(2R,3S,5S,6R)-6-(2,5-Dimethoxy-phenyl)-2,6-dimethoxy-5-methyl-hexane-1,3-diol | 143470-45-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2R,3S,5S,6R)-6-(2,5-Dimethoxy-phenyl)-2,6-dimethoxy-5-methyl-hexane-1,3-diol
• 英文别名: (2R,3S,5S,6R)-6-(2,5-dimethoxyphenyl)-2,6-dimethoxy-5-methylhexane-1,3-diol
• CAS: 143470-45-5
• 化学式: C₁₇H₂₈O₆
• 分子量: 328.406
• InChiKey: CHYOZSSUBBAPGM-HYEYJGRESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  23
• 可旋转键数：
  10
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  77.4
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  (2S,5S,6R)-(E)-methyl 6-(2,5-dimethoxyphenyl)-2,6-dimethoxy-5-methylhex-3-enoate 在 sodium hydroxide 、 dimethyl sulfide borane 、 双氧水 作用下， 生成 (2R,3S,5S,6R)-6-(2,5-Dimethoxy-phenyl)-2,6-dimethoxy-5-methyl-hexane-1,3-diol 、 (2R,3R,5S,6R)-6-(2,5-Dimethoxy-phenyl)-2,6-dimethoxy-5-methyl-hexane-1,3-diol
  参考文献：
  名称：

  Diastereoselectivity in the borane methyl sulfide promoted hydroboration of .alpha.-alkoxy-.beta.,.gamma.-unsaturated esters. Documentation of an alkoxy-directed hydroboration reaction

  摘要：

  Alpha-Alkoxy-beta,gamma-unsaturated methyl esters of structural type 1 undergo an alkoxy-directed hydroboration with the mild hydroborating reagent borane-methyl sulfide complex (BH3-SMe2) in THF from 0-degrees-C to room temperature, and after standard alkaline hydrogen peroxide oxidation the 1,3-diol product 2 is produced with useful levels of selectivity favoring the anti diastereomer.

  DOI：

  10.1021/jo00046a006

文献信息

• Diastereoselectivity in the borane methyl sulfide promoted hydroboration of .alpha.-alkoxy-.beta.,.gamma.-unsaturated esters. Documentation of an alkoxy-directed hydroboration reaction
  作者：James S. Panek、Feng Xu

  DOI：10.1021/jo00046a006

  日期：1992.9

  Alpha-Alkoxy-beta,gamma-unsaturated methyl esters of structural type 1 undergo an alkoxy-directed hydroboration with the mild hydroborating reagent borane-methyl sulfide complex (BH3-SMe2) in THF from 0-degrees-C to room temperature, and after standard alkaline hydrogen peroxide oxidation the 1,3-diol product 2 is produced with useful levels of selectivity favoring the anti diastereomer.