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| 1415724-89-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1415724-89-8
化学式
C45H54Cl3NO15Si
mdl
——
分子量
983.366
InChiKey
VWDXOVFYTFVUOJ-RVIFKECYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    7.06
  • 重原子数:
    65.0
  • 可旋转键数:
    17.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.51
  • 拓扑面积:
    181.84
  • 氢给体数:
    1.0
  • 氢受体数:
    15.0

反应信息

  • 作为反应物:
    描述:
    吡啶triflic azidecopper(II) sulfate溶剂黄146三乙胺 作用下, 以 乙腈 为溶剂, 反应 4.0h, 生成
    参考文献:
    名称:
    First Synthesis of a Pentasaccharide Moiety of Ganglioside GAA-7 Containing Unusually Modified Sialic Acids through the Use of N-Troc-sialic Acid Derivative as a Key Unit
    摘要:
    The pentasaccharide part of the potent neuritogenic ganglioside GAA-7 has been synthesized for the first time. The unique branched terminus constituting partially modified sialic acids and N-acetylgalactosamine was successfully established by stereoselective double-sialylation using 8-O-methyl-N-Troc-sialic acid as a donor. The final 4 + 1 coupling reaction provided a high yield of pentasaccharide, which was deprotected to deliver the target molecule.
    DOI:
    10.1021/ol303122w
  • 作为产物:
    描述:
    phenyl 4,6-O-benzylidene-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-1-thio-β-D-galactopyranoside 在 三乙基硅烷4-二甲氨基吡啶 作用下, 以 吡啶二氯甲烷 为溶剂, 反应 16.0h, 生成
    参考文献:
    名称:
    First Synthesis of a Pentasaccharide Moiety of Ganglioside GAA-7 Containing Unusually Modified Sialic Acids through the Use of N-Troc-sialic Acid Derivative as a Key Unit
    摘要:
    The pentasaccharide part of the potent neuritogenic ganglioside GAA-7 has been synthesized for the first time. The unique branched terminus constituting partially modified sialic acids and N-acetylgalactosamine was successfully established by stereoselective double-sialylation using 8-O-methyl-N-Troc-sialic acid as a donor. The final 4 + 1 coupling reaction provided a high yield of pentasaccharide, which was deprotected to deliver the target molecule.
    DOI:
    10.1021/ol303122w
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