Examples of 'pyridine' in a sentence
Meaning of "pyridine"
pyridine (noun): A colorless liquid with a strong, foul odor that is often used as a solvent or reagent in chemical processes. Pyridine is a common compound in organic chemistry and is known for its distinctive properties and reactions
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- Any of a class of aromatic heterocyclic compounds containing a ring of five carbon atoms and an nitrogen atom; especially the simplest one, C₅H₅N.
How to use "pyridine" in a sentence
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pyridine
Typical bases include pyridine and triethylamine.
Pyridine is also used as a base in condensation reactions.
Related to these are pyridine and its derivatives.
Pyridine and dimethylformamide are the preferred solvents.
Computational studies of pyridine related supramolecular structures.
Pyridine can also serve as the solvent.
Typical bases used are pyridine and triethylamine.
The pyridine recovered by distillation may be recycled.
Examples thereof include pyridine and dimethylaminopyridine.
The pyridine was evaporated under high vacuum.
It is possible to use pyridine also as the solvent.
Pyridine was removed by concentration under reduced pressure.
Preferred bases are pyridine and potassium carbonate.
The pyridine was removed leaving a brown residue.
It contains chiefly phenols and pyridine bases.
See also
The excess pyridine was distilled under vacuum.
Pyridinium is the cationic conjugate acid of pyridine.
Traces of pyridine were removed under high vacuum.
Examples of basic aromatic rings are pyridine or quinoline.
Preferably the pyridine or pyrmidine ring is subsituted.
With cyanogen bromide mediated pyridine activation.
Pyridine may be added but is not required.
Pyridyne in chemistry is the pyridine analogue of benzyne.
Traces of pyridine were removed using high vacuum.
This yellow crystalline solid is a derivative of pyridine.
Then pyridine was removed under reduced pressure.
Acetylation by acetic anhydride in the presence of pyridine.
The pyridine was removed as much as possible in vacuo.
Syntheses of the sulfonic acids of pyridine compounds.
Pyridine can be used as a solvent for recrystallisation.
It is evaporated and the pyridine is driven off.
Preferred solvents are aprotic solvents such a pyridine.
Pyridine might be evaluated differently now.
One suitable method is using an anhydride in pyridine.
A series of pyridine derivatives can be produced in this way.
Preferred bases include triethylamine and pyridine.
Pyridine can be replaced by the same amount of acetonitrile.
Examples of such groups are pyridine and pyrazine.
The pyridine analog is quinoline or isoquinoline.
Examples of suitable bases are triethylamine and pyridine.
Pyridine forms numerous complexes with transition metals.
These solvents are found to be advantageous over pyridine.
The structures of pyridine and pyridinium are almost identical.
Suitable bases include triethylamine and pyridine.
Pyridine has been used as the base in this case.
Preferably the reaction is carried out in pyridine.
Pyridine is usually employed as the base.
Most preferred among monodentate ligands is pyridine.
Epibatidine is a pyridine with a structure similar to that of nicotine.
One exemplary such solvent is anhydrous pyridine.
