RifamycinMode of Action, Resistance, and Biosynthesis

Floss, Heinz G., Yu, Tin-Wein·2005·Chemical Reviews

Cited by (553)

Items 201–300 of 553

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  12. Formation, characterization and pH dependence of rifampicin: heptakis(2,6-di- O -methyl)-β-cyclodextrin complexes
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  14. Application of The [4+3] Cycloaddition Reaction To The Synthesis of Natural Products
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  15. HelR is a helicase-like protein that protects RNA polymerase from rifamycin antibiotics
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  20. Application of intramolecular Dötz reaction to the synthesis of ansa-compounds: concise synthesis of arnebinol
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  21. Inhibition of translation by cytotrienin A—a member of the ansamycin family
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  22. Semi-synthetic zwitterionic rifamycins: a promising class of antibiotics; survey of their chemistry and biological activities
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  30. Redetermination of rifampicin pentahydrate revealing a zwitterionic form of the antibiotic
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  47. Preparation and in vitro anti-staphylococcal activity of novel 11-deoxy-11-hydroxyiminorifamycins
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  48. 8-Deoxy-Rifamycin Derivatives from Amycolatopsis mediterranei S699 ΔrifT Strain
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  57. Evaluation of the Synthetic Potential of an AHBA Knockout Mutant of the Rifamycin Producer Amycolatopsis mediterranei
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  58. Macrolactam formation catalyzed by the thioesterase domain of vicenistatin polyketide synthase
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  59. Synthesis and antibacterial evaluation of a novel series of rifabutin-like spirorifamycins
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