(2S,3R,4S,5S)-3,4-O-isopropylidene-5-phenyl-2-((naphthalen-2-yl)methyl)tetrahydrofuran-3,4-diol

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (2S,3R,4S,5S)-3,4-O-isopropylidene-5-phenyl-2-((naphthalen-2-yl)methyl)tetrahydrofuran-3,4-diol
• 英文别名: (3aS,4S,6S,6aR)-2,2-dimethyl-6-(naphthalen-2-ylmethyl)-4-phenyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxole
• 化学式: C₂₄H₂₄O₃
• 分子量: 360.453
• InChiKey: OUISOWSDDRCSPR-GPJHCHHRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  27
• 可旋转键数：
  3
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  27.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2-溴萘 、 (2S,3R)-2,3-O-isopropylidene-1-phenyl-pent-4-ene-1,2,3-triol 在 双(2-二苯基磷苯基)醚 、 bis(dibenzylideneacetone)-palladium⁽⁰⁾ 、 sodium t-butanolate 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 生成 (2S,3R,4S,5S)-3,4-O-isopropylidene-5-phenyl-2-((naphthalen-2-yl)methyl)tetrahydrofuran-3,4-diol 、 (2R,3R,4S,5R)-3,4-O-isopropylidene-5-phenyl-2-((naphthalen-2-yl)methyl)tetrahydrofuran-3,4-diol
  参考文献：
  名称：

  Domino reaction: Pd(II)-catalyzed cyclization of unsaturated polyols and cross-coupling

  摘要：

  The Pd-catalyzed cyclization and cross-coupling of hydroxylated alkenes in domino reactions are described. The alkenols undergo Pd-catalyzed cyclization and subsequent cross-coupling reactions with aryl bromides to afford (poly)hydroxylated tetrahydrofuran derivatives. The relationship between the stereoselectivity of the transformation and the steric and/or electronic effects of the substrates has also been studied. The diastereoselectivity of the cyclization of gamma-hydroxyalkenes 1.4-6 is influenced by the allylic hydroxyl functionality in favor of 2,3-cis stereoselectivity. Substitution at the C-1 carbon in alkenitols 7 and 8 ensured the formation of products with 2,5-trans diastereoselectivity (up to >19:1), independent of additional substituents. (c) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2012.05.020

文献信息

• Domino reaction: Pd(II)-catalyzed cyclization of unsaturated polyols and cross-coupling
  作者：Angelika Lásiková、Jana Doháňošová、Lucia Hlavínová、Martial Toffano、Giang Vo-Thanh、Jozef Kožíšek、Tibor Gracza

  DOI：10.1016/j.tetasy.2012.05.020

  日期：2012.6

  The Pd-catalyzed cyclization and cross-coupling of hydroxylated alkenes in domino reactions are described. The alkenols undergo Pd-catalyzed cyclization and subsequent cross-coupling reactions with aryl bromides to afford (poly)hydroxylated tetrahydrofuran derivatives. The relationship between the stereoselectivity of the transformation and the steric and/or electronic effects of the substrates has also been studied. The diastereoselectivity of the cyclization of gamma-hydroxyalkenes 1.4-6 is influenced by the allylic hydroxyl functionality in favor of 2,3-cis stereoselectivity. Substitution at the C-1 carbon in alkenitols 7 and 8 ensured the formation of products with 2,5-trans diastereoselectivity (up to >19:1), independent of additional substituents. (c) 2012 Elsevier Ltd. All rights reserved.