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Vicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorArisara Issareeen_US
dc.contributor.authorLaddawan Sampaongoenen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:18:46Z
dc.date.available2018-07-24T03:18:46Z
dc.date.issued2003-10-20en_US
dc.description.abstractVicinal dianions of diethyl α-aroylsuccinates react with aromatic aldehydes to provide functionalized 2,3-dihydrofurans as the major products together with γ-butyrolactones after treatment of the adducts obtained with a catalytic amount of p-toluenesulfonic acid in refluxing toluene. cis-2,3-Dihydrofurans are used as precursors for the preparation of tetrasubstituted furans and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanes. © 2003 Published by Elsevier Ltd.en_US
dc.identifier.citationTetrahedron Letters. Vol.44, No.43 (2003), 7937-7940en_US
dc.identifier.doi10.1016/j.tetlet.2003.09.005en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0141708670en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/20685
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0141708670&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleVicinal dianions of diethyl α-aroylsuccinates: Preparation of functionalized-2,3-dihydrofurans and -furans, and diaxial 2,4-diaryl-3,7-dioxabicyclo[3.3.0]octanesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0141708670&origin=inwarden_US

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