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  1. Aldol–Tishchenko reactionCondensation The Aldol–Tishchenko reaction is a tandem reaction involving an aldol reaction and a Tishchenko reaction. Named reaction · Wikipedia
  2. Dieckmann condensationCondensation The Dieckmann condensation is the intramolecular chemical reaction of diesters with base to give β-keto esters. Named reaction · Wikipedia
  3. Grieco three-component condensationCondensation The Grieco three-component condensation is an organic chemistry reaction that produces nitrogen-containing six-member heterocycles via a multi-component reaction of an aldehyde, a nitrogen component, such as aniline, and an electron-rich alkene. Named reaction · Wikipedia
  4. Japp–Maitland condensationCondensation The Japp–Maitland condensation is an organic reaction and a type of Aldol reaction and a tandem reaction. Named reaction · Wikipedia
  5. Knoevenagel condensationCondensation In organic chemistry, the Knoevenagel condensation (pronounced [ˈknøːvənaːɡl̩]) reaction is a type of chemical reaction named after German chemist Emil Knoevenagel. Named reaction · Wikipedia
  6. 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). Named reaction · Wikipedia
  7. 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. Named reaction · Wikipedia
  8. Pechmann condensationCondensation The Pechmann condensation is a synthesis of coumarins, starting from a phenol and a carboxylic acid or ester containing a β-carbonyl group. Named reaction · Wikipedia
  9. Perkin reactionCondensation The Perkin reaction is an organic reaction developed by English chemist William Henry Perkin in 1868 that is used to make cinnamic acids. Named reaction · Wikipedia
  10. Perkin rearrangementCondensation The Perkin rearrangement (coumarin–benzofuran ring contraction) is a rearrangement reaction in which a 2-halocoumarin in the presence of hydroxide undergoes a ring contraction to form a benzofuran. Named reaction · Wikipedia
  11. Stobbe condensationCondensation The Stobbe condensation entails the reaction of an aldehyde or ketone with an ester of succinic acid to generate alkylidene succinic acid or related derivatives. Named reaction · Wikipedia
  12. Ullmann condensationCondensation The Ullmann condensation or Ullmann-type reaction is the copper-promoted conversion of aryl halides to aryl ethers, aryl thioethers, aryl nitriles, and aryl amines. Named reaction · Wikipedia