Bis(amino)cyclopropenylidene-Catalyzed 1,6-Conjugate Addition of Aromatic Aldehydes to para-Quinone Methides: Expedient Access to α,α′-Diarylated Ketones

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DC Field	Value	Language
dc.contributor.author	Ramanjaneyulu, B.T.	-
dc.contributor.author	Mahesh, S.	-
dc.contributor.author	Anand, R.V.	-
dc.date.accessioned	2020-12-08T10:09:37Z	-
dc.date.available	2020-12-08T10:09:37Z	-
dc.date.issued	2015	-
dc.identifier.citation	Organic Letters, 17(16)	en_US
dc.identifier.other	10.1021/acs.orglett.5b01724	-
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/acs.orglett.5b01724	-
dc.identifier.uri	http://hdl.handle.net/123456789/2830	-
dc.description.abstract	A bis(amino)cyclopropenylidene-catalyzed direct method for the synthesis of α,α′-diarylated ketones from aromatic as well as heteroaromatic aldehydes has been developed. This unprecedented organocatalytic protocol offers access to a wide range of α,α′-diarylated ketones in moderate to excellent yields under mild conditions through umpolung of aldehydes followed by 1,6-conjugate addition with para-quinone methides.	en_US
dc.language.iso	en_US	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Carbonyls	en_US
dc.subject	Chemical reactions	en_US
dc.subject	Aromatic compounds	en_US
dc.subject	etones	en_US
dc.title	Bis(amino)cyclopropenylidene-Catalyzed 1,6-Conjugate Addition of Aromatic Aldehydes to para-Quinone Methides: Expedient Access to α,α′-Diarylated Ketones	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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