(1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-[(hydroxy)methyl]-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,17-dioxabicyclo[11.3.1]heptadecane-3,10-dione | 223693-26-3

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酯类和类似物
• 英文名称: (1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-[(hydroxy)methyl]-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,17-dioxabicyclo[11.3.1]heptadecane-3,10-dione
• 英文别名: (1S,5S,7R,9R,13S,15S,16R)-11-(benzenesulfonyl)-5-(hydroxymethyl)-7-[(4-methoxyphenyl)methoxy]-6,6,9,16-tetramethyl-15-phenylmethoxy-4,17-dioxabicyclo[11.3.1]heptadecane-3,10-dione
• CAS: 223693-26-3
• 化学式: C₄₁H₅₂O₁₀S
• 分子量: 736.924
• InChiKey: MUYVGROPHYTWHD-LBJJGPCSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.1
• 重原子数：
  52
• 可旋转键数：
  10
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.51
• 拓扑面积：
  143
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  (1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-[(hydroxy)methyl]-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,17-dioxabicyclo[11.3.1]heptadecane-3,10-dione 在 chromium dichloride 、 potassium tert-butylate 、 戴斯-马丁氧化剂 、 (+)-8,8-二氯樟脑磺哑嗪 作用下， 以 四氢呋喃 、 二氯甲烷 、 叔丁醇 为溶剂， 反应 4.5h， 生成 (1S,5R,7R,9R,13S,15S,16R)-15-Benzyloxy-5-((E)-2-iodo-vinyl)-7-(4-methoxy-benzyloxy)-6,6,9,16-tetramethyl-4,17-dioxa-bicyclo[11.3.1]heptadecane-3,10,11-trione
  参考文献：
  名称：

  Stereocontrolled Elaboration of Natural (−)-Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudai

  摘要：

  A stereoselective total synthesis of natural levorotatory polycavemoside A (1) has been achieved. initial investigations produced the properly activated disaccharide unit 18b via the conjoining of building blocks originating from L-fucose and D-xylose. This objective was followed by preparation of the phenylsulfonyl-substituted tetrahydropyran 23 and aldehyde 30. After proper linking of these key compounds, important information had to be garnered on the sequence of steps that would ultimately result in successful access to 1. Although oxidation to generate alpha-diketone 35 and unmasking of the C-13 hydroxyl did give rise efficiently to lactol 36, this functionality did not pave the way for ensuring macrolactonization. When this sequence of steps was reversed, it was indeed possible to arrive at the heavily functionalized precursor 43. However, numerous experiments failed to result in the requisite activation of C-16 for attachment of the trienyl side chain. However, if the E-vinyl iodide was elaborated in advance of alpha-diketone generation, glycosidation, and complete side chain construction, arrival at 1 proceeded without unsurmountable complications to furnish the targeted marine toxin.

  DOI：

  10.1021/ja993487o
• 作为产物：
  描述：

  (benzenesulfonyl)methyllithium 在 吡啶 、 甲醇 、 六甲基磷酰三胺 、 4-二甲氨基吡啶 、 sodium chlorite 、 sodium periodate 、 sodium dihydrogenphosphate 、 四氧化锇 、 正丁基锂 、 N-甲基吲哚酮 、 2-甲基-2-丁烯 、 2,4,6-三氯苯甲酰氯 、 戴斯-马丁氧化剂 、 对甲苯磺酸 、 氟化氢吡啶 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 叔丁醇 为溶剂， 反应 6.0h， 生成 (1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-[(hydroxy)methyl]-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,17-dioxabicyclo[11.3.1]heptadecane-3,10-dione
  参考文献：
  名称：

  A Convergent Total Synthesis of the Macrolactone Disaccharide Toxin (−)-Polycavernoside A

  摘要：

  DOI：

  10.1021/ja990384x

文献信息

• Stereocontrolled Elaboration of Natural (−)-Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga <i>Polycavernosa</i> <i>tsudai</i>
  作者：Leo A. Paquette、Louis Barriault、Dmitri Pissarnitski、Jeffrey N. Johnston

  DOI：10.1021/ja993487o

  日期：2000.2.1

  A stereoselective total synthesis of natural levorotatory polycavemoside A (1) has been achieved. initial investigations produced the properly activated disaccharide unit 18b via the conjoining of building blocks originating from L-fucose and D-xylose. This objective was followed by preparation of the phenylsulfonyl-substituted tetrahydropyran 23 and aldehyde 30. After proper linking of these key compounds, important information had to be garnered on the sequence of steps that would ultimately result in successful access to 1. Although oxidation to generate alpha-diketone 35 and unmasking of the C-13 hydroxyl did give rise efficiently to lactol 36, this functionality did not pave the way for ensuring macrolactonization. When this sequence of steps was reversed, it was indeed possible to arrive at the heavily functionalized precursor 43. However, numerous experiments failed to result in the requisite activation of C-16 for attachment of the trienyl side chain. However, if the E-vinyl iodide was elaborated in advance of alpha-diketone generation, glycosidation, and complete side chain construction, arrival at 1 proceeded without unsurmountable complications to furnish the targeted marine toxin.
• A Convergent Total Synthesis of the Macrolactone Disaccharide Toxin (−)-Polycavernoside A
  作者：Leo A. Paquette、Louis Barriault、Dmitri Pissarnitski

  DOI：10.1021/ja990384x

  日期：1999.5.1