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Named Organic Reaction
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Deepak Kansal
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1
Introduction to the second edition
Acyloin Ester Condensation
Aldol Reaction
Alkene Metathesis
Arbuzov Reaction
Arndt–Eistert Synthesis
Baeyer–Villiger Oxidation
Bamford–Stevens Reaction
Barton Reaction
Baylis–Hillman Reaction
Beckmann Rearrangement
Benzidine Rearrangement
Benzilic Acid Rearrangement
Benzoin Condensation
Bergman Cyclization
Birch Reduction
Blanc Reaction
Bucherer Reaction
Cannizzaro Reaction
Chugaev Reaction
Claisen Ester Condensation
Claisen Rearrangement
Clemmensen Reduction
Cope Elimination Reaction
Cope Rearrangement
Corey–Winter Fragmentation
Curtius Reaction
1,3-Dipolar Cycloaddition
[2 Y2 ] Cycloaddition
Darzens Glycidic Ester Condensation
Del ́ pine Reaction
Diazo Coupling
Diazotization
Diels–Alder Reaction
Di-p-Methane Rearrangement
vi Contents
D ̈ tz Reaction
Elbs Reaction
Ene Reaction
Ester Pyrolysis
Favorskii Rearrangement
Finkelstein Reaction
Fischer Indole Synthesis
Friedel–Crafts Acylation
Friedel–Crafts Alkylation
Friedl ̈ nder Quinoline Synthesis
Fries Rearrangement
Gabriel Synthesis
Gattermann Synthesis
Glaser Coupling Reaction
Glycol Cleavage
Gomberg–Bachmann Reaction
Grignard Reaction
Haloform Reaction
Hantzsch Pyridine Synthesis
Heck Reaction
Hell–Volhard–Zelinskii Reaction
Hofmann Elimination Reaction
Hofmann Rearrangement
Hunsdiecker Reaction
Hydroboration
Japp-Klingemann Reaction
Knoevenagel Reaction
Knorr Pyrrole Synthesis
Kolbe Electrolytic Synthesis
Kolbe Synthesis of Nitriles
Kolbe–Schmitt Reaction
Leuckart–Wallach Reaction
Lossen Reaction
Malonic Ester Synthesis
Mannich Reaction
McMurry Reaction
Meerwein–Ponndorf–Verley Reduction
Michael Reaction
Mitsunobu Reaction
Nazarov Cyclization
Neber Rearrangement
Nef Reaction
Contents vii
Norrish Type I Reaction
Norrish Type II Reaction
Ozonolysis
Paterno–B ̈ chi Reaction
Pauson–Khand Reaction
Perkin Reaction
Peterson Olefination
Pinacol Rearrangement
Prilezhaev Reaction
Prins Reaction
Ramberg–B'cklund Reaction
Reformatsky Reaction
Reimer–Tiemann Reaction
Robinson Annulation
Rosenmund Reduction
Sakurai Reaction
Sandmeyer Reaction
Schiemann Reaction
Schmidt Reaction
Sharpless Epoxidation
Simmons–Smith Reaction
Skraup Quinoline Synthesis
Stevens Rearrangement
Stille Coupling Reaction
Stork Enamine Reaction
Strecker Synthesis
Suzuki Reaction
Swern Oxidation
Tiffeneau–Demjanov Reaction
Vilsmeier Reaction
Vinylcyclopropane Rearrangement
Wagner–Meerwein Rearrangement
Weiss Reaction
Willgerodt Reaction
Williamson Ether Synthesis
Wittig Reaction
Wittig Rearrangement
Wohl–Ziegler Bromination
Wolff Rearrangement
Wolff–Kishner Reduction
Wurtz Reaction
Index
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