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| 1350309-62-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1350309-62-4
化学式
C41H58O11Si
mdl
——
分子量
754.99
InChiKey
DHLUVQJNIQJFDW-LRAGNMSPSA-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):
    5.99
  • 重原子数:
    53.0
  • 可旋转键数:
    17.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    134.53
  • 氢给体数:
    3.0
  • 氢受体数:
    11.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    溴甲苯 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 生成
    参考文献:
    名称:
    Synthetic Study and Structural Analysis of the Antifreeze Agent Xylomannan from Upis ceramboides
    摘要:
    The novel antifreeze factor, xylomannan, first isolated from the freeze-tolerant Alaskan beetle Upis ceramboides, demonstrates a high degree of thermal hysteresis, comparable to that of the most active insect antifreeze proteins. Although the presence of a lipid component in this factor has not yet been verified, it has been proposed that the glycan backbone consists of a beta-D-mannopyranosyl-(1 -> 4)-beta-D-xylopyranose-disaccharide-repeating structure according to MS and NMR analyses. In this contribution, we report the stereoselective synthesis of the tetrasaccharide beta-D-mannopyranosyl-(1 -> 4)-beta-D-xylopyranosyl-(1 -> 4)-beta-D-mannopyranosyl-(1 -> 4)-D-xylopyranoside, a structural component of xylomannan. Our synthesis features the use of 2-naphthylmethyl (NAP)-ether-mediated intramolecular aglycon delivery (IAD) as the key reaction in obtaining beta-mannopyranoside stereoselectively. Various donors for NAP-IAD were tested to determine the most suitable for the purposes of this synthesis. Fragment coupling between a disaccharyl fluoride and a disaccharide acceptor obtained from a common beta-D-mannopyranosyl-(1 -> 4)-beta-D-xylopyranoside derivative was successfully carried out to afford the desired tetrasaccharide in the presence of Cp2HfCl2-AgClO4. Structural analysis of the resulting synthetic tetrasaccharide using NMR techniques and molecular modeling was performed in order to demonstrate the presence of the proposed xylomannan linkages in this molecule.
    DOI:
    10.1021/ja208528c
  • 作为产物:
    参考文献:
    名称:
    Synthetic Study and Structural Analysis of the Antifreeze Agent Xylomannan from Upis ceramboides
    摘要:
    The novel antifreeze factor, xylomannan, first isolated from the freeze-tolerant Alaskan beetle Upis ceramboides, demonstrates a high degree of thermal hysteresis, comparable to that of the most active insect antifreeze proteins. Although the presence of a lipid component in this factor has not yet been verified, it has been proposed that the glycan backbone consists of a beta-D-mannopyranosyl-(1 -> 4)-beta-D-xylopyranose-disaccharide-repeating structure according to MS and NMR analyses. In this contribution, we report the stereoselective synthesis of the tetrasaccharide beta-D-mannopyranosyl-(1 -> 4)-beta-D-xylopyranosyl-(1 -> 4)-beta-D-mannopyranosyl-(1 -> 4)-D-xylopyranoside, a structural component of xylomannan. Our synthesis features the use of 2-naphthylmethyl (NAP)-ether-mediated intramolecular aglycon delivery (IAD) as the key reaction in obtaining beta-mannopyranoside stereoselectively. Various donors for NAP-IAD were tested to determine the most suitable for the purposes of this synthesis. Fragment coupling between a disaccharyl fluoride and a disaccharide acceptor obtained from a common beta-D-mannopyranosyl-(1 -> 4)-beta-D-xylopyranoside derivative was successfully carried out to afford the desired tetrasaccharide in the presence of Cp2HfCl2-AgClO4. Structural analysis of the resulting synthetic tetrasaccharide using NMR techniques and molecular modeling was performed in order to demonstrate the presence of the proposed xylomannan linkages in this molecule.
    DOI:
    10.1021/ja208528c
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