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3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose | 1007885-91-7

中文名称
——
中文别名
——
英文名称
3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose
英文别名
——
3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose化学式
CAS
1007885-91-7
化学式
C55H54ClIO12
mdl
——
分子量
1069.38
InChiKey
NSHIYBKKRPDPHW-UTAKRQDDSA-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):
    10.29
  • 重原子数:
    69.0
  • 可旋转键数:
    17.0
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    110.76
  • 氢给体数:
    0.0
  • 氢受体数:
    12.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose二异丁基氢化铝 作用下, 以 二氯甲烷甲苯 为溶剂, 以56%的产率得到3,4,4'-tri-O-benzyl-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose
    参考文献:
    名称:
    Synthetic Studies toward Mycobacterium tuberculosis Sulfolipid-I
    摘要:
    [GRAPHICS]Sulfolipid-I (SL-I) is an abundant metabolite found in the cell wall of Mycobacterium tuberculosis that is comprised of a trehalose 2-sulfate core modified with four fatty acyl substituents. The correlation of its abundance with the virulence of clinical isolates suggests a role for SL-I in pathogenesis, although its biological functions remain unknown. Here we describe the synthesis of a SL-I analogue bearing unnatural lipid substituents. A key feature of the synthesis was application of an intramolecular aglycon delivery reaction to join two differentially protected glucose monomers, one prepared with a novel alpha-selective glycosylation. The route developed for the model compound can be readily extended to the synthesis of native SL-I as well as additional analogues for use in the investigation of SL-I's functions.
    DOI:
    10.1021/jo702032c
  • 作为产物:
    描述:
    3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-α,α-D-trehalose1-(碘甲基)-4-甲氧基苯 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以4.15 g的产率得到3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose
    参考文献:
    名称:
    Synthetic Studies toward Mycobacterium tuberculosis Sulfolipid-I
    摘要:
    [GRAPHICS]Sulfolipid-I (SL-I) is an abundant metabolite found in the cell wall of Mycobacterium tuberculosis that is comprised of a trehalose 2-sulfate core modified with four fatty acyl substituents. The correlation of its abundance with the virulence of clinical isolates suggests a role for SL-I in pathogenesis, although its biological functions remain unknown. Here we describe the synthesis of a SL-I analogue bearing unnatural lipid substituents. A key feature of the synthesis was application of an intramolecular aglycon delivery reaction to join two differentially protected glucose monomers, one prepared with a novel alpha-selective glycosylation. The route developed for the model compound can be readily extended to the synthesis of native SL-I as well as additional analogues for use in the investigation of SL-I's functions.
    DOI:
    10.1021/jo702032c
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