A new and efficient chemoenzymatic route to both enantiomers of α′-acetoxy and α′-hydroxy-α-methoxy cyclic enones

Tetrahedron Asymmetry

Volumn 17, Issue 5, 2006, Pages 786-791

  Demir, Ayhan S ^a   Caliskan, Zerrin ^a,b   Aydin, A Ebru ^c   Bicer, Isil ^a  

^a MIDDLE EAST TECHNICAL UNIVERSITY   (Turkey)

^b YILDIZ TECHNICAL UNIVERSITY   (Turkey)

^c MUSTAFA KEMAL UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

3 ETHYL 5 HYDROXY 2 METHOXY 2 CYCLOPENTEN 1 ONE; 3 METHOXY 4 METHYL 2 OXOCYCLOHEX 3 ENYLACETATE; 3 METHOXY 4 METHYL 2 OXOCYCLOPENT 3 ENYLACETATE; 3 METHOXY 4,6,6 TRIMETHYL 2 OXOCYCLOHEX 3 ENYLACETATE; 4 ETHYL 3 METHOXY 2 OXOCYCLOPENT 3 ENYLACETATE; 5 HYDROXY 3 METHYL 2 METHOXY 2 CYCLOPENTEN 1 ONE; 6 HYDROXY 2 METHOXY 3 METHYLCYCLOHEX 2 EN 1 ONE; 6 HYDROXY 2 METHOXY 3,5,5 TRIMETHYLCYCLOHEX 2 EN 1 ONE; ACETIC ACID DERIVATIVE; CYCLOPENTENE DERIVATIVE; HYDROXYL GROUP; MANGANESE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION KINETICS; DRUG SYNTHESIS; ENANTIOMER; HYDROLYSIS KINETICS; PRIORITY JOURNAL; TRANSESTERIFICATION;

EID: 33645833444     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.01.025     Document Type: Article

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