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p-methoxyphenyl 6-deoxy-α-L-talopyranosyl-(1->3)-β-D-glucopyranosyl-(1->3)-6-deoxy-α-L-talopyranosyl-(1->3)-α-D-glucopyranoside | 1347739-62-1

中文名称
——
中文别名
——
英文名称
p-methoxyphenyl 6-deoxy-α-L-talopyranosyl-(1->3)-β-D-glucopyranosyl-(1->3)-6-deoxy-α-L-talopyranosyl-(1->3)-α-D-glucopyranoside
英文别名
——
p-methoxyphenyl 6-deoxy-α-L-talopyranosyl-(1->3)-β-D-glucopyranosyl-(1->3)-6-deoxy-α-L-talopyranosyl-(1->3)-α-D-glucopyranoside化学式
CAS
1347739-62-1
化学式
C31H48O20
mdl
——
分子量
740.71
InChiKey
SPAJPNOADFNFCN-DPXROKLSSA-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):
    -5.6
  • 重原子数:
    51.0
  • 可旋转键数:
    11.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    305.6
  • 氢给体数:
    11.0
  • 氢受体数:
    20.0

反应信息

  • 作为产物:
    描述:
    p-methoxyphenyl 2,3,4-tri-O-benzoyl-6-deoxy-α-L-talopyranosyl-(1->3)-2,4,6-tri-O-benzoyl-β-D-glucopyranosyl-(1->3)-2,4-di-O-benzoyl-6-deoxy-α-L-talopyranosyl-(1->3)-2,4,6-tri-O-benzoyl-α-D-glucopyranoside 作用下, 以 甲醇 为溶剂, 反应 168.0h, 以84%的产率得到p-methoxyphenyl 6-deoxy-α-L-talopyranosyl-(1->3)-β-D-glucopyranosyl-(1->3)-6-deoxy-α-L-talopyranosyl-(1->3)-α-D-glucopyranoside
    参考文献:
    名称:
    Facile syntheses of the disaccharide repeating unit of the O-antigenic polysaccharide of Burkholderia pseudomallei strain 304b and its dimer and trimer
    摘要:
    A highly efficient strategy for the preparation of a disaccharide-repeating unit of the O-antigenic polysaccharide of Burkholderia pseudomallei strain 304b, and its dimer and trimer, has been developed through a regio- and stereoselective manner using p-methoxylphenyl 2,4,6-tri-O-benzoyl-alpha-D-glucopyranoside and 3-O-allyloxycarbonyl-2,4-di-O-benzoy1-6-deoxy-alpha-L-talopyranosyl trichloroacetimidate as the key synthons. The target molecules were equipped with a p-methoxylphenyl handle at the reducing terminus to allow for their further functionalization and attachment to a carrier protein. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.09.001
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