(1S,3R,7R,10R,12S,13R)-13-(methoxymethoxy)-1,3,12-trimethyl-12-[(1S)-1-(naphthalen-2-ylmethoxy)but-3-enyl]-2,6,11-trioxatricyclo[8.4.0.03,7]tetradecan-5-one | 934810-57-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (1S,3R,7R,10R,12S,13R)-13-(methoxymethoxy)-1,3,12-trimethyl-12-[(1S)-1-(naphthalen-2-ylmethoxy)but-3-enyl]-2,6,11-trioxatricyclo[8.4.0.03,7]tetradecan-5-one
• CAS: 934810-57-8
• 化学式: C₃₁H₄₀O₇
• 分子量: 524.654
• InChiKey: DIHXIWGXZYUZFD-WTYSFWMLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  38
• 可旋转键数：
  9
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.58
• 拓扑面积：
  72.4
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  (1S,3R,7R,10R,12S,13R)-13-(methoxymethoxy)-1,3,12-trimethyl-12-[(1S)-1-(naphthalen-2-ylmethoxy)but-3-enyl]-2,6,11-trioxatricyclo[8.4.0.03,7]tetradecan-5-one 在 草酰氯 、 二异丁基氢化铝 、 二甲基亚砜 、 三乙胺 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 生成 (2S,3R,4aS,6R,7S,9aR)-6-[(Z)-4-hydroxy-3-methoxybut-2-enyl]-3-(methoxymethoxy)-2,4a,6-trimethyl-2-[(1S)-1-(naphthalen-2-ylmethoxy)but-3-enyl]-3,4,7,8,9,9a-hexahydropyrano[3,2-b]oxepin-7-ol
  参考文献：
  名称：

  Synthesis of the LMN-ring fragment of the Caribbean ciguatoxin C-CTX-1

  摘要：

  Ciguatoxin C-CTX-1 was isolated as a principal causative toxin of ciguatera seafood poisoning in the Caribbean Sea, and is structurally classified as a ladder-shaped polycyclic ether. In this Letter, we report the synthesis of the tricyclic LMN-ring system of C-CTX-1. SmI2-mediated reductive cyclization efficiently constructed the seven-membered M-ring with the axially oriented 1,3-dimethyl structure. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.01.103
• 作为产物：
  描述：

  在 咪唑 、 4-二甲氨基吡啶 、 samarium diiodide 、 草酰氯 、 四丁基氟化铵 、 potassium tri-sec-butyl-borohydride 、 二甲基亚砜 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 甲苯 、 叔丁醇 为溶剂， 反应 24.0h， 生成 (1S,3R,7R,10R,12S,13R)-13-(methoxymethoxy)-1,3,12-trimethyl-12-[(1S)-1-(naphthalen-2-ylmethoxy)but-3-enyl]-2,6,11-trioxatricyclo[8.4.0.03,7]tetradecan-5-one
  参考文献：
  名称：

  Synthesis of the LMN-ring fragment of the Caribbean ciguatoxin C-CTX-1

  摘要：

  Ciguatoxin C-CTX-1 was isolated as a principal causative toxin of ciguatera seafood poisoning in the Caribbean Sea, and is structurally classified as a ladder-shaped polycyclic ether. In this Letter, we report the synthesis of the tricyclic LMN-ring system of C-CTX-1. SmI2-mediated reductive cyclization efficiently constructed the seven-membered M-ring with the axially oriented 1,3-dimethyl structure. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.01.103

文献信息

• Synthesis of the LMN-ring fragment of the Caribbean ciguatoxin C-CTX-1
  作者：Keita Yoshikawa、Masayuki Inoue、Masahiro Hirama

  DOI：10.1016/j.tetlet.2007.01.103

  日期：2007.3

  Ciguatoxin C-CTX-1 was isolated as a principal causative toxin of ciguatera seafood poisoning in the Caribbean Sea, and is structurally classified as a ladder-shaped polycyclic ether. In this Letter, we report the synthesis of the tricyclic LMN-ring system of C-CTX-1. SmI2-mediated reductive cyclization efficiently constructed the seven-membered M-ring with the axially oriented 1,3-dimethyl structure. (c) 2007 Elsevier Ltd. All rights reserved.