Access to Naphthalene Derivatives from 2-Alkeny1-pheny1- substituted para-quinone methodes

dc.contributor.authorBaranwal, Divyanshu
dc.contributor.authorPrasad, Shambhu
dc.date.accessioned2022-10-13T10:11:53Z
dc.date.available2022-10-13T10:11:53Z
dc.date.issued2022-04
dc.description.abstractA base-mediated and Lewis acid catalyzed one-pot reaction between 2-alkenylphenyl- substituted p-quinone methides and bromo-malonates has been developed to access a wide range of naphthalene derivatives. Basically, this transformation involves two different steps, i.e., (i) base-mediated cyclopropanation of 2-alkenylphenyl-substituted p-quinone methides with bromo-malonates (ii) Lewis acid catalyzed intramolecular annulation of cyclopropenyl- alkenes to form the naphthalene derivatives.en_US
dc.guideAnand, R. Vijayaen_US
dc.identifier.urihttp://hdl.handle.net/123456789/4066
dc.language.isoen_USen_US
dc.publisherIISER Mohalien_US
dc.subjectsubstituted para-quinoneen_US
dc.subjectNaphthalene Derivativesen_US
dc.subject2-Alkeny1-pheny1en_US
dc.titleAccess to Naphthalene Derivatives from 2-Alkeny1-pheny1- substituted para-quinone methodesen_US
dc.typeThesisen_US

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