Publication:
Samarium dienolate mediated stereoselective synthesis of anti-1,3-diol monoesters via aldol-Tishchenko reaction

dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorJaray Jaratjaroonphongen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorPalangpon Kongsaereeen_US
dc.contributor.authorSamran Prabpaien_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-20T06:50:50Z
dc.date.available2018-08-20T06:50:50Z
dc.date.issued2006-07-03en_US
dc.description.abstractThe reaction of an (E)-samarium dienolate, generated by the regioselective reductive cleavage of a phenylsulfonyl activated cyclopropyl ketone with samarium(II) iodide, with aliphatic and aromatic aldehydes gives the 2-substituted anti-1,3-diol monoester derivatives, stereoselectively, in good to excellent yields. The results represent the first report of a dienolate in the aldol-Tishchenko reaction and also provide an optically active polyol with (R)-glyceraldehyde. © 2006 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.47, No.27 (2006), 4753-4757en_US
dc.identifier.doi10.1016/j.tetlet.2006.04.091en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-33744532073en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/23008
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33744532073&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleSamarium dienolate mediated stereoselective synthesis of anti-1,3-diol monoesters via aldol-Tishchenko reactionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33744532073&origin=inwarden_US

Files

Collections