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The Pummerer-type reaction mediated ring-opening of 2-alkyl substituted 1-[(2-methoxyethoxy)methoxy]-2-(phenylsulfinyl)cyclopropanes

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorPanawan Moosophonen_US
dc.contributor.authorSomchai Pisutjaroenpongen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-07T09:38:03Z
dc.date.available2018-09-07T09:38:03Z
dc.date.issued2001-06-25en_US
dc.description.abstractα-Lithiated 1-[(2-methoxyethoxy)methoxy]-2-(phenylsylfinyl)cyclopropane reacted smoothly with alkylating agents to afford the corresponding α-alkylated cyclopropylsulfoxides, which underwent the Pummerer-type reaction mediated ring-opening at low temperature (-78°C) by employing TFAA/Pri2NEt/CH2Cl2to give mixtures of β-(phenylthio)-α,β- and γ,δ-unsaturated aldehydes. © 2001 Elsevier Science Ltd.en_US
dc.identifier.citationTetrahedron Letters. Vol.42, No.26 (2001), 4389-4391en_US
dc.identifier.doi10.1016/S0040-4039(01)00723-7en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0035948272en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/26458
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035948272&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleThe Pummerer-type reaction mediated ring-opening of 2-alkyl substituted 1-[(2-methoxyethoxy)methoxy]-2-(phenylsulfinyl)cyclopropanesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035948272&origin=inwarden_US

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