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• Volume 1: Early Studies
• Electrophilic Aromatic Substitution
• Friedel-Crafts Chemistry
• Stable (Persistent), Long Lived Carbocations: General Aspects
• Trivalent Alkyl (Cycloalkyl) Cations (Carbenium Ions)
• - and -Delocalized Carbocations
• Heteroatom and Metal Substituted Carbocations
• Carbodications
• Aromatic and Homoaromatic Cations and Dications
• Five and Higher Coordinate (Nonclassical) Carbonium Ions: Controversy and Significance
• Magic Acid and Superacid Chemistry
• Solid Superacid Catalysis
• From Kekule's Four-Valent Carbon to Higher Coordinate Hypercarbon
• Electrophilic Chemistry of Saturated Hydrocarbons
• Onium Ions: General Aspects
• Volume 2: Oxonium, Sulfonium, Selenonium and Telluronium Ions
• Azonium Ions
• Halonium Ions
• Miscellaneous Onium Ions
• Gitonic Onium Di(Poly)cations and Superelectrophilic Activation
• Synthetic Reagents, Methods and Reactions
• Oxygenation and Sulfuration
• Nitration and Nitrosation Chemistry
• Organofluorine Chemistry
• Organometallic Chemistry
• Polymer Chemistry
• New Approaches to Future of Hydrocarbon Needs
• Miscellaneous Studies.
• (source: Nielsen Book Data)

In the course of his distinguished career spanning about half a century, George A. Olah, winner of the 1994 Nobel Prize for Chemistry, has been exceedingly prolific and has published more than 1000 scientific papers and 15 books and holds more than 100 patents. This volume contains about 250 of his papers, selected for their breadth and current importance.
(source: Nielsen Book Data)

• pt. A. Structure and mechanisms
• pt. B. Reactions and synthesis.

• Chemical Bonding and Molecular Structure.- Stereochemical Principles.- Conformational, Steric, and Stereoelectronic Effects.- Study and Description of Organic Reaction Mechanisms.- Nucleophilic Substitution.- Polar Addition and Elimination Reactions.- Carbanions and Other Nucleophilic Carbon Species.- Reactions of Carbonyl Compounds.- Aromaticity and Electrophilic Aromatic Substitution.- Concerted Reactions.- Photochemistry.- Free-Radical Reactions.
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The purpose of this edition is the same as that of the first edition, that is, to provide a deeper understanding of the structures of organic compounds and the mechanisms of organic reactions. The level is aimed at advanced undergraduates and beginning graduate students. Our goal is to solidify the student's understanding of basic concepts provided in an introduction to organic chemistry and to fill in much more information and detail, including quantitative information, than can be presented in the first course in organic chemistry. The first three chapters consider the fundamental topics of bonding theory, stereochemistry, and conformation. Chapter 4 discusses the techniques that are used to study and characterize reaction mechanisms. The remaining chapters consider basic reaction types with a broad coverage of substituent effects and stereochemistry being provided so that each reaction can be described in good, if not entirely complete, detail. The organization is very similar to the first edition with only a relative shift in emphasis having been made. The major change is the more general application of qualitative molecular orbital theory in presenting the structural basis of substituent and stereoelectronic effects. The primary research literature now uses molecular orbital approaches very widely, while resonance theory serves as the primary tool for explanation of structural and substituent effects at the introductory level. Our intention is to illustrate the use of both types of interpretation, with the goal of facilitating the student's ability to understand and apply the molecular orbital concepts now widely in use.
(source: Nielsen Book Data)

• pt. A. Structure and metabolism.--pt. B. Reactions and synthesis.

• Localized Chemical Bonding
• Delocalized Chemical Bonding
• Bonding Weaker than Covalent
• Stereochemistry
• Carbocations, Carbanions, Free Radicals, Carbenes, and Nitrenes
• Mechanisms and Methods of Determining Them
• Photochemistry
• Acids and Bases
• Effects of Structure on Reactivity
• Aliphatic Nucleophilic Substitution
• Aromatic Electrophilic Substitution
• Aliphatic Electrophilic Substitution
• Aromatic Nucleophilic Substitution
• Free-Radical Substitution
• Addition to Carbon-Carbon Multiple Bonds
• Addition to Carbon-Hetero Multiple Bonds
• Eliminations
• Rearrangements
• Oxidations and Reductions
• Appendices
• Indexes.
• (source: Nielsen Book Data)

Covering virtually every useful chemical reaction, this revised reference work discusses scope, limitation and mechanism. The text is organized by reaction type in order to facilitate ease of use. It contains over 10,000 references.
(source: Nielsen Book Data)

• Localized Chemical bonding
• Delocalized Chemical Bonding
• Bonding Weaker than Covalent
• Stereochemistry
• Carbocations, Carbanions, Free Radicals, Carbenes and Nitrenes
• Mechanisms and Methods of Determining Them
• Photochemistry
• Acids and Bases
• Effects of Structure on Reactivity
• Aliphatic Nucleophilic Substitution
• Aromatic Electrophilic Substitution
• Aliphatic Electrophilic Substitution
• Free-Radical Substitution
• Addition to Carbon-Carbon Multiple Bonds
• Addition to Carbon- Hetero Multiple Bonds
• Eliminations
• Rearrangements
• Oxidations and Reductions
• The Literature of Organic Chemistry
• Classifications of Reactions by Type of Compound Synthesized.
• (source: Nielsen Book Data)

This survey of advanced chemistry covers virtually all the useful reactions - 600 all told - with the scope, limitations and mechanism of each described in detail. Extensive general sections on the mechanisms of the important reaction types and five chapters on the structure and stereochemistry of organic compounds and reactive intermediates are included as well. Of the more than 10,000 references included, 5000 are new in this edition.
(source: Nielsen Book Data)

• Safety
• keeping records of laboratory work
• equipping the laboratory and the bench
• purification and drying of solvents
• reagents - purification and handling
• gases
• vacuum pumps
• carrying out the reaction
• working up the reaction
• purification
• small-scale reactions
• large-scale reactions
• characterization
• the chemical literature
• special procedures
• trouble shooting.
• (source: Nielsen Book Data)

Any research which uses new organic chemicals or those which are not available commercially will at some time require the synthesis of such compounds. This practical book covers the most up-to-date techniques commonly used in organic synthesis, and updates the first edition. This book should be of interest to: postgraduate industrial and advanced undergraduate organic chemists; biologists, biochemists and genetic engineers; material scientists; polymer researchers; and pharmaceutical, agrochemical and others involved with fine chemicals research and electronics.
(source: Nielsen Book Data)

• Selected Problems: A tandem route to 1,2,3,4-tetrasubstituted naphthalenes. The Hooker oxidation. Benzopyrene synthesis - by accident. Lactone ammonolysis. Acid-catalysed condensation of indole with acetone. Flash vacuum pyrolysis of o-xylylene dimers. A "stable enol" that doesn't exist. Reaction of benzothiazole with DMAD. Ring contractions of a dibenzothiepinone. Rearrangement of 6-hydroxyprotopine to dihydrosanguinarine. An intramolecular Wittig reaction. Easy contruction of a tricyclic indole related to the mitomycins. A flavone from a chromanone. Lewis acid-catalysed condensation of indole with 1,3-cyclohexanedione. Two syntheses of dehydrorotenone.
• (source: Nielsen Book Data)

Covering all major areas of modern organic chemistry, this text consists of 300 problems which challenge the user in terms of providing reasonable mechanistic interpretations of sets of experimental observations.
(source: Nielsen Book Data)
"The Elsevier Tetrahedron Organic Chemistry Series" is a topical series of monographs by world-renowned scientists in several fields of organic chemistry. "The Tetrahedron Organic Chemistry Series" has been very successful in providing some of the very best scholarly works in these topical areas that have proven to be of lasting quality as indispensable reference sources. These books have provided the practicing researcher, student and scholar with an invaluable source of comprehensive reviews in organic chemistry, predominantly in the areas of synthesis and structure determination, including: Reagents; Reaction mechanisms; Molecular Diversity; Asymmetric Synthesis; Multi-dimensional nmr; Enzymatic Synthesis; Organometallic Chemistry; and, Biologically Important Molecules.
(source: Nielsen Book Data)

• The setting
• old and new reactions of diazo compounds
• medium-sized ring effects
• electrophilic azo compounds and azomethine imines
• benzyne chemistry
• azoles and azides
• 1,3-dipolar cycloadditions
• electrocyclic reactions
• 1,4-dipolar cycloadditions
• (2+2) cycloadditions of ketenes
• (2+2) cycloadditions of donor and acceptor olefins
• glimpses and reflections - more on my life and thoughts.
• (source: Nielsen Book Data)

The "Profiles, Pathways and Dreams" series is a "who's who" of organic chemistry that follows the lives of some of chemistry's most eminent and prolific scientists. Each contributor describes his research and science over the range of his career. Together, these autobiographies illustrate how various disciplines of chemistry have progressed over the past 50 years. Noted for his discoveries in the field of heterocyclic chemistry, Rolf Huisgen "invented" numerous reactions, including the 2 + 3 dipolar cycloaddition. In this book, he tells of rebuilding the famous Munich laboratory from rubble after the destruction due to the bombings of Munich in World War II. Huisgen's philosophies of life and science are discussed in detail in academia. Many photographs depict both the professional, as well as the personal side of this renowned scientist.
(source: Nielsen Book Data)

• IR maxima sequence.--Melting point sequence.--Refractive index sequence.--Boiling point sequence.--Molecular weight sequence.--Density sequence.

• I. Introduction, alcohols, yeast, malt and malt liquors, wines and potable spirits, neutral alcohol derivatives, sugars, starch and its isomerides, paper and pulp testing, aliphatic acids.- II. Fixed oils, fats and waxes, special characters and methods, butter fat, lard,linseed oil, higher fatty acids, soap, glycerin, wool-fat, cloth oils, sterol alcohols.- III. Hydrocarbons, bitumens, naphthale and its derivatives, anthracene and its associates, phenols, aromatic acids, gallic acid, and its allies, phthalic acid and the phthaleins, modern explosives.- IV. Special characters of essential oils; resins, india-rubber, gutta percha, balata, and allied substances; the constituents of essential oils, and allied substances; the general characters and analysis of essential oils.- V. Tannins, writing inks, stamping, typing and marking inks, printing inks, amines and ammonium bases, analysis of leather, colouring matters of natural origin, colouring substances in foods, benzene and its homoloues, aniline and its allies, naphthylamines, pyridine, quinoline and acridine bases.-

• Partial table of contents: The Rules of the Game. Slow Motion, Deep Insight. Clear Drawings, Three--Dimensional Structures. Preserve Atoms in Place, Keep Things Simple. Atom and Bond Budgets. Fragmentation of Bicyclobutane by Way of Anti--Bredt Intermediates. Acidic Fragmentation in the Course of a Clever Synthesis of Alpha----Methylene Butyrolactones. A Local Oxidation at the Unexpected Site by Bromination at the Expected Site. Vicinal Migrations with Stereocontrol. Hydrazine Used for Ring Mutation. A Stepwise Electron Transfer That Requires Two Moles of Oxidant. Circuitous Oxidation With Lead Tetraacetate. Multifaceted Performance of Grignard Reagent. A Potentially Complex Wagner----Meerwein Rearrangement Made Simple. Strange Involvement of Nonfunctionalized Isopentyl Side Chain. A Case of X--Ray Data Yielding the Wrong Structure Due to Interference of Organic Chemistry. Reaction Index.
• (source: Nielsen Book Data)

For students of advanced organic chemistry, this text develops problem-solving skills using fifty-six challenging, organic chemistry problems covering a wide variety of chemical systems. Concentrates on necessary and fundamental concepts in the introductory chapters. Valuable not only as a study guide and source of interesting problems, but also as an illustration of reactions and phenomena of general interest.
(source: Nielsen Book Data)

• Introduction in organic chemistry
• the structural model of classical organic chemistry
• optical activity, chirality, and symmetry of molecules
• configurational analysis (demonstrated using carbohydrates examples)
• conformational analysis (demonstrated using steroid examples)
• macromolecular and supramolocular chemistry
• the qualitative MO model
• documentation and retrieval of chemical knowledge
• symmetry point groups and space groups
• determination of absolute configuration
• NMR-spectroscopy
• the special case of benzene
• base-pairing in biology
• and chemistry.
• (source: Nielsen Book Data)

Gerhard Quinkert Ernst Egert Christian Griesinger Aspects of Organic Chemistry Structure Praise for the German Edition This up-to-date picture of organic chemistry presented in a rather unconventional fashion is well-founded yet fascinating. One really feels the enthusiasm of the authors for this exciting area, and it easily springs over onto the reader. Surely, I would have studied organic chemistry, if I had had such a book during my course. Richard R. Ernst This is the documentation of an extraordinary, future-oriented educational concept for organic chemistry. Albert Eschenmoser Being a beneficiary of Aspects of Organic Chemistry by Quinkert, Egert, and Griesinger, I want to point out that this book is an excellent source of information yet a gripping reading matter, not only for advanced students, but also for chemists more advanced in years. Vladimir Prelog The series has good chance to become such a standard work for organic chemists as Lectures on Physics (Feynman, Leighton, Sands) has been for the physics students since the last two generations passing a change in paradigms, which is essential for science itself, onto the education. The logical structure of organic chemistry is elucidated in a really uniquely conclusive way. Crossing the borders is considered not an exception, but the rule, no matter, whether links to topology, group or graph theories are discussed, or connections between chemistry and biology are worked out. Indeed, the basic concept of the authors to emphasize the close relationship between modern biology and chemistry is proved convincingly as a thread running through the whole text. This is not and wants not to be a lowbrow text. It is not a conventional textbook as you can find them on the market more than enough. It is a work made to help think about organic chemistry, to understand its logical structure, without neglecting the numerous important details. Helmut Schwarz.
(source: Nielsen Book Data)

• A reminiscence or two on Professor Sir Derek Barton, Nobel Laureate, A.G.M. Barrett
• inventing radical chain reactions with Derek Barton at the Institut de Chimie des Substances Naturelle, D. Crich
• Derek Barton as "hidden advisor", E.L. Eliel
• Derek H.R. Barton - the lighter side, G. Stork
• some memories of my 45-year association with Derek Barton, H.H. Wasserman
• a memoir - two years with Derek Barton at Imperial College (1971-1973), R.N. Young
• some personal recollections of Sir Derek Barton FRS - a gentleman, a scholar, and a very human being, W.B. Motherwell
• Professor D.H.R. Barton, my spiritual mentor, S. Ito. (Part contents).
• (source: Nielsen Book Data)

A collection of memoirs, reminiscences and biographical details regarding Sir Derek Barton (1918-1998), who was one of the most influential organic chemists of the 20th century. The chapters are contributed by some of his many students, co-workers and scientific colleagues, all of whom testify to his fascinating character and true genius. They offer glimpses at Sir Derek's scientific life, his sense of humour and his "modus operandi" as a teacher of research methods.
(source: Nielsen Book Data)

• The Beilstein Online Database: An Introduction
• Computerizing Beilstein
• STN Implementation of Factual and Structure Databases
• An Overview of DIALOG
• Chemical Structure Searching: Using S4/MOLKICK on DIALOG
• Support of Industry Information Needs
• Searching for Chemical Reaction Information
• Physical Property Data: Capabilities for Search and Retrieval
• Experiences of Two Academic Users: Evaluation of Applications in an Academic Environment
• The Lawson Similarity Number (LN): Offline Generation and Online Use.
• (source: Nielsen Book Data)

The computer-based Beilstein Handbook is the most complete and systematic collection of evaluated data on organic compounds. This book begins with an introduction and overview of the database. It then discusses the development of the database, the implementations of the two operating systems (STN and DIALOG), chemical structure searches, and the physical properties data stored in the handbook. It also describes the Lawson Similarity Number, a valuable new tool for searching for structure similarity.
(source: Nielsen Book Data)

• 1. The Beilstein System-An Introduction
• 2. The Beilstein Handbook
• 3. The Beilstein Online Database
• 4. Current Facts in Chemistry on CD-ROM
• 5. Computer Systems for Substructure Searching
• 6. CrossFireplus Reactions
• 7. Using the Beilstein Reaction Database in an Academic Environment
• 8. Beilstein's CrossFire: A Milestone in Chemical Information and Interlibrary Cooperation in Academia
• 9. Use of the Beilstein System in the Chemical and Pharmaceutical Industries
• 10. AutoNom.
• (source: Nielsen Book Data)

The Beilstein System is a comprehensive online database for information on organic molecules, reactions, structures, and related topics in organic chemistry. This book describes the growth of the Beilstein System, the new CrossFire search system, and the CrossFire-plus-Reactions database. It provides complete overviews of Current Facts in Chemistry on CD-ROM and the Beilstein database of structures, data, and literature citations. The book also discusses Autonom, a software program that gives chemical names of structures following IUPAC nomenclature rules. It will be an invaluable tool for anyone using the Beilstein System.
(source: Nielsen Book Data)

• v. 1. Enzyme action.--
• v. 2. Substrate behavior.--
• v. 3. Macro- and multimolecular systems.--
• v. 4. Electron transfer and energy conversion; cofactors; probes.

• Biogenerat+.
• (source: Nielsen Book Data)