(R)-1-(4-hydroxy-2,6-dimethoxy-3,5-dimethylphenyl)-2-methylbutan-1-one | 1080023-65-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (R)-1-(4-hydroxy-2,6-dimethoxy-3,5-dimethylphenyl)-2-methylbutan-1-one
• 英文别名: (2R)-1-(4-hydroxy-2,6-dimethoxy-3,5-dimethylphenyl)-2-methylbutan-1-one
• CAS: 1080023-65-9
• 化学式: C₁₅H₂₂O₄
• 分子量: 266.337
• InChiKey: QGDUOWXVJKWKPN-MRVPVSSYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (R)-1-(4-hydroxy-2,6-dimethoxy-3,5-dimethylphenyl)-2-methylbutan-1-one 在 2-碘酰基苯甲酸 作用下， 以 四氢呋喃 为溶剂， 反应 15.0h， 生成 (6S)-4-((2R)-2-methylbutanoyl)-6-hydroxy-3,5-dimethoxy-2,6-dimethylcyclohexa-2,4-dienone 、 (6R)-4-((2R)-2-methylbutanoyl)-6-hydroxy-3,5-dimethoxy-2,6-dimethylcyclohexa-2,4-dienone
  参考文献：
  名称：

  Total Synthesis of Wasabidienones B₁ and B₀ via SIBX-Mediated Hydroxylative Phenol Dearomatization

  摘要：

  The first total synthesis of the natural nondimerizing o-quinol (+)-wasabidienone B-1 was achieved from commercially available 1,3,5-trimethoxybenzene. The key dearomatizing transformation was efficiently accomplished via a hydroxylative phenol dearomatization reaction using the stabilized lambda(5)-iodane reagent IBX (SIBX). (+)-Wasabidienone B-1 was then converted into its congener (-)-wasabidienone B-0 via an improved thermally induced ring-contracting isomerization reaction.

  DOI：

  10.1021/ol802183p
• 作为产物：
  描述：

  1-(4-hydroxy-2,6-dimethoxy-3,5-dimethylphenyl)-2-methylbutan-1-one 以87 mg的产率得到(R)-1-(4-hydroxy-2,6-dimethoxy-3,5-dimethylphenyl)-2-methylbutan-1-one
  参考文献：
  名称：

  Total Synthesis of Wasabidienones B₁ and B₀ via SIBX-Mediated Hydroxylative Phenol Dearomatization

  摘要：

  The first total synthesis of the natural nondimerizing o-quinol (+)-wasabidienone B-1 was achieved from commercially available 1,3,5-trimethoxybenzene. The key dearomatizing transformation was efficiently accomplished via a hydroxylative phenol dearomatization reaction using the stabilized lambda(5)-iodane reagent IBX (SIBX). (+)-Wasabidienone B-1 was then converted into its congener (-)-wasabidienone B-0 via an improved thermally induced ring-contracting isomerization reaction.

  DOI：

  10.1021/ol802183p

文献信息

• Total Synthesis of Wasabidienones B₁ and B₀ via SIBX-Mediated Hydroxylative Phenol Dearomatization
  作者：Laurent Pouységu、Mélanie Marguerit、Julien Gagnepain、Gildas Lyvinec、Andrew J. Eatherton、Stéphane Quideau

  DOI：10.1021/ol802183p

  日期：2008.11.20

  The first total synthesis of the natural nondimerizing o-quinol (+)-wasabidienone B-1 was achieved from commercially available 1,3,5-trimethoxybenzene. The key dearomatizing transformation was efficiently accomplished via a hydroxylative phenol dearomatization reaction using the stabilized lambda(5)-iodane reagent IBX (SIBX). (+)-Wasabidienone B-1 was then converted into its congener (-)-wasabidienone B-0 via an improved thermally induced ring-contracting isomerization reaction.