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dc.contributor.authorVaishali
dc.contributor.authorSingh, Virender
dc.date.accessioned2024-01-21T10:33:07Z
dc.date.available2024-01-21T10:33:07Z
dc.date.issued2023-04-25T00:00:00
dc.identifier.issn21935807
dc.identifier.urihttp://kr.cup.edu.in/handle/32116/3272
dc.description.abstractA simple, facile, and highly efficient approach has been unfolded for the syntheses of ?-carboline tethered imidazole derivatives. This expeditious catalyst-free strategy proceeds through the assembly of 1-formyl-9H-?-carbolines, glyoxal derivatives and ammonium acetate via the formation of concomitant four C?N bonds in a one-pot operation. The current approach has various advantages, including multicomponent nature, simple reaction conditions, short reaction time, broad substrate scope, and high product yield. Importantly, the ?-carboline tethered imidazole derivatives displayed excellent photophysical properties with quantum yield up to 90%. � 2023 Wiley-VCH GmbH.en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.subjectCatalyst-freeen_US
dc.subjectImidazoleen_US
dc.subjectKumujian Cen_US
dc.subjectPhenyl glyoxalen_US
dc.subject?-Carbolineen_US
dc.titleA Catalyst- and Metal-free Approach towards the Synthesis of ?-Carboline tethered Imidazole Derivatives and Assessment of their Photophysical Propertiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ajoc.202300068
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/ajoc.202300068
dc.title.journalAsian Journal of Organic Chemistryen_US
dc.type.accesstypeOpen Accessen_US


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