(S)-1-[4-((S)-2-Hydroxy-dec-4-ynyloxy)-phenoxy]-dec-4-yn-2-ol | 201477-84-1

• 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: (S)-1-[4-((S)-2-Hydroxy-dec-4-ynyloxy)-phenoxy]-dec-4-yn-2-ol
• 英文别名: (2S)-1-[4-[(2S)-2-hydroxydec-4-ynoxy]phenoxy]dec-4-yn-2-ol
• CAS: 201477-84-1
• 化学式: C₂₆H₃₈O₄
• 分子量: 414.585
• InChiKey: XZFMUWFMQDPBCG-ZEQRLZLVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.9
• 重原子数：
  30
• 可旋转键数：
  14
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  58.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (S)-1-[4-((S)-2-Hydroxy-dec-4-ynyloxy)-phenoxy]-dec-4-yn-2-ol 在 lithium aluminium tetrahydride 作用下， 以 二乙二醇二甲醚 为溶剂， 反应 24.0h， 以95%的产率得到(E,2S)-1-[4-[(E,2S)-2-hydroxydec-4-enoxy]phenoxy]dec-4-en-2-ol
  参考文献：
  名称：

  Enantiocontrolled Construction of Functionalized Tetrahydrofurans:  Total Synthesis of (6S,7S,9R,10R)-6,9-Epoxynonadec-18-ene-7,10-diol, a Marine Natural Product

  摘要：

  An efficient strategy has been developed for the construction of highly functionalized tetrahydrofurans. The key feature involves the use of Sharpless asymmetric dihydroxylation and the choice of a new bis-C-3 building block 5 as-the starting material which increased the efficiency. On the basis of this methodology, a marine natural product, (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol(1), was successfully synthesized in high enantioselectivity.

  DOI：

  10.1021/jo971324h
• 作为产物：
  描述：

  1,4-二(丙-2-烯氧基)苯 在 正丁基锂 、 三氟化硼乙醚 、 氢溴酸 、 potassium carbonate 、 氢化奎尼定 1,4-(2,3-二氮杂萘)二醚 、 potassium hexacyanoferrate(III) 作用下， 以 四氢呋喃 、 甲醇 、 正己烷 、 水 、 叔丁醇 为溶剂， 反应 65.5h， 生成 (S)-1-[4-((S)-2-Hydroxy-dec-4-ynyloxy)-phenoxy]-dec-4-yn-2-ol
  参考文献：
  名称：

  Enantiocontrolled Construction of Functionalized Tetrahydrofurans:  Total Synthesis of (6S,7S,9R,10R)-6,9-Epoxynonadec-18-ene-7,10-diol, a Marine Natural Product

  摘要：

  An efficient strategy has been developed for the construction of highly functionalized tetrahydrofurans. The key feature involves the use of Sharpless asymmetric dihydroxylation and the choice of a new bis-C-3 building block 5 as-the starting material which increased the efficiency. On the basis of this methodology, a marine natural product, (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol(1), was successfully synthesized in high enantioselectivity.

  DOI：

  10.1021/jo971324h

文献信息

• Enantiocontrolled Construction of Functionalized Tetrahydrofurans:  Total Synthesis of (6<i>S</i>,7<i>S</i>,9<i>R</i>,10<i>R</i>)-6,9-Epoxynonadec-18-ene-7,10-diol, a Marine Natural Product
  作者：Zhi-Min Wang、Ming Shen

  DOI：10.1021/jo971324h

  日期：1998.3.1

  An efficient strategy has been developed for the construction of highly functionalized tetrahydrofurans. The key feature involves the use of Sharpless asymmetric dihydroxylation and the choice of a new bis-C-3 building block 5 as-the starting material which increased the efficiency. On the basis of this methodology, a marine natural product, (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol(1), was successfully synthesized in high enantioselectivity.