(R)-2-((tert-butyldimethylsilyl)oxy)-3-fluoropropan-1-ol | 1338560-72-7

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: (R)-2-((tert-butyldimethylsilyl)oxy)-3-fluoropropan-1-ol
• 英文别名: (2R)-2-[tert-butyl(dimethyl)silyl]oxy-3-fluoropropan-1-ol
• CAS: 1338560-72-7
• 化学式: C₉H₂₁FO₂Si
• 分子量: 208.348
• InChiKey: NMLPPVGOMFCEFZ-QMMMGPOBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.34
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (R)-2-((tert-butyldimethylsilyl)oxy)-3-fluoropropan-1-ol 在 2,6-二甲基吡啶 、 六甲基磷酰三胺 、 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成
  参考文献：
  名称：

  Design and synthesis of C35-fluorinated solamins and their growth inhibitory activities against human cancer cell lines

  摘要：

  The convergent synthesis of C35-fluorinated analogues of solamin, a mono-THF Annonaceous acetogenin, has been achieved by the Sonogashira coupling of the THF ring fragment and the fluorinated gamma-lactone fragment. It was revealed that the number of fluorine atoms on the gamma-lactone moiety affects the growth inhibitory activities against human cancer cell lines. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.08.011
• 作为产物：
  描述：

  叔丁基二甲基氯硅烷 在 咪唑 、 对甲苯磺酸 作用下， 以 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 生成 (R)-2-((tert-butyldimethylsilyl)oxy)-3-fluoropropan-1-ol
  参考文献：
  名称：

  Design and synthesis of C35-fluorinated solamins and their growth inhibitory activities against human cancer cell lines

  摘要：

  The convergent synthesis of C35-fluorinated analogues of solamin, a mono-THF Annonaceous acetogenin, has been achieved by the Sonogashira coupling of the THF ring fragment and the fluorinated gamma-lactone fragment. It was revealed that the number of fluorine atoms on the gamma-lactone moiety affects the growth inhibitory activities against human cancer cell lines. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.08.011

文献信息

• Synthesis and Liver Microsomal Metabolic Stability Studies of a Fluorine‐Substituted δ‐Tocotrienol Derivative
  作者：Xingui Liu、Saikat Poddar、Lin Song、Howard Hendrickson、Xuan Zhang、Yaxia Yuan、Daohong Zhou、Guangrong Zheng

  DOI：10.1002/cmdc.201900676

  日期：2020.3.18

  A fluoro-substituted δ-tocotrienol derivative, DT3-F2, was synthesized. This compound was designed to stabilize the metabolically labile terminal methyl groups of δ-tocotrienol by replacing one C-H bond on each of the two methyl groups with a C-F bond. However, in vitro metabolic stability studies using mouse liver microsomes revealed an unexpected rapid enzymatic C-F bond hydrolysis of DT3-F2. To

  合成了氟取代的δ-生育三烯酚衍生物DT3-F2。该化合物被设计为通过用CF键取代两个甲基上每个的一个CH键来稳定δ-生育三烯酚的代谢不稳定的甲基。但是，使用小鼠肝微粒体进行的体外代谢稳定性研究表明，DT3-F2发生了意外的快速酶促CF键水解。据我们所知，这是烯丙基CF键异常代谢水解的第一个报道。
• Design and synthesis of C35-fluorinated solamins and their growth inhibitory activities against human cancer cell lines
  作者：Naoto Kojima、Yuki Suga、Hiromi Hayashi、Takao Yamori、Takehiko Yoshimitsu、Tetsuaki Tanaka

  DOI：10.1016/j.bmcl.2011.08.011

  日期：2011.10

  The convergent synthesis of C35-fluorinated analogues of solamin, a mono-THF Annonaceous acetogenin, has been achieved by the Sonogashira coupling of the THF ring fragment and the fluorinated gamma-lactone fragment. It was revealed that the number of fluorine atoms on the gamma-lactone moiety affects the growth inhibitory activities against human cancer cell lines. (C) 2011 Elsevier Ltd. All rights reserved.