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3-Methoxy-2-methyl-6-(3-methylbut-2-enyl)phenol | 1006054-43-8

中文名称
——
中文别名
——
英文名称
3-Methoxy-2-methyl-6-(3-methylbut-2-enyl)phenol
英文别名
3-methoxy-2-methyl-6-(3-methylbut-2-enyl)phenol
3-Methoxy-2-methyl-6-(3-methylbut-2-enyl)phenol化学式
CAS
1006054-43-8
化学式
C13H18O2
mdl
——
分子量
206.285
InChiKey
GDENVPVCKHMFQN-UHFFFAOYSA-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):
    3.8
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Construction of the 3-prenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-one core of caged xanthonoid natural products via tandem Wessely oxidation–intramolecular [4+2] cycloaddition
    摘要:
    A two-step protocol based on tandem Wessely oxidation/intramolecular Diels-Alder reaction to provide general access to the 3-prenyl-4-oxa-tricyclo[4.3. 1.0(3,7)]dec-8-en-2-one core present in the caged Garcinia xanthonoids is demonstrated. These readily accessible tricyclic scaffolds also provide ready entry into a variety of substituted gamma-lactones through a photochemical 1,3-acyl shift and decarbonylation. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.11.050
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文献信息

  • Construction of the 3-prenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-one core of caged xanthonoid natural products via tandem Wessely oxidation–intramolecular [4+2] cycloaddition
    作者:Goverdhan Mehta、Pulakesh Maity
    DOI:10.1016/j.tetlet.2007.11.050
    日期:2008.1
    A two-step protocol based on tandem Wessely oxidation/intramolecular Diels-Alder reaction to provide general access to the 3-prenyl-4-oxa-tricyclo[4.3. 1.0(3,7)]dec-8-en-2-one core present in the caged Garcinia xanthonoids is demonstrated. These readily accessible tricyclic scaffolds also provide ready entry into a variety of substituted gamma-lactones through a photochemical 1,3-acyl shift and decarbonylation. (C) 2007 Elsevier Ltd. All rights reserved.
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