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Organic Mechanisms

by Bruckner, Reinhard.
Authors: Harmata, Michael.%editor. | SpringerLink (Online service) Physical details: XXXII, 856p. 900 illus. in color. online resource. ISBN: 3642036511 Subject(s): Chemistry. | Chemistry, Organic. | Polymers. | Biochemistry. | Chemistry. | Organic Chemistry. | Biochemistry, general. | Polymer Sciences. | Medicinal Chemistry.
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E-Book E-Book AUM Main Library 547 (Browse Shelf) Not for loan

Radical Substitution Reactions at the Saturated C Atom -- Nucleophilic Substitution Reactions at the Saturated C Atom -- Electrophilic Additions to the C=C Double Bond -- ?-Eliminations -- Substitution Reactions on Aromatic Compounds -- Nucleophilic Substitution Reactions at the Carboxyl Carbon -- Carboxylic Compounds, Nitriles, and Their Interconversion -- Carbonic Acid Derivatives and Heterocumulenes and Their Interconversion -- Additions of Heteroatom Nucleophiles to Carbonyl Compounds and Subsequent Reactions—Condensations of Heteroatom Nucleophiles with Carbonyl Compounds -- Addition of Hydride Donors and of Organometallic Compounds to Carbonyl Compounds -- Conversion of Phosphorus- or Sulfur-Stabilized C Nucleophiles with Carbonyl Compounds: Addition-induced Condensations -- The Chemistry of Enols and Enamines -- Chemistry of the Alkaline Earth Metal Enolates -- Rearrangements -- Thermal Cycloadditions -- Transition Metal-Mediated Alkenylations, Arylations, and Alkynylations -- Oxidations and Reductions.

This English edition of a best-selling and award-winning German textbook Reaction Mechanisms: Organic Reactions · Stereochemistry · Modern Synthetic Methods is aimed at those who desire to learn organic chemistry through an approach that is facile to understand and easily committed to memory. Michael Harmata, Norman Rabjohn Distinguished Professor of Organic Chemistry (University of Missouri) surveyed the accuracy of the translation, made certain contributions, and above all adapted its rationalizations to those prevalent in the organic chemistry community in the English-speaking world. Throughout the book fundamental and advanced reaction mechanisms are presented with meticulous precision. The systematic use of red "electron-pushing arrows" allows students to follow each transformation elementary step by elementary step. Mechanisms are not only presented in the traditional contexts of rate laws and substituent effects but, whenever possible, are illustrated using practical, useful and state-of-the-art reactions. The abundance of stereoselective reactions included in the treatise makes the reader familiar with key concepts of stereochemistry. The fundamental topics of the book address the needs of upper-level undergraduate students, while its advanced sections are intended for graduate-level audiences. Accordingly, this book is an essential learning tool for students and a unique addition to the reference desk of practicing organic chemists, who as life-long learners desire to keep abreast of both fundamental and applied aspects of our science. In addition, it will well serve ambitious students in chemistry-related fields such as biochemistry, medicinal chemistry and pharmaceutical chemistry. From the reviews: "Professor Bruckner has further refined his already masterful synthetic organic chemistry classic; the additions are seamless and the text retains the magnificent clarity, rigour and precision which were the hallmark of previous editions. The strength of the book stems from Professor Bruckner’s ability to provide lucid explanations based on a deep understanding of physical organic chemistry and to limit discussion to very carefully selected reaction classes illuminated by exquisitely pertinent examples, often from the recent literature. The panoply of organic synthesis is analysed and dissected according to fundamental structural, orbital, kinetic and thermodynamic principles with an effortless coherence that yields great insight and never over-simplifies. The perfect source text for advanced Undergraduate and Masters/PhD students who want to understand, in depth, the art of synthesis ." Alan C. Spivey, Imperial College London "Bruckner’s ‘Organic Mechanisms’ accurately reflects the way practicing organic chemists think and speak about organic reactions. The figures are beautifully drawn and show the way organic chemists graphically depict reactions. It uses a combination of basic valence bond pictures with more sophisticated molecular orbital treatments. It handles mechanisms both from the "electron pushing perspective" and from a kinetic and energetic view. The book will be very useful to new US graduate students and will help bring them to the level of sophistication needed to be serious researchers in organic chemistry." Charles P. Casey, University of Wisconsin-Madison "This is an excellent advanced organic chemistry textbook that provides a key resource for students and teachers alike." Mark Rizzacasa, University of Melbourne, Australia.

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