Asymmetric transfer hydrogenation reaction in water: Comparison of chiral proline amide/amine ruthenium(II) complexes
Makaleler > Tam Makale · 2014
Yazarlar: Serpil DENİZALTI, Deniz MERCAN, Betul Sen, Aytac Gurhan Gokce, BEKİR ÇETİNKAYA
Journal of Organometallic Chemistry, SCI Expanded İndekslerine Giren Dergi, Uluslararası, Wos, 2014, cilt 779, ss 62-66
DOI: 10.1016/j.jorganchem.2014.12.023
Özet
Chiral proline amide/amine ligands (2, 3), synthesized by multi-step reaction starting from L-proline (1), were evaluated as catalyst generated in situ from [RuCl2(p-cymene)](2) for asymmetric transfer hydrogenation of aromatic ketones in the presence of sodium formiate and sodium dodecyl sulfate (SDS). The results revealed that efficiencies and enantioselectivities strongly depend on the N-substituents. (C) 2014 Elsevier B.V. All rights reserved.