Bis(amino)cyclopropenium salt Catalyzed 1,6-Conjugate Addition of Thiols to p-Quinone Methides

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dc.contributor.authorRana, Prabhat Singh
dc.date.accessioned2020-10-28T07:02:59Z
dc.date.available2020-10-28T07:02:59Z
dc.date.issued2019-12
dc.description.abstractBis(amino)cyclopropenium salt has been utilized as a H-bond donor catalyst for the 1,6- conjugate addition of thiols to para-quinone methides. Here the bis(amino)cyclopropenium salt acts as a Brønsted acid for the catalysis. The transformation occurs at mild conditions and is tolerant to a variety of functional groups. This protocol provides an easy and simple access to various unsymmetrical diarylmethyl thioether in good to excellent yield.en_US
dc.guideAnand, R.V.
dc.identifier.urihttp://hdl.handle.net/123456789/1607
dc.language.isoen_USen_US
dc.subjectH-bond donor catalysisen_US
dc.subjectPara-quinone methidesen_US
dc.subjectCyclopropenium ionen_US
dc.titleBis(amino)cyclopropenium salt Catalyzed 1,6-Conjugate Addition of Thiols to p-Quinone Methidesen_US
dc.typeThesisen_US

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