Organic Mechanisms: Reactions, Stereochemistry and Synthesis

Much of life can be understood in rational terms if expressed in the language of chemistry. It is an international language, a language without dialects, a language for all time, a language that explains where we came from, what we are, and where the physical world will allow us to go. Chemical Language has great esthetic beauty and links the physical sciences to the b- logical sciences. from The Two Cultures: Chemistry and Biology by Arthur Kornberg (Nobel Prize in Physiology and Medicine, 1959) Over the past two centuries, chemistry has evolved from a relatively pure disciplinary pursuit to a position of central importance in the physical and life sciences. More generally, it has p- vided the language and methodology that has unified, integrated and, indeed, molecularized the sciences, shaping our understanding of the molecular world and in so doing the direction, development and destiny of scientific research. The language of chemistry referred to by my former Stanford colleague is made up of atoms and bonds and their interactions. It is a s- tem of knowledge that allows us to understand structure and events at a molecular level and increasingly to use that understanding to create new knowledge and beneficial change. The words on this page, for example, are detected by the eye in a series of events, now generally understood at the molecular level.

Clear and concise treatment Strength is thoroughness and systematology Overall concepts are given in special boxes Distinct marking of lower and higher level sections English edition of a bestselling German textbook Includes supplementary material: sn.pub/extras

Autorentext
Professor Dr. Reinhard Brückner arbeitet seit 1998 am Institut für Organische Chemie und Biochemie der Universität Freiburg. Seine Forschungsgebiete sind Naturstoffsynthese und die Entwicklung neuer Methoden im Bereich der Stereoselektiven Synthese. Zuvor war er Professor für Organische Chemie an den Universitäten Würzburg und Göttingen bzw. Gastprofessor an der University of Wisconsin in Madison (USA), der Universidade de Santiago de Compostela (Spanien), der Indiana University Bloomington (USA) und der Tokyo University (Center of Excellence Program).

Inhalt
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 ReactionsCondensations 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.

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