(10S,3R,5R,6R)-10-(Methoxycarbonyl)-5-[(methoxycarbonyl)methyl]-6,10-dimethyl-4-methylenebicyclo[4.4.0]dec-3-yl 2,2,2-trifluoroacetate | 291748-45-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (10S,3R,5R,6R)-10-(Methoxycarbonyl)-5-[(methoxycarbonyl)methyl]-6,10-dimethyl-4-methylenebicyclo[4.4.0]dec-3-yl 2,2,2-trifluoroacetate
• 英文别名: methyl (1S,4aR,5R,7R,8aR)-5-(2-methoxy-2-oxoethyl)-1,4a-dimethyl-6-methylidene-7-(2,2,2-trifluoroacetyl)oxy-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate
• CAS: 291748-45-3
• 化学式: C₂₀H₂₇F₃O₆
• 分子量: 420.426
• InChiKey: UMBJGKAGIKSTNT-YLWMSMLNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  29
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  78.9
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  (10S,3R,5R,6R)-10-(Methoxycarbonyl)-5-[(methoxycarbonyl)methyl]-6,10-dimethyl-4-methylenebicyclo[4.4.0]dec-3-yl 2,2,2-trifluoroacetate 在 四(三苯基膦)钯 potassium carbonate 、 1-丙烷硫醇钠 作用下， 以 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 33.0h， 生成 13,14,15,16-tetranorlabda-6,8(17)-diene-12,19-dioic acid
  参考文献：
  名称：

  Preparation of bioactive podolactones via a new Pd-catalysed bislactonisation reaction. Synthesis of oidiolactone C

  摘要：

  A new route towards podolactone skeleton compounds, including the recently discovered Oidiolactone C, is described, using Pd-catalysed elimination of allylic trifluoroacetates and Pd-catalysed bislactonisation as key steps. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(00)00815-7
• 作为产物：
  描述：

  dimethyl 13,14,15,16-tetranorlabd-8(17)-ene-12,19-dioate 在 叔丁基过氧化氢 、 4-二甲氨基吡啶 、 selenium(IV) oxide 作用下， 以 正己烷 、 二氯甲烷 为溶剂， 反应 2.75h， 生成 (10S,3R,5R,6R)-10-(Methoxycarbonyl)-5-[(methoxycarbonyl)methyl]-6,10-dimethyl-4-methylenebicyclo[4.4.0]dec-3-yl 2,2,2-trifluoroacetate
  参考文献：
  名称：

  First Synthesis of the Antifungal Oidiolactone C from trans-Communic Acid:  Cytotoxic and Antimicrobial Activity in Podolactone-Related Compounds

  摘要：

  The synthesis of the fungicide oidiolactone C starting from diterpenic trans-communic acid was carried out with an overall yield of 11.7%. The key step in the process consists of a new bislactonization reaction catalyzed by Pd(H), which gives rise to the podolactone-type tetracyclic skeleton from a norlabdadienedioic acid. We also carried out a study of the structure-biological activity of different natural podolactones and their synthetic precursors. Thus, the highest cytotoxic activity was found in dienic dilactones with ether-type substitutions on C-17, whereas the closure of the gamma-lactone ring is not critical for presenting a maximal antimicrobial activity.

  DOI：

  10.1021/jo0161882

文献信息

• Preparation of bioactive podolactones via a new Pd-catalysed bislactonisation reaction. Synthesis of oidiolactone C
  作者：Alejandro F Barrero、José F Quı́lez Del Moral、Juan M Cuerva、E Cabrera、David Jiménez-González

  DOI：10.1016/s0040-4039(00)00815-7

  日期：2000.7

  A new route towards podolactone skeleton compounds, including the recently discovered Oidiolactone C, is described, using Pd-catalysed elimination of allylic trifluoroacetates and Pd-catalysed bislactonisation as key steps. (C) 2000 Elsevier Science Ltd. All rights reserved.
• First Synthesis of the Antifungal Oidiolactone C from <i>trans</i>-Communic Acid:  Cytotoxic and Antimicrobial Activity in Podolactone-Related Compounds
  作者：Alejandro F. Barrero、Siméon Arseniyadis、José F. Quílez del Moral、M. Mar Herrador、M. Valdivia、D. Jiménez

  DOI：10.1021/jo0161882

  日期：2002.4.1

  The synthesis of the fungicide oidiolactone C starting from diterpenic trans-communic acid was carried out with an overall yield of 11.7%. The key step in the process consists of a new bislactonization reaction catalyzed by Pd(H), which gives rise to the podolactone-type tetracyclic skeleton from a norlabdadienedioic acid. We also carried out a study of the structure-biological activity of different natural podolactones and their synthetic precursors. Thus, the highest cytotoxic activity was found in dienic dilactones with ether-type substitutions on C-17, whereas the closure of the gamma-lactone ring is not critical for presenting a maximal antimicrobial activity.