顺式-1,3-二乙酰氧基环己烷 | 832-09-7

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 顺式-1,3-二乙酰氧基环己烷
• 英文名称: cis-1.3-Diacetoxy-cyclohexan
• 英文别名: cis-1,3-Diacetoxycyclohexane；[(1S,3R)-3-acetyloxycyclohexyl] acetate
• CAS: 832-09-7
• 化学式: C₁₀H₁₆O₄
• 分子量: 200.235
• InChiKey: PIAZUOCNDRREHF-AOOOYVTPSA-N

物化性质

• 沸点：
  249.7±33.0 °C(Predicted)
• 密度：
  1.09±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 海关编码：
  2915390090

反应信息

• 作为产物：
  描述：

  cis-1,3-cyclohexanediol 生成 顺式-1,3-二乙酰氧基环己烷
  参考文献：
  名称：

  339.间苯二酚。第一部分

  摘要：

  DOI：

  10.1039/jr9490001586

文献信息

• Rhodium(I)-catalyzed hydroboration of olefins. The documentation of regio- and stereochemical control in cyclic and acyclic systems
  作者：David A. Evans、Gregory C. Fu、Amir H. Hoveyda

  DOI：10.1021/ja00228a068

  日期：1988.9

  Catalyse par les complexes Rh(PPh 3 ) 3 Cl et [Rh(nbd)(diphos-4)]BF 4 (nbd=norbornadiene, diphos-4=bis-diphenylphosphino-1,4 butane)

  催化复合物 Rh(PPh 3 ) 3 Cl et [Rh(nbd)(diphos-4)]BF 4 (nbd=降冰片二烯，diphos-4=双-二苯基膦基-1,4丁烷)
• Rhodium(I)- and iridium(I)-catalyzed hydroboration reactions: scope and synthetic applications
  作者：David A. Evans、Gregory C. Fu、Amir H. Hoveyda

  DOI：10.1021/ja00043a009

  日期：1992.8

  A study of the rhodium(1)- and iridium(1)-catalyzed hydroboration of olefins with catecholborane is described. Applications to organic synthesis were one focus of this investigation. The scope of the reaction was defined, and issues of stereoselection were addressed. The rhodium-catalyzed hydroboration of several classes of allylic alcohols was found to be highly diastereoselective, preferentially

  描述了铑 (1)-和铱 (1)-催化烯烃与儿茶酚硼烷硼氢化的研究。有机合成的应用是这项研究的重点之一。定义了反应的范围，并解决了立体选择问题。发现几类烯丙醇的铑催化硼氢化反应具有高度的非对映选择性，优先提供与未催化反应变体 (9-BBN) 提供的异构体互补的异构体。开发了实现定向烯烃硼氢化的前两种通用方法。亚膦酸盐和酰胺都证明能够传递过渡金属试剂。
• METHOD FOR THE PRODUCTION OF DIARYLCYCLOALKYL DERIVATIVES
  申请人：Salagnad Christophe

  公开号：US20070197614A1

  公开（公告）日：2007-08-23

  The invention relates generally to a process for preparing diarylcycloalkyl derivatives of the formula (I). wherein the respective R-group substituents are defined herein. These compounds of formula (I) are activators for peroxisome proliferator-activated receptors (PPAR activators) which are useful in the therapeutic treatment of a number of diseases and disorders of the central nervous system such as multiple sclerosis, Parkinson's Disease, psychiatric disorders and the like. The present invention is a novel process for preparing PPAR activators of the formula (I) which do not have the disadvantages of the processes known in the prior art. In particular, a process is provided with which the PPAR activators of formula (I) can be prepared in a suitable enantiomeric excess, i.e. high enantioselectivity, without the need for subsequent chiral chromatography.

  本发明涉及一种制备公式（I）的二芳基环烷基衍生物的方法，其中各自的R基取代基如本文所定义。公式（I）化合物是过氧化物酶体增殖物激活受体（PPAR激活剂），在治疗多发性硬化症、帕金森病、精神障碍等中枢神经系统疾病和疾病方面非常有用。本发明提供了一种新的制备公式（I）的PPAR激活剂的方法，该方法不具有先前技术中已知的缺点。特别是，提供了一种方法，可以在不需要后续手性色谱的情况下以适当的对映选择性制备公式（I）的PPAR激活剂，即高对映选择性。
• NOVEL INTERMEDIATE COMPOUNDS USEFUL IN THE PRODUCTION OF DIARYLCYCLOALKYL DERIVATIVES
  申请人：Salagnad Christophe

  公开号：US20080051583A1

  公开（公告）日：2008-02-28

  The invention relates generally to intermediate compounds derived during the process for preparing diarylcycloalkyl derivatives which are activators for peroxisome proliferator-activated receptors (PPAR activators) and are therefore useful in the therapeutic treatment of a number of diseases and disorders of the central nervous system such as multiple sclerosis, Parkinson's Disease, psychiatric disorders and the like. The intermediate compounds of the present invention are defined structurally by the formulae (Ia): and formula (II): wherein the respective substituent groups are defined herein.

  本发明涉及制备二苯基环烷衍生物的过程中产生的中间化合物，该化合物是过氧化物酶体增殖物活化受体（PPAR活化剂），因此在治疗多发性硬化症、帕金森病、精神障碍等中枢神经系统疾病和疾病方面具有用处。本发明的中间化合物在结构上由公式（Ia）和公式（II）定义，其中各取代基在此定义。
• Method for the production of diarylcycloalkyl derivatives
  申请人：Sanofi-Aventis Deutschland GmbH

  公开号：US07803950B2

  公开（公告）日：2010-09-28

  The invention relates generally to a process for preparing diarylcycloalkyl derivatives of the formula (I). wherein the respective R-group substituents are defined herein. These compounds of formula (I) are activators for peroxisome proliferator-activated receptors (PPAR activators) which are useful in the therapeutic treatment of a number of diseases and disorders of the central nervous system such as multiple sclerosis, Parkinson's Disease, psychiatric disorders and the like. The present invention is a novel process for preparing PPAR activators of the formula (I) which do not have the disadvantages of the processes known in the prior art. In particular, a process is provided with which the PPAR activators of formula (I) can be prepared in a suitable enantiomeric excess, i.e. high enantioselectivity, without the need for subsequent chiral chromatography.

  本发明涉及一种制备公式（I）的二芳基环烷基衍生物的过程，其中各自的R基取代基在此定义。这些公式（I）化合物是过氧化物酶体增殖物激活受体（PPAR激活剂），可用于治疗中枢神经系统的多种疾病和障碍，如多发性硬化症，帕金森病，精神障碍等。本发明是一种新型制备公式（I）的PPAR激活剂的过程，其不具有先前技术中已知的缺点。特别是，提供了一种方法，可以在不需要后续手性色谱的情况下制备公式（I）的PPAR激活剂，即高对映选择性，以适当的对映异构体过量。