benzyl 3,5-di-O-benzyl-α-D-arabinofuranoside | 917591-02-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: benzyl 3,5-di-O-benzyl-α-D-arabinofuranoside
• CAS: 917591-02-7
• 化学式: C₂₆H₂₈O₅
• 分子量: 420.505
• InChiKey: WNQZNYYPMPLCNA-ZJSPYRCASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.09
• 重原子数：
  31.0
• 可旋转键数：
  10.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  57.15
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  benzyl 3,5-di-O-benzyl-α-D-arabinofuranoside 、 p-tolyl 5-O-t-butyldiphenylsilyl-2,3-O-(tetraisopropylsiloxane-1,3-diyl)-1-thio-α-D-arabinofuranoside 在 N-碘代丁二酰亚胺 、 3 A molecular sieve 、 silver trifluoromethanesulfonate 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成 benzyl 5-O-tert-butyldiphenylsilyl-2,3-O-(tetraisopropylsiloxane-1,3-diyl)-α-D-arabinofuranosyl-(1->2)-3,5-O-dibenzyl-α-D-arabinofuranoside 、 benzyl 5-O-tert-butyldiphenylsilyl-2,3-O-(tetraisopropylsiloxane-1,3-diyl)-β-D-arabinofuranosyl-(1->2)-3,5-O-dibenzyl-α-D-arabinofuranoside
  参考文献：
  名称：

  Stereoselective Synthesis of a Fragment of Mycobacterial Arabinan

  摘要：

  Strategies for the stereoselective synthesis of mycobacterial arabinan were explored. Arabinofuranosyl donors with various protective groups were screened in terms of suitability for beta-( 1,2- cis)- selective glycosylation. The protective group was found to affect the stereoselectivity of arabinofuranosylation. beta-Selectivity was drastically enhanced by using donors protected with 3,5- TIDPS, possibly due to conformational constraints on the furanose ring. Synthesis of heptaarabinofuranoside was then performed to demonstrate the practicality of this methodology.

  DOI：

  10.1021/ol062198j
• 作为产物：
  描述：

  benzyl 2-O-acetyl-3,5-di-O-benzyl-α-D-arabinofuranoside 在 sodium methylate 作用下， 以 甲醇 为溶剂， 反应 1.0h， 以85%的产率得到benzyl 3,5-di-O-benzyl-α-D-arabinofuranoside
  参考文献：
  名称：

  Stereoselective Synthesis of a Fragment of Mycobacterial Arabinan

  摘要：

  Strategies for the stereoselective synthesis of mycobacterial arabinan were explored. Arabinofuranosyl donors with various protective groups were screened in terms of suitability for beta-( 1,2- cis)- selective glycosylation. The protective group was found to affect the stereoselectivity of arabinofuranosylation. beta-Selectivity was drastically enhanced by using donors protected with 3,5- TIDPS, possibly due to conformational constraints on the furanose ring. Synthesis of heptaarabinofuranoside was then performed to demonstrate the practicality of this methodology.

  DOI：

  10.1021/ol062198j