KI-assisted Sulfur Activation/Insertion/Denitration Strategy towards Dual C?S Bond Formation for One-pot Synthesis of ?-Carboline-tethered 2-Acylbenzothiophenes

dc.contributor.authorSingh, Manpreet
dc.contributor.authorJamra., Rahul
dc.contributor.authorPaul, Avijit K.
dc.contributor.authorMalakar, Chandi C.
dc.contributor.authorSingh, Virender
dc.date.accessioned2024-01-21T10:32:58Z
dc.date.accessioned2024-08-13T11:16:40Z
dc.date.available2024-01-21T10:32:58Z
dc.date.available2024-08-13T11:16:40Z
dc.date.issued2021-12-13T00:00:00
dc.description.abstractA simple and efficient KI promoted sulfur activation-insertion/de-nitration strategy has been developed for the synthesis of ?-carboline C1 tethered 2-acylbenzothiophenes via one-pot assembly of 1-acetyl ?-carbolines (an alkaloid based scaffold), 2-nirobenzaldehydes and elemental sulfur. This expeditious reaction proceeds through the formation of ?-carboline linked nitro-chalcones followed by embodiment of elemental sulfur to generate the multifunctional ?-carboline linked benzothiophene derivatives. The highlighted features of this efficient methodology are transition metal-free conditions, use of inexpensive and non-toxic catalyst, easy procedure, short reaction time, and broad substrate scope with good yields. The scope of this protocol has been extended for the synthesis of a range of novel compounds with significant diversity. � 2021 Wiley-VCH GmbHen_US
dc.identifier.doi10.1002/ajoc.202100653
dc.identifier.issn21935807
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3226
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/ajoc.202100653
dc.language.isoen_USen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.subject1-Acetyl ?-carbolineen_US
dc.subject2-Acylbenzothiopheneen_US
dc.subjectDe-nitrationen_US
dc.subjectSulfur insertionen_US
dc.subjectTransition metal-freeen_US
dc.titleKI-assisted Sulfur Activation/Insertion/Denitration Strategy towards Dual C?S Bond Formation for One-pot Synthesis of ?-Carboline-tethered 2-Acylbenzothiophenesen_US
dc.title.journalAsian Journal of Organic Chemistryen_US
dc.typeArticleen_US
dc.type.accesstypeClosed Accessen_US

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