Please use this identifier to cite or link to this item: http://hdl.handle.net/2080/3623
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dc.contributor.authorPanda, Jeetendra-
dc.contributor.authorSahoo, Jigyansa-
dc.contributor.authorSahoo, Gokarneswar-
dc.date.accessioned2022-02-09T06:20:55Z-
dc.date.available2022-02-09T06:20:55Z-
dc.date.issued2022-01-
dc.identifier.citationJ-NOST- 2022;University of Hydrabad, Date: 6-9 Jan 2022en_US
dc.identifier.urihttp://hdl.handle.net/2080/3623-
dc.descriptionCopyright of this paper is with proceedings publisheren_US
dc.description.abstractUmpolung mode of reactivity of the “Br” species; from cationic bromine to an anionic bromine species using an organocatalyst has been newly developed, and used for regioselective bromination of various alkenes. This one-pot synthetic tool, using a stable, inexpensive halogen source (NBS) along with organocatalysts (pyrrolidine, L-proline, MacMillan catalyst) at room temperature is expeditious compared to conventional methodologies.en_US
dc.language.isoenen_US
dc.subjectOrganocatalysisen_US
dc.subjectUmpolungen_US
dc.subjectBrominationen_US
dc.titleUmpolung of Cationic Bromine; Organocatalyzed Halogenation of Olefinsen_US
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