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• 1305155-02-5 1,3,5-tris(2-carbomethoxyphenylamino)benzene 

Relevant academic research and scientific papers

Bottom-Up Synthesis of Nitrogen-Doped Polycyclic Aromatic Hydrocarbons

Bottom-up organic synthesis serves as an efficient method to provide atomically precise heteroatom-doped polycyclic aromatic hydrocarbons (PAHs) with not only well-defined size and edge structures but also specific concentrations and positions of the heteroatoms. We provide a plenary account of the preparation of nitrogen-doped PAHs (N-PAHs) through 1,3-dipolar cycloaddition between different dipolarophiles, as well as pyrazine-type N-doped diaza-hexa-peri-hexabenzocoronene (diaza-HBC). Additionally, we present the synthesis of a class of helical N-charged PAHs, including one charged aza[5]helicene and two charged aza[4]helicenes. Moreover, the bottom-up organic synthesis strategy is further extended to the construction of novel nitrogen-boron-nitrogen (NBN)-containing PAHs. Finally, we discuss the synthesis of four-coordinate boron chromophores containing 6,12,18-tris(alkyl amine)-5,11,17-triazatrinaphthylene derivative ligands. 1 Introduction 2 Nitrogen-Doped PAHs Based on Dibenzo-9a-azaphenalene (DBAP) 3 Cationic Nitrogen-Doped Helical PAHs 4 Nitrogen-Boron-Nitrogen-Doped PAHs 5 Conclusion and Outlook.

6,12,18-triaryl-5,11,17-benzotriquinoline derivative and synthetic method thereof

The invention discloses a 6,12,18-triaryl-5,11,17-benzotriquinoline derivative and a synthetic method thereof. The 6,12,18-triaryl-5,11,17-benzotriquinoline derivative, shown as a structural formula below, has a large planar rigid aromatic nucleus, has a

Recognition of G-quadruplex DNA by triangular star-shaped compounds: With or without side chains?

We report the synthesis of two new series of triangular aromatic platforms, either with three aminoalkyl side chains (triazatrinaphthylene series, TrisK: six compounds), or without side chains (triazoniatrinaphthylene, TrisQ). The quadruplex-DNA binding b