(10E,14E)-(6S,7R,18S,19R)-6,18,19-tris(methoxymethoxy)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraen-7-ol | 124018-82-2

• 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: (10E,14E)-(6S,7R,18S,19R)-6,18,19-tris(methoxymethoxy)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraen-7-ol
• 英文别名: (6S,7R,10E,14E,18S,19R)-6,18,19-tris(methoxymethoxy)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraen-7-ol
• CAS: 124018-82-2
• 化学式: C₃₆H₆₆O₇
• 分子量: 610.916
• InChiKey: UDLGUCOBJUEJTB-UBQCMQKKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.82
• 重原子数：
  43.0
• 可旋转键数：
  26.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  75.61
• 氢给体数：
  1.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  (10E,14E)-(6S,7R,18S,19R)-6,18,19-tris(methoxymethoxy)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraen-7-ol 在 bis(acetylacetonate)oxovanadium 叔丁基过氧化氢 、 溶剂黄146 作用下， 以 二氯甲烷 、 苯 为溶剂， 反应 7.0h， 生成 (2R,5R)-tetrahydro-2-<(E)-(1S,8S,9R)-1-hydroxy-8,9-bis(methoxymethoxy)-5,9,13-trimethyltetradeca-4,12-dienyl>-5-<(S)-1-(methoxymethoxy)-1,5-dimethylhex-4-enyl>-2-methylfuran 、 (2R,5R)-tetrahydro-2-<(2S,5R)-tetrahydro-5-<(1S,4S,5R)-1-hydroxy-4,5-bis(methoxymethoxy)-1,5,9-trimethyldec-8-enyl>furan-2-yl>-5-<(S)-1-(methoxymethoxy)-1,5-dimethylhex-4-enyl>-2-methylfuran
  参考文献：
  名称：

  Total synthesis of the meso-triterpene polyether teurilene

  摘要：

  The first total synthesis of the triterpene ether teurilene (1) has been accomplished utilizing two vanadium(V)-catalyzed oxidation-cyclization reactions with different stereoselectivities. The synthesis involved stereoselective and step-by-step construction of 2,5-cis- and 2,5-trans-tetrahydrofuran rings, vanadium(V)-catalyzed oxidation of 4-substituted 4-en-1-ol 40 and subsequent cyclization of the resulting anti-epoxy alcohol 41, and a similar oxidation-cyclization of 5-substituted 4-en-1-ol 49 by way of syn-epoxy alcohol 50. This was followed by construction of a third tetrahydrofuran ring by more conventional means. An improved synthesis of 1, which featured direct formation of bis(tetrahydrofuran) 51 from squalene derivative 66 by simultaneous double oxidation-cyclization, was also accomplished.

  DOI：

  10.1021/jo00007a013
• 作为产物：
  描述：

  6-辛烯-1,3-二醇,3,7-二甲基-,1-(4-甲基苯磺酸酯),(3R)- 在 四氯化碳 、 4-二甲氨基吡啶 、 正丁基锂 、 四甲基乙二胺 、 氨 、 sodium 、 lithium 、 potassium carbonate 、 N,N-二异丙基乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 苯 为溶剂， 反应 69.34h， 生成 (10E,14E)-(6S,7R,18S,19R)-6,18,19-tris(methoxymethoxy)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraen-7-ol
  参考文献：
  名称：

  Total synthesis of the meso-triterpene polyether teurilene

  摘要：

  The first total synthesis of the triterpene ether teurilene (1) has been accomplished utilizing two vanadium(V)-catalyzed oxidation-cyclization reactions with different stereoselectivities. The synthesis involved stereoselective and step-by-step construction of 2,5-cis- and 2,5-trans-tetrahydrofuran rings, vanadium(V)-catalyzed oxidation of 4-substituted 4-en-1-ol 40 and subsequent cyclization of the resulting anti-epoxy alcohol 41, and a similar oxidation-cyclization of 5-substituted 4-en-1-ol 49 by way of syn-epoxy alcohol 50. This was followed by construction of a third tetrahydrofuran ring by more conventional means. An improved synthesis of 1, which featured direct formation of bis(tetrahydrofuran) 51 from squalene derivative 66 by simultaneous double oxidation-cyclization, was also accomplished.

  DOI：

  10.1021/jo00007a013

文献信息

• A short step synthesis of teurilene. Stereocontrolled sequential double cyclization of the C30-tetraenetetraol to the tandem tetrahydrofuran system
  作者：Masaru Hashimoto、Hiroko Harigaya、Mitsutoshi Yanagiya、Haruhisa Shirahama

  DOI：10.1016/s0040-4039(00)82236-4

  日期：1988.1
• HASHIMOTO, MASARU;HARIGAYA, HIROKO;YANAGIYA, MITSUTOSHI;SHIRAHAMA, HARUHI+, J. ORG. CHEM., 56,(1991) N, C. 2299-2311
  作者：HASHIMOTO, MASARU、HARIGAYA, HIROKO、YANAGIYA, MITSUTOSHI、SHIRAHAMA, HARUHI+

  DOI：——

  日期：——
• HASHIMOTO, MASARU;HARIGAYA, HIROKO;YANAGIYA, MITSUTOSHI;SHIRAHAMA, HARUHI+, TETRAHEDRON LETT., 29,(1988) N 46, C. 5947-5948
  作者：HASHIMOTO, MASARU、HARIGAYA, HIROKO、YANAGIYA, MITSUTOSHI、SHIRAHAMA, HARUHI+

  DOI：——

  日期：——