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allyl 2-azido-3,6-di-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside | 1628714-96-4

中文名称
——
中文别名
——
英文名称
allyl 2-azido-3,6-di-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside
英文别名
——
allyl 2-azido-3,6-di-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside化学式
CAS
1628714-96-4
化学式
C81H94N8O20
mdl
——
分子量
1499.68
InChiKey
LKOFCJVSNHXTBX-GAZHRAQRSA-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

反应信息

  • 作为反应物:
    描述:
    allyl 2-azido-3,6-di-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside 在 10 wt% Pd(OH)2 on carbon 、 氢气溶剂黄146 作用下, 以 甲醇二氯甲烷 为溶剂, 以55%的产率得到n-propyl 2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-2-deoxy-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of Partially N-Acetylated Chitooligosaccharides and Muropeptides
    摘要:
    Partially N-acetylated chitooligosaccharides and muropeptides are referred to as microbial associated molecular patterns (MAMPs). To shed light on the molecular basis of their recognition by the innate immunity system of living organisms, their production in pure form is necessary. To this end, we present here the first synthetic strategy for the obtainment of a series of partially N-acetylated muropeptides as well as of a chitodisaccharide and a chitotetrasaccharide, all possessing a well-defined N-acetylation pattern.
    DOI:
    10.1055/s-0033-1340323
  • 作为产物:
    描述:
    乙酸酐甲醇二氯甲烷 为溶剂, 反应 4.0h, 以15.2 mg的产率得到allyl 2-azido-3,6-di-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of Partially N-Acetylated Chitooligosaccharides and Muropeptides
    摘要:
    Partially N-acetylated chitooligosaccharides and muropeptides are referred to as microbial associated molecular patterns (MAMPs). To shed light on the molecular basis of their recognition by the innate immunity system of living organisms, their production in pure form is necessary. To this end, we present here the first synthetic strategy for the obtainment of a series of partially N-acetylated muropeptides as well as of a chitodisaccharide and a chitotetrasaccharide, all possessing a well-defined N-acetylation pattern.
    DOI:
    10.1055/s-0033-1340323
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