887-94-5

Upstream product

• 14886-84-1 N-methyl-2-phenylquinolium iodide 
• 91-22-5 quinoline 
• 591-51-5 phenyllithium 
• 74-88-4 methyl iodide 
• 6120-94-1 N-methylanilinochlorophenylborane 
• 14371-10-9 (E)-3-phenylpropenal 
• 100-52-7 benzaldehyde 
• 3867-18-3 2-vinylaniline 
• 33149-71-2 trans-β-methyl-o-aminostyrene 
• 615-43-0 2-iodophenylamine 
• 936637-46-6 (E)-1-phenyl-N-(2-((E)-prop-1-en-1-yl)phenyl)methanimine 
• 875897-55-5 (E)-1-phenyl-N-(2-vinylphenyl)methanimine 
• 936637-51-3 C₁₈H₁₉N 
• 936637-50-2 C₁₉H₂₁N 

Downstream Products

• 130210-69-4 C₂₀H₁₉N₂O₄S₂^(1-)*C₁₆H₁₄N⁽¹⁺⁾ 
• 24005-23-0 2-phenyl-1,2,3,4-tetrahydroquinoline 
• 118848-62-7 1-Methyl-2-phenyl-1,2,3,4-tetrahydro-6-quinolinecarbaldehyde 
• 99338-55-3 1-methyl-2-phenylquinolinium 3-p-toluenesulfonylamino-4-hydroxyphenyl-p-toluenesulfonyliminate 
• 16524-11-1 2-(N-benzoyl-N-methylamino)benzoic acid 
• 79461-71-5 1-methyl-2-phenyl-1,2,3,4-tetrahydroquinoline 
• 99354-78-6 C₂₀H₁₈ClN₂O₅S₂^(1-)*C₁₆H₁₄N⁽¹⁺⁾ 
• 99338-41-7 N-methyl-2-phenylquinolinium 1-p-toluenesulfonylimino-3-p-toluenesulfonylaminocyclohexadienate-1,5-one 
• 99338-65-5 C₁₈H₁₄ClN₂O₅S₂^(1-)*C₁₆H₁₄N⁽¹⁺⁾ 
• 97984-21-9 C₁₆H₁₄N⁽¹⁺⁾*C₁₂H₅N₄^(1-) 
• 97984-21-9 C₁₆H₁₄N⁽¹⁺⁾*C₁₂H₄N₄^(1-) 
• 14886-84-1 N-methyl-2-phenylquinolium iodide 
• 612-96-4 2-Phenylquinoline 
• 34557-54-5 methane 

Relevant academic research and scientific papers

Rapid synthesis of the tetrahydroquinoline alkaloids: angustureine, cuspareine and galipinine

A one-pot method for the preparation of 1,2-substituted dihydroquinolines is described. This method features the C-2 addition of a range of organolithium reagents to quinoline followed by the in-situ addition of an electrophile. Standard palladium-catalys

Pd-catalyzed arylation/ring-closing metathesis approach to azabicycles

Palladium-catalyzed arylation followed by Grignard addition to imines and ring-closing metathesis, using Grubbs' catalysts, provides a route to six-, seven-, and eight-membered azabicycles.

Preparation of ortho-hydroxyalkylanilines as ortho-quinone methide imine precursors via an aminoborane complex

A general process for ortho-specific hydroxyalkylation of secondary anilines has been developed.N-Methylanilinochlorophenylboranes react readily with aryl aldehydes, and with α,β-unsaturated or saturated aliphatic aldehydes to give the corresponding ortho-hydroxyalkylanilines in good yield.Thermolysis of the latter generated the corresponding ortho-quinone methide imine, which can participate in an electrocyclic or intramolecular cycloaddition reaction to give various dihydro- and tetrahydroquinoline derivatives.Application of the method to the syntheses of 5-aza anal ogs of hexahydrocannabinol is demonstrated.Key words: quinone methide imine, ortho-hydroxyalkylaniline, azacannabinoids.