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  2. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    4-Methylpyridine is the organic compound with the formula CH 3 C 5 H 4 N. It is one of the three isomers of methylpyridine. This pungent liquid is a building block for the synthesis of other heterocyclic compounds. Its conjugate acid, the 4-methylpyridinium ion, has a pK a of 5.98, about 0.7 units above that of pyridine itself. [1]

  3. Chichibabin pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Chichibabin_pyridine_synthesis

    The Chichibabin pyridine synthesis (/ ˈ tʃ iː tʃ iː ˌ b eɪ b iː n /) is a method for synthesizing pyridine rings. The reaction involves the condensation reaction of aldehydes , ketones , α,β-Unsaturated carbonyl compounds , or any combination of the above, with ammonia . [ 1 ]

  4. 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]

  5. 2,6-Di-tert-butylpyridine - Wikipedia

    en.wikipedia.org/wiki/2,6-Di-tert-butylpyridine

    The synthesis is reminiscent of the Chichibabin reaction. Some related bulky pyridine compounds have been described, including 2,4,6-tri-t-butylpyridine [ 3 ] and 2,6-di-tert-butyl-4-methylpyridine. [ 4 ]

  6. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Methylpyridine or 3-picoline, is an organic compound with formula 3-CH 3 C 5 H 4 N. It is one of three positional isomers of methylpyridine, whose structures vary according to where the methyl group is attached around the pyridine ring. This colorless liquid is a precursor to pyridine derivatives that have applications in the pharmaceutical ...

  7. Oligonucleotide synthesis - Wikipedia

    en.wikipedia.org/wiki/Oligonucleotide_synthesis

    In the early 1950s, Alexander Todd's group pioneered H-phosphonate and phosphate triester methods of oligonucleotide synthesis. [5] [6] The reaction of compounds 1 and 2 to form H-phosphonate diester 3 is an H-phosphonate coupling in solution while that of compounds 4 and 5 to give 6 is a phosphotriester coupling (see phosphotriester synthesis ...

  8. Ribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Ribonucleotide

    DNA is defined by containing 2'-deoxy-ribose nucleic acid while RNA is defined by containing ribose nucleic acid. [1] In some occasions, DNA and RNA may contain some minor bases. Methylated forms of the major bases are most common in DNA. In viral DNA, some bases may be hydroxymethylated or glucosylated.

  9. Pyrosequencing - Wikipedia

    en.wikipedia.org/wiki/Pyrosequencing

    Pyrosequencing is a method of DNA sequencing (determining the order of nucleotides in DNA) based on the "sequencing by synthesis" principle, in which the sequencing is performed by detecting the nucleotide incorporated by a DNA polymerase. Pyrosequencing relies on light detection based on a chain reaction when pyrophosphate is released. Hence ...