1-[(2S,3R,5S,6R)-3,5-Bis-benzyloxy-6-methyl-6-((S)-2-methyl-but-3-enyl)-tetrahydro-pyran-2-yl]-propan-2-one | 126694-12-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-[(2S,3R,5S,6R)-3,5-Bis-benzyloxy-6-methyl-6-((S)-2-methyl-but-3-enyl)-tetrahydro-pyran-2-yl]-propan-2-one
• CAS: 126694-12-0
• 化学式: C₂₈H₃₆O₄
• 分子量: 436.591
• InChiKey: FUWPWNFHVAMAIW-JPJACQMESA-N

物化性质

• 沸点：
  533.4±50.0 °C(predicted)
• 密度：
  1.07±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  32.0
• 可旋转键数：
  11.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  44.76
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  1-[(2S,3R,5S,6R)-3,5-Bis-benzyloxy-6-methyl-6-((S)-2-methyl-but-3-enyl)-tetrahydro-pyran-2-yl]-propan-2-one 在 四氧化锇 、 水 、 N-甲基吗啉氧化物 作用下， 以 四氢呋喃 为溶剂， 反应 5.0h， 生成 1-[(2S,3R,5S,6R)-3,5-Bis-benzyloxy-6-((S)-3,4-dihydroxy-2-methyl-butyl)-6-methyl-tetrahydro-pyran-2-yl]-propan-2-one
  参考文献：
  名称：

  Total Synthesis of Brevetoxin A: Part 1: First Generation Strategy and Construction of BCD Ring System

  摘要：

  Discussed herein is our first generation strategy for the total synthesis of brevetoxin A. This approach relies upon dissection of the molecule at the nine-membered ring site (ring E), A Wittig coupling of requisite polycyclic fragments 3 and 4 followed by hydroxy dithioketal cyclization was expected to furnish the polycyclic framework of brevetoxin A (1). Intermediate 8 was anticipated to be a valid synthetic precursor to phosphonium salt 3, and its synthesis was accomplished by a bis(lactonization)/thionolactone formation/functionalization sequence. In order to test our synthetic strategy, the synthesis of an advanced model system (36) was attempted. Aldehyde 38 and phosphonium salt 37 were successfully synthesized and coupled through a:Wittig reaction. Unfortunately, the planned hydroxy dithioketal cyclization to form the crucial nonacene (ring E) did not proceed as anticipated and this synthetic approach was discontinued.

  DOI：

  10.1002/(sici)1521-3765(19990201)5:2<599::aid-chem599>3.0.co;2-n
• 作为产物：
  描述：

  (3S,5S,6S,8R)-6,8-Bis-benzyloxy-9,9-bis-ethylsulfanyl-3,5-dimethyl-non-1-en-5-ol 在 2,6-二甲基吡啶 、 N-氯代丁二酰亚胺 、 水 、 sodium hydride 作用下， 以 四氢呋喃 、 甲苯 、 乙腈 、 paraffin 为溶剂， 反应 14.08h， 生成 1-[(2S,3R,5S,6R)-3,5-Bis-benzyloxy-6-methyl-6-((S)-2-methyl-but-3-enyl)-tetrahydro-pyran-2-yl]-propan-2-one
  参考文献：
  名称：

  Total Synthesis of Brevetoxin A: Part 1: First Generation Strategy and Construction of BCD Ring System

  摘要：

  Discussed herein is our first generation strategy for the total synthesis of brevetoxin A. This approach relies upon dissection of the molecule at the nine-membered ring site (ring E), A Wittig coupling of requisite polycyclic fragments 3 and 4 followed by hydroxy dithioketal cyclization was expected to furnish the polycyclic framework of brevetoxin A (1). Intermediate 8 was anticipated to be a valid synthetic precursor to phosphonium salt 3, and its synthesis was accomplished by a bis(lactonization)/thionolactone formation/functionalization sequence. In order to test our synthetic strategy, the synthesis of an advanced model system (36) was attempted. Aldehyde 38 and phosphonium salt 37 were successfully synthesized and coupled through a:Wittig reaction. Unfortunately, the planned hydroxy dithioketal cyclization to form the crucial nonacene (ring E) did not proceed as anticipated and this synthetic approach was discontinued.

  DOI：

  10.1002/(sici)1521-3765(19990201)5:2<599::aid-chem599>3.0.co;2-n