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IBX/n-Bu<inf>4</inf>NBr/CH<inf>2</inf>Cl<inf>2</inf>-H<inf>2</inf>O: A new mild system for selective oxidation of secondary alcohols

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dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorKrisada Kittigowittanaen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-21T08:08:14Z
dc.date.available2018-06-21T08:08:14Z
dc.date.issued2005-09-19en_US
dc.description.abstractA new alternative system for the chemoselective oxidation of secondary hydroxyl group to ketone with IBX/n-Bu4NBr in CH2Cl2-H2O has been developed. Under the reaction conditions, the secondary hydroxyl group was highly chemoselectively oxidized to the corresponding ketone, in moderate to good yields at rt, in the presence of primary hydroxyl group within the same molecule. © 2005 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron. Vol.61, No.38 (2005), 8995-9000en_US
dc.identifier.doi10.1016/j.tet.2005.07.051en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-23944511343en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16295
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=23944511343&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleIBX/n-Bu<inf>4</inf>NBr/CH<inf>2</inf>Cl<inf>2</inf>-H<inf>2</inf>O: A new mild system for selective oxidation of secondary alcoholsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=23944511343&origin=inwarden_US

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