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8α-hydroxy-9-epi-4,6,11-tri-O-methyl-ζ-rhodomycinone | 75332-03-5

中文名称
——
中文别名
——
英文名称
8α-hydroxy-9-epi-4,6,11-tri-O-methyl-ζ-rhodomycinone
英文别名
——
8α-hydroxy-9-epi-4,6,11-tri-O-methyl-ζ-rhodomycinone化学式
CAS
75332-03-5
化学式
C25H26O9
mdl
——
分子量
470.476
InChiKey
SXQBRJYOASDRNO-XZLBEJRYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为产物:
    描述:
    8,9-dehydro-9-epi-4,6,11-tri-O-methyl-ζ-rhodomycinone 8,9-epoxide 在 高氯酸 作用下, 以 丙酮 为溶剂, 反应 64.0h, 以18%的产率得到8α-hydroxy-9-epi-4,6,11-tri-O-methyl-ζ-rhodomycinone
    参考文献:
    名称:
    8-Hydroxyanthracyclinones from .epsilon.-rhodomycinone
    摘要:
    epsilon-Rhodomycinone was converted into 8,9-dehydro-zeta-rhodomycinone, which gave a cis diol with osmium tetroxide and a pair of epimeric epoxides with m-chloroperbenzoic acid. Acid-catalyzed opening of the epoxides gave the corresponding trans diols. In contrast, acid treatment of the trimethyl ethers of these epoxides gave predominantly a lactone and an eta-rhodomycinone derivative, with only small amounts of the diols. None of the new rhodomycinones were active against Bacillus subtilis, but 8,9-dehydro-zeta-rhodomycinone was active in the induction of lytic phage in Escherichia coli.
    DOI:
    10.1021/jm00185a020
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