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(2S)-2-((E)-2-(4-methoxyphenyl)vinyl)piperidine | 1565872-59-4

中文名称
——
中文别名
——
英文名称
(2S)-2-((E)-2-(4-methoxyphenyl)vinyl)piperidine
英文别名
(2S)-2-[(E)-2-(4-methoxyphenyl)ethenyl]piperidine
(2S)-2-((E)-2-(4-methoxyphenyl)vinyl)piperidine化学式
CAS
1565872-59-4
化学式
C14H19NO
mdl
——
分子量
217.311
InChiKey
MLGWSRRUEOPTAW-LJLILKBBSA-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):
    2.8
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-Boc-哌啶 在 lithium aluminium tetrahydride 、 四丁基溴化铵仲丁基锂 、 palladium diacetate 、 三乙胺1,3-二-叔丁基咪唑氯化物(+)-鹰爪豆碱 作用下, 以 四氢呋喃乙醚乙醇 为溶剂, 反应 14.08h, 生成 (2S)-2-((E)-2-(4-methoxyphenyl)vinyl)piperidine
    参考文献:
    名称:
    Pd- N -heterocyclic carbene catalyzed synthesis of piperidine alkene–alkaloids and their anti-cancer evaluation
    摘要:
    A facile synthesis of piperidine alkene-alkaloids including natural (+)-Caulophyllumine B in high yields has been developed by Heck cross-coupling reaction catalyzed by simple in situ formed palladium-N-heterocyclic carbenes (Pd-NHCs). Formation of Pd(0) nanoparticles has been noticed during the reaction course. The synthesized piperidine alkene-alkaloids were evaluated for in vitro anti-cancer activity against a panel of human tumor cell lines of lung, breast and ovarian. Several of these piperidine alkene-alkaloids were found to possess highest growth inhibition activity than the standard drug cisplatin and support the concept to modulate drug receptor interaction. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.12.108
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文献信息

  • Pd- N -heterocyclic carbene catalyzed synthesis of piperidine alkene–alkaloids and their anti-cancer evaluation
    作者:Shravankumar Kankala、Ranjith Kumar Kankala、Ramesh Balaboina、Narasimha Swamy Thirukovela、Ravinder Vadde、Chandra Sekhar Vasam
    DOI:10.1016/j.bmcl.2013.12.108
    日期:2014.2
    A facile synthesis of piperidine alkene-alkaloids including natural (+)-Caulophyllumine B in high yields has been developed by Heck cross-coupling reaction catalyzed by simple in situ formed palladium-N-heterocyclic carbenes (Pd-NHCs). Formation of Pd(0) nanoparticles has been noticed during the reaction course. The synthesized piperidine alkene-alkaloids were evaluated for in vitro anti-cancer activity against a panel of human tumor cell lines of lung, breast and ovarian. Several of these piperidine alkene-alkaloids were found to possess highest growth inhibition activity than the standard drug cisplatin and support the concept to modulate drug receptor interaction. (C) 2013 Elsevier Ltd. All rights reserved.
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