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新一代大环内酯类抗生素telithromycin 被引量:2

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出处 《国外医药(抗生素分册)》 CAS 2001年第6期282-283,共2页 World Notes on Antibiotics
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  • 1易红,许先栋.2’-乙酰基-3-酮基-10,11-脱水-6-O-甲氧基红霉素的合成[J].中国新药杂志,2005,14(5):581-582. 被引量:1
  • 2王翀,郑忠辉.3-脱克拉定糖-3-酮基-6-O-甲基-10,11-脱氢-12-O-咪唑酰基-2′-苯甲酰基红霉素A的合成[J].齐鲁药事,2006,25(10):617-618. 被引量:1
  • 3尤启冬,魏新,赵英.泰利霉素的合成改进[J].中国医药工业杂志,2007,38(4):318-320. 被引量:9
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  • 7Elliott R L, Pireh D, Griesgraber G. Anhydrolide macrolides. 1. synthesis and antibacterial activity of 2,3-anhydro-6-methyl 11,12-carbamate erythromycin A analogues [ J ]. J Med Chem, 1998,41 (10) :1651-1659.
  • 8George R C, Thomas H, Grace C L. The synthesis of phenyl and phridyl-glyoxalines[J]. J Chem Soc, 1938,753 -755.
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  • 10Ma Zhen-kun, Clark R F, Antony B, et al. Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens [ J ]. J Med Chem, 2001,44(24) :4137 -4156.

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