Tümerdem, RTopal, GTurgut, Y2024-04-242024-04-2420050957-4166https://doi.org/10.1016/j.tetasy.2004.12.020https://hdl.handle.net/11468/16095Some new chiral Schiff bases have been prepared in good yields from various carbonyl groups and two 2-amino alcohols. LiAlH4 was treated with different equivalents of the Schiff bases. Enantioselective reduction of acetophenone is achieved in high chemical yield (up to 93%) with moderate enantiomeric excess (up to 22%) by use of the new reducing agents. (C) 2005 Elsevier Ltd. All rights reserved.eninfo:eu-repo/semantics/closedAccess[No Keyword]Article164865868WOS:0002272667000162-s2.0-1384427504610.1016/j.tetasy.2004.12.020N/AQ2