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(3aR)-3a-methyl-3-methylidene-2,4,5,6-tetrahydro-1H-indene-5,6-diol | 1065490-67-6

中文名称
——
中文别名
——
英文名称
(3aR)-3a-methyl-3-methylidene-2,4,5,6-tetrahydro-1H-indene-5,6-diol
英文别名
——
(3aR)-3a-methyl-3-methylidene-2,4,5,6-tetrahydro-1H-indene-5,6-diol化学式
CAS
1065490-67-6
化学式
C11H16O2
mdl
——
分子量
180.247
InChiKey
SMASCUDVOGKDHK-VQXHTEKXSA-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):
    0.6
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (3aR)-3a-methyl-3-methylidene-2,4,5,6-tetrahydro-1H-indene-5,6-diol 、 lead(IV) tetraacetate 以 甲苯 为溶剂, 反应 0.08h, 以34 mg的产率得到
    参考文献:
    名称:
    Microwave-assisted domino reactions: function-compatibility, modulation, and greening efforts
    摘要:
    Herein we report a microwave-assisted version of a domino protocol, providing ready access to a wide variety of complex oxygen heterocycles. The latter can be converted to stereochemically, well-defined, variously substituted carbocycles, since reaction conditions and the substitution pattern can be tailored to fit a particular type of transformation. Microwave assistance, the influence of solvent, temperature, the function compatibility, and the use of PhI(OAc)(2) as a domino promoter are investigated. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2008.06.026
  • 作为产物:
    描述:
    [(3aR)-6-[tert-butyl(dimethyl)silyl]oxy-3a-methyl-3-methylidene-2,4,5,6-tetrahydro-1H-inden-5-yl]oxy-tert-butyl-dimethylsilane 在 四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以81%的产率得到(3aR)-3a-methyl-3-methylidene-2,4,5,6-tetrahydro-1H-indene-5,6-diol
    参考文献:
    名称:
    Microwave-assisted domino reactions: function-compatibility, modulation, and greening efforts
    摘要:
    Herein we report a microwave-assisted version of a domino protocol, providing ready access to a wide variety of complex oxygen heterocycles. The latter can be converted to stereochemically, well-defined, variously substituted carbocycles, since reaction conditions and the substitution pattern can be tailored to fit a particular type of transformation. Microwave assistance, the influence of solvent, temperature, the function compatibility, and the use of PhI(OAc)(2) as a domino promoter are investigated. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2008.06.026
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