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dc.contributor.authorREDDY, MALLU CHENNAen_US
dc.contributor.authorJEGANMOHAN, MASILAMANIen_US
dc.date.accessioned2019-02-25T09:02:09Z
dc.date.available2019-02-25T09:02:09Z
dc.date.issued2014-09en_US
dc.identifier.citationOrganic Letters, 16(18), 4866-4869.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1965-
dc.identifier.urihttps://doi.org/10.1021/ol502375pen_US
dc.description.abstractAromatic 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.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectRuthenium-catalyzeden_US
dc.subjectAromatic boronic acidsen_US
dc.subjectPhenanthridines and carbazolesen_US
dc.subjectAromatic boronicen_US
dc.subjectCoordinating oxygenen_US
dc.subjectAromatic Nitrilesen_US
dc.subjectRuthenium catalysten_US
dc.subjectAromatic amidesen_US
dc.subject2014en_US
dc.titleRuthenium-Catalyzed Cyclization of Aromatic Nitriles with Alkenes: Stereoselective Synthesis of (Z)-3-Methyleneisoindolin-1-onesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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