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  2. Arylcyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Arylcyclohexylamine

    History. Phencyclidine (PCP) is believed to be the first arylcyclohexylamine with recognized anesthetic properties, but several arylcyclohexylamines were described before PCP in the scientific literature, beginning with PCA (1-phenylcyclohexan-1-amine) the synthesis of which was first published in 1907. PCP itself was discovered in 1926 but not ...

  3. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide-based reagents used as accelerators for vulcanization. It is a building block for pharmaceuticals (e.g., mucolytics, analgesics, and bronchodilators). The amine itself is an effective corrosion inhibitor.

  4. Eticyclidine - Wikipedia

    en.wikipedia.org/wiki/Eticyclidine

    Eticyclidine ( PCE, CI-400) is a dissociative anesthetic drug with hallucinogenic effects. It is similar in effects to phencyclidine but is slightly more potent. PCE was developed by Parke-Davis in the 1970s and evaluated for anesthetic potential under the code name CI-400, [2] but research into PCE was not continued after the development of ...

  5. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    i. mechanism. In organic chemistry, the Ei mechanism ( Elimination Internal/Intramolecular ), also known as a thermal syn elimination or a pericyclic syn elimination, is a special type of elimination reaction in which two vicinal (adjacent) substituents on an alkane framework leave simultaneously via a cyclic transition state to form an alkene ...

  6. Dicyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Dicyclohexylamine

    Synthesis. Dicyclohexylamine, as a mixture with cyclohexylamine, is prepared by the catalytic hydrogenation of aniline (phenylamine), with a catalyst of ruthenium and/or palladium. This method produces mainly cyclohexylamine with little dicyclohexylamine.

  7. Gabriel synthesis - Wikipedia

    en.wikipedia.org/wiki/Gabriel_synthesis

    The Gabriel synthesis is a chemical reaction that transforms primary alkyl halides into primary amines. Traditionally, the reaction uses potassium phthalimide . [1] [2] [3] The reaction is named after the German chemist Siegmund Gabriel .

  8. Phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Phenethylamine

    A much more convenient method for the synthesis of β-phenethylamine is the reduction of ω-nitrostyrene by lithium aluminium hydride in ether, whose successful execution was first reported by R. F. Nystrom and W. G. Brown in 1948. Phenethylamine can also be produced via the cathodic reduction of benzyl cyanide in a divided cell.

  9. Chemical synthesis - Wikipedia

    en.wikipedia.org/wiki/Chemical_synthesis

    In chemistry, chemical synthesis (chemical combination) is the artificial execution of chemical reactions to obtain one or several products. This occurs by physical and chemical manipulations usually involving one or more reactions.

  10. Electrosynthesis - Wikipedia

    en.wikipedia.org/wiki/Electrosynthesis

    In electrochemistry, electrosynthesis is the synthesis of chemical compounds in an electrochemical cell. Compared to ordinary redox reactions, electrosynthesis sometimes offers improved selectivity and yields. Electrosynthesis is actively studied as a science and also has industrial applications.

  11. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    In organic chemistry, peptide synthesis is the production of peptides, compounds where multiple amino acids are linked via amide bonds, also known as peptide bonds. Peptides are chemically synthesized by the condensation reaction of the carboxyl group of one amino acid to the amino group of another.