(2S)-1-[2-[(2S,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-[(4S,6R)-2,2-dimethyl-6-(phenylmethoxymethyl)-1,3-dioxan-4-yl]pent-4-enyl]-1,3-dithian-2-yl]-5-[2-[(2R,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-(2-phenyl-1,3-dithian-2-yl)pentyl]-1,3-dithian-2-yl]pentan-2-ol | 585535-24-6

• 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: (2S)-1-[2-[(2S,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-[(4S,6R)-2,2-dimethyl-6-(phenylmethoxymethyl)-1,3-dioxan-4-yl]pent-4-enyl]-1,3-dithian-2-yl]-5-[2-[(2R,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-(2-phenyl-1,3-dithian-2-yl)pentyl]-1,3-dithian-2-yl]pentan-2-ol
• CAS: 585535-24-6
• 化学式: C₅₉H₉₈O₆S₆Si₂
• 分子量: 1151.99
• InChiKey: AQHDCPVUQHISBR-YRFFEHHKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  17.28
• 重原子数：
  73
• 可旋转键数：
  27
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.76
• 拓扑面积：
  218
• 氢给体数：
  1
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  (2S)-1-[2-[(2S,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-[(4S,6R)-2,2-dimethyl-6-(phenylmethoxymethyl)-1,3-dioxan-4-yl]pent-4-enyl]-1,3-dithian-2-yl]-5-[2-[(2R,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-(2-phenyl-1,3-dithian-2-yl)pentyl]-1,3-dithian-2-yl]pentan-2-ol 在 2,6-二甲基吡啶 、 [双(三氟乙酰氧基)碘]苯 作用下， 以 四氢呋喃 、 水 为溶剂， 生成 (2S,3R,9S,13S,14S)-14-((4S,6R)-6-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-3,9,13-tris-(tert-butyl-dimethyl-silanyloxy)-2-ethyl-1-phenyl-hexadec-15-ene-1,5,11-trione
  参考文献：
  名称：

  (+)-Rimocidin Synthetic Studies. Construction of an Advanced C(1−18) Polyol Fragment

  摘要：

  The synthesis of an appropriately functionalized advanced C(1-18) polyol fragment of the mycosamine-glycosylated polyene macrolide, (+)-rimocidin (1), has been achieved in a highly efficient manner. Highlights of the strategy include the S(N)2/S(N)2' addition of dithiane anions to vinyl epoxides and the multicomponent linchpin union of 2-TBS-1,3-dithiane with two advanced epoxides.

  DOI：

  10.1021/ol034989g
• 作为产物：
  描述：

  2-(叔丁基二甲基甲硅烷基)-1,3-二噻烷 、 (4R,6S)-4-Benzyloxymethyl-2,2-dimethyl-6-((S)-(R)-1-oxiranyl-allyl)-[1,3]dioxane 、 tert-Butyl-dimethyl-[(1R,2S)-1-[2-((S)-3-oxiranyl-propyl)-[1,3]dithian-2-ylmethyl]-2-(2-phenyl-[1,3]dithian-2-yl)-butoxy]-silane 在 叔丁基锂 、 六甲基磷酰三胺 作用下， 以 乙醚 、 正戊烷 为溶剂， 反应 5.0h， 以56%的产率得到(2S)-1-[2-[(2S,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-[(4S,6R)-2,2-dimethyl-6-(phenylmethoxymethyl)-1,3-dioxan-4-yl]pent-4-enyl]-1,3-dithian-2-yl]-5-[2-[(2R,3S)-2-[tert-butyl(dimethyl)silyl]oxy-3-(2-phenyl-1,3-dithian-2-yl)pentyl]-1,3-dithian-2-yl]pentan-2-ol
  参考文献：
  名称：

  (+)-Rimocidin Synthetic Studies. Construction of an Advanced C(1−18) Polyol Fragment

  摘要：

  The synthesis of an appropriately functionalized advanced C(1-18) polyol fragment of the mycosamine-glycosylated polyene macrolide, (+)-rimocidin (1), has been achieved in a highly efficient manner. Highlights of the strategy include the S(N)2/S(N)2' addition of dithiane anions to vinyl epoxides and the multicomponent linchpin union of 2-TBS-1,3-dithiane with two advanced epoxides.

  DOI：

  10.1021/ol034989g

文献信息

• (+)-Rimocidin Synthetic Studies. Construction of an Advanced C(1−18) Polyol Fragment
  作者：Amos B. Smith、Suresh M. Pitram、Michael J. Fuertes

  DOI：10.1021/ol034989g

  日期：2003.7.1

  The synthesis of an appropriately functionalized advanced C(1-18) polyol fragment of the mycosamine-glycosylated polyene macrolide, (+)-rimocidin (1), has been achieved in a highly efficient manner. Highlights of the strategy include the S(N)2/S(N)2' addition of dithiane anions to vinyl epoxides and the multicomponent linchpin union of 2-TBS-1,3-dithiane with two advanced epoxides.