3-((3aS,4R,6R,7S,7aR)-2-Ethoxy-7-methoxy-6-methoxymethyl-4-methyl-hexahydro-furo[3,2-c]pyran-4-yl)-propionaldehyde | 401625-11-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-((3aS,4R,6R,7S,7aR)-2-Ethoxy-7-methoxy-6-methoxymethyl-4-methyl-hexahydro-furo[3,2-c]pyran-4-yl)-propionaldehyde
• CAS: 401625-11-4
• 化学式: C₁₆H₂₈O₆
• 分子量: 316.395
• InChiKey: XCRKZKZOWAGNIB-PQLLZTCYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.55
• 重原子数：
  22.0
• 可旋转键数：
  8.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.94
• 拓扑面积：
  63.22
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  烯丙基三苯基溴化膦 、 3-((3aS,4R,6R,7S,7aR)-2-Ethoxy-7-methoxy-6-methoxymethyl-4-methyl-hexahydro-furo[3,2-c]pyran-4-yl)-propionaldehyde 在 正丁基锂 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 生成 (3aS,4R,6R,7S,7aR)-2-ethoxy-4-[(3Z)-3,5-hexadienyl]-7-methoxy-6-(methoxymethyl)-4-methylhexahydro-4H-furo[3,2-c]pyran 、 (3aS,4R,6R,7S,7aR)-2-ethoxy-4-[(3E)-3,5-hexadienyl]-7-methoxy-6-(methoxymethyl)-4-methylhexahydro-4H-furo[3,2-c]pyran
  参考文献：
  名称：

  Stereocontrolled entry to β-C-glycosides and bis-C,C-glycosides from C-glycals: preparation of a highly functionalized triene from d-mannose

  摘要：

  The C(3) hydroxyl group of C-glycals can be readily converted into mixed halo-acetals of 2-bromo-acetaldehyde. Radical reaction of the latter mediated by tri-n-butyltin hydride, with or without a radical acceptor, led diastereoselectively to either beta -C-glycosides or bis-C,C-glycosides, respectively. The latter have been transformed into a highly functionalized triene, which is a potential precursor in a proposed synthesis of labdane type diterpenes from D-mannose. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(01)00363-9
• 作为产物：
  描述：

  2,3:4,6-di-O-isopropylidene-D-mannopyranose 在 四氯化碳 、 偶氮二异丁腈 、 dimethyl sulfide borane 、 四丁基碘化铵 、 sodium hydride 、 对甲苯磺酸 、 三乙胺 、 三苯基膦 、 pyridinium chlorochromate 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 甲苯 为溶剂， 反应 109.0h， 生成 3-((3aS,4R,6R,7S,7aR)-2-Ethoxy-7-methoxy-6-methoxymethyl-4-methyl-hexahydro-furo[3,2-c]pyran-4-yl)-propionaldehyde
  参考文献：
  名称：

  Stereocontrolled entry to β-C-glycosides and bis-C,C-glycosides from C-glycals: preparation of a highly functionalized triene from d-mannose

  摘要：

  The C(3) hydroxyl group of C-glycals can be readily converted into mixed halo-acetals of 2-bromo-acetaldehyde. Radical reaction of the latter mediated by tri-n-butyltin hydride, with or without a radical acceptor, led diastereoselectively to either beta -C-glycosides or bis-C,C-glycosides, respectively. The latter have been transformed into a highly functionalized triene, which is a potential precursor in a proposed synthesis of labdane type diterpenes from D-mannose. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(01)00363-9