endo-1-methyl-7-phenyl-4-oxatetracyclo<5.5.1.0^2,6.0^8,12>trideca-8,11-diene-3,5-dione | 141613-61-8

• 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: endo-1-methyl-7-phenyl-4-oxatetracyclo<5.5.1.0^2,6.0^8,12>trideca-8,11-diene-3,5-dione
• 英文别名: endo-1-methyl-7-phenyl-4-oxatetracyclo[5.5.1.0^2,6.0^8,12]trideca-8,11-diene-3,5-dione；(1R,2S,6R,7S)-1-methyl-7-phenyl-4-oxatetracyclo[5.5.1.02,6.08,12]trideca-8,11-diene-3,5-dione
• CAS: 141613-61-8
• 化学式: C₁₉H₁₆O₃
• 分子量: 292.334
• InChiKey: YUPSWQWDNSCCMC-PDWMJMLSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  22
• 可旋转键数：
  1
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.37
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  endo-1-methyl-7-phenyl-4-oxatetracyclo<5.5.1.0^2,6.0^8,12>trideca-8,11-diene-3,5-dione 、 4-甲基-1,2,4-三吖啉-3,5-二酮 以 二氯甲烷 为溶剂， 反应 2.0h， 生成 anti,endo-1,6-dimethyl-11-phenyl-14-oxa-4,6,8-triazahexacyclo<9.5.1.13,9.02,10.04,8.012,16>octadec-2(10)-ene-5,7,13,15-tetrone
  参考文献：
  名称：

  Generation and interception of isodicyclopentadiene tautomers by diene transmissive Diels-Alder reaction of a 1,5-dihydropentalene with a variety of dienophiles

  摘要：

  The cycloaddition of N-methyl-1,2,4-triazoline-3,5-dione (MTAD), dimethyl acetylenedicarboxylate (DMAD), maleic anhydride (MA), and p-benzoquinone (BQ) with 6-methyl-4-phenyl-1,5-dihydropentalene (1) afforded the mono- and bis-adducts which depended on the dienophilic strength and reaction conditions (temperature, concentration). Thus, for the highly reactive dienophiles MTAD and DMAD, exclusively the bis-adducts (2, 3) were isolated in high yields as products of diene transmissive Diels-Alder reactions; the corresponding mono-adducts (substituted isodicyclopentadienes) were not detected even as transients. The pi-facial selectivity was high (>95% anti selectivity for 2 and 3) for the second addition step, but it decreased to 75% when high substrate concentrations were used (formation of 25% of the syn product 3b). In the case of the less reactive dienophiles MA or BQ, the corresponding intermediary mono-adducts could be detected by H-1 NMR spectroscopy and their conversion to the more stable isodicyclopentadiene tautomers (e.g. 4a to 4b) monitored directly in the reaction mixture. Both tautomers could be trapped intermolecularly for the MA case by addition of MTAD (5, 7) or another equivalent of MA (6, 8). The intramolecular cycloaddition of the isodicyclopentadiene tautomer derived from BQ and 1, namely the mono-adduct 10b, led to the cage compound 11. The double cycloaddition of dienophiles to 1,5-dihydropentalenes provides an efficient and convenient methodology for the synthesis of complex polycyclic ring skeletons.

  DOI：

  10.1021/jo00040a047
• 作为产物：
  描述：

  马来酸酐 、 4-Phenyl-6-methyl-1,5-dihydropentalene 以 二氯甲烷 为溶剂， 生成 endo-1-methyl-7-phenyl-4-oxatetracyclo<5.5.1.0^2,6.0^8,12>trideca-8,11-diene-3,5-dione
  参考文献：
  名称：

  Generation and interception of isodicyclopentadiene tautomers by diene transmissive Diels-Alder reaction of a 1,5-dihydropentalene with a variety of dienophiles

  摘要：

  The cycloaddition of N-methyl-1,2,4-triazoline-3,5-dione (MTAD), dimethyl acetylenedicarboxylate (DMAD), maleic anhydride (MA), and p-benzoquinone (BQ) with 6-methyl-4-phenyl-1,5-dihydropentalene (1) afforded the mono- and bis-adducts which depended on the dienophilic strength and reaction conditions (temperature, concentration). Thus, for the highly reactive dienophiles MTAD and DMAD, exclusively the bis-adducts (2, 3) were isolated in high yields as products of diene transmissive Diels-Alder reactions; the corresponding mono-adducts (substituted isodicyclopentadienes) were not detected even as transients. The pi-facial selectivity was high (>95% anti selectivity for 2 and 3) for the second addition step, but it decreased to 75% when high substrate concentrations were used (formation of 25% of the syn product 3b). In the case of the less reactive dienophiles MA or BQ, the corresponding intermediary mono-adducts could be detected by H-1 NMR spectroscopy and their conversion to the more stable isodicyclopentadiene tautomers (e.g. 4a to 4b) monitored directly in the reaction mixture. Both tautomers could be trapped intermolecularly for the MA case by addition of MTAD (5, 7) or another equivalent of MA (6, 8). The intramolecular cycloaddition of the isodicyclopentadiene tautomer derived from BQ and 1, namely the mono-adduct 10b, led to the cage compound 11. The double cycloaddition of dienophiles to 1,5-dihydropentalenes provides an efficient and convenient methodology for the synthesis of complex polycyclic ring skeletons.

  DOI：

  10.1021/jo00040a047

文献信息

• Generation and interception of isodicyclopentadiene tautomers by diene transmissive Diels-Alder reaction of a 1,5-dihydropentalene with a variety of dienophiles
  作者：Waldemar Adam、Thomas Deufel、Ralf Finzel、Axel G. Griesbeck、Joachim Hirt

  DOI：10.1021/jo00040a047

  日期：1992.7

  The cycloaddition of N-methyl-1,2,4-triazoline-3,5-dione (MTAD), dimethyl acetylenedicarboxylate (DMAD), maleic anhydride (MA), and p-benzoquinone (BQ) with 6-methyl-4-phenyl-1,5-dihydropentalene (1) afforded the mono- and bis-adducts which depended on the dienophilic strength and reaction conditions (temperature, concentration). Thus, for the highly reactive dienophiles MTAD and DMAD, exclusively the bis-adducts (2, 3) were isolated in high yields as products of diene transmissive Diels-Alder reactions; the corresponding mono-adducts (substituted isodicyclopentadienes) were not detected even as transients. The pi-facial selectivity was high (>95% anti selectivity for 2 and 3) for the second addition step, but it decreased to 75% when high substrate concentrations were used (formation of 25% of the syn product 3b). In the case of the less reactive dienophiles MA or BQ, the corresponding intermediary mono-adducts could be detected by H-1 NMR spectroscopy and their conversion to the more stable isodicyclopentadiene tautomers (e.g. 4a to 4b) monitored directly in the reaction mixture. Both tautomers could be trapped intermolecularly for the MA case by addition of MTAD (5, 7) or another equivalent of MA (6, 8). The intramolecular cycloaddition of the isodicyclopentadiene tautomer derived from BQ and 1, namely the mono-adduct 10b, led to the cage compound 11. The double cycloaddition of dienophiles to 1,5-dihydropentalenes provides an efficient and convenient methodology for the synthesis of complex polycyclic ring skeletons.