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dc.contributor.authorPadala, Kishoren_US
dc.contributor.authorJEGANMOHAN, MASILAMANIen_US
dc.date.accessioned2019-07-23T11:09:21Z
dc.date.available2019-07-23T11:09:21Z
dc.date.issued2012-02en_US
dc.identifier.citationOrganic Letters, 1 4 (4), 1134-1137.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3653-
dc.identifier.urihttps://doi.org/10.1021/ol3000684en_US
dc.description.abstractVarious aromatic and heteroaromatic aldehydes reacted with activated alkenes in the presence of a catalytic amount of [{RuCl2(p-cymene)}2], AgSbF6, and Cu(OAc)2·H2O to give substituted alkene derivatives in a highly regio- and stereoselective manner. The corresponding alkene derivatives were further converted into unusual four-membered cyclic ketones or a polycyclic isochromanone derivative via a photochemical rearrangement. Notably, the catalytic reaction was conducted under an open atmosphere.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectStereoselective Rutheniumen_US
dc.subjectOpen Atmosphereen_US
dc.subjectActivated Alkenesen_US
dc.subjectHeteroaromatic aldehydesen_US
dc.subject2012en_US
dc.titleHighly Regio- and Stereoselective Ruthenium(II)-Catalyzed Direct ortho-Alkenylation of Aromatic and Heteroaromatic Aldehydes with Activated Alkenes under Open Atmosphereen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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