Bis(amino)cyclopropenium Salt Catalyzed 1,6-Conjugate Addition of 2-Naphthols to p-Quinone Methides

dc.contributor.authorPrashant
dc.date.accessioned2020-10-05T09:42:01Z
dc.date.available2020-10-05T09:42:01Z
dc.date.issued2020-04
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.guideAnand, R.V.
dc.identifier.urihttp://hdl.handle.net/123456789/1492
dc.language.isoenen_US
dc.publisherIISER Mohalien_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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