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3'-O-(p-methoxybenzyl)-6'-O-(t-butyldimethylsilyl)-D-lactal | 688317-17-1

中文名称
——
中文别名
——
英文名称
3'-O-(p-methoxybenzyl)-6'-O-(t-butyldimethylsilyl)-D-lactal
英文别名
(2R,3S,4S,5R,6S)-2-[[tert-butyl(dimethyl)silyl]oxymethyl]-6-[[(2R,3S,4R)-4-hydroxy-2-(hydroxymethyl)-3,4-dihydro-2H-pyran-3-yl]oxy]-4-[(4-methoxyphenyl)methoxy]oxane-3,5-diol
3'-O-(p-methoxybenzyl)-6'-O-(t-butyldimethylsilyl)-D-lactal化学式
CAS
688317-17-1
化学式
C26H42O10Si
mdl
——
分子量
542.699
InChiKey
KUMNSYRDFCAQQM-PAWGEYITSA-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):
    1.7
  • 重原子数:
    37
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    136
  • 氢给体数:
    4
  • 氢受体数:
    10

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

反应信息

  • 作为反应物:
    描述:
    3'-O-(p-methoxybenzyl)-6'-O-(t-butyldimethylsilyl)-D-lactal碳酸氢钠 间氯过氧苯甲酸 作用下, 以 乙醚 为溶剂, 反应 3.0h, 生成 (2S,3S,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-3,5-dihydroxy-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yloxy]-6-hydroxymethyl-tetrahydro-pyran-2,3,4-triol
    参考文献:
    名称:
    A facile and novel route to the antigenic branched phosphoglycan of the protozoan Leishmania major parasite
    摘要:
    A novel approach for the iterative synthesis of the antigenic branched phosphoglycan of the protozoan parasite Leishmania major is presented that exploits remarkable dual selectivity in the functionalization of D-lactal, providing flexibility to extend the PG chain either towards the reducing or nonreducing end. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.01.155
  • 作为产物:
    描述:
    D-lactal18-冠醚-6 sodium hydride 、 二正丁基氧化锡 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 52.5h, 生成 3'-O-(p-methoxybenzyl)-6'-O-(t-butyldimethylsilyl)-D-lactal
    参考文献:
    名称:
    A facile and novel route to the antigenic branched phosphoglycan of the protozoan Leishmania major parasite
    摘要:
    A novel approach for the iterative synthesis of the antigenic branched phosphoglycan of the protozoan parasite Leishmania major is presented that exploits remarkable dual selectivity in the functionalization of D-lactal, providing flexibility to extend the PG chain either towards the reducing or nonreducing end. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.01.155
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文献信息

  • A facile and novel route to the antigenic branched phosphoglycan of the protozoan Leishmania major parasite
    作者:Dipali Ruhela、Ram A. Vishwakarma
    DOI:10.1016/j.tetlet.2004.01.155
    日期:2004.3
    A novel approach for the iterative synthesis of the antigenic branched phosphoglycan of the protozoan parasite Leishmania major is presented that exploits remarkable dual selectivity in the functionalization of D-lactal, providing flexibility to extend the PG chain either towards the reducing or nonreducing end. (C) 2004 Elsevier Ltd. All rights reserved.
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