Chemistry Heterocyclic Building Blocks Pyridines 2,4,6-triphenylpyridine
Ambeed provide 7 derivatives of 2,4,6-triphenylpyridine.
These compounds have the same murcko framework: 2,4,6-triphenylpyridine.
Substitution Reactions: Due to the presence of the phenyl groups, 2,4,6-triphenylpyridine can undergo substitution reactions where one or more hydrogen atoms are replaced by other groups or atoms. For example, it might react with electrophiles to form substituted derivatives.
Oxidation Reactions: Depending on the conditions, 2,4,6-triphenylpyridine may undergo oxidation reactions. This could involve the conversion of a hydrogen atom to a more oxidized state, for example, converting a methyl group to a carboxyl group.
Reduction Reactions: Conversely, 2,4,6-triphenylpyridine could also undergo reduction reactions, where a more oxidized group is converted to a less oxidized state.
Metalation Reactions: The pyridine ring can act as a ligand and coordinate with metal ions. This can lead to the formation of metal complexes.
Lewis Acid-Base Reactions: Depending on the conditions and the reagents present, 2,4,6-triphenylpyridine can act as either a Lewis acid (electron pair acceptor) or a Lewis base (electron pair donor).
Condensation Reactions: It could potentially participate in condensation reactions with appropriate reagents, leading to the formation of larger molecules.
Arylation Reactions: Given the presence of phenyl groups, it could potentially undergo reactions where aryl groups are introduced or substituted.
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5,5',5''-(Pyridine-2,4,6-triyl)triisophthalic acid
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4,4',4''-(Pyridine-2,4,6-triyl)trianiline
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4-(3,5-Dimethylphenyl)-2,6-di-p-tolylpyridine
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N,N-Dimethyl-4-(2-(2-(octyloxy)phenyl)-6-phenylpyridin-4-yl)aniline
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4,4',4''-(Pyridine-2,4,6-triyl)tribenzoic acid
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4,4',4''-(Pyridine-2,4,6-triyl)tribenzaldehyde