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tetradecyl 2,3,6-tri-O-Bn-β-D-glucopyranoside | 1093982-56-9

中文名称
——
中文别名
——
英文名称
tetradecyl 2,3,6-tri-O-Bn-β-D-glucopyranoside
英文别名
——
tetradecyl 2,3,6-tri-O-Bn-β-D-glucopyranoside化学式
CAS
1093982-56-9
化学式
C41H58O6
mdl
——
分子量
646.908
InChiKey
QNNSHEAQMNWRQD-PGSFLWIGSA-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):
    9.18
  • 重原子数:
    47.0
  • 可旋转键数:
    24.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    66.38
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    tetradecyl 2,3,6-tri-O-Bn-β-D-glucopyranoside 、 2-O-benzoyl-6-O-benzyl-3-O-(methyl 7-O-acetyl-5-amino-9-O-benzyl-5-N,4-O-carbonyl-3,5-dideoxy-8-O-(methyl 7-O-acetyl-5-amino-9-O-benzyl-5-N,4-O-carbonyl-3,5-dideoxy-8-O-(methyl 7,8-di-O-acetyl-5-amino-9-O-benzyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-4-O-(2,2,2-trichloroethoxycarbonyl)-D-galactopyranosyl 在 三氟甲磺酸三甲基硅酯 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以93%的产率得到tetradecyl 4-O-(2-O-benzoyl-6-O-benzyl-3-O-(methyl 7-O-acetyl-5-amino-9-O-benzyl-5-N,4-O-carbonyl-3,5-dideoxy-8-O-(methyl 7-O-acetyl-5-amino-9-O-benzyl-5-N,4-O-carbonyl-3,5-dideoxy-8-O-(methyl 7,8-di-O-acetyl-5-amino-9-O-benzyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-4-O-(2,2,2-trichloroethoxycarbonyl)-β-D-galactopyranoside)-2,3,6-tri-O-Bn-β-D-glucopyranoside
    参考文献:
    名称:
    An Efficient Convergent Synthesis of GP1c Ganglioside Epitope
    摘要:
    In this report, we describe an efficient convergent synthesis of the GP1c glycolipid epitope, which is one of the most complex c-series gangliosides. The alpha(2,3) and alpha(2,8) sialylations were accomplished by use of 5N,4O-carbonyl and 7,8-O-isopropyliden as well as 5N,4O-carbonyl- and 7,8-di-O-chloroacetyl-protected sialyl donors in good yields with excellent alpha-selectivity, respectively. The two sialyl donors enable synthesis of the di- and trisialylgalactosides by simple glycosylation and deprotection. We synthesized the protected GP1c glycolipid epitope, which is a compact, rigid, branched structure, via direct coupling of tetarasaccharide and pentasaccharide units.
    DOI:
    10.1021/ja807482t
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