摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[3-[2-(p-anisylethynyl)phenyl]-1-m-tolylpropa-1,2-dienyl]-trimethylsilane | 1422529-08-5

中文名称
——
中文别名
——
英文名称
[3-[2-(p-anisylethynyl)phenyl]-1-m-tolylpropa-1,2-dienyl]-trimethylsilane
英文别名
——
[3-[2-(p-anisylethynyl)phenyl]-1-m-tolylpropa-1,2-dienyl]-trimethylsilane化学式
CAS
1422529-08-5
化学式
C28H28OSi
mdl
——
分子量
408.615
InChiKey
MFTMMHYWINVKEG-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):
    6.98
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Nonstatistical Dynamic Effects in the Thermal C2–C6 Diels–Alder Cyclization of Enyne–Allenes
    摘要:
    The Diels-Alder (DA) reaction channel of the thermal C-2-C-6 (Schmittel) cyclization of enyne-allenes is studied computationally and experimentally evaluating the influence of temperature on product ratios. Remote substituents at the alkyne terminus influence the mechanism of the C-2-C-6/DA cyclization steering it either to a stepwise or a concerted course. Temperature independent product ratios, selectivity of product formation, and computational results obtained at (U)BLYP/6-31G(d) level unveil a mechanism that is strongly controlled by nonstatistical dynamics.
    DOI:
    10.1021/jo302524a
  • 作为产物:
    描述:
    1-{2-[2-(4-methoxyphenyl)-1-ethynyl]phenyl}-3-(trimethylsilyl)-2-propyn-1-ol 在 4-二甲氨基吡啶三乙胺 、 zinc(II) chloride 作用下, 以 四氢呋喃乙醚二氯甲烷 为溶剂, 反应 14.75h, 生成 [3-[2-(p-anisylethynyl)phenyl]-1-m-tolylpropa-1,2-dienyl]-trimethylsilane
    参考文献:
    名称:
    Nonstatistical Dynamic Effects in the Thermal C2–C6 Diels–Alder Cyclization of Enyne–Allenes
    摘要:
    The Diels-Alder (DA) reaction channel of the thermal C-2-C-6 (Schmittel) cyclization of enyne-allenes is studied computationally and experimentally evaluating the influence of temperature on product ratios. Remote substituents at the alkyne terminus influence the mechanism of the C-2-C-6/DA cyclization steering it either to a stepwise or a concerted course. Temperature independent product ratios, selectivity of product formation, and computational results obtained at (U)BLYP/6-31G(d) level unveil a mechanism that is strongly controlled by nonstatistical dynamics.
    DOI:
    10.1021/jo302524a
点击查看最新优质反应信息

文献信息

  • Nonstatistical Dynamic Effects in the Thermal C<sup>2</sup>–C<sup>6</sup> Diels–Alder Cyclization of Enyne–Allenes
    作者:Debabrata Samanta、Mehmet Emin Cinar、Kalpataru Das、Michael Schmittel
    DOI:10.1021/jo302524a
    日期:2013.2.15
    The Diels-Alder (DA) reaction channel of the thermal C-2-C-6 (Schmittel) cyclization of enyne-allenes is studied computationally and experimentally evaluating the influence of temperature on product ratios. Remote substituents at the alkyne terminus influence the mechanism of the C-2-C-6/DA cyclization steering it either to a stepwise or a concerted course. Temperature independent product ratios, selectivity of product formation, and computational results obtained at (U)BLYP/6-31G(d) level unveil a mechanism that is strongly controlled by nonstatistical dynamics.
查看更多