1-Methyl-5-trimethylsilanyl-4-trimethylsilanylmethyl-pent-3-enylamine | 185814-68-0

• 分子结构分类: 有机化合物 - 有机盐 - 有机金属盐
• 英文名称: 1-Methyl-5-trimethylsilanyl-4-trimethylsilanylmethyl-pent-3-enylamine
• 英文别名: 6-Trimethylsilyl-5-(trimethylsilylmethyl)hex-4-en-2-amine
• CAS: 185814-68-0
• 化学式: C₁₃H₃₁NSi₂
• 分子量: 257.567
• InChiKey: LJNWUIHKOPEYRL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.33
• 重原子数：
  16
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.85
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-Methyl-5-trimethylsilanyl-4-trimethylsilanylmethyl-pent-3-enylamine 在 三乙胺 、 三氯氧磷 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 28.0h， 生成 N-(1-Methyl-5-trimethylsilanyl-4-trimethylsilanylmethyl-pent-3-enyl)-2-oxo-butyrimidoyl chloride
  参考文献：
  名称：

  Stereocontrolled Synthesis of 5-Acyl-3,4-dihydro-2H-pyrroles and Related Heterocycles via Intramolecular 2-Propylidene-1,3-bis(silane)−Acylnitrilium Ion Cyclizations

  摘要：

  2-Propylidene-1,3-bis(silane)s have been shown to be highly effective terminators in heteroannulations initiated by C-acylnitrilium ions. These cyclizations proceed under exceedingly mild reaction conditions with good to excellent levels of substrate-derived stereocontrol to provide the corresponding Delta(1)-pyrrolines possessing a functionalizable allylsilane moiety. Sequential reduction/N-tosylation of these products leads to the stereoselective formation of cis-pyrrolidine derivatives.

  DOI：

  10.1021/jo961452q
• 作为产物：
  描述：

  2-(1-Methyl-5-trimethylsilanyl-4-trimethylsilanylmethyl-pent-3-enyl)-isoindole-1,3-dione 在 一水合肼 作用下， 以 乙醇 为溶剂， 以92%的产率得到1-Methyl-5-trimethylsilanyl-4-trimethylsilanylmethyl-pent-3-enylamine
  参考文献：
  名称：

  Stereocontrolled Synthesis of 5-Acyl-3,4-dihydro-2H-pyrroles and Related Heterocycles via Intramolecular 2-Propylidene-1,3-bis(silane)−Acylnitrilium Ion Cyclizations

  摘要：

  2-Propylidene-1,3-bis(silane)s have been shown to be highly effective terminators in heteroannulations initiated by C-acylnitrilium ions. These cyclizations proceed under exceedingly mild reaction conditions with good to excellent levels of substrate-derived stereocontrol to provide the corresponding Delta(1)-pyrrolines possessing a functionalizable allylsilane moiety. Sequential reduction/N-tosylation of these products leads to the stereoselective formation of cis-pyrrolidine derivatives.

  DOI：

  10.1021/jo961452q

文献信息

• Stereocontrolled Synthesis of 5-Acyl-3,4-dihydro-2<i>H</i>-pyrroles and Related Heterocycles via Intramolecular 2-Propylidene-1,3-bis(silane)−Acylnitrilium Ion Cyclizations
  作者：Timothy Kercher、Tom Livinghouse

  DOI：10.1021/jo961452q

  日期：1997.2.1

  2-Propylidene-1,3-bis(silane)s have been shown to be highly effective terminators in heteroannulations initiated by C-acylnitrilium ions. These cyclizations proceed under exceedingly mild reaction conditions with good to excellent levels of substrate-derived stereocontrol to provide the corresponding Delta(1)-pyrrolines possessing a functionalizable allylsilane moiety. Sequential reduction/N-tosylation of these products leads to the stereoselective formation of cis-pyrrolidine derivatives.