| 143817-33-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• CAS: 143817-33-8
• 化学式: C₁₉H₂₄O₄S₂
• 分子量: 380.529
• InChiKey: AOZQBOUQZWLOJI-PWSUYJOCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.63
• 重原子数：
  25.0
• 可旋转键数：
  3.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  48.67
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  在 吡啶 、 sodium tetrahydroborate 、 硫酸 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 23.5h， 生成 methyl 2-[(8'S,8'aR)-3',8'-dimethyl-4'-oxospiro[1,3-dithiolane-2,2'-1,7,8,8a-tetrahydroazulene]-5'-yl]prop-2-enoate
  参考文献：
  名称：

  Bis-heteroannulation. 16. A synthetic approach to geigerin

  摘要：

  Furano alcohol 5, the key intermediate in our proposed synthesis of the guaianolide sesquiterpene geigerin (1), was prepared by a novel sequence of reactions which includes a chemoselective oxy-Cope transformation of enynols of general structure 42. Although 42 itself underwent oxy-Cope reaction with exclusive triple-bond participation, the corresponding tert-butyldimethylsilyl ether 46 gave the desired vinyl silyloxy Cope product 48 with 100% selectivity. The conversion of acetylenic oxazole 48 to 5 was then effected by a highly efficient (Diels-Alder)-(retro-Diels-Alder) transformation to generate the guaiane ketone 20, followed by hydride reduction.

  DOI：

  10.1021/jo00049a044
• 作为产物：
  描述：

  (R^*,S^*)-6-<9-Methyl-8-(4-methyl-5-methoxy-2-oxazolyl)-1,4-dithiaspiro<4.4>non-8-en-7-yl>-1-methoxyhept-2-yn-4-one 在 碳酸氢钠 、 对苯二酚 作用下， 以 甲苯 为溶剂， 反应 4.5h， 以90%的产率得到
  参考文献：
  名称：

  Bis-heteroannulation. 16. A synthetic approach to geigerin

  摘要：

  Furano alcohol 5, the key intermediate in our proposed synthesis of the guaianolide sesquiterpene geigerin (1), was prepared by a novel sequence of reactions which includes a chemoselective oxy-Cope transformation of enynols of general structure 42. Although 42 itself underwent oxy-Cope reaction with exclusive triple-bond participation, the corresponding tert-butyldimethylsilyl ether 46 gave the desired vinyl silyloxy Cope product 48 with 100% selectivity. The conversion of acetylenic oxazole 48 to 5 was then effected by a highly efficient (Diels-Alder)-(retro-Diels-Alder) transformation to generate the guaiane ketone 20, followed by hydride reduction.

  DOI：

  10.1021/jo00049a044