(1R,2R,6R,7R,8R,9R)-9-Allyl-6-isopropyl-3,9-dimethyl-12-oxa-tricyclo[6.3.1.0^2,7]dodec-3-en-10-one | 876748-92-4

• 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: (1R,2R,6R,7R,8R,9R)-9-Allyl-6-isopropyl-3,9-dimethyl-12-oxa-tricyclo[6.3.1.0^2,7]dodec-3-en-10-one
• 英文别名: (1R,2R,6R,7R,8R,9R)-3,9-dimethyl-6-propan-2-yl-9-prop-2-enyl-12-oxatricyclo[6.3.1.02,7]dodec-3-en-10-one
• CAS: 876748-92-4
• 化学式: C₁₉H₂₈O₂
• 分子量: 288.43
• InChiKey: IICXNDRMIBPMKP-JMCDZUJHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (1R,2R,6R,7R,8R,9R)-9-Allyl-6-isopropyl-3,9-dimethyl-12-oxa-tricyclo[6.3.1.0^2,7]dodec-3-en-10-one 在 bis(cyclohexanyl)borane 、 sodium perborate 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 5.0h， 以94%的产率得到(1R,2R,6R,7R,8R,9R)-9-(3-Hydroxy-propyl)-6-isopropyl-3,9-dimethyl-12-oxa-tricyclo[6.3.1.0^2,7]dodec-3-en-10-one
  参考文献：
  名称：

  A General Route toward the Synthesis of the Cladiellin Skeleton Utilizing a SmI₂-Mediated Cyclization

  摘要：

  [graphics]An efficient synthesis of the cladiellin skeleton is reported utilizing methods that were previously developed in this laboratory. The approach is based on a SmI2-mediated cyclization reaction for the construction of the oxacyclononane unit. A [4 + 3] annulation strategy was used to create the octahydroisobenzofuran moiety. This route provides the cladiellin skeleton in only 14 steps without the use of protecting groups. The present approach also enabled the synthesis of the 3,7-diastereomer of the natural product polyanthellin A.

  DOI：

  10.1021/jo052290d
• 作为产物：
  描述：

  (1R,2R,6R,7R,8R,9S)-6-Isopropyl-3,9-dimethyl-12-oxa-tricyclo[6.3.1.0^2,7]dodec-3-en-10-one 在 silver trifluoroacetate 、 potassium hydride 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 3.0h， 生成 (1R,2R,6R,7R,8R,9R)-9-Allyl-6-isopropyl-3,9-dimethyl-12-oxa-tricyclo[6.3.1.0^2,7]dodec-3-en-10-one
  参考文献：
  名称：

  A General Route toward the Synthesis of the Cladiellin Skeleton Utilizing a SmI₂-Mediated Cyclization

  摘要：

  [graphics]An efficient synthesis of the cladiellin skeleton is reported utilizing methods that were previously developed in this laboratory. The approach is based on a SmI2-mediated cyclization reaction for the construction of the oxacyclononane unit. A [4 + 3] annulation strategy was used to create the octahydroisobenzofuran moiety. This route provides the cladiellin skeleton in only 14 steps without the use of protecting groups. The present approach also enabled the synthesis of the 3,7-diastereomer of the natural product polyanthellin A.

  DOI：

  10.1021/jo052290d

文献信息

• A General Route toward the Synthesis of the Cladiellin Skeleton Utilizing a SmI₂-Mediated Cyclization
  作者：Gary A. Molander、Barbara Czakó、David J. St. Jean

  DOI：10.1021/jo052290d

  日期：2006.2.1

  [graphics]An efficient synthesis of the cladiellin skeleton is reported utilizing methods that were previously developed in this laboratory. The approach is based on a SmI2-mediated cyclization reaction for the construction of the oxacyclononane unit. A [4 + 3] annulation strategy was used to create the octahydroisobenzofuran moiety. This route provides the cladiellin skeleton in only 14 steps without the use of protecting groups. The present approach also enabled the synthesis of the 3,7-diastereomer of the natural product polyanthellin A.