(3S,4aS,8aR)-3-isopropyl-4a,8,8a-trimethyl-4a,5-dihydrobenzo[e][1,2,4]trioxin-6(8aH)-one | 1393526-77-6

• 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: (3S,4aS,8aR)-3-isopropyl-4a,8,8a-trimethyl-4a,5-dihydrobenzo[e][1,2,4]trioxin-6(8aH)-one
• CAS: 1393526-77-6
• 化学式: C₁₃H₂₀O₄
• 分子量: 240.299
• InChiKey: GXBQQPVPYYZELZ-RWMBFGLXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.38
• 重原子数：
  17.0
• 可旋转键数：
  1.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  44.76
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  4-hydroperoxy-3,4,5-trimethyl-2,5-cyclohexadien-1-one 、 异丁醛 在 1-(3,5-bis(trifluoromethyl)phenyl)-3-phenylthiourea 、 (Ra)-12-hydroxy-1,10-bis(2,4,6-triisopropylphenyl)-4,5,6,7-tetrahydrodiindeno[1,3,2]dioxaphosphocine 12-oxide 作用下， 以 1,2-二氯乙烷 为溶剂， 以63%的产率得到(3S,4aS,8aR)-3-isopropyl-4a,8,8a-trimethyl-4a,5-dihydrobenzo[e][1,2,4]trioxin-6(8aH)-one
  参考文献：
  名称：

  An Asymmetric Synthesis of 1,2,4-Trioxane Anticancer Agents via Desymmetrization of Peroxyquinols through a Brønsted Acid Catalysis Cascade

  摘要：

  The desymmetrization of p-peroxyquinols using a Bronsted acid-catalyzed acetalization/oxa-Michael cascade was achieved in high yields and selectivities for a variety of aliphatic and aryl aldehydes. Mechanistic studies, suggest that the reaction proceeds through a dynamic kinetic resolution of the peroxy hemiacetal intermediate. The resulting 1,2,4-trioxane products were derivatized and show potent cancer cell-growth inhibition.

  DOI：

  10.1021/ja3052427