Colak, MehmetDemirel, Nadir2024-04-242024-04-2420080957-4166https://doi.org/10.1016/j.tetasy.2008.02.005https://hdl.handle.net/11468/16101Chiral Schiff-bases 2, 3, 4 and 5 were designed for the enantioselective nitroaldol (Henry) reaction. The highest enantioselectivity was observed for ligand 4 (82% ee) when CH2Cl2 was used as a solvent. (C) 2008 Elsevier Ltd. All rights reserved.eninfo:eu-repo/semantics/closedAccess[No Keyword]Article195635639WOS:0002548020000182-s2.0-4084909400310.1016/j.tetasy.2008.02.005N/AQ2