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  2. Electrophilic amination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_amination

    Other electron-deficient, sp 3 amination reagents react by similar mechanisms to give substitution products. [3] In aminations involving oxaziridines, nucleophilic attack takes place on the nitrogen atom of the three-membered ring. For some substrates (α-cyano ketones, for example), the resulting alkoxide reacts further to afford unexpected ...

  3. Cross electrophile coupling - Wikipedia

    en.wikipedia.org/wiki/Cross_Electrophile_Coupling

    Cross electrophile coupling is a type of cross-coupling reaction that occurs between two electrophiles. It is often catalyzed by transition metal catalyst(s). Unlike conventional cross-coupling reactions of an electrophile with an organometallic reagent, [1] the coupling partners in cross electrophile coupling reactions are both electrophiles. [2]

  4. Electrophile - Wikipedia

    en.wikipedia.org/wiki/Electrophile

    In chemistry, an electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron pair. [1] Because electrophiles accept electrons, they are Lewis acids . [ 2 ] Most electrophiles are positively charged , have an atom that carries a partial positive charge, or have an atom that does not have an octet of electrons.

  5. Stille reaction - Wikipedia

    en.wikipedia.org/wiki/Stille_reaction

    The mechanism of the Stille reaction has been extensively studied. [11] [23] The catalytic cycle involves an oxidative addition of a halide or pseudohalide (2) to a palladium catalyst (1), transmetalation of 3 with an organotin reagent (4), and reductive elimination of 5 to yield the coupled product (7) and the regenerated palladium catalyst (1).

  6. Electrophilic fluorination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_fluorination

    The mechanism of electrophilic fluorination remains controversial. At issue is whether the reaction proceeds via an S N 2 or single-electron transfer (SET) process. In support of the S N 2 mechanism, aryl Grignard reagents and aryllithiums give similar yields of fluorobenzene in combination with N-fluoro-o-benzenedisulfonimide (NFOBS), even though the tendencies of these reagents to ...

  7. Electrophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_substitution

    This reaction is similar to nucleophilic aliphatic substitution where the reactant is a nucleophile rather than an electrophile. The four possible electrophilic aliphatic substitution reaction mechanisms are S E 1, S E 2(front), S E 2(back) and S E i (Substitution Electrophilic), which are also similar to the nucleophile counterparts S N 1 and ...

  8. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    Therefore, they are generated by adding iron filings to bromine or chlorine. Here is the mechanism of this reaction: The mechanism for bromination of benzene. The mechanism for iodination is slightly different: iodine (I 2) is treated with an oxidizing agent such as nitric acid to obtain the electrophilic iodine ("I +", probably IONO 2).

  9. Electrophilic addition - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_addition

    The overall reaction for electrophilic addition to ethylene.. In organic chemistry, an electrophilic addition (A E) reaction is an addition reaction where a chemical compound containing a double or triple bond has a π bond broken, with the formation of two new σ bonds.