(2S,3S)-dimethyl 3-((E)-3,3-dimethylbut-1-en-1-yl)-2-hydroxy-2-(trifluoromethyl)succinate | 1594882-52-6

• 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: (2S,3S)-dimethyl 3-((E)-3,3-dimethylbut-1-en-1-yl)-2-hydroxy-2-(trifluoromethyl)succinate
• CAS: 1594882-52-6
• 化学式: C₁₃H₁₉F₃O₅
• 分子量: 312.286
• InChiKey: LYEYNNMXKRCROT-WCAZPSEFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.84
• 重原子数：
  21.0
• 可旋转键数：
  4.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.69
• 拓扑面积：
  72.83
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  甲醇 、 三氟丙酮酸甲酯 、 在 (5aR,10bS)-5a,10b-dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b]-1,2,4-triazolo[4,3-d]-1,4-oxazinium chloride 、 dipotassium hydrogenphosphate 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 51.0h， 以95%的产率得到
  参考文献：
  名称：

  Catalytic Asymmetric α-Aldol Reaction of Vinylogous N-Heterocyclic Carbene Enolates: Formation of Quaternary and Labile Tertiary Stereocenters

  摘要：

  Simple N-heterocyclic carbene (NHC)-enolates are widely studied versatile species. However, their vinylogous siblings (i.e., vinylogous NHC-enolates) have been much less studied. Here we disclose the first catalytic asymmetric a-aldol reaction of vinylogous NHC-enolates. With trifluoropyruvate as the carbon electrophile, the efficient C C bond formation process displays not only complete alpha-regioselectivity but also excellent stereocontrol over the two newly established challenging stereocenters (one quaternary and the other labile tertiary), furnishing a range of highly enantioenriched beta,gamma-unsaturated alpha-fluoroalkylated esters.

  DOI：

  10.1021/ol500830a