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  2. Kröhnke pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Kröhnke_pyridine_synthesis

    The Kröhnke method in this synthesis was crucial due to the failure of other cyclization techniques such as the Glaser coupling or Ullmann coupling. Figure 13. Another use of the Kröhnke pyridine synthesis was the generation of a number of 2,4,6-trisubstituted pyridines that were investigated as potential topoisomerase 1 inhibitors.

  3. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C 5 H 5 NH +) ions.For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts.

  4. 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

  5. Hantzsch ester - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_ester

    Hantzsch ester refers to an organic compound with the formula HN(MeC=C(CO 2 Et)) 2 CH 2 where Me = methyl (CH 3) and Et = ethyl (C 2 H 5).It is a light yellow solid. The compound is an example of a 1,4-dihydropyridine.

  6. Hantzsch pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_pyridine_synthesis

    Upon metabolism, 1,4-DHP based antihypertensive drugs undergo oxidation by way of cytochrome P-450 in the liver and are thus converted to their pyridine derivatives. [11] As a result, particular attention has been paid to the aromatization of 1,4-DHPs as a means to understand biological systems and so as to develop new methods of accessing ...

  7. 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] It was reported by Aleksei Chichibabin in 1924.

  8. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    In one alternative method, formation of toxic chromyl chloride (CrO 2 Cl 2) fumes during the making of the aforementioned solution were minimized by simply changing the order of addition: a cold solution of pyridine in concentrated hydrochloric acid was added to solid chromium trioxide under stirring. [5]

  9. Basement waterproofing - Wikipedia

    en.wikipedia.org/wiki/Basement_waterproofing

    The drainage system collects any water entering the basement and drains it to an internally placed sump pump system, which will then pump the water out of the basement. The Federal Emergency Management Agency (FEMA) recommends basement waterproofing with a water alarm and "battery-operated backup pump" as a preventive measure against the high ...