Pentanal, 4-oxo-5-(phenylthio)- | 142841-43-8

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: Pentanal, 4-oxo-5-(phenylthio)-
• 英文别名: 4-oxo-5-phenylsulfanylpentanal
• CAS: 142841-43-8
• 化学式: C₁₁H₁₂O₂S
• 分子量: 208.281
• InChiKey: ZDTAHUJMNHOIOW-UHFFFAOYSA-N

物化性质

• 沸点：
  338.9±27.0 °C(Predicted)
• 密度：
  1.15±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  59.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Pentanal, 4-oxo-5-(phenylthio)- 在 六甲基磷酰三胺 、 samarium diiodide 、 三氟甲磺酸三甲基硅酯 、 对甲苯磺酸 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 二氯甲烷 、 苯 为溶剂， 反应 245.33h， 生成 (1R*,2R*)-1-hydroxy-2-(methoxycarbonyl)-2-methyl-5-methylenecycloheptan-3-one, ethylene acetal
  参考文献：
  名称：

  [3 + 4] and [3 + 5] Annulation Reactions of .alpha.-(Phenylthio)Dicarbonyl Electrophiles with Bis(trimethylsilyl) Enol Ethers: Synthesis of Highly Functionalized Medium Ring Carbocycles

  摘要：

  The [3 + 4] and [3 + 5] annulations of bis(trimethylsilyl) enol ethers with 1,4- and 1,5-dicarbonyl electrophiles bearing alpha-phenylthio substituents leads to the formation of bicyclic [3.2.1] and [3.3.1] ethers with good regiochemical and stereochemical control, Subsequent oxidation of the phenylthio moiety followed by reduction with SmI2 constitutes a high-yielding and regioselective process for cleavage of the bridging ether linkage. The overall strategy provides a synthetic pathway for the synthesis of highly functionalized medium ring carbocycles.

  DOI：

  10.1021/jo00131a013
• 作为产物：
  描述：

  9-((R)-5-Phenylsulfanylmethyl-2,3-dihydro-furan-2-yl)-9H-purin-6-ylamine 在 水 作用下， 以 甲醇 为溶剂， 生成 Pentanal, 4-oxo-5-(phenylthio)-
  参考文献：
  名称：

  Nucleotide C4′ radical fragmentation is base-dependent

  摘要：

  Nucleotide C4' radicals undergo radical ionic fragmentation with expulsion of the 3'-phosphate giving a 3',4'-radical cation. With a series of mononucleotides it is shown that the rate of this fragmentation is a function of the base (T similar to G > ABz > A similar to C) with the least basic, less-hydrogen bonded nucleotides fragmenting more rapidly in aqueous methanol. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4039(97)10249-0

文献信息

• Synthesis of Cyclic Bis(trimethysilyl) Enol Ethers and Their [3 + 4] and [3 + 5] Annulation Reactions with Dicarbonyl Electrophiles. Access to Highly Functionalized Tricyclic Ethers Possessing Trans Intrabridgehead Stereochemistry
  作者：Gary A. Molander、Bernard Bessières、Paul R. Eastwood、Bruce C. Noll

  DOI：10.1021/jo9902547

  日期：1999.5.1

  The synthesis of cyclic bis(trimethylsilyl) enol ethers from cycloalkanone carboxylates is described. The [3 + 4] and [3 + 5] annulation reactions of these bis(dinucleophilic), synthons with various 1,4- and 1,5-dicarbonyl electrophiles leads to the formation of tricyclic keto ethers with good regio- and stereochemical control. An interesting trans intrabridgehead stereochemistry is observed when using bis(trimethylsilyl) enol ethers derived from nine- to 12-membered ring beta-keto esters.
• [3 + 4] and [3 + 5] Annulation Reactions of .alpha.-(Phenylthio)Dicarbonyl Electrophiles with Bis(trimethylsilyl) Enol Ethers: Synthesis of Highly Functionalized Medium Ring Carbocycles
  作者：Gary A. Molander、Paul R. Eastwood

  DOI：10.1021/jo00131a013

  日期：1995.12

  The [3 + 4] and [3 + 5] annulations of bis(trimethylsilyl) enol ethers with 1,4- and 1,5-dicarbonyl electrophiles bearing alpha-phenylthio substituents leads to the formation of bicyclic [3.2.1] and [3.3.1] ethers with good regiochemical and stereochemical control, Subsequent oxidation of the phenylthio moiety followed by reduction with SmI2 constitutes a high-yielding and regioselective process for cleavage of the bridging ether linkage. The overall strategy provides a synthetic pathway for the synthesis of highly functionalized medium ring carbocycles.
• Nucleotide C4′ radical fragmentation is base-dependent
  作者：David Crich、Xue-Sheng Mo

  DOI：10.1016/s0040-4039(97)10249-0

  日期：1997.11

  Nucleotide C4' radicals undergo radical ionic fragmentation with expulsion of the 3'-phosphate giving a 3',4'-radical cation. With a series of mononucleotides it is shown that the rate of this fragmentation is a function of the base (T similar to G > ABz > A similar to C) with the least basic, less-hydrogen bonded nucleotides fragmenting more rapidly in aqueous methanol. (C) 1997 Elsevier Science Ltd.