{(2R,4R,5S,6R)-4-[(2,5-Dimethoxy-phenyl)-hydroxy-methyl]-2-phenyl-6-vinyl-[1,3]dioxan-5-yl}-methyl-carbamic acid methyl ester | 205868-42-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: {(2R,4R,5S,6R)-4-[(2,5-Dimethoxy-phenyl)-hydroxy-methyl]-2-phenyl-6-vinyl-[1,3]dioxan-5-yl}-methyl-carbamic acid methyl ester
• 英文别名: methyl N-[(2R,4R,5S,6R)-4-[(2,5-dimethoxyphenyl)-hydroxymethyl]-6-ethenyl-2-phenyl-1,3-dioxan-5-yl]-N-methylcarbamate
• CAS: 205868-42-4
• 化学式: C₂₄H₂₉NO₇
• 分子量: 443.497
• InChiKey: YRLMUWVVPFHXLW-XEABEPSOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  32
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  86.7
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  {(2R,4R,5S,6R)-4-[(2,5-Dimethoxy-phenyl)-hydroxy-methyl]-2-phenyl-6-vinyl-[1,3]dioxan-5-yl}-methyl-carbamic acid methyl ester 在 重铬酸吡啶 、 乙酸酐 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 3.0h， 生成 {(2R,4R,5S,6R)-4-[(S)-1-(2,5-Dimethoxy-phenyl)-1-hydroxy-ethyl]-2-phenyl-6-vinyl-[1,3]dioxan-5-yl}-methyl-carbamic acid methyl ester
  参考文献：
  名称：

  Studies on the Synthesis of the C-Glycosidic Part of Nogalamycin, Part 3

  摘要：

  The addition of the metalated 1,4-dimethoxybenzenes 17a-c to the methyl ketone 14 was investigated in connection with the construction of the C-glycosidic part of nogalamycin. In most reactions, a selectivity towards the undesired Q-isomer 16a was observed, However, the reaction of the lithiated aromate 17c with 14 at low temperatures in THF favored the formation of the desired (R)-alcohol 15a (15a:16a = 4.8:1) in accordance with the chelate model A. The selectivity was considerably enhanced in the addition of the more hindered lithiated naphthalene 18 yielding the (R)-isomer 15b exclusively. Reduction of 15b afforded the dimethylamino compound 19b, a direct precursor of the CDEF-ring system of nogalamycin.

  DOI：

  10.1080/07328309808002322
• 作为产物：
  描述：

  3-deoxy-3-(N-methoxycarbonyl-N-methylamino)-1,2-O-isopropylidene-α-D-glucofuranose 在 正丁基锂 、 碘 、 碳酸氢钠 、 对甲苯磺酸 、 三乙胺 、 sodium iodide 、 zinc(II) chloride 作用下， 以 四氢呋喃 、 二氯甲烷 、 丙酮 、 丁酮 为溶剂， 反应 47.0h， 生成 {(2R,4R,5S,6R)-4-[(2,5-Dimethoxy-phenyl)-hydroxy-methyl]-2-phenyl-6-vinyl-[1,3]dioxan-5-yl}-methyl-carbamic acid methyl ester
  参考文献：
  名称：

  Studies on the Synthesis of the C-Glycosidic Part of Nogalamycin, Part 3

  摘要：

  The addition of the metalated 1,4-dimethoxybenzenes 17a-c to the methyl ketone 14 was investigated in connection with the construction of the C-glycosidic part of nogalamycin. In most reactions, a selectivity towards the undesired Q-isomer 16a was observed, However, the reaction of the lithiated aromate 17c with 14 at low temperatures in THF favored the formation of the desired (R)-alcohol 15a (15a:16a = 4.8:1) in accordance with the chelate model A. The selectivity was considerably enhanced in the addition of the more hindered lithiated naphthalene 18 yielding the (R)-isomer 15b exclusively. Reduction of 15b afforded the dimethylamino compound 19b, a direct precursor of the CDEF-ring system of nogalamycin.

  DOI：

  10.1080/07328309808002322