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methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-2)-[2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1-6)]-3,4-O-(2,3-dimethoxybutane-2,3-diyl)-α-D-mannopyranoside | 1057668-97-9

中文名称
——
中文别名
——
英文名称
methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-2)-[2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1-6)]-3,4-O-(2,3-dimethoxybutane-2,3-diyl)-α-D-mannopyranoside
英文别名
——
methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-2)-[2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1-6)]-3,4-O-(2,3-dimethoxybutane-2,3-diyl)-α-D-mannopyranoside化学式
CAS
1057668-97-9
化学式
C39H54N2O24
mdl
——
分子量
934.857
InChiKey
FMUHGPYTTDWWOG-DDIYPIPTSA-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):
    -0.82
  • 重原子数:
    65.0
  • 可旋转键数:
    14.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    290.72
  • 氢给体数:
    0.0
  • 氢受体数:
    24.0

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

  • 作为产物:
    描述:
    ethyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranosidemethyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-2)-3,4-O-(2,3-dimethoxybutane-2,3-diyl)-α-D-mannopyranoside2,6-二叔丁基-4-甲基吡啶 、 dimethyl(methylthio)sulfonium triflate 作用下, 以 二氯甲烷 为溶剂, 反应 20.33h, 以77%的产率得到methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-2)-[2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1-6)]-3,4-O-(2,3-dimethoxybutane-2,3-diyl)-α-D-mannopyranoside
    参考文献:
    名称:
    Investigations of Glycosylation Reactions with 2-N-Acetyl-2N,3O-oxazolidinone-Protected Glucosamine Donors
    摘要:
    NIS/AgOTf-promoted glycosylations with ethyl 2,3-N,O-carbonyl-2-deoxy-1-thio-beta-D-glueopyranoside donors can be performed with either alpha- or beta-selectivity by tuning the reaction conditions. Small amounts of AgOTf (0.1 equiv) and short reaction times give beta-selectivity, whereas 0.4 equiv of AgOTf and prolonged reaction times afford alpha-linked products. NMR-monitored glycosylation and anomerization experiments show initial formation of exclusively the beta-linkage, which anomerizes, through an intramolecular mechanism involving an endocyclic C - O bond cleavage, to the alpha-linkage.
    DOI:
    10.1021/jo800971s
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