(4S,5S)-5-((R)-1-(tert-butyldimethylsilyloxy)-2-methylallyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid | 1448243-37-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (4S,5S)-5-((R)-1-(tert-butyldimethylsilyloxy)-2-methylallyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid
• 英文别名: (4S,5S)-5-[(1R)-1-[tert-butyl(dimethyl)silyl]oxy-2-methylprop-2-enyl]-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid
• CAS: 1448243-37-5
• 化学式: C₁₆H₃₀O₅Si
• 分子量: 330.497
• InChiKey: LMYAFZTUGUZQOM-UPJWGTAASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.56
• 重原子数：
  22
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.81
• 拓扑面积：
  65
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (4S,5S)-5-((R)-1-(tert-butyldimethylsilyloxy)-2-methylallyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid 在 甲醇 、 三甲基氯硅烷 作用下， 反应 3.0h， 以89%的产率得到(3S,4S,5R)-3,4-dihydroxy-5-(prop-1-en-2-yl)dihydrofuran-2(3H)-one
  参考文献：
  名称：

  A C2-Symmetric Pool Based Synthesis of the Furanoside of Hygromycin A

  摘要：

  The readily available and inexpensive D-tartaric acid serves as the chiral building block for synthesis of the furanoside of hygromycin A. Key to our successes in the asymmetric synthesis of the furanose segment was the melding of several key reactions, such as the successful application of the monosilylation of C-2-symmetric diol, diastereocontrolled di(2-propenyl)zinc addition to the aldehyde, and TMSCl-MeOH promoted desilylation, acetal-cleavage, and intramolecular esterification in one-step.

  DOI：

  10.3987/com-12-s(n)19
• 作为产物：
  描述：

  (-)-2,3-O-亚异丙基-D-苏力糖醇 在 camphor-10-sulfonic acid 、 三氧化硫吡啶 、 sodium hydride 、 戴斯-马丁氧化剂 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 乙二醇二甲醚 、 二氯甲烷 、 二甲基亚砜 为溶剂， 反应 35.49h， 生成 (4S,5S)-5-((R)-1-(tert-butyldimethylsilyloxy)-2-methylallyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid
  参考文献：
  名称：

  A C2-Symmetric Pool Based Synthesis of the Furanoside of Hygromycin A

  摘要：

  The readily available and inexpensive D-tartaric acid serves as the chiral building block for synthesis of the furanoside of hygromycin A. Key to our successes in the asymmetric synthesis of the furanose segment was the melding of several key reactions, such as the successful application of the monosilylation of C-2-symmetric diol, diastereocontrolled di(2-propenyl)zinc addition to the aldehyde, and TMSCl-MeOH promoted desilylation, acetal-cleavage, and intramolecular esterification in one-step.

  DOI：

  10.3987/com-12-s(n)19