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| 1046465-60-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1046465-60-4
化学式
C46H38O11
mdl
——
分子量
766.801
InChiKey
MBIMHVANYJZODX-MDDBISMWSA-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

物化性质

  • 沸点:
    862.1±65.0 °C(Predicted)
  • 密度:
    1.37±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.67
  • 重原子数:
    57.0
  • 可旋转键数:
    15.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    143.89
  • 氢给体数:
    1.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Synthesis of a tetrasaccharide phosphate from the linkage region of the arabinogalactan–peptidoglycan complex in the mycobacterial cell wall
    摘要:
    The synthesis of dibenzyl 6-O-naphthylmethyl-2,3,5-tri-O-benzoyl-beta-D-galactofuranosyl-(1 -> 5)-2,3-di-O-benzoyl-6-O-benzyl- beta-D-galactofuranosyl-(1 -> 4)-3-O-benzyl-2-O-pivaloyl-alpha-L-rhamnopyranosyl-(1 -> 3)-2-acetamido-2-deoxy-4,6-di-O-benzoyl-alpha-glucopyranosyl phosphate (1), a protected form of the tetrasaccharide phosphate of the linkage region of the arabinogalactan-peptidoglycan complex in the mycobacterial cell wall, has been accomplished. Key steps include the coupling of four monosaccharide building blocks with complete stereoselectivity by glycosylations employing thioglycosides, 2'-carboxybenzyl glycosides, and glycosyl fluorides as glycosyl donors. The alpha-glycosyl phosphate linkage was also stereoselectively elaborated by reaction of a tetrasaccharide hermacetal with tetrabenzyl pyrophosphate in the presence of a base. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2008.05.009
  • 作为产物:
    描述:
    在 palladium on activated charcoal 乙酸铵氢气 作用下, 以 甲醇乙酸乙酯 为溶剂, 反应 1.0h, 以89%的产率得到
    参考文献:
    名称:
    Synthesis of a tetrasaccharide phosphate from the linkage region of the arabinogalactan–peptidoglycan complex in the mycobacterial cell wall
    摘要:
    The synthesis of dibenzyl 6-O-naphthylmethyl-2,3,5-tri-O-benzoyl-beta-D-galactofuranosyl-(1 -> 5)-2,3-di-O-benzoyl-6-O-benzyl- beta-D-galactofuranosyl-(1 -> 4)-3-O-benzyl-2-O-pivaloyl-alpha-L-rhamnopyranosyl-(1 -> 3)-2-acetamido-2-deoxy-4,6-di-O-benzoyl-alpha-glucopyranosyl phosphate (1), a protected form of the tetrasaccharide phosphate of the linkage region of the arabinogalactan-peptidoglycan complex in the mycobacterial cell wall, has been accomplished. Key steps include the coupling of four monosaccharide building blocks with complete stereoselectivity by glycosylations employing thioglycosides, 2'-carboxybenzyl glycosides, and glycosyl fluorides as glycosyl donors. The alpha-glycosyl phosphate linkage was also stereoselectively elaborated by reaction of a tetrasaccharide hermacetal with tetrabenzyl pyrophosphate in the presence of a base. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2008.05.009
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