ethyl (3R)-3-(methoxymethoxy)-5-oxohept-6-enoate

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: ethyl (3R)-3-(methoxymethoxy)-5-oxohept-6-enoate
• 化学式: C₁₁H₁₈O₅
• 分子量: 230.26
• InChiKey: YWDGQUSEFQNKHT-SNVBAGLBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  16
• 可旋转键数：
  10
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  61.8
• 氢给体数：
  0
• 氢受体数：
  5

文献信息

• PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL IN THE SYNTHESIS OF STATIN DERIVATIVES ESPECIALLY 7-AMINO 3,5-DIHYDROXY HEPTANOIC ACID DERIVATIVES, AND INTERMEDIATES THEREOF
  申请人：Ciba Specialty Chemicals Holding Inc.

  公开号：EP1404639A1

  公开（公告）日：2004-04-07
• Synthesis and intermediates
  申请人：Ohrlein Reinhold

  公开号：US20080312466A1

  公开（公告）日：2008-12-18

  The invention relates to novel synthesis methods for the preparation of statin derivatives, which methods proceed by way of a key intermediate of formula I wherein X is halogen, acyloxy, activated hydrocarbyloxy, activated hydrocarbylthio or —N(CH 3 )OCH 3 , R a is a hydroxy-protecting group and R b is a carboxy-protecting group, and, as well as to the compound of formula I, to further new intermediates and methods for their preparation by Friedel-Crafts acylation.
• [EN] PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL IN THE SYNTHESIS OF STATIN DERIVATIVES ESPECIALLY 7-AMINO 3,5-DIHYDROXY HEPTANOIC ACID DERIVATIVES, AND INTERMEDIATES THEREOF<br/>[FR] PREPARATION D'INTERMEDIAIRES CONVENANT BIEN POUR LA SYNTHESE DE DERIVES DE STATINE, EN PARTICULIER DE DERIVES D'ACIDE 7-AMINO 3,5-DIHYDROXY HEPTANOIQUE ET DE DERIVES DE CET ACIDE
  申请人：CIBA SC HOLDING AG

  公开号：WO2003004450A1

  公开（公告）日：2003-01-16

  The invention relates to synthesis methods for the preparation of statin derivatives, which methods proceed by way of a key intermediate of formula I wherein X is halogen, acyloxy, activated hydrocarbyloxy, activated hydrocarbylthio or N(CH3)OCH3, Ra is a hydroxy-protecting group, and Rb is a carboxy-protecting group, and, as well as to the compound of formula I, to further intermediates and methods for their preparation by Friedel-Crafts acylation.