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  2. Curtius rearrangement - Wikipedia

    en.wikipedia.org/wiki/Curtius_rearrangement

    Curtius rearrangement. The Curtius rearrangement (or Curtius reaction or Curtius degradation ), first defined by Theodor Curtius in 1885, is the thermal decomposition of an acyl azide to an isocyanate with loss of nitrogen gas. [1] [2] The isocyanate then undergoes attack by a variety of nucleophiles such as water, alcohols and amines, to yield ...

  3. Arylcyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Arylcyclohexylamine

    An arylcyclohexylamine is composed of a cyclohexylamine unit with an aryl moiety attachment. The aryl group is positioned geminal to the amine. In the simplest cases, the aryl moiety is typically a phenyl ring, sometimes with additional substitution. The amine is usually not primary; secondary amines such as methylamine or ethylamine, or ...

  4. Dynamic kinetic resolution in asymmetric synthesis - Wikipedia

    en.wikipedia.org/wiki/Dynamic_Kinetic_Resolution...

    Dynamic kinetic resolution in chemistry is a type of kinetic resolution where 100% of a racemic compound can be converted into an enantiopure compound. It is applied in asymmetric synthesis. Asymmetric synthesis has become a much explored field due to the challenge of creating a compound with a single 3D structure. [1]

  5. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    Williamson ether synthesis. The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol ( alkoxide ). This reaction was developed by Alexander Williamson in 1850. [2] Typically it involves the reaction of an alkoxide ion with a primary alkyl halide via an S N 2 reaction.

  6. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    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 in ...

  7. 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, but research into PCE was not continued after the development of ketamine, a similar drug with more favourable properties.

  8. Haber process - Wikipedia

    en.wikipedia.org/wiki/Haber_process

    Haber process. The Haber process, [1] also called the Haber–Bosch process, is the main industrial procedure for the production of ammonia. [2] [3] It converts atmospheric nitrogen (N 2) to ammonia (NH 3) by a reaction with hydrogen (H 2) using a finely divided iron metal catalyst: This reaction is slightly favorable in terms of enthalpy, but ...

  9. Pummerer rearrangement - Wikipedia

    en.wikipedia.org/wiki/Pummerer_rearrangement

    The organic group "R2" shown in the diagram above on the bottom right is the methyl violet carbocation, whose pK R+ of 9.4 is not sufficient to out-compete loss of H + and therefore a classical Pummerer rearrangement occurs. The reaction on the left is a fragmentation because the leaving group with pK R+ = 23.7 is particularly stable.