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undeca-1,4,5-triene | 127871-49-2

中文名称
——
中文别名
——
英文名称
undeca-1,4,5-triene
英文别名
1-allyl-3-pentylallene
undeca-1,4,5-triene化学式
CAS
127871-49-2
化学式
C11H18
mdl
——
分子量
150.264
InChiKey
MUEVWLUQWIELTK-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

物化性质

  • 沸点:
    197.8±10.0 °C(Predicted)
  • 密度:
    0.760±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    苯胺undeca-1,4,5-trienegold(III) bromide 作用下, 以 四氢呋喃 为溶剂, 反应 3.08h, 生成 、
    参考文献:
    名称:
    Gold-catalyzed hydrofunctionalization of allenes with nitrogen and oxygen nucleophiles and its mechanistic insight
    摘要:
    A wide range of nucleophiles, such as amines and alcohols, reacted intermolecularly with various allenes in the presence of gold catalysts to give the corresponding hydrofunctionalization products in high yields. The intermolecular hydroamination of chiral allenes with aromatic and aliphatic amines proceeded with high to good enantioface selectivities to afford the corresponding chiral allylic amines. On the other hand, in the case of the intermolecular hydroalkoxylation of chiral allenes, no chirality transfer was observed. This marked contrast on the chirality transfer indicates that the mechanisms of gold-catalysis between hydroamination and hydroalkoxylation are different. (C) 2008 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tet.2008.11.106
  • 作为产物:
    描述:
    4-(<1-(prop-2-enyl)oct-2-ynyl>sulfinyl)morpholine三氟化硼乙醚 作用下, 以 四氢呋喃 为溶剂, 以46%的产率得到undeca-1,4,5-triene
    参考文献:
    名称:
    Baudin Jean-Bernard; Julia, Sylvestre A; Wang, Yuan, Bulletin de la Societe Chimique de France, 1995, vol. 132, # 7, p. 754 - 760
    摘要:
    DOI:
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文献信息

  • Construction of 1,5-Enynes by Stereospecific Pd-Catalyzed Allyl–Propargyl Cross-Couplings
    作者:Michael J. Ardolino、James P. Morken
    DOI:10.1021/ja302329f
    日期:2012.5.30
    The palladium-catalyzed cross-coupling of chiral propargyl acetates and allyl boronates delivers chiral 1,5-enynes with excellent levels of chirality transfer and can be applied across a broad range of substrates.
  • Gold-Catalyzed Intermolecular Hydroamination of Allenes with Arylamines and Resulting High Chirality Transfer
    作者:Naoko Nishina、Yoshinori Yamamoto
    DOI:10.1002/anie.200600331
    日期:2006.5.12
  • BAUDIN, JEAN-BERNARD;JULIA, SYLVESTRE A.;RUEL, ODILE;WANG, YUAN, TETRAHEDRON LETT., 31,(1990) N, C. 213-216
    作者:BAUDIN, JEAN-BERNARD、JULIA, SYLVESTRE A.、RUEL, ODILE、WANG, YUAN
    DOI:——
    日期:——
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