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Volumn 26, Issue 4, 2008, Pages 321-326

Two-step, one-pot enzymatic synthesis of cefprozil from -phenylacetamido-3-propenyl-cephalosporanic acid (GPRA)

Author keywords

7 phenylacetamido 3 propenyl cephalosporanic acid (GPRA); Cefprozil; One pot enzymatic synthesis; Penicillin acylase

Indexed keywords

AMINES; ESCHERICHIA COLI; ESTERS;

EID: 45849114356     PISSN: 10242422     EISSN: 10292446     Source Type: Journal    
DOI: 10.1080/10242420802090925     Document Type: Article
Times cited : (8)

References (12)
  • 1
    • 45849125875 scopus 로고
    • Hydrolysis of penicillin G by immobilized penicillin acylase-ionic exchange combition system
    • Chen, J., Omasa, T., Katakura, Y., Shioya, S. and Suga, KI (1995) Hydrolysis of penicillin G by immobilized penicillin acylase-ionic exchange combition system. Chin J Biotechnol, 11, pp. 343-349.
    • (1995) Chin J Biotechnol , vol.11 , pp. 343-349
    • Chen, J.1    Omasa, T.2    Katakura, Y.3    Shioya, S.4    Suga, K.I.5
  • 2
    • 0023103550 scopus 로고
    • Comparative antibacterial activity of a new oral cephalosporin, BMY-28100
    • Chin, NX and Neu, HC (1987) Comparative antibacterial activity of a new oral cephalosporin, BMY-28100. Antimicrob Agents Chemother, 31, pp. 483-490.
    • (1987) Antimicrob Agents Chemother , vol.31 , pp. 483-490
    • Chin, N.X.1    Neu, H.C.2
  • 3
    • 0040822514 scopus 로고
    • Dicarbonylverbindungen als aminoschutzgruppen bei peptidsynthesen
    • Dane, E., Drees, F., Konrad, P. and Dockner, T. (1962) Dicarbonylverbindungen als aminoschutzgruppen bei peptidsynthesen. Angew Chimie, 74, p. 873.
    • (1962) Angew Chimie , vol.74 , pp. 873
    • Dane, E.1    Drees, F.2    Konrad, P.3    Dockner, T.4
  • 4
    • 0343446120 scopus 로고    scopus 로고
    • Synthesis of antibiotics (cephaloglycin) catalysed by penicillin G acylase: Evaluation and optimization of different synthetic approaches
    • Fernandez-Lafuente, R., Rossell, CM, Pitatkowska, B. and Guisan, JM (1996) Synthesis of antibiotics (cephaloglycin) catalysed by penicillin G acylase: Evaluation and optimization of different synthetic approaches. Enzyme Microb Technol, 19, pp. 9-14.
    • (1996) Enzyme Microb Technol , vol.19 , pp. 9-14
    • Fernandez-Lafuente, R.1    Rossell, C.M.2    Pitatkowska, B.3    Guisan, J.M.4
  • 5
    • 2342517327 scopus 로고    scopus 로고
    • Optimization of cephalexin synthesis with immobilized penicillin acylase in ethylene glycol medium at low temperatures
    • Illanes, A., Anjari, MS, Altamirano, C. and Aguirre, C. (2004) Optimization of cephalexin synthesis with immobilized penicillin acylase in ethylene glycol medium at low temperatures. J Mol Catal B: Enzym, 30, pp. 95-103.
    • (2004) J Mol Catal B: Enzym , vol.30 , pp. 95-103
    • Illanes, A.1    Anjari, M.S.2    Altamirano, C.3    Aguirre, C.4
  • 6
    • 0032486573 scopus 로고    scopus 로고
    • Use an aqueous two-phase systems for in situ extraction of water soluble antibiotics during their synthesis by enzymes immobilized on porous supports
    • Justiz, OH, Fernandez-Lafuente, R., Terreni, M. and Guisan, JM (1998) Use an aqueous two-phase systems for in situ extraction of water soluble antibiotics during their synthesis by enzymes immobilized on porous supports. Biotechnol Bioeng, 59, pp. 73-79.
    • (1998) Biotechnol Bioeng , vol.59 , pp. 73-79
    • Justiz, O.H.1    Fernandez-Lafuente, R.2    Terreni, M.3    Guisan, J.M.4
  • 7
    • 0031466064 scopus 로고    scopus 로고
    • One-pot chemoenzymatic synthesis of 3′-functionalized cephalosporines (Cefazolin) by three consecutive biotransformations in fully aqueous medium
    • Justiz, OH, Fernandez-Lafuente, R., Guisan, JM, Negri, P., Pagani, G., Pregnolato, M. and Terreni, M. (1997) One-pot chemoenzymatic synthesis of 3′-functionalized cephalosporines (Cefazolin) by three consecutive biotransformations in fully aqueous medium. J Org Chem, 62, pp. 9099-9106.
    • (1997) J Org Chem , vol.62 , pp. 9099-9106
    • Justiz, O.H.1    Fernandez-Lafuente, R.2    Guisan, J.M.3    Negri, P.4    Pagani, G.5    Pregnolato, M.6    Terreni, M.7
  • 9
    • 34047220282 scopus 로고    scopus 로고
    • Synthesis of β-lactam antibacterials using soluble side chain esters and enzymatic acylase
    • WO Patent
    • Usher, JJ and Romancik, G. (1998) Synthesis of β-lactam antibacterials using soluble side chain esters and enzymatic acylase. WO Patent
    • (1998)
    • Usher, J.J.1    Romancik, G.2
  • 11
    • 0042904786 scopus 로고    scopus 로고
    • Quantitative characterization of the nucleophile reactivity in penicillin acylase-catalysed acyl transfer reactions
    • Youshko, MI, Chilov, GG, Shcherbakova, TA and Svedas, VK (2002) Quantitative characterization of the nucleophile reactivity in penicillin acylase-catalysed acyl transfer reactions. Biochim Biophys Acta, 1599, pp. 134-140.
    • (2002) Biochim Biophys Acta , vol.1599 , pp. 134-140
    • Youshko, M.I.1    Chilov, G.G.2    Shcherbakova, T.A.3    Svedas, V.K.4
  • 12
    • 45849085515 scopus 로고    scopus 로고
    • Process for the enzymatic synthesis of beta-lactam antibiotics in the presence of an enzyme inhibitor
    • Zenoni, M., Tagliani, AR, Cannas, E. and Venturelli, A. (1996) Process for the enzymatic synthesis of beta-lactam antibiotics in the presence of an enzyme inhibitor. Eur Patent
    • (1996) Eur Patent
    • Zenoni, M.1    Tagliani, A.R.2    Cannas, E.3    Venturelli, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.