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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1301
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dc.contributor.authorM. S. S. SHANKER, R. B. REDDY-
dc.contributor.authorG. V. P. CHANDRA MOULI and, Y. D. REDDY-
dc.date.accessioned2024-10-30T05:53:23Z-
dc.date.available2024-10-30T05:53:23Z-
dc.date.issued1989-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1301-
dc.description.abstractA few benzothiazepinyl chromones (I1 & IV) were prepared by the reaction of 2-amino benzenethiol with new types of chromonyl chalcones (I & 111). One representative compound (IVb) was cleaved with hydrazine hydrate and with hydroxylamine hydrochloride to afford pyrazole (V) and isoxazole (VI) derivatives. The structures of these compounds were confirmed by their analytical and spectral analysis. Some of the above compounds were screened for their anti-microbial activity.en_US
dc.description.sponsorshipNITWen_US
dc.language.isoenen_US
dc.publisherPhosphorw. Sulfur, and Siliconen_US
dc.subjectBenzothiazepineen_US
dc.subjectchromonyl chalconesen_US
dc.subjectfungicidalen_US
dc.subjectantibacterialen_US
dc.titleSYNTHESIS AND CLEAVAGE REACTIONS OF BENZOTHIAZEPINYL CHROMONE DERIVATIVESen_US
dc.typeArticleen_US
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