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| 1178528-97-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1178528-97-6
化学式
C79H103N3O38Si
mdl
——
分子量
1730.77
InChiKey
GEIJXYSKFMDGRO-SFWKHBTHSA-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):
    4.18
  • 重原子数:
    121.0
  • 可旋转键数:
    39.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    512.27
  • 氢给体数:
    3.0
  • 氢受体数:
    38.0

反应信息

  • 作为反应物:
    描述:
    乙酸酐 在 Pearlman catalyst 、 氢气 作用下, 以 乙酸乙酯 为溶剂, 以61%的产率得到
    参考文献:
    名称:
    Synthetic study on α(2→8)-linked oligosialic acid employing 1,5-lactamization as a key step
    摘要:
    An attempt to synthesize alpha(2 -> 8)-linked oligosialic acid utilizing a 1,5-lactamized sialyl acceptor is described. 1,5-Lactamization was experimentally proven to proceed only for alpha-sialoside, which was integrated into the synthetic cycle of oligosialic acid as a chemical sorting step to collect the desired alpha-sialoside and as a transformation step to produce a reactive sialyl acceptor for the next sialylation. Lactarnized oligosialyl acceptors served as favorable coupling partners for sialylation, providing high stereoselectivities and high yields. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.05.057
  • 作为产物:
    描述:
    乙酸酐碘甲烷三乙胺potassium carbonate4-二甲氨基吡啶 作用下, 以 乙腈N,N-二甲基甲酰胺吡啶 为溶剂, 以22%的产率得到
    参考文献:
    名称:
    Synthetic study on α(2→8)-linked oligosialic acid employing 1,5-lactamization as a key step
    摘要:
    An attempt to synthesize alpha(2 -> 8)-linked oligosialic acid utilizing a 1,5-lactamized sialyl acceptor is described. 1,5-Lactamization was experimentally proven to proceed only for alpha-sialoside, which was integrated into the synthetic cycle of oligosialic acid as a chemical sorting step to collect the desired alpha-sialoside and as a transformation step to produce a reactive sialyl acceptor for the next sialylation. Lactarnized oligosialyl acceptors served as favorable coupling partners for sialylation, providing high stereoselectivities and high yields. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.05.057
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