[1-(4-Bromophenyl)-3-phenylmethoxypropan-2-yl]oxy-tert-butyl-dimethylsilane | 157035-16-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: [1-(4-Bromophenyl)-3-phenylmethoxypropan-2-yl]oxy-tert-butyl-dimethylsilane
• CAS: 157035-16-0
• 化学式: C₂₂H₃₁BrO₂Si
• 分子量: 435.476
• InChiKey: PUXQBXXJYYSAIT-UHFFFAOYSA-N

物化性质

• 沸点：
  456.5±45.0 °C(predicted)
• 密度：
  1.145±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.6
• 重原子数：
  26
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 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：

  [1-(4-Bromophenyl)-3-phenylmethoxypropan-2-yl]oxy-tert-butyl-dimethylsilane 在 palladium on activated charcoal lithium hydroxide 、 copper(I) bromide dimethylsulfide complex 、 氢气 、 potassium carbonate 作用下， 以 四氢呋喃 、 吡啶 、 甲醇 、 乙酸乙酯 为溶剂， 反应 12.0h， 生成 3-[3-[4-[2-[Tert-butyl(dimethyl)silyl]oxy-3-hydroxypropyl]phenoxy]-4-methoxyphenyl]propanoic acid
  参考文献：
  名称：

  Synthesis of combretastatin D-2. An efficient route to caffrane macrolactones

  摘要：

  Combretastatin D-2, (1), was synthesized via a 10 step sequence. Macrolactonization was performed on saturated substrate 12 in high yield and the double bond was established via dehalogenation of intermediate 15.

  DOI：

  10.1016/s0040-4039(00)73369-7
• 作为产物：
  描述：

  3-(4-溴苯基)丙-2-烯-1-醇 在 咪唑 、 四丁基碘化铵 、 sodium hydride 、 二异丁基氢化铝 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 10.67h， 生成 [1-(4-Bromophenyl)-3-phenylmethoxypropan-2-yl]oxy-tert-butyl-dimethylsilane
  参考文献：
  名称：

  Total Synthesis of Combretastatins D

  摘要：

  The 15-membered caffrane ring of the natural product group of combretastatins D is synthesized in high yield with suitably functionalized saturated seco acids. The key step is a Mitsunobu-type macrolactonization. A common synthon is used for the construction of both combretastatins. The synthesis of combretastatin D-2 is completed by the use of Sammuelson's dehydroxylation protocol, The asymmetric epoxide of combretastatin D-1 is constructed in two separate operations: one asymmetric center is fixed at an early stage of the synthetic route by Sharpless AD of a trans-styrene derivative, inducing the intramolecular formation of the asymmetric epoxide at the final stages. The synthesis of the title compounds is accomplished in high overall yields (37% for D-1 and 41% for D-2, 9 steps in both cases). X-ray crystallographic analysis of the (S)-(+) acetylmandelic ester of (-)-combretastatin D-1 verified its revised structure.

  DOI：

  10.1002/(sici)1521-3765(199801)4:1<33::aid-chem33>3.0.co;2-8

文献信息

• Total Synthesis of Combretastatins D
  作者：Elias A. Couladouros、Ioanna C. Soufli、Vassilios I. Moutsos、Raj K. Chadha

  DOI：10.1002/(sici)1521-3765(199801)4:1<33::aid-chem33>3.0.co;2-8

  日期：1998.1

  The 15-membered caffrane ring of the natural product group of combretastatins D is synthesized in high yield with suitably functionalized saturated seco acids. The key step is a Mitsunobu-type macrolactonization. A common synthon is used for the construction of both combretastatins. The synthesis of combretastatin D-2 is completed by the use of Sammuelson's dehydroxylation protocol, The asymmetric epoxide of combretastatin D-1 is constructed in two separate operations: one asymmetric center is fixed at an early stage of the synthetic route by Sharpless AD of a trans-styrene derivative, inducing the intramolecular formation of the asymmetric epoxide at the final stages. The synthesis of the title compounds is accomplished in high overall yields (37% for D-1 and 41% for D-2, 9 steps in both cases). X-ray crystallographic analysis of the (S)-(+) acetylmandelic ester of (-)-combretastatin D-1 verified its revised structure.
• Synthesis of combretastatin D-2. An efficient route to caffrane macrolactones
  作者：Elias A. Couladouros、Ioanna C. Soufli

  DOI：10.1016/s0040-4039(00)73369-7

  日期：1994.6

  Combretastatin D-2, (1), was synthesized via a 10 step sequence. Macrolactonization was performed on saturated substrate 12 in high yield and the double bond was established via dehalogenation of intermediate 15.