Ruthenium(II)-Catalyzed Redox-Neutral Oxidative Cyclization of Benzimidates with Alkenes with Hydrogen Evolution

dc.contributor.author	Manikandan, Rajendran	en_US
dc.contributor.author	Tamizmani, Masilamani	en_US
dc.contributor.author	JEGANMOHAN, MASILAMANI	en_US
dc.date.accessioned	2019-07-01T05:34:35Z
dc.date.available	2019-07-01T05:34:35Z
dc.date.issued	2017-12	en_US
dc.identifier.citation	Organic Letters, 19 (24), 6678-6681.	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/123456789/3254
dc.identifier.uri	https://doi.org/10.1021/acs.orglett.7b03405	en_US
dc.description.abstract	1H-Isoindoles and 2H-isoindoles are synthesized via a ruthenium-catalyzed oxidant-free cyclization of benzimidates with alkenes at room temperature with the liberation of H2. Later, 1H-isoindoles were converted into nitrogen-containing heterocycles. The proposed reaction mechanism was strongly supported by experimental evidence and DFT calculations.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Redox-Neutral Oxidative	en_US
dc.subject	Cyclization	en_US
dc.subject	Hydrogen Evolution	en_US
dc.subject	DFT calculations	en_US
dc.subject	Nitrogen-containing heterocycles	en_US
dc.subject	2017	en_US
dc.title	Ruthenium(II)-Catalyzed Redox-Neutral Oxidative Cyclization of Benzimidates with Alkenes with Hydrogen Evolution	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