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Please use this identifier to cite or link to this item: http://10.10.120.238:8080/xmlui/handle/123456789/919
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dc.contributor.authorVetica F.en_US
dc.contributor.authorDr.en_US
dc.contributor.authorBailey S.J.en_US
dc.contributor.authorKumar M.en_US
dc.contributor.authorMahajan S.en_US
dc.contributor.authorVon Essen C.en_US
dc.contributor.authorRissanen K.en_US
dc.contributor.authorEnders D.en_US
dc.date.accessioned2023-11-30T08:56:01Z-
dc.date.available2023-11-30T08:56:01Z-
dc.date.issued2020-
dc.identifier.issn0039-7881-
dc.identifier.otherEID(2-s2.0-85087570929)-
dc.identifier.urihttps://dx.doi.org/10.1055/s-0040-1707472-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/919-
dc.description.abstractA mild and efficient palladium-catalyzed [3+2] cycloaddition of vinylaziridine and indane-1,3-diones has been realized. The resulting spiro-pyrrolidines were provided in excellent yields and, with the introduction of the leucine-derived phosphine ligand, moderate to good enantio- and diastereoselectivities. © 2020. Thieme. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlagen_US
dc.sourceSynthesis (Germany)en_US
dc.subjectasymmetric synthesisen_US
dc.subjectaziridinesen_US
dc.subjectindane-1,3-dionesen_US
dc.subjectpalladium catalysisen_US
dc.subjectsprio-pyrrolidinesen_US
dc.titlePalladium-Catalyzed [3+2] Cycloaddition of Vinylaziridine and Indane-1,3-diones: Diastereo- And Enantioselective Access to Spiro-Pyrrolidinesen_US
dc.typeJournal Articleen_US
Appears in Collections:Journal Article

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