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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-3-O-[(R)-1'-(ethoxycarbonyl)ethyl]-α-D-glucopyranoside | 1215016-58-2

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-3-O-[(R)-1'-(ethoxycarbonyl)ethyl]-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-3-O-[(R)-1'-(ethoxycarbonyl)ethyl]-α-D-glucopyranoside化学式
CAS
1215016-58-2
化学式
C51H62N4O13
mdl
——
分子量
939.072
InChiKey
HVOSYNAMRAFHEZ-QQVAICGESA-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):
    7.16
  • 重原子数:
    68.0
  • 可旋转键数:
    26.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    196.46
  • 氢给体数:
    1.0
  • 氢受体数:
    14.0

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-3-O-[(R)-1'-(ethoxycarbonyl)ethyl]-α-D-glucopyranoside 在 lithium hydroxide 作用下, 以 四氢呋喃1,4-二氧六环 为溶剂, 反应 2.0h, 以82%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-3-O-[(R)-1'-carboxyethyl]-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:
    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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文献信息

  • Synthesis of a β-GlcN-(1→4)-MurNAc building block en route to N-deacetylated peptidoglycan fragments
    作者:Luigi Cirillo、Emiliano Bedini、Antonio Molinaro、Michelangelo Parrilli
    DOI:10.1016/j.tetlet.2009.12.124
    日期:2010.2
    Some bacteria present a variation in their peptidoglycan structure that is the absence of the N-acetyl substituent in the glucosamine residue. Very recently, this structural modification was demonstrated to be critical for host innate immune evasion in Listeria monocytogenes. To shed light on the molecular details of the evasion mechanism, the synthesis of some N-deacetylated peptidoglycan fragments is needed. En route to this goal a high-yielding synthesis of a GlcN-MurNAc disaccharide building block has been accomplished. A careful study of the optimal protecting groups and reaction conditions was done to have a complete beta-stereoselectivity in glycosylation as well as to ensure a high versatility to the disaccharide building block. (C) 2009 Elsevier Ltd. All rights reserved.
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