216-00-2

Usage

InChI:InChI=1/C26H16/c1-2-8-18-14-20-16-26-24-12-6-4-10-22(24)21-9-3-5-11-23(21)25(26)15-19(20)13-17(18)7-1/h1-16H

Upstream product

• 119505-34-9 o-tolyl-triphenylen-2-yl ketone 
• 39013-98-4 2,3-bis(triphenylphosphonium-methyl)-naphthalene dibromide 
• 84-11-7 9,10-phenanthrenequinone 
• 118522-15-9 9,16-dihydro-9,16-epoxydibenzonaphthacene 
• 110-86-1 pyridine 
• 872294-17-2 dibenzo[a,c]naphthacene-10,15-dione 
• 64-19-7 acetic acid 
• 77037-23-1 1,4,epoxy-1,4-dihydrotriphenylene 
• 7651-80-1 1-fluoroanthracene 
• 77037-26-4 1,2,3,4-tetrahydro-1,4-epoxytriphenylene 
• 235-94-9 Phenanthro[9,10-c]furan 
• 31540-88-2 (E)-3-(2-Chloro-phenyl)-2-{3-[(E)-2-(2-chloro-phenyl)-1-cyano-vinyl]-naphthalen-2-yl}-acrylonitrile 
• 859745-96-3 dibenzo[a,c]naphthacene-9,16-dione 

Relevant academic research and scientific papers

Segregation of Charge in Ions of Dibenzonaphthacene: Relation of Topology and Electronic Structure. An NMR, ESR, and ENDOR Study

1H- and 13C-chemical shifts of the dianion of dibenzonaphthacene (1) have unambiguously been assigned by 2D-NMR spectroscopy.They indicate a remarkable charge distribution, as most of the negative charge is localized on the 'anthracenic' moiety, whil

Aluminium-mediated aromatic C-F bond activation: Regioswitchable construction of benzene-fused triphenylene frameworks

Selective synthesis of benzo[f]tetraphenes or benzo[g]chrysenes was achieved via aromatic C-F bond cleavage and unprecedented regioselective C-C bond formation depending upon the choice of aluminium reagents. On treatment with AlCl3, 2-(bipheny

Benzannulated Isobenzofurans

A number of arynes, generated by treatment of haloarenes with sodium or potassium amide in tetrahydrofuran, were trapped with furan.The resulting dihydro epoxy arenes were converted into the following annulated isobenzofuran derivatives by using reverse Diels-Alder methodology: naphthofuran, phenanthrofuran, pyrenofuran, pyrenofuran, anthrafuran, phenanthrofuran and phenathrofuran.Bimolecular rate constants for the addition of maleic anhydride to these furans were measured, and were correlated with the Herndon structure count.Addition of arynes to selected members of this furan series yielded adducts which were deoxygenated to afford polycyclic aromatic hydrocarbons.