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Facile oxidative hydrolysis of acetals to esters using hypervalent iodine(III)/LiBr combination in water

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dc.contributor.authorWaraporn Panchanen_US
dc.contributor.authorSupanimit Chiampanichayakulen_US
dc.contributor.authorDeanna L. Snyderen_US
dc.contributor.authorSiriporn Yodbuntungen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorThaworn Jaipetchen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-24T08:46:11Z
dc.date.available2018-09-24T08:46:11Z
dc.date.issued2010-04-03en_US
dc.description.abstractThe combination of (diacetoxy)iodobenzene (PhI(OAc)2, DIB) and lithium bromide (LiBr) efficiently oxidized cyclic and acyclic acetals to the corresponding hydroxyalkyl carboxylic esters and simple esters in good to excellent yields. The merits of this reaction are that it employs commercially available and non-explosive hypervalent iodine(III) reagent, water as the solvent, a short reaction time, and mild reaction conditions. © 2010 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron. Vol.66, No.14 (2010), 2732-2735en_US
dc.identifier.doi10.1016/j.tet.2010.01.098en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-77649182466en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/28738
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77649182466&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFacile oxidative hydrolysis of acetals to esters using hypervalent iodine(III)/LiBr combination in wateren_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77649182466&origin=inwarden_US

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