Named Organic Reactions By Thomas Lauer 2nd Edition (informative)

Free download Named Organic Reactions By Thomas Lauer 2nd Edition
2nd Edition
Authors of: Named Organic Reactions By Thomas Lauer 2nd Edition
Thomas Lauer
Andreas Plagens
Table of Contents in Named Organic Reactions By Thomas Lauer 2nd Edition
Named Organic Reactions by Thomas Lauer, in its second edition, serves as a comprehensive guide to the critical reactions in organic chemistry that are named after the chemists who discovered or developed them. This book not only provides essential information about these reactions but also offers insights into their mechanisms, applications, and historical significance, making it an invaluable resource for students, educators, and professionals in the field of chemistry.
The primary focus of this book is on reactions that have become foundational in synthetic organic chemistry due to their reliability, selectivity, and versatility. Named organic reactions are often seen as landmarks in the evolution of organic chemistry, as they introduced novel methods for bond formation, functional group transformations, and stereochemical control.
Each reaction is thoroughly explained, detailing the starting materials, reagents, conditions, and products, along with the mechanistic pathways involved. The book breaks down complex processes into clear, understandable steps, helping readers to grasp both the theoretical and practical aspects of these reactions.
One of the strengths of Named Organic Reactions is its organized and systematic approach. Lauer categorizes reactions based on their types and functions, such as substitution, addition, elimination, rearrangement, and oxidation-reduction reactions.
This classification not only aids in understanding but also facilitates the application of these reactions in the synthesis of various organic compounds, from pharmaceuticals to polymers. Moreover, the second edition incorporates recent advancements and updates in the field, including newer reactions and modifications to classic ones that enhance their efficiency or broaden their applicability.
The historical context provided in this book adds a unique layer, illustrating how these reactions were discovered and refined over time. By including biographical notes on the chemists associated with each reaction, Lauer connects readers to the human side of scientific discovery, underscoring the trial-and-error nature of research in organic chemistry.
In essence, Named Organic Reactions by Thomas Lauer is more than just a compilation of reactions. It is a narrative of organic chemistry’s progression, showcasing the ingenuity and persistence of chemists whose work laid the groundwork for modern synthetic methods. This edition is essential for anyone seeking a deeper understanding of organic synthesis, making it an ideal reference for academic and professional settings alike.
Introduction to the 2nd 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
[2Y2 ] Cycloaddition
Darzens Glycidic Ester Condensation
Del´epine Reaction
Diazo Coupling
Diazotization
Diels–Alder Reaction
Di-p-Methane Rearrangement
D¨otz 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
Index
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