(1Z,3E)-5-oxo-1-phenylhexa-1,3-dien-1-yl dimethylcarbamate | 1573114-43-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (1Z,3E)-5-oxo-1-phenylhexa-1,3-dien-1-yl dimethylcarbamate
• 英文别名: [(1Z,3E)-5-oxo-1-phenylhexa-1,3-dienyl] N,N-dimethylcarbamate
• CAS: 1573114-43-8
• 化学式: C₁₅H₁₇NO₃
• 分子量: 259.305
• InChiKey: ZYBSUIGTXKQHRF-UWWXTLEHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  苯乙酮 在 silver hexafluoroantimonate 、 dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer 、 copper diacetate 、 sodium hydride 作用下， 以 甲醇 、 二甲基亚砜 、 mineral oil 为溶剂， 反应 16.5h， 生成 (1Z,3E)-5-oxo-1-phenylhexa-1,3-dien-1-yl dimethylcarbamate 、 (Z)-5-oxo-1-phenylhex-1-en-1-yl dimethylcarbamate
  参考文献：
  名称：

  Using Rh(III)-Catalyzed C–H Activation as a Tool for the Selective Functionalization of Ketone-Containing Molecules

  摘要：

  Due to the strong potential of C H activation in many areas of organic chemistry, the use of a pre-existing carbonyl group for the installation of a directing group to enable selective and predictable alpha-alkenylation with activated olefins as coupling partners is described. This Heck-type reaction would then lead either to beta,gamma-unsaturated ketones or to variously substituted 1,4-butadienes depending on the conditions used for the cleavage of the directing group.

  DOI：

  10.1021/ol500258q

文献信息

• Using Rh(III)-Catalyzed C–H Activation as a Tool for the Selective Functionalization of Ketone-Containing Molecules
  作者：Mélissa Boultadakis-Arapinis、Matthew N. Hopkinson、Frank Glorius

  DOI：10.1021/ol500258q

  日期：2014.3.21

  Due to the strong potential of C H activation in many areas of organic chemistry, the use of a pre-existing carbonyl group for the installation of a directing group to enable selective and predictable alpha-alkenylation with activated olefins as coupling partners is described. This Heck-type reaction would then lead either to beta,gamma-unsaturated ketones or to variously substituted 1,4-butadienes depending on the conditions used for the cleavage of the directing group.