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Electrophilic Addition Reactions

electrophilic addition reactions   Named Reactions in Organic Synthesis

Featured reactions:

 

An addition reaction occurs when two molecules join together to create a more complex compound and all of the atoms in the original molecules are usually incorporated into the larger one. Electrophilic addition involves the attack of a primary substrate by an electrophile. The substrate generally possesses a carbon–carbon double or triple bond.

One of the first named reactions featuring electrophilic addition was the Prilezhaev reaction, named after the Russian chemist Nikolai Alexandrovich Prilezhaev who in 1909 was the first to use peroxycarboxylic acids to oxidize isolated double bonds to the corresponding oxiranes. Because of its wide utility, epoxidation is one of the most frequently used reactions in organic chemistry and epoxides such as epichlorohydrin are used in the manufacture of epoxy resins, a group of adhesives.

In this series, we feature the following electrophilic addition reactions:

 

Other named reactions that utilize electrophilic addition include:
  • Brown hydroboration reaction
  • Davis oxaziridine oxidation
  • Jacobsen–Katsuki epoxidation
  • Sharpless asymmetric epoxidation


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Other reaction categories:

Electrophilic aromatic substitution

Nucleophilic substitution reactions

Heterocycle-formation

Transition metal-catalyzed couplings

Oxidation

Reactions involving carbonyl compounds

Reduction reactions

Rearrangement reactions


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