Synthesis of new chiral 2-functionalized-1, 2, 3, 4-tetrahydroquinoline derivatives via asymmetric hydrogenation of substituted quinolines
AM Maj, I Suisse, C Hardouin, F Agbossou-Niedercorn
Index: Maj, Anna M.; Suisse, Isabelle; Hardouin, Christophe; Agbossou-Niedercorn, Francine Tetrahedron, 2013 , vol. 69, # 44 p. 9322 - 9328
Full Text: HTML
Citation Number: 7
Abstract
Abstract The asymmetric hydrogenation of a series of quinolines substituted by a variety of functionalized groups linked to the C2 carbon atom is providing access to optically enriched 2-functionalized 1, 2, 3, 4-tetrahydroquinolines in the presence of in situ generated catalysts from [Ir (cod) Cl] 2, a bisphosphine, and iodine. The enantioselectivity levels were as high as 96% ee.
Related Articles:
[Lipshutz, Bruce H.; Kim, Sung-Kyu; Mollard, Paul; Blomgren, Peter A.; Stevens, Kirk L. Tetrahedron, 1998 , vol. 54, # 25 p. 6999 - 7012]
[Wachi, Kazuyuki; Terada, Atsusuke Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 3020 - 3028]