Ruthenium-catalyzed direct α-alkylation of amides using alcohols

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DC Field	Value	Language
dc.contributor.author	CHAUDHARI, MORESHWAR B.	en_US
dc.contributor.author	BISHT, GIRISH SINGH	en_US
dc.contributor.author	KUMARI, POOJA	en_US
dc.contributor.author	GNANAPRAKASAM, BOOPATHY	en_US
dc.date.accessioned	2019-04-26T09:12:30Z
dc.date.available	2019-04-26T09:12:30Z
dc.date.issued	2016-09	en_US
dc.identifier.citation	Organic and Biomolecular Chemistry, 14(39), 9215-9220.	en_US
dc.identifier.issn	1477-0520	en_US
dc.identifier.issn	1477-0539	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2498	-
dc.identifier.uri	https://doi.org/10.1039/C6OB01786J	en_US
dc.description.abstract	The highly efficient direct α-alkylation of unactivated amides has been accomplished using alcohols in the presence of the Ru-PNN catalyst (0.1 mol%) with a high turnover number. Using this approach, 2-oxindole was directly transformed into C3-alkylated 3-hydroxyindolin-2-one in one step without the use of any oxidant.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Ruthenium-catalyzed	en_US
dc.subject	Direct ?-alkylation	en_US
dc.subject	Pharmaceutical compounds	en_US
dc.subject	Ru-PNN catalyst	en_US
dc.subject	NMR and mass analysis	en_US
dc.subject	2016	en_US
dc.title	Ruthenium-catalyzed direct α-alkylation of amides using alcohols	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Organic and Biomolecular Chemistry	en_US
dc.publication.originofpublisher	Foreign	en_US
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