3,4,6-tri-O-benzyl-1-O-(3,4-dimethoxybenzyl)-5-O-tert-butyldimethylsilyl-D-glucitol

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3,4,6-tri-O-benzyl-1-O-(3,4-dimethoxybenzyl)-5-O-tert-butyldimethylsilyl-D-glucitol
• 英文别名: (2S,3R,4S,5R)-5-[tert-butyl(dimethyl)silyl]oxy-1-[(3,4-dimethoxyphenyl)methoxy]-3,4,6-tris(phenylmethoxy)hexan-2-ol
• 化学式: C₄₂H₅₆O₈Si
• 分子量: 716.987
• InChiKey: JORKRGDSXRJEME-FXVJFNHDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.36
• 重原子数：
  51
• 可旋转键数：
  22
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  84.8
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  3,4,6-tri-O-benzyl-D-glucopyranose 在 咪唑 、 sodium tetrahydroborate 、 硼烷四氢呋喃络合物 、 3 A molecular sieve 、 硫酸 作用下， 以 四氢呋喃 、 二氯甲烷 、 溶剂黄146 、 N,N-二甲基甲酰胺 为溶剂， 反应 22.5h， 生成 3,4,6-tri-O-benzyl-1-O-(3,4-dimethoxybenzyl)-5-O-tert-butyldimethylsilyl-D-glucitol
  参考文献：
  名称：

  Total Synthesis of Caloporoside

  摘要：

  The first total synthesis of the fungal metabolite caloporoside 1, a strong and selective inhibitor of phospholipase C, is described. Both sugar units of its complex disaccharidic segment were obtained from 3,4,6-tri-O-benzyl-D-glucopyranose 14 as a common building block, with D-gluco-->D-manno inversions as the key strategic elements. This particular substitution reaction occurred readily on the acyclic segment (27-->28), whereas ultrasonication was required to override adverse stereoelectronic effects upon formation of beta-D-mannopyranoside unit 34. The (16R)-hydroxyheptadecylsalicylic acid part of 1 was efficiently prepared by a palladium-catalyzed Suzuki cross coupling reaction of aryltriflate 7 with the 9-alkyl-9-BBN derivative formed from alkene 6 and 9-H-9-BBN.

  DOI：

  10.1021/jo9800098

文献信息

• Total Synthesis of Caloporoside
  作者：Alois Fürstner、Ingo Konetzki

  DOI：10.1021/jo9800098

  日期：1998.5.1

  The first total synthesis of the fungal metabolite caloporoside 1, a strong and selective inhibitor of phospholipase C, is described. Both sugar units of its complex disaccharidic segment were obtained from 3,4,6-tri-O-benzyl-D-glucopyranose 14 as a common building block, with D-gluco-->D-manno inversions as the key strategic elements. This particular substitution reaction occurred readily on the acyclic segment (27-->28), whereas ultrasonication was required to override adverse stereoelectronic effects upon formation of beta-D-mannopyranoside unit 34. The (16R)-hydroxyheptadecylsalicylic acid part of 1 was efficiently prepared by a palladium-catalyzed Suzuki cross coupling reaction of aryltriflate 7 with the 9-alkyl-9-BBN derivative formed from alkene 6 and 9-H-9-BBN.