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3-O-α-D-glucopyranosyl-D-arabino-2-hexosulose bis(phenylhydrazone) | 172909-81-8

中文名称
——
中文别名
——
英文名称
3-O-α-D-glucopyranosyl-D-arabino-2-hexosulose bis(phenylhydrazone)
英文别名
3-O-β-a-D-Glucosyl-fructose-phenylosazon; 3-O-α-D-Glucosyl-mannose-phenylosazon;3-O-α-D-Glucosylmannose-phenylosazon
3-O-α-D-glucopyranosyl-D-arabino-2-hexosulose bis(phenylhydrazone)化学式
CAS
172909-81-8
化学式
C24H32N4O9
mdl
——
分子量
520.539
InChiKey
SWQBOFUTBWUOAT-VZGVZGJCSA-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:
    苯肼,盐酸盐黑曲霉二糖sodium acetate 作用下, 反应 14.0h, 以41.6%的产率得到3-O-α-D-glucopyranosyl-D-arabino-2-hexosulose bis(phenylhydrazone)
    参考文献:
    名称:
    Sequential Removal of Monosaccharides from the Reducing End of Oligosaccharides. 2. Fundamental Studies of a Reaction between Hydrazino Compounds and Sugars Having a Glycosyl Moiety on a Carbon Atom Adjacent to a Carbonyl Group
    摘要:
    Hydrazine and certain hydrazino derivatives react with sugars having a glycosidic substituent, where the glycosyl moiety is located on a carbon atom adjacent to an aldehyde or keto group of the aglycon, resulting in cleavage of the glycosidic linkage. The reaction proceeds whether the glycon is of the alpha or beta configuration. The released glycosyl moiety, in the presence of excess hydrazino compound, reacts further to give a hydrazone derivative. Removal of the hydrazone group gives the reducing sugar derived from the glycon.
    DOI:
    10.1021/jo00130a026
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