Publication:

Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: stereoselective access to all-carbon quaternary centers

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Date

Date
2008
Journal Article
Published version
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cris.lastimport.scopus2025-07-03T03:44:29Z
cris.lastimport.wos2025-01-02T02:30:15Z
cris.virtual.orcidhttps://orcid.org/0000-0002-9343-9180
cris.virtualsource.orcid583798eb-3ab4-47b8-a603-8db9be1b8d4f
dc.contributor.institutionUniversity of Zurich
dc.date.accessioned2009-01-19T16:03:51Z
dc.date.available2009-01-19T16:03:51Z
dc.date.issued2008
dc.description.abstract

A camphor-based alpha'-hydroxy enone reagent acts as a chiral acrylate equivalent in copper-catalyzed Michael reactions of beta-keto esters and affords products that possess all-carbon quaternary stereocenters of high enantiomeric purity.

dc.identifier.doi10.1021/ol800564d
dc.identifier.issn1523-7052
dc.identifier.scopus2-s2.0-54849408611
dc.identifier.urihttps://www.zora.uzh.ch/handle/20.500.14742/36602
dc.identifier.wos000257211400006
dc.language.isoeng
dc.subject.ddc540 Chemistry
dc.title

Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: stereoselective access to all-carbon quaternary centers

dc.typearticle
dcterms.accessRightsinfo:eu-repo/semantics/restrictedAccess
dcterms.bibliographicCitation.journaltitleOrganic Letters
dcterms.bibliographicCitation.number13
dcterms.bibliographicCitation.originalpublishernameAmerican Chemical Society
dcterms.bibliographicCitation.pageend2640
dcterms.bibliographicCitation.pagestart2637
dcterms.bibliographicCitation.pmid18517215
dcterms.bibliographicCitation.volume10
dspace.entity.typePublicationen
uzh.contributor.affiliationUniversidad del Pais Vasco
uzh.contributor.affiliationUniversidad del Pais Vasco
uzh.contributor.affiliation#PLACEHOLDER_PARENT_METADATA_VALUE#
uzh.contributor.affiliation#PLACEHOLDER_PARENT_METADATA_VALUE#
uzh.contributor.affiliationUniversidad Pública de Navarra
uzh.contributor.affiliationUniversidad Pública de Navarra
uzh.contributor.affiliationUniversity of Zurich
uzh.contributor.authorPalomo, C
uzh.contributor.authorOiarbide, M
uzh.contributor.authorGarcía, J M
uzh.contributor.authorBañuelos, P
uzh.contributor.authorOdriozola, J M
uzh.contributor.authorRazkin, J
uzh.contributor.authorLinden, Anthony
uzh.contributor.correspondenceYes
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.document.availabilitycontent_undefined
uzh.eprint.datestamp2009-01-19 16:03:51
uzh.eprint.lastmod2025-07-03 03:44:30
uzh.eprint.statusChange2009-01-19 16:03:51
uzh.funder.projectTitleUniversidad del Paı´s Vasco, Gobierno Vasco
uzh.funder.projectTitleMEC
uzh.funder.projectTitleUPNA
uzh.harvester.ethYes
uzh.harvester.nbNo
uzh.identifier.doi10.5167/uzh-8797
uzh.jdb.eprintsId20837
uzh.oastatus.unpaywallclosed
uzh.oastatus.zoraClosed
uzh.publication.citationPalomo, C; Oiarbide, M; García, J M; Bañuelos, P; Odriozola, J M; Razkin, J; Linden, Anthony (2008). Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: stereoselective access to all-carbon quaternary centers. Organic Letters, 10(13):2637-2640.
uzh.publication.originalworkoriginal
uzh.publication.publishedStatusfinal
uzh.scopus.impact16
uzh.scopus.subjectsBiochemistry
uzh.scopus.subjectsPhysical and Theoretical Chemistry
uzh.scopus.subjectsOrganic Chemistry
uzh.workflow.doajuzh.workflow.doaj.false
uzh.workflow.eprintid8797
uzh.workflow.fulltextStatusrestricted
uzh.workflow.revisions134
uzh.workflow.rightsCheckkeininfo
uzh.workflow.statusarchive
uzh.wos.impact13
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