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  2. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Osazone formation was developed by Emil Fischer, [3] who used the reaction as a test to identify monosaccharides. The formation of a pair of hydrazone functionalities involves both oxidation and condensation reactions. [4] Since the reaction requires a free carbonyl group, only "reducing sugars" participate.

  3. Trimethylsulfoxonium iodide - Wikipedia

    en.wikipedia.org/wiki/Trimethylsulfoxonium_iodide

    It is used to generate dimethyloxosulfonium methylide by reaction with sodium hydride. [1] The latter compound is used as a methylene-transfer reagent, and is used to prepare epoxides. This compound is commercially available. It may be prepared by the reaction of dimethyl sulfoxide and iodomethane: [2] (CH 3) 2 SO + CH 3 I → (CH 3) 3 SO + I −

  4. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Hydrazones are converted to azines when used in the preparation of 3,5-disubstituted 1H-pyrazoles, [12] a reaction also well known using hydrazine hydrate. [ 13 ] [ 14 ] With a transition metal catalyst , hydrazones can serve as organometallic reagent surrogates to react with various electrophiles.

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