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Corey化学酶与不对称合成 被引量:4

Corey's Chemzyme and Asymmetric Synthesis
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摘要 本文从立体化学和反应机理方面综述了Corey化学酶的催化作用及其在有机不对称合成中的应用,指出了Corey化学酶与酶的相同点和不同点,对于关键的反应过程态均以空间关系更为清楚的构象式表示。 This review examines the catalysis and application of Corey' s chemzyme in asymmetric organic synthesis from the viewpoint of stereochemistry and reaction mechanism. The similarities and differences between chemzyme and enzyme are shown clearly in the paper. In order to give more clear the spacial relationship some key transient states are described by the comformational formula.
机构地区 北京大学化学系
出处 《有机化学》 SCIE CAS CSCD 北大核心 1996年第5期403-414,共12页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金
关键词 化学酶 不对称合成 醇胺 邻二胺 催化作用 chemzyme, asymmetric synthesis, hydroxy amine, vicinal diamine
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同被引文献37

  • 1黄世文,单自兴,段标,赵德杰.由(1R,2S)-麻黄碱制备的硼杂噁唑烷催化甲硼烷不对称还原苯乙酮[J].有机化学,1995,15(5):550-554. 被引量:3
  • 2蒋耀忠,泰勇,宓爱巧,李智,陈新滋,杨登贵.手性噁唑硼烷结构与还原苯基乙基甲酮的对映选择性研究~≠[J].有机化学,1996,16(1):29-33. 被引量:4
  • 3蒋耀忠 冯小明.以氨基醇为手性配体的不对称催化反应[J].化学(台湾),1997,55(1):67-67.
  • 4Hirao A, Itsuno S, NaKahama S et al. Asymmetric reduction of aromatic ketones with chiral alkoxy -amine - borane complexes [ J ] . J. Chem. Soe. Commun, 1981,315 - 317.
  • 5Corey E J, Bakshi R K, Shibata S. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines mechanism and synthetic implieations[J].J. Am. Chem. Soe. ,1987,109:5 551-5 553.
  • 6Corey E J, Bakshi R K, Shibata S et al. A stableand easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses[J] .J.Am. Chem. Soe., 1987, 109:7 925-7926.
  • 7Corey E J, Shibata S, Bakshi R K. An efficient and catalytically enantioselective route to (s) - ( - ) -phenyloxirane[J] .J. Org. Chem., 1988,53:2 861- 2 863.
  • 8Corey E J. New enantioselective routes to biologically interesting compounds [ J ] . Pure & Appl. Chem.,1990, 62:(7),1 209- 1 216.
  • 9Wallbaum S, Martens J. Asymmetric syntheses with chiral oxazaborolidines [ J ]. Tetrahedron: Asymmetry,1992,3(12):1 475-1 504.
  • 10Li X S, Xie R G. Enantioselective reduction of prochiral ketones catalyzed by new (R) -4-(phenylmercapto) methyl - 5,5 - diphenyl - 1,3,2 oxazahorolidine and bis - [( R, R ) - 5, 5 -diphenyl - 1,3, 2 - oxazahorolidine methyl ] disulfide from L- cystine[J]. Tetrahedron:Asymmetry,1997,8(14) :2 283 - 2 285.

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