(2S,4aS,6aS,6bR,8aR,10S,12aS,12bR)-10-((2R,4S,5R,6S)-4,5-Dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13-octadecahydro-picene-2-carboxylic acid methyl ester

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S,4aS,6aS,6bR,8aR,10S,12aS,12bR)-10-((2R,4S,5R,6S)-4,5-Dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13-octadecahydro-picene-2-carboxylic acid methyl ester
• 英文别名: methyl (2S,4aS,6aR,6aS,6bR,8aR,10S,12aS)-10-[(2R,4S,5R,6S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-4,5,6,6a,7,8,8a,10,11,12-decahydro-3H-picene-2-carboxylate
• 化学式: C₃₇H₅₆O₇
• 分子量: 612.847
• InChiKey: AUFDFTYBPJZDDK-WURDGPPUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  44
• 可旋转键数：
  4
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.84
• 拓扑面积：
  102
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  3,4-二-O-乙酰-1,5-酐-2,6-双脱氧-L-阿拉伯-己-1-糖醇 在 palladium on activated charcoal 氢氧化钾 、 iodonium di(2,4,6-trimethylpyridine) perchlorate 、 4 A molecular sieve 、 氢气 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 144.0h， 生成 (2S,4aS,6aS,6bR,8aR,10S,12aS,12bR)-10-((2R,4S,5R,6S)-4,5-Dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13-octadecahydro-picene-2-carboxylic acid methyl ester
  参考文献：
  名称：

  Stereoselective synthesis of triterpene and steroid 2-deoxy-α-glycosides using iodonium dicollidine perchlorate

  摘要：

  2-Deoxy-alpha-glycosides of oleonane type triterpene alcohols and deoxycholic acid were synthesized by glycosylation with glycal acetates in the presence of iodonium dicollidine perchlorate followed by deiodination and deprotection.

  DOI：

  10.1007/bf02495419

文献信息

• Stereoselective synthesis of triterpene and steroid 2-deoxy-α-glycosides using iodonium dicollidine perchlorate
  作者：L. A. Baltina、O. B. Flekhter、E. V. Vasil'eva、G. A. Tolstikov

  DOI：10.1007/bf02495419

  日期：1997.3

  2-Deoxy-alpha-glycosides of oleonane type triterpene alcohols and deoxycholic acid were synthesized by glycosylation with glycal acetates in the presence of iodonium dicollidine perchlorate followed by deiodination and deprotection.