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(1R)-1-[(1S,2R,3S)-2-(hydroxymethyl)-2,3-dimethylcyclohexyl]ethane-1,2-diol | 325982-00-1

中文名称
——
中文别名
——
英文名称
(1R)-1-[(1S,2R,3S)-2-(hydroxymethyl)-2,3-dimethylcyclohexyl]ethane-1,2-diol
英文别名
——
(1R)-1-[(1S,2R,3S)-2-(hydroxymethyl)-2,3-dimethylcyclohexyl]ethane-1,2-diol化学式
CAS
325982-00-1
化学式
C11H22O3
mdl
——
分子量
202.294
InChiKey
GDCQLWDRJUFQPJ-ZRUFSTJUSA-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):
    1.2
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (1R)-1-[(1S,2R,3S)-2-(hydroxymethyl)-2,3-dimethylcyclohexyl]ethane-1,2-diolsodium periodatepyridinium chlorochromate 作用下, 以 乙醚乙醇 为溶剂, 反应 6.0h, 生成 (3aR,4S,7aS)-3a,4-Dimethyl-hexahydro-isobenzofuran-1-one
    参考文献:
    名称:
    Regiocontrol of Radical Cyclization by Lewis Acids. Efficient Synthesis of Optically Active Functionalized Cyclopentanes and Cyclohexanes
    摘要:
    [GRAPHICS]Treatment of alpha -alkylidenelactones 3a-d with Bu3SnH and a catalytic amount of Et3B effected a 5-exo radical cyclization preferentially to provide the corresponding 1 and 2 in a ratio of 70:30 to 100:0, Meanwhile, the reaction of 3a and 3b in the presence of Et2AlCl proceeded via a B-endo cyclization pathway predominantly to afford 2a and 2b with 90% and 92% regioselectivity, respectively.
    DOI:
    10.1021/ol0067890
  • 作为产物:
    描述:
    (3E,4S,5R)-3-ethylidene-4-(3-iodopropyl)-5-(phenylmethoxymethyl)oxolan-2-one 在 palladium on activated charcoal lithium aluminium tetrahydride 、 三乙基硼氢气三正丁基氢锡lithium diisopropyl amide 作用下, 以 四氢呋喃甲醇甲苯 为溶剂, -78.0~20.0 ℃ 、101.33 kPa 条件下, 反应 7.0h, 生成 (1R)-1-[(1S,2R,3S)-2-(hydroxymethyl)-2,3-dimethylcyclohexyl]ethane-1,2-diol
    参考文献:
    名称:
    Regiocontrol of Radical Cyclization by Lewis Acids. Efficient Synthesis of Optically Active Functionalized Cyclopentanes and Cyclohexanes
    摘要:
    [GRAPHICS]Treatment of alpha -alkylidenelactones 3a-d with Bu3SnH and a catalytic amount of Et3B effected a 5-exo radical cyclization preferentially to provide the corresponding 1 and 2 in a ratio of 70:30 to 100:0, Meanwhile, the reaction of 3a and 3b in the presence of Et2AlCl proceeded via a B-endo cyclization pathway predominantly to afford 2a and 2b with 90% and 92% regioselectivity, respectively.
    DOI:
    10.1021/ol0067890
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