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  2. 4-Pyrone - Wikipedia

    en.wikipedia.org/wiki/4-Pyrone

    4-Pyrone (γ-pyrone or pyran-4-one) is an unsaturated cyclic chemical compound with the molecular formula C 5 H 4 O 2.It is isomeric with 2-pyrone. Preparation [ edit ]

  3. Nazarov cyclization reaction - Wikipedia

    en.wikipedia.org/wiki/Nazarov_cyclization_reaction

    The key step of the reaction mechanism involves a cationic 4π-electrocyclic ring closure which forms the cyclopentenone product (See Mechanism below). As the reaction has been developed, variants involving substrates other than divinyl ketones and promoters other than Lewis acids have been subsumed under the name Nazarov cyclization provided ...

  4. Category:4-Pyrones - Wikipedia

    en.wikipedia.org/wiki/Category:4-Pyrones

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  5. Pyrone - Wikipedia

    en.wikipedia.org/wiki/Pyrone

    2-Pyrone 4-Pyrone. Pyrones or pyranones are a class of heterocyclic chemical compounds. They contain an unsaturated six-membered lactone ring, which has one oxygen atom and an adjacent ketone functional group. [1] There are two isomers denoted as 2-pyrone and 4-pyrone.

  6. 4-Pyridone - Wikipedia

    en.wikipedia.org/wiki/4-Pyridone

    4-Pyridone is an organic compound with the formula C 5 H 4 ... Preparation. 4-Pyridone, and its derivatives, are prepared from 4-pyrone and amines in protic solvents ...

  7. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    Initial steps in the Buchner–Curtius–Schlotterbeck reaction mechanism. The reaction is then completed either by the reformation of the carbonyl through an 1,2-rearrangement or by the formation of the epoxide. There are two possible carbonyl products: one formed by migration of R 1 (4) and the other by migration of R 2 (5). The relative ...

  8. Ring expansion and contraction - Wikipedia

    en.wikipedia.org/wiki/Ring_expansion_and_contraction

    Ring expansion and ring contraction reactions expand or contract rings, usually in organic chemistry. The term usually refers to reactions involve making and breaking C-C bonds, [1] Diverse mechanisms lead to these kinds of reactions. The bond migration step of the pinacol type rearrangement

  9. Reaction step - Wikipedia

    en.wikipedia.org/wiki/Reaction_step

    In chemistry, a reaction step of a chemical reaction is defined as: "An elementary reaction, constituting one of the stages of a stepwise reaction in which a reaction intermediate (or, for the first step, the reactants) is converted into the next reaction intermediate (or, for the last step, the products) in the sequence of intermediates between reactants and products". [1]