Book Named Organic Reactions 2nd Edition in pdf
Volkswagen AG, Wolfsburg, Germany published by John Wiley & Sons Ltd, 2005 of professors of science faculties universities Germany.
Number of chapters: 24 chapters
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+2 ] Cycloaddition.
Darzens Glycidic Ester Condensation.
Del´epine Reaction.
Diazo Coupling.
Diazotization.
Diels–Alder Reaction.
Di-pp-Methane Rearrangement.
Do¨tz Reaction.
Elbs Reaction.
Ene Reaction.
Ester Pyrolysis.
Favorskii Rearrangement.
Finkelstein Reaction.
Fischer Indole Synthesis.
Friedel–Crafts Acylation.
Friedel–Crafts Alkylation.
Friedl¨ander 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.
Norrish Type I Reaction.
Norrish Type II Reaction.
Ozonolysis.
Paterno–B¨uchi Reaction.
Pauson–Khand Reaction.
Perkin Reaction.
Peterson Olefination.
Pinacol Rearrangement.
Prilezhaev Reaction.
Prins Reaction.
Ramberg–B¨acklund 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.
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