Lipase-catalyzed resolution of racemic 2-aklyl substituted 1-alkanols

dc.contributor.authorBarth, Stefande
dc.contributor.authorEffenberger, Franzde
dc.date.accessioned2009-08-28de
dc.date.accessioned2016-03-31T07:47:48Z
dc.date.available2009-08-28de
dc.date.available2016-03-31T07:47:48Z
dc.date.issued1993de
dc.description.abstract(R)-2-alkyl-1-alkanoids (R)-1 with high optical purities were obtained by lipase-catalyzed esterification of the racemic substrates (R,S)-1 with vinyl acetate in dichloromethane. The alcohols (R)-1 were oxidized without racemization to the corresponding carboxylic acids (R)-4. The enriched (S)-acetates (S)-3 either were saponified to the alcohols (S)-1 which are substrates for a second lipase-catalyzed transesterification to give (S)-1 in high optical purity or were racemized and applied once again in the kinetic resolution to prepare (R)-1.en
dc.identifier.other316226270de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-44477de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/1183
dc.identifier.urihttp://dx.doi.org/10.18419/opus-1166
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationAlkanole , Enzymkatalyse , Racemisierungde
dc.subject.ddc540de
dc.titleLipase-catalyzed resolution of racemic 2-aklyl substituted 1-alkanolsen
dc.typearticlede
ubs.fakultaetFakultät Chemiede
ubs.institutInstitut für Organische Chemiede
ubs.opusid4447de
ubs.publikation.sourceTetrahedron / Asymmetry 4 (1993), S. 823-833. URL http://dx.doi.org./10.1016/S0957-4166(00)80120-2de
ubs.publikation.typZeitschriftenartikelde

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