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Volumn 20, Issue 35, 2014, Pages 11225-11228

Biocontrolled formal inversion or retention of L -α-amino acids to enantiopure (R)- or (S)-hydroxyacids

Author keywords

asymmetric catalysis; biocatalysis; cascades; inversion; retention

Indexed keywords

CARBOXYLIC ACIDS; CASCADES (FLUID MECHANICS); CHROMATOGRAPHIC ANALYSIS;

EID: 84906788805     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201403195     Document Type: Article
Times cited : (42)

References (59)
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    • Such a biocatalytic reaction sequence has only been reported in a stepwise fashion using divergent reaction conditions in a patent:, 2002, WO 2002/033110, or using growing cultures of Clostridium butyricum with low yield (max. 6.2 %)
    • Such a biocatalytic reaction sequence has only been reported in a stepwise fashion using divergent reaction conditions in a patent:, R. F. Senkpeil, D. P. Pantaleone, P. P. Taylor, 2002, WO 2002/033110, or using growing cultures of Clostridium butyricum with low yield (max. 6.2 %)
    • Senkpeil, R.F.1    Pantaleone, D.P.2
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    • For instance; hydroxy acids (R)- and (S)- 3 c are, respectively, 1286 and 86 times more expensive than the starting material L - 1 c (see Supporting Information Table S1 for additional details).
    • For instance; hydroxy acids (R)- and (S)- 3 c are, respectively, 1286 and 86 times more expensive than the starting material L-1 c (see Supporting Information Table S1 for additional details).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.