Azizoglu, MuratErdogan, AsliArslan, NevinTurgut, YilmazHosgoren, HalilPirinccioglu, Necmettin2024-04-242024-04-2420160957-4166https://doi.org/10.1016/j.tetasy.2016.06.003https://hdl.handle.net/11468/16115The enantioselective reduction of prochiral ketones with borane in the presence of a chiral ligand has received considerable attention. Hydroxylamine-based chiral ligands with amide and hydroxyl functions in the presence of other co-ordinating groups are highly effective in these asymmetric reductions. The current work presents a simple one step synthesis of a series of beta-hydroxyamide-based ligands from the reaction between 3-hydroxy-2-naphthoic acid and chiral amino alcohols and their applications as catalysts in asymmetric borane-mediated reductions of aromatic prochiral ketones in THE The reductions provided the corresponding secondary alcohols with up to 96% ee and in good to excellent yields (89-99%). OFF calculations at B3LYP/6-31+g(d) level offered theoretical models to account for the enantioselectivity imposed by the chiral ligands in the reductions of the ketones. (C) 2016 Elsevier Ltd. All rights reserved.eninfo:eu-repo/semantics/closedAccess[No Keyword]Article2714-15614622WOS:0003804198000042-s2.0-8497709856310.1016/j.tetasy.2016.06.003N/AQ2