(3'S, 4'R)-1,2-O-isopropylidene-3-O-(3'-dimethylphenylsilylazetidin-2'-on-4'-yl)-α-D-xylofuranose | 218146-86-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (3'S, 4'R)-1,2-O-isopropylidene-3-O-(3'-dimethylphenylsilylazetidin-2'-on-4'-yl)-α-D-xylofuranose
• CAS: 218146-86-2
• 化学式: C₁₉H₂₇NO₆Si
• 分子量: 393.512
• InChiKey: UCFRLFVFZBRTFV-CNVOCDGBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.68
• 重原子数：
  27.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  86.25
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  (3'S, 4'R)-1,2-O-isopropylidene-3-O-(3'-dimethylphenylsilylazetidin-2'-on-4'-yl)-α-D-xylofuranose 在 四丁基溴化铵 、 potassium carbonate 作用下， 以 乙腈 为溶剂， 生成 (4'R)-5-deoxy-1,2-O-isopropylidene-3-O:5-C-(3'-azetidin-2'-on-1',4'-di-yl)-α-D-xylofuranose
  参考文献：
  名称：

  [2+2]cycloaddition of chlorosulfonyl isocyanate to (Z) 3-O-(2′-silylvinyl) ethers of 1,2-O-isopropylidene-5-O-trityl-α-D-xylofuranose

  摘要：

  The asymmetric [2+2]cycloaddition of chlorosulfonyl isocyanate to 1,2-O-isopropylidene-3-O-2'-silylvinyl)-5-O-trityl-alpha-D-xylofuranose proceeds with high steroselectivity in a good yield to afford the corresponding azetidin-2-ones with (R) configuration at the newly formed stereogenic center. The bulky t-butyl-dimethyisilyl substituent causes partial epimerization at C-3' carbon atom of the azetidin-2-one ring. Intramolecular alkylation of the nitrogen atom by the terminal carbon of the sugar chain gives 1-oxacephams; basic conditions of cyclization cause desilylation or partial desilylation of products. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00857-6
• 作为产物：
  描述：

  1,2-O-(异丙亚基)-5-O-(三苯基甲基)-alpha-D-呋喃木糖 在 Pd-BaSO₄ 喹啉 、 正丁基锂 、 氢气 、 sodium carbonate 、 对甲苯磺酸 、 红铝 作用下， 以 四氢呋喃 、 甲醇 、 正己烷 、 乙酸乙酯 、 甲苯 为溶剂， 反应 9.0h， 生成 (3'S, 4'R)-1,2-O-isopropylidene-3-O-(3'-dimethylphenylsilylazetidin-2'-on-4'-yl)-α-D-xylofuranose
  参考文献：
  名称：

  [2+2]cycloaddition of chlorosulfonyl isocyanate to (Z) 3-O-(2′-silylvinyl) ethers of 1,2-O-isopropylidene-5-O-trityl-α-D-xylofuranose

  摘要：

  The asymmetric [2+2]cycloaddition of chlorosulfonyl isocyanate to 1,2-O-isopropylidene-3-O-2'-silylvinyl)-5-O-trityl-alpha-D-xylofuranose proceeds with high steroselectivity in a good yield to afford the corresponding azetidin-2-ones with (R) configuration at the newly formed stereogenic center. The bulky t-butyl-dimethyisilyl substituent causes partial epimerization at C-3' carbon atom of the azetidin-2-one ring. Intramolecular alkylation of the nitrogen atom by the terminal carbon of the sugar chain gives 1-oxacephams; basic conditions of cyclization cause desilylation or partial desilylation of products. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00857-6