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

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1607

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DC Field	Value	Language
dc.contributor.author	Rana, Prabhat Singh	-
dc.date.accessioned	2020-10-28T07:02:59Z	-
dc.date.available	2020-10-28T07:02:59Z	-
dc.date.issued	2019-12	-
dc.identifier.uri	http://hdl.handle.net/123456789/1607	-
dc.description.abstract	Bis(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.language.iso	en_US	en_US
dc.subject	H-bond donor catalysis	en_US
dc.subject	Para-quinone methides	en_US
dc.subject	Cyclopropenium ion	en_US
dc.title	Bis(amino)cyclopropenium salt Catalyzed 1,6-Conjugate Addition of Thiols to p-Quinone Methides	en_US
dc.type	Thesis	en_US
dc.guide	Anand, R.V.	-
Appears in Collections:	MS-14

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