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Volumn , Issue 15, 2006, Pages 2395-2398

Enantioselective hydrogenation of β-ketoesters using a MeO-PEG-supported Biphep ligand under atmospheric pressure: A practical synthesis of (S)-fluoxetine

Author keywords

Asymmetric synthesis; Biphenyl ligands; Fluoxetine; Hydrogenation; Supported catalysis

Indexed keywords

6,6' BIS(DIPHENYLPHOSPHANYL)BIPHENYL; BENZENE DERIVATIVE; BETA KETOESTER DERIVATIVE; BIPHENYL DERIVATIVE; ESTER DERIVATIVE; ETHYL 3 HYDROXY 3 PHENYLPROPANOATE; FLUOXETINE; OXALIC ACID; RUTHENIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 33749335267     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-949650     Document Type: Article
Times cited : (11)

References (31)
  • 8
    • 0030000726 scopus 로고    scopus 로고
    • (b) Lily Co. Drugs Future 1996, 21, 83.
    • (1996) Drugs Future , vol.21 , pp. 83
  • 25
    • 33749339820 scopus 로고    scopus 로고
    • note
    • th International Symposium on Fine Chemistry and Functional Polymers held at Shanghai during October 2005.
  • 28
    • 33749326455 scopus 로고    scopus 로고
    • note
    • 3): δ = -14.05 (s).
  • 29
    • 33749321009 scopus 로고    scopus 로고
    • note
    • Catalyst Preparation: To a mixture of diphosphine ligand 3 (60 mg, 0.0126 mmol) and bis(2-methylallyl)cycloocta-1,5-diene ruthenium (II) complex (4 mg, 0.0126 mmol) in anhydrous degassed acetone (1.5 mL) was added 0.18 M methanolic HBr (0.14 mL, 0.025 mmol). The amber mixture was stirred at room temperature for 0.5 h and the solvent removed thoroughly in vacuo to leave the active catalyst, which was used immediately as a hydrogenation catalyst.
  • 31
    • 33749325199 scopus 로고    scopus 로고
    • note
    • 2O (30 mL). The precipitated polymeric catalyst was collected by filtration for reuse in the next run. Both the yield and the ee value of the alcohol were determined from the filtrate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.