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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
Title: Palladium-Catalyzed [3+2] Cycloaddition of Vinylaziridine and Indane-1,3-diones: Diastereo- And Enantioselective Access to Spiro-Pyrrolidines
Authors: Vetica F.
Dr.
Bailey S.J.
Kumar M.
Mahajan S.
Von Essen C.
Rissanen K.
Enders D.
Keywords: asymmetric synthesis
aziridines
indane-1,3-diones
palladium catalysis
sprio-pyrrolidines
Issue Date: 2020
Publisher: Georg Thieme Verlag
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.
URI: https://dx.doi.org/10.1055/s-0040-1707472
http://localhost:8080/xmlui/handle/123456789/919
ISSN: 0039-7881
Appears in Collections:Journal Article

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