(2R)-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (2R)-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman
• 英文别名: (2R)-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydrochromene
• 化学式: C₂₉H₅₀O
• 分子量: 414.715
• InChiKey: ZQJBTZSSRCFVQZ-RZRYPWFSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.1
• 重原子数：
  30
• 可旋转键数：
  12
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (2R)-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman 在 N-氟代双苯磺酰胺 作用下， 以 乙腈 为溶剂， 以44%的产率得到(2R)-6-fluoro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman
  参考文献：
  名称：

  Vitamin E-inspired multi-scale imaging agent

  摘要：

  The production and use of multi-modal imaging agents is on the rise. The vast majority of these imaging agents are limited to a single length scale for the agent (e.g. tissues only), which is typically at the organ or tissue scale. This work explores the synthesis of such an imaging agent and discusses the applications of our vitamin E-inspired multi-modal and multi-length scale imaging agents TB-Toc ((S,E)-5,5-difluoro-7-(2-(5-((6-hydroxy-2,5,7,8-tetramethylchroman-2-yl) methyl) thiophen-2-yl) vinyl)-9-methyl-5H-dipyrrolo-[1,2-c:2',1'-f] [1,3,2] diazaborinin-4-ium-5-uide). We investigate the toxicity of TB-Toc along with the starting materials and lipid based delivery vehicle in mouse myoblasts and fibroblasts. Further we investigate the uptake of TB-Toc delivered to cultured cells in both solvent and liposomes. TB-Toc has low toxicity, and no change in cell viability was observed up to concentrations of 10 mM. TB-Toc shows time-dependent cellular uptake that is complete in about 30 min. This work is the first step in demonstrating our vitamin E derivatives are viable multi-modal and length scale diagnostic tools.

  DOI：

  10.1016/j.bmcl.2018.10.052

文献信息

• Regioselective C–H Amidation of (Alkyl)arenes by Iron(II) Catalysis
  作者：Yao Ding、Shen-Yuan Zhang、Yu-Chen Chen、Shuai-Xin Fan、Jie-Sheng Tian、Teck-Peng Loh

  DOI：10.1021/acs.orglett.9b00697

  日期：2019.4.19

  nondirected amidation reaction of aromatic C–H bond was developed under iron(II) catalysis, using sulfonyl azides as the nitrogen source. The reaction displayed a broad substrate scope and good regioselectivities in the aspects of aromatic ring vs alkyl chain and different aromatic position of (alkyl)arenes. This method provided a new protocol for the synthesis of some aromatic amines, which were hard

  在铁（II）催化下，使用磺酰基叠氮化物作为氮源，开发了芳香族CH键的非定向酰胺化反应。该反应在芳族环对烷基链和（烷基）芳烃的不同芳族位置方面显示出较宽的底物范围和良好的区域选择性。该方法为合成某些芳族胺提供了新的方案，在先前的报告中很难实现。