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  2. Ylide - Wikipedia

    en.wikipedia.org/wiki/Ylide

    An ylide (/ ˈ ɪ l aɪ d /) [1] or ylid (/ ˈ ɪ l ɪ d /) is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached to a heteroatom with a formal positive charge (usually nitrogen, phosphorus or sulfur), and in which both atoms have full octets of electrons.

  3. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    Pyridinium refers to the cation [C 5 H 5 NH] +. It is the conjugate acid of pyridine. Many related cations are known involving substituted pyridines, e.g. picolines ...

  4. Zincke reaction - Wikipedia

    en.wikipedia.org/wiki/Zincke_reaction

    The first reaction is the formation of the N-2,4-dinitrophenyl-pyridinium salt (2). This salt is typically isolated and purified by recrystallization. The formation of the DNP-pyridinium salt. Upon heating a primary amine with the N-2,4-dinitrophenyl-pyridinium salt (2), the addition

  5. Zincke aldehyde - Wikipedia

    en.wikipedia.org/wiki/Zincke_aldehyde

    Zincke aldehydes, or 5-aminopenta-2,4-dienals, are the product of the reaction of a pyridinium salt with two equivalents of any secondary amine, followed by basic hydrolysis. Using secondary amines (as opposed to primary amines) the Zincke reaction takes on a different shape forming Zincke aldehydes in which the pyridine ring is ring-opened ...

  6. Kröhnke pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Kröhnke_pyridine_synthesis

    The Kröhnke synthesis is generally performed in either glacial acetic acid or methanol, but it can also be done under aqueous conditions, and more recently under solvent-free conditions. 1,3-dicarbonyl compounds have also been shown to be viable starting materials in place of the α-pyridinium methyl ketone salts. [ 7 ]

  7. Pyrylium - Wikipedia

    en.wikipedia.org/wiki/Pyrylium

    Pyrylium salts are easily produced from simple starting materials through a condensation reaction. [2]Pyrylium salts with aromatic substituents, such 2,4,6-triphenylpyrylium tetrafluoroborate, can be obtained from two moles of acetophenone, one mole of benzaldehyde, and excess tetrafluoroboric acid. [3]

  8. Red Dye 3 Just Got Banned. These Are the Foods to Avoid If ...

    www.aol.com/red-dye-3-just-got-134800003.html

    Experts recommend that if you're concerned about red food colorings or synthetic dyes, one of the most impactful changes is to prioritize whole, real foods over ultra-processed ones and carefully ...

  9. Category:Pyridines - Wikipedia

    en.wikipedia.org/wiki/Category:Pyridines

    Pyridinium compounds (37 P) T. Thienopyridines (10 P) Pages in category "Pyridines" The following 200 pages are in this category, out of approximately 253 total.