OBJECTIVE To synthesize benzoxazinorifamycin derivatives to study the antibacterial activities.
目的设计合成苯并口恶嗪利福霉素衍生物,并研究其抗菌活性.
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CONCLUSION The antibacterial activities of benzoxazinorifamycin derivatives etherified on 3 ? ? - position may be changed.
结论3′-苯并口恶嗪酚利福霉素的3′位酚 羟基 醚化对抗菌活性有影响.
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