Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3242
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dc.contributor.authorCHAUDHARI, MORESHWAR B.en_US
dc.contributor.authorSutar, Yogeshen_US
dc.contributor.authorMALPATHAK, SHREYASen_US
dc.contributor.authorHAZRA, ANIRBANen_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2019-07-01T05:34:34Z
dc.date.available2019-07-01T05:34:34Z
dc.date.issued2017-07en_US
dc.identifier.citationOrganic Letters, 19 (13), 3628-3631.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3242-
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.7b01616en_US
dc.description.abstractTransition metal and reductant free ?-C(sp3)-H hydroxylation of carbonyl compounds are reported. This method is promoted by commercially available inexpensive KO-t-Bu and atmospheric air as an oxidant at room temperature. This unified strategy is also very facile for hydroxylation of various carbonyl compound derivatives to obtain quaternary hydroxyl compounds in excellent yield. A preliminary mechanistic investigation, supported by isotope labeling and computational studies, suggests the formation of a peroxide bond and its cleavage by in situ generated enolate.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectTransition-Metal-Freeen_US
dc.subjectC-H Hydroxylationen_US
dc.subjectCarbonyl Compoundsen_US
dc.subjectHydrocarbonsen_US
dc.subjectOrganic synthesisen_US
dc.subject2017en_US
dc.titleTransition-Metal-Free CH Hydroxylation of Carbonyl Compoundsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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