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p-methoxyphenyl β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-β-D-galactopyranoside | 1374633-18-7

中文名称
——
中文别名
——
英文名称
p-methoxyphenyl β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-β-D-galactopyranoside
英文别名
Galf(b1-3)Gal(a1-3)Galf(b1-3)Gal(a1-3)Galf(b1-3)Gal(b)-O-Ph(4-OMe);(2R,3R,4S,5S,6R)-2-[(2S,3R,4R,5R)-2-[(1R)-1,2-dihydroxyethyl]-5-[(2R,3R,4S,5S,6R)-2-[(2S,3R,4R,5R)-2-[(1R)-1,2-dihydroxyethyl]-5-[(2R,3S,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-(4-methoxyphenoxy)oxan-4-yl]oxy-4-hydroxyoxolan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-4-hydroxyoxolan-3-yl]oxy-4-[(2S,3R,4R,5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,5-diol
p-methoxyphenyl β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-β-D-galactopyranoside化学式
CAS
1374633-18-7
化学式
C43H68O32
mdl
——
分子量
1096.99
InChiKey
WXTFCNIWOGCJMG-YWFVHBBISA-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):
    -9.3
  • 重原子数:
    75
  • 可旋转键数:
    22
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    504
  • 氢给体数:
    19
  • 氢受体数:
    32

反应信息

  • 作为产物:
    描述:
    在 palladium 10% on activated carbon 、 氢气 作用下, 以 甲醇 为溶剂, 45.0 ℃ 、4.05 MPa 条件下, 反应 20.0h, 以26 mg的产率得到p-methoxyphenyl β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-α-D-galactopyranosyl-(1->3)-β-D-galactofuranosyl-(1->3)-β-D-galactopyranoside
    参考文献:
    名称:
    Synthesis of tetra- and hexasaccharide fragments corresponding to the O-antigenic polysaccharide of Klebsiella pneumoniae
    摘要:
    The preparation of linear tetra- (1) and hexasaccharides (2), containing the repeating unit [-> 3)-beta-Galf-(1 -> 3)-alpha-Galp-(1 -> ] present in the O-polysaccharide of the lipopolysaccharide of Klebsiella pneumoniae is described. The key step in their synthesis is the alpha-selective galactopyranosylation of 3-OH di- and tetrasaccharide acceptors (20 and 22) with a disaccharide trichloroacetimidate donor 19 in the presence of trimethylsilyl triflate in a diethyl ether-CH2Cl2 mixture as solvent. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.03.074
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