Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4379
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dc.contributor.authorGuruprasad, BV
dc.contributor.authorMruthyunjayaswamy, BHM
dc.date.accessioned2020-06-12T15:03:43Z-
dc.date.available2020-06-12T15:03:43Z-
dc.date.issued2012
dc.identifier.citationINDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY , Vol. 51 , 3 , p. 514 - 520en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4379-
dc.description.abstract(E)-3-Chloro-N'-((6-substituted-2-hydroxy quinolin-3-yl) methylene)-6-substituted benzo[b]thiophene-2-carbohydrazides 3a-d obtained by the reaction of 3-chloro-6-substituted benzo[b]thiophene-2-carbohydrazides 1a and 1b and 6-substituted-2-hydroxy quinoline-3-carboxaldehyde 2a and 2b, on reduction with sodium borohydride gives the respective 3-chloro-N'-((6-substituted-2-hydroxy quinolin-3-yl) methyl)-6-substituted benzo[b]thiophene-2-carbohydrazides 4a-d. These on further reaction with formalin yield 3-chloro-6-substituted-N- (6-substituted 2H-[1,3]oxazino[6,5-b]quinolin-3-(4H,5aH,9aH)-yl)benzo[b]thiophene-2-carboxamides 5a-d. The structures of all the newly synthesized compounds have been confirmed by IR, H-1 NMR and mass spectral data. All these compounds have been screened for their antibacterial activity against Gram (+ve) S. aureus and B. subtilus, Gram (-ve) E. coli and K. pneumonia and antifungal activity against A. niger and C. albi cans.en_US
dc.publisherCOUNCIL SCIENTIFIC & INDUSTRIAL RES
dc.subjectBenzothiopene
dc.subjectquinoline
dc.subjectoxazinoquinolines
dc.subjectantimicrobial activity
dc.titleSynthesis and antimicrobial activity of some new 3-chloro-6-substituted-N-(substituted 2H-[1,3]oxazino[6,5-b]quinolin-3-(4H,5aH,9aH)-yl) benzo[b]thiophene-2-carboxamidesen_US
dc.typeArticle
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