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(4R,6R,8S,10R,12S,14R,16S,18R,20S,22S)-4,6:8,10:12,14:16,18:20,22-Pentakis-O-(1-methylethylidene)-1-heptacosene-4,6,8,10,12,14,16,18,20,22-decol | 139071-33-3

中文名称
——
中文别名
——
英文名称
(4R,6R,8S,10R,12S,14R,16S,18R,20S,22S)-4,6:8,10:12,14:16,18:20,22-Pentakis-O-(1-methylethylidene)-1-heptacosene-4,6,8,10,12,14,16,18,20,22-decol
英文别名
(4R,6S)-4-[[(4S,6R)-6-[[(4S,6S)-2,2-dimethyl-6-pentyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]-6-[[(4R,6S)-6-[[(4R,6R)-2,2-dimethyl-6-prop-2-enyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]-2,2-dimethyl-1,3-dioxane
(4R,6R,8S,10R,12S,14R,16S,18R,20S,22S)-4,6:8,10:12,14:16,18:20,22-Pentakis-O-(1-methylethylidene)-1-heptacosene-4,6,8,10,12,14,16,18,20,22-decol化学式
CAS
139071-33-3
化学式
C42H74O10
mdl
——
分子量
739.044
InChiKey
OIIRPVUNSFACOR-KFLVAVFTSA-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):
    8.5
  • 重原子数:
    52
  • 可旋转键数:
    14
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    92.3
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    (4R,6R,8S,10R,12S,14R,16S,18R,20S,22S)-4,6:8,10:12,14:16,18:20,22-Pentakis-O-(1-methylethylidene)-1-heptacosene-4,6,8,10,12,14,16,18,20,22-decol 在 Dowex W50-X1 作用下, 以 甲醇 为溶剂, 以50.5 mg的产率得到(4R,6R,8S,10R,12R,14S,16S,18S,20S,22S)-Decahydroxy-1-heptacosene
    参考文献:
    名称:
    An iterative and convergent synthesis of syn polyols
    摘要:
    We have developed a new iterative and convergent synthesis of alternating (1,3,5...) polyol chains based on enantiomerically enriched (94% ee) chloro nitrile 1. Chloro nitrile 1 is both a potential nucleophile and a potential electrophile; orthogonal nucleophilic or electrophilic activation leads to a highly efficient synthetic strategy for alternating polyol chains. As an illustration permethylated polyol 2 (n = 10), a natural product with 10 stereogenic centers isolated from the blue green alga Tolypothrix conglutinata var. chlorata, was prepared in 10 steps from 1.
    DOI:
    10.1021/jo00031a041
  • 作为产物:
    描述:
    (4R,6R,8S,10R,12S,14R,16S,18R,20S,22S)-4,8,12,16,20-Penta-C-cyano-4,6:8,10:12,14:16,18:20,22-pentakis-O-(1-methylethylidene)-1-heptacosene-4,6,8,10,12,14,16,18,20,22-decollithium 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以85%的产率得到(4R,6R,8S,10R,12S,14R,16S,18R,20S,22S)-4,6:8,10:12,14:16,18:20,22-Pentakis-O-(1-methylethylidene)-1-heptacosene-4,6,8,10,12,14,16,18,20,22-decol
    参考文献:
    名称:
    An iterative and convergent synthesis of syn polyols
    摘要:
    We have developed a new iterative and convergent synthesis of alternating (1,3,5...) polyol chains based on enantiomerically enriched (94% ee) chloro nitrile 1. Chloro nitrile 1 is both a potential nucleophile and a potential electrophile; orthogonal nucleophilic or electrophilic activation leads to a highly efficient synthetic strategy for alternating polyol chains. As an illustration permethylated polyol 2 (n = 10), a natural product with 10 stereogenic centers isolated from the blue green alga Tolypothrix conglutinata var. chlorata, was prepared in 10 steps from 1.
    DOI:
    10.1021/jo00031a041
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