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  2. 2-Pyridone - Wikipedia

    en.wikipedia.org/wiki/2-Pyridone

    The amide group can be involved in hydrogen bonding to other nitrogen- and oxygen-containing species.. The predominant solid state form is 2-pyridone. This has been confirmed by X-ray crystallography which shows that the hydrogen in solid state is closer to the nitrogen than to the oxygen (because of the low electron density at the hydrogen the exact positioning is difficult), and IR ...

  3. Pyridone - Wikipedia

    en.wikipedia.org/wiki/Pyridone

    4-Pyridone These can adopt three tautomers , a oxo form, a zwitterion form, and a enol form. Whereas 2-pyridone (α) and 4-pyridone (γ) predominantly adopt the oxo form, the 3-pyridone (β) cannot, and instead adopts an equilibrium of the zwitterion form, pyridin-1-ium-3-olate, and the enol form, 3-hydroxypyridine (the canonical form).

  4. Category:2-Pyridones - Wikipedia

    en.wikipedia.org/wiki/Category:2-Pyridones

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  5. Petrenko-Kritschenko piperidone synthesis - Wikipedia

    en.wikipedia.org/wiki/Petrenko-Kritschenko...

    The synthesis of tropinone can be seen as a variation of the Petrenko-Kritschenko reaction in which the two aldehyde functions are covalently linked in a single molecule. Apart from the Hantzsch synthesis the Petrenko-Kritschenko reaction is one of the few examples in which a symmetric pyridine precursor can be obtained in a multicomponent ring ...

  6. Pyridyne - Wikipedia

    en.wikipedia.org/wiki/Pyridyne

    The reaction of 3-bromo-4-chloropyridine with furan and lithium amalgam gives 1,4-epoxy-dihydroquinoline through the 2,3-pyridyne intermediate. The reaction of 4-bromopyridine with sodium in liquid ammonia gives both 3-aminopyridine and 4-aminopyridine through the 3,4-pyridyne intermediate and an E1cB-elimination reaction .

  7. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .

  8. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    The reaction is then completed either by the reformation of the carbonyl through an 1,2-rearrangement or by the formation of the epoxide. There are two possible carbonyl products: one formed by migration of R 1 (4) and the other by migration of R 2 (5). The relative yield of each possible carbonyl is determined by the migratory preferences of ...

  9. C7H8N2O2 - Wikipedia

    en.wikipedia.org/wiki/C7H8N2O2

    The molecular formula C 7 H 8 N 2 O 2 may refer to: N 1-Methyl-2-pyridone-5-carboxamide; N 1-Methyl-4-pyridone-3-carboxamide