2-methoxymethoxy-6-methyl-hept-5-en-1-ol | 1301247-87-9

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 2-methoxymethoxy-6-methyl-hept-5-en-1-ol
• 英文别名: (2S)-2-(methoxymethoxy)-6-methylhept-5-en-1-ol
• CAS: 1301247-87-9
• 化学式: C₁₀H₂₀O₃
• 分子量: 188.267
• InChiKey: SEWPBMTZLYEGQP-JTQLQIEISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  13
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-methoxymethoxy-6-methyl-hept-5-en-1-ol 在 吡啶 、 咪唑 、 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 、 4-二甲氨基吡啶 、 四丙基高钌酸铵 、 palladium 10% on activated carbon 、 三氟化硼乙醚 、 四丁基氟化铵 、 氢气 、 氧气 、 copper diacetate 、 四丁基碘化铵 、 sodium hydride 、 碳酸氢钠 、 potassium carbonate 、 臭氧 、 溶剂黄146 、 N-甲基吗啉氧化物 、 N,N-二异丙基乙胺 、 间氯过氧苯甲酸 、 (+)-B-methoxydiisocamphenylborane 、 palladium dichloride 、 tetramethylammonium triacetoxyborohydride 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 乙腈 、 mineral oil 为溶剂， 反应 146.5h， 生成 3-hydroxy-7,9,16-tris(methoxymethoxy)-13-methyl-12,19-dioxa-tricyclo-[13.3.1.0(5,10)]nonadeca-5,7,9-trien-11-one
  参考文献：
  名称：

  Synthesis of the Purported ent-Pochonin J Structure Featuring a Stereoselective Oxocarbenium Allylation

  摘要：

  The synthesis of the alleged natural product pochonin J is presented. Key steps of this convergent synthesis include a chemoselective Wacker oxidation, and an Evans' anti-reduction of the resulting ketone. Upon ozonolysis, this intermediate undergoes a 6-exo-trig cyclization to give a hemiketal intermediate, the key oxocarbenium precursor. The construction of the alpha-C-glycoside subunit is highlighted by a mismatched oxocarbenium cation formation/allylation sequence. An olefin metathesis afforded the 14-membered macrolactone, and final oxidation provided the "desired" compound that does not spectroscopically correlate to the initially described natural product.

  DOI：

  10.1021/jo200332d
• 作为产物：
  描述：

  1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-hept-5-en-2-ol 在 4-二甲氨基吡啶 、 四丁基氟化铵 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 2-methoxymethoxy-6-methyl-hept-5-en-1-ol
  参考文献：
  名称：

  Synthesis of the Purported ent-Pochonin J Structure Featuring a Stereoselective Oxocarbenium Allylation

  摘要：

  The synthesis of the alleged natural product pochonin J is presented. Key steps of this convergent synthesis include a chemoselective Wacker oxidation, and an Evans' anti-reduction of the resulting ketone. Upon ozonolysis, this intermediate undergoes a 6-exo-trig cyclization to give a hemiketal intermediate, the key oxocarbenium precursor. The construction of the alpha-C-glycoside subunit is highlighted by a mismatched oxocarbenium cation formation/allylation sequence. An olefin metathesis afforded the 14-membered macrolactone, and final oxidation provided the "desired" compound that does not spectroscopically correlate to the initially described natural product.

  DOI：

  10.1021/jo200332d

文献信息

• Synthesis of the Purported <i>ent</i>-Pochonin J Structure Featuring a Stereoselective Oxocarbenium Allylation
  作者：Dionicio Martinez-Solorio、Kenneth A. Belmore、Michael P. Jennings

  DOI：10.1021/jo200332d

  日期：2011.5.20

  The synthesis of the alleged natural product pochonin J is presented. Key steps of this convergent synthesis include a chemoselective Wacker oxidation, and an Evans' anti-reduction of the resulting ketone. Upon ozonolysis, this intermediate undergoes a 6-exo-trig cyclization to give a hemiketal intermediate, the key oxocarbenium precursor. The construction of the alpha-C-glycoside subunit is highlighted by a mismatched oxocarbenium cation formation/allylation sequence. An olefin metathesis afforded the 14-membered macrolactone, and final oxidation provided the "desired" compound that does not spectroscopically correlate to the initially described natural product.