Ruthenium-Catalyzed Cyclization of Aromatic Nitriles with Alkenes: Stereoselective Synthesis of (Z)-3-Methyleneisoindolin-1-ones

dc.contributor.author	REDDY, MALLU CHENNA	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	2014-09	en_US
dc.identifier.citation	Organic Letters, 16(18), 4866-4869.	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/123456789/1965
dc.identifier.uri	https://doi.org/10.1021/ol502375p	en_US
dc.description.abstract	Aromatic nitriles underwent cyclization with activated alkenes in the presence of a ruthenium catalyst, AgSbF6, and Cu(OAc)2·H2O providing substituted 3-methyleneisoindolin-1-ones with high Z-stereoselectivity. The Z-stereoselectivity of the 3-methyleneisoindolin-1-one moiety was controlled by the intramolecular hydrogen bonding.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Ruthenium-catalyzed	en_US
dc.subject	Aromatic boronic acids	en_US
dc.subject	Phenanthridines and carbazoles	en_US
dc.subject	Aromatic boronic	en_US
dc.subject	Coordinating oxygen	en_US
dc.subject	Aromatic Nitriles	en_US
dc.subject	Ruthenium catalyst	en_US
dc.subject	Aromatic amides	en_US
dc.subject	2014	en_US
dc.title	Ruthenium-Catalyzed Cyclization of Aromatic Nitriles with Alkenes: Stereoselective Synthesis of (Z)-3-Methyleneisoindolin-1-ones	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