TINDAK BALAS CINTA KU.....

LIST OF ORGANIC REACTIONS..

0-9

• 1,3-dipolar cycloaddition

A

• Abramovitch-Shapiro tryptamine synthesis
• Acetoacetic ester condensation
• Achmatowicz reaction
• Acyloin condensation
• Adams catalyst
• Adkins catalyst
• Adkins-Peterson reaction
• Akabori amino acid reaction
• Alder ene reaction
• Alder-Stein rules
• Aldol addition
• Aldol condensation
• Algar-Flynn-Oyamada reaction
• Allan-Robinson reaction
• Allylic rearrangement
• Amadori rearrangement
• Angeli-Rimini reaction
• Andrussov oxidation
• Appel reaction
• Arbuzov reaction, Arbusow reaction
• Arens-van Dorp synthesis, Isler modification
• Arndt-Eistert synthesis
• Auwers synthesis
• Azo coupling

B

• 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 rearrangement
• Bamberger triazine synthesis
• Bamford-Stevens reaction
• Barbier-Wieland degradation
• Bardhan-Senguph phenanthrene synthesis
• Bartoli indole synthesis
• Bartoli reaction
• Barton reaction
• Barton-McCombie reaction, Barton deoxygenation
• Baudisch reaction
• Bayer test
• Baylis-Hillman reaction
• Bechamp reaction
• Bechamp reduction
• Beckmann fragmentation
• Beckmann rearrangement
• Bellus-Claisen rearrangement
• Belousov-Zhabotinsky reaction
• Benary reaction
• Benzidine rearrangement
• Benzilic acid rearrangement
• Benzoin condensation
• Bergman cyclization
• Bergmann azlactone peptide synthesis
• Bergmann degradation
• Bergmann-Zervas carbobenzoxy method
• Bernthsen acridine synthesis
• Bestmann's reagent
• Betti reaction
• Biginelli pyrimidine synthesis
• Biginelli reaction
• Birch reduction
• Bischler-Möhlau indole synthesis
• Bischler-Napieralski reaction
• Blaise ketone synthesis
• Blaise reaction
• Blanc reaction
• Blanc chloromethylation
• Bodroux reaction
• Bodroux-Chichibabin aldehyde synthesis
• Bogert-Cook synthesis
• Bohn-Schmidt reaction
• Boord olefin synthesis
• Borodin reaction
• Borsche-Drechsel cyclization
• Bosch-Meiser urea process
• Bouveault aldehyde synthesis
• Bouveault-Blanc reduction
• Boyland-Sims oxidation
• Boyer Reaction
• Bredt's rule
• Brown hydroboration
• Bucherer carbazole synthesis
• Bucherer reaction
• Bucherer-Bergs reaction
• Buchner ring enlargement
• Buchner-Curtius-Schlotterbeck reaction
• Buchwald-Hartwig amination
• Bunnett reaction

C

• Cadiot-Chodkiewicz coupling
• Camps quinoline synthesis
• Cannizzaro reaction
• Carroll reaction
• Catalytic reforming
• CBS reduction
• Chan-Lam coupling
• Chapman rearrangement
• Chichibabin pyridine synthesis
• Chichibabin reaction
• Chugaev elimination
• Ciamician-Dennstedt rearrangement
• Claisen condensation
• Claisen rearrangement
• Claisen-Schmidt condensation
• Clemmensen reduction
• Collins-Reagent
• Combes quinoline synthesis
• Conia reaction
• Conrad-Limpach synthesis
• Corey-Gilman-Ganem oxidation
• Cook-Heilbron thiazole synthesis
• Cope elimination
• Cope rearrangement
• Corey reagent
• Corey-Bakshi-Shibata reduction
• Corey-Fuchs reaction
• Corey-Kim oxidation
• Corey-Posner, Whitesides-House reaction
• Corey-Winter olefin synthesis
• Corey-Winter reaction
• Coupling 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, Curtius reaction

D

• Dakin reaction
• Dakin-West reaction
• Danheiser Annulation
• 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
• Diazotisation
• DIBAL-H selective reduction
• Dieckmann condensation
• Dieckmann reaction
• Diels-Alder reaction
• Diels Reese reaction
• Dienol benzene rearrangement
• Dienone phenol rearrangement
• Dimroth rearrangement
• Di-pi-methane rearrangement
• Directed ortho metalation
• Doebner modification
• Doebner reaction
• Doebner-Miller reaction, Beyer method for quinolines
• Doering-LaFlamme carbon chain extension
• Dötz reaction
• Dowd-Beckwith ring expansion reaction
• Duff reaction
• Dutt-Wormall reaction

E

• E1cB elimination reaction
• Eder reaction
• Edman degradation
• Eglinton reaction
• Ehrlich-Sachs reaction
• Einhorn variant
• Einhorn-Brunner reaction
• Elbs persulfate oxidation
• Elbs reaction
• Elimination reaction
• Emde degradation
• Emmert reaction
• Ene reaction
• Epoxidation
• Erlenmeyer synthesis, Azlactone synthesis
• Erlenmeyer-Plöchl azlactone and amino acid synthesis
• Eschenmoser fragmentation
• Eschweiler-Clarke reaction
• Ester pyrolysis
• Étard reaction
• Evans aldol

F

• Favorskii reaction
• Favorskii rearrangement
• Favorskii-Babayan synthesis
• Feist-Benary synthesis
• Fenton reaction
• Ferrario reaction
• Ferrier carbocyclization
• Ferrier rearrangement
• Finkelstein reaction
• Fischer indole synthesis
• Fischer oxazole synthesis
• Fischer peptide synthesis
• Fischer phenylhydrazine and oxazone reaction
• Fischer glycosidation
• Fischer-Hepp rearrangement
• Fischer-Speier esterification
• Fischer Tropsch synthesis
• Fleming-Tamao oxidation
• Flood reaction
• Forster reaction
• Forster-Decker method
• Franchimont reaction
• Frankland synthesis
• Frankland-Duppa reaction
• Freund reaction
• Friedel-Crafts Acylation
• Friedel-Crafts Alkylation
• Friedländer synthesis
• Fries rearrangement
• Fritsch-Buttenberg-Wiechell rearrangement
• Fujimoto-Belleau reaction
• Fukuyama coupling
• Fukuyama indole synthesis

G

• Gabriel ethylenimine method
• Gabriel synthesis
• Gabriel-Colman rearrangement, Gabriel isoquinoline synthesis
• Gallagher-Hollander degradation
• Gassman indole synthesis
• Gastaldi synthesis
• Gattermann aldehyde synthesis
• Gattermann Koch reaction
• Gattermann reaction
• Gewald reaction
• Gibbs phthalic anhydride process
• Gilman reagent
• Glaser coupling
• Glycol cleavage
• Gogte synthesis
• Gomberg-Bachmann reaction
• Gomberg-Bachmann-Hey reaction
• Gomberg-Free radical reaction
• Gould-Jacobs reaction
• Graebe-Ullmann synthesis
• Grignard degradation
• Grignard reaction
• Grob fragmentation
• Grubbs' catalyst in Olefin metathesis
• Grundmann aldehyde synthesis
• Gryszkiewicz-Trochimowski and McCombie method
• Guareschi-Thorpe condensation
• Guerbet reaction
• Gutknecht pyrazine synthesis

H

• Haller-Bauer reaction
• Haloform reaction
• Hammett equation
• Hammick reaction
• Hammond-Principle or Hammond postulate
• Hantzsch pyrrole synthesis
• Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis
• Hantzsch Pyridine synthesis, Gattermann-Skita synthesis, Guareschi-Thorpe condensation, Knoevenagel-Fries modification
• Hantzsch-Collidin-synthesis
• Harber-Weiss reaction
• Harries Ozonide reaction
• Haworth Methylation
• Haworth Phenanthrene synthesis
• Haworth-reaction
• Hay coupling
• Hayashi rearrangement
• Heck reaction
• Helferich method
• Hell-Volhard-Zelinsky halogenation
• Hemetsberger indole synthesis
• Hemetsberger-Knittel synthesis
• 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 oxindole 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
• Hoesch reaction
• Hosomi-Sakurai reaction
• Houben-Fischer synthesis
• Hunsdiecker reaction
• Hydroboration
• Hydrohalogenation

I

• Ing-Manske procedure
• Ipso substitution
• Ivanov reagent, Ivanov reaction

[edit] J

• Jacobsen rearrangement
• Janovsky reaction
• Japp-Klingemann reaction
• Japp-Maitland condensation
• Johnson-Claisen rearrangement
• Jones oxidation
• Jordan-Ullmann-Goldberg synthesis
• Julia olefination
• Julia-Lythgoe olefination

K

• 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 reaction
• Kolbe electrolysis
• Kolbe-Schmitt reaction
• Kondakov rule
• Kontanecki acylation
• Kornblum oxidation
• Kornblum–DeLaMare rearrangement
• Kowalski ester homologation
• Krafft degradation
• Krapcho decarboxylation
• Kröhnke aldehyde synthesis
• Kröhnke oxidation
• Kröhnke pyridine synthesis
• Kucherov reaction
• Kuhn-Winterstein reaction
• Kulinkovich reaction
• Kumada coupling

L

• Larock indole synthesis
• Lebedev process
• Lehmstedt-Tanasescu reaction
• Leimgruber-Batcho indole synthesis
• Letts nitrile synthesis
• Leuckart reaction
• Leuckart thiophenol reaction
• Leuckart-Wallach reaction
• Leuckert amide synthesis
• Levinstein process
• Ley Oxidation
• Lieben iodoform reaction, Haloform reaction
• Liebeskind-Srogl coupling
• Lindlar catalyst
• Lobry-de Bruyn-van Ekenstein transformation
• Lossen rearrangement
• Luche reduction

M

• Madelung synthesis
• Malaprade reaction, Periodic acid oxidation
• Malonic ester synthesis
• Mannich reaction
• Markovnikov's rule, Markownikoff rule, Markownikow rule
• Martinet dioxindole synthesis
• McDougall monoprotection
• McFadyen-Stevens reaction
• McMurry reaction
• Meerwein arylation
• Meerwein-Ponndorf-Verley reduction
• Meisenheimer rearrangement
• Meissenheimer complex
• Menshutkin reaction
• Mentzer pyrone synthesis
• Metal-ion-catalyzed σ-bond rearrangement
• Mesylation
• Merckwald asymmetric synthesis
• Meyer and Hartmann reaction
• Meyer reaction
• Meyer synthesis
• Meyer-Schuster rearrangement
• 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
• Myers' asymmetric alkylation

N

• Nametkin rearrangement
• Nazarov cyclization reaction
• Neber rearrangement
• Nef reaction
• Negishi coupling
• Negishi-Zipper reaction
• Nenitzescu indole synthesis
• Nenitzescu reductive acylation
• Nicholas reaction
• Niementowski quinazoline synthesis
• Niementowski quinoline synthesis
• Nierenstein reaction
• Nitroaldol reaction
• Normant reagents
• Noyori asymmetric hydrogenation
• Nozaki-Hiyama-Kishi Nickel/Chromium Coupling reaction
• Nucleophilic acyl substitution

O

• Ohira-Bestmann reaction
• Olefin metathesis
• Oppenauer oxidation
• Ostromyslenskii reaction, Ostromisslenskii reaction
• Oxidative decarboxylation
• Oxo synthesis
• Oxy-Cope rearrangement
• Oxymercuration
• Ozonolysis

[edit] P

• 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
• Petasis reaction
• Petasis reagent
• Peterson olefination
• Peterson reaction
• Petrenko-Kritschenko piperidone synthesis
• Pfan-Plattner azulene synthesis
• Pfitzinger reaction
• Pfitzner-Moffatt oxidation
• Pictet-Gams isoquinoline synthesis
• Pictet-Hubert reaction
• Pictet-Spengler tetrahydroisoquinoline 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 rearrangement
• Purdie methylation, Irvine-Purdie methylation

Q

• Quelet reaction

R

• Ramberg-Backlund reaction
• Raney-Nickel
• Rap-Stoermer condensation
• Raschig phenol process
• Rauhut-Currier reaction
• 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 annulation
• Robinson-Gabriel synthesis
• Robinson Schopf reaction
• Rosenmund reaction
• Rosenmund reduction
• Rosenmund-von Braun synthesis
• Rothemund reaction
• Rowe rearrangement
• Rupe reaction
• Rubottom oxidation
• Ruff-Fenton degradation
• Ruzicka large ring synthesis

S

• Sakurai reaction
• Salol reaction
• Sandheimer
• Sandmeyer diphenylurea isatin synthesis
• Sandmeyer isonitrosoacetanilide isatin synthesis
• Sandmeyer reaction
• Sanger reagent
• Sarett oxidation
• Saytzeff rule, Saytzeff's Rule
• Schiemann reaction
• 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
• Screttas-Yus reaction
• Semidine rearrangement
• Semmler-Wolff reaction
• Serini reaction
• Seyferth-Gilbert homologation
• Shapiro reaction
• Sharpless asymmetric dihydroxylation
• Sharpless epoxidation
• Sharpless oxyamination or aminohydroxylation
• Simmons-Smith reaction
• Simonini reaction
• Simonis chromone cyclization
• Skraup chinolin synthesis
• Skraup reaction
• Smiles rearrangement
• S_NAr nucleophilic aromatic substitution
• SN1
• SN2
• SNi
• Sommelet reaction
• Sonn-Müller method
• Sonogashira coupling
• Sørensen formol titration
• Staedel-Rugheimer pyrazine synthesis
• Staudinger reaction
• Stephen aldehyde synthesis
• Stetter reaction
• Stevens rearrangement
• Stieglitz rearrangement
• Stille coupling
• Stobbe condensation
• Stollé synthesis
• Stork acylation
• Stork enamine alkylation
• Strecker amino acid synthesis
• Strecker degradation
• Strecker sulfite alkylation
• Strecker synthesis
• Suzuki coupling
• Swain equation
• Swarts reaction
• Swern oxidation

T

• Tamao oxidation
• Tafel rearrangement
• Takai olefination
• Tebbe olefination
• ter Meer reaction
• Thermite reactions
• Thiele reaction
• Thorpe reaction
• 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

• Ugi reaction
• Ullmann reaction
• Upjohn dihydroxylation
• Urech cyanohydrin method
• Urech hydantoin synthesis

V

• Van Slyke determination
• Varrentrapp reaction
• Vilsmeier reaction
• Vilsmeier-Haack reaction
• Voight amination
• Volhard-Erdmann cyclization
• von Braun amide degradation
• von Braun reaction
• von Richter cinnoline synthesis
• von Richter reaction

W

• 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
• Wharton reaction
• 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
• Wolffenstein-Böters reaction
• Wolff rearrangement
• Wolff-Kishner reduction
• Woodward cis-hydroxylation
• Woodward-Hoffmann rule

• Wulff-Dötz reaction
• Wurtz coupling, Wurtz reaction
• Wurtz-Fittig reaction

X

Y

• Yamaguchi esterification

Z

• Zeisel determination
• Zerevitinov determination, Zerewitinoff determination
• Ziegler condensation
• Ziegler method
• Zimmermann reaction
• Zincke disulfide cleavage
• Zinke nitration
• Zincke reaction
• Zincke-Suhl reaction