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dc.contributor.authorNisha-
dc.date.accessioned2026-09-17T10:55:03Z-
dc.date.available2026-09-17T10:55:03Z-
dc.date.issued2022-04-
dc.identifier.urihttp://localhost:8081/jspui/handle/123456789/21461-
dc.guideGnanamani, E.en_US
dc.description.abstractCarbazole containing compounds have its separate predominance in the field of drug development. Now a days it is also utilizing for the development of fluorescent probes and solar cells. Generally different type of drugs which contains carbazole moiety have substitution on nitrogen atom but at the same time it is also known that synthesizing N-substituted carbazoles is a tedious task because these compounds are quite unstable and easily decomposed.Here in this work, N-alkylated carbazole product with 2-benzylidenemalononitrile by using inorganic base under mild reaction conditions. This is first N-alkylated carbazole product obtained by the reaction between 2-benzylidenemalononitrile and carbazole. The N-alkylated product obtained up to 55% yield.en_US
dc.language.isoenen_US
dc.publisherIIT Roorkeeen_US
dc.titleRegioselective N-Alkylation of Carbazole under Mild Conditionen_US
dc.typeDissertationsen_US
Appears in Collections:MASTERS' THESES (Chemistry)

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