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Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones

dc.contributor.authorB. Chitkulen_US
dc.contributor.authorY. Pinyopronpanichen_US
dc.contributor.authorC. Thebtaranonthen_US
dc.contributor.authorY. Thebtaranonthen_US
dc.contributor.authorW. C. Tayloren_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThe University of Sydneyen_US
dc.date.accessioned2018-02-27T04:25:25Z
dc.date.available2018-02-27T04:25:25Z
dc.date.issued1994-02-14en_US
dc.description.abstractSpiro[4.4]non- and spiro[4.5] dec-2-ene-1,6-diones [2; n = 0 and 1] were prepared in moderate to high enantiomeric purities via asymmetric allylation of enamines 6 and ketal derivatives 7 and 8 formed from keto-esters 5, followed by a carbanionic cyclization process. © 1994.en_US
dc.identifier.citationTetrahedron Letters. Vol.35, No.7 (1994), 1099-1102en_US
dc.identifier.doi10.1016/S0040-4039(00)79975-8en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0028354367en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/9517
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028354367&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleEnantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-dionesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028354367&origin=inwarden_US

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