The Nobel Prize in Chemistry 2009 The Nobel Prize in Biology and Medicine 2009
Source link: www.organic-chemistry.org/namedreactions/
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 Condensation
Acetoacetic Ester Synthesis
Acyloin Condensation
Alder-Ene Reaction
Aldol Addition
Aldol Condensation
Appel Reaction
Arbuzov Reaction
Arndt-Eistert Synthesis
Azo Coupling
b
Baeyer-Villiger Oxidation
Baker-Venkataraman Rearrangement
Balz-Schiemann Reaction
Bamford-Stevens Reaction
Barton Decarboxylation
Barton-McCombie Reaction (Barton Desoxygenation)
Baylis-Hillman Reaction
Beckmann Rearrangement
Benzilic Acid Rearrangement
Benzoin Condensation
Bergman Cyclization
Bestmann-Ohira Reagent
Biginelli Reaction
Birch Reduction
Blanc Reaction
Bohlmann-Rahtz Pyridine Synthesis
Boronic Acid Mannich Reaction
Bouveault-Blanc Reduction
Brook Rearrangement
Brown Hydroboration
Bucherer-Bergs Reaction
Buchwald-Hartwig Cross Coupling Reaction
c
Cadiot-Chodkiewicz Coupling
Cannizzaro Oxidation Reduction
CBS Reduction
Chan-Lam Coupling
Claisen Condensation
Claisen Rearrangement
Clemmensen Reduction
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
Delépine 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
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-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
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-Büchi Reaction
Pauson-Khand Reaction
Pechmann Condensation
Petasis Reaction
Peterson Olefination
Pinacol Coupling Reaction
Pinacol Rearrangement
Pinner Reaction
Prévost Reaction
Prilezhaev Reaction
Prins Reaction
Pschorr Reaction
q
r
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
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
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
