methyl L-2-O-benzyl-3,4-O-cyclohexylidene-6-deoxy-β-arabino-hex-5-enopyranoside | 156593-33-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl L-2-O-benzyl-3,4-O-cyclohexylidene-6-deoxy-β-arabino-hex-5-enopyranoside
• CAS: 156593-33-8
• 化学式: C₂₀H₂₆O₅
• 分子量: 346.423
• InChiKey: NZVQCVUZVCGQJU-INDMIFKZSA-N

物化性质

• 沸点：
  470.4±45.0 °C(predicted)
• 密度：
  1.18±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.53
• 重原子数：
  25.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  46.15
• 氢给体数：
  0.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  methyl L-2-O-benzyl-3,4-O-cyclohexylidene-6-deoxy-β-arabino-hex-5-enopyranoside 在 溶剂黄146 、 lithium tri-t-butoxyaluminum hydride 、 硫脲 、 mercury dichloride 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 反应 16.0h， 生成 L-2,4-di-O-benzoyl-1-O-benzyl-3-deoxy-chiro-inositol
  参考文献：
  名称：

  Stereoselective synthesis of 6-deoxy and 3,6-dideoxy-D-myo-inositol precursors of deoxy-myo-inositol phosphate analogues from D-galactose

  摘要：

  The synthesis of chiral protected D-6-deoxy-myo-inositol derivatives from D-galactose is described. Ferrier rearrangement of hexenogalactopyranosides has been employed to produce the corresponding 6-deoxy-cyclohexanone polyols. The stereoselectivity of the carbocyclic transformation was discussed on the basis of the experimental data and a mechanism has been proposed. From deoxy-inososes, the access to a variety of 6-deoxy and 3,6-dideoxy-myo-inositol was performed to prepare suitable monool, diol and triol precursors for the synthesis of D-deoxy-myo-inositol phosphate analogues. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)10101-6
• 作为产物：
  描述：

  环己酮二甲缩酮 在 吡啶 、 四氯化碳 、 氢氧化钾 、 硫酸 、 苄基三甲基氯化铵 、 sodium hydride 、 三苯基膦 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 35.17h， 生成 methyl L-2-O-benzyl-3,4-O-cyclohexylidene-6-deoxy-β-arabino-hex-5-enopyranoside
  参考文献：
  名称：

  Stereoselective synthesis of 6-deoxy and 3,6-dideoxy-D-myo-inositol precursors of deoxy-myo-inositol phosphate analogues from D-galactose

  摘要：

  The synthesis of chiral protected D-6-deoxy-myo-inositol derivatives from D-galactose is described. Ferrier rearrangement of hexenogalactopyranosides has been employed to produce the corresponding 6-deoxy-cyclohexanone polyols. The stereoselectivity of the carbocyclic transformation was discussed on the basis of the experimental data and a mechanism has been proposed. From deoxy-inososes, the access to a variety of 6-deoxy and 3,6-dideoxy-myo-inositol was performed to prepare suitable monool, diol and triol precursors for the synthesis of D-deoxy-myo-inositol phosphate analogues. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)10101-6