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phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside | 159734-75-5

中文名称
——
中文别名
——
英文名称
phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
英文别名
——
phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside化学式
CAS
159734-75-5
化学式
C54H50N2O15S
mdl
——
分子量
999.061
InChiKey
BFLSZSPXYVHTRO-GRWMNXBOSA-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):
    6.17
  • 重原子数:
    72.0
  • 可旋转键数:
    17.0
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    199.81
  • 氢给体数:
    0.0
  • 氢受体数:
    16.0

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:
    phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranosidep-methoxyphenyl 2,3,6-tri-O-benzyl-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosideN-碘代丁二酰亚胺三氟甲磺酸 、 4 A molecular sieve 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以88%的产率得到p-methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl0(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
    参考文献:
    名称:
    Synthesis and biological evaluation of oligosaccharides related to the molecule signals in plant defence and the Rhizobium-legume symbiosis
    摘要:
    The synthesis of tetrasaccharides related to the chitinoligosaccharides involved in plant defence and Rhizobium-legume symbiosis is reported. One and two central GlcNAc residues of the chitin backbone have been replaced by Glc units. A biological evaluation using Catharanthus roseaus assay indicates that the replacement of the two central units produces a total loss of activity. However, the replacement of the GlcNAc moiety close to the reducing end by Glc in the chitin tetramer, does not reduce its activity. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)01148-6
  • 作为产物:
    描述:
    3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-D-glucopyranose 在 三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 、 potassium carbonate 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 136.0h, 生成 phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
    参考文献:
    名称:
    Synthesis and biological evaluation of oligosaccharides related to the molecule signals in plant defence and the Rhizobium-legume symbiosis
    摘要:
    The synthesis of tetrasaccharides related to the chitinoligosaccharides involved in plant defence and Rhizobium-legume symbiosis is reported. One and two central GlcNAc residues of the chitin backbone have been replaced by Glc units. A biological evaluation using Catharanthus roseaus assay indicates that the replacement of the two central units produces a total loss of activity. However, the replacement of the GlcNAc moiety close to the reducing end by Glc in the chitin tetramer, does not reduce its activity. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)01148-6
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文献信息

  • Orthogonal Glycosylation Strategy in Oligosaccharide Synthesis
    作者:Osamu Kanie、Yukishige Ito、Tomoya Ogawa
    DOI:10.1021/ja00105a066
    日期:1994.12
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