Publication:
Recent trends of chromene syntheses

dc.contributor.authorDas, Samarpita
dc.contributor.authorAsati, Pulkit
dc.contributor.authorIndurthi, Harish K.
dc.contributor.authorDash, Ashutosh Kumar
dc.contributor.authorSharma, Deepak K.
dc.date.accessioned2025-01-28T09:38:30Z
dc.date.available2025-01-28T09:38:30Z
dc.date.issued2023
dc.description.abstract2H/4H-chromenes (2H/4H-Ch) structural scaffolds have been widely employed in the synthesis of many natural products and medicinal agents. 2H/4H-Ch have attracted considerable attention due to their various pharmacological activities, such as anticonvulsant, anticholinesterase, anticancer, anti-tuberculosis, antimicrobial, and inhibitory activity against monoamine oxidase (MAO), and anti-diabetic activities. In literature, the synthesis of 4H-chromenes was performed by one-pot Knoevenagel condensation of resorcinol, aryl aldehydes, and malononitrile in the presence of basic catalysts. Also, 2H-Ch analogs were performed by the Wittig-Horner-Emmons and Suzuki-Miyaura cross-coupling reactions. A description of recent advances in the syntheses of chromenes is presented in this chapter. The strategies for the synthesis of 2H/4H-Ch discussed in this chapter are organocatalysts, organometallic or metal catalysts, heterogeneous base catalysts, enzymatic catalysts, and green chemistry-based approaches. � 2023 Bentham Science Publishers. All rights reserved.
dc.identifier.isbn978-981512433-0; 978-981512434-7
dc.identifier.urihttps://dl.bhu.ac.in/ir/handle/123456789/21871
dc.language.isoen
dc.publisherBentham Science Publishers
dc.subject2H/4H-chromenes
dc.subjectEnzymatic catalyst
dc.subjectGreen chemistry approaches
dc.subjectHeterogeneous base catalyst
dc.subjectKnoevenagel condensation
dc.subjectOrgano-base-catalyst
dc.subjectPharmacological activities
dc.subjectWittig-Horner-Emmons
dc.titleRecent trends of chromene syntheses
dc.typeBook chapter
dspace.entity.typePublication
journal.titleThe Role of Chromenes in Drug Discovery and Development

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