(R)-4-Allyl-4-[(S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-cyclohex-2-enone | 226546-04-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (R)-4-Allyl-4-[(S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-cyclohex-2-enone
• 英文别名: (4R)-4-[(2S)-1-[tert-butyl(diphenyl)silyl]oxybut-3-en-2-yl]-4-prop-2-enylcyclohex-2-en-1-one
• CAS: 226546-04-9
• 化学式: C₂₉H₃₆O₂Si
• 分子量: 444.689
• InChiKey: BSIPQTVYOOWYKF-FUFSCUOVSA-N

物化性质

• 沸点：
  505.561±43.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.030±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.85
• 重原子数：
  32
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (R)-4-Allyl-4-[(S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-cyclohex-2-enone 在 Grubbs catalyst first generation 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 4.0h， 以89%的产率得到(1S,5R)-1-(tert-Butyl-diphenyl-silanyloxymethyl)-spiro[4.5]deca-2,6-dien-8-one
  参考文献：
  名称：

  An Asymmetric Route to Novel Chiral Cyclohexenones with Spiro-Connected Cyclopentenes. Further Utility of Chiral Bicyclic Thiolactams and the [3,3] Thio-Claisen Products

  摘要：

  Sequential allylation of chiral, nonracemic thiolactam 8 affords clean thio-Claisen [3,3] products ii. The stereoselectivity of the rearrangement was found to be on the order of 10-11:1, with the exo-endo products responsible for the mixture. Addition of hydride or methyllithium-cerium chloride gave clean addition to the thiolactam in the form of its iminium salts 12. Hydrolysis gave 4,4-dialkylcyclohexenones 16, which were cyclized to the cyclopentene derivatives 16 using Grubbs' catalyst.

  DOI：

  10.1021/jo982426q
• 作为产物：
  描述：

  (E)-4-(tert-butyldiphenylsilyloxy)-2-buten-1-ol 在 N-溴代丁二酰亚胺(NBS) 、 二甲基硫 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 1.0h， 生成 (R)-4-Allyl-4-[(S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-cyclohex-2-enone
  参考文献：
  名称：

  An Asymmetric Route to Novel Chiral Cyclohexenones with Spiro-Connected Cyclopentenes. Further Utility of Chiral Bicyclic Thiolactams and the [3,3] Thio-Claisen Products

  摘要：

  Sequential allylation of chiral, nonracemic thiolactam 8 affords clean thio-Claisen [3,3] products ii. The stereoselectivity of the rearrangement was found to be on the order of 10-11:1, with the exo-endo products responsible for the mixture. Addition of hydride or methyllithium-cerium chloride gave clean addition to the thiolactam in the form of its iminium salts 12. Hydrolysis gave 4,4-dialkylcyclohexenones 16, which were cyclized to the cyclopentene derivatives 16 using Grubbs' catalyst.

  DOI：

  10.1021/jo982426q