(Z)-1-butyl-4,6,7,10-tetrahydro-3-methyl-4-phenylfuro[3,4-c]oxonine | 1188491-59-9

• 分子结构分类: 有机化合物 - 苯类化合物
• 英文名称: (Z)-1-butyl-4,6,7,10-tetrahydro-3-methyl-4-phenylfuro[3,4-c]oxonine
• CAS: 1188491-59-9
• 化学式: C₂₁H₂₆O₂
• 分子量: 310.436
• InChiKey: AGSGGHJXXRNLIX-TWGQIWQCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.54
• 重原子数：
  23.0
• 可旋转键数：
  4.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  22.37
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为产物：
  描述：

  3-allyl-4-((but-3-enyloxy)(phenyl)methyl)-2-butyl-5-methylfuran 在 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 作用下， 以 1,2-二氯乙烷 为溶剂， 以44%的产率得到(Z)-1-butyl-4,6,7,10-tetrahydro-3-methyl-4-phenylfuro[3,4-c]oxonine
  参考文献：
  名称：

  2-（1-炔基）-2-烯-1-酮与亲核试剂的钯（II）催化多米诺反应：范围，机理及在3,4-氟代双环四取代呋喃合成中的合成应用

  摘要：

  Abstractmagnified imageDescribed herein is the development of a palladium(II)‐catalyzed two‐ or three‐component reaction of 2‐(1‐alkynyl)‐2‐alken‐1‐ones with nucleophiles and allylic chlorides. Various types of nucleophiles such as O‐, N‐, C‐based nucleophiles and olefin‐tethered O‐, N‐, C‐based nucleophiles were investigated. The scope, mechanism and application of this Pd(II)‐catalyzed domino reaction were studied. In these transformations, the palladium catalyst exhibits a dual role, serving simultaneously as a Lewis acid and a transition metal. Two possible reaction pathways (cross‐coupling reaction vs. Heck reaction) from the same intermediate furanylpalladium species were observed. The reaction pathway is dependent on the property of the nucleophile and the length of the tethered chain as well. When olefin‐tethered O‐based nucleophiles were used, only the cross‐coupling reaction pathway was observed, in contrast, both reaction pathways were observed when olefin‐tethered C‐based nucleophiles were employed. The product ratio is dependent on the length of the tethered chain. Furthermore, ring‐closing metathesis (RCM) of corresponding furans with CC bonds provides an easy method for the preparation of functionalized oxygen‐heterocycles – 3,4‐fused bicyclic furans. It is also noteworthy that allylic chloride can be as an oxidant besides its well known function as an alkylating reagent.

  DOI：

  10.1002/adsc.200800715