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  2. Hydrazide - Wikipedia

    en.wikipedia.org/wiki/Hydrazide

    An applied example is a synthesis of sunitinib begins by mixing 5-fluoroisatin slowly into hydrazine hydrate. [10] After 4 hours at 110 °C, the indole ring structure has been broken into (2-amino-5-fluoro-phenyl)-acetic acid hydrazide with reduction of the ketone at the 3-position.

  3. Pellizzari reaction - Wikipedia

    en.wikipedia.org/wiki/Pellizzari_reaction

    The Pellizzari reaction was discovered in 1911 by Guido Pellizzari, and is the organic reaction of an amide and a hydrazide to form a 1,2,4-triazole. [1] The product is similar to that of the Einhorn-Brunner reaction, but the mechanism itself is not regioselective. An overview of the Pellizzari reaction

  4. McFadyen–Stevens reaction - Wikipedia

    en.wikipedia.org/wiki/McFadyen–Stevens_reaction

    Dudman et al. have developed an alternative hydrazide reagent. ... "Use of 2,4,6-tri-isopropylbenzenesulphonyl hydrazide in the mcfadyen-stevens aldehyde synthesis". ...

  5. Shapiro reaction - Wikipedia

    en.wikipedia.org/wiki/Shapiro_reaction

    The Shapiro reaction or tosylhydrazone decomposition is an organic reaction in which a ketone or aldehyde is converted to an alkene through an intermediate hydrazone in the presence of 2 equivalents of organolithium reagent.

  6. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).

  7. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Pigment Yellow 97, a popular yellow colorant, is a hydrazone. [6]Hydrazones are the basis for various analyses of ketones and aldehydes. For example, dinitrophenylhydrazine coated onto a silica sorbent is the basis of an adsorption cartridge.

  8. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  9. p-Toluenesulfonyl hydrazide - Wikipedia

    en.wikipedia.org/wiki/P-toluenesulfonyl_hydrazide

    p-Toluenesulfonyl hydrazide is the organic compound with the formula CH 3 C 6 H 4 SO 2 NHNH 2. It is a white solid that is soluble in many organic solvents but not water or alkanes. It is a reagent in organic synthesis. [1]