58841-73-9

Upstream product

• 10016-52-1 2,8-dibromodibenzofuran 
• 98-80-6 phenylboronic acid 
• 132-64-9 dibenzofuran 
• 5943-11-3 2,8-diiodo-dibenzo[b,d]furan 

Downstream Products

• 949925-64-8 2,8-diphenyldibenzofuran-4-boronic acid 
• 1307859-72-8 4-(3-bromophenyl)-2,8-diphenyldibenzofuran> 
• 1307859-75-1 3-(2,8-diphenyldibenzofuran-4-yl)phenylboronic acid 
• 1307859-78-4 4-[3-(9,10-diphenyl-2-anthryl)phenyl]-2,8-diphenyldibenzofuran 
• 24253-53-0 2,11-diphenyltriphenylene 

Relevant academic research and scientific papers

Aromatic Metamorphosis of Dibenzofurans into Triphenylenes Starting with Nickel-Catalyzed Ring-Opening C-O Arylation

A new class of aromatic metamorphosis has been developed in which dibenzofurans were converted into triphenylenes. This transformation is composed of three successive operations: (1) nickel-catalyzed ring-opening C-O bond arylation with arylmagnesium bromides, (2) trifluoromethanesulfonylation (triflation) of the resulting hydroxy moiety with Tf2O, and (3) palladium-catalyzed or photoinduced ring closure. In the last ring-closing step, the photoinduced process has proven to be more productive than the palladium-catalyzed one. By employing π-extended dinaphthofuran as the substrate, dorsally benzo-fused [5]helicene was obtained in a satisfactory yield.

Heterocyclic compound, light-emitting element, light-emitting device, electronic device, and lighting device

Provided are a heterocyclic compound which emits blue light and is represented by General Formula (G1) below, and a light-emitting element, a light-emitting device, an electronic device and a lighting device which are formed using the heterocyclic compound represented by General Formula (G1) below. The use of the heterocyclic compound represented by General Formula (G1) makes it possible to provide a light-emitting element which has high emission efficiency, and also a light-emitting device, an electronic device and a lighting device which have reduced power consumption.