期刊文献+

1β-甲基碳青霉烯类抗生素关键中间体的合成进展 被引量:4

Progress in synthesis of the key intermediates of 1 β-methyl carbapenem antibiotics
下载PDF
导出
摘要 合成碳青霉烯类抗生素的关键中间体主要有两类 ,本文针对这两类关键中间体的合成新进展作一简单综述。 1 β-Methylcarbapenems have important activities of an antibacterial.There are two kinds of key intermediates of syntheses of carbapenem antibiotics,acetoxy azetidinone and 11 β -methylcarbapenems -methyl azetidinone.This review accounts for the recent development in the synthesis of 1 β -methylcarbapenems′ key intermediates.
出处 《中国药物化学杂志》 CAS CSCD 2003年第4期241-248,共8页 Chinese Journal of Medicinal Chemistry
关键词 药物化学 合成进展 综述 1β-甲基碳青霉烯关键中间体 medicinal chemistry synthesis progress review 1 β-methyl carbapenem's key intermediates
  • 相关文献

参考文献30

  • 1郑珩,顾觉奋.碳青霉烯类抗生素研究新进展[J].国外医药(抗生素分册),1999,20(1):1-5. 被引量:24
  • 2沐芳.注射用泰宁[J].中国新药杂志,1992,1(1):42-43. 被引量:2
  • 3仲兆金,刘浚.新型碳青霉烯类抗生素[J].中国新药杂志,2002,11(2):116-123. 被引量:8
  • 4王燕云,刘浚,屈传星,胡来兴.(3R,4R)-3-[(R)-1-叔丁基二甲基硅氧乙基]-4-乙酰氧基-2-氮杂环丁酮的合成[J].中国医药工业杂志,1998,29(3):128-129. 被引量:6
  • 5Cainelli G, Contento M, Giacomine D. Stereocontrolled total synthesis of the chiral building block (3S,4R)-3-[ ( R )-1-hydroxyethyl] -4-acetyloxy-azetidin-2-one: a useful synthon for the synthesis of ( + )-thienamycin ,carbapenerns and peaems[J]. Tetrahedrcm Lett, 1985, 26(7) :937 - 940.
  • 6Nakatsuka T, Iwata H, Tanaka R, et al. A facile conversion of the phenylthlo group to acetoxy by copper reagents for a practical synthesis of 4-acetoxyazetidin-2-ne derivatives from ( R )-butane-1, 3-diol [J ]. J Chem Soc Chem Commun, 1991, (8) :662- 664.
  • 7Kita Y, Shibata N, Tohjo T, et al. An efficient synthesis of 4-heterofunction substituted 3-(1-hydroxy)ethylazetidin-2-ones from 3-(1-hydroxy) ethyl-4-phenylsulfinylazetin-2-one by reaction with silylated heteronucleophiles[J]. Chem Pharm Bull, 1992, 40(7) : 1733 - 1736.
  • 8Akira Sasaki, Koshiro Coda, Masao Enomoto, et al.Synthetic studies of carbapenem and penem antibiotics.Ⅱ. Synthesis of 3-acetyl-2-azetidinone (2 + 2 )cycloaddition of diketene and schiff bases [ J ]. Chem Pharm Bull, 1992, 40(5) :1094 - 1097.
  • 9Gianfranco Cainelli, Paoa Galletti, Daria Giacomini, et al. A practical synthesis of a key intermediate for the production of β-lactam antibiotics [J]. Tetrahedron Letters, 1998, 39(42) :7779 - 7782.
  • 10Franco Cozzi, Rita Annunzziata, Mauro Cinquini, et al. A short, stereosdective synthesis of (3 R, 4R )-4-acetoxy-3-[ ( R )-1' (( t-butyldimethylsilyl ) oxy) ethyl ]-2-azetidinone, key intermediate for the preparation of carbapenem antibiotics[J]. Chirality, 1998,10:91 - 94.

二级参考文献4

共引文献33

同被引文献48

引证文献4

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部