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.
337–360 of 3,374
- Miyaura borylation Miyaura borylation, also known as the Miyaura borylation reaction, is a named reaction in organic chemistry that allows for the generation of boronates from vinyl or aryl halides with the cross-coupling of bis(pinacolato)diboron in basic conditions with a catalyst such as PdCl2(dppf).
- Mozingo reductionReduction The Mozingo reduction, also known as Mozingo reaction or thioketal reduction, is a chemical reaction capable of fully reducing a ketone or aldehyde to the corresponding alkane via a dithioacetal.
- Mukaiyama aldol additionCondensation In organic chemistry, the Mukaiyama aldol addition is an organic reaction and a type of aldol reaction between a silyl enol ether (R2C=CR−O−Si(CH3)3) and an aldehyde (R−CH=O) or formate (R−O−CH=O).
- Mukaiyama hydrationCondensation The Mukaiyama hydration is an organic reaction involving formal addition of an equivalent of water across an olefin by the action of catalytic bis(acetylacetonato)cobalt(II) complex, phenylsilane and atmospheric oxygen to produce an alcohol with Markovnikov selectivity.
- Mumm rearrangementRearrangement The Mumm rearrangement is an organic reaction and a rearrangement reaction.
- Murahashi couplingCross-coupling The Murahashi Coupling is a cross coupling reaction.
- Myers allene synthesis In organic chemistry, the Myers allene synthesis is a chemical reaction that converts a propargyl alcohol into an allene by way of an arenesulfonylhydrazine as a key intermediate.
- Myers deoxygenation In organic chemistry, the Myers deoxygenation reaction is an organic redox reaction that reduces an alcohol into an alkyl position by way of an arenesulfonylhydrazine as a key intermediate.
- Narasaka–Prasad reductionReduction The Narasaka–Prasad reduction, sometimes simply called Narasaka reduction, is a diastereoselective reduction of β-hydroxy ketones to the corresponding syn-dialcohols.
- Nazarov cyclizationCyclization The Nazarov cyclization, also known as the Nazarov reaction, is a chemical reaction used in organic chemistry for the synthesis of cyclopentenones.
- Neber rearrangementRearrangement The Neber rearrangement is an organic reaction in which a ketoxime is converted into an alpha-aminoketone via a rearrangement reaction.
- Nef isocyanide reaction The Nef isocyanide reaction is an addition reaction that takes place between isocyanides and acyl chlorides to form imidoyl chloride products, a process first discovered by John Ulrich Nef.
- Nef reaction In organic chemistry, the Nef reaction is an organic reaction describing the acid hydrolysis of a salt of a primary or secondary nitroalkane (R−NO2) to an aldehyde (R−CH=O) or a ketone (R2C=O) and nitroxyl (HNO), which rapidly converts to nitrous oxide (N2O).
- Nef synthesis In organic chemistry, Nef synthesis is the addition of sodium acetylides to aldehydes and ketones to yield propargyl alcohols.
- Negishi couplingCross-coupling The Negishi coupling is a widely employed transition metal catalyzed cross-coupling reaction.
- Nenitzescu indole synthesis The Nenitzescu indole synthesis is a chemical reaction that forms 5-hydroxyindole derivatives from benzoquinone and β-aminocrotonic esters.
- Newman–Kwart rearrangementRearrangement The Newman–Kwart rearrangement is a type of rearrangement reaction in which the aryl group of an O-aryl thiocarbamate, ArOC(=S)NMe2, migrates from the oxygen atom to the sulfur atom, forming an S-aryl thiocarbamate, ArSC(=O)NMe2.
- Nicholas reaction The Nicholas reaction is an organic reaction where a dicobalt octacarbonyl-stabilized propargylic cation is reacted with a nucleophile.
- Niementowski quinazoline synthesis The Niementowski quinazoline synthesis is the chemical reaction of anthranilic acids with amides to form 4-oxo-3,4-dihydroquinazolines (3H-quinazolin-4-ones).
- Niementowski quinoline synthesis The Niementowski quinoline synthesis is the chemical reaction of anthranilic acids and ketones (or aldehydes) to form γ-hydroxyquinoline derivatives.
- Nierenstein reaction The Nierenstein reaction is an organic reaction describing the conversion of an acid chloride into a haloketone with diazomethane.
- Nitro-Mannich reactionAddition The nitro-Mannich reaction (or aza-Henry reaction) is the nucleophilic addition of a nitroalkane (or the corresponding nitronate anion) to an imine, resulting in the formation of a beta-nitroamine.
- Noise-induced order Noise-induced order is a mathematical phenomenon appearing in the Matsumoto-Tsuda model of the Belosov-Zhabotinski reaction.
- Norrish reaction A Norrish reaction, named after Ronald George Wreyford Norrish who developed the reaction(s) during the 1930's primarily through his work at Cambridge University.
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