6-Methyl-7-(5-oxazolyl)-α,α-di-1-propynyl-1,4-dioxaspiro<4.4>non-7-ene-6-methanol | 122277-71-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-Methyl-7-(5-oxazolyl)-α,α-di-1-propynyl-1,4-dioxaspiro<4.4>non-7-ene-6-methanol
• 英文别名: 4-[9-methyl-8-(1,3-oxazol-5-yl)-1,4-dioxaspiro[4.4]non-7-en-9-yl]hepta-2,5-diyn-4-ol
• CAS: 122277-71-8
• 化学式: C₁₈H₁₉NO₄
• 分子量: 313.353
• InChiKey: CVFNWZFAZMWCSY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  64.7
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  6-Methyl-7-(5-oxazolyl)-α,α-di-1-propynyl-1,4-dioxaspiro<4.4>non-7-ene-6-methanol 生成 (Z)-2-[9-methyl-8-(1,3-oxazol-5-yl)-1,4-dioxaspiro[4.4]non-7-en-7-yl]hept-2-en-5-yn-4-one
  参考文献：
  名称：

  JACOBI, PETER A.;ARMACOSI, LISA M.;KRAVITZ, JOSEPH I.;MARTINELLI, MICHAEL+, TETRAHEDRON LETT., 29,(1988) N 52, C. 6865-6868

  摘要：

  DOI：
• 作为产物：
  描述：

  6-Carbomethoxy-6-methyl-7-(5-oxazolyl)-1,4-dioxaspiro<4.4>non-7-ene 、 丙炔 在 乙基溴化镁 作用下， 生成 6-Methyl-7-(5-oxazolyl)-α,α-di-1-propynyl-1,4-dioxaspiro<4.4>non-7-ene-6-methanol
  参考文献：
  名称：

  Enynones in Organic Synthesis. 6. Synthesis of Spirocyclic Methylenecyclopentenones and Analogs of the Methylenomycin Class of Antibiotics. Mechanism of Phenol Catalysis

  摘要：

  Spirocyclic methylenecyclopentenones of general structure 18 were prepared in a single step from bis-acetylenic alcohols 29 by a process involving initial oxy-Cope rearrangement to afford (Z)-enynones 30-Z followed by electrocyclic ring closure. Mechanistic studies indicate that the initial step leading from 30-Z to 18 is a thermal 1,5-prototropic shift to afford dienols which can cyclize by a symmetry-allowed (pi(4)s + sigma(2)s + pi(2)a) process. This last step is catalyzed by certain phenols having low oxidation potentials, most likely by a mechanism involving single electron transfer. Dramatic rate enhancements were also observed for the cyclization of simple enynones 37 to methylenecyclopentenones 39 upon catalysis with either a-tocopherol (vitamin E, 40) or tert-butylcatechol(41). Further enhancements in both rate and yield were obtained under conditions of photoassisted single electron transfer (PET), which afforded 39 in yields of 80-98%.

  DOI：

  10.1021/jo00097a035

文献信息

• Enynones in organic synthesis. I. Spiroannulation by tandem oxy-cope rearrangement-electrocyclic ring closure
  作者：Peter A. Jacobi、Lisa M. Armacost、Joseph I. Kravitz、Michael J. Martinelli、Harold G. Selnick

  DOI：10.1016/s0040-4039(00)88461-0

  日期：1988.1

  Bis-acetylenic alcohols of proper design undergo a facile oxy-Cope rearrangement to afford mixtures of E- and Z-enynones. These latter compounds afford methylenecyclopentenones upon enolization and electrocyclic ring closure.

  适当设计的双炔醇容易进行oxy-Cope重排，得到E-和Z-烯炔酮的混合物。后面的这些化合物在烯醇化和电环闭合时提供亚甲基环戊烯。