(2S,3R,4S,5R)-4-benzyloxy-2-(4-bromo-2,5-dimethoxyphenyl)-hept-6-en-2,3,5-triol | 205816-30-4

• 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: (2S,3R,4S,5R)-4-benzyloxy-2-(4-bromo-2,5-dimethoxyphenyl)-hept-6-en-2,3,5-triol
• 英文别名: (2S,3R,4S,5R)-2-(4-bromo-2,5-dimethoxyphenyl)-4-phenylmethoxyhept-6-ene-2,3,5-triol
• CAS: 205816-30-4
• 化学式: C₂₂H₂₇BrO₆
• 分子量: 467.357
• InChiKey: XLFIIIRXLYCVCL-YCZSINBZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.17
• 重原子数：
  29.0
• 可旋转键数：
  10.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  88.38
• 氢给体数：
  3.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  (2S,3R,4S,5R)-4-benzyloxy-2-(4-bromo-2,5-dimethoxyphenyl)-hept-6-en-2,3,5-triol 在 Sudan-B 、 臭氧 作用下， 以 二氯甲烷 为溶剂， 以73%的产率得到3-O-benzyl-6-deoxy-5-C-(4-bromo-2,5-dimethoxyphenyl)-α,β-D-idohexofuranose
  参考文献：
  名称：

  Studies on the Synthesis of the C-Glycosidic Part of Nogalamycin, Part 1

  摘要：

  Studies aimed at the construction of the C-glycosidic part of nogalamycin (1) and menogarol (2) are described. The stereochemistry of the addition of aryl lithiums to 4-acetyl-1,3-dioxolane 16, prepared from D-glucose via 10a-15, was studied. The major isomers were the Q-isomers 17a and 17b as shown by X-ray analysis of 17a with the unnatural configuration. The adduct 17a was further converted to the anomeric naphthoquinones 22a and 22b by acetal cleavage, ozonolysis, acetalization and Diels-Alder reaction with 1-methoxybutadiene.

  DOI：

  10.1080/07328309808002320
• 作为产物：
  描述：

  (2R,4S,5S,6R)-(5-benzyloxy-2-phenyl-6-vinyl-[1,3]dioxan-4-yl)-methanol 在 正丁基锂 、 chromium trioxide-pyridine complex 、 乙酸酐 、 对甲苯磺酸 、 二甲基亚砜 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 水 为溶剂， 反应 43.34h， 生成 (2S,3R,4S,5R)-4-benzyloxy-2-(4-bromo-2,5-dimethoxyphenyl)-hept-6-en-2,3,5-triol
  参考文献：
  名称：

  Studies on the Synthesis of the C-Glycosidic Part of Nogalamycin, Part 1

  摘要：

  Studies aimed at the construction of the C-glycosidic part of nogalamycin (1) and menogarol (2) are described. The stereochemistry of the addition of aryl lithiums to 4-acetyl-1,3-dioxolane 16, prepared from D-glucose via 10a-15, was studied. The major isomers were the Q-isomers 17a and 17b as shown by X-ray analysis of 17a with the unnatural configuration. The adduct 17a was further converted to the anomeric naphthoquinones 22a and 22b by acetal cleavage, ozonolysis, acetalization and Diels-Alder reaction with 1-methoxybutadiene.

  DOI：

  10.1080/07328309808002320