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(E)-1-(1-cyclohexyl-1-octenyl)cyclohexanol | 125642-03-7

中文名称
——
中文别名
——
英文名称
(E)-1-(1-cyclohexyl-1-octenyl)cyclohexanol
英文别名
1-[(E)-1-cyclohexyloct-1-enyl]cyclohexan-1-ol
(E)-1-(1-cyclohexyl-1-octenyl)cyclohexanol化学式
CAS
125642-03-7
化学式
C20H36O
mdl
——
分子量
292.505
InChiKey
LTKGKKJIGKHWRJ-XDJHFCHBSA-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):
    7.4
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

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文献信息

  • Reactions between tantalum- or niobium-alkyne complexes and carbonyl compounds
    作者:Yasutaka Kataoka、Jiro Miyai、Koichiro Oshima、Kazuhiko Takai、Kiitiro Utimoto
    DOI:10.1021/jo00033a015
    日期:1992.3
    A variety of tantalum-alkyne complexes are generated in situ by treatment of alkynes with low-valent tantalum derived from TaCl5 and zinc. These complexes add regioselectively to carbonyl compounds in a one-to-one fashion to yield (E)-allylic alcohols stereoselectively. Iodinolysis of the oxatantalacyclopentene, which is postulated as an intermediate of the reaction, gives a (Z)-3-iodo-2-propen-1-ol derivation. In contrast to tantalum-alkyne complexes, niobium-alkyne complexes, prepared with low-valent niobium derived from NbCl5 and zinc, add in situ to aldehydes in a one-to-two fashion to give 1,3-diene derivatives. The dienes are produced through (i) addition of the alkyne complexes with 2 equiv of aldehydes at cis vicinal positions of the alkenes and (ii) deoxygenative elimination of 2,7-dioxanioba-4-cycloheptene complexes.
  • Tantalum-alkyne complexes as synthetic intermediates. Stereoselective preparation of trisubstituted allylic alcohols from acetylenes and aldehydes
    作者:Kazuhiko Takai、Y. Kataoka、K. Utimoto
    DOI:10.1021/jo00293a008
    日期:1990.3
  • TAKAI, KAZUHIKO;KATAOKA, YASUTAKA;UTIMOTO, KIITIRO, J. ORG. CHEM., 55,(1990) N, C. 1707-1708
    作者:TAKAI, KAZUHIKO、KATAOKA, YASUTAKA、UTIMOTO, KIITIRO
    DOI:——
    日期:——
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