2-二甲氧基甲基-5-(2-甲氧羰基乙基)呋喃 | 102865-14-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 中文名称: 2-二甲氧基甲基-5-(2-甲氧羰基乙基)呋喃
• 英文名称: 2-dimethoxymethyl-5-(2-methoxycarbonylethyl)furan
• 英文别名: Methyl 3-[5-(dimethoxymethyl)furan-2-yl]propanoate
• CAS: 102865-14-5
• 化学式: C₁₁H₁₆O₅
• 分子量: 228.245
• InChiKey: SCMIQNNYMJNCRP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  16
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  57.9
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-二甲氧基甲基-5-(2-甲氧羰基乙基)呋喃 在 disodium hydrogenphosphate 、 水合氯醛 、 溴 、 sodium carbonate 、 三乙胺 、 柠檬酸 作用下， 以 1,4-二氧六环 、 乙酸乙酯 为溶剂， 生成 (+/-)-3-dimethoxymethyl-4-hydroxy-2-methoxycarbonylmethylcyclopent-2-en-1-one
  参考文献：
  名称：

  Enzymatic kinetic resolution of a functionalized 4-hydroxy-cyclopentenone: synthesis of the key intermediates in the total synthesis of isoprostanes

  摘要：

  The enzymatic kinetic resolution of racemic alcohol 4-hydroxy-cyclopentenone 1 was investigated using four different lipases for enantioselective transacetylation, as well as for enantioselective hydrolysis, leading to the pure (R)- and (S)-enantiomers 2 and 3. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.03.028
• 作为产物：
  描述：

  methyl 3-(2-furyl)propionate 在 对甲苯磺酸 、 APTS 、 三氯氧磷 作用下， 生成 2-二甲氧基甲基-5-(2-甲氧羰基乙基)呋喃
  参考文献：
  名称：

  Enzymatic kinetic resolution of a functionalized 4-hydroxy-cyclopentenone: synthesis of the key intermediates in the total synthesis of isoprostanes

  摘要：

  The enzymatic kinetic resolution of racemic alcohol 4-hydroxy-cyclopentenone 1 was investigated using four different lipases for enantioselective transacetylation, as well as for enantioselective hydrolysis, leading to the pure (R)- and (S)-enantiomers 2 and 3. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.03.028

文献信息

• Total Synthesis of the Four Enantiomerically Pure Diasteroisomers of the Phytoprostanes E₁Type II and of the 15-E_2t-Isoprostanes
  作者：Edith Pinot、Alexandre Guy、Anais Fournial、Laurence Balas、Jean-Claude Rossi、Thierry Durand

  DOI：10.1021/jo702455g

  日期：2008.4.1

  Syntheses of the four enantiomerically pure diastereoisomers of the phytoprostanes E1 type II and 15-E2t-isoprostanes (1−4) are described. The key steps included the preparation of the Freïmanis (±)-hydroxycyclopentenone 5, enzymatic resolution of this racemic hydroxycyclopentenone, Wittig and Horner−Wadsworth−Emmons (HWE) coupling reactions and finally enantioselective reductions.

  所述phytoprostanes的四个对映体纯非对映体的合成ë 1 II型和15-E 2吨-isoprostanes（1 - 4）中有所描述。关键步骤包括弗雷曼尼斯（±）-羟基环戊烯酮5的制备，该外消旋羟基环戊烯酮的酶促拆分，Wittig和Horner-Wadsworth-Emmons（HWE）偶联反应，最后是对映选择性还原。
• LOZHA, EH. V.;LOLYA, D. O.;FREJMANIS, YA. F.;TUROVSKIJ, I. V.;GAVARS, M. +, IZV. AN LATVSSR. CEP. XIM., 1985, N 4, 465-472
  作者：LOZHA, EH. V.、LOLYA, D. O.、FREJMANIS, YA. F.、TUROVSKIJ, I. V.、GAVARS, M. +

  DOI：——

  日期：——
• Enzymatic kinetic resolution of a functionalized 4-hydroxy-cyclopentenone: synthesis of the key intermediates in the total synthesis of isoprostanes
  作者：Edith Pinot、Alexandre Guy、Ann-Laure Guyon、Jean-Claude Rossi、Thierry Durand

  DOI：10.1016/j.tetasy.2005.03.028

  日期：2005.6

  The enzymatic kinetic resolution of racemic alcohol 4-hydroxy-cyclopentenone 1 was investigated using four different lipases for enantioselective transacetylation, as well as for enantioselective hydrolysis, leading to the pure (R)- and (S)-enantiomers 2 and 3. (c) 2005 Elsevier Ltd. All rights reserved.