(3aR,7R,9aR)-3a,6,7,9a-Tetrahydro-7-methylspirofuran-5(3H),2'-<1,3>dioxolan>-1(4H)-one | 132537-60-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (3aR,7R,9aR)-3a,6,7,9a-Tetrahydro-7-methylspirofuran-5(3H),2'-<1,3>dioxolan>-1(4H)-one
• 英文别名: (3aR,7R,9aR)-3a,6,7,9a-Tetrahydro-7-methylspiro(cycloocta[c]furan-5(3H),2'-[1,3]dioxolan)-1(4H)-one；(3'aR,4'Z,6'R,9'aR)-6'-methylspiro[1,3-dioxolane-2,8'-1,3a,6,7,9,9a-hexahydrocycloocta[c]furan]-3'-one
• CAS: 132537-60-1
• 化学式: C₁₃H₁₈O₄
• 分子量: 238.284
• InChiKey: JINMMNLUAWDYTD-MVCSARHOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  17
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  44.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (3aR,7R,9aR)-3a,6,7,9a-Tetrahydro-7-methylspirofuran-5(3H),2'-<1,3>dioxolan>-1(4H)-one 在 sodium periodate 、 diethylzinc 、 双(三甲基硅烷基)氨基钾 、 碳酸氢钠 作用下， 以 甲醇 、 水 为溶剂， 生成 (7R,7aS,8aS)-4,6,7,7a,8,8a-Hexahydro-7-methylspiro<1H-cyclopropa<3,4>cycloocta<1,2-c>furan-5(3H),2'-<1,3>dioxolan>-1-one
  参考文献：
  名称：

  Enantiospecific synthesis of the the tricyclxc nucleus of acetoxycrenulide by claisen ring exfansion

  摘要：

  DOI：

  10.1016/s0040-4039(00)97221-6
• 作为产物：
  描述：

  (R)-4-allyldihydrofuran-2(3H)-one 在 sodium periodate 、 碳酸氢钠 、 对甲苯磺酸 、 二乙胺 、 lithium diisopropyl amide 、 原甲酸三甲酯 作用下， 以 四氢呋喃 、 甲醇 、 正己烷 、 二氯甲烷 、 均三甲苯 为溶剂， 反应 21.0h， 生成 (3aR,7R,9aR)-3a,6,7,9a-Tetrahydro-7-methylspirofuran-5(3H),2'-<1,3>dioxolan>-1(4H)-one
  参考文献：
  名称：

  Suitability of the Claisen ring expansion protocol for crenulide diterpene construction

  摘要：

  An enantiospecific synthesis of optically pure 2 a molecule possessing the ring system characteristic of the crenulide diterpenes, is reported. The nine-step sequence began with the previously described R lactone 6. The early bond-forming reactions include an aldol condensation with crotonaldehyde and intramolecular selenonium ion-promoted cyclization with participation by the neighboring hydroxyl group. Selenoxide elimination made possible the acquisition of allyl vinyl ether 4. Thermal activation of the latter in hot mesitylene proceeded via a Claisen ring expansion pathway to give 36a. This key intermediate was then ketalized, subjected to Simmons-Smith cyclopropanation, and carried through a selenoxide elimination step to arrive ultimately at 2. Selected transformations of the medium-ring bicyclic lactones are described, accompanied by X-ray crystallographic studies to substantiate the stereochemical assignments advanced throughout the investigation.

  DOI：

  10.1021/jo00110a053

文献信息

• Enantiospecific synthesis of the the tricyclxc nucleus of acetoxycrenulide by claisen ring exfansion
  作者：Jesus Ezquerra、Wei He、Leo A. Paquette

  DOI：10.1016/s0040-4039(00)97221-6

  日期：1990.1
• Suitability of the Claisen ring expansion protocol for crenulide diterpene construction
  作者：Leo A. Paquette、Jesus Ezquerra、Wei He

  DOI：10.1021/jo00110a053

  日期：1995.3

  An enantiospecific synthesis of optically pure 2 a molecule possessing the ring system characteristic of the crenulide diterpenes, is reported. The nine-step sequence began with the previously described R lactone 6. The early bond-forming reactions include an aldol condensation with crotonaldehyde and intramolecular selenonium ion-promoted cyclization with participation by the neighboring hydroxyl group. Selenoxide elimination made possible the acquisition of allyl vinyl ether 4. Thermal activation of the latter in hot mesitylene proceeded via a Claisen ring expansion pathway to give 36a. This key intermediate was then ketalized, subjected to Simmons-Smith cyclopropanation, and carried through a selenoxide elimination step to arrive ultimately at 2. Selected transformations of the medium-ring bicyclic lactones are described, accompanied by X-ray crystallographic studies to substantiate the stereochemical assignments advanced throughout the investigation.