2-<(S)-1-<(tert-Butyldimethylsilyl)oxy>-2-propyl>-3-(triisopropylsiloxy)-5,9,9-trimethyl-6,7,8,9-tetrahydroanthran-1-ol | 157731-73-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 蒽
• 英文名称: 2-<(S)-1-<(tert-Butyldimethylsilyl)oxy>-2-propyl>-3-(triisopropylsiloxy)-5,9,9-trimethyl-6,7,8,9-tetrahydroanthran-1-ol
• 英文别名: 2-[(2R)-1-[tert-butyl(dimethyl)silyl]oxypropan-2-yl]-8,8,10-trimethyl-3-tri(propan-2-yl)silyloxy-6,7-dihydro-5H-anthracen-1-ol
• CAS: 157731-73-2
• 化学式: C₃₅H₆₀O₃Si₂
• 分子量: 585.031
• InChiKey: JLJGANPUMZQOJV-VWLOTQADSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.15
• 重原子数：
  40
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-<(S)-1-<(tert-Butyldimethylsilyl)oxy>-2-propyl>-3-(triisopropylsiloxy)-5,9,9-trimethyl-6,7,8,9-tetrahydroanthran-1-ol 在 四丁基氟化铵 、 氧气 作用下， 以 四氢呋喃 为溶剂， 反应 14.0h， 以87%的产率得到1,4-Anthracenedione,5,6,7,8-tetrahydro-2-hydroxy-3-[(1R)-2-hydroxy-1-methylethyl]-5,5,9-trimethyl-
  参考文献：
  名称：

  Total Synthesis of Aegyptinones A and B

  摘要：

  This paper describes the first total syntheses of the diterpene quinones aegyptinones A and B via an extremely direct route which should easily accommodate the production of gram quantities of each compound. The key step in the synthetic strategy involves the application of a recently developed ''second-generation'' photochemical aromatic annulation method for the construction of highly substituted aromatic systems. The synthesis of one of the annulation components, the diazo ketone 5, was achieved using a Diels-Alder-based benzannulation strategy employing cyanoallene and the dienamine 13. Cyanoallene proved to be uniquely effective for this cycloaddition, which either failed or proceeded in poor yield using several substituted acetylenes as dienophiles. The pivotal aromatic annulation reaction was accomplished by irradiating a solution of the diazo ketone 5 and the readily available siloxyalkyne 4 in a Pyrex vessel with a 450-W medium-pressure Hanovia lamp at room temperature for 17-20 h. The desired tricyclic phenol 3 was produced in 58-70% yield and was then converted to aegyptinone B (2) by treatment with tetra-n-butylammonium fluoride in the presence of oxygen. Finally, cyclization to generate aegyptinone A was accomplished in high yield by brief exposure of 2 to an ethanolic solution of concentrated sulfuric acid at room temperature. Overall, this strategy provides efficient routes (six and seven steps, respectively) to aegyptinones A and B which should facilitate the systematic investigation of the pharmacological activity of these novel diterpenes.

  DOI：

  10.1021/jo00096a027
• 作为产物：
  描述：

  (E)-<2-<(6',6'-Dimethylcyclohex-1'-enyl)>ethenyl>pyrrolidine 在 silica gel 作用下， 以 乙醚 、 苯 为溶剂， 反应 110.0h， 生成 2-<(S)-1-<(tert-Butyldimethylsilyl)oxy>-2-propyl>-3-(triisopropylsiloxy)-5,9,9-trimethyl-6,7,8,9-tetrahydroanthran-1-ol
  参考文献：
  名称：

  Total Synthesis of Aegyptinones A and B

  摘要：

  This paper describes the first total syntheses of the diterpene quinones aegyptinones A and B via an extremely direct route which should easily accommodate the production of gram quantities of each compound. The key step in the synthetic strategy involves the application of a recently developed ''second-generation'' photochemical aromatic annulation method for the construction of highly substituted aromatic systems. The synthesis of one of the annulation components, the diazo ketone 5, was achieved using a Diels-Alder-based benzannulation strategy employing cyanoallene and the dienamine 13. Cyanoallene proved to be uniquely effective for this cycloaddition, which either failed or proceeded in poor yield using several substituted acetylenes as dienophiles. The pivotal aromatic annulation reaction was accomplished by irradiating a solution of the diazo ketone 5 and the readily available siloxyalkyne 4 in a Pyrex vessel with a 450-W medium-pressure Hanovia lamp at room temperature for 17-20 h. The desired tricyclic phenol 3 was produced in 58-70% yield and was then converted to aegyptinone B (2) by treatment with tetra-n-butylammonium fluoride in the presence of oxygen. Finally, cyclization to generate aegyptinone A was accomplished in high yield by brief exposure of 2 to an ethanolic solution of concentrated sulfuric acid at room temperature. Overall, this strategy provides efficient routes (six and seven steps, respectively) to aegyptinones A and B which should facilitate the systematic investigation of the pharmacological activity of these novel diterpenes.

  DOI：

  10.1021/jo00096a027