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Volumn 43, Issue 37, 2002, Pages 6617-6620

Highly enantioselective biotransformations of 2-aryl-4-pentenenitriles, a novel chemoenzymatic approach to (R)-(-)-baclofen

Author keywords

(R) ( ) baclofen; Amidase; Biotransformations; Chemoenzymatic synthesis; Nitrile hydratase

Indexed keywords

AMIDE; BACLOFEN; NITRILE;

EID: 0037048478     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01449-1     Document Type: Article
Times cited : (47)

References (32)
  • 19
    • 0011164957 scopus 로고    scopus 로고
    • 4), removal of solvent, and column chromatography, the unconverted nitrile 1 and amide 2. The aqueous solution was then acidified using aqueous HCl (2 M) to pH 2 and extracted with ethyl acetate to give acid 3.
    • 4), removal of solvent, and column chromatography, the unconverted nitrile 1 and amide 2. The aqueous solution was then acidified using aqueous HCl (2 M) to pH 2 and extracted with ethyl acetate to give acid 3.
  • 20
    • 0011247427 scopus 로고    scopus 로고
    • note
    • 2Cl requires 209.0374.
  • 21
    • 0011166088 scopus 로고    scopus 로고
    • Enantiomeric excess values were obtained from HPLC analysis using a Chiracel OD, OJ or OB column with a mixture of n-hexane and 2-propanol (9:1) as the mobile phase.
    • Enantiomeric excess values were obtained from HPLC analysis using a Chiracel OD, OJ or OB column with a mixture of n-hexane and 2-propanol (9:1) as the mobile phase.
  • 23
    • 4244159951 scopus 로고
    • Makosza, M.; Serafin, B. Rocz. Chem. 1965, 39, 1401-1409. Chem. Abs. 1966, 64, 17474g.
    • (1966) Chem. Abs. , vol.64
  • 31
    • 0011209104 scopus 로고    scopus 로고
    • 15NCl requires: 196.0887.
    • 15NCl requires: 196.0887.
  • 32
    • 0011196219 scopus 로고    scopus 로고
    • 2O) δ 179.4, 138.1, 132.9, 129.3, 129.1, 44.0, 42.1, 40.7.
    • 2O) δ 179.4, 138.1, 132.9, 129.3, 129.1, 44.0, 42.1, 40.7.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.