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  2. Phenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/Phenylhydrazine

    Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875. [7] [8] He prepared it by reduction of a phenyl diazonium salt using sulfite salts. Fischer used phenylhydrazine to characterize sugars via formation of hydrazones known as osazones with the sugar aldehyde. He also demonstrated in this ...

  3. Fischer indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Fischer_indole_synthesis

    The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions. [1] [2] The reaction was discovered in 1883 by Emil Fischer. Today antimigraine drugs of the triptan class are often synthesized by this method. The Fischer ...

  4. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Since the reaction requires a free carbonyl group, only "reducing sugars" participate. Sucrose, which is nonreducing, does not form an osazone. A typical reaction showing the formation of an osazone. D-glucose reacts with phenylhydrazine to give glucosazone. The same product is obtained from fructose and mannose.

  5. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Hydrazones can also be synthesized by the Japp–Klingemann reaction via β-keto acids or β-keto-esters and aryl diazonium salts. Hydrazones are converted to azines when used in the preparation of 3,5-disubstituted 1H-pyrazoles, [11] a reaction also well known using hydrazine hydrate.

  6. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Phenylhydrazine and 2,4-dinitrophenylhydrazine had been used historically in analytical chemistry to detect and identify compounds with carbonyl groups. Phenylhydrazine was used to study the structure of carbohydrates, because the reaction of the sugar's aldehyde groups lead to well crystallizing phenylhydrazones or osazones.

  7. Borsche–Drechsel cyclization - Wikipedia

    en.wikipedia.org/wiki/Borsche–Drechsel_cyclization

    Borsche–Drechsel cyclization is the central step in Borsche–Drechsel carbazole synthesis, where in the first step phenylhydrazine is condensed with cyclohexanone to form the cyclohexanone phenylhydrazone, and in the final step the resulting tetrahydrocarbazole is oxidized to carbazole itself.

  8. Moral Injury: The Grunts - The Huffington Post

    projects.huffingtonpost.com/moral-injury/the...

    Can we imagine ourselves back on that awful day in the summer of 2010, in the hot firefight that went on for nine hours? Men frenzied with exhaustion and reckless exuberance, eyes and throats burning from dust and smoke, in a battle that erupted after Taliban insurgents castrated a young boy in the village, knowing his family would summon nearby Marines for help and the Marines would come ...

  9. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Reaction 3: 4 NH 3 + N 2 H 4 → 3 N 2 + 8 H 2. The first two reactions are extremely exothermic (the catalyst chamber can reach 800 °C in a matter of milliseconds, [28]) and they produce large volumes of hot gas from a small volume of liquid, [29] making hydrazine a fairly efficient thruster propellant with a vacuum specific impulse of about ...