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dc.contributor.authorConnon, Stephen
dc.date.accessioned2021-10-20T15:53:13Z
dc.date.available2021-10-20T15:53:13Z
dc.date.issued2018
dc.date.submitted2018en
dc.identifier.citationCraig, R. and Sorrentino, E. and Connon, S.J., Enantioselective Alkylation of 2-Oxindoles Catalyzed by a Bifunctional Phase-Transfer Catalyst: Synthesis of (â )-Debromoflustramine B, Chemistry - A European Journal, 24, 18, 2018, 4528-4531en
dc.identifier.otherY
dc.identifier.urihttp://hdl.handle.net/2262/97401
dc.description.abstractA new bifunctional phase-transfer catalyst that employs hydrogen bonding as a control element was developed to promote efficient enantioselective SN2 reactions for the construction all-carbon quaternary stereocenters in high yield and excellent enantioselectivity (up to 97 % ee) utilizing the alkylation of a malleable oxindole substrate. The utility of the methodology was demonstrated through a concise and highly enantioselective synthesis of (−)-debromoflustramine B.en
dc.format.extent4528-4531en
dc.language.isoenen
dc.relation.ispartofseriesChemistry - A European Journal;
dc.relation.ispartofseries24;
dc.relation.ispartofseries18;
dc.rightsYen
dc.subjectdebromoflustramine Ben
dc.subjectPhase-transferen
dc.subjectEnantioselectivityen
dc.titleEnantioselective Alkylation of 2-Oxindoles Catalyzed by a Bifunctional Phase-Transfer Catalyst: Synthesis of (− )-Debromoflustramine Ben
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/connons
dc.identifier.rssinternalid189079
dc.identifier.doihttp://dx.doi.org/10.1002/chem.201800313
dc.rights.ecaccessrightsopenAccess


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