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Lemon juice catalyzed C–C bond formation via C–H activation of methylarene: a sustainable synthesis of chromenopyrimidines

dc.contributor.authorKumari, S.
dc.contributor.authorSingh, S.
dc.contributor.authorSrivastava, V.
dc.date.accessioned2020-12-09T05:28:29Z
dc.date.available2020-12-09T05:28:29Z
dc.date.issued2020-08-01
dc.description.abstractAbstract: An economical and proficient approach has been developed for the synthesis of chromenopyrimidines via three-component reaction of thiobarbituric acid/barbituric acid, methylarenes and dimedone/1,3-cyclohexanedione by using lemon juice as a natural, biodegradable catalyst and TBHP as an oxidant. This transformation involves metal-free C–C bond formation via C–H activation of methylarenes under mild reaction conditions. Graphical abstract: [Figure not available: see fulltext.]. © 2019, Springer Nature Switzerland AG.en_US
dc.description.sponsorshipBanaras Hindu Universityen_US
dc.identifier.issn13811991
dc.identifier.urihttps://idr-sdlib.iitbhu.ac.in/handle/123456789/1111
dc.language.isoen_USen_US
dc.publisherSpringeren_US
dc.relation.ispartofseriesMolecular Diversity;Vol. 24 Issue 3
dc.subjectC–H activationen_US
dc.subjectMulticomponent reactionen_US
dc.subjectChromenopyrimidineen_US
dc.subjectTBHPen_US
dc.subjectLemon juiceen_US
dc.titleLemon juice catalyzed C–C bond formation via C–H activation of methylarene: a sustainable synthesis of chromenopyrimidinesen_US
dc.typeArticleen_US

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