| 1236037-86-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• CAS: 1236037-86-7
• 化学式: C₇₁H₁₀₈NO₁₁P
• 分子量: 1182.61
• InChiKey: GUVABOWJESSCBO-RBIZVNQESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  17.92
• 重原子数：
  84.0
• 可旋转键数：
  49.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  120.45
• 氢给体数：
  0.0
• 氢受体数：
  12.0

反应信息

• 作为反应物：
  描述：

  、 在 四氮唑 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 6.0h， 生成
  参考文献：
  名称：

  Synthesis of the lipoteichoic acid of the Streptococcus species DSM 8747

  摘要：

  The lipoteichoic acid (LTA) of the Streptococcus species DSM 8747 consists of a beta-D-galactofuranosyl diacylglycerol moiety (with different acyl groups) that is linked via 6-O to a poly(glycerophosphate) backbone; about 30% of the glycerophosphate moieties carry at 2-O hydrolytically labile D-alanyl residues. As typical LTA for this array of compounds LTA 1a was synthesized. To this end, from D-galactose the required galactofuranosyl building block 5 was obtained. The anomeric stereocontrol in the glycosylation step with 1,2-O-cyclohexylidene-sn-glycerol (4) was based on anchimeric assistance, thus finally leading to the unprotected core glycolipid 16. Regioselective protection and deprotection procedures permitted the defined attachment of the pentameric glycerophosphate 3 to the 6-hydroxy group of the galactose residue. Introduction of four D-alanyl residues led after global deprotection and purification to target molecule 1a possessing on average about two D-alanyl residues at 2-O of the pentameric glycerophosphate backbone, thus being in close accordance with the structure of the natural material. (C) 2010 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmc.2010.04.006
• 作为产物：
  描述：

  3-O-(2,3,5-tri-O-benzyl-β-D-galactofuranosyl)-1,2-di-O-myristoyl-sn-glycerol 、 苄基N,N,N',N'-四异丙基亚磷酰二胺 在 二异丙基铵盐四氮唑 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以81%的产率得到
  参考文献：
  名称：

  Synthesis of the lipoteichoic acid of the Streptococcus species DSM 8747

  摘要：

  The lipoteichoic acid (LTA) of the Streptococcus species DSM 8747 consists of a beta-D-galactofuranosyl diacylglycerol moiety (with different acyl groups) that is linked via 6-O to a poly(glycerophosphate) backbone; about 30% of the glycerophosphate moieties carry at 2-O hydrolytically labile D-alanyl residues. As typical LTA for this array of compounds LTA 1a was synthesized. To this end, from D-galactose the required galactofuranosyl building block 5 was obtained. The anomeric stereocontrol in the glycosylation step with 1,2-O-cyclohexylidene-sn-glycerol (4) was based on anchimeric assistance, thus finally leading to the unprotected core glycolipid 16. Regioselective protection and deprotection procedures permitted the defined attachment of the pentameric glycerophosphate 3 to the 6-hydroxy group of the galactose residue. Introduction of four D-alanyl residues led after global deprotection and purification to target molecule 1a possessing on average about two D-alanyl residues at 2-O of the pentameric glycerophosphate backbone, thus being in close accordance with the structure of the natural material. (C) 2010 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmc.2010.04.006