(4R)-trans-N,N,N',N'-tetramethyl-2-methyl-2-(3-hydroxypent-2-yl)-1,3-dioxolan-4,5-dicarboxamide | 140430-30-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (4R)-trans-N,N,N',N'-tetramethyl-2-methyl-2-(3-hydroxypent-2-yl)-1,3-dioxolan-4,5-dicarboxamide
• 英文别名: (4R,5R)-2-(3-hydroxypentan-2-yl)-4-N,4-N,5-N,5-N,2-pentamethyl-1,3-dioxolane-4,5-dicarboxamide
• CAS: 140430-30-4
• 化学式: C₁₅H₂₈N₂O₅
• 分子量: 316.398
• InChiKey: ATCVURSVQJVRIU-KIDURHIOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  79.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  (4R)-trans-N,N,N',N'-tetramethyl-2-methoxy-2-methyl-1,3-dioxolan-4,5-dicarboxamide 在 四氯化钛 、 L-Selectride 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 20.0h， 生成 (4R)-trans-N,N,N',N'-tetramethyl-2-methyl-2-(3-hydroxypent-2-yl)-1,3-dioxolan-4,5-dicarboxamide
  参考文献：
  名称：

  Chiral orthoesters in organic synthesis: Novel reagents for the enantioselective acylation of silylenolethers

  摘要：

  Dialkyl trans-2-alkoxy-2-alkyl-1,3-dioxolan-4,5-dicarboxylates and the corresponding N,N,N,N-tetramethyl-4,5-diamides have been prepared respectively from dialkyl tartrates or tartaric acid diamides. They smoothly reacted with silylenolethers in the presence of Lewis acids to give enantiomerically enriched (up to 90% d.e.) monoprotected 1,3-diketones. A dramatic dependence of the stereochemical outcome from the configuration of the enolic double bond of 4 has been observed. The products can be stereoselectively reduced to give configurationally defined monoprotected 3-ketols.

  DOI：

  10.1016/s0040-4020(01)90792-6

文献信息

• Chiral orthoesters in organic synthesis: Novel reagents for the enantioselective acylation of silylenolethers
  作者：Luigi Longobardo、Giovanna Mobbili、Emilio Tagliavini、Claudio Trombini、Achille Umani-Ronchi

  DOI：10.1016/s0040-4020(01)90792-6

  日期：1992.1

  Dialkyl trans-2-alkoxy-2-alkyl-1,3-dioxolan-4,5-dicarboxylates and the corresponding N,N,N,N-tetramethyl-4,5-diamides have been prepared respectively from dialkyl tartrates or tartaric acid diamides. They smoothly reacted with silylenolethers in the presence of Lewis acids to give enantiomerically enriched (up to 90% d.e.) monoprotected 1,3-diketones. A dramatic dependence of the stereochemical outcome from the configuration of the enolic double bond of 4 has been observed. The products can be stereoselectively reduced to give configurationally defined monoprotected 3-ketols.