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  2. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.

  3. Kröhnke pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Kröhnke_pyridine_synthesis

    The mechanism of this Kröhnke-type reaction likely proceeds via a vinylogous cyanamide 23 which undergoes elimination of hydrocyanic acid, deprotonation to form enamine 24 and cyclization to form intermediate 25, which is then dehydrated to form the desired pyridine product. Figure 6. A clean one-pot Kröhnke method in aqueous media generates ...

  4. 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 ...

  5. Oxidation with chromium(VI) complexes - Wikipedia

    en.wikipedia.org/wiki/Oxidation_with_chromium(VI...

    One family of reagents employs the complex CrO 3 (pyridine) 2. [2] Sarett's reagent: a solution of CrO 3 (pyridine) 2 in pyridine. It was popularized for selective oxidation of primary and secondary alcohols to carbonyl compounds. Collins reagent is a solution of the same CrO 3 (pyridine) 2 but in dichloromethane. The Ratcliffe variant of ...

  6. 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 ...

  7. Transition metal pyridine complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_pyridine...

    The role of pyridine as a Lewis base extends also to main group chemistry. Examples include sulfur trioxide pyridine complex SO 3 (py) and pyridine adduct of borane, BH 3 py. Pyridine is classified as L ligand in the Covalent bond classification method. In the usual electron counting method, it is a two-electron ligand.

  8. Chichibabin reaction - Wikipedia

    en.wikipedia.org/wiki/Chichibabin_reaction

    Different aromatic nitrogen heterocyclic compounds proceed through the Chichibabin reaction in a matter of minutes and others can take hours. Factors that influence the reaction rate include: Basicity - The ideal pKa range is 5-8 and the reaction either does not proceed, or proceeds poorly outside of this range. The reaction occurs faster under ...

  9. Bipyridine - Wikipedia

    en.wikipedia.org/wiki/Bipyridine

    Bipyridines are a family of organic compounds with the formula (C 5 H 4 N) 2, consisting of two pyridyl (C 5 H 4 N) rings. Pyridine is an aromatic nitrogen-containing heterocycle. The bipyridines are all colourless solids, which are soluble in organic solvents and slightly soluble in water. Bipyridines, especially the 4,4' isomer, are mainly of ...