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3-iodo-6,6-dimethyl-cyclohex-2-enol | 1020202-91-8

中文名称
——
中文别名
——
英文名称
3-iodo-6,6-dimethyl-cyclohex-2-enol
英文别名
——
3-iodo-6,6-dimethyl-cyclohex-2-enol化学式
CAS
1020202-91-8
化学式
C8H13IO
mdl
——
分子量
252.095
InChiKey
CCRAETLRXKSQJU-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):
    2.49
  • 重原子数:
    10.0
  • 可旋转键数:
    0.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    20.23
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    3-iodo-6,6-dimethyl-cyclohex-2-enol三异丙基硅基三氟甲磺酸酯2,6-二甲基吡啶 作用下, 以94%的产率得到(3-iodo-6,6-dimethyl-cyclohex-2-enyloxy)-triisopropylsilane
    参考文献:
    名称:
    Allenyl Azide Cycloaddition Chemistry. 2,3-Cyclopentennelated Indole Synthesis through Indolidene Intermediates
    摘要:
    The thermal, photochemical, and photochemical/CuI-mediated cascade cyclizations of a range of substituted 1-(2-azidophenyl)-3-alkenylallenes are described. These reactions provide both 1,2- and 2,3-cyclopentennelated indole products in varying ratios. In most cases, high regioselectivity for the 2,3-annelated isomer can be achieved under the hv/CuI conditions. Computational studies of this multistep reaction support the intermediacy of indolidene intermediates whose electrocyclizations (with or without copper present) define the regioselectivity branch point in the sequence.
    DOI:
    10.1021/jo900659w
  • 作为产物:
    描述:
    3-碘-6,6-二甲基-环己-2-烯酮 在 sodium tetrahydroborate 、 cerium(III) chloride heptahydrate 作用下, 以 甲醇 为溶剂, 以99%的产率得到3-iodo-6,6-dimethyl-cyclohex-2-enol
    参考文献:
    名称:
    Allenyl Azide Cycloaddition Chemistry. Photochemical Initiation and CuI Mediation Leads to Improved Regioselectivity
    摘要:
    Irradiation of 2-(3-alkenyl)allenylphenyl azides in the presence of excess Cul furnished functionalized 2,3-cyclopentenylindoles in good yield with only trace amounts of competitive C-N-bonded regioisomeric products. These results represent a significant departure from the modestto-nonexistent regioselectivity that attended thermal cyclization of these allenyl azide substrates.
    DOI:
    10.1021/ol800429j
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