Organometallic addition reactions
3,374 reactions: 10 worked examples with a reagent table you can scale, 503 named reactions and 2,861 checked procedures from Organic Syntheses.
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- Barbier reactionOrganometallic addition The Barbier reaction is an organometallic reaction between an alkyl halide (chloride, bromide, iodide), a carbonyl group and a metal.
- Barbier–Wieland degradationOrganometallic addition The Barbier–Wieland degradation is a procedure for shortening the carbon chain of a carboxylic acid by one carbon.
- Grignard reactionOrganometallic addition The Grignard reaction (French: [ɡʁiɲaʁ]) is an organometallic chemical reaction in which, according to the classical definition, carbon alkyl, allyl, vinyl, or aryl magnesium halides (Grignard reagent) are added to the carbonyl groups of either an aldehyde or ketone under anhydrous conditions.
- Lumière–Barbier methodOrganometallic addition The Lumière–Barbier method is a method of acetylating aromatic amines in aqueous solutions.
- Reformatsky reactionOrganometallic addition The Reformatsky reaction (sometimes transliterated as Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones with α-halo esters using metallic zinc to form β-hydroxy-esters.