Baysal, AkinKarakas, Duygu ElmaMeric, NerminAk, BunyaminAydemir, MuratDurap, Feyyaz2024-12-242024-12-2420170340-42851572-901Xhttps://doi.org/10.1007/s11243-017-0140-1https://hdl.handle.net/20.500.12604/6132Metal-catalyzed enantioselective transfer reduction of ketones to enantiomerically enriched chiral alcohols has recently attracted attention. Therefore, a series of methyl alkyl or alkyl/aryl ketones have been reduced by using Ru(II), Rh(I) and Ir(III) catalysts based on C (2)-symmetric chiral ferrocenyl phosphinite ligands. The corresponding optically active secondary alcohols were obtained in excellent conversions and moderate-to-good enantioselectivities. The best results were obtained with an iridium catalyst, giving up to 98% conversion and 80% ee.eninfo:eu-repo/semantics/closedAccessChiral phosphinites as efficient ligands for enantioselective Ru(II), Rh(I) and Ir(III)-catalyzed transfer hydrogenation reactionsArticle424365372Q3WOS:000399456900011Q22-s2.0-8501648205910.1007/s11243-017-0140-1