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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1766
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dc.contributor.authorPrashant-
dc.contributor.authorAnand, R.V.-
dc.date.accessioned2021-12-13T10:50:01Z-
dc.date.available2021-12-13T10:50:01Z-
dc.date.issued2020-04-
dc.identifier.urihttp://hdl.handle.net/123456789/1766-
dc.description.abstractBis(amino)cyclopropenium salt has been utilized as a hydrogen-bond donor catalyst for the 1,6- conjugate addition of 2-naphthols to para-quinone methides. Here the bis(amino)cyclopropenium salt acts as a Brønsted acid. This transformation occurs at mild conditions and is tolerant to a variety of functional groups. This protocol provides an easy and straightforward access to various unsymmetrical triarylmethanes in good to excellent yields.en_US
dc.language.isoenen_US
dc.publisherIISERMen_US
dc.subjectBis(amino)cyclopropenylidene (BAC)en_US
dc.subjectPhase transfer catalysis by the TDAC saltsen_US
dc.subjectintroduction on p-Quinone methidesen_US
dc.subject2-Naphtholsen_US
dc.titleBis(amino)cyclopropenium Salt Catalyzed 1,6-Conjugate Addition of 2-Naphthols to p-Quinone Methidesen_US
dc.typeThesisen_US
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