A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
A
- Acetoacetic-Ester Synthesis
- Acetoacetic-Ester Condensation (Claisen Condensation)
- Appel Reaction
- Acyloin Condensation
- Alder (Ene) Reaction (Hydro-Allyl Addition)
- Aldol Reaction
- Alkene (Olefin) Metathesis
- Alkyne Metathesis
- Amadori Reaction/Rearrangement
- Arbuzov Reaction (Michaelis-Arbuzov Reaction)
- Arndt-Eistert Homologation/Synthesis
- Aza-Claisen Rearrangement
- Aza-Cope Rearrangement
- Aza-Wittig Reaction
- Aza-[2,3]-Wittig Rearrangement
- Alkylation Enyne Metathesis.
B
- Baeyer-Villiger Oxidation/Rearrangement
- Baker-Venkataraman Rearrangement
- Baldwin’s Rules/Guidelines for Ring-Closing Reactions
- Balz-Schiemann Reaction (Schiemann Reaction)
- Bamford-Stevens-Shapiro Olefination
- Barbier Coupling Reaction
- Bartoli Indole synthesis
- Barton Nitrite Ester Reaction
- Barton Radical Decarboxylation Reaction
- Barton-McCombie Radical Deoxygenation Reaction
- Baylis-Hillman Reaction Beckmann Rearrangement
- Beckmann Rearrangement
- Benzilic Acid Rearrangement
- Benzoin and Retro-Benzoin Condensation
- Bergman Cycloaromatization Reaction
- Biginelli Reaction.
- Birch Reduction.
- Bischler-Napieralski Isoquinoline Synthesis
- Brook Rearrangement
- Brown Hydroboration Reaction
- Buchner Method of Ring Expansion (Buchner Reaction)
- Buchwald-Hartwig Cross-Coupling
- Burgess Dehydration Reaction
C
- Cannizzaro Reaction
- Carroll Rearrangement (Kimel-Cope Rearrangement)
- Castro-Stephens Coupling
- Chichibabin Amination Reaction (Chichibabin Reaction)
- Chugaev Elimination Reaction (Xanthate Ester Pyrolysis)
- Ciamician-Dennstedt Rearrangement
- Claisen Condensation/Claisen Reaction
- Claisen Rearrangement
- Claisen-Ireland Rearrangement
- Clemmensen Reduction
- Combes Quinoline Synthesis
- Cope Elimination / Cope Reaction
- Cope Rearrangement
- Corey-Bakshi-Shibata Reduction (CBS Reduction)
- Corey-Chaykovsky Epoxidation and Cyclopropanation
- Corey-Fuchs Alkyne Synthesis
- Corey-Kim Oxidation
- Corey-Nicolaou Macrolactonization
- Corey-Winter Olefination Cornforth Rearrangement
- Criegee Oxidation
- Curtius Rearrangement
D
- Dakin Oxidation
- Dakin-West Reaction
- Danheiser Benzannulation
- Danheiser Cyclopentene Annulation
- Danishefsky’s Diene Cycloaddition
- Darzens Glycidic Ester Condensation
- Davis’ Oxaziridine Oxidations
- De Mayo Cycloaddition (Enone-Alkene [2+2] Photocycloaddition)
- Demjanov Rearrangement and Tiffeneau-Demjanov Rearrangement
- Dess-Martin Oxidation
- Dieckmann Condensation
- Diels-Alder Cycloaddition
- Dienone-Phenol Rearrangement
- Dimroth Rearrangement
- Doering-LaFlamme Allene Synthesis
- Dötz Benzannulation Reaction Enders SAMP/RAMP Hydrazone
E
- Eschenmoser Methenylation
- Eschenmoser-Claisen Rearrangement
- Eschenmoser-Tanabe Fragmentation
- Eschweiler-Clarke Methylation (Reductive Alkylation)
- Evans Aldol Reaction
F
- Favorskii and Homo-Favorskii Rearrangement
- Favorskii Rearrangement
- Feist-Bénary Furan Synthesis Ferrier Reaction/Rearrangement
- Finkelstein Reaction
- Fischer Indole Synthesis
- Fleming-Tamao Oxidation
- Friedel-Crafts Acylation
- Friedel-Crafts Alkylation
- Fries-, Photo-Fries, and Anionic Ortho-Fries Rearrangement
G
- Gabriel Synthesis
- Gattermann and Gattermann-Koch Formylation
- Glaser Coupling
- Grignard Reaction
- Grob Fragmentation
H
- Hajos-Parrish Reaction
- Hantzsch Dihydropyridine Synthesis
- Heck Reaction
- Heine Reaction.
- Hell-Volhard-Zelinsky Reaction
- Henry Reaction
- Hetero Diels-Alder Cycloaddition (HDA)
- Hofmann Elimination
- Hofmann-Löffler-Freytag Reaction (Remote Functionalization)
- Hofmann Rearrangement
- Horner-Wadsworth-Emmons Olefination
- Horner-Wadsworth-Emmons Olefination – Still-Gennari Modification
- Houben-Hoesch Reaction/Synthesis
- Hunsdiecker Reaction
J
- Jacobsen Hydrolytic Kinetic Resolution
- Jacobsen-Katsuki Epoxidation
- Japp-Klingemann Reaction
- Johnson-Claisen Rearrangement
- Jones Oxidation/Oxidation of Alcohols by Chromium Reagents
- Julia-Lythgoe Olefination.
K
- Kagan-Molander Samarium Diiodide-Mediated Coupling
- Kahne Glycosidation
- Keck Asymmetric Allylation
- Keck Macrolactonization
- Keck Radical Allylation
- Knoevenagel Condensation Knorr Pyrrole Synthesis
- Koenigs-Knorr Glycosidation
- Kolbe-Schmitt Reaction
- Kornblum Oxidation
- Krapcho Dealkoxycarbonylation (Krapcho reaction)
- Kröhnke Pyridine Synthesis
- Kulinkovich Reaction
- Kumada Cross-Coupling
- Larock Indole Synthesis
L
- Ley Oxidation
- Lieben Haloform Reaction
- Lossen Rearrangement
- Luche Reduction
M
- Madelung Indole Synthesis
- Malonic Ester Synthesis
- Mannich Reaction
- McMurry Coupling
- Meerwein Arylation
- Meerwein-Ponndorf-Verley Reduction
- Meisenheimer Rearrangement
- Meyer-Schuster and Rupe Rearrangement
- Michael Addition Reaction
- Midland Alpine Borane Reduction
- Minisci Reaction
- Mislow-Evans Rearrangement
- Mitsunobu Reaction
- Miyaura Boration
- Mukaiyama Aldol Reaction
- Myers Asymmetric Alkylation
N
- Nagata Hydrocyanation
- Nazarov Cyclization
- Neber Rearrangement
- Nef Reaction
- Negishi Cross-Coupling
- Nenitzescu Indole Synthesis
- Nicholas Reaction
- Noyori Asymmetric Hydrogenation
- Nozaki-Hiyama-Kishi Reaction
O
- Oppenauer Oxidation
- Overman Rearrangement
- Oxy-Cope Rearrangement
- Anionic Oxy-Cope Rearrangement
P
- Paal-Knorr Furan Synthesis
- Paal-Knorr Pyrrole Synthesis
- Passerini Multicomponent Reaction
- Paterno-Büchi Reaction
- Pauson-Khand Reaction
- Payne Rearrangement
- Perkin Reaction
- Petasis Boronic Acid-Mannich Reaction
- Petasis-Ferrier Rearrangement
- Peterson Olefination
- Pfitzner-Moffatt Oxidation
- Pictet-Spengler Tetrahydroisoquinoline Synthesis
- Pinacol and Semi-pinacol Rearrangement
- Pinner Reaction
- Pinnick Oxidation
- Polonovski Reaction
- Pomeranz-Fritsch Reaction
- Prévost Reaction
- Prilezhaev Reaction
- Prins Reaction
- Prins-Pinacol Rearrangement
- Pummerer Rearrangement
Q
- Quasi-Favorskii Rearrangement
R
- Ramberg-Bäcklund Rearrangement
- Reformatsky Reaction
- Regitz Diazo Transfer
- Reimer-Tiemann Reaction
- Riley Selenium Dioxide Oxidation
- Ritter Reaction
- Robinson Annulation
- Roush Asymmetric Allylation
- Rubottom Oxidation
S
- Saegusa Oxidation
- Sakurai Allylation
- Sandmeyer Reaction
- Schmidt Reaction
- Schotten-Baumann Reaction
- Schwartz Hydrozirconation
- Seyferth-Gilbert Homologation
- Sharpless Asymmetric Aminohydroxylation
- Sharpless Asymmetric Dihydroxylation
- Sharpless Asymmetric Epoxidation.
- Shi Asymmetric Epoxidation
- Simmons-Smith Cyclopropanation
- Skraup and Doebner-Miller Quinoline Synthesis
- Smiles Rearrangement
- Smith-Tietze Multicomponent Dithiane Linchpin Coupling
- Snieckus Directed Ortho Metalation
- Sommelet-Hauser Rearrangement
- Sonogashira Cross-Coupling
- Staudinger Ketene Cycloaddition
- Staudinger Reaction
- Stephen Aldehyde Synthesis (Stephen Reduction)
- Stetter Reaction
- Stevens Rearrangement
- Stille Carbonylative Cross-Coupling
- Stille Cross-Coupling (Migita-Kosugi-Stille Coupling)
- Stille-Kelly Coupling
- Stobbe Condensation
- Stork Enamine Synthesis
- Strecker Reaction
- Suzuki Cross-Coupling (Suzuki-Miyaura Cross-Coupling
- Swern Oxidation
T
- Takai-Utimoto Olefination (Takai Reaction)
- Tebbe Olefination/Petasis-Tebbe Olefination
- Tishchenko Reaction
- Tsuji-Trost Reaction/Allylation
- Tsuji-Wilkinson Decarbonylation Reaction
U
- Ugi Multicomponent Reaction
- Ullmann Biaryl Ether and Biaryl Amine Synthesis
- Ullmann Reaction/Coupling/Biaryl Synthesis
V
- Vilsmeier-Haack Formylation
- Vinylcyclopropane-Cyclopentene Rearrangement
- Von Pechman Reaction
W
- Wacker Oxidation
- Willgerodt-Kindler Reaction
- Wagner-Meerwein Rearrangement
- Weinreb Ketone Synthesis
- Wharton Fragmentation
- Wharton Olefin Synthesis (Wharton Transposition)
- Williamson Ether Synthesis
- Wittig Reaction
- Wittig Reaction – Schlosser Modification
- Wittig-[1,2]- and [2,3]-Rearrangement
- Wohl-Ziegler Bromination
- Wolff Rearrangement
- Wolff-Kishner Reduction
References :
- Name Reactions A Collection of Detailed Reaction Mechanisms By Jie Jack Li · 2013 “
- Name Reactions and Reagents in Organic Synthesis Bradford P. Mundy, Michael G. Ellerd, Frank G. Favaloro, Jr. · 2005 “
- Named Organic Reactions By Thomas Laue, Andreas Plagens · 2005 “
- Name Reactions – Organic Chemistry Portal “
- Name reaction – Wikipedia “
Related Topic- All Reagents and there Use with mechanism and Examples
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