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| 1262658-55-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1262658-55-8
化学式
C85H86N2O18Si
mdl
——
分子量
1451.71
InChiKey
ZXEOETXPGUXOGJ-QEEOSURVSA-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):
    9.74
  • 重原子数:
    106.0
  • 可旋转键数:
    28.0
  • 环数:
    14.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    236.98
  • 氢给体数:
    3.0
  • 氢受体数:
    18.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Encouraging Progress in the ω-Aspartylation of Complex Oligosaccharides as a General Route to β-N-Linked Glycopolypeptides
    摘要:
    Described herein is a method for the joining of complex peptides to complex oligosaccharides via an N-linkage. The omega-aspartylation is conducted by coupling fully deprotected glycosylamine with a peptide containing a unique thioacid at the omega-aspartate carboxyl. In the presence of HOBT, under conditions that, in principle, allow for oxidation, complex components are combined in encouraging yields to produce structurally and stereochemically defined N-linked glycopolypeptides wherein the carbohydrate domain can be quite complex. Various mechanisms for oxidative coupling are proposed.
    DOI:
    10.1021/ja110115a
  • 作为产物:
    描述:
    三氟乙酸乙硫醇 作用下, 以 二氯甲烷 为溶剂, 反应 0.25h, 以72%的产率得到
    参考文献:
    名称:
    Encouraging Progress in the ω-Aspartylation of Complex Oligosaccharides as a General Route to β-N-Linked Glycopolypeptides
    摘要:
    Described herein is a method for the joining of complex peptides to complex oligosaccharides via an N-linkage. The omega-aspartylation is conducted by coupling fully deprotected glycosylamine with a peptide containing a unique thioacid at the omega-aspartate carboxyl. In the presence of HOBT, under conditions that, in principle, allow for oxidation, complex components are combined in encouraging yields to produce structurally and stereochemically defined N-linked glycopolypeptides wherein the carbohydrate domain can be quite complex. Various mechanisms for oxidative coupling are proposed.
    DOI:
    10.1021/ja110115a
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