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  2. Transition metal carboxylate complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carboxyl...

    A common reaction of metal carboxylates is their displacement by more basic ligands. Acetate is a common leaving group. They are especially prone to protonolysis, which is widely used to introduce ligands, displacing the carboxylic acid. In this way octachlorodimolybdate is produced from dimolybdenum tetraacetate:

  3. McMurry reaction - Wikipedia

    en.wikipedia.org/wiki/McMurry_reaction

    The reaction is named after its co-discoverer, John E. McMurry. The McMurry reaction originally involved the use of a mixture TiCl 3 and LiAlH 4 , which produces the active reagents. Related species have been developed involving the combination of TiCl 3 or TiCl 4 with various other reducing agents, including potassium , zinc , and magnesium .

  4. Calconcarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Calconcarboxylic_acid

    Calconcarboxylic acid (IUPAC name 3-hydroxy-4-[(2-hydroxy-4-sulfonaphthalen-1-yl)diazenyl]naphthalene-2-carboxylic acid; commonly called Patton and Reeder's Indicator) is an azo dye that is used as an indicator for complexometric titrations of calcium with ethylenediaminetetraacetic acid (EDTA) in the presence of magnesium. [2]

  5. Insertion reaction - Wikipedia

    en.wikipedia.org/wiki/Insertion_reaction

    This reaction happens via a SET mechanism ( single-electron-transfer mechanism ). If magnesium reacts with an alkyl halide, it forms a Grignard reagent, or if lithium reacts, an organolithium reagent is formed. Thus, this type of insertion reactions has important applications in chemical synthesis. Insertion reactions of magnesium and lithium

  6. Carboxylation - Wikipedia

    en.wikipedia.org/wiki/Carboxylation

    Carboxylation is a chemical reaction in which a carboxylic acid is produced by treating a substrate with carbon dioxide. [1] The opposite reaction is decarboxylation.In chemistry, the term carbonation is sometimes used synonymously with carboxylation, especially when applied to the reaction of carbanionic reagents with CO 2.

  7. Shiina macrolactonization - Wikipedia

    en.wikipedia.org/wiki/Shiina_macrolactonization

    Shiina macrolactonization (or Shiina lactonization) is an organic chemical reaction that synthesizes cyclic compounds by using aromatic carboxylic acid anhydrides as dehydration condensation agents. In 1994, Prof. Isamu Shiina ( Tokyo University of Science , Japan) reported an acidic cyclization method using Lewis acid catalyst , [ 1 ] [ 2 ...

  8. Metallacarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Metallacarboxylic_acid

    A metallacarboxylic acid is a metal complex with the ligand CO 2 H. These compounds are intermediates in reactions that involve carbon monoxide and carbon dioxide, these species are intermediates in the water gas shift reaction. Metallacarboxylic acids are also called hydroxycarbonyls. [1]

  9. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    The carboxylic acid Schmidt reaction starts with acylium ion 1 obtained from protonation and loss of water. Reaction with hydrazoic acid forms the protonated azido ketone 2 , which goes through a rearrangement reaction with the alkyl group R, migrating over the C-N bond with expulsion of nitrogen.