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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9425
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:59Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:59Z-
dc.date.issued2013-
dc.identifier.citationSingh, V., Das, B., & Mobin, S. (2013). Oxidative dearomatization of o -hydroxymethylphenol and intramolecular π4s+π2s cycloaddition: An expedient synthesis of a tricyclic intermediate for platencin. Synlett, 24(12), 1583-1587. doi:10.1055/s-0033-1339196en_US
dc.identifier.issn0936-5214-
dc.identifier.otherEID(2-s2.0-84879064997)-
dc.identifier.urihttps://doi.org/10.1055/s-0033-1339196-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9425-
dc.description.abstractA synthesis of a tricyclic intermediate for platencin from a simple aromatic precursor is described. Oxidative dearomatization and intramolecular Diels-Alder reaction are key features of the approach. © Georg Thieme Verlag Stuttgart. New York.en_US
dc.language.isoenen_US
dc.sourceSynletten_US
dc.subjectbenzyl derivativeen_US
dc.subjectcarbonyl derivativeen_US
dc.subjectcyclohexane derivativeen_US
dc.subjecthydroxyl groupen_US
dc.subjectortho hydroxymethylphenolen_US
dc.subjectphenol derivativeen_US
dc.subjectplatencinen_US
dc.subjecttricyclic aromatic compounden_US
dc.subjectunclassified drugen_US
dc.subjectaromatizationen_US
dc.subjectarticleen_US
dc.subjectchemical structureen_US
dc.subjectcycloadditionen_US
dc.subjectdecarboxylationen_US
dc.subjectDiels Alder reactionen_US
dc.subjectoxidation reduction reactionen_US
dc.subjectprecursoren_US
dc.subjectstereochemistryen_US
dc.subjectsynthesisen_US
dc.titleOxidative dearomatization of o -hydroxymethylphenol and intramolecular π4s+π2s Cycloaddition: An expedient synthesis of a tricyclic intermediate for platencinen_US
dc.typeJournal Articleen_US
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