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This page aims to list well-known chemical reactions , name reactions , name reagents , and name rules to stimulate the creation of Wikipedia articles.
reaction instead of synthesis ). I would suggest to give new articles a descriptive title if possible (e.g. Birch reduction instead of Birch reaction , Williamson ether synthesis instead of Williamson reaction ).
http://themerckindex.cambridgesoft.com/TheMerckIndex/NameReactions/ http://www.organic-chemistry.org/namedreactions/index.htm http://fachschaft.cup.uni-muenchen.de/~schleifi/reaktion/reaction/ http://www.stolaf.edu/depts/chemistry/courses/toolkits/247/practice/medialib/data/
See also
Contents
1 (back up )
1,3-dipolar cycloaddition
A (back up )
Abramovitch-Shapiro tryptamine synthesis Acetoacetic ester condensation Acyloin condensation Adams catalyst Adkins catalyst Adkins-Peterson reaction Akabori amino acid reaction Alder ene reaction Alder-Rickert rule Alder-Stein rules Aldol addition Aldol condensation Algar-Flynn-Olyamada reaction Allan-Robinson reaction Allylic rearrangement Amadori rearrangement Andrussov oxidation Appel reaction Arbuzov reaction, Arbusow reaction Arens-van Dorp synthesis, Isler modification Arndt-Eistert reaction Auwers synthesis Azo coupling
B (back up )
Baeyer-Drewson indigo synthesis Baeyer-Villiger oxidation Baeyer-Villiger rearrangement Bakeland process (Bakelite) Baker-Venkataraman rearrangement Baker-Venkataraman transformation Bally-Scholl synthesis Balz-Schiemann reaction Bamberger triazine synthesis Bamford-Stevens reaction Barbier-Wieland degradation Bardhan-Senguph phenanthrene synthesis Barton reaction Barton-McCombie reaction, Barton desoxigenation Baudisch reaction Bayer test Baylis-Hillman reaction Bechamp reaction Beckmann rearrangement Belousov-Zhabotinsky reaction Benary reaction Benzidine rearrangement Benzilic acid rearrangement Benzoin condensation Bergamann-Zevars carbobenzoxy method Bergmann azlactone peptide synthesis Bergmann degradation Bernthsen acridine synthesis Betti reaction Biginelli pyrimidine synthesis Biginelli reaction Birch reduction Bischler indole synthesis Bischler triazine synthesis Bischler-Napieralski reaction Blaise ketone synthesis Blaise reaction Blanc reaction, Chloromethylation Bodroux reaction Bodroux-Chichibabin aldehyde synthesis Bogert-Cook synthesis Bohn-Schmidt reaction Boord Olefin synthesis Borsche-Drechsel cyclization Bosch-Meiser urea process Bouveault aldehyde synthesis Bouveault-Blanc reduction Brown hydroboration Bucherer carbazole synthesis Bucherer reaction Bucherer-Bergs reaction Buchner ring enlargement Buchner-Curtius-Schlotterbeck reaction Buchwald-Hartwig Cross coupling reaction Bunnett reaction
C (back up )
Cadiot-Chodkiewicz coupling Camps quinoline synthesis Cannizzaro reaction Carroll reaction CBS reduction Chan-Lam coupling Chapman rearrangement Chichibabin pyridine synthesis Chichibabin reaction Chugaev Method Ciamician-Dennstedt rearrangement Claisen condensation Claisen rearrangement Claisen Schmidt condensation Clemmensen reduction Collins-Reagenz Combes Quinoline synthesis Conrad-Limpach synthesis Cope elimination Cope rearrangement Corey reagent Corey-Bakshi-Shibata reduction Corey-Fuchs reaction Corey-Kim oxidation Corey-Winter olefin synthesis Corey-Winter reaction Craig method Cram's rule of asymmetric induction Creighton process Criegee reaction Criegee rearrangement Cross metathesis Crum Brown-Gibson rule Curtius degradation Curtius rearrangement, Curtious reaction
D (back up )
Dakin reaction Dakin-West reaction Darapsky degradation Darzens condensation, Darzens-Claisen reaction, Glycidic ester condensation Darzens synthesis of unsaturated ketones Darzens tetralin synthesis Delepine reaction Demjanov rearrangement Demjanow desamination Dess-Martin oxidation Dewer-Evans-Zimmermann reaction Diazotisation Dieckmann condensation Dieckmann reaction Dieckmann-condensation Diels-Alder reaction Diels Reese reaction Dienol benzene rearrangement Dienone phenol rearrangement Dimroth rearrangement Di-pi-methane rearrangement Directed ortho metalation Doebner modification Doebner-Miller synthesis, Beyer method for quinolines Doering-LaFlamme carbon chain extension Dötz-reaction Duff reaction Dutt-Wormall reaction
E (back up )
E1 E1cb E2 Eder reaction Edman degradation Egling coupling Eglinton reaction Ehrlich-Sachs reaction Einhorn variant Einhorn-Brunner reaction Elbs persulfate oxidation Elbs reaction Eltekoff reaction Emde degradation Emmert reaction Ene reaction Epoxidation Erlenmeyer synthesis, Azlactone synthesis Erlenmeyer-Plochl azlactone and amino acid synthesis Eschweiler-Clarke reaction Ester pyrolysis Etard reaction
F (back up )
Favorskii reaction Favorskii rearrangement Favorskii-Babayan synthesis Feist-Benary synthesis Fenton reaction Ferrario reaction Finkelstein reaction Fischer indole synthesis Fischer oxazole synthesis Fischer peptide synthesis Fischer phenylhydrazine and oxazone reaction Fischer reduction Fischer-Hepp rearrangement Fischer-Speier esterification Flood reaction Foster reaction Foster-Decker method Franchimont reaction Frankland synthesis Frankland-Duppa reaction Freund reaction Friedel-Crafts Acylation Friedel-Crafts-Alkylation Friedländer-synthesis Fries rearrangement Fritsch-Buttenberg-Wischell rearrangement Fukuyama coupling
G (back up )
Gabriel ethylenimine method Gabriel synthesis Gabriel-Coleman rearrangement, Gabriel isoquinoline synthesis Gallagher-Hollander degradation Gastaldi synthesis Gattermann aldehyde synthesis Gattermann Koch reaction Gattermann reaction Gewald reaction Gibbs phthalic anhydride process Glaser coupling Glycol cleavage Gogte synthesis Gomberg-Bachmann reaction Gomberg-Free radical reaction Gould-Jacobs reaction Graebe-Ullmann synthesis Grignard degradation Grignard reaction Grob fragmentation Gromberg-Bachmann-Hey reaction Grubbs reaction Grundmann aldehyde synthesis Gryszkiewicz-Trochimowski and McCombie method Guareschi-Thorpe condensation Guerbet reaction Gutknecht pyrazine synthesis
H (back up )
Haller-Bauer reaction Haloform reaction Hammett equation Hammick picolinic acid decarboxylation Hammond-Prinzip Hantzch pyrrole synthesis Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis Hantzsch Pyridine synthesis, Gattermann-Skita synthesis , Guareschi-Thorpe condensation, Knoevenagel-Fries modification Hantzsch-Collidin-synthesis Harries Ozonide reaction Haworth Methylation Haworth Phenanthrene synthesis Haworth-reaction Hay coupling Hayashi rearrangement Heck reaction Helferich method Hell-Volhard-Zelinsky halogenation Henkel reaction, Raecke process, Henkel process Henry reaction, Kamlet reaction Herz reaction, Herz compounds Herzig-Meyer alkimide group determination Heumann indigo synthesis Hinsberg indole synthesis Hinsberg reaction Hinsberg separation Hinsberg sulfone synthesis Hoch-Campbell ethylenimine synthesis Hofmann degradation, Exhaustive methylation Hofmann Elimination Hofmann Isonitrile synthesis, Carbylamine reaction Hofmann produkt Hofmann rearrangement Hofmann-Löffler reaction, Löffler-Freytag reaction, Hofmann-Löffler-Freytag reaction Hofmann-Martius rearrangement Hofmann's Rule Hofmann-Sand reaction Homo rearrangement of steroids Hooker reaction Horner-Wadsworth-Emmons reaction Hösch reaction Hosomi-Sakurai reaction Houben-Fischer synthesis Hunsdiecker reaction, Borodine reaction Hydride Hydroboration
I (back up )
J (back up )
Jacobsen rearrangement Janovsky reaction Japp-Klingemann reaction Jones oxidation Jordan-Ullmann-Goldberg synthesis
K (back up )
Kabachnik-Fields reaction Kendall-Mattox reaction Kiliani-Fischer synthesis Kindler reaction Kishner cyclopropane synthesis Knoevenagel condensation Knoop-Oesterlin amino acid synthesis Knorr pyrazole synthesis Knorr pyrrole synthesis Knorr quinoline synthesis Koch-Haaf reaction Kochi reaction Koenigs-Knorr synthesis Kolbe Electrolysis Kolbe elektrolysis Kolbe-Schmitt reaction Kondakov rule Kontanecki acylation Kornblum reaction Krafft degradation Krohnke aldehyde synthesis Kucherov reaction Kuhn-Winterstein reaction Kumada coupling
L (back up )
Latts Nitrile synthesis Lebedev process Lehmstedt-Tanasescu reaction Leuckart thiophenol reaction Leuckart-Wallach reaction Leuckert amide synthesis Levinstein process Lieben iodoform reaction, Haloform reaction Lindlar catalyst Lobry-de Bruyn-van Ekenstein transformation Lossen rearrangement Luche reduction
M (back up )
Madelung synthesis Malaprade reaction, Periodic acid oxidation Malonic ester synthesis Mannich reaction Markovnikov rule, Markownikoff rule, Markownikow rule Martinet dioxindole synthesis McFadyen-Stevens reaction McLafferty rearrangement McMurry reaction Meerwein arylation Meerwein-Ponndorf-Verley reduction Meisenheimer rearrangement Meissenheimer complex Meldrum acid Menshutkin reaction Mentzer pyrone synthesis Merckwald asymmetric synthesis Metathese Meyer and Hartmann reaction Meyer reaction Meyer synthesis Meyer-Schuster rearrangement; Rupe reaction Michael addition Michael addition, Michael system Michael condensation Michaelis-Arbuzov reaction Miescher degradation Mignonac reaction Milas hydroxylation of olefins Mitsunobu reaction Mukaiyama aldol addition Mukaiyama reaction
N (back up )
Nametkin rearrangement Nazarov cyclization reaction Neber rearrangement Nef reaction Negishi coupling Negishi-Zipper reaction Nenitzescu indole synthesis Nenitzescu reductive acylation Niementowski quinazoline reaction Nierenstein reaction Nitroaldol reaction Normant reagents Nozaki-Hiyama coupling
O (back up )
Olefin metathesis Oppenauer oxidation Oppenauer reaction Ostromyslenskii reaction, Ostromisslenskii reaction Oxidative decarboxylation Oxo synthesis Oxy-Cope rearrangement Oxymercuration Ozonolysis
P (back up )
Paal-Knorr pyrrole synthesis Paal-Knorr synthesis Paneth technique Paolini reaction Passerini reaction Paterno-Büchi reaction Pauson-Khand reaction Pechmann condensation Pechmann pyrazole synthesis Pellizzari reaction Pelouze synthesis Perkin alicyclic synthesis Perkin reaction Perkin rearrangement Perkow reaction Peterson olefination Petrenko-Kritschenko piperidone synthesis Pfan-Plattner azulene synthesis Pfitzinger reaction Pictet-Gams isoquinoline synthesis Pictet-Hubert reaction Pictet-Spengler isoquinoline synthesis Pictet-Spengler reaction Piloty alloxazine synthesis Piloty-Robinson pyrrole synthesis Pinacol coupling reaction Pinacol rearrangement Pinner amidine synthesis Pinner method for ortho esters Pinner reaction Pinner triazine synthesis Piria reaction Pitzer strain Polonovski reaction Pomeranz-Fritsch reaction Ponzio reaction Prelog strain Prevost reaction Prileschajew reaction Prilezhaev reaction Prins reaction Prinzbach synthesis Pschorr reaction Pummerer reaction Purdie methylation, Irvine-Purdie methylation
Q (back up )
R (back up )
Ramberg-Backlund reaction Raney-Nickel Rap-Stoermer condensation Raschig phenol process Reed reaction Reformatskii reaction Reilly-Hickinbottom rearrangement Reimer-Tiemann reaction Reissert indole synthesis Reissert reaction, Reissert compound Reppe synthesis Retropinacol rearrangement Reverdin reaction Riehm quinoline synthesis Riemschneider thiocarbamate synthesis Riley oxidations Ring closing metathesis Ring opening metathesis Ritter reaction Robinson annelation, Robinson annulation Robinson Schopf reaction Rosenmund reaction Rosenmund reduction Rosenmund-von Braun synthesis Rothemund reaction Rowe rearrangement Rubottom oxidation Ruff-Fenton degradation Ruzicka large ring synthesis
S (back up )
Sabather catalyst Sakurai reaction Salol reaction Sandheimer Sandmeyer diphenylurea isatin synthesis Sandmeyer isonitrosoacetanilide isatin synthesis Sandmeyer reaction Sanger reagent Sarett oxidation Saytzeff rule, Saytzeff's Rule Saytzew product Schiemann reaction Schiff base Schlenk equilibrium Schlosser modification Schlosser variant Schlosser-Lochmann reaction Schmidlin ketene synthesis Schmidt degradation Schmidt reaction Scholl reaction Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction Schotten Baumann reaction Semidine rearrangement Semmler-Wolff reaction Serini reaction Shapiro reaction Sharpless bishydroxylation Sharpless epoxidation Simmons-Smith reaction Simonini reaction Simonis chromone cyclization Skell Skraup chinolin synthesis Skraup reaction Smiles rearrangement SNAr nucleophilic aromatic substitution SN1 SN2 SNi Sommelet reaction Sonn-Müller method Sonogashira coupling Sonogashira reaction Sorenson formol titration Staedel-Rugheimer pyrazine synthesis Staudinger reaction Stephen aldehyde synthesis Stetter reaction Stevens rearrangement Stieglitz rearrangement Stille coupling Stobbe condensation Stolle synthesis Stork acylation Stork enamine alkylation Strecker amino acid synthesis Strecker degradation Strecker sulfite alkylation Strecker synthesis Stuffer disulfone hydrolysis rule Süs reaction Suzuki coupling Swain equation Swarts reaction Swern oxidation
T (back up )
Tafel rearrangement Takai olefination Tebbe olefination ter Meer reaction Thiele reaction Thorpe reactions Tiemann rearrangement Tiffeneau ring enlargement reaction Tiffeneau-Demjanow rearrangement Tischtschenko reaction Tishchenko reaction, Tischischenko-Claisen reaction Tollens reagent Trapp mixture Traube purine synthesis Truce-Smiles rearrangement Tscherniac-Einhorn reaction Tschitschibabin reaction Tschugajeff reaction Twitchell process Tyrer sulfonation process
U (back up )
Ugi reaction Ullmann reaction Urech cyanohydrin method Urech Hydantoin synthesis Van Slyke determination Varrentrapp reaction Vilsmeier reaction Vilsmeier-Haack reaction Voight amination Volhard-Erdmann cyclization von Braun degradation, von Braun cyanogen bromide reaction von Meyer reduction von Richter cinnoline synthesis von Richter reaction
W (back up )
Wacker-Tsuji oxidation Wagner-Jauregg reaction Wagner-Meerwein rearrangement Walden inversion Wallach rearrangement Weerman degradation Weinreb ketone synthesis Wenker ring closure Wenker synthesis Wessely-Moser rearrangement Westphalen-Lettré rearrangement Whiting reaction Wichterle reaction Widman-Stoermer synthesis Wilkinson catalyst Willgerodt rearrangement Willgerodt-Kindler reaction Williamson ether synthesis Winstein reaction Wittig reaction Wittig rearrangement Wittig-Horner reaction Wohl degradation Wohl-Aue reaction Wohler synthesis Wohl-Ziegler reaction Wolfenstein-Boters reaction Wolff rearrangement Wolff-Kishner reduction Woodward cis-hydroxylation Woodward-Hoffmann rule Wurtz coupling Wurtz reaction Wurtz-Fittig reaction
X (back up )
Y (back up )
Z (back up )
Zeisel determination Zerevitinov determination, Zerewitinoff determination Ziegler condensation Ziegler method Zimmermann reaction Zincke disulfide cleavage Zinke nitration Zinke-Suhl reaction
Results from FactBites:
Flexeril Side Effects, and Drug Interactions - Cyclobenzaprine Hcl - RxList Monographs (515 words)
Adverse reactions which were reported in 1% to 3% of the patients were: abdominal pain, acid regurgitation, constipation, diarrhea, dizziness, nausea, irritability, mental acuity decreased, nervousness, upper respiratory infection, and pharyngitis. The following list of adverse reactions is based on the experience in 473 patients treated with FLEXERIL 10 mg in additional controlled clinical studies, 7607 patients in the post-marketing surveillance program, and reports received since the drug was marketed. The overall incidence of adverse reactions among patients in the surveillance program was less than the incidence in the controlled clinical studies.
Guidance: Adverse Reactions Section of Labeling for Human Prescription Drug and Biological Products - Content and Format (3789 words)
Exhaustive lists of every reported adverse event, including those that are infrequent and minor, commonly observed in the absence of drug therapy or not plausibly related to drug therapy should be avoided (see § 201.57(c)(7) and the Glossary at the end of this guidance for a definition of Adverse Reaction ). The rates for reactions that are specific to a subgroup (e.g., gender-specific reactions such as menstrual irregularity) should be determined using the appropriate denominator, and that denominator should be identified in a footnote. Adverse Reaction (21 CFR 201.57(c)(7)): For purposes of prescription drug labeling and this guidance, an adverse reaction is an undesirable effect, reasonably associated with the use of a drug, that may occur as part of the pharmacological action of the drug or may be unpredictable in its occurrence.
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