174713-32-7

Upstream product

• 629-03-8 1 ,6-dibromohexane 
• 22937-68-4 1,6-Bis(3,5-bis(methoxycarbonyl)phenoxy)hexane 
• 618-83-7 5-Hydroxyisophthalic acid 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 948888-32-2 {3-[6-(3,5-Bis-hydroxymethyl-phenoxy)-hexyloxy]-5-hydroxymethyl-phenyl}-methanol 

Relevant academic research and scientific papers

Pyridinium N-heteroarylaminides: synthesis of N-heteroaryltetramines based on 1,6-bis(phenoxy)hexane and 1,3-bis(phenoxymethyl)benzene

The synthesis of a set of new N-heteroaryltetramines is reported. A regioselective alkylation on the N-exo nitrogen of pyridinium N-(heteroaryl)aminide with the corresponding tetrabromo compounds, followed by a clean N-N bond reduction of the correspondin

Pyridinium N-heteroarylaminides: synthesis of N-heteroarylpolyamines

The synthesis of a set of new N-heteroarylpolyamines is reported. A multiple and regioselective alkylation on the exo nitrogen of pyridinium N-(heteroaryl)aminides with several polybromo compounds, followed by a clean N-N bond reduction of the corresponding pyridinium salts, provides an easy and general method to obtain the title compounds.

Curved aromatic compounds, part 2[?]: 1,7-dioxa[7](2,7)pyrenophane: The pyrene moiety is more bent than that of C70

The synthesis of the highly strained title compound 8 a was achieved by the valence isomerization and in situ dehydrogenation of the cyclophanediene 7 a at only 80°C. A single-crystal X-ray structure determination of 8 a revealed that the pyrene moiety is

Dioxa(2,7)pyrenophan, ein stark verzerrter, polycyclischer, aromatischer Kohlenwasserstoff

Keywords: Cyclophane; Fullerenfragmente; Gespannte Ringe; Pyrene