Oxidation 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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- Pfitzner–Moffatt oxidationOxidation The Pfitzner–Moffatt oxidation, sometimes referred to as simply the Moffatt oxidation, is a chemical reaction for the oxidation of primary and secondary alcohols to aldehydes and ketones, respectively.
- Pinnick oxidationOxidation The Pinnick oxidation is an organic reaction by which aldehydes can be oxidized into their corresponding carboxylic acids using sodium chlorite (NaClO2) under mild acidic conditions.
- Riley oxidationOxidation The Riley oxidation is a selenium dioxide-mediated oxidation of methylene groups adjacent to carbonyls.
- Rubottom oxidationOxidation The Rubottom oxidation is a useful, high-yielding chemical reaction between silyl enol ethers and peroxyacids to give the corresponding α-hydroxy carbonyl product.
- Saegusa–Ito oxidationOxidation The Saegusa–Ito oxidation is a chemical reaction used in organic chemistry.
- Sarett oxidationOxidation The Sarett oxidation is an organic reaction that oxidizes primary and secondary alcohols to aldehydes and ketones, respectively, using chromium trioxide and pyridine.
- Sharpless epoxidationOxidation The Sharpless epoxidation reaction is an enantioselective chemical reaction to prepare 2,3-epoxyalcohols from primary and secondary allylic alcohols.
- Shi epoxidationOxidation The Shi epoxidation is a chemical reaction, as the asymmetric epoxidation of alkenes with oxone (potassium peroxymonosulfate) and a fructose-derived catalyst (1).
- Stahl oxidationOxidation The Stahl oxidation is a copper-catalyzed aerobic oxidation of primary and secondary alcohols to aldehydes and ketones.
- Swern oxidationOxidation In organic chemistry, the Swern oxidation also known as Moffatt–Swern, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol (−OH) is oxidized to an aldehyde (−CH=O) or ketone (>C=O) using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine.
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