65443-83-6

Upstream product

• 459-57-4 4-fluorobenzaldehyde 
• 91-59-8 naphthalen-2-ylamine 

Downstream Products

• 110582-26-8 1-But-3-enyl-3-(4-fluoro-phenyl)-benzo[f]quinoline 
• 110582-24-6 1-(4-Fluoro-phenyl)-1-(naphthalen-2-ylamino)-hept-6-en-3-one 
• 107805-75-4 1-(5-acenaphthenyl)-3-(p-fluorophenyl)-2-propen-1-one 
• 107805-76-5 1-Acenaphthen-5-yl-3-(4-fluoro-phenyl)-benzo[f]quinoline 
• 247138-65-4 8-(4-fluoro-phenyl)-7,8-dihydro-7-aza-indeno[2,1-c]phenanthren-9-one 
• 247138-28-9 5-(4-fluoro-phenyl)-2,3,5,6-tetrahydro-1H-benzo[a]phenanthridin-4-one 
• 328117-91-5 5-(4-fluorophenyl)-1,2,3,4-tetrahydrobenzo[a]phenanthridine 
• 912288-86-9 13-(4-fluorophenyl)-7,13-dihydro-12H-benzo[f]indeno[1,2-b]quinolin-12-one 
• 1218777-51-5 1-(3-pyridyl)-3-(4-fluorophenyl)benzo[f]quinoline 
• 28707-36-0 3-(4-fluorophenyl)benzo[f]quinoline 
• 1429117-80-5 8-(4-fluorophenyl)-13H-benzo[f]indolo[3,2-c]quinoline 
• 250719-17-6 2,3-dihydro-4-(4-fluorophenyl)-1H-benzo[f]cyclopenta[c]quinoline 
• 331674-50-1 4-(4-fluorophenyl)-2,3,4,5-tetrahydro-1H-cyclopenta[c]benzo[f]quinoline 

Relevant academic research and scientific papers

Rhodium-Catalyzed Dehydrogenative Annulation of N-Arylmethanimines with Vinylene Carbonate for Synthesizing Quinolines

Here we report a novel Rh-catalyzed C-H/C-H alkenylation of N-arylmethanimines with vinylene carbonate acting as a vinylene unit. Forty examples of C3,C4-nonsubstituted quinolines were achieved from commercially available starting materials. This identified process features an exceedingly simple system, a lower loading of catalyst, and the capacity for postfunctionalization with bioactive molecules.

An efficient method for the synthesis of indolo[3,2-c]quinoline derivatives catalyzed by iodine

The reaction of Schiff base and indole catalyzed by iodine in DMA, subsequently treated with DDQ, gave indolo[3,2-c]quinoline derivatives in good yields. The structure of 3e was confirmed by X-ray diffraction analysis. The reaction of Schiff base and indo

A stereoselective Povarov reaction leading to exo-tetrahydroindolo[3,2-c] quinoline derivatives catalyzed by iodine

We report an iodine-catalyzed Povarov reaction using indole as dienophile carried out in toluene at room temperature. This three-component reaction, coupling an aldehyde, an amine, and an indole, proved to be an efficient method for synthesizing exo-indol

Condensation of fluorine-substituted benzaldehydes with amines and cyclic ketones

Condensation of fluorine-containing benzaldehydes with naphthalen-2-amine or quinolin-6-amine and cyclic ketones (cyclopentanone, cyclohexanone, and 4-methylcyclohexanone) gave new fluorine-containing derivatives of cyclopenta[c]benzo[f]quinoline, benzo[a

Synthesis of 5-aryl-1,2,3,4-tetrahydrobenzo[a]phenanthridines

Previously unknown derivatives of tetrahydro[a]phenanthridine containing annelated benzoquinoline and cyclohexene nuclei were prepared by condensation of azomethines of the 2-naphthylamine series with cyclohexanone. The possibility of synthesis of such compounds without preliminarily preparing Schiff bases was demonstrated. The effect of substituents in the aromatic ring of the azomethine on the yield of the target products was elucidated. The IR, UV, 1H NMR, and mass spectra of the synthesized compounds were discussed.