dimethyl (2aα,3β,8β,8aα)-2a,3,8,8a-tetrahydro-3,8-methano-4,7-dimethoxycyclobutanaphthalene-1,2-dicarboxylate | 124751-65-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: dimethyl (2aα,3β,8β,8aα)-2a,3,8,8a-tetrahydro-3,8-methano-4,7-dimethoxycyclobutanaphthalene-1,2-dicarboxylate
• 英文别名: dimethyl (2aα,3β,8β,8aα)-4,7-dimethoxy-2a,3,8,8a-tetrahydro-3,8-methanocyclobutanaphthalene-1,2-dicarboxylate；dimethyl-(2aα,3β,8β,8aα)-2a,3,8,8a-tetrahydro-1,4-dimethoxy-5,8-methanocyclobutanaphthalene-1,2-dicarboxylate；3,4-Bis-methoxycarbonyl-3',6'-dimethoxy-7,8-benzo-tricyclo<4.2.1.0^2,5>nonen-(3)；3,4-Bis-methoxycarbonyl-3',6'-dimethoxy-7,8-benzo-tricyclo[4.2.1.0^2,5]nonen-(3)；dimethyl (1R,8S,9R,12S)-3,6-dimethoxytetracyclo[6.4.1.02,7.09,12]trideca-2,4,6,10-tetraene-10,11-dicarboxylate
• CAS: 124751-65-1
• 化学式: C₁₉H₂₀O₆
• 分子量: 344.364
• InChiKey: XNZQCMFOOPBCNP-NWQDQBDJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.18
• 重原子数：
  25.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  71.06
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  dimethyl (2aα,3β,8β,8aα)-2a,3,8,8a-tetrahydro-3,8-methano-4,7-dimethoxycyclobutanaphthalene-1,2-dicarboxylate 、 四环庚烷 反应 72.0h， 以72%的产率得到dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-1,4,4a,4b,4c,5,10,10a,10b,10c-decahydro-1,4:5,10-dimethano-6,9-dimethoxybenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2-b>naphthalene-4b,10b-dicarboxylate
  参考文献：
  名称：

  Antolovich, Michael; Oliver, Anna M.; Paddon-Row, Michael N., Journal of the Chemical Society. Perkin transactions II, 1989, p. 783 - 790

  摘要：

  DOI：
• 作为产物：
  描述：

  8,11-dimethoxybenzonorbornadiene 、 丁炔二酸二甲酯 在 RuH₂(CO)(PPh₃)₃ 作用下， 以 苯 为溶剂， 反应 120.0h， 以91%的产率得到dimethyl (2aα,3β,8β,8aα)-2a,3,8,8a-tetrahydro-3,8-methano-4,7-dimethoxycyclobutanaphthalene-1,2-dicarboxylate
  参考文献：
  名称：

  一对新的刚性非对映异构三联体的合成与结构表征

  摘要：

  描述了一种用于构建完全刚性的三联体（发色团）系统D 2 -B 1 -D 1 -B 2 -A的方法，其中发色团D 2（=二甲基苯胺），D 1（= 1,4-二甲氧基萘），和A（＝二氰基ovyl）稠合到刚性烃桥B 1和B 2，其包括线性稠合的降冰片烷和双环[2.2.0]己烷单元。

  DOI：

  10.1016/0040-4020(95)00107-j

文献信息

• Synthesis of a Variety of Bichromophoric “Ball-and-Chain” Systems Based on Buckminsterfullerene (C₆₀) for the Study of Intramolecular Electron and Energy Transfer Processes
  作者：James M. Lawson、Anna M. Oliver、Daniel F. Rothenfluh、Yi-Zhong An、George A. Ellis、Millagahamada G. Ranasinghe、Saeed I. Khan、Andreas G. Franz、Padma S. Ganapathi、Michael J. Shephard、Michael N. Paddon-Row、Yves Rubin

  DOI：10.1021/jo960512p

  日期：1996.1.1

  Diels-Alder reaction of C-60 with the 1,3-dienes 7e-h, 8a, 8b, and 8d-h affords the ''ball-and-chain'' systems 2e-h, 3a, 3b, and 3d-h bearing two chromophores linked via a rigid, hybrid saturated polynorbornane-bicyclo[2.2.0]hexane (''norbornylogous'') hydrocarbon bridge. Analogous reaction with the bis(diene) 9 affords the soluble dumbbell system 4 bearing two C-60, chromophores. The norbornylogous bridge is a strong mediator of electron and energy transfer via a through-bond coupling mechanism. The norbornylogous donor-bridge-diene units 7d-h, 8a, 8b, and 8d-h were prepared in a straightforward manner from bicyclo[2.2.2]octane precursors by extending the bridges with linearly fused norbornane-bicyclo[2.2.0]hexane moieties through execution of the tandem Mitsudo-Smith series of reactions. The X-ray structure of the dimethoxybenzene-bridge-C-60 system 3a reveals favorable self-complementarity manifested by the unusual packing structure of 3a in the crystal. Molecular mechanics, semiempirical, and ab initio conformational analyses of compounds 2e, 3a, 3b, 3e, 3f, 3h, 68, and 70 (MM2, Sybyl, CVFF, AM1, HF/3-21G) were performed to quantify their ability to adopt two nondegenerate boat conformations, i.e,, extended and folded conformers, as well as their kinetic barrier of interconversion. A similar treatment of the C-60-bridge-C-60 system 4 revealed unusual preference for the folded-folded conformer (18.9 kcal/mol at CVFF level), which was not reproduced by the AM1 method (0.11 kcal/mol). The reduction potentials of the systems 2e, 3a, and 3e were about 0.1-0.5 V more negative than C-60, and the third reduction potential (E(3)) Of the 6-bond system 2e was 0.14 V more negative than the corresponding wave for the 10-bond system 3e. This shift was attributed to the closer proximity of the dimethylaniline donor group to the C-60 surface for 2e vs 3e.
• ANTOLOVICH, MICHAEL;OLIVER, ANNA M.;PADDON-ROW, MICHAEL N., J. CHEM. SOC. PERKIN TRANS. PT 2,(1989) N, C. 783-789
  作者：ANTOLOVICH, MICHAEL、OLIVER, ANNA M.、PADDON-ROW, MICHAEL N.

  DOI：——

  日期：——