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氧化还原酶在有机合成中的应用

Application of Oxidoreductases in Ogranic Synthesis
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摘要 概述氧化还原酶在有机合成中的还原作用和氧化作用,展望氧化还原酶的应用前景。 Oxidoructases are widely used in organic synthesis, including both oxidation and reduction of related compounds. This paper reviews the latest progress in their application, with the emphasis placed on chiral synthesis. The paper also discusses the prospect of oxidoreductases.
作者 刘振杰 李从发 刘四新 明飞平
机构地区 华南热带农业大学工学院
出处 《华南热带农业大学学报》 2004年第3期29-33,共5页 Journal of South China University of Tropical Agriculture
关键词 氧化还原酶 有机合成 还原作用 氧化作用 oxidoreductase organic synthesis chiral synthesis application
分类号 O629.8 [理学—有机化学]
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参考文献17

  • 1薛兴涛,陈志春,施长年,吕德水,林贤福.氧化还原酶催化合成芳香聚合物的研究进展[J].功能高分子学报,2002,15(1):82-86. 被引量：5
  • 2[2]Patrick Boutoute, Guy Mousset, Henri Veschambre.Regioselective or enantiogenic electrochemical and microbial reductions of 1,2-diketones. New J. Chem, 1998(3):247～251
  • 3[3]Cotterill I C, Cox P B, Drake A F, et al. Synthesis of Three Metabolites of Icosapentaenoic and Docosahexaenoic acids. J. Chem Soc, Perkin Trans.1991(1):3071～3075
  • 4[4]Bradshaw C W, Hummel W, Wong C H.A Pseudomonas sp. alcohol dehydrogenase with broad substrate specificity and unusual stereospecificity for organic synthesis. J. Org Chem, 1992, 57:1526～1532
  • 5[5]Dodds D R, Jones J B. Biocatalysis and enzymes in organic synthesis. Nat Prod Rep, 2001,18:618～640
  • 6[6]Baldoli C, Buttero P Del, Maiorana S, et al. Studies on enantiotopic differentiation in the horse liver alcohol dehydrogenase catalysed reduction of chiral tricarbonyl-(6-ben-zaldehyde)chromium complexes. Tetrahedron: Asymmetry, 1998,9:1497～1504
  • 7[7]Keinan E, Sinha S C, Singh S P. Thermostable enzymes in organic synthesis. 5. Total synthesis of S-(+)-Z-dodec-3-en-11-olide (ferrulactone Ⅱ)using a TBADH-generated bifunctional chiron. Tetrahedron, 1991,47:4631～4636
  • 8[8]Hayakawa R, Nozawa K, Shimizu M, et al. Control of enantioselectivity in the Baker's yeast reduction of keto ester derivatives in the presence of a sulfur compound. Tetrahedron Lett,1998,39:67～70
  • 9[9]Dao D H, Okamura M, Akasaka T, et al. Stereochemical Control in Microbial Reduction. 31. Reduction of Alkyl 20xo-4-arylbutylates by Bakers'Yeast under Selected Reaction Conditions.Tetrahedron:Asymmmetry, 1998,9:2725～2730
  • 10[10]Maguire A R, Kelleher L L. Enantioselective Introduction of a Benzenesulfonylmethyl Substituent at an Unactivated Carbon Atom via Chemoenzymatic Methods. Tetrahedron Lett, 1997,38:7459～7462

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华南热带农业大学学报
2004年 第3期

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