:05:43Z-
dc.date.available2020-06-12T15:05:43Z-
dc.date.issued2009
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 18 , 4 , p. 321 - 324en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4938-
dc.description.abstractEthyl 5-substituted-3-phenylindol-2-carboxylates (1a-d) were converted to 5-substituted-3-phenylindol-2-carbohydrazides (2a-d), by treating with hydrazine hydrate. Carbohydrazides 2 on reaction with carbon disulphide and potassium hydroxide yielded 5-substituted-3-phenyl-2-(5'-mercapto-1',3',4'-oxadiazol-2'-yl) indoles (3a-d), which on reaction with chloroacetic acid gave 2-(5'-substituted-3'-phenylindol-2'-yl)-1,3,4-oxadiazol-5-thioacetic acids (4a-d). These thioacetic acid derivatives 4 on reaction with orthophenylenediamine dihydrochloride furnished the title compounds 5. Newly synthesized compounds were screened for their anthelmintic activity.en_US
dc.publisherDR R S VARMA
dc.titleSYNTHESIS AND ANTHELMINTIC ACTIVITY OF TRIHETEROCYCLES: [5 '-(5 ''-SUBSTITUTED-3 ''-PHENYLINDOL-2 '-YL)-1 ',3 ',4 '-OXADIAZOL-2 '-YL-THIOMETHYL] BENZIMIDAZOLESen_US
dc.typeArticle
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