New chiral synthon from the PLE catalyzed enantiomeric separation of 6-acetoxy-3-methylcyclohex-2-en-1-one

1996-08-01
Tanyeli, Cihangir
Demir, AS
Dikici, E
(+/-)-6-Acetoxy-3-methylcyclohex-2-en-1-one was resolved by PLE catalyzed hydrolysis to afford (+)-6-hydroxy-3-methylcyclohex-2-en-1-one in >95% e.e. (+)-6-Hydroxy-3-methylcyclohex-2-en-1-one was transformed to its (S)-O-acetyllactyl ester derivative to determine the e.e. %. Copyright (C) 1996 Elsevier Science Ltd
Citation Formats
C. Tanyeli, A. Demir, and E. Dikici, “New chiral synthon from the PLE catalyzed enantiomeric separation of 6-acetoxy-3-methylcyclohex-2-en-1-one,” pp. 2399–2402, 1996, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/44987.