Regioselective Ortho-Arylation and Alkenylation of N-Alkyl Benzamides with Boronic Acids via Ruthenium-Catalyzed C-H Bond Activation: An Easy Route to Fluorenones Synthesis

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DC Field	Value	Language
dc.contributor.author	Chinnagolla, Ravi Kiran	en_US
dc.contributor.author	JEGANMOHAN, MASILAMANI	en_US
dc.date.accessioned	2019-07-23T11:09:55Z
dc.date.available	2019-07-23T11:09:55Z
dc.date.issued	2012-10	en_US
dc.identifier.citation	Organic Letters, 1 4 (20), 5246-5249.	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/123456789/3656	-
dc.identifier.uri	https://doi.org/10.1021/ol3024067	en_US
dc.description.abstract	A highly regioselective ruthenium-catalyzed ortho-arylation of substituted N-alkyl benzamides with aromatic boronic acids in the presence of [{RuCl2(p-cymene)}2], AgSbF6, and Ag2O is described. Further, ortho-arylated N-alkyl benzamides were converted into fluorenones in the presence of trifluoroacetic anhydride and HCl.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Regioselective	en_US
dc.subject	Easy Route	en_US
dc.subject	Fluorenones Synthesis	en_US
dc.subject	Boronic Acids	en_US
dc.subject	C-H Bond Activation	en_US
dc.subject	2012	en_US
dc.title	Regioselective Ortho-Arylation and Alkenylation of N-Alkyl Benzamides with Boronic Acids via Ruthenium-Catalyzed C-H Bond Activation: An Easy Route to Fluorenones Synthesis	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
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