[(2R,3R,4R)-2,4-dimethyl-1-oxo-6-trityloxyhexan-3-yl] acetate | 1361130-24-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: [(2R,3R,4R)-2,4-dimethyl-1-oxo-6-trityloxyhexan-3-yl] acetate
• CAS: 1361130-24-6
• 化学式: C₂₉H₃₂O₄
• 分子量: 444.571
• InChiKey: AJTKGPATZCEURR-AWVRMFGXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  33
• 可旋转键数：
  12
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  [(2R,3R,4R)-2,4-dimethyl-1-oxo-6-trityloxyhexan-3-yl] acetate 在 chromium dichloride 、 氟化铵 、 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) 、 C₁₇H₂₆N₂O₆S 、 palladium 10% on activated carbon 、 氢气 、 N,N-二异丙基乙胺 作用下， 以 甲醇 、 乙醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 85.15h， 生成 (3R,4R,5S,6R,9S,10S,12S)-12-((tert-butyldimethylsilyl)oxy)-6-(((3,4-dimethoxybenzyl)oxy)methoxy)-14-hydroxy-10-methoxy-3,5,9-trimethyl-1-(trityloxy)tetradecan-4-yl acetate
  参考文献：
  名称：

  Design, Synthesis, and Biological Evaluations of Aplyronine A–Mycalolide B Hybrid Compound

  摘要：

  A hybrid compound consisting of aplyronine A and mycalolide B was synthesized, and its biological activities were evaluated. The hybrid compound was found to have somewhat more potent actin-depolymerizing activity than aplyronine A. In contrast, the hybrid compound possessed about 1000-fold less cytotoxicity than aplyronine A. These results indicated that there is no direct correlation between actin-depolymerizing activity and cytotoxicity.

  DOI：

  10.1021/ol300182r
• 作为产物：
  描述：

  在 吡啶 、 4-二甲氨基吡啶 、 sodium periodate 、 四氧化锇 、 水 、 戴斯-马丁氧化剂 、 N-甲基吗啉氧化物 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 、 甲苯 为溶剂， 反应 23.5h， 生成 [(2R,3R,4R)-2,4-dimethyl-1-oxo-6-trityloxyhexan-3-yl] acetate
  参考文献：
  名称：

  Design, Synthesis, and Biological Evaluations of Aplyronine A–Mycalolide B Hybrid Compound

  摘要：

  A hybrid compound consisting of aplyronine A and mycalolide B was synthesized, and its biological activities were evaluated. The hybrid compound was found to have somewhat more potent actin-depolymerizing activity than aplyronine A. In contrast, the hybrid compound possessed about 1000-fold less cytotoxicity than aplyronine A. These results indicated that there is no direct correlation between actin-depolymerizing activity and cytotoxicity.

  DOI：

  10.1021/ol300182r

文献信息

• Second-generation total synthesis of aplyronine A featuring Ni/Cr-mediated coupling reactions
  作者：Ichiro Hayakawa、Keita Saito、Sachiko Matsumoto、Shinichi Kobayashi、Ayaka Taniguchi、Kenichi Kobayashi、Yusuke Fujii、Takahiro Kaneko、Hideo Kigoshi

  DOI：10.1039/c6ob02241c

  日期：——

  Second-generation total synthesis of aplyronine A, a potent antitumor marine macrolide, was achieved using Ni/Cr-mediated coupling reactions as key steps. The overall yield of the second-generation synthetic pathway of aplyronine A was 1.4%, obtained in 38 steps based on the longest linear sequence. Compared to our first-generation synthetic pathway of aplyronine A, the second-generation synthesis greatly improved

  使用Ni / Cr介导的偶联反应作为关键步骤，实现了有效的抗肿瘤海洋大环内酯aplyronine A的第二代全合成。基于最长的线性序列，分38步获得的第二代aplyronine A合成途径的总产率为1.4％。与我们的第一代合成的邻苯丙氨酸A路径相比，第二代合成极大地提高了收率和步骤数。特别是，我们在C13立体中心和C14–C15（ENi / Cr介导的不对称偶联反应））-三取代双键。此外，我们为C21–C28和C29–C34之间的不对称Ni / Cr介导的偶联反应建立了有效的反应条件。因此，该偶联反应以各链段的等摩尔比进行。