Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2719
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dc.contributor.authorManoharan, Ramasamyen_US
dc.contributor.authorJAYAKANNAN, MANICKAMen_US
dc.date.accessioned2019-04-29T10:15:50Z
dc.date.available2019-04-29T10:15:50Z
dc.date.issued2016-08en_US
dc.identifier.citationEuropean Journal of Organic Chemistry, 2016(23), 4013-4019.en_US
dc.identifier.issn1434-193Xen_US
dc.identifier.issn1099-0690en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2719-
dc.identifier.urihttps://doi.org/10.1002/ejoc.201600505en_US
dc.description.abstractA highly regioselective ruthenium‐catalyzed C–H amidation of cyclic N‐sulfonyl ketimines with organic sulfonyl azides is described. An alkenylation at the C–H bond of cyclic N‐sulfonyl ketimines with various alkenes was also carried out. Only a catalytic amount of the oxidant Cu(OAc)2 was used in the reaction; the remainder of the required amount of oxidant was formed by regeneration of Cu(OAc)2 under an air atmosphere.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectRuthenium?Catalyzeden_US
dc.subjectC-H Amidationen_US
dc.subjectAlkenylationen_US
dc.subjectCyclic N?Sulfonyl Ketiminesen_US
dc.subjectHeteroaromatic compounden_US
dc.subject2016en_US
dc.titleRuthenium‐Catalyzed C–H Amidation and Alkenylation of Cyclic N‐Sulfonyl Ketiminesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleEuropean Journal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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