(6S,7S)-bis(tert-butyldimethylsilyloxy)dec-1-en-8-yne | 306287-24-1

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: (6S,7S)-bis(tert-butyldimethylsilyloxy)dec-1-en-8-yne
• 英文别名: tert-butyl-[(4S,5S)-4-[tert-butyl(dimethyl)silyl]oxydec-9-en-2-yn-5-yl]oxy-dimethylsilane
• CAS: 306287-24-1
• 化学式: C₂₂H₄₄O₂Si₂
• 分子量: 396.761
• InChiKey: LIYPGSWIWIRCDM-PMACEKPBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.15
• 重原子数：
  26
• 可旋转键数：
  11
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (6S,7S)-bis(tert-butyldimethylsilyloxy)dec-1-en-8-yne 在 dicobalt octacarbonyl 、 N-丁基甲基硫醚 、 ammonium cerium(IV) nitrate 作用下， 以 乙醚 、 1,2-二氯乙烷 、 甲醇 为溶剂， 反应 4.0h， 生成 (E)-(6S,7S)-6,7-Bis-(tert-butyl-dimethyl-silanyloxy)-dec-2-en-8-yne
  参考文献：
  名称：

  Pauson−Khand Reaction of Optically Active 6,7-Bis(tert-butyldimethylsiloxy)non-1-en-8-ynes

  摘要：

  Treatment of(6S, 7S)-7-bis(tert-butyldimethylsiloxy)non-1-en-8-ynes with dicobalt octacarbonyl gave the corresponding cobalt complex. This complex was subsequently exposed to the Pauson-Khand conditions in the presence of a promoter such as cyclohexylamine, thioanisole, methyl isopropyl sulfide, and butyl methyl sulfide ending up with the stereoselective production of the (2S, 3S, 6S, 7S)-7-methylbicyclo[4.3.0]nonenone derivatives instead of the expected (2S, 3S, 7S)-bicyclo[5.3.0]decenone species.

  DOI：

  10.1021/jo0008082
• 作为产物：
  描述：

  (3S,4S)-1,1-dibromo-3,4-(isopropylidenedioxy)nona-1,8-diene 在 咪唑 、 盐酸 、 正丁基锂 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 生成 (6S,7S)-bis(tert-butyldimethylsilyloxy)dec-1-en-8-yne 、 alkaline earth salt of/the/ methylsulfuric acid
  参考文献：
  名称：

  Pauson−Khand Reaction of Optically Active 6,7-Bis(tert-butyldimethylsiloxy)non-1-en-8-ynes

  摘要：

  Treatment of(6S, 7S)-7-bis(tert-butyldimethylsiloxy)non-1-en-8-ynes with dicobalt octacarbonyl gave the corresponding cobalt complex. This complex was subsequently exposed to the Pauson-Khand conditions in the presence of a promoter such as cyclohexylamine, thioanisole, methyl isopropyl sulfide, and butyl methyl sulfide ending up with the stereoselective production of the (2S, 3S, 6S, 7S)-7-methylbicyclo[4.3.0]nonenone derivatives instead of the expected (2S, 3S, 7S)-bicyclo[5.3.0]decenone species.

  DOI：

  10.1021/jo0008082

文献信息

• Pauson−Khand Reaction of Optically Active 6,7-Bis(<i>tert</i>-butyldimethylsiloxy)non-1-en-8-ynes
  作者：Chisato Mukai、Hiroshi Sonobe、Jin Sung Kim、Miyoji Hanaoka

  DOI：10.1021/jo0008082

  日期：2000.10.1

  Treatment of(6S, 7S)-7-bis(tert-butyldimethylsiloxy)non-1-en-8-ynes with dicobalt octacarbonyl gave the corresponding cobalt complex. This complex was subsequently exposed to the Pauson-Khand conditions in the presence of a promoter such as cyclohexylamine, thioanisole, methyl isopropyl sulfide, and butyl methyl sulfide ending up with the stereoselective production of the (2S, 3S, 6S, 7S)-7-methylbicyclo[4.3.0]nonenone derivatives instead of the expected (2S, 3S, 7S)-bicyclo[5.3.0]decenone species.