222622-96-0

Upstream product

• 33693-48-0 4-benzyloxy-3-methoxybenzyl alcohol 
• 121-33-5 vanillin 
• 100-39-0 benzyl bromide 
• 40705-22-4 4-benzyloxy-6-bromo-3-methoxybenzaldehyde 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 65341-82-4 [4-(benzyloxy)-2-bromo-5-methoxyphenyl]methanol 

Downstream Products

• 331248-70-5 dimethyl 2-bromo-4-benzyloxy-5-methoxybenzylphosphonate 
• 348618-45-1 3-(4-benzyloxy-2-bromo-5-methoxyphenyl)propionitrile 
• 891202-07-6 3-(4-benzyloxy-2-bromo-5-methoxybenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylic acid methyl ester 
• 222621-24-1 N-(4-benzyloxy-2-bromo-5-methoxy)benzyl-N'-(pyridin-2-yl)piperazine 
• 1417801-80-9 (Z)-1-(4-(benzyloxy)-2-bromo-5-methoxystyryl)-2-bromo-3-isopropoxy-4-methoxybenzene 
• 1417801-81-0 1-(4-(benzyloxy)-2-bromo-5-methoxyphenethyl)-2-bromo-3-isopropoxy-4-methoxybenzene 
• 1417801-83-2 (4-(benzyloxy)-2-bromo-5-methoxybenzyl)triphenylphosphonium bromide 
• 331248-82-9 4-{4-[(E)-2-(4-Benzyloxy-2-bromo-5-methoxy-phenyl)-vinyl]-phenoxy}-6-[(E)-2-(5-benzyloxy-2-bromo-phenyl)-vinyl]-2,2-diphenyl-benzo[1,3]dioxole 
• 331248-79-4 (E)-1-[[4-(5-dimethylphosphonomethyl-2,3-diphenylmethylenedioxy)phenoxy]phenyl]-2-[2-bromo-4-benzyloxy-5-methoxyphenyl]ethene 
• 331248-77-2 (E)-1-[[4-(5-methoxycarbonyl-2,3-diphenylmethylenedioxy)phenoxy]phenyl]-2-[2-bromo-4-benzyloxy-5-methoxyphenyl]ethene 
• 348618-46-2 4-Benzyloxy-7-(4-chloro-phenylsulfanyl)-3-methoxybicyclo [4.2.0]octa-1,3,5-triene-7-carbonitrile 
• 348618-49-5 3-amino-6-benzyloxy-7-methoxynaphthalene-2-carboxylic acid tert-butyl ester 
• 348618-47-3 4-benzyloxy-3-methoxy-7-phenylsulfanylbicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile 
• 629652-75-1 4-benzyloxy-3-methoxy-7-methylsulfanyl-bicyclo[4.2.0]octa-1⁽⁶⁾,2,4-triene-7-carbonitrile 

Relevant academic research and scientific papers

Regioselective synthesis of a potent Src kinase inhibitor: 4-(2,4-Dichloro-5-methoxyphenylamino)-7-methoxy-8-(2-morpholin-4-ylethoxy) benzo[g]quinoline-3-carbonitrile

The regioselective synthesis of compound 3, a potent Src kinase inhibitor is described. A key step in this synthesis is the regioselective thermal rearrangement of a substituted benzocyclobutene to provide a 2,3,6,7-tetrasubstituted naphthalene. An effici

Method for the regioselective preparation of substituted benzo[g]quinoline3-carbonitriles and benzo[g]quinazolines

This invention relates to a method for the regioselective synthesis of 4,6,7,8-substituted benzo[g]quinoline-3-carbonitriles and 4,6,7,8-substituted benzo[g]quinazolines as well as intermediates thereof. The compounds derived from this invention are usefu

Total syntheses of plagiochins A and D, macrocyclic bis(bibenzyls), by Pd(0) catalyzed intramolecular Stille-Kelly reaction

Total syntheses of plagiochins A (1) and D (4), the former of which exhibits a significant neurotrophic activity, have been accomplished. The key 16-membered ring closure in 4 has been achieved directly from the dibromoperrottetin derivative (7) by Pd(0)

Tricyclic protein kinase inhibitors

This invention provides compounds of formula 1, having the structure which are useful as inhibitors of protein tyro sine kinase and are antiproliferative agents.