methyl (5Z,8S)-8,9-dihydroxynon-5-enoate | 885481-78-7

• 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 (5Z,8S)-8,9-dihydroxynon-5-enoate
• 英文别名: methyl (Z,8S)-8,9-dihydroxynon-5-enoate
• CAS: 885481-78-7
• 化学式: C₁₀H₁₈O₄
• 分子量: 202.251
• InChiKey: XMLDAGVZSOKZFG-MDHMXLOGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  14
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  66.8
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl (5Z,8S)-8,9-dihydroxynon-5-enoate 在 4-二甲氨基吡啶 、 sodium tetrahydroborate 、 草酰氯 、 cerium(III) chloride heptahydrate 、 2,4,6-三氯苯甲酰氯 、 水 、 对甲苯磺酸 、 二甲基亚砜 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 、 2,3-二氯-5,6-二氰基-1,4-苯醌 、 lithium chloride 、 lithium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 37.58h， 生成
  参考文献：
  名称：

  Synthesis of marine oxylipin topsentolide A1 and its stereoisomers, and determination of the absolute configuration of the natural product

  摘要：

  Four possible stereoisomers of topsentolide A(1), a cytotoxic oxylipin against human solid tumor cell lines, were efficiently synthesized in a stereoselective manner in order to determine the stereochemistry of natural product. The absolute configuration of topsentolide A(1) was determined to be 8R,11R,12S by comparing NMR spectra and specific rotations of the synthetic isomers and the natural product. Cytotoxicity of the synthetic isomers was also examined. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2015.09.013
• 作为产物：
  描述：

  4-羧丁基三苯基溴化膦 在 盐酸 、 水 、 sodium hexamethyldisilazane 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 为溶剂， 反应 22.17h， 生成 methyl (5Z,8S)-8,9-dihydroxynon-5-enoate
  参考文献：
  名称：

  Synthesis of marine oxylipin topsentolide A1 and its stereoisomers, and determination of the absolute configuration of the natural product

  摘要：

  Four possible stereoisomers of topsentolide A(1), a cytotoxic oxylipin against human solid tumor cell lines, were efficiently synthesized in a stereoselective manner in order to determine the stereochemistry of natural product. The absolute configuration of topsentolide A(1) was determined to be 8R,11R,12S by comparing NMR spectra and specific rotations of the synthetic isomers and the natural product. Cytotoxicity of the synthetic isomers was also examined. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2015.09.013

文献信息

• Stereochemical assignment of topsentolide C2 by stereodivergent synthesis of its four diastereomers
  作者：Ryo Towada、Yusuke Kurashina、Shigefumi Kuwahara

  DOI：10.1016/j.tetlet.2013.10.032

  日期：2013.12

  Four diastereomers of topsentolide C-2, a cytotoxic nine-membered lactone isolated from the marine sponge Topsentia sp., were synthesized stereodivergently from a common chiral seco acid by the combined use of the Yamaguchi and Mitsunobu lactonizations. Comparison of the NMR spectra of the four diastereomers with those of an authentic sample of topsentolide C-2 led to the stereochemical determination of topsentolide C-2 as 8R, 11S, and 12S. (C) 2013 Elsevier Ltd. All rights reserved.
• Determination of the absolute configuration of marine oxylipin topsentolide A1 by the synthesis of the enantiomer of the natural product
  作者：Munetaka Kobayashi、Ken Ishigami、Hidenori Watanabe

  DOI：10.1016/j.tetlet.2010.03.071

  日期：2010.5

  Two possible stereoisomers of topsentolide A(1), a cytotoxic oxylipin against human solid tumor cell lines, were prepared in order to determine the stereochemistry of natural product. That is, the enantiomer of topsentolide A(1), (85,115,12R)-isomer, and its diastereomer was efficiently synthesized in a stereoselective manner. The stereochemistry of topsentolide A(1) was determined to be 8R,11R,12S by comparing NMR spectra and specific rotations of the synthetic isomers and the natural product. (C) 2010 Elsevier Ltd. All rights reserved.