(1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(tert-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-6(S)-O-acetylundecanol | 1190739-03-7

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(tert-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-6(S)-O-acetylundecanol
• 英文别名: ethyl 2-[(4aR,6S,9R,9aR)-9-acetyloxy-2,2-ditert-butyl-4a,6,7,8,9,9a-hexahydro-4H-[1,3,2]dioxasilino[5,4-b]oxepin-6-yl]-2-methylpropanoate
• CAS: 1190739-03-7
• 化学式: C₂₃H₄₂O₇Si
• 分子量: 458.668
• InChiKey: ZBJFXBIZJQDFPS-AKHDSKFASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.51
• 重原子数：
  31
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  80.3
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  (1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(t-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-6(S)-undecanol 、 乙酸酐 在 吡啶 、 4-二甲氨基吡啶 作用下， 以 二氯甲烷 为溶剂， 以68%的产率得到(1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(tert-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-6(S)-O-acetylundecanol
  参考文献：
  名称：

  Heptanosides from Galactose-Derived Oxepenes via Stereoselective Addition Reactions

  摘要：

  Addition reactions to a 3,4-anhydroheptanose gave heptanoside analogues of carbohydrate derivatives in good to excellent stereochemical purity. Characterization of the products by H-1 and C-13 NMR, COSY, HSQC-DEPT, HMBC, 1D TOCSY, and NOE experiments were performed to obtain the stereochemistry of addition. The 3,4-anhydroheptanose used in this study is obtained from the ring-expansion of a cyclopropanated galactal and thus demonstrates the synthetic utility of heptanose synthesis via cyclopropanated carbohydrates.

  DOI：

  10.1021/jo901706e