5-methyl-3-[1-(1-naphthyl)-2-propynyl]-1-triisopropylsilylindole | 1004517-34-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 5-methyl-3-[1-(1-naphthyl)-2-propynyl]-1-triisopropylsilylindole
• 英文别名: [5-methyl-3-[(1R)-1-naphthalen-1-ylprop-2-ynyl]indol-1-yl]-tri(propan-2-yl)silane
• CAS: 1004517-34-3
• 化学式: C₃₁H₃₇NSi
• 分子量: 451.727
• InChiKey: WIBFGKZVMYOIGB-AREMUKBSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.89
• 重原子数：
  33
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  4.9
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  5-methyl-3-[1-(1-naphthyl)-2-propynyl]-1-triisopropylsilylindole 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 生成 5-methyl-3-[1-(1-naphthyl)-2-propynyl]indole
  参考文献：
  名称：

  Remarkable Effect of N-Substituent on Enantioselective Ruthenium-Catalyzed Propargylation of Indoles with Propargylic Alcohols

  摘要：

  Ruthenium-catalyzed enantioselective propargylation of indoles with propargylic alcohols affords the corresponding beta-propargylated indoles in good yields with a high enantioselectivity (up to 95% ee). A remarkable effect of the nature of the N-substituent of indoles is observed for the enantioselectivity of the propargylated indoles. The preparative method described in this paper may provide a novel protocol for asymmetric Friedel-Crafts alkylation of indoles using propargylic alcohols as a new type of electrophiles.

  DOI：

  10.1021/ol7025203
• 作为产物：
  描述：

  5-methyl-1-triisopropylsilylindole 、 1-(1'-naphthyl)-2-propyn-1-ol 在 chiral di(1-phenyl)propyl disulfide-based ruthenium complex ammonium tetrafluoroborate 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 20.0h， 生成 5-methyl-3-[1-(1-naphthyl)-2-propynyl]-1-triisopropylsilylindole 、 5-methyl-3-[1-(1-naphthyl)-2-propynyl]-1-triisopropylsilylindole
  参考文献：
  名称：

  Remarkable Effect of N-Substituent on Enantioselective Ruthenium-Catalyzed Propargylation of Indoles with Propargylic Alcohols

  摘要：

  Ruthenium-catalyzed enantioselective propargylation of indoles with propargylic alcohols affords the corresponding beta-propargylated indoles in good yields with a high enantioselectivity (up to 95% ee). A remarkable effect of the nature of the N-substituent of indoles is observed for the enantioselectivity of the propargylated indoles. The preparative method described in this paper may provide a novel protocol for asymmetric Friedel-Crafts alkylation of indoles using propargylic alcohols as a new type of electrophiles.

  DOI：

  10.1021/ol7025203

文献信息

• Remarkable Effect of <i>N</i>-Substituent on Enantioselective Ruthenium-Catalyzed Propargylation of Indoles with Propargylic Alcohols
  作者：Hiroshi Matsuzawa、Keiichiro Kanao、Yoshihiro Miyake、Yoshiaki Nishibayashi

  DOI：10.1021/ol7025203

  日期：2007.12.1

  Ruthenium-catalyzed enantioselective propargylation of indoles with propargylic alcohols affords the corresponding beta-propargylated indoles in good yields with a high enantioselectivity (up to 95% ee). A remarkable effect of the nature of the N-substituent of indoles is observed for the enantioselectivity of the propargylated indoles. The preparative method described in this paper may provide a novel protocol for asymmetric Friedel-Crafts alkylation of indoles using propargylic alcohols as a new type of electrophiles.