6-((2S,3S)-3-Isopropyl-oxiranyl)-hexan-2-one | 133909-65-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-((2S,3S)-3-Isopropyl-oxiranyl)-hexan-2-one
• CAS: 133909-65-6
• 化学式: C₁₁H₂₀O₂
• 分子量: 184.279
• InChiKey: DYSGBKACKUOSIT-QWRGUYRKSA-N

反应信息

• 作为反应物：
  描述：

  6-((2S,3S)-3-Isopropyl-oxiranyl)-hexan-2-one 在 三氟化硼乙醚 作用下， 以 二氯甲烷 为溶剂， 以70%的产率得到rel-(1R,6S,8S)-6-methyl-8-(1-methylethyl)-7,9-dioxabicyclo<4.2.1>nonane
  参考文献：
  名称：

  Stereochemical control in reactions of nucleophiles with oxocarbenium ions formed by intramolecular opening of activated epoxides by neighboring carbonyl groups

  摘要：

  Tandem cyclization/reduction and cyclization/alkylation processes for the stereoselective synthesis of 2,5-disubstituted tetrahydrofurans, 2,6-disubstituted tetrahydropyrans, and 2,7-disubstituted oxepanes are described. In the presence of Lewis acids or TMSOTf, gamma,delta-, delta,epsilon- and epsilon,zeta-epoxy ketones and esters undergo cyclization to the corresponding oxocarbenium ions, which react in situ with a variety of organosilanes and organoaluminum reagents to give the substituted oxacyclic products. For the synthesis of substituted tetrahydrofurans, the stereochemical control of the addition process was much higher with TMSOTf than BF3.OEt2.

  DOI：

  10.1021/jo00013a013