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(E)-chlorogold(I)(1-(2,4,6-tri-tert-butylphenyl)2-benzyl-2-methyl-1-phosphaethene) | 1211351-72-2

中文名称
——
中文别名
——
英文名称
(E)-chlorogold(I)(1-(2,4,6-tri-tert-butylphenyl)2-benzyl-2-methyl-1-phosphaethene)
英文别名
——
(E)-chlorogold(I)(1-(2,4,6-tri-tert-butylphenyl)2-benzyl-2-methyl-1-phosphaethene)化学式
CAS
1211351-72-2
化学式
C27H39AuClP
mdl
——
分子量
627.0
InChiKey
LLCFAVCWTSTDNX-UHFFFAOYSA-M
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

反应信息

  • 作为产物:
    描述:
    (tetrahydrothiophene)gold(I) chloride(E)-(1-(2,4,6-tri-tert-butylphenyl)(2-benzyl-2-methyl-1-phosphaethene))二氯甲烷 为溶剂, 以72%的产率得到(E)-chlorogold(I)(1-(2,4,6-tri-tert-butylphenyl)2-benzyl-2-methyl-1-phosphaethene)
    参考文献:
    名称:
    Ligand effect of bulky 2,2-dialkyl-1-phosphaethenes on Au-catalyzed cycloisomerization of 1,6-enynes and lactonization of pent-4-ynoic acids
    摘要:
    2,2-Dimethyl- and 2-benzyl-2-methyl-1-(2,4,6-tri-tert-butylphenyl)-1-phosphaethenes were employed as ligand of mononuclear chlorogold(I) complexes, which catalyzed cycloisomerization of 1,6-enyne affording vinylcyclopentene exclusively in the absence of silver co-catalyst. The reaction mechanisms are discussed based on DFT calculations. In addition to the cycloisomerization, the phosphaalkene-chlorogold(I) complexes catalyzed cyclization of pent-4-ynoic acids providing gamma-methylene-gamma-lactones under basic conditions. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2009.09.040
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