Morita-Baylis-Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

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dc.contributor.authorDevi, Nisha
dc.contributor.authorSingh, Virender
dc.date.accessioned2024-01-21T10:33:02Z
dc.date.accessioned2024-08-13T11:16:45Z
dc.date.available2024-01-21T10:33:02Z
dc.date.available2024-08-13T11:16:45Z
dc.date.issued2022-07-26T00:00:00
dc.description.abstract?-Carboline is a privileged class of the alkaloid family and is associated with a broad spectrum of biological properties. 3-Formyl-9H-pyrido[3,4-b]indole is a such potent precursor belonging to this family which can be tailored for installing diversity at various positions of ?-carboline to generate unique molecular hybrids of biological importance. The present work is a step towards this and assimilates the results related to the exploration of 3-formyl-9H-?-carbolines for the synthesis of ?-carboline C-3 substituted MBH adducts followed by evaluation of their fluorescent characteristic. The effect of contact time, solvent system, concentration and substituents was also studied during investigation of fluorescence properties of these derivatives. � 2022 Devi and Singh; licensee Beilstein-Institut.en_US
dc.identifier.doi10.3762/bjoc.18.92
dc.identifier.issn18605397
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3246
dc.identifier.urlhttps://www.beilstein-journals.org/bjoc/articles/18/92
dc.language.isoen_USen_US
dc.publisherBeilstein-Institut Zur Forderung der Chemischen Wissenschaftenen_US
dc.subjectDABCOen_US
dc.subjectfluorescenceen_US
dc.subjectMBH reactionen_US
dc.subjectMichael additionen_US
dc.subjectstructure-fluorescence activity relationshipen_US
dc.subject?-carbolineen_US
dc.titleMorita-Baylis-Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the productsen_US
dc.title.journalBeilstein Journal of Organic Chemistryen_US
dc.typeArticleen_US
dc.type.accesstypeOpen Accessen_US

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