Synthetic strategies and pharmacological activities of chromene and its derivatives: An overview

dc.contributor.authorKatiyar, Madhurendra K.
dc.contributor.authorDhakad, Govind Kumar
dc.contributor.authorShivani
dc.contributor.authorArora, Sahil
dc.contributor.authorBhagat, Srikant
dc.contributor.authorArora, Taruna
dc.contributor.authorKumar, Raj
dc.date.accessioned2024-01-21T10:38:20Z
dc.date.accessioned2024-08-13T12:05:16Z
dc.date.available2024-01-21T10:38:20Z
dc.date.available2024-08-13T12:05:16Z
dc.date.issued2022-04-07T00:00:00
dc.description.abstractChromene is commonly found in nature and is considered one of the most frequently used scaffolds in heterocyclic chemistry for the designing of chemical probes for therapeutic and diagnostic purposes. The chromene nucleus comprises an oxine ring fused with a phenyl ring. Owing to existing several useful biological applications of chromenes have generated wide interest among chemists to synthesize its derivatives frequently. Here, in this review, we have compiled and analysed various recently reported synthetic strategies of chromene and its derivatives through numerous approaches such as microwave-assisted, catalyst based, green solvents, solvent-free conditions, etc. along with their biological applications such as anticancer, antimicrobial, anti-inflammatory, AChE inhibition, antiviral, and antioxidant activities. � 2022 Elsevier B.V.en_US
dc.identifier.doi10.1016/j.molstruc.2022.133012
dc.identifier.issn222860
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3539
dc.identifier.urlhttps://linkinghub.elsevier.com/retrieve/pii/S0022286022006731
dc.language.isoen_USen_US
dc.publisherElsevier B.V.en_US
dc.subjectAmino acid catalysisen_US
dc.subjectBase catalysisen_US
dc.subjectChromeneen_US
dc.subjectNanocatalysisen_US
dc.subjectPharmacological activitiesen_US
dc.subjectSynthesisen_US
dc.titleSynthetic strategies and pharmacological activities of chromene and its derivatives: An overviewen_US
dc.title.journalJournal of Molecular Structureen_US
dc.typeReviewen_US
dc.type.accesstypeClosed Accessen_US

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