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[α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[ β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-α-D-glucopyranosyl fluoride | 1002354-74-6

中文名称
——
中文别名
——
英文名称
[α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[ β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-α-D-glucopyranosyl fluoride
英文别名
——
[α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[ β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-α-D-glucopyranosyl fluoride化学式
CAS
1002354-74-6
化学式
C51H85FO42
mdl
——
分子量
1389.21
InChiKey
QCMKXGBUAIDOGL-CEDXMTSKSA-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:
    [(2,3,4-tri-O-acetyl-α-D-xylopyranosyl)-(1->6)]-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1->4)-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->2)-(3,4-di-O-acetyl-α-D-xylopyranosyl)-(1->6)]-(2,3-di-O-acetyl-β-D-glucopyranosyl)-(1->4)-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->2)-(3,4-di-O-acetyl-α-D-xylopyranosyl)-(1->6)]-(2,3-di-O-acetyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride 在 甲醇sodium methylate 作用下, 以93%的产率得到[α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[ β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-[β-D-galactopyranosyl-(1->2)-α-D-xylopyranosyl-(1->6)]-β-D-glucopyranosyl-(1->4)-α-D-glucopyranosyl fluoride
    参考文献:
    名称:
    Chemo-enzymatic synthesis of xylogluco-oligosaccharides and their interactions with cellulose
    摘要:
    A novel class of complex oligosaccharides with a backbone made of twelve beta-(1 -> 4)-D-glucosyl units that may be regularly substituted on their primary position with alpha-D-xylosyl or beta-D-(1 -> 2)-galactosyl-alpha-D-xylosyl residues were readily synthesized using enzymatic hydrolysis of the plant polysaccharide xyloglucan (XG), followed by chemical modifications of the well-defined oligosaccharides and their enzymatic coupling catalyzed by the Cel7B E197A glycosynthase from Humicola insolens. These complex oligosaccharides proved useful for a better understanding of the effects of structural variation of xyloglucan on interactions with bacterial microcrystalline cellulose (BMCC). (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carbpol.2011.11.085
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