0% found this document useful (0 votes)
132 views10 pages

List of Named Reaxns

This document lists over 200 chemical reactions organized alphabetically, including common organic reactions like the Aldol reaction, Diels-Alder reaction, Friedel-Crafts reaction, Grignard reaction, and Wittig reaction. Some reactions listed include the Acetoacetic Ester Condensation, Baylis-Hillman reaction, Blaise reaction, Cope rearrangement, Darzens reaction, Favorskii reaction, Gabriel synthesis, Hofmann elimination, Ireland-Claisen rearrangement, Kabachnik-Fields reaction, Mitsunobu reaction, Nazarov cyclization, Oppenauer oxidation, Pauson-Khand reaction, Reformatsky reaction, Robinson annulation,

Uploaded by

Surya Vamsi
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
132 views10 pages

List of Named Reaxns

This document lists over 200 chemical reactions organized alphabetically, including common organic reactions like the Aldol reaction, Diels-Alder reaction, Friedel-Crafts reaction, Grignard reaction, and Wittig reaction. Some reactions listed include the Acetoacetic Ester Condensation, Baylis-Hillman reaction, Blaise reaction, Cope rearrangement, Darzens reaction, Favorskii reaction, Gabriel synthesis, Hofmann elimination, Ireland-Claisen rearrangement, Kabachnik-Fields reaction, Mitsunobu reaction, Nazarov cyclization, Oppenauer oxidation, Pauson-Khand reaction, Reformatsky reaction, Robinson annulation,

Uploaded by

Surya Vamsi
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
You are on page 1/ 10

a Acetoacetic Ester Condensation Acetoacetic Ester Synthesis Acyloin Condensation Alder-Ene Reaction Aldol Addition

Appel Reaction Arbuzov Reaction Azide-Alkyne 1,3-Dipolar Cycloaddition Azo Coupling b Baker-Venkataraman Rearrangement Balz-Schiemann Reaction Bamford-Stevens Reaction Barton Decarboxylation Barton-McCombie Reaction (Barton Desoxygenation) Baylis-Hillman Reaction Beckmann Rearrangement Benzilic Acid Rearrangement Bergman Cyclization Bestmann-Ohira Reagent Biginelli Reaction Bischler-Napieralski Reaction Blaise Reaction Blanc Reaction Bohlmann-Rahtz Pyridine Synthesis

Boronic Acid Mannich Reaction Brook Rearrangement Brown Hydroboration Bucherer-Bergs Reaction Buchwald-Hartwig Cross Coupling Reaction c Cadiot-Chodkiewicz Coupling CBS Reduction Chan-Lam Coupling Clemmensen Reduction Click Chemistry Collins Reagent Cope Elimination Cope Rearrangement Conia-Ene Reaction Corey-Bakshi-Shibata Reduction Corey-Chaykovsky Reaction Corey-Fuchs Reaction Corey-Kim Oxidation Corey-Seebach Reaction Corey-Suggs Reagent Corey-Winter Olefin Synthesis Coumarin Synthesis Criegee Mechanism for Ozonolysis Cross Metathesis Curtius Rearrangement (Reaction) d

Dakin Reaction Darzens Condensation Darzens Reaction Delpine Reaction Dess-Martin Oxidation Diazotisation Dieckmann Condensation Diels-Alder Reaction 1,3-Dipolar Cycloaddition Directed ortho Metalation Doebner Modification e Eglinton Reaction Ene Reaction Enyne Metathesis Epoxidation Eschweiler-Clarke Reaction Ester Pyrolysis Esterification f Favorskii Reaction Finkelstein Reaction Fischer Esterification Fischer Indole Synthesis Fleming-Tamao Oxidation Friedel-Crafts Acylation Friedel-Crafts Alkylation

Friedlaender Synthesis Fries Rearrangement Fukuyama Coupling Fukuyama Reduction g Gabriel Synthesis Gewald Reaction Glaser Coupling Griesbaum Coozonolysis Grignard Reaction Grubbs Reaction h Haloform Reaction Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis) Hay Coupling Heck Reaction Hell-Volhard-Zelinsky Reaction Henry Reaction Hiyama Coupling Hiyama-Denmark Coupling Hofmann Elimination Hofmann's Rule Horner-Wadsworth-Emmons Reaction Hosomi-Sakurai Reaction Huisgen Cycloaddition Hunsdiecker Reaction Hydroboration

i Ireland-Claisen Rearrangement Itsuno-Corey Reduction Iwanow Reaction (Reagent) j Jacobsen Epoxidation Jacobsen-Katsuki Epoxidation Jocic Reaction Johnson-Corey-Chaykovsky Reaction Jones Oxidation Julia-Lythgoe Olefination Julia-Kocienski Olefination k Kabachnik-Fields Reaction Kindler Reaction Knoevenagel Condensation Kochi Reaction Kolbe Electrolysis Kolbe Nitrile Synthesis Kolbe-Schmitt Reaction Koser's Reagent Kulinkovich Reaction Kulinkovich-de Meijere Reaction Kulinkovich-Szymoniak Reaction Kumada Coupling l Lawesson's Reagent

Leuckart Thiophenol Reaction Luche Reduction m Malonic Ester Synthesis Mannich Reaction Markovnikov's Rule McMurry Reaction Meerwein-Ponndorf-Verley Reduction Myers' Modification of the Ramberg-Bcklund Reaction Myers-Saito Cyclization Michael Addition Michaelis-Arbuzov Reaction Mitsunobu Reaction Miyaura Borylation Reaction Modified Julia Olefination Mukaiyama Aldol Addition n Nazarov Cyclization Nef Reaction Negishi Coupling Newman-Kwart Rearrangement Nitroaldol Reaction Nozaki-Hiyama Coupling Nucleophilic Substitution (SN1 / SN2) o Ohira-Bestmann Reagent Olefin Metathesis

Oppenauer Oxidation Overman Rearrangement Oxy-Cope Rearrangement Ozonolysis p Paal-Knorr Furan Synthesis Paal-Knorr Pyrrole Synthesis Paal-Knorr Thiophene Synthesis Passerini Reaction Paterno-Bchi Reaction Pauson-Khand Reaction Pechmann Condensation Petasis Reaction Peterson Olefination Pinacol Coupling Reaction Pinacol Rearrangement Pinner Reaction Prvost Reaction Prilezhaev Reaction Prins Reaction Pschorr Reaction q r Ramberg-Bcklund Reaction Reformatsky Reaction Ring Closing Metathesis Ring Opening Metathesis (Polymerization)

Ritter Reaction Robinson Annulation Rosenmund Reduction Rosenmund-von Braun Reaction Rubottom Oxidation s Sakurai Reaction Sandmeyer Reaction Saytzeff's Rule Schiemann Reaction Schlosser Modification Schmidt Reaction Schotten-Baumann Reaction Seebach Umpolung Seyferth-Gilbert Homologation Sarett Reagent Shapiro Reaction Sharpless Aminohydroxylation Sharpless Dihydroxylation Sharpless Epoxidation Shi Epoxidation Simmons-Smith Reaction Sonogashira Coupling Staudinger Cycloaddition Staudinger Reaction Staudinger Reduction Staudinger Synthesis

Steglich Esterification Stetter Reaction Stille Coupling Strecker Synthesis Suzuki Coupling Swern Oxidation t Tamao-Kumada Oxidation Tebbe Olefination Tishchenko Reaction Tsuji-Trost Reaction Trost Allylation u Ugi Reaction Ullmann Reaction Upjohn Dihydroxylation v Van Leusen Imidazole Synthesis Van Leusen Oxazole Synthesis Van Leusen Reaction Vicarious Nucleophilic Substitution Vilsmeier Reaction w Wacker-Tsuji Oxidation Weinreb Ketone Synthesis Wenker Synthesis Willgerodt-Kindler Reaction

Williamson Synthesis Wittig-Horner Reaction Wittig Reaction [1,2]-Wittig Rearrangement [2,3]-Wittig Rearrangement Wohl-Ziegler Reaction Wolff-Kishner Reduction Wolff Rearrangement Woodward cis-Hydroxylation Woodward Reaction Wurtz Reaction Wurtz-Fittig Reaction x y Yamaguchi Esterification z

You might also like