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  2. Persistent radical effect - Wikipedia

    en.wikipedia.org/wiki/Persistent_radical_effect

    The persistent radical effect (PRE) in chemistry describes and explains the selective product formation found in certain free-radical cross-reactions. In these type of reactions, different radicals compete in secondary reactions. The so-called persistent (long-lived) radicals do not self-terminate and only react in cross-couplings.

  3. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    Organic reactions can be organized into several basic types. Some reactions fit into more than one category. For example, some substitution reactions follow an addition-elimination pathway. This overview isn't intended to include every single organic reaction. Rather, it is intended to cover the basic reactions.

  4. Kharasch addition - Wikipedia

    en.wikipedia.org/wiki/Kharasch_addition

    The Kharasch addition is an organic reaction and a metal-catalysed free radical ... An example of Kharasch addition is the synthesis of 1,1,3-trichloro-n ...

  5. Radical initiator - Wikipedia

    en.wikipedia.org/wiki/Radical_initiator

    Radical initiators are utilized in industrial processes such as polymer synthesis. Typical examples are molecules with a nitrogen-halogen bond, azo compounds , and organic and inorganic peroxides . [ 2 ]

  6. Barton reaction - Wikipedia

    en.wikipedia.org/wiki/Barton_reaction

    Large excesses of activated alkenes can be used to intercept the alkyl radical and results in formation of a C-C bond from an unactivated C-H bond. [21] In the presence of oxygen, the alkyl radical is trapped and forms an organic peroxy radical. This intermediate is trapped by the nitrosyl radical and then isomerizes to give a δ-nitrate ester ...

  7. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    In organic chemistry, the Michael reaction or Michael 1,4 addition is a reaction between a Michael donor (an enolate or other nucleophile) and a Michael acceptor (usually an α,β-unsaturated carbonyl) to produce a Michael adduct by creating a carbon-carbon bond at the acceptor's β-carbon.

  8. Cascade reaction - Wikipedia

    en.wikipedia.org/wiki/Cascade_reaction

    The high reactivity of free radical species renders radical-based synthetic approaches decidedly suitable for cascade reactions. [4] One of the most widely recognized examples of the synthetic utility of radical cascades is the cyclization sequence employed in the total synthesis of (±)-hirsutene, in 1985 (Scheme 6).

  9. Radical (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Radical_(chemistry)

    Radical elimination can be viewed as the reverse of radical addition. In radical elimination, an unstable radical compound breaks down into a spin-paired molecule and a new radical compound. Shown below is an example of a radical elimination reaction, where a benzoyloxy radical breaks down into a phenyl radical and a carbon dioxide molecule. [7]