methyl (2E,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-4-{(1'R,2'S,4'S)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[(1''E,6''R)-6-hydroxyocta-1,7-dien-1-yl]cyclopentyl}but-2-enoate | 1267910-36-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: methyl (2E,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-4-{(1'R,2'S,4'S)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[(1''E,6''R)-6-hydroxyocta-1,7-dien-1-yl]cyclopentyl}but-2-enoate
• 英文别名: methyl (2E,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-4-{(1R,2S,4S)-4-{[tert-butyl(dimethyl)-silyl]oxy}-2-[(1E,6R)-6-hydroxyocta-1,7-dien-1-yl]cyclopentyl}but-2-enoate
• CAS: 1267910-36-0
• 化学式: C₃₀H₅₆O₅Si₂
• 分子量: 552.943
• InChiKey: FQTVPQOSYBLZJS-MSRRIRRBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.8
• 重原子数：
  37.0
• 可旋转键数：
  13.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  64.99
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  methyl (2E,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-4-{(1'R,2'S,4'S)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[(1''E,6''R)-6-hydroxyocta-1,7-dien-1-yl]cyclopentyl}but-2-enoate 在 甲醇 、 triethylamine tris(hydrogen fluoride) 、 sodium hydroxide 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 16.0h， 生成 (1R,6S,11aS,13S,14aR)-1,13-bis{[tert-butyl(dimethyl)silyl]oxy}-6-vinyl-1,6,7,8,9,11a,12,13,14,14a-decahydro-4H-cyclopenta[f]oxacyclotridecin-4-one
  参考文献：
  名称：

  Synthesis and Biological Properties of Novel Brefeldin A Analogues

  摘要：

  New brefeldin A (1) analogues were obtained by introducing a variety of substituents at C15. Most of the analogues exhibited significant biological activity. (15R)-Trifluoromethyl-nor-brefeldin A (3), (15R)-vinyl-nor-brefeldin A (5), their epimers 4 and 6 as well as (15S)-ethyl-nor-brefeldin A (2) were prepared from the key building blocks 12 or 24 by Julia-Kocienski olefination with tetrazolyl sulfones and subsequent macrolactonization. The vinyl derivative 5 allowed analogues to be synthesized by hydroboration and Suzuki-Miyaura coupling. The following biological properties were assessed: (a) inhibition of cell growth of human cancer cells (NCI), (b) induction of morphological changes of the Golgi apparatus of plant and mammalian cells, and (c) influence on the replication of the enterovirus CVB3. Furthermore, conformational aspects were studied by X-ray crystal structure analysis and molecular mechanics calculations, including docking of the analogues into the brefeldin A binding site of an Arf1/Sec7-complex.

  DOI：

  10.1021/jm400615g
• 作为产物：
  描述：

  methyl (2E,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-4-((1R,2S,4S)-4-{[tert-butyl(dimethyl)-silyl]oxy}-2-{(1E,6E)-8-[(methoxycarbonyl)oxy]octa-1,6-dien-1-yl}cyclopentyl)but-2-enoate 在 palladium di-μ-chlorobis (η-allyl) 、 potassium hydrogencarbonate 作用下， 以 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 以95%的产率得到methyl (2E,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-4-{(1'R,2'S,4'S)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[(1''E,6''R)-6-hydroxyocta-1,7-dien-1-yl]cyclopentyl}but-2-enoate
  参考文献：
  名称：

  Synthesis and Biological Properties of Novel Brefeldin A Analogues

  摘要：

  New brefeldin A (1) analogues were obtained by introducing a variety of substituents at C15. Most of the analogues exhibited significant biological activity. (15R)-Trifluoromethyl-nor-brefeldin A (3), (15R)-vinyl-nor-brefeldin A (5), their epimers 4 and 6 as well as (15S)-ethyl-nor-brefeldin A (2) were prepared from the key building blocks 12 or 24 by Julia-Kocienski olefination with tetrazolyl sulfones and subsequent macrolactonization. The vinyl derivative 5 allowed analogues to be synthesized by hydroboration and Suzuki-Miyaura coupling. The following biological properties were assessed: (a) inhibition of cell growth of human cancer cells (NCI), (b) induction of morphological changes of the Golgi apparatus of plant and mammalian cells, and (c) influence on the replication of the enterovirus CVB3. Furthermore, conformational aspects were studied by X-ray crystal structure analysis and molecular mechanics calculations, including docking of the analogues into the brefeldin A binding site of an Arf1/Sec7-complex.

  DOI：

  10.1021/jm400615g

文献信息

• Enantio- and Regioselective Iridium-Catalyzed Allylic Hydroxylation
  作者：Martin Gärtner、Steffen Mader、Kai Seehafer、Günter Helmchen

  DOI：10.1021/ja109953v

  日期：2011.2.23

  The first enantioselective allylic hydroxylation to prepare branched allylic alcohols directly is described. Bicarbonate was used as nucleophile in conjunction with new single component Ir-catalysts, which are stable to air and water. Excellent regio- and enantioselectivities have been achieved with a representative set of substrates.