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4-methoxyphenyl (3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside | 1064679-20-4

中文名称
——
中文别名
——
英文名称
4-methoxyphenyl (3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
英文别名
——
4-methoxyphenyl (3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside化学式
CAS
1064679-20-4
化学式
C81H83NO21
mdl
——
分子量
1406.54
InChiKey
MLYHDKBZPDLGRZ-QQTKUNDVSA-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):
    10.89
  • 重原子数:
    103.0
  • 可旋转键数:
    32.0
  • 环数:
    12.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    236.27
  • 氢给体数:
    0.0
  • 氢受体数:
    21.0

反应信息

  • 作为反应物:
    描述:
    4-methoxyphenyl (3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside甲醇sodium methylate 作用下, 反应 0.5h, 以98%的产率得到4-methoxyphenyl (6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
    参考文献:
    名称:
    Concise synthesis of two pentasaccharides corresponding to the α-chain oligosaccharides of Neisseria gonorrhoeae and Neisseria meningitidis
    摘要:
    Two pentasaccharides containing a common tetrasaccharide (lacto-N-neotetraose) core, and D-galactosamine and N-acetyl neuraminic acid in the non-reducing ends, respectively, corresponding to the lipooligosaccharides of Neisseria gonorrhoeae and Neisseria meningitidis were synthesized in a very concise manner from a common trisaccharide derivative using minimum number of steps. Thioglycosides and glycosyl trichloroacetimidate have been used as glycosyl donors for glycosylations and yields were excellent in every step. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.07.004
  • 作为产物:
    描述:
    4-methoxyphenyl (4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranosideethyl 3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 在 4 A molecular sieve 、 N-碘代丁二酰亚胺三氟甲磺酸三甲基硅酯 作用下, 以 二氯甲烷 为溶剂, 反应 1.5h, 以90%的产率得到4-methoxyphenyl (3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
    参考文献:
    名称:
    Concise synthesis of two pentasaccharides corresponding to the α-chain oligosaccharides of Neisseria gonorrhoeae and Neisseria meningitidis
    摘要:
    Two pentasaccharides containing a common tetrasaccharide (lacto-N-neotetraose) core, and D-galactosamine and N-acetyl neuraminic acid in the non-reducing ends, respectively, corresponding to the lipooligosaccharides of Neisseria gonorrhoeae and Neisseria meningitidis were synthesized in a very concise manner from a common trisaccharide derivative using minimum number of steps. Thioglycosides and glycosyl trichloroacetimidate have been used as glycosyl donors for glycosylations and yields were excellent in every step. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.07.004
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