Category:Name reactions
A name reaction is a chemical reaction named after its discoverers or developers.
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Pages in category "Name reactions"
The following 177 pages are in this category, out of approximately 532 total. This list may not reflect recent changes.
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- Nametkin rearrangement
- Narasaka–Prasad reduction
- Nazarov cyclization reaction
- Neber rearrangement
- Nef isocyanide reaction
- Nef reaction
- Negishi coupling
- Nenitzescu indole synthesis
- Newman–Kwart rearrangement
- Nicholas reaction
- Niementowski quinazoline synthesis
- Niementowski quinoline synthesis
- Nierenstein reaction
- Nitro-Mannich reaction
- Noise-induced order
- Norrish reaction
- Nozaki–Hiyama–Kishi reaction
P
- Paal–Knorr synthesis
- Parikh–Doering oxidation
- Passerini reaction
- Paternò–Büchi reaction
- Pauson–Khand reaction
- Payne rearrangement
- Pechmann condensation
- Pellizzari reaction
- Perkin reaction
- Perkin rearrangement
- Perkow reaction
- Petasis reaction
- Peterson olefination
- Petrenko-Kritschenko piperidone synthesis
- Pfitzinger reaction
- Pfitzner–Moffatt oxidation
- Piancatelli rearrangement
- Pictet–Hubert reaction
- Pictet–Spengler reaction
- Pinner reaction
- Pinnick oxidation
- Pomeranz–Fritsch reaction
- Povarov reaction
- Prato reaction
- Prévost reaction
- Prilezhaev reaction
- Prins reaction
- Pschorr cyclization
- Pudovik reaction
- Pummerer rearrangement
R
- Ramberg–Bäcklund reaction
- Rauhut–Currier reaction
- Jaffe reaction
- Reed reaction
- Reformatsky reaction
- Reilly–Hickinbottom rearrangement
- Reimer–Tiemann reaction
- Reissert indole synthesis
- Reissert reaction
- Reppe synthesis
- Retro-Diels–Alder reaction
- Retropinacol rearrangement
- Rieche formylation
- Riemschneider thiocarbamate synthesis
- Riley oxidation
- Ritter reaction
- Robinson annulation
- Robinson–Gabriel synthesis
- Rosenmund reduction
- Rosenmund–von Braun reaction
- Roskamp reaction
- Rothemund reaction
- Rubottom oxidation
- Ruff degradation
- Ružička reaction
S
- Sabatier reaction
- Saegusa–Ito oxidation
- Sakurai reaction
- Salol reaction
- Sandmeyer reaction
- Sarett oxidation
- Saville reaction
- Balz–Schiemann reaction
- Schikorr reaction
- Schmidt reaction
- Scholl reaction
- Schöllkopf method
- Schotten–Baumann reaction
- Seyferth–Gilbert homologation
- Shapiro reaction
- Sharpless asymmetric dihydroxylation
- Sharpless epoxidation
- Sharpless oxyamination
- Shi epoxidation
- Shiina macrolactonization
- Simmons–Smith reaction
- Skattebøl rearrangement
- Skraup reaction
- Smiles rearrangement
- Soai reaction
- Sommelet reaction
- Sommelet–Hauser rearrangement
- Sonogashira coupling
- Staudinger reaction
- Staudinger synthesis
- Steglich esterification
- Stephen aldehyde synthesis
- Stetter reaction
- Stevens rearrangement
- Stickland fermentation
- Stieglitz rearrangement
- Stille reaction
- Stobbe condensation
- Stollé synthesis
- Stork enamine alkylation
- Strecker amino acid synthesis
- Strecker degradation
- Suzuki reaction
- Swarts fluorination
- Swern oxidation
T
U
V
W
- Wacker process
- Wagner-Jauregg reaction
- Wagner–Meerwein rearrangement
- Wallach degradation
- Wallach rearrangement
- Weerman degradation
- Weinreb ketone synthesis
- Wenker synthesis
- Westphalen–Lettré rearrangement
- Wharton reaction
- Whiting reaction
- Widman–Stoermer synthesis
- Willgerodt rearrangement
- Williamson ether synthesis
- Wittig reaction
- Wohl degradation
- Wohl–Aue reaction
- Wohl–Ziegler bromination
- Wöhler synthesis
- Wolff rearrangement
- Wolff–Kishner reduction
- Wolffenstein–Böters reaction
- Woodward cis-hydroxylation
- Wurtz reaction
- Wurtz–Fittig reaction