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7-cyclohexylidenebicyclo[4.2.1]nona-2,4-diene

中文名称
——
中文别名
——
英文名称
7-cyclohexylidenebicyclo[4.2.1]nona-2,4-diene
英文别名
(1S,6S)-7-cyclohexylidenebicyclo[4.2.1]nona-2,4-diene
7-cyclohexylidenebicyclo[4.2.1]nona-2,4-diene化学式
CAS
——
化学式
C15H20
mdl
——
分子量
200.324
InChiKey
QCPRNYLBNUUOTB-GXTWGEPZSA-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):
    4.2
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    环己乙炔环庚三烯二氯二(戊烷-2,4-二酮酸根-O,O')钛氯化二乙基铝 作用下, 以 为溶剂, 反应 8.0h, 以79%的产率得到7-cyclohexylidenebicyclo[4.2.1]nona-2,4-diene
    参考文献:
    名称:
    Catalytic [6π+2π]-cycloaddition of alkynes, 1,2- and 1,3-dienes to 1,3,5-cycloheptatrienes involving Ti complexes
    摘要:
    Novel two-component Ti-based catalytic systems, R2TiCl2 R'nAlCl(3-n) (R=acac, (PrO)-Pr-i, (BuO)-Bu-t; R'=Et, Bu, n=2, 3), for [6 pi+2 pi]-cycloaddition of acetylenes and 1,2- and 1,3-dienes, including functionally substituted ones, to 1,3,5-cycloheptatrienes to give bi-, tri-, and polycyclic hydrocarbons were developed. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.04.019
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文献信息

  • Chromium(0)-Promoted [6π + 2π] Cycloadditions of Allenes with Cycloheptatriene
    作者:James H. Rigby、Stéphane B. Laurent、Zeeshan Kamal、Mary Jane Heeg
    DOI:10.1021/ol802401a
    日期:2008.12.18
    Photoinitiated [6pi + 2pi] cycloadditions of allenes with (eta(6)-cycloheptatriene)tricarbonylchromium(0) (1) are described. An example of asymmetric induction obtained by reaction of 1 with a chiral 1,3-disubstituted allene is also reported.
    描述了丙二烯与 (eta(6)-环庚三烯)tricarbonylchromium(0) (1) 的光引发 [6pi + 2pi] 环加成。还报道了通过 1 与手性 1,3-二取代丙二烯反应获得的不对称诱导的例子。
  • Ti-catalyzed [6π+2π] cycloadditions of allenes with 1,3,5-cycloheptatriene
    作者:Vladimir A. D’yakonov、Gulnara N. Kadikova、Usein M. Dzhemilev
    DOI:10.1016/j.tetlet.2011.03.131
    日期:2011.5
    The reaction between 1,2-dienes and 1,3,5-cycloheptatriene in the presence of the two-component catalyst, TiCl(4)-Et(2)AlCl leads to the regioselective formation of endo-bicyclo[4.2.1]nona-2,4-diene derivatives in yields of up to 80%. (C) 2011 Elsevier Ltd. All rights reserved.
  • Catalytic [6π+2π]-cycloaddition of alkynes, 1,2- and 1,3-dienes to 1,3,5-cycloheptatrienes involving Ti complexes
    作者:Usein M. Dzhemilev、Gulnara N. Kadikova、Dmitry I. Kolokol'tsev、Vladimir A. D'yakonov
    DOI:10.1016/j.tet.2013.04.019
    日期:2013.6
    Novel two-component Ti-based catalytic systems, R2TiCl2 R'nAlCl(3-n) (R=acac, (PrO)-Pr-i, (BuO)-Bu-t; R'=Et, Bu, n=2, 3), for [6 pi+2 pi]-cycloaddition of acetylenes and 1,2- and 1,3-dienes, including functionally substituted ones, to 1,3,5-cycloheptatrienes to give bi-, tri-, and polycyclic hydrocarbons were developed. (C) 2013 Elsevier Ltd. All rights reserved.
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