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dibenzyl (3,4,6-tri-O-benzyl-2-deoxy-α-D-lyxo-hexopyranosyl)-1-phosphate | 1190870-90-6

中文名称
——
中文别名
——
英文名称
dibenzyl (3,4,6-tri-O-benzyl-2-deoxy-α-D-lyxo-hexopyranosyl)-1-phosphate
英文别名
——
dibenzyl (3,4,6-tri-O-benzyl-2-deoxy-α-D-lyxo-hexopyranosyl)-1-phosphate化学式
CAS
1190870-90-6
化学式
C41H43O8P
mdl
——
分子量
694.761
InChiKey
YVWPURDCFLQYJY-GAKQXGIYSA-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:
    dibenzyl (3,4,6-tri-O-benzyl-2-deoxy-α-D-lyxo-hexopyranosyl)-1-phosphate 在 10% palladium on activated carbon 、 氢气 作用下, 以 甲醇乙酸乙酯 为溶剂, 20.0 ℃ 、5.0 MPa 条件下, 反应 10.0h, 以65%的产率得到Gal2deoxy-1-P
    参考文献:
    名称:
    En route to deoxygenated N-acetyllactosamine analogues employing uridyl and galactosyl transferases
    摘要:
    All monodeoxygenated galactoses were treated with galactokinase, and for the 2-, 3-, and 4-deoxy compounds, transformation into the corresponding galactopyranosyl phosphates could be observed. In case of the 2-deoxy derivative, further reaction via UDP-2-deoxy-D-lyxo-hexose (UDP-2-deoxygalactose), which was also obtained chemically, the multiple enzymatic system could be employed to prepare 2'-deoxy-N-acetyllactosamine. (C) 2009 Elsevier Ltd. Ail rights reserved.
    DOI:
    10.1016/j.carres.2009.05.015
  • 作为产物:
    参考文献:
    名称:
    En route to deoxygenated N-acetyllactosamine analogues employing uridyl and galactosyl transferases
    摘要:
    All monodeoxygenated galactoses were treated with galactokinase, and for the 2-, 3-, and 4-deoxy compounds, transformation into the corresponding galactopyranosyl phosphates could be observed. In case of the 2-deoxy derivative, further reaction via UDP-2-deoxy-D-lyxo-hexose (UDP-2-deoxygalactose), which was also obtained chemically, the multiple enzymatic system could be employed to prepare 2'-deoxy-N-acetyllactosamine. (C) 2009 Elsevier Ltd. Ail rights reserved.
    DOI:
    10.1016/j.carres.2009.05.015
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