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Showing posts with label Organic Chemistry. Show all posts
Showing posts with label Organic Chemistry. Show all posts

Friday, January 16, 2015

Peptides: Chemistry and Biology



Peptides: Chemistry and Biology
Edited by Norbert Sewald & Hans-Dieter Jakubke

Thoroughly updated, incorporating around 25 % new material, Sewald/Jakubke remains the only modern and scientifically up-to-date advanced textbook on peptide biochemistry, distilling the knowledge of hundreds of publications into a highly readable synopsis of this diverse field.
The authors explain the broad fundamentals of peptide synthesis and structure, systematically addressing important families of biologically active peptides, and adopting an interdisciplinary approach that covers application areas in biotechnology, pharmaceutical science, and biomedicine. One major focus is on such "hot" research topics as pseudopeptides, peptidomimetics, and combinatorial synthesis.
This new edition also features study questions for each learning unit, for easier self-study and classroom teaching

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Tuesday, January 13, 2015

Dictionary of Chemistry, 2nd Edition



Dictionary of Chemistry
McGraw-Hill, Second Edition

McGraw-Hill Dictionary of Chemistry (2nd Edition) is compiled by McGraw-Hill and it is published in 2003. The McGraw-Hill Dictionary of Chemistry provides a compendium of 8000 terms that are central to chemistry and related fields of science and technology. The coverage in this Second Edition is focused on the the areas of analytical chemistry, general chemistry, inorganic chemistry, organic chemistry, physical chemistry, and spectroscopy, with new terms added and others revised as necessary.

more than 8000 essential terms
covers every discipline of chemistry
provides synonyms, acronyms and abbreviations

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Saturday, January 10, 2015

Solving General Chemistry Problems



Solving General Chemistry Problems
Edited by Robert Nelson Smith

With the birth of the electronic hand calculator and the death of the slide rule, the teaching of general chemistry entered a new era. Unfortunately, the alculator did not bring automatic understanding of chemistry; analyzing and solving problems is just as difficult as ever. The need for detailed explanations, drill, and review problems is still with us. This book, "Solving General Chemistry Problems", by R.N. Smith, is a replication of a book originally published before 1980. It has been restored by human beings, page by page, so that you may enjoy it in a form as close to the original as possible. This book was created using print-on-demand technology

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Friday, January 9, 2015

Principles and Applications of Asymmetric Synthesis


Principles and Applications of Asymmetric Synthesis

Asymmetric synthesis remains a challenge to practicing scientists as the need for enantiomerically pure or enriched compounds continues to increase. Over the last decade, a large amount of literature has been published in this field. Principles and Applications of Asymmetric Synthesis consolidates and evaluates the most useful methodologies into a one-volume resource for the convenience of practicing scientists and students.
Authored by internationally renowned scientists in the field, this reliable reference covers more than 450 reactions and includes important stoichiometric as well as catalytic asymmetric reactions. The first chapter reviews the basic principles, common nomenclature, and analytical methods, and the remainder of the book is organized according to reaction type. The text examines such topics as:
Carbon-carbon bond formations involving carbonyls, enamines, imines, and enolates
Asymmetric C-O bond formations including epoxidation, dihydroxylation, and aminohydroxylation
Asymmetric synthesis using the Diels-Alder reaction and other cyclizations
Applications to the total synthesis of natural products
Use of enzymes in asymmetric synthesis
Practicing chemists in the pharmaceutical, fine chemical, and agricultural professions as well as graduate students will find that Principles and Applications of Asymmetric Synthesis affords comprehensive and current coverage

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Visions of the Future: Chemistry and Life Science


Visions of the Future: Chemistry and Life Science

What does the future of science hold? Who is making the discoveries that will help shape this future? What areas of research show the greatest promise? Find definitive and insightful answers to such questions as these in the three volumes of Visions of the Future: Astronomy and Earth Science, Chemistry and Life Science, and Physics and Electronics. Representing a careful selection of authoritative articles published in a special issue of Philosophical Transactions--the world's longest-running scientific journal--the chapters explore such themes as:
The Big Bang
Humankind's exploration of the solar system
The deep interior of the Earth
Global warming and climate change
Atoms and molecules in motion
New materials and processes
Nature's secrets of biological growth and form
Understanding the human body and mind
Quantum physics and its relationship to relativity theory and human consciousness
Exotic quantum computing and data storage

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Thursday, January 8, 2015

The Art of Writing Reasonable Organic Mechanisms


The Art of Writing Reasonable Organic Mechanisms
Edited by Robert B. Grossman

Intended for students of intermediate organic chemistry, this text shows how to write a reasonable mechanism for an organic chemical transformation. The discussion is organized by types of mechanisms and the conditions under which the reaction is executed, rather than by the overall reaction as is the case in most textbooks. Each chapter discusses common mechanistic pathways and suggests practical tips for drawing them. Worked problems are included in the discussion of each mechanism, and "common error alerts" are scattered throughout the text to warn readers about pitfalls and misconceptions that bedevil students. Each chapter is capped by a large problem set

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Organic Reaction Mechanisms


Organic Reaction Mechanisms, 1997
Edited by A. C. Knipe

Includes such mechanisms as addition and elimination reactions, nucleophilic and electrophilic aromatic substitutions, and molecular rearrangements.
* Each chapter deals with specific reaction types, reviewing the previous year's developments in the area.
* Extensively referenced to previous volumes and primary journals

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Wednesday, January 7, 2015

A Guidebook to Mechanism in Organic Chemistry


A Guidebook to Mechanism in Organic Chemistry
Edited by Peter Sykes

A classic textbook on mechanistic organic chemistry which is characterised particularly by its clarity, careful choice of examples and its general approach that is designed to lead to a ready understanding of the subject matter. This guidebook is aimed clearly at the needs of the student, with a thorough understanding of, and provision for, the potential conceptual difficulties he or she is likely to encounter

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Schaum's Outlines of Beginning Chemistry


Schaum's Outlines of Beginning Chemistry

More than 40 million students have trusted Schaum's to help them succeed in the classroom and on exams. Schaum's is the key to faster learning and higher grades in every subject. Each Outline presents all the essential course information in an easy-to-follow, topic-by-topic format. You also get hundreds of examples, solved problems, and practice exercises to test your skills.

This Schaum's Outline gives you

673 fully solved problems
Hundreds of examples with explanations of chemistry concepts
Support for all the major textbooks for beginning chemistry courses
Fully compatible with your classroom text, Schaum's highlights all the important facts you need to know. Use Schaum’s to shorten your study time--and get your best test scores!

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Tuesday, January 6, 2015

Side Reactions in Organic Synthesis


Side Reactions in Organic Synthesis
A Guide to Successful Synthesis Design

Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reactivity relationship of organic compounds.
This textbook highlights the competing processes and limitations of the most important reactions used in organic synthesis. By allowing chemists to quickly recognize potential problems this book will help to improve their efficiency and success-rate. A must for every graduate student but also for every chemist in industry and academia

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The Logic of Chemical Synthesis


The Logic of Chemical Synthesis
By E.J. Corey and Xue-Min Cheng

The Logic of Chemical Synthesis The title of this three-part volume derives from a key theme of the book-the logic underlying the rational analysis of complex synthetic problems. Although the book deals almost exclusively with molecules of biological origin, which are ideal for developing the fundamental ideas of multistep synthetic design because of their architectural complexity and variety, the approach taken is fully applicable to other types of carbon-based structures. Part One outlines the basic concepts of retrosynthetic analysis and the general strategies for generating possible synthetic pathways by logical reduction of molecular complexity. Systematic retrosynthetic analysis and the concurrent use of multiple independent strategies to guide problem solving greatly simplify the task of devising a new synthesis. This way of thinking has been used for more than two decades by one of the authors to teach the analysis of difficult synthetic problems to many hundreds of chemists. A substantial fraction of the intricate syntheses which have appeared in the literature in recent years have been produced by these individuals and their students. Part Two, a collection of multistep syntheses, provides much integrated information on synthetic methods and pathways for the construction of interesting target molecules. These syntheses are the result of synthetic planning which was based on the general principles summarized in Part One. Thus, Part Two serves to supplement Part One with emphasis on the reactions of synthesis and on specific examples of retrosynthetically planned syntheses.

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Saturday, December 20, 2014

Good Laboratory Practice


Good Laboratory Practice

After more than twenty years of use Good Laboratory Practice, or GLP, has attained a secure place in the world of testing chemicals and other “test items” with regard to their safety for humans and the environment. Gone are the days when the GLP regulations were hotly debated amongst scientists in academia and industry and were accused of stifling flexibility in, imaginative approaches to, and science-based conduct of, all kinds of studies concerned with toxic effects and other parameters important for the evaluation and assessment of products submitted for registration and permission to market. The GLP regulations have developed from rules on how to exactly document the planning, conduct and reporting of toxicity studies to a quality system for the management of a multitude of study types, from the simple determination of a physical/chemical parameter to the most complex field studies or ecotoxicology studies. At the same time the term “Good Laboratory Practice” has become somewhat of a slogan with the aim to characterise any reliably conducted laboratory work.

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Laboratory Experiments for General, Organic and Bio-Chemistry


Laboratory Experiments for General, Organic and Bio-Chemistry

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Laboratory Methods of Organic Chemistry


Laboratory Methods of Organic Chemistry

Edited by L. Gattermann

Completely Revised by Heinrich Wieland 

Hardcover: 435 pages
Publisher: Macmillan; Completely rev. / by Heinrich Wieland edition (1937)
ASIN: B000889DIO

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Research Techniques in Organic Chemistry


Research Techniques in Organic Chemistry

The text is crystal clear, to the point; the graph is large and nicely done. The combination of these two greatly reduced the size of the book.

Personally the best part was about reaction - some counter-flow reaction design and continuous reaction setup may only be met in chemical industry settings. Some reaction designs get very deep into the advanced organic chemistry and industrial reaction engineering, such as the Grignard reaction where alkyl halide and ketone were added simultaneously after Grignard initiation.

The purification part was good too, filled with practical guidance in a few pages.

The characterization is exclusive, with some rarely mentioned techniques by organic chemists. Of course the advances of mass spectrometry in recent decades did not show in this 1971 text.

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Monday, December 8, 2014

Organic Chemistry of Drug Synthesis


Organic Chemistry of Drug Synthesis

The classic reference on the synthesis of medicinal agents --now completely updated The seventh volume in the definitive series that provides a quick yet thorough overview of the synthetic routes used to access specific classesof therapeutic agents, this volume covers approximately 220 new non-proprietary drug entities introduced since the publication of Volume 6.Many of these compounds represent novel structural types firstidentified by sophisticated new cell-based assays. Specifically, a significant number of new antineoplastic and antiviral agents are covered. As in the previous volumes, materials are organized by chemical class and syntheses originate with available starting materials. Organized to make the information accessible, this resource covers disease state, rationale for method of drug therapy, and the biological activities of each compound and preparation. The Organic Chemistry of Drug Synthesis, Volume 7 is a hands-on reference for medicinal and organic chemists, and a great resource for graduate and advanced undergraduate students in organic and medicinal chemistry.

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Saturday, December 6, 2014

Essential Chemistry: Atoms, Molecules and Compounds


Essential Chemistry: Atoms, Molecules and Compounds

"Atoms, Molecules, and Compounds" goes behind the scenes of day-to-day chemistry to explore the atoms that govern chemical processes. In clear language, this exciting book shows how the interactions between simple substances such as salt and water are crucial to life on Earth and how those interactions are predestined by the atoms that make up the molecules. In addition, the stories of the scientists whose discoveries shaped the modern world, such as Niels Bohr and Albert Einstein, are presented here in gripping detail. Brimming with full-color photographs and illustrations and enhanced by sidebars and a glossary, "Atoms, Molecules, and Compounds" enables readers to explore the incredible discoveries highlighted in this book.

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Periodic Table of Elements: Los Alamos National Laboratory


Periodic Table of Elements
Los Alamos National Laboratory's Chemistry Division

The periodic table is the most important chemistry reference there is. It arranges all the known elements in an informative array. Elements are arranged left to right and top to bottom in order of increasing atomic number. Order generally coincides with increasing atomic mass.

The different rows of elements are called periods. The period number of an element signifies the highest energy level an electron in that element occupies (in the unexcited state). The number of electrons in a period increases as one traverses down the periodic table; therefore, as the energy level of the atom increases, the number of energy sub-levels per energy level increases.

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Saturday, January 4, 2014

Theoretical Organic Chemistry



Theoretical Organic Chemistry


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Hazardous Chemicals Handbook


Hazardous Chemicals Handbook


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