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2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-galactopyranosyl-(1->3)-1-O-acetyl-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranose | 1186313-73-4

中文名称
——
中文别名
——
英文名称
2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-galactopyranosyl-(1->3)-1-O-acetyl-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranose
英文别名
——
2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-galactopyranosyl-(1->3)-1-O-acetyl-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranose化学式
CAS
1186313-73-4
化学式
C38H56N4O21
mdl
——
分子量
904.877
InChiKey
WYDFIOUCILUMSL-TZRZYAFWSA-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

  • 作为产物:
    描述:
    乙酸酐吡啶 作用下, 反应 10.0h, 生成 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-galactopyranosyl-(1->3)-1-O-acetyl-2,4-diacetamido-2,4,6-trideoxy-β-D-glucopyranose 、 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-galactopyranosyl-(1->3)-1-O-acetyl-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranose
    参考文献:
    名称:
    Synthesis of undecaprenyl pyrophosphate-linked glycans as donor substrates for bacterial protein N-glycosylation
    摘要:
    Synthesis of undecaprenyl pyrophosphate (Und-PP)-linked glycans is described. Bacterial ([E](3),[Z](7))-undecaprenol was synthesized from trans-geranylgeranyl sulfone and isoprenoid building blocks, which was converted to undecaprenyl phosphate (Und-P). It was coupled with glycosyl phosphates to afford Und-PP-linked glycans, including core trisaccharide of Campylobacter jejuni N-glycan. Our synthetic method for Und-PP-linked glycan would provide various substrates as a useful tool for systematic analysis of bacterial protein N-glycosylation. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.06.032
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