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Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7675
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dc.contributor.authorMOHANTA, NIRMALAen_US
dc.contributor.authorSamal, PragnyaParamitaen_US
dc.contributor.authorKrishnamurty, Sailajaen_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2023-03-24T09:11:02Z-
dc.date.available2023-03-24T09:11:02Z-
dc.date.issued2023-02en_US
dc.identifier.citationAdvanced Synthesis & Catalysis, 365(4), 515-521.en_US
dc.identifier.issn1615-4150en_US
dc.identifier.issn1615-4169en_US
dc.identifier.urihttps://doi.org/10.1002/adsc.202201308en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7675-
dc.description.abstractWe report an FeCl2-catalyzed radical rearrangement of aryl peroxyoxindoles into 1,3-benzooxazin-2-ones to obtain a variety of aryl substituted 1,3-benzooxazin-4-ones in moderate to good yields. Mechanistically, this skeletal rearrangement of peroxyoxindoles proceeded via radical pathway and was well supported with a series of experimental findings and DFT studies.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectPeroxyoxindoleen_US
dc.subjectFeCl2en_US
dc.subjectRearrangementen_US
dc.subject1,3-Benzooxazin-4-oneen_US
dc.subjectRing expansionen_US
dc.subject2023-MAR-WEEK3en_US
dc.subjectTOC-MAR-2023en_US
dc.subject2023en_US
dc.titleFeCl2-Catalyzed Rearrangement of Aryl Peroxyoxindole into 1,3-Benzooxazin-4-Oneen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleAdvanced Synthesis & Catalysisen_US
dc.publication.originofpublisherForeignen_US
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