(R)-4-((S)-(tert-butyldimethylsilyloxy)(4-(tert-butyldimethylsilyloxy)-3-methoxyphenyl)methyl)dihydrofuran-2(3H)-one | 1428741-25-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (R)-4-((S)-(tert-butyldimethylsilyloxy)(4-(tert-butyldimethylsilyloxy)-3-methoxyphenyl)methyl)dihydrofuran-2(3H)-one
• 英文别名: (4R)-4-[(S)-[tert-butyl(dimethyl)silyl]oxy-[4-[tert-butyl(dimethyl)silyl]oxy-3-methoxyphenyl]methyl]oxolan-2-one
• CAS: 1428741-25-6
• 化学式: C₂₄H₄₂O₅Si₂
• 分子量: 466.765
• InChiKey: CLCWXVRJTVUADO-XMSQKQJNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.71
• 重原子数：
  31
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (R)-4-((S)-(tert-butyldimethylsilyloxy)(4-(tert-butyldimethylsilyloxy)-3-methoxyphenyl)methyl)dihydrofuran-2(3H)-one 在 六甲基磷酰三胺 、 四丁基氟化铵 、 双(三甲基硅烷基)氨基钾 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 30.25h， 生成 (─)-7'(S)-hydroxymatairesinol
  参考文献：
  名称：

  Asymmetric aldol approach to dibenzylbutyrolactone lignans: synthesis of (−)-(7′S)-hydroxymatairesinol and (−)-(7′S)-hydroxyarctigenin

  摘要：

  A competent and general asymmetric synthesis of 7'-hydroxydibenzylbutyrolactone lignans such as (7'S)-hydroxymatairesinol and (7'S)-hydroxyarctigenin has been reported from N-succinyl-2-oxazolidinone in six steps where diastereoselective aldol reaction and stereoselective alkylation serve as the key steps. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.02.044
• 作为产物：
  描述：

  O-tert-butyldimethylsilylvanillin 在 2,6-二甲基吡啶 、 4-二甲氨基吡啶 、 lithium hydroxide monohydrate 、 dimethyl sulfide borane 、 双氧水 、 双环己基(三氟甲烷磺酰氧基)硼烷 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 反应 36.0h， 生成 (R)-4-((S)-(tert-butyldimethylsilyloxy)(4-(tert-butyldimethylsilyloxy)-3-methoxyphenyl)methyl)dihydrofuran-2(3H)-one
  参考文献：
  名称：

  Asymmetric aldol approach to dibenzylbutyrolactone lignans: synthesis of (−)-(7′S)-hydroxymatairesinol and (−)-(7′S)-hydroxyarctigenin

  摘要：

  A competent and general asymmetric synthesis of 7'-hydroxydibenzylbutyrolactone lignans such as (7'S)-hydroxymatairesinol and (7'S)-hydroxyarctigenin has been reported from N-succinyl-2-oxazolidinone in six steps where diastereoselective aldol reaction and stereoselective alkylation serve as the key steps. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.02.044

文献信息

• Asymmetric aldol approach to dibenzylbutyrolactone lignans: synthesis of (−)-(7′S)-hydroxymatairesinol and (−)-(7′S)-hydroxyarctigenin
  作者：Saumen Hajra、Abhisek Mandal、Sunit Hazra

  DOI：10.1016/j.tetlet.2013.02.044

  日期：2013.4

  A competent and general asymmetric synthesis of 7'-hydroxydibenzylbutyrolactone lignans such as (7'S)-hydroxymatairesinol and (7'S)-hydroxyarctigenin has been reported from N-succinyl-2-oxazolidinone in six steps where diastereoselective aldol reaction and stereoselective alkylation serve as the key steps. (C) 2013 Elsevier Ltd. All rights reserved.