(2S)-2-(t-Butyldimethylsilyloxy)-2-<(4R)-2,2-dimethyl-1,3-dioxolan-4-yl>-3-butynal | 140429-13-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S)-2-(t-Butyldimethylsilyloxy)-2-<(4R)-2,2-dimethyl-1,3-dioxolan-4-yl>-3-butynal
• CAS: 140429-13-6
• 化学式: C₁₅H₂₆O₄Si
• 分子量: 298.455
• InChiKey: OMFXBPMLRVFQGL-DOMZBBRYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.73
• 重原子数：
  20.0
• 可旋转键数：
  4.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  44.76
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (2S)-2-(t-Butyldimethylsilyloxy)-2-<(4R)-2,2-dimethyl-1,3-dioxolan-4-yl>-3-butynal 在 四(三苯基膦)钯 copper(l) iodide 、 二乙胺 作用下， 以 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 1.09h， 生成 (2S)-2-(t-Butyldimethylsilyloxy)-2-<(4R)-2,2-dimethyl-1,3-dioxolan-4-yl>-4-<(5Z)-5-(3-trimethylsilyl-2-propynylidene)-1-cyclopenten-1-yl>-3-butynal
  参考文献：
  名称：

  Synthetic studies on the compounds related to neocarzinostatin chromophore. 1. Synthesis of the acyclic (E)- and (Z)-dienediyne systems

  摘要：

  The stereo-defined (E)- and (Z)-dienediyne systems related to neocarzinostatin chromophore (1) could be prepared by the coupling reaction of (E)- and (Z)-enol triflates with optically active acetylynes hearing the correct absolute stereochemistries as found in 1. Comparison of cytotoxic level of the (E)- and (Z)-dienediyne diols (32 and 33) revealed that the stereochemistry of exo-trisubstituted double bond might have a posibility to control the cytotoxicity of the acyclic analogues related to I.

  DOI：

  10.1016/s0040-4020(01)88124-2
• 作为产物：
  描述：

  叔丁基二甲硅基三氟甲磺酸酯 在 2,6-二甲基吡啶 、 pyridine-SO3 complex 、 二异丁基氢化铝 、 三乙胺 作用下， 以 正己烷 、 二氯甲烷 、 二甲基亚砜 为溶剂， 反应 4.0h， 生成 (2S)-2-(t-Butyldimethylsilyloxy)-2-<(4R)-2,2-dimethyl-1,3-dioxolan-4-yl>-3-butynal
  参考文献：
  名称：

  Synthetic studies on the compounds related to neocarzinostatin chromophore. 1. Synthesis of the acyclic (E)- and (Z)-dienediyne systems

  摘要：

  The stereo-defined (E)- and (Z)-dienediyne systems related to neocarzinostatin chromophore (1) could be prepared by the coupling reaction of (E)- and (Z)-enol triflates with optically active acetylynes hearing the correct absolute stereochemistries as found in 1. Comparison of cytotoxic level of the (E)- and (Z)-dienediyne diols (32 and 33) revealed that the stereochemistry of exo-trisubstituted double bond might have a posibility to control the cytotoxicity of the acyclic analogues related to I.

  DOI：

  10.1016/s0040-4020(01)88124-2

文献信息

• Synthetic studies on the compounds related to neocarzinostatin chromophore. 1. Synthesis of the acyclic (E)- and (Z)-dienediyne systems
  作者：Kazuhiko Nakatani、Katsuko Arai、Noriaki Hirayama、Fuyuhiko Matsuda、Shiro Terashima

  DOI：10.1016/s0040-4020(01)88124-2

  日期：——

  The stereo-defined (E)- and (Z)-dienediyne systems related to neocarzinostatin chromophore (1) could be prepared by the coupling reaction of (E)- and (Z)-enol triflates with optically active acetylynes hearing the correct absolute stereochemistries as found in 1. Comparison of cytotoxic level of the (E)- and (Z)-dienediyne diols (32 and 33) revealed that the stereochemistry of exo-trisubstituted double bond might have a posibility to control the cytotoxicity of the acyclic analogues related to I.