(2R,3S,8R)-8-(tert-Butyl-diphenyl-silanyloxymethyl)-2-ethyl-5-(toluene-4-sulfonyl)-oxocan-3-ol | 185012-50-4

• 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: (2R,3S,8R)-8-(tert-Butyl-diphenyl-silanyloxymethyl)-2-ethyl-5-(toluene-4-sulfonyl)-oxocan-3-ol
• 英文别名: (2R,3S,8R)-8-[[tert-butyl(diphenyl)silyl]oxymethyl]-2-ethyl-5-(4-methylphenyl)sulfonyloxocan-3-ol
• CAS: 185012-50-4
• 化学式: C₃₃H₄₄O₅SSi
• 分子量: 580.861
• InChiKey: ROVJBQPJYANVBE-WEEZNATMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.42
• 重原子数：
  40
• 可旋转键数：
  9
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  81.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (2R,3S,8R)-8-(tert-Butyl-diphenyl-silanyloxymethyl)-2-ethyl-5-(toluene-4-sulfonyl)-oxocan-3-ol 在 草酰氯 、 TEA 、 sodium hydride 、 二甲基亚砜 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 potassium iodide 作用下， 以 甲苯 为溶剂， 反应 26.33h， 生成 (2R,3R,8R)-8-(((tert-butyldiphenylsilyl)oxy)methyl)-3-(benzyloxy)-2-ethyl-3,4,7,8-tetrahydro-2H-oxocin
  参考文献：
  名称：

  Enantioselective Synthesis of α,β,α‘-Trisubstituted Cyclic Ethers

  摘要：

  A synthetic strategy for the preparation of trisusbstituted cyclic ethers is presented, in which the stereochemistry at the carbon atoms adjacent to the oxygen of the ether was controlled by means of a hetero Diels-Alder reaction between a monoactivated diene and a chiral aldehyde. The adducts were transformed into linear ethers, which were then used for the preparation of cis and trans cyclic ethers of different sizes. A cis-oxepane, cis-oxonane, and cis-oxocane and a trans-oxocane were prepared as examples of the scope of the strategy.

  DOI：

  10.1021/jo981188w
• 作为产物：
  描述：

  tert-Butyl-[(R)-2-((R)-(S)-1-oxiranyl-propoxy)-5-(toluene-4-sulfonyl)-pentyloxy]-diphenyl-silane 在 lithium diisopropyl amide 作用下， 以 四氢呋喃 为溶剂， 反应 0.42h， 生成 (2R,3S,8R)-8-(tert-Butyl-diphenyl-silanyloxymethyl)-2-ethyl-5-(toluene-4-sulfonyl)-oxocan-3-ol
  参考文献：
  名称：

  Enantioselective Synthesis of α,β,α‘-Trisubstituted Cyclic Ethers

  摘要：

  A synthetic strategy for the preparation of trisusbstituted cyclic ethers is presented, in which the stereochemistry at the carbon atoms adjacent to the oxygen of the ether was controlled by means of a hetero Diels-Alder reaction between a monoactivated diene and a chiral aldehyde. The adducts were transformed into linear ethers, which were then used for the preparation of cis and trans cyclic ethers of different sizes. A cis-oxepane, cis-oxonane, and cis-oxocane and a trans-oxocane were prepared as examples of the scope of the strategy.

  DOI：

  10.1021/jo981188w