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头孢克肟侧链的合成研究 被引量:5

Study on Synthesis of Cefixime Side Chain
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摘要 介绍了头孢克肟的抗菌活性。综述了头孢克肟侧链的合成方法 ,提出了从氯乙酰乙酸乙酯为原料经肟化、缩合 2步反应合成头孢克肟侧链是一条适合于工业化生产的工艺路线。参考文献 2 The medical properties of Cefixime are introduced. Synthesis of Cefixime side chain several synthetic methods from different raw materials were discussed in detail. A preparation method sutiable for industrial application was also suggested. 20 References were quoted.
出处 《合成化学》 CAS CSCD 2004年第4期348-350,364,J002,共5页 Chinese Journal of Synthetic Chemistry
关键词 头孢克肟 合成 铡链 综述 Cefixime synthesis review side chain
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参考文献5

二级参考文献2

  • 1Yamanaka H, Chiba T, Kawabata K, et al. Studies on β-lactam antibiotics IX. Synthesis and biological activity of a new orally active cephalosphorin, cefixime(FK027).J Antibiotics. 1985,38(12):1738-1751.
  • 2王玉芬 王洛生.Ceftazidime对β—内酰胺酶稳定性研究[J].抗生索,1988,13(2):122-126.

共引文献24

同被引文献22

  • 1段冀江.头孢克肟的药理与临床应用[J].广东药学,1995,5(4):7-8. 被引量:2
  • 2Debashish D.Novel intermediates for synthesis of cephalo-sporins and process for preparation of such intermediates:US,20060135761[P].2006-06-22.
  • 3Martin D.Proces for purification of a cephalesporin derivative:US,6825345B2[P].2004-11-30.
  • 4Walter C.Process for preparation of cefixime via alkyl-or arylsulfonates,US:20050032771A1,2005-02-10.
  • 5ateson JH,Burton G,Fell S.Preparation of 3 - (oxotetra-hydrofuryl. ceph--3 --em ---4 --carboxylates as antibaeterials[P].EP395219,1990- 10-31(CA 1991,114:8142g).
  • 6Martin gomezpatriclo,Alpeglani marco,Cabri walter,Olivafrancesco.A process for the Preparation of Cefixime via M ky-loraryl-Sulfonates[P]. WO 03 040 148,2003.
  • 7Picomell dardes carlos,Marcham rrading,InvestmentLProcessfor the Preparation of Trihydrated Cefixime[P].WO 9 533753,1995.
  • 8Ascher Gerd.Process for the Producing Cephalosporin Antibi-otics, and Novel Intermediates for Use in Such Process and Their Produc- tion(P].US 500 3073,1991.
  • 9Sandoz GmbH .Process for Purification of a Cephalosporin Deriva- tive[P].US 4 652 651,1987--03-24.
  • 10Rosenblum barnettb,Khan shaheer,Menchen stevenm.Propar- gylethoxyamino Nucleotides[P].WO 9 806 732,1998.

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