http://10.10.120.238:8080/xmlui/handle/123456789/919
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Vetica F. | en_US |
dc.contributor.author | Dr. | en_US |
dc.contributor.author | Bailey S.J. | en_US |
dc.contributor.author | Kumar M. | en_US |
dc.contributor.author | Mahajan S. | en_US |
dc.contributor.author | Von Essen C. | en_US |
dc.contributor.author | Rissanen K. | en_US |
dc.contributor.author | Enders D. | en_US |
dc.date.accessioned | 2023-11-30T08:56:01Z | - |
dc.date.available | 2023-11-30T08:56:01Z | - |
dc.date.issued | 2020 | - |
dc.identifier.issn | 0039-7881 | - |
dc.identifier.other | EID(2-s2.0-85087570929) | - |
dc.identifier.uri | https://dx.doi.org/10.1055/s-0040-1707472 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/919 | - |
dc.description.abstract | A 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.iso | en | en_US |
dc.publisher | Georg Thieme Verlag | en_US |
dc.source | Synthesis (Germany) | en_US |
dc.subject | asymmetric synthesis | en_US |
dc.subject | aziridines | en_US |
dc.subject | indane-1,3-diones | en_US |
dc.subject | palladium catalysis | en_US |
dc.subject | sprio-pyrrolidines | en_US |
dc.title | Palladium-Catalyzed [3+2] Cycloaddition of Vinylaziridine and Indane-1,3-diones: Diastereo- And Enantioselective Access to Spiro-Pyrrolidines | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Journal Article |
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