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  1. Suzuki–Miyaura coupling: 4-bromobenzonitrile + phenylboronic acid → 4-cyanobiphenylCross-couplingC-C Canonical Pd(0)-catalysed cross-coupling of an aryl halide with an aryl boronic acid. Worked example · after Suzuki 1979 Scale
  2. Buchwald–Hartwig aminationCross-coupling In organic chemistry, the Buchwald–Hartwig amination is a chemical reaction for the synthesis of carbon–nitrogen bonds via the palladium-catalyzed coupling reactions of amines with aryl halides. Named reaction · Wikipedia
  3. Cadiot–Chodkiewicz couplingCross-coupling The Cadiot–Chodkiewicz coupling in organic chemistry is a coupling reaction between a terminal alkyne and a haloalkyne catalyzed by a copper(I) salt such as copper(I) bromide and an amine base. Named reaction · Wikipedia
  4. Castro–Stephens couplingCross-coupling The Castro–Stephens coupling is a cross coupling reaction between a copper(I) acetylide and an aryl halide in pyridine, forming a disubstituted alkyne and a copper(I) halide. Named reaction · Wikipedia
  5. Chan–Lam couplingCross-coupling The Chan–Lam coupling reaction, also known as the Chan–Evans–Lam coupling, is a cross-coupling reaction between an aryl boronic acid and an alcohol or an amine to form the corresponding secondary aryl amines or aryl ethers, respectively. Named reaction · Wikipedia
  6. Fukuyama couplingCross-coupling The Fukuyama coupling is a coupling reaction taking place between a thioester and an organozinc halide in the presence of a palladium catalyst. Named reaction · Wikipedia
  7. Glaser couplingCross-coupling The Glaser coupling is a type of coupling reaction. Named reaction · Wikipedia
  8. Heck reactionCross-coupling The Heck reaction (also called the Mizoroki–Heck reaction) is the chemical reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst to form a substituted alkene. Named reaction · Wikipedia
  9. Heck–Matsuda reactionCross-coupling The Heck–Matsuda (HM) reaction is an organic reaction and a type of palladium catalysed arylation of olefins that uses arenediazonium salts as an alternative to aryl halides and triflates. Named reaction · Wikipedia
  10. Hirao couplingCross-coupling In organic chemistry, Hirao coupling is a chemical reaction for the formation of carbon-phosphorus bonds using palladium cross-coupling. Named reaction · Wikipedia
  11. Hiyama couplingCross-coupling The Hiyama coupling is a palladium-catalyzed cross-coupling reaction of organosilanes with organic halides used in organic chemistry to form carbon–carbon bonds (C-C bonds). Named reaction · Wikipedia
  12. Kumada couplingCross-coupling In organic chemistry, the Kumada coupling is a type of cross coupling reaction, useful for generating carbon–carbon bonds by the reaction of a Grignard reagent and an organic halide. Named reaction · Wikipedia
  13. Liebeskind–Srogl couplingCross-coupling The Liebeskind–Srogl coupling reaction is an organic reaction forming a new carbon–carbon bond from a thioester and a boronic acid using a metal catalyst. Named reaction · Wikipedia
  14. Murahashi couplingCross-coupling The Murahashi Coupling is a cross coupling reaction. Named reaction · Wikipedia
  15. Negishi couplingCross-coupling The Negishi coupling is a widely employed transition metal catalyzed cross-coupling reaction. Named reaction · Wikipedia
  16. Sonogashira couplingCross-coupling The Sonogashira reaction is a cross-coupling reaction used in organic synthesis to form carbon–carbon bonds. Named reaction · Wikipedia
  17. Stille reactionCross-coupling The Stille reaction is a chemical reaction widely used in organic synthesis. Named reaction · Wikipedia
  18. Suzuki reactionCross-coupling The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. Named reaction · Wikipedia
  19. Accelerated Suzuki coupling via a ligandless palladium catalyst: 4-methoxy-2'-methylbiphenylCross-coupling Org. Synth. Vol. 75, p. 61 · Goodson et al.
  20. Alkynyl(phenyl)iodonium tosylates: preparation and stereospecific coupling with vinylcopper reagents. Formation of conjugated enynes. 1-Hexynyl(phenyl)iodonium tosylate and (E)-5-phenyldodec-5-en-7-yneCross-coupling Org. Synth. Coll. Vol. 9, p. 477; Vol. 70, p. 215 · Stang and Kitamura
  21. Coupling of o-tolidine and chicago acidCross-coupling Org. Synth. Coll. Vol. 2, p. 145; Vol. 16, p. 12 · Hartwell and Fieser
  22. Discussion addendum for: 4-methoxy-4'-nitrophenyl. Recent advances in the Stille biaryl coupling reaction and applications in complex natural products synthesisCross-coupling Org. Synth. Vol. 88, p. 197 · Williams*
  23. Discussion Addendum for: palladium catalyzed cross-coupling of (Z)-1-heptenyldimethylsilanol with 4-iodoanisole: (Z)-(1-heptenyl)-4-methoxybenzeneCross-coupling Org. Synth. Vol. 88, p. 102 · * and Liu
  24. Discussion Addendum for: Suzuki-Miyaura Cross-Coupling: Preparation of 2'-VinylacetanilideCross-coupling Org. Synth. Vol. 89, p. 202 · O'Shea.*