1-{(1S,2S)-2-[2-(tert-Butyl-dimethyl-silanyloxy)-5-(1,2-dihydroxy-1-methyl-ethyl)-cyclopentylmethyl]-2-methyl-cyclopentyl}-3-methyl-butane-2,3-diol | 141461-45-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 1-{(1S,2S)-2-[2-(tert-Butyl-dimethyl-silanyloxy)-5-(1,2-dihydroxy-1-methyl-ethyl)-cyclopentylmethyl]-2-methyl-cyclopentyl}-3-methyl-butane-2,3-diol
• CAS: 141461-45-2
• 化学式: C₂₆H₅₂O₅Si
• 分子量: 472.781
• InChiKey: PLRHHNWNDFWNGD-PAYYFGPKSA-N

物化性质

• 沸点：
  558.4±25.0 °C(Predicted)
• 密度：
  1.04±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.86
• 重原子数：
  32.0
• 可旋转键数：
  9.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  90.15
• 氢给体数：
  4.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  1-{(1S,2S)-2-[2-(tert-Butyl-dimethyl-silanyloxy)-5-(1,2-dihydroxy-1-methyl-ethyl)-cyclopentylmethyl]-2-methyl-cyclopentyl}-3-methyl-butane-2,3-diol 在 sodium periodate 、 TiCl₃-1,2-dimethoxyethane 、 四丁基氟化铵 、 铜 、 锌 作用下， 以 四氢呋喃 、 乙二醇二甲醚 、 水 、 丙酮 为溶剂， 反应 98.0h， 生成 (Z)-(1S,3aR,6aS,9aS,10aS)-4,9a-Dimethyl-1,2,3,3a,6,6a,7,8,9,9a,10,10a-dodecahydro-dicyclopenta[a,d]cycloocten-1-ol
  参考文献：
  名称：

  A short enantiospecific synthesis of the ceroplastin nucleus.

  摘要：

  The tricyclic nucleus 9b of ceroplastol I and ceroplasteric acid has been synthesized stereoselectively and enantiospecifically in only 10 steps from 1-cyclopentenecarboxaldehyde. Addition of (3-methyl-3-butenyl)magnesium bromide to imine 13b and methylation with methyl iodide by Koga's procedure gave 94% of optically pure aldehyde 40 as previously described in our reiswigin A synthesis. Isomerization of the double bond of aldehyde 40 with HI afforded aldehyde 17b. Coupling of the enolate prepared from silyl enol ether 45 with aldehyde 17b gave a 1:1 mixture of 46a and 46b, which contain the complete carbon skeleton of 9b, in only three steps. Dehydration provided enones 47a and 47b. Reduction of 47a and 47b with Li/NH3 afforded saturated ketones 48at and 48bt that were reduced with LiAlH4 to the saturated alcohols 49att and 49btt. Protection of the alcohols as the TBDMS ethers and oxidative cleavage of the dienes afforded readily separable keto aldehydes 51 and 56. McMurry coupling of 51, cleavage of the silyl ether, and oxidation of the alcohol with PCC completed the synthesis of 9b.

  DOI：

  10.1021/jo00039a021
• 作为产物：
  描述：

  tert-Butyl-{3-isopropenyl-2-[(1S,2S)-1-methyl-2-(3-methyl-but-2-enyl)-cyclopentylmethyl]-cyclopentyloxy}-dimethyl-silane 在 四氧化锇 、 N-甲基吗啉氧化物 作用下， 以 水 、 丙酮 、 叔丁醇 为溶剂， 反应 24.0h， 以138 mg的产率得到1-{(1S,2S)-2-[2-(tert-Butyl-dimethyl-silanyloxy)-5-(1,2-dihydroxy-1-methyl-ethyl)-cyclopentylmethyl]-2-methyl-cyclopentyl}-3-methyl-butane-2,3-diol
  参考文献：
  名称：

  A short enantiospecific synthesis of the ceroplastin nucleus.

  摘要：

  The tricyclic nucleus 9b of ceroplastol I and ceroplasteric acid has been synthesized stereoselectively and enantiospecifically in only 10 steps from 1-cyclopentenecarboxaldehyde. Addition of (3-methyl-3-butenyl)magnesium bromide to imine 13b and methylation with methyl iodide by Koga's procedure gave 94% of optically pure aldehyde 40 as previously described in our reiswigin A synthesis. Isomerization of the double bond of aldehyde 40 with HI afforded aldehyde 17b. Coupling of the enolate prepared from silyl enol ether 45 with aldehyde 17b gave a 1:1 mixture of 46a and 46b, which contain the complete carbon skeleton of 9b, in only three steps. Dehydration provided enones 47a and 47b. Reduction of 47a and 47b with Li/NH3 afforded saturated ketones 48at and 48bt that were reduced with LiAlH4 to the saturated alcohols 49att and 49btt. Protection of the alcohols as the TBDMS ethers and oxidative cleavage of the dienes afforded readily separable keto aldehydes 51 and 56. McMurry coupling of 51, cleavage of the silyl ether, and oxidation of the alcohol with PCC completed the synthesis of 9b.

  DOI：

  10.1021/jo00039a021