Aerobic Dehydrogenative α-Diarylation of Benzyl Ketones with Aromatics through Carbon–Carbon Bond Cleavage

dc.contributor.author	More, Nagnath Yadav	en_US
dc.contributor.author	JEGANMOHAN, MASILAMANI	en_US
dc.date.accessioned	2019-02-25T09:02:09Z
dc.date.available	2019-02-25T09:02:09Z
dc.date.issued	2014-02	en_US
dc.identifier.citation	Organic Letters, 16(3), 804-807.	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.issn	1523-7052	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1962
dc.identifier.uri	https://doi.org/10.1021/ol500079y	en_US
dc.description.abstract	Substituted benzyl ketones reacted with aromatics in the presence of K2S2O8 in CF3COOH at room temperature, yielding α-diaryl benzyl ketones through a carbon–carbon bond cleavage. In the reaction, two new carbon–carbon bonds were formed and one carbon–carbon bond was cleaved. It is very interesting that two different nucleophiles such as benzyl ketones and aromatics were coupled together without metal, which is unusual in organic synthesis.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Aerobic Dehydrogenative	en_US
dc.subject	Aromatics	en_US
dc.subject	Carbon Bond Cleavage	en_US
dc.subject	Organic synthesis	en_US
dc.subject	2014	en_US
dc.title	Aerobic Dehydrogenative α-Diarylation of Benzyl Ketones with Aromatics through Carbon–Carbon Bond Cleavage	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Organic Letters	en_US
dc.publication.originofpublisher	Foreign	en_US