Acetic acid (3S,5S)-2-oxo-5-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-tetrahydro-furan-3-yl ester | 203173-12-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: Acetic acid (3S,5S)-2-oxo-5-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-tetrahydro-furan-3-yl ester
• 英文别名: [(3S,5S)-2-oxo-5-[(4R,5R)-2,2,5-trimethyl-1,3-dioxolan-4-yl]oxolan-3-yl] acetate
• CAS: 203173-12-0
• 化学式: C₁₂H₁₈O₆
• 分子量: 258.271
• InChiKey: DJEWVFRWDVYQCO-DOWZNPNQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  71.1
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  Acetic acid (3S,5S)-2-oxo-5-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-tetrahydro-furan-3-yl ester 在 盐酸 作用下， 以 甲醇 为溶剂， 反应 72.0h， 以76%的产率得到(3S,5S)-5-((1R,2R)-1,2-Dihydroxy-propyl)-3-hydroxy-dihydro-furan-2-one
  参考文献：
  名称：

  Highly Functionalized Cyclopentanes by Radical Cyclization of Unsaturated Bromolactones. 2. A Facile Synthesis of the First Carbaaldohexofuranoses and Their Conversion to Carbapentofuranoses

  摘要：

  A novel type of carbasugars, carbaaldohexofuranoses, has been prepared using a 5-exo-trig radical cyclization of C-2 substituted 2,3-unsaturated 7-bromoheptono-1,4-lactones as the key step. During the cyclization step, two-stereogenic centers were farmed with high stereoselectivity. The lactone moieties of the cyclopentane derivatives were reduced to the alcohols, and the following carbahexofuranoses were synthesized: carba-beta-D-mannofuranose, carba-alpha-L-glucofuranose and 5-amino-5-deoxycarba-alpha-L-glucofuranose. Side chain degradation of the two former compounds gave the carbapentofuranoses: carba-alpha-L-xylofuranose and carba-beta-D-lyxofuranose.

  DOI：

  10.1021/jo971928l
• 作为产物：
  描述：

  (3R,4R,5R)-5-((4S,5S)-5-Bromomethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-3,4-dihydroxy-dihydro-furan-2-one 在 palladium on activated charcoal 吡啶 、 氢气 、 三乙胺 作用下， 以 二氯甲烷 、 乙酸乙酯 为溶剂， 25.0 ℃ 、10.0 MPa 条件下， 反应 42.0h， 生成 Acetic acid (3S,5S)-2-oxo-5-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-tetrahydro-furan-3-yl ester
  参考文献：
  名称：

  Highly Functionalized Cyclopentanes by Radical Cyclization of Unsaturated Bromolactones. 2. A Facile Synthesis of the First Carbaaldohexofuranoses and Their Conversion to Carbapentofuranoses

  摘要：

  A novel type of carbasugars, carbaaldohexofuranoses, has been prepared using a 5-exo-trig radical cyclization of C-2 substituted 2,3-unsaturated 7-bromoheptono-1,4-lactones as the key step. During the cyclization step, two-stereogenic centers were farmed with high stereoselectivity. The lactone moieties of the cyclopentane derivatives were reduced to the alcohols, and the following carbahexofuranoses were synthesized: carba-beta-D-mannofuranose, carba-alpha-L-glucofuranose and 5-amino-5-deoxycarba-alpha-L-glucofuranose. Side chain degradation of the two former compounds gave the carbapentofuranoses: carba-alpha-L-xylofuranose and carba-beta-D-lyxofuranose.

  DOI：

  10.1021/jo971928l