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Vicinal dianions of diethyl α-aroylsuccinates: A general synthetic route to α-aroyl- and α-arylidene-γ-butyrolactones

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorLaddawan Sampaongoenen_US
dc.contributor.authorArisara Issareeen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:19:07Z
dc.date.available2018-07-24T03:19:07Z
dc.date.issued2003-08-25en_US
dc.description.abstractVicinal dianions derived from diethyl α-aroylsuccinates were found to react with carbonyl compounds β-regioselectively to afford α-aroyl-γ-butyrolactones, which were converted into α-arylidene-γ-butyrolactones by reduction with H2/Pd-C followed by elimination employing methanesulfonyl chloride in pyridine. The method provides a general and convenient route to α-aroyl- and α-arylidene-γ-butyrolactones. © 2003 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.44, No.35 (2003), 6717-6720en_US
dc.identifier.doi10.1016/S0040-4039(03)01622-8en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0043172234en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/20699
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0043172234&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: A general synthetic route to α-aroyl- and α-arylidene-γ-butyrolactonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0043172234&origin=inwarden_US

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