Pentafluorobenzoic Acid Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methides

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1628

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DC Field	Value	Language
dc.contributor.author	Chowdhury, Arjun.	-
dc.contributor.author	Anand, R.V.	-
dc.date.accessioned	2021-12-09T19:22:42Z	-
dc.date.available	2021-12-09T19:22:42Z	-
dc.date.issued	2021-07-28	-
dc.identifier.uri	http://hdl.handle.net/123456789/1628	-
dc.description.abstract	Pentafluorobenzoic acid has been utilized as a non-covalent Br Ø nsted acid catalyst for the 1,6- conjugate addition of indoles to para-quinone methides. This transformation tolerant to a variety of functional groups and occurs in mild conditions. This methodology provides an easy and straightforward access to a set of unsymmetrical diarylindolylmethanes in moderate to good yields.	en_US
dc.language.iso	en_US	en_US
dc.publisher	IISERM	en_US
dc.subject	Pentafluorobenzoic	en_US
dc.subject	p-Quinone	en_US
dc.subject	Methides	en_US
dc.title	Pentafluorobenzoic Acid Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methides	en_US
dc.type	Thesis	en_US
Appears in Collections:	MS-16

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