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Books > Science & Mathematics > Chemistry > Organic chemistry
In this book importance of Asymmetric Synthesis are given with examples. It has underlined concepts developed starting with basic principles of stereochemistry. It is based on drug required, four methodologies are given. The text is written in a simple and lucid style. The topics have been dealt with systematically, diagrammatically and in a lucid language. The book is based on three important principles. First, concepts and terminology used in asymmetric synthesis, second, the four types of asymmetric synthesis and third, applications of asymmetric synthesis. Students, teachers and researchers need to understand the methodology of asymmetric synthesis, because of the crucial role this plays in the organic synthesis, especially in synthesis of drugs. An understanding of different methods of asymmetric synthesis is essential for the planning of drug synthesis using the knowledge of QSAR.
During recent years, stereochemistry has undergone a phenomenal growth both in theory and practice, with a concomitant increase of interest among the organic chemists, biological chemists, medicinal chemists, and pharmacologists. The present text provides an up-to-date, coherent, and comprehensive account of the subject starting from the fundamentals and leading up to the latest developments as far as practicable. Emphasis has been placed on a symmetry-based approach to molecular chirality, stereochemical terminologies (modern stereochemistry is replete with them), topicity and prostereoisomerism, conformational analysis, dynamic stereochemistry, chiroptical properties, and assignment of absolute configuration to chiral molecules. Dynamic stereochemistry has been discussed with reference to conformation-reactivity correlation, stereoselective synthesis, and pericyclic reactions. A large crosssection of organic reactions with stereochemical implication has been incorporated. Attempts have been made to familiarise the readers with modern instrumental techniques, nuclear magnetic resonance in particular, used for stereochemical investigation. Each chapter is provided with a summary which highlights the main points of the text.
This long awaited fourth edition continues with its popular and outstanding methodologies for the elucidation of reaction mechanisms. This book has constantly tried to assist the students in learning mechanisms considering a broad coverage of every important aspect of mechanistic techniques. It has been extensively used as a text for the last 30 years by both graduate and postgraduate level students. In addition, research workers have also enormously benefited because of the in-depth discussion of the subject and inclusion of recent bibliography. The book consists of 14 chapters and is written in a reader friendly language. The contents of this edition provide a concrete and compact description of the subject. New end-of-chapter problems have been appended. This book will hopefully continue to inspire its readers in focussing on the mechanistic approach to chemistry.
This profusely illustrated book is intended to provide a comprehensive exposition of different aspects of organic and name reactions in detail including rearrangements such as mechanisms, stereochemistry and their applications with illustrations, figures, schemes and reaction series in such a way that it should not be difficult for the reader to evaluate typical reaction condition, workup procedure etc. Each chapter is accompanied with conceptual, theoretical and numerical problems along with references. The reaction series of schemes of organic and name reactions provide the way for rapid revision of the topics. All this should be of great help to research scholars, postgraduate students and teachers.
The book is designed to provide a comprehensive coverage in the area of organic reaction mechanism for a chemistry major/graduate student. The practice of medicine now increasingly demands a knowledge of the behaviour of molecules. Therefore, the biologist of tomorrow will have to be more of an organic chemist, among other things. The books is thus aimed at Pharmacologists, Medical chemists and Biochemists also.
This completely new and innovative textbook provides a comprehensive account of pericyclic reactions and organic photochemistry for undergraduate and postgraduate courses. The approach is based on mechanism and reaction type, and the subject matter is developed and concentrated on better understanding rather than on merely grasping factual knowledge. Basics of the subject are explained in thorough details in this title. Important points are revisited and mentioned wherever they are relevant. This title provides over 200 excellent thought-provoking textual problems. Glossary and questions for self-assessment are given at the end of each chapter. The most important aspect of this book is Chapter 14 which contains about 400 problems and their solutions based on pericyclic reactions and photochemistry. Applied photochemistry is also discussed in the book.
The text is ideal for under and postgraduate students of biophysical chemistry and as a handy guide for researchers in industry and biotechnology. This text covers: The study of biological cell and its organisation Bioenergetics Statistical Mechanics in biopolymers Forces involved in biopolymer interactions Cell membrane and solute transport Biopolymers and their molecular weights Thermodynamics of biopolymer solutions Diffraction methods and study of macromolecules
Chemistry of Love and Sex is a chemist's guide to the chemical
phenomena and molecules associated with endogenous hormonal
mechanisms and brain neurotransmission - the basis of many emotions
associated with love, passion, and sex.
""This book should become an indispensable asset on the bookshelves of pharmaceutical laboratories in academia and in industry, as well as of laboratories devoted to plant protection. I am convinced that studying this book will be an eye-opener for many scientists in the field of life sciences. Furthermore, for teachers in this area it will not only be a useful compilation of the various languages and definitions of organic stereochemistry, but also a welcome source of examples for demonstrating to their students the intricate and intriguing role stereochemistry plays in the chemistry of life."" -Prof. Dr. Dieter Seebach, Laboratory of Organic Chemistry, ETH Zurich, Switzerland This textbook presents the molecular scale of matter in the broad diversity and richness of its three dimensions, giving due attention when relevant to the temporal dimension in which molecules exist, act, and react. The focus is on two significant fields of three-dimensional chemistry: a presentation of the guiding principles in organic stereochemistry, followed by a focus on the biochemical and medicinal relevance of this discipline. The treatment of "Guiding Principles "gives priority to didactic clarity and nomenclature issues, as detailed and illustrated in Parts 1 to 4: '"Symmetry Elements and Operations, Classification of Stereoisomers"''"Stereoisomerism Resulting from One or Several Stereogenic Centers"''"Other Stereogenic Elements: Axes of Chirality, Planes of Chirality, Helicity, and ("E," "Z")-Diastereoisomerism"''"Isomerisms about Single Bonds and in Cyclic Systems"' This is followed by Parts 5 to 8 which focus on the biomedicinal relevance of stereochemistry, with special reference to the biochemistry and pharmacology of medicinal compounds. Here, examples and applications are discussed and illustrated based on their relevance to a given specific stereochemical aspect: '"Chirality in Molecular and Clinical Pharmacology"''"The Conformational Factor in Molecular Pharmacology"''"The Concept of Substrate Stereoselectivity in Biochemistry and Xenobiotic Metabolism"''"Prostereoisomerism and the Concept of Product Stereoselectivity in Xenobiotic Metabolism"' Finally, the book contains a gift for broad-minded readers with an interest in the historical roots of stereochemistry: Part 9: '"Molecular Chirality in Chemistry and Biology: Historical Milestones"' Key features: Consists entirely of beautifully produced colored figuresIncludes marginal notes, giving clear-cut short definitions of terms used in the corresponding captionProvides an alphabetic glossary of termsOffers an extensive index
The identification and quantification of the widespread occurrence of trace organic chemicals at minute concentrations in the aqueous environment impacted by human activities is a result of rapid advances in environmental analytical chemistry. The body of knowledge regarding the characterization, fate and transport of these chemicals of emerging concern (CECs) in the natural water environment and engineered water treatment processes, as well as their toxicity, has grown substantially over the last two decades. Recently, the focus in the environmental chemistry community has shifted from these CEC parent compounds to the fate, transport, and toxicity of transformation products, which are generated through abiotic and biotic mechanisms in natural systems and during engineered advanced water treatment processes. This two-part book focuses on the studies and recent advancements towards the development of more harmonized strategies and workflows using non-target and suspects screening methods, including suitable bioassay approaches to assess the overall relevance of transformation products. Volume I covers the relevance of transformation products and international strategies to manage CECs, new methods for a comprehensive assessment of transformation products, and the fate and transport of transformation products in natural systems. This book is ideal for environmental scientists and engineers, particularly chemists, environmental engineers, public health officials, regulators, other chemistry-related professionals, and students.
Information literacy-the ability to find, evaluate, and use information resources-is an important skill for future chemists. Students and scientists need to distinguish between information provided by Wikipedia, ChemSpider, research journals, and The New York Times, depending on the intended use of the information sought. Instructors and librarians may often teach these skills through stand-alone database demonstrations, video tutorials, and lectures. However, it is possible to teach these skills in a more contextual and integrated manner by designing chemistry assignments that incorporate information literacy as a learning outcome. This book will prove useful for librarians and chemistry instructors who are designing courses in which students develop information literacy in the context of a chemistry course at two-year colleges, public and private universities, and high schools. The chapters in this book review the current state of information literacy in chemistry and provide concrete examples of assignments and interventions aimed at teaching information literacy skills in chemistry curricula. A wide range of options are offered for integrating information literacy into college-level chemistry courses, including general chemistry, organic chemistry, science courses for students not majoring in science, and chemistry capstone research courses.
This book, based primarily on late breaking work ... provides an
interesting snapshot at some of the main lines of current and new
research within the field, such as investigation of the novel
properties of ionic liquids and their uses in separations (e.g.,
gases, organics, and metal ions), biochemistry, medicine, and
nanochemistry. The chapters also reflect the growing theoretical
and computational work within the field leading to new predictive
capability.
This book examines the history and fundamentals of the physical organic chemistry discipline. With the recent flowering of the organic synthesis field, physical organic chemistry has seemed to be shrinking or perhaps is just being absorbed into the toolkit of the synthetic chemist. The only Nobel Prize that can be reasonably attributed to a physical organic chemist is the 1994 award to George Olah, although Jeffrey I. Seeman has recently made a strong case that R. B. Woodward was actually a physical organic chemist in disguise (I). 2014 saw the awarding of the 50th James Flack Norris Award in Physical Organic Chemistry. James Flack Norris was an early physical organic chemist, before the discipline received its name. This book provides insight into the fundamentals of the field, and each chapter is devoted to a major discovery or to noted physical organic chemists, including Paul Schleyer, William Doering, and Glen A. Russell.
"Progress in Medicinal Chemistry" provides a review of eclectic developments in medicinal chemistry. This volume continues in the serial's tradition of providing an insight into the skills required of the modern medicinal chemist; in particular, the use of an appropriate selection of the wide range of tools now available to solve key scientific problems, including g-secretase modulators, P2X7 antagonists as therapeutic agents for CNS disorders, N-type calcium channel modulators for the treatment of pain, and more.
This book is focused on recent progress in the dynamically developing field of controlled/living radical polymerization. It is a sequel to ACS Symposium Series 685, 768, 854, and 944. The volume contains 24 chapters on other controlled/living radical polymerization techniques including kinetics and mechanism of RAFT, DT, NMP, and OMRP, macromolecular architecture by RAFT, DT, and NMP, materials prepared by RAFT and NMP, and industriral aspects of RAFT and NMP.
Homework help! Develop the solid problem-solving strategies you need for success in organic chemistry with this Study Guide/Solutions Manual. Contains answers to all problems in the text.
This book is focused on recent progress in the dynamically developing field of controlled/living radical polymerization. It is a sequel to ACS Symposium Series 685, 768, 854, and 944. Volume 1023 contains 26 chapters on mechanistic, synthetic and materials aspects of ATRP. Volume 1024 contains 24 chapters on other controlled/living radical polymerization techniques.
Chirality as an environmental phenomenon was dealt with in a
thorough and interesting manner in a series of three symposia
entitled "Modern Chiral Pesticides: Enantioselectivity and Its
Consequences," sponsored by the Agrochemical Division of the
American Chemical Society and held in Washington, DC (2005),
Boston, MA (2007) and San Francisco, CA (2010). All three symposia
included speakers from industry, government and academia,
representing several European countries, China, and the United
States. Corresponding to this broad group of countries,
institutions and speakers, the range of topics touched on almost
all facets of chirality as it is manifested in environmental and
human exposure and toxicity. The 40 oral and 20 poster
presentations indeed approached comprehensive coverage: analysis of
enantiomers and other stereoisomers; preparative separation of
enantiomers; stereoselective occurrences of chiral pesticides in
environment soil and water and in wildlife and human tissues and
fluids; stereoselective degradation and metabolism of chiral
pesticides; and stereoselective toxicity.
This volume consists of written chapters taken from the
presentations at the symposium "100+ Years of Plastics: Leo
Baekeland and Beyond," held March 22, 2010, at the 239th ACS
National Meeting in San Francisco. The symposium celebrates the
100th anniversary of the formation of General Bakelite Corp., which
was preceded by Leo Baekland's synthesis of Bakelite in 1907 and
the unveiling of the Bakelite process in 1909. It is quite
reasonable to use the synthesis of Bakelite as the starting point
of the Age of Plastics. Indeed, Time magazine in its June 14, 1999,
issue on the 100 most influential people of the 20th century chose
Leo Baekeland and his Bakelite synthesis as the sole representative
of chemistry.
This third volume of NMR Spectroscopy in the Undergraduate Curriculum continues the work we started with the first and second volumes in providing effective approaches for using nuclear magnetic resonance spectrometers as powerful tools for investigating a wide variety of phenomena at the undergraduate level. This volume focuses on upper-level courses and NMR spectroscopy across the curriculum. The applications and strategies in this volume will be helpful to those who are looking to transform their curriculum by integrating more NMR spectroscopy, to those who might not have considered NMR spectroscopy as a tool for solving certain types of problems, or for those seeking funding for a new or replacement NMR spectrometer.
This ACS Symposium Series is the product of a symposium held at the 241st National Meeting of the American Chemical Society in Anaheim, CA on March 27-31, 2011. It includes chapters on new biobased building blocks such as the furandicarboxylic acid, polyesters and polyamides from adipic, succinic and sebacic acids with aliphatic diols such as 1,3-propylene glycol, 1,4-butanediol, 1,12-dodecylenediol and isosorbide. The conversion of hydroxymethylfurfural, the dehydration product of hexose sugars, to succinic acid and 1,4-butanediol to produce poly(butylene succinate) is described in one chapter. Also the synthesis of new polymers from plant-derived olefinic monomers such as tulipalin A and studies of composites from cotton by-products are featured in other chapters. There is a strong emphasis on biocatalytic synthesis and polymerization within the book. Chapter topics include the synthesis of ?-hydroxyfatty acids and polymers therefrom, an interesting discussion on the structural differences of the products of the biocatalytic and chemical catalytic synthesis of polyesters from oleic diacid and glycerol and the ability to produce polylactic acid (PLA) and PLA-PHA copolyesters within a "microbial cell factory". Other areas of interest explored in other chapters include recent developments of biobased polymer fibers and oleate-based pressure sensitive adhesives and composites. One chapter describes a large increase in cold-drawn fiber tensile strength by the blending of a small amount of ultrahigh molecular weight (MW) poly(3-hydroxybutyrate) with a much lower MW 3-hydroxybutyrate polymer. The addition of a rubber and inorganic fillers to normally brittle PLA was found to dramatically improve its ductility. Finally, there are several chapters on seed oil-based polyurethanes, one on fibers from soy proteins and composites from starch.
This book will explore our forests as the most readily available and renewable source of carbon as well as the building block of chemicals, plastics, and pharmaceuticals as the next 100 years gradually push consumers toward alternate sources of chemicals. Meeting these needs from trees requires that new chemistry be developed so that plant materials is converted to commodity chemicals. This focused discussion on ongoing global efforts at creativity using forest and biomass based renewable materials will include six different mechanisms for bringing about change on this very innovative topic.
Assessing Exposures and Reducing Risks to People from the Use of Pesticides will focus on practices that have been developed in the past 10 years marked from the passage of the Food Quality Protection Act and other pertinent legislation (eg the Clean Air Act Amendments), which deal all, or in part with reducing risks associated with pesticides.
This book is meant to be a companion volume for the ACS Symposium Series Book entitled Nuts and Bolts of Chemical Education Research. In the Nuts and Bolts book (edited by Diane M. Bunce and Renee Cole), readers were presented with information on how to conduct quality chemical education research. In the Myth book, exemplars of chemical education research are featured. In the cases where the chapter in the book is describing research that has already been published (typically in the Journal of Chemical Education), additional information is provided either in terms of research questions investigated that were not reported in the published article or background information on decisions made in the research that helped the investigation. The main focus of this type of discussion is to engage the reader in the reality of doing chemical education research including a discussion of the authors' motivation. It is expected that these two books could be used as textbooks for graduate chemical education courses showing how to do chemical education research and then providing examples of quality research.
A major strength of American Chemical Society (ACS) is the large number of volunteers who help to grow and sustain the organization, from local sections to technical divisions, from regional to national meetings, from task forces to national committees, and from conducting research to writing and reviewing manuscripts for journals. Some of them spend literally thousands of hours on behalf of ACS and the global chemistry enterprise, helping students or fellow scientists, organizing meetings and symposia, and reaching out to the local communities. One of the people who excelled in these efforts was the late Prof. Ernest L. Eliel. For many years he taught at the University of Notre Dame and the University of North Carolina and was an acknowledged leader in organic stereochemistry and conformational analysis. He was also a leader at ACS, serving as ACS President in 1992 and Chair of ACS Board of Directors in 1987-89. Unfortunately Prof. Eliel died in 2008, but the ACS held a symposium in 2016 honoring his work. This book features two volumes highlighting stereochemistry and global connectivity, which represent two of the key legacies of Prof. Eliel. Because stereochemistry is a fundamental chemistry concept, ongoing research is carried out in different subfields of chemistry (such as organic, medicinal, carbohydrates, polymers), using various analytical techniques (such as NMR, X-ray crystallography, and circular dichroism). The two volumes of this book contain many research papers that represent cutting-edge research in all the above areas. Because chemistry is now a world-wide enterprise, global connectivity is important to chemistry practitioners, and the chapters on international activities should be of great interest as well. |
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