75573-11-4

Upstream product

• 2373-89-9 4,4'-dimethoxychalcone 
• 17282-38-1 1-(4-methylphenacyl)pyridinium bromide 
• 41564-67-4 (E)-1,3-bis(4-methoxyphenyl)-2-propene-1-one 
• 76337-69-4 4-Methylphenacyl-β-picolinium bromide 
• 20691-74-1 Triphenylarsin-p-anisoylmethylen 
• 50990-40-4 (2E)-3-(4-methoxyphenyl)-1-(4-methylphenyl)prop-2-en-1-one 
• 25407-31-2 N-(p-methoxyphenacyl)pyridinium bromide 
• 619-41-0 4-(bromoacetyl)toluene 
• 119-65-3 isoquinoline 

Relevant academic research and scientific papers

Studies on Benzopyridinium Ylids: Synthesis of Substituted 2,4,6-Triarylpyridines via Isoquinolinium Ylids

Aroylmethylene-isoquinolinium ylids (1) on reaction with substituted benzylideneacetophenones (2) in gl.acetic acid containing ammonium acetate afford 2,4,6-triarylpyridines (4).The reaction seems to proceed via N-(1,5-dioxo-2-pentyl)-isoquinolium derivat

Studies on Cycloimmonium Ylides. Synthesis of Some 2,4,6-Triaryl-Substituted Pyridines via Picolinium Ylides

A wide variety of 2,4,6-triaryl-substituted pyridines have been synthesized by the interaction of aroylmethylenepicolinium ylides with different α,β-unsaturated ketones.The structural assignments were based on microanalytical and spectral data.

Synthesis of Some New 2,4,6-Triaryl Substituted Pyridines via Pyridinium Ylides

Reactions of 4-methoxy phenacyl pyridinium ylide and 4-chlorophenacyl pyridinium ylide with different substituted α-β unsaturated ketones gave a wide variety of 2,4,6-triaryl substituted pyridines which are expected to possess marked biological activities

REACTION OF PHENACYLIDENETRIPHENYLARSENANES WITH α,β-UNSATURATED KETONES: SYNTHESIS OF SOME NEW 2,4,6-TRIARYLPYRIDINES

The reaction of some phenacylidenetriphenylarsenanes with substituted benzylideneacetophenones in the presence of ammonium acetate in acetic acid or methanol gave new 2,4,6-triarylpyridines.Ammonium acetate in acetic acid and ammonium acetate in methanol

Studies on Cycloimmonium Ylids. Synthesis of some New 2,4,6-Triaryl-substituted Pyridines via Pyridinium, Picolinium and Isoquinolinium Ylids

Reaction of pyridinium phenacylids and their picolinium and isoquinolinium counterparts with substituted benzylideneacetophenones gave a wide variety of 2,4,6-triaryl-substituted pyridines which are expected to have some potential biological activities.Ammonium acetate in glacial acetic acid was used as the cyclization agent.The structures of resulting pyridines are supported by nmr and ir spectral data.