(S,3E,5Z)-6-bromo-1-{(1R,2R)-2-[(4-methoxybenzyloxy)methyl]cyclopentyl}-7-(triisopropylsilyloxy)hepta-3,5-dien-1-ol | 935872-18-7

• 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: (S,3E,5Z)-6-bromo-1-{(1R,2R)-2-[(4-methoxybenzyloxy)methyl]cyclopentyl}-7-(triisopropylsilyloxy)hepta-3,5-dien-1-ol
• 英文别名: (1S,3E,5Z)-6-bromo-1-[(1R,2R)-2-[(4-methoxyphenyl)methoxymethyl]cyclopentyl]-7-tri(propan-2-yl)silyloxyhepta-3,5-dien-1-ol
• CAS: 935872-18-7
• 化学式: C₃₀H₄₉BrO₄Si
• 分子量: 581.706
• InChiKey: IIBPGUPUQCDUHN-QILYRGQLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.41
• 重原子数：
  36
• 可旋转键数：
  15
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  47.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (S,3E,5Z)-6-bromo-1-{(1R,2R)-2-[(4-methoxybenzyloxy)methyl]cyclopentyl}-7-(triisopropylsilyloxy)hepta-3,5-dien-1-ol 、 在 4-二甲氨基吡啶 、 三乙胺 作用下， 以 苯 为溶剂， 反应 2.0h， 生成
  参考文献：
  名称：

  Total Synthesis of Borrelidin

  摘要：

  The total synthesis of borrelidin has been achieved. The best feature of our synthetic route is macrocyclization at C11-C12 for the construction of an 18-membered ring after esterification between two segments. A detailed examination of the macrocyclization led us to the samarium(II) iodide-mediated intramolecular Reformatsky-type reaction as the most efficient synthetic approach. The two key segments were synthesized through regioselective methylation, directed hydrogenation, stereoselective Reformatsky-type reaction, and MgBr2 center dot Et2O-mediated chelation-controlled allylation.

  DOI：

  10.1021/jo062089i
• 作为产物：
  描述：

  ((1R,2R)-cyclopentane-1,2-diyl)dimethanol 在 吡啶 、 2,6-二甲基吡啶 、 sodium periodate 、 四氧化锇 、 N-甲基吲哚酮 、 水 、 sodium hydride 、 二异丁基氢化铝 、 戴斯-马丁氧化剂 、 氟化氢吡啶 、 magnesium bromide 作用下， 以 四氢呋喃 、 甲醇 、 正己烷 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 丙酮 、 苯 为溶剂， 反应 93.0h， 生成 (S,3E,5Z)-6-bromo-1-{(1R,2R)-2-[(4-methoxybenzyloxy)methyl]cyclopentyl}-7-(triisopropylsilyloxy)hepta-3,5-dien-1-ol
  参考文献：
  名称：

  Total Synthesis of Borrelidin

  摘要：

  The total synthesis of borrelidin has been achieved. The best feature of our synthetic route is macrocyclization at C11-C12 for the construction of an 18-membered ring after esterification between two segments. A detailed examination of the macrocyclization led us to the samarium(II) iodide-mediated intramolecular Reformatsky-type reaction as the most efficient synthetic approach. The two key segments were synthesized through regioselective methylation, directed hydrogenation, stereoselective Reformatsky-type reaction, and MgBr2 center dot Et2O-mediated chelation-controlled allylation.

  DOI：

  10.1021/jo062089i

文献信息

• Total Synthesis of Borrelidin
  作者：Tohru Nagamitsu、Daisuke Takano、Kaori Marumoto、Takeo Fukuda、Kentaro Furuya、Kazuhiko Otoguro、Kazuyoshi Takeda、Isao Kuwajima、Yoshihiro Harigaya、Satoshi Ōmura

  DOI：10.1021/jo062089i

  日期：2007.4.1

  The total synthesis of borrelidin has been achieved. The best feature of our synthetic route is macrocyclization at C11-C12 for the construction of an 18-membered ring after esterification between two segments. A detailed examination of the macrocyclization led us to the samarium(II) iodide-mediated intramolecular Reformatsky-type reaction as the most efficient synthetic approach. The two key segments were synthesized through regioselective methylation, directed hydrogenation, stereoselective Reformatsky-type reaction, and MgBr2 center dot Et2O-mediated chelation-controlled allylation.