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

Date

1996-08-01

Author

Tanyeli, Cihangir
Dikici, E

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(+/-)-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

Subject Keywords

Manganese(İii) acetate, Oxidation, Enones, Acids

URI

https://hdl.handle.net/11511/44987

Journal

TETRAHEDRON-ASYMMETRY

DOI

https://doi.org/10.1016/0957-4166(96)00296-0

Collections

Department of Chemistry, Article

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Citation Formats

C. Tanyeli and E. Dikici, “New chiral synthon from the PLE catalyzed enantiomeric separation of 6-acetoxy-3-methylcyclohex-2-en-1-one,” TETRAHEDRON-ASYMMETRY, pp. 2399–2402, 1996, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/44987.