(1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(t-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-5(R),6(R)-undecanediol | 1190738-99-8

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: (1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(t-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-5(R),6(R)-undecanediol
• 英文别名: ethyl 2-[(4aR,6S,8S,9S,9aR)-2,2-ditert-butyl-8,9-dihydroxy-4a,6,7,8,9,9a-hexahydro-4H-[1,3,2]dioxasilino[5,4-b]oxepin-6-yl]-2-methylpropanoate
• CAS: 1190738-99-8
• 化学式: C₂₁H₄₀O₇Si
• 分子量: 432.63
• InChiKey: QPYKCUSAERZZDM-QEOTZNIISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.91
• 重原子数：
  29
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.95
• 拓扑面积：
  94.4
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  (1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(t-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-5(R),6(R)-undecanediol 、 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79%的产率得到(1R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(t-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-5(R),6(R)-di-O-acetylundecanediol
  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
• 作为产物：
  描述：

  ethyl 2-[(4aR,6S,9aR)-2,2-ditert-butyl-4a,6,7,9a-tetrahydro-4H-[1,3,2]dioxasilino[5,4-b]oxepin-6-yl]-2-methylpropanoate 在 四氧化锇 、 水 、 N-甲基吗啉氧化物 作用下， 以 乙醚 为溶剂， 反应 1.0h， 以59%的产率得到(1R,7R)-3-(ethyl 2-methyl-2-propanoate)-9,9-di-(t-butyl)-2,8,10-trioxa-9-silabicyclo[5.4.0]-5(R),6(R)-undecanediol
  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