(2S,3R)-1-(2-ethyl-1H-pyrrol-1-yl)-2,3-dihydroxy-4-methylpentan-1-one | 1449799-15-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: (2S,3R)-1-(2-ethyl-1H-pyrrol-1-yl)-2,3-dihydroxy-4-methylpentan-1-one
• 英文别名: (2S,3R)-1-(2-ethylpyrrol-1-yl)-2,3-dihydroxy-4-methylpentan-1-one
• CAS: 1449799-15-8
• 化学式: C₁₂H₁₉NO₃
• 分子量: 225.288
• InChiKey: QHALNXDPEXCDQQ-MNOVXSKESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.58
• 拓扑面积：
  62.5
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2-乙基吡咯 在 正丁基锂 、 diethylzinc 、 三溴化硼 、 2,6-bis[(S)-2-Ph2(OH)C-pyrrolidinomethyl]-3,5-Me2-phenol 作用下， 以 四氢呋喃 、 正己烷 、 正庚烷 、 二氯甲烷 为溶剂， 反应 73.0h， 生成 (2S,3R)-1-(2-ethyl-1H-pyrrol-1-yl)-2,3-dihydroxy-4-methylpentan-1-one 、 1-(2-ethyl-1H-pyrrol-1-yl)-2,3-dihydroxy-4-methylpentan-1-one
  参考文献：
  名称：

  Dinuclear Zinc–ProPhenol-Catalyzed Enantioselective α-Hydroxyacetate Aldol Reaction with Activated Ester Equivalents

  摘要：

  An enantioselective alpha-hydroxyacetate aldol reaction that employs N-acetyl pyrroles as activated ester equivalents and generates syn 1,2-diols in good yield and diastereoselectivity is reported. This dinuclear zinc-ProPhenol-catalyzed transformation proceeds with high enantioselectivity with a wide variety of substrates including aryl, alyl, and alkenyl aldehydes. The resulting alpha,beta-dihydroxy activated esters are versatile intermediates for the synthesis of a variety of carboxylic acid derivatives including amides, esters, and unsymmetrical ketones.

  DOI：

  10.1021/ol402081p

文献信息

• Dinuclear Zinc–ProPhenol-Catalyzed Enantioselective α-Hydroxyacetate Aldol Reaction with Activated Ester Equivalents
  作者：Barry M. Trost、David J. Michaelis、Mihai I. Truica

  DOI：10.1021/ol402081p

  日期：2013.9.6

  An enantioselective alpha-hydroxyacetate aldol reaction that employs N-acetyl pyrroles as activated ester equivalents and generates syn 1,2-diols in good yield and diastereoselectivity is reported. This dinuclear zinc-ProPhenol-catalyzed transformation proceeds with high enantioselectivity with a wide variety of substrates including aryl, alyl, and alkenyl aldehydes. The resulting alpha,beta-dihydroxy activated esters are versatile intermediates for the synthesis of a variety of carboxylic acid derivatives including amides, esters, and unsymmetrical ketones.