Chemo-enzymatic route for (R)-terbutaline hydrochloride based on microbial asymmetric reduction of a substituted α-chloroacetophenone derivative

Journal of Molecular Catalysis B: Enzymatic

Volumn 84, Issue , 2012, Pages 83-88

  Taketomi, Shohei ^a   Asano, Masayoshi ^a   Higashi, Toshinori ^a   Shoji, Mitsuru ^a   Sugai, Takeshi ^a  

^a KEIO UNIVERSITY   (Japan)

Author keywords

Asymmetric reduction; Hydrolysis; Lipase; Yeast

Indexed keywords

ASYMMETRIC REDUCTION; CARBON SOURCE; CHLOROACETOPHENONE; ENANTIOSELECTIVE; KEY REACTIONS; TERBUTALINE; WHOLE CELL BIOCATALYSTS;

GLYCEROL; HYDROLYSIS; LIPASES;

YEAST;

1 [3',5' BIS(METHOXYMETHOXY)PHENYL] 2 (TERTBUTYLAMINO); 2 CHLORO 1 [3',5' BIS(METHOXYMETHOXY)PHENYL]ETHANOL; 2 CHLORO 1 [3',5' BIS(METHOXYMETHOXY)PHENYL]ETHANONE; CARBON; GLYCEROL; PHENACYL CHLORIDE; TERBUTALINE; UNCLASSIFIED DRUG;

BIOCATALYST; CANDIDA NITRATOPHILA; CATALYSIS; CONFERENCE PAPER; DRUG SYNTHESIS; ENANTIOSELECTIVITY; FUNGUS; KLUYVEROMYCES MARXIANUS; PICHIA FARINOSA; PICHIA MINUTA; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; SUBSTITUTION REACTION; WILLIOPSIS CALIFORNICA;

WILLIOPSIS CALIFORNICA;

EID: 84866431759     PISSN: 13811177     EISSN: 18733158     Source Type: Journal    
DOI: 10.1016/j.molcatb.2012.01.020     Document Type: Conference Paper

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