3,4,4'-tri-O-benzyl-3'-O-(p-chlorobenzyl)-6,6'-di-O-(3,4-dimethoxybenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose | 1007885-83-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3,4,4'-tri-O-benzyl-3'-O-(p-chlorobenzyl)-6,6'-di-O-(3,4-dimethoxybenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose
• 英文别名: (2R,3R,4S,5R,6R)-2-[(2R,3R,4S,5R,6R)-4-[(4-chlorophenyl)methoxy]-6-[(3,4-dimethoxyphenyl)methoxymethyl]-3-[(4-iodophenyl)methoxy]-5-phenylmethoxyoxan-2-yl]oxy-6-[(3,4-dimethoxyphenyl)methoxymethyl]-3-[(4-methoxyphenyl)methoxy]-4,5-bis(phenylmethoxy)oxane
• CAS: 1007885-83-7
• 化学式: C₇₃H₇₈ClIO₁₆
• 分子量: 1373.77
• InChiKey: PZEGMPAAPHOETF-OUNFDWQWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  12.1
• 重原子数：
  91
• 可旋转键数：
  33
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  148
• 氢给体数：
  0
• 氢受体数：
  16

反应信息

• 作为产物：
  描述：

  3-O-benzyl-4,6;4',6'-di-O-benzylidene-3'-O-(p-chlorobenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose 、 3,4-二甲氧基苄氯 在 二异丁基氢化铝 、 四丁基碘化铵 、 sodium hydride 作用下， 以 二氯甲烷 、 甲苯 、 N,N-二甲基甲酰胺 为溶剂， 生成 (2R,3R,4S,5R,6R)-2-[(2R,3R,4S,5R,6R)-4-[(4-chlorophenyl)methoxy]-6-[(3,4-dimethoxyphenyl)methoxymethyl]-3,5-bis(phenylmethoxy)oxan-2-yl]oxy-6-[(3,4-dimethoxyphenyl)methoxymethyl]-3-[(4-methoxyphenyl)methoxy]-4,5-bis(phenylmethoxy)oxane 、 3,4,4'-tri-O-benzyl-3'-O-(p-chlorobenzyl)-6,6'-di-O-(3,4-dimethoxybenzyl)-2'-O-(p-iodobenzyl)-2-O-(p-methoxybenzyl)-α,α-D-trehalose
  参考文献：
  名称：

  Synthetic Studies toward Mycobacterium tuberculosis Sulfolipid-I

  摘要：

  [GRAPHICS]Sulfolipid-I (SL-I) is an abundant metabolite found in the cell wall of Mycobacterium tuberculosis that is comprised of a trehalose 2-sulfate core modified with four fatty acyl substituents. The correlation of its abundance with the virulence of clinical isolates suggests a role for SL-I in pathogenesis, although its biological functions remain unknown. Here we describe the synthesis of a SL-I analogue bearing unnatural lipid substituents. A key feature of the synthesis was application of an intramolecular aglycon delivery reaction to join two differentially protected glucose monomers, one prepared with a novel alpha-selective glycosylation. The route developed for the model compound can be readily extended to the synthesis of native SL-I as well as additional analogues for use in the investigation of SL-I's functions.

  DOI：

  10.1021/jo702032c