4,4-dimethyl-1-trimethylsilylhept-6-en-1-yn-3-ol | 155785-37-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4,4-dimethyl-1-trimethylsilylhept-6-en-1-yn-3-ol
• CAS: 155785-37-8
• 化学式: C₁₂H₂₂OSi
• 分子量: 210.392
• InChiKey: MSCFXBGURWIDLA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.83
• 重原子数：
  14.0
• 可旋转键数：
  3.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  20.23
• 氢给体数：
  1.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  4,4-dimethyl-1-trimethylsilylhept-6-en-1-yn-3-ol 在 氢氧化钾 作用下， 生成 (+/-)-4,4-Dimethyl-6-hepten-1-yn-3-ol
  参考文献：
  名称：

  Pd-Catalyzed Cycloisomerization to 1,2- Dialkylidenecycloalkanes. 1

  摘要：

  Enhancing synthetic efficiency requires the development of synthetic reactions that, to the extent possible, are simple additions wherein everything else is required only in catalytic amounts. The Alder ene reaction constitutes a classical reaction that meets this requirement that has much unrealized potential. A transition-metal-catalyzed version helps to increase that potential by permitting this reaction to proceed under mild conditions. A significant benefit of transition metal catalysis is the feasibility of diverting the reaction along pathways not feasible under thermal conditions. The synthesis of 1,3-dienes rather than 1,4-dienes is a very important diversion because of the utility of 1,3-dienes as reaction partners in the Diels-Alder reaction, another highly atom economical process. A catalyst derived from palladium acetate cycloisomerizes 1,6- and 1,7-enynes to dialkylidenecyclopentanes and -cyclohexanes. 1,3-Diene formation is favored over the Alder ene process by both steric and electronic effects. The reaction is highly chemoselective-tolerating a wide diversity of functionality including hydroxyl groups, ketones, esters, alkynyl and enol ethers, alkynyl and vinyl silanes, and enones. Many of the substrates are available by palladium-catalyzed alkylation reactions-highlighting the effectiveness of palladium catalyzed methodology in organic synthesis. The atom-economical nature of these reactions combined with the Diels-Alder reaction permit butadiene and dimethyl propargylmalonate to be molded into a polyhydro-as-indacene. The mechanism of this reaction may involve a tautomerization of an enyne-Pd(+2) complex to a pallada(+4)cyclopentene intermediate as a key step.

  DOI：

  10.1021/ja00089a015
• 作为产物：
  描述：

  2,2-二甲基-4-戊烯醛 、 magnesium,ethynyl(trimethyl)silane,bromide 生成 4,4-dimethyl-1-trimethylsilylhept-6-en-1-yn-3-ol
  参考文献：
  名称：

  A preparation of haloalkylidene cyclopentanones

  摘要：

  A radical-based 5-exo-dig cyclisation, initiated by addition of a trichloromethyl radical to an acyclic acetylenic ketone with an appropriately positioned double bond, has been employed to produce a variety of cyclic haloalkylidene cyclopentanones in moderate to excellent yields and with a high degree of stereoselectivity for the (E)-isomer. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4039(97)00503-0

文献信息

• Lemiere, Gilles; Gandon, Vincent; Cariou, Kevin, Journal of the American Chemical Society, 2009, vol. 131, p. 2993 - 3006
  作者：Lemiere, Gilles、Gandon, Vincent、Cariou, Kevin、Hours, Alexandra、Fukuyama, Takahide、et al.

  DOI：——

  日期：——
• Pearson Anthony J., Dubbert Robert A., Organometallics, 13 (1994) N 5, S 1656-1661
  作者：Pearson Anthony J., Dubbert Robert A.

  DOI：——

  日期：——