6-(1-ethoxy-vinyl)-2-non-1-enyl-3,4-dihydro-2H-pyran-4-ol

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-(1-ethoxy-vinyl)-2-non-1-enyl-3,4-dihydro-2H-pyran-4-ol
• 英文别名: (2S,4S)-6-(1-ethoxyethenyl)-2-[(E)-non-1-enyl]-3,4-dihydro-2H-pyran-4-ol
• 化学式: C₁₈H₃₀O₃
• 分子量: 294.434
• InChiKey: AKBAXXKQWXWYAN-PUENXVRKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  21
• 可旋转键数：
  10
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 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：

  6-(1-ethoxy-vinyl)-2-non-1-enyl-3,4-dihydro-2H-pyran-4-ol 在 三乙胺 、 magnesium bromide 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 48.0h， 生成 8-ethoxy-9-heptyl-13-hydroxy-tricyclo[6.5.1.0^2,6]tetradec-10-ene-3,14-dione
  参考文献：
  名称：

  Rapid Assembly of the Bicyclo[5.3.1]undecenone Core of Penostatin F:  A Successive Diels−Alder/Claisen Reaction Strategy with an Efficient Stereochemical Relay

  摘要：

  The first synthesis of the tricyclic core of Penostatin F (1) using a stereocontrolled Diels-Alder reaction and a Claisen rearrangement in succession has been achieved in nine steps from commercially available methyl acetoacetate and (E)-2-decenal. Penostatin F is a metabolite isolated from a fungal strain of Penicillium sp., OUPS-79, separated from the marine alga Enteromorphia intestinalis and exhibits significant cytotoxicity against cultured P388 Leukemia cells (ED50 = 1.4 mumol/mL).

  DOI：

  10.1021/ol049680r
• 作为产物：
  描述：

  反式-2-癸烯醛 在 4-二甲氨基吡啶 、 tetramethylammonium borohydride 、 sodium hydride 、 溶剂黄146 、 三乙胺 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 96.66h， 生成 6-(1-ethoxy-vinyl)-2-non-1-enyl-3,4-dihydro-2H-pyran-4-ol
  参考文献：
  名称：

  Rapid Assembly of the Bicyclo[5.3.1]undecenone Core of Penostatin F:  A Successive Diels−Alder/Claisen Reaction Strategy with an Efficient Stereochemical Relay

  摘要：

  The first synthesis of the tricyclic core of Penostatin F (1) using a stereocontrolled Diels-Alder reaction and a Claisen rearrangement in succession has been achieved in nine steps from commercially available methyl acetoacetate and (E)-2-decenal. Penostatin F is a metabolite isolated from a fungal strain of Penicillium sp., OUPS-79, separated from the marine alga Enteromorphia intestinalis and exhibits significant cytotoxicity against cultured P388 Leukemia cells (ED50 = 1.4 mumol/mL).

  DOI：

  10.1021/ol049680r

文献信息

• Rapid Assembly of the Bicyclo[5.3.1]undecenone Core of Penostatin F:  A Successive Diels−Alder/Claisen Reaction Strategy with an Efficient Stereochemical Relay
  作者：Louis Barriault、Patrick J. A. Ang、Roch M. A. Lavigne

  DOI：10.1021/ol049680r

  日期：2004.4.1

  The first synthesis of the tricyclic core of Penostatin F (1) using a stereocontrolled Diels-Alder reaction and a Claisen rearrangement in succession has been achieved in nine steps from commercially available methyl acetoacetate and (E)-2-decenal. Penostatin F is a metabolite isolated from a fungal strain of Penicillium sp., OUPS-79, separated from the marine alga Enteromorphia intestinalis and exhibits significant cytotoxicity against cultured P388 Leukemia cells (ED50 = 1.4 mumol/mL).