(3-(benzyloxy)-5-(6-(hydroxymethyl)-2,3,4-trimethoxyphenoxy)-4-methoxyphenyl)methanol | 1010094-01-5

• 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: (3-(benzyloxy)-5-(6-(hydroxymethyl)-2,3,4-trimethoxyphenoxy)-4-methoxyphenyl)methanol
• CAS: 1010094-01-5
• 化学式: C₂₅H₂₈O₈
• 分子量: 456.493
• InChiKey: CNWZCLXSBWLLJN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.08
• 重原子数：
  33.0
• 可旋转键数：
  11.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  95.84
• 氢给体数：
  2.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  (3-(benzyloxy)-5-(6-(hydroxymethyl)-2,3,4-trimethoxyphenoxy)-4-methoxyphenyl)methanol 在 吡啶 、 4-二甲氨基吡啶 、 硼烷四氢呋喃络合物 、 palladium 10% on activated carbon 、 potassium tert-butylate 、 氢气 、 sodium acetate 、 palladium diacetate 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三苯基膦 、 (S)-2-甲基-CBS-恶唑硼烷 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 N,N-二甲基乙酰胺 为溶剂， -40.0~20.0 ℃ 、101.33 kPa 条件下， 反应 170.25h， 生成 (S)-6-acetoxymethyl-6'-hydroxymethyl-4-(6-acetoxymethyl-2,3,4-trimethoxyphenoxy)-2,2',3,3',4'-pentamethoxy-1,1'-biphenyl
  参考文献：
  名称：

  Syntheses of all-methylated ellagitannin, isorugosin B and rugosin B

  摘要：

  Ellagitannins possess a wide range of biological activities and remarkable structural diversity, which commonly include an axially chiral biaryl unit. This paper describes syntheses of all-methylated versions of isorugosin B and rugosin B, which are regioisomeric, ellagitannin-related compounds. The key features of these syntheses involve the construction of an axially chiral biaryl function on a sugar moiety through a Pd-catalyzed intramolecular biaryl coupling reaction, Bringmann's atroposelective lactone opening reaction, and a two-step ester formation. This is the first synthetic approach for generating ellagitannins featuring a valoneoyl group. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.01.004
• 作为产物：
  描述：

  methyl 3-(benzyloxy)-5-hydroxy-4-methoxybenzoate 在 lithium aluminium tetrahydride 、 铜 作用下， 以 四氢呋喃 为溶剂， 反应 6.0h， 生成 (3-(benzyloxy)-5-(6-(hydroxymethyl)-2,3,4-trimethoxyphenoxy)-4-methoxyphenyl)methanol
  参考文献：
  名称：

  Syntheses of all-methylated ellagitannin, isorugosin B and rugosin B

  摘要：

  Ellagitannins possess a wide range of biological activities and remarkable structural diversity, which commonly include an axially chiral biaryl unit. This paper describes syntheses of all-methylated versions of isorugosin B and rugosin B, which are regioisomeric, ellagitannin-related compounds. The key features of these syntheses involve the construction of an axially chiral biaryl function on a sugar moiety through a Pd-catalyzed intramolecular biaryl coupling reaction, Bringmann's atroposelective lactone opening reaction, and a two-step ester formation. This is the first synthetic approach for generating ellagitannins featuring a valoneoyl group. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.01.004

文献信息

• Enantioselective synthesis of valoneic acid derivative
  作者：Hitoshi Abe、Yusuke Sahara、Yuki Matsuzaki、Yasuo Takeuchi、Takashi Harayama

  DOI：10.1016/j.tetlet.2007.11.154

  日期：2008.1

  The enantioselective synthesis of trimethyl octa-O-methylvaloneate (1) was accomplished using the Bringniann's 'lactone concept', which involves the intramolecular biaryl coupling reaction of a phenyl benzoate derivative and the asymmetric lactone-opening reaction. (c) 2007 Elsevier Ltd. All rights reserved.