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Ru Catalyzed Asymmetric Hydrogenation of Quinolines

Subsequently, some commercially available chiral bidentate phosphine ligands [Pg.299]

Chiral Amine Synthesis Methods, Developments and Applications. Edited by Thomas C. Nugent Copyright 2010 WILEY-VCH Verlag GmbH Co. KGaA, Weinheim ISBN 978-3-527-32509-2 [Pg.299]

Having established the optimal condition, the scope ofthe Ir catalyzed asymmetric hydrogenation of quinoline derivatives was explored. A variety of 2 substituted and [Pg.300]

Zhou and coworkers also studied the asymmetric hydrogenation of 2 functiona [Pg.300]

0mol% of catalysts prepared in situ from [Ir(COD)Cl]2 and 2.2 equiv of chiral [Pg.300]


See other pages where Ru Catalyzed Asymmetric Hydrogenation of Quinolines is mentioned: [Pg.299]    [Pg.310]   


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Hydrogen catalyzed

Hydrogenation of quinoline

Hydrogenation of quinolines

Hydrogenation, catalyzed

Of [Ru

Quinoline, hydrogenation

Quinolines hydrogenation

Ru-Catalyzed Asymmetric Hydrogenation

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