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  2. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    These reaction partners can interact specifically with the strained alkene, staying bioorthogonal to endogenous alkenes found in lipids, fatty acids, cofactors and other natural products. [ 38 ] Alkene and azide [3+2] cycloaddition

  3. Hypochlorous acid - Wikipedia

    en.wikipedia.org/wiki/Hypochlorous_acid

    Hypochlorous acid is an inorganic compound with the chemical formula Cl O H, also written as HClO, HOCl, or ClHO. [2] [3] Its structure is H−O−Cl.It is an acid that forms when chlorine dissolves in water, and itself partially dissociates, forming a hypochlorite anion, ClO −.

  4. Enone–alkene cycloadditions - Wikipedia

    en.wikipedia.org/wiki/Enone–alkene_cycloadditions

    The less hindered faces of the enone and alkene react. [9] Intramolecular enone–alkene cycloaddition may give either "bent" or "straight" products depending on the reaction regioselectivity. When the tether between the enone and alkene is two atoms long, bent products predominate due to the rapid formation of five-membered rings. [10]

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The Wittig reaction involves reaction of an aldehyde or ketone with a Wittig reagent (or phosphorane) of the type Ph 3 P=CHR to produce an alkene and Ph 3 P=O. The Wittig reagent is itself prepared easily from triphenylphosphine and an alkyl halide.

  6. Ene reaction - Wikipedia

    en.wikipedia.org/wiki/Ene_reaction

    In organic chemistry, the ene reaction (also known as the Alder-ene reaction by its discoverer Kurt Alder in 1943) is a chemical reaction between an alkene with an allylic hydrogen (the ene) and a compound containing a multiple bond (the enophile), in order to form a new σ-bond with migration of the ene double bond and 1,5 hydrogen shift.

  7. Intramolecular Heck reaction - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_Heck_reaction

    The intramolecular Heck reaction (IMHR) in chemistry is the coupling of an aryl or alkenyl halide with an alkene in the same molecule. The reaction may be used to produce carbocyclic or heterocyclic organic compounds with a variety of ring sizes. Chiral palladium complexes can be used to synthesize chiral intramolecular Heck reaction products ...

  8. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    In polymer chemistry, polymerization (American English), or polymerisation (British English), is a process of reacting monomer molecules together in a chemical reaction to form polymer chains or three-dimensional networks. [1] [2] [3] There are many forms of polymerization [4] and different systems exist to categorize them. IUPAC definition for ...

  9. McMurry reaction - Wikipedia

    en.wikipedia.org/wiki/McMurry_reaction

    The McMurry reaction of benzophenone. The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent. The reaction is named after its co-discoverer, John E. McMurry.