Publication:
First catalytic, enantioselective aldol-Tishchenko reactions with ketone aldols as enol equivalents

dc.bibliographiccitation.firstpage837
dc.bibliographiccitation.issue6
dc.bibliographiccitation.journalSynlett
dc.bibliographiccitation.lastpage840
dc.contributor.authorSchneider, C.
dc.contributor.authorHansch, M.
dc.date.accessioned2018-11-07T10:39:28Z
dc.date.available2018-11-07T10:39:28Z
dc.date.issued2003
dc.description.abstractChiral zirconiumTADDOLates were found to catalyze the aldol-Tishchenko reaction of diacetone alcohol (1a) and two other ketone aldol adducts 1b and 1c with a range of aldehydes giving rise to differentiated 1,3-anti-diol monoesters in good yields, complete diastereocontrol and moderate enantioselectivities.
dc.identifier.doi10.1055/s-2003-38741
dc.identifier.isi000182776600016
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/46055
dc.notes.statuszu prüfen
dc.notes.submitterNajko
dc.publisherGeorg Thieme Verlag Kg
dc.relation.issn0936-5214
dc.titleFirst catalytic, enantioselective aldol-Tishchenko reactions with ketone aldols as enol equivalents
dc.typejournal_article
dc.type.internalPublicationyes
dc.type.peerReviewedyes
dc.type.statuspublished
dspace.entity.typePublication

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