Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164462
Title: Highly enantioselective iridium-catalyzed hydrogenation of 2-aryl allyl phthalimides
Author: Cabré, Albert
Romagnoli, Elia
Martínez-Balart, Pol
Verdaguer i Espaulella, Xavier
Riera i Escalé, Antoni
Keywords: Hidrogenació
Catàlisi asimètrica
Amines
Hydrogenation
Enantioselective catalysis
Amines
Issue Date: 8-Nov-2019
Publisher: American Chemical Society
Abstract: The iridium-catalyzed asymmetric hydrogenation of 2-aryl allyl phthalimides to afford enantioenriched β-aryl-β-methyl amines is presented. Recently developed Ir-MaxPHOX catalysts are used for this enantioselective transformation. The mild reaction conditions and the feasible removal of the phthalimido group makes this catalytic method easily scalable and of great interest to afford chiral amines. The importance of this new methodology is exemplified by the formal synthesis of (R)-Lorcaserin, OTS514 and enantiomerically enriched 3-methyl indolines.
Note: Versió postprint del document publicat a: https://doi.org/10.1021/acs.orglett.9b03865
It is part of: Organic Letters, 2019, vol. 21, num. 23, p. 9709-9713
URI: http://hdl.handle.net/2445/164462
Related resource: https://doi.org/10.1021/acs.orglett.9b03865
ISSN: 1523-7060
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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