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  2. Annulation - Wikipedia

    en.wikipedia.org/wiki/Annulation

    In organic chemistry, annulation (from Latin anellus 'little ring'; occasionally annelation) is a chemical reaction in which a new ring is constructed on a molecule. [1] Examples are the Robinson annulation, Danheiser annulation and certain cycloadditions.

  3. Ring expansion and contraction - Wikipedia

    en.wikipedia.org/wiki/Ring_expansion_and_contraction

    A common method for expanding a ring involves opening cyclopropane-containing bicyclic intermediate. The strategy can start with a Simmons-Smith-like cyclopropanation of a cyclic alkene. [8] A related cyclopropane-based ring expansion is the Buchner ring expansion. The Buchner ring expansion is used to convert arenes to cycloheptatrienes. The ...

  4. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    A cyclic compound or ring compound is a compound in which at least some its atoms are connected to form a ring. [1] Rings vary in size from three to many tens or even hundreds of atoms. Examples of ring compounds readily include cases where: all the atoms are carbon (i.e., are carbocycles),

  5. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...

  6. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined. Cross-couplings are a subset of the more general coupling reactions. Often cross-coupling reactions require metal catalyst

  7. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    nucleophilic substitution especially to small strained rings like epoxy [12] and aziridines; carbonyl-chemistry-like formation of ureas but not reactions of the aldol type due to low thermodynamic driving force. addition reactions to carbon-carbon double bonds like dihydroxylation or the alkynes in the thiol-yne reaction. [5] Sulfur (VI ...

  8. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    In commercial applications, the alkylating agents are generally alkenes, some of the largest scale reactions practiced in industry.Such alkylations are of major industrial importance, e.g. for the production of ethylbenzene, the precursor to polystyrene, from benzene and ethylene and for the production of cumene from benzene and propene in cumene process:

  9. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    The fluorine atom is para with respect to the substituent Z in the benzene ring. The image on the right shows four distinguished ring carbon atoms, C1, C2, C3, C4 in p-F-C 6 H 4-Z molecule. The carbon with Z is defined as C1(ipso) and fluorinated carbon as C4(para). This definition is followed even for Z = H.

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