Aydin, A. E.2024-09-182024-09-1820221070-42801608-3393https://doi.org/10.1134/S1070428022060100https://hdl.handle.net/20.500.12483/9769Chiral norephedrine-based beta-amino alcohol bearing a substituted thiophene ring were applied as catalysts for the enantioselective aldol reaction of isatins with ketones. Using enantiomeric chiral amino alco-hols, the desired aldol products were obtained in high yields and excellent enantioselectivities (up to 95% ee) under optimized conditions.eninfo:eu-repo/semantics/closedAccessenantioselective reactionaldol reactionchiral amino alcoholsisatinEnantioselective Aldol Reaction between Isatins and Ketones, Catalyzed by Chiral Norephedrine-Derived ?-Amino Alcohols with a Thiophene MoietyArticle58682082910.1134/S10704280220601002-s2.0-85135604307Q4WOS:000837686700010Q4