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  2. Phenylpiperazine - Wikipedia

    en.wikipedia.org/wiki/Phenylpiperazine

    1-Phenylpiperazine (1-PP or PP) is a simple chemical compound and drug featuring a phenyl group bound to a piperazine ring. [1] The suffix ‘-piprazole’ is sometimes used in the names of drugs to indicate they belong to this class. [2] It is a rigid analogue of amphetamine.

  3. Ruff degradation - Wikipedia

    en.wikipedia.org/wiki/Ruff_degradation

    Ruff degradation is a reaction used to shorten the open chain forms of monosaccharides. [1] It is functionally the reverse reaction of Kiliani-Fischer synthesis.. In 1898, Otto Ruff published his work on the transformation of D-Glucose to D-Arabinose later called the Ruff degradation.

  4. Piperazine - Wikipedia

    en.wikipedia.org/wiki/Piperazine

    Two common salts in the form of which piperazine is usually prepared for pharmaceutical or veterinary purposes are the citrate, 3C 4 H 10 N 2 ·2C 6 H 8 O 7 (i.e. containing 3 molecules of piperazine to 2 molecules of citric acid), and the adipate, C 4 H 10 N 2 ·C 6 H 10 O 4 (containing 1 molecule each of piperazine and adipic acid).

  5. Buchwald–Hartwig amination - Wikipedia

    en.wikipedia.org/wiki/Buchwald–Hartwig_amination

    The first example of a palladium catalyzed C–N cross-coupling reaction was published in 1983 by Migita and coworkers and described a reaction between several aryl bromides and N,N-diethylamino-tributyltin using 1 mol% PdCl 2 [P(o-tolyl) 3] 2.

  6. Carbohydrate synthesis - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_synthesis

    Anything larger than ten monosacharide units is called a polysaccharide, this broad category includes very large molecules such as starch, a plant glucose polymer which can contain millions of glucose residues. [2] The synthesis of carbohydrates is very important to the study of biochemistry and certain kinds of synthetic chemistry since ...

  7. N-Methylpiperazine - Wikipedia

    en.wikipedia.org/wiki/N-Methylpiperazine

    N-Methylpiperazine is a common building block used in organic synthesis. [2] For example, N-methylpiperazine is used in the manufacture of various pharmaceutical drugs including cyclizine, [3] meclizine, and sildenafil. The lithium salt, lithium N-methylpiperazide, is used as a reagent in organic synthesis for protection of aryl aldehydes. [4]

  8. 2,3-Dichlorophenylpiperazine - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichlorophenylpiperazine

    It is both a precursor in the synthesis of aripiprazole and one of its metabolites. [1] [2] It is unclear whether 2,3-DCPP is pharmacologically active as a serotonin receptor agonist similar to its close analogue 3-chlorophenylpiperazine (mCPP), though it has been shown to act as a partial agonist of the dopamine D 2 and D 3 receptors. [3]

  9. 2,5-Diketopiperazine - Wikipedia

    en.wikipedia.org/wiki/2,5-Diketopiperazine

    It is the parent of a large class of 2,5-Diketopiperazines (2,5-DKPs) with the formula (NHCH 2 (R)C(O)) 2 (R = H, CH 3, etc.). They are ubiquitous peptide in nature. They are often found in fermentation broths and yeast cultures as well as embedded in larger more complex architectures in a variety of natural products as well as several drugs. [ 2 ]