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Volumn 32, Issue 5-6, 2005, Pages 167-174

Assessing substrate acceptance and enantioselectivity of yeast reductases in reactions with substituted α-keto β-lactams

Author keywords

Hydroxy lactams; Keto lactams; Bioreductions; Yeast reductases; Yeast catalyzed reductions

Indexed keywords

ESCHERICHIA COLI; REACTION KINETICS; REDUCTION; YEAST;

EID: 13944278021     PISSN: 13811177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcatb.2004.10.005     Document Type: Article
Times cited : (10)

References (66)
  • 15
    • 0002674759 scopus 로고
    • Stereocontrolled ketene-imine cycloaddition reactions
    • G.I. Georg VCH New York, NY
    • G.I. Georg, and V.T. Ravikumar Stereocontrolled ketene-imine cycloaddition reactions G.I. Georg The Organic Chemistry of β-Lactams 1993 VCH New York, NY 295 368
    • (1993) The Organic Chemistry of β-Lactams , pp. 295-368
    • Georg, G.I.1    Ravikumar, V.T.2
  • 57
    • 13944278467 scopus 로고    scopus 로고
    • Bruker XSCANS, SHELXS-97, SHELXL-97 and SHELXTL, Bruker Analytical X-Ray Systems, Madison, Wisconsin, USA. The CIF tables have been deposited with the Cambridge Data File Centre. The deposit numbers are CCDC 247144-247146. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK [Fax: +44 (1223) 336 033; E-mail: deposit@ccdc.cam.ac.uk]
    • Bruker XSCANS, SHELXS-97, SHELXL-97 and SHELXTL, Bruker Analytical X-Ray Systems, Madison, Wisconsin, USA. The CIF tables have been deposited with the Cambridge Data File Centre. The deposit numbers are CCDC 247144-247146. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK [Fax: +44 (1223) 336 033; E-mail: deposit@ccdc.cam.ac.uk].
  • 64
    • 13944253274 scopus 로고    scopus 로고
    • Ph.D. Dissertation, University of Florida, Gainesville, FL, USA
    • S. Rodríguez Giordano, Ph.D. Dissertation, University of Florida, Gainesville, FL, USA, 2000.
    • (2000)
    • Rodríguez Giordano, S.1
  • 65
    • 13944273758 scopus 로고    scopus 로고
    • note
    • The corresponding numerical values are available in the Supplementary data.
  • 66
    • 13944280273 scopus 로고    scopus 로고
    • note
    • The ketones have lower UV absorptions than the alcohols, and the margin of error in the determining the extent of conversion and the product distribution for compounds 1d and 1e is therefore slightly larger than for 1a-c. The trends observed, however, are quite consistent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.