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盐酸氯洁霉素的合成 被引量:5

SYNTHESIS OF CLINDAMYCIN HYDROCHLORIDE
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摘要 盐酸氯洁霉素(clindamycin hydrochloride,1)属洁霉素衍生物。化学名为7-氯-6,7,8-三脱氧-6-反-(-甲基-4-丙基-L-吡咯烷-2-羧酰胺基)-1-硫代-L-苏型-α-D-半乳型-辛吡喃糖甲甙盐酸盐。 1的抗菌谱与洁霉素(2)相似,但对大多数敏感菌的抗菌作用比2强,疗效也较好。Birkenmeyer等最先用三条路线合成1,其中三苯膦-氯气法收率最高,达73%,操作也较简便。但关键是三苯膦来源困难,副产物氧化三苯膦的后处理也存在问题。
出处 《中国医药工业杂志》 CAS CSCD 北大核心 1990年第3期103-104,共2页 Chinese Journal of Pharmaceuticals
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同被引文献32

  • 1张骁,束梅英.林可霉素产销现状及展望[J].中国药房,1995,6(6):5-6. 被引量:3
  • 2夏万东,李少华.林可酰胺类抗生素研究进展[J].江西医学院学报,2005,45(5):183-184. 被引量:5
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  • 6Martens-Lobenhoffer J,Banditt P.Sensitive and specific determination of clindamycin in human serum and bone tissue applying liquid chromatographyatmospheric pressure chemical ionization-mass spectrometry[J].J Chromatogr B,2001,755:143-149.
  • 7Szunyog J,Adams E,Liekens K,et al.Analysis of a formulation containing lincomycin and spectinomycin by liquid chromatography with pulsed electrochemical detection[J].J Pharm Biomed Anal,2002,29:213-220.
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  • 9Bowden K,Stevens GP.An alternative synthesis of clindamycin[J].J Serbian Chem Soc,2000,65(10):691-693.
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