76017-15-7

Upstream product

• 1493-13-6 trifluorormethanesulfonic acid 
• 35339-16-3 (E)-2-(3-oxo-1,3-diphenylpropylidene)-3,4-dihydronaphthalen-1(2H)-one 
• 94-41-7 benzalacetophenone 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 100-52-7 benzaldehyde 
• 98-86-2 acetophenone 

Downstream Products

• 76017-62-4 N-(4-Pyridyl)-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 76017-61-3 N-(2-Pyridyl)-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 76017-64-6 N-(2-Benzothiazolyl)-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 76017-38-4 N-n-Octyl-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 76017-55-5 N-(4-Methylphenyl)-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 76017-36-2 N-Amyl-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 74864-01-0 5,6-dihydro-2,4-diphenyl-1-phenethylnaphtho<1,2-b>pyridinium trifluoromethanesulphonate 
• 83698-52-6 Trifluoro-methanesulfonate1-(3-dimethylamino-propyl)-2,4-diphenyl-5,6-dihydro-benzo[h]quinolinium; 
• 83698-45-7 Trifluoro-methanesulfonate1-(2-diethylamino-ethyl)-2,4-diphenyl-5,6-dihydro-benzo[h]quinolinium; 
• 104745-45-1 1-(2-pentyl)-5,6-dihydro-2,4-diphenylnaphto<1,2-b>pyridinium trifluoromethanesulphonate 
• 76017-58-8 N-(m-Nitrophenyl)-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 
• 76017-40-8 N-o-Chlorobenzyl-5,6-dihydro-2,4-diphenylnaphtho<1,2-b>pyridinium triflate 

Relevant academic research and scientific papers

Radical C?N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent

Herein, we report a radical borylation of aromatic amines through a homolytic C(sp2)?N bond cleavage. This method capitalizes on a simple and mild activation via a pyrylium reagent (ScPyry-OTf) thus priming the amino group for reacti

Pyrylium Mediated Transformations of Neopentylamine

A series of 2,4-diphenyl-5,6-dihydrobenzochromenylium salts have been prepared.They react with neopentylamine to form the corresponding 1-neopentylquinolinium salts which on thermolysis afford neopentyl halides, trifluoracetate, and thiocyanate, in good yields without rearrangements.

Trifluoromethanesulphonic Acid as Cyclodehydrating Agent: Synthesis of Nitrogen Heterocycles via 5,6-Dihydro-2,4-diphenylpyrylium Cation

N-Substituted 5,6-dihydro-2,4-diphenylnaphtho-pyridinium triflates (5a-q) have been prepared in high yields by the condensation of 5,6-dihydro-2,4-diphenylnaphthopyrylium triflate (4) with different amines.The pyrylium salt (4) in turn can b

Improved Methods for Conversion of Primary Amines into Bromides

N-Alkyl- and N-benzyl-4-p-chlorophenyl-2,3,5,6-tetraphenyl- N-alkyl- and N-benzyl-2,3,4,5,6-pentaphenyl-, and N-alkyl- and N-benzyl-2,4,6-triphenyl-pyridinium bromides on pyrolysis at 180-220 deg C give the corresponding alkyl and benzyl bromides in high yield. 1-Benzyl-5,6-dihydro-2,4-diphenylbenzoquinolinium trifluoromethanesulphonate gave benzyl bromide on heating with KBr in dimethylformamide at 100 deg C, and n-octyl bromide (80percent) was obtained from the corresponding pentacyclic bromide in refluxing acetonitrile.

The Preparation of 2,4,6-Triphenylpyrylium Trifluoromethanesulphonate, Fluorosulphonate, Ethoxysulphonate, Naphthalene-2-sulphonate, Stannochloride, Trichloroacetate, and Trifluoroacetate and other Pyrylium Trifluoromethanesulphonates and their Reactions

The title pyrylium salts are all readily prepared in high yield from 1,3,5-triphenylpent-2-ene-1,5-dione.Amines react with the trifluoromethanesulphonate, naphthalene-2-sulphonate, and trifluoroacetate to give the corresponding pyridinium salts in high yi