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(2S,4S)-2,4-Dihydroxy-2,4-O-isopropylidene-6-heptenal | 171598-98-4

中文名称
——
中文别名
——
英文名称
(2S,4S)-2,4-Dihydroxy-2,4-O-isopropylidene-6-heptenal
英文别名
(4S,6S)-2,2-dimethyl-6-prop-2-enyl-1,3-dioxane-4-carbaldehyde
(2S,4S)-2,4-Dihydroxy-2,4-O-isopropylidene-6-heptenal化学式
CAS
171598-98-4
化学式
C10H16O3
mdl
——
分子量
184.235
InChiKey
XGTUJFDKDKJTRH-IUCAKERBSA-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):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    (2S,4S)-2,4-Dihydroxy-2,4-O-isopropylidene-6-heptenal 在 palladium on activated charcoal 盐酸正丁基锂氢气 作用下, 以 四氢呋喃乙醇 为溶剂, 生成 (4S,6R)-Tridecane-4,6-diol
    参考文献:
    名称:
    Studies on the Stereochemistry of Theonezolides A-C: Elucidation of the Relative Configurations of 1,3-Diol Moieties of the C-4Å`C-17 Fragment
    摘要:
    Four model compounds having syn and anti 1,3-diol type moieties corresponding to C-8/C-10 and C-14/C-16 positions contained in the C-4 similar to C-17 fragment of theonezolides A-C were prepared. Comparison of their spectral data suggested that the 1,3-diol at C-8/C-10 and the OH/OMe groups at C-14/C-16 positions of theonezolides A-C were both syn.
    DOI:
    10.3987/com-97-s6-1
  • 作为产物:
    描述:
    (2S,4'S)-2-(N-Benzylamino)-4-<oxy>-6-hepten-1-ol 在 盐酸sodium hydroxide四丁基氯化铵sodium acetate二异丁基氢化铝potassium carbonate 、 magnesium monoperoxyphthalate hexahydrate 作用下, 以 四氢呋喃甲醇正己烷二氯甲烷氯仿叔丁醇 为溶剂, 反应 5.49h, 生成 (2S,4S)-2,4-Dihydroxy-2,4-O-isopropylidene-6-heptenal
    参考文献:
    名称:
    Synthetic Studies on the Polyene Macrolide Antibiotics. Development of syn- and anti-1,3-Diol Subunits and Assembly of the Polyacetate Region of Amphotericin B
    摘要:
    The synthesis of syn- and anti-1,3-diol subunits from thiol ester oxazoline 4 has been described. The key features of these synthetic sequences include the stereodivergent allylation of an asymmetric beta-amino aldehyde (7) and the stereospecific transformation of a vicinal amino alcohol to an epoxide. The resultant diasteromeric silyl-protected epoxy alcohols (10s and 10a) serve as convenient precursors to the isomeric diol aldehyde derivatives 13, 13-ent, and 16. One of these fragments, compound 13, has been exploited in a highly convergent synthesis of the C1-C13 polyacetate segment of amphotericin B.
    DOI:
    10.1021/jo00129a019
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文献信息

  • Synthetic Studies on the Polyene Macrolide Antibiotics. Development of syn- and anti-1,3-Diol Subunits and Assembly of the Polyacetate Region of Amphotericin B
    作者:Glenn J. McGarvey、Jeffrey A. Mathys、Kenneth J. Wilson、Kenneth R. Overly、Paul T. Buonora、P. Grant Spoors
    DOI:10.1021/jo00129a019
    日期:1995.12
    The synthesis of syn- and anti-1,3-diol subunits from thiol ester oxazoline 4 has been described. The key features of these synthetic sequences include the stereodivergent allylation of an asymmetric beta-amino aldehyde (7) and the stereospecific transformation of a vicinal amino alcohol to an epoxide. The resultant diasteromeric silyl-protected epoxy alcohols (10s and 10a) serve as convenient precursors to the isomeric diol aldehyde derivatives 13, 13-ent, and 16. One of these fragments, compound 13, has been exploited in a highly convergent synthesis of the C1-C13 polyacetate segment of amphotericin B.
  • Studies on the Stereochemistry of Theonezolides A-C: Elucidation of the Relative Configurations of 1,3-Diol Moieties of the C-4Å`C-17 Fragment
    作者:Jun'ichi Kobayashi、Makiko Yonezawa、Shinji Takeuchi、Masami Ishibashi
    DOI:10.3987/com-97-s6-1
    日期:——
    Four model compounds having syn and anti 1,3-diol type moieties corresponding to C-8/C-10 and C-14/C-16 positions contained in the C-4 similar to C-17 fragment of theonezolides A-C were prepared. Comparison of their spectral data suggested that the 1,3-diol at C-8/C-10 and the OH/OMe groups at C-14/C-16 positions of theonezolides A-C were both syn.
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