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Books > Science & Mathematics > Chemistry > Organic chemistry > General
Published continuously since 1944, the "Advances in Protein
Chemistry and Structural Biology" serial has been a continuous,
essential resource for protein chemists. Covering reviews of
methodology and research in all aspects of protein chemistry,
including purification/expression, proteomics, modeling and
structural determination and design, each volume brings forth new
information about protocols and analysis of proteins while
presenting the most recent findings from leading experts in a broad
range of protein-related topics. Coversreviews of methodology and research in all aspects of protein chemistry. Brings forth new information about protocols and analysis of proteins while presentingthe most recent findings from leading experts in a broad range of protein-related topics. "
Established in 1960, "Advances in Heterocyclic Chemistry" is the
definitive serial in the area one of great importance to organic
chemists, polymer chemists and many biological scientists. Written
by established authorities in the field, the comprehensive reviews
combine descriptive chemistry and mechanistic insight and yield an
understanding of how the chemistry drives the properties.
Provides a synthetic armory of tools to aid the practicing
chemist by reviewing the most reliable historical methods alongside
new methods/ Written by scientists who have actually used these in
synthesis. By emphasizing tricks and tips to optimize reactions for
the best yields and purity, which are often missing from the
primary literature, this book provides another dimension for the
synthetic chemist. A combined academic and industrial approach
evaluates the best methods for different scales of reaction and
discusses practical tips (e.g. when to stop a reaction early to
maximize purity or when to re-use side products). Chapters also
assess whether to make or source starting materials, how to connect
them and what are the best synthetic routes. The book is designed
to be a stand-alone reference, but also provides cross references
to leading reviews and the "Comprehensive Heterocyclic Chemistry"
reference works for those who want to learn more.
The series Topics in Current Chemistry presents critical reviews of the present and future trends in modern chemical research. The scope of coverage is all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science. The goal of each thematic volume is to give the non-specialist reader, whether in academia or industry, a comprehensive insight into an area where new research is emerging which is of interest to a larger scientific audience. Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field. Review articles for the individual volumes are invited by the volume editors. Readership: research chemists at universities or in industry, graduate students
This volume deals with the chemistry of five-membered heterocycles containing at least two nitrogen atoms, or those with one, or more, nitrogens and one or more atoms from group 6 of the Peri tables. It includes chapters on: oxadiazoles and thiadiazoles; five-memebered heterocyclic compounds with four-heter-atoms in the ring; five-membered rings containing two nitrogen atoms; and five-membered heterocyclic compounds with three hetero-atoms in the ring.
Since the industrial revolution, chlorine remains an iconic molecule even though its production by the electrolysis of sodium chloride is extremely energy intensive. The rationale behind this book is to present useful and industrially relevant examples for alternatives to chlorine in synthesis. This multi-authored volume presents numerous contributions from an international spectrum of authors that demonstrate how to facilitate the development of industrially relevant and implementable breakthrough technologies. This volume will interest individuals working in organic synthesis in industry and academia who are working in Green Chemistry and Sustainable Technologies.
This volume contains a survey of 51 ring systems in which an imidazole ring is fused to an additional five-membered ring system. Ring systems included are those appearing in the Chemical Abstracts Index of Ring Systems under the 2-ring 5-5 citation and including a C3N2 fragment. The material is subsequently subdivided into chapters based on the number and types of hetero atoms in the additional 5-membered ring. The synthesis, physiochemical properties and reactions of compounds in each ring system are covered; reactions are organized on a mechanistic basis and the survey includes compounds that are both partially and fully saturated.
Find out how theoretical calculations are used to determine, elucidate and propose mechanisms for Pd-catalyzed C-C cross-coupling reactions in Max Garcia Melchor's outstanding thesis. Garcia Melchor investigates one of the most significant and useful types of reactions in modern organic synthesis; the Pd-cross coupling reaction. Due to its versatility, broad scope and selectivity under mild conditions, this type of reaction can now be applied in fields as diverse as the agrochemical and pharmaceutical industry. Garcia Melchor studies the reaction intermediates and transition states involved in the Negishi, the copper-free Sonogashira and the asymmetric version of Suzuki-Miyaura coupling. He also characterizes and provides a detailed picture of the associated reaction mechanisms. The author has won numerous prizes for this work which has led to over eight publications in internationally renowned journals.
Based on presentations made during the 6th International Symposium
on Natural Product Chemistry, this book is divided into two broad
sections. Section A includes articles on synthetic routes developed
to complex natural products, while Section B is a compilation of
discoveries of new natural products and their pharmacological
properties.
This anthological description of the history and applications of photochemistry provides photochemistry practitioners with complementary information about the field, currently not covered in existing textbooks and handbooks. The first part focuses on the historical development of the field, including light-matter interaction, the discovery of photochemical reactions and the development of modern photochemical mechanisms. This section provides useful background to the second part which outlines applications of photochemistry in the present day, such as in synthesis, green chemistry, diagnostics, medicine and nanotechnology. Furthermore, the author provides an outlook on promising areas for future developments. The broad scope of "Photochemistry: Past, Present and Future" is also of interest to the wider chemical audience and it makes a pleasant read while not compromising on scientific rigor.
Established in 1960, "Advances in Heterocyclic Chemistry" is the
definitive serial in the area one of great importance to organic
chemists, polymer chemists and many biological scientists. Written
by established authorities in the field, the comprehensive reviews
combine descriptive chemistry and mechanistic insight and yield an
understanding of how the chemistry drives the properties.
The Chemistry of Heterocyclic Compounds, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects - properties, synthesis, reactions, physiological and industrial significance - of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors are recognized authorities, the Chemistry of Heterocyclic Chemistry is considered worldwide as the indispensable resource for organic, bioorganic, and medicinal chemists.
Each volume reviews the total synthesis of a set of compounds looking at syntheses reported historically and at the practice current at the time of publication. From volume 1 focusing on carbohydrates, prostagladins, nucleic acids, antibiotics, naturally occurring oxygen ring compounds and pyrrole pigments, the series continues with coverage of aromatic steroids, monoterpenes, triterpenes, sesquiterpenes, cannabinoids, natural inophores, insect pheromones and alkaloids. Volumes revisit the total synthesis of key compounds such as carbohydrates, nucleic acids and pyrrole pigments several times during the series building a picture of the historic development of total synthesis techniques for these major groups. Chapters are edited by experts in their field to give a complete overview of the best in the field at the time.
In this volume, contributions covering the theoretical and practical aspects of multicomponent crystals provide a timely and contemporary overview of the state-of-the art of this vital aspect of crystal engineering/materials science. With a solid foundation in fundamentals, multi-component crystals can be formed, for example, to enhance pharmaceutical properties of drugs, for the specific control of optical responses to external stimuli and to assemble molecules to allow chemical reactions that are generally intractable following conventional methods. Contents Pharmaceutical co-crystals: crystal engineering and applications Pharmaceutical multi-component crystals: improving the efficacy of anti-tuberculous agents Qualitative and quantitative crystal engineering of multi-functional co-crystals Control of photochromism in N-salicylideneaniline by crystal engineering Quinoline derivatives for multi-component crystals: principles and applications N-oxides in multi-component crystals and in bottom-up synthesis and applications Multi-component crystals and non-ambient conditions Co-crystals for solid-state reactivity and thermal expansion Solution co-crystallisation and its applications The salt-co-crystal continuum in halogen-bonded systems Large horizontal displacements of benzene-benzene stacking interactions in co-crystals Simultaneous halogen and hydrogen bonding to carbonyl and thiocarbonylfunctionality Crystal chemistry of the isomeric N,N'-bis(pyridin-n-ylmethyl)-ethanediamides, n = 2, 3 or 4 Solute solvent interactions mediated by main group element (lone-pair) (aryl) interactions
Chemistry and Technology of Isocyanates Henri Ulrich Chemical
Consultant, Guilford, USA The production of both mono- and
diisocyanates is of ever increasing importance to the chemical
industry. The annual global consumption of polyurethanes, derived
from diisocyanates, has reached over six million metric tons. This
book highlights the syntheses, reactions and the industrial
importance of this group. Chemistry and Technology of Isocyanates:
"Introduction to Biological and Small Molecule Drug Research and Development "provides, for the first time, an introduction to the science behind successful pharmaceutical research and development programs. The book explains basic principles, then compares and contrasts approaches to both biopharmaceuticals (proteins) and small molecule drugs, presenting an overview of the business and management issues of these approaches. The latter part of the book provides carefully selected real-life case studies illustrating how the theory presented in the first part of the book is actually put into practice. Studies include Herceptin/T-DM1, erythropoietin (Epogen/Eprex/NeoRecormon), anti-HIV protease inhibitor Darunavir, and more. "Introduction to Biological and Small Molecule Drug Research and
Development" is intended for late-stage undergraduates or
postgraduates studying chemistry (at the biology interface),
biochemistry, medicine, pharmacy, medicine, or allied subjects. The
book is also useful in a wide variety of science degree courses, in
post-graduate taught material (Masters and PhD), and as basic
background reading for scientists in the pharmaceutical
industry.
Since its inception in 1945, this serial has provided critical
and integrating articles written by research specialists that
integrate industrial, analytical, and technological aspects of
biochemistry, organic chemistry, and instrumentation methodology in
the study of carbohydrates. The articles provide a definitive
interpretation of the current status and future trends in
carbohydrate chemistry and biochemistry.
This book reviews the fundamental aspects of quinoxaline chemistry: synthesis, reactions, mechanisms, structure, properties, and uses. The first four chapters present a survey of the developments in quinoxaline chemistry since the publication of the monograph on "Condensed Pyrazines" by Cheeseman and Cookson in 1979. These chapters give comprehensive coverage of all the methods of the synthesis of quinoxalines and the important quinoxaline-containing ring systems such as thiazolo[3,4-a]-, pyrrolo[1,2-a]-, and imidazo[1,5-a]quinoxalines. Chapter five describes many new methods for the construction of quinoxaline macrocycles, which are important in applications such as optical devices and materials. The final chapter reviews all previously known rearrangements of heterocyclic systems that lead to benzimidazole derivatives. Mamedov critically analyses these transformations to reveal a novel acid-catalyzed rearrangement of quinoxalinones giving 2-heteroarylbenzimidazoles and 1-heteroarylbenzimidazolones in the presence of nucleophilic reactants (MAMEDOV Heterocycle Rearrangement). This book is of interest to researchers in the fields of heterocyclic and synthetic organic chemistry.
Natural products present in the plant and animal kingdom offer a
huge diversity of chemical structures, which are the result of
biosynthetic processes that have been modulated over the millennia
through genetic effects. With the rapid developments in
spectroscopic techniques and accompanying advances in
high-throughput screening techniques, it has become possible to
isolate and then determine the structures and biological activity
of natural products rapidly, thus opening up to the pharmaceutical
industry exciting opportunities in the field of new drug
development. The series covers all of the above as well as the
synthesis, testing and recording of the medicinal properties of
natural products.
The purpose of "Ligand Efficiency Indices for Drug Discovery:
Towards an Atlas-Guided Paradigm" is to introduce in a concise and
self-contained form the concepts, ideas, applications and examples
of efficiency-driven drug discovery to the biomedical community at
large. The book emphasizes the use of 'new variables' and more
objective numerical methods to drive drug discovery in an
encompassing way. These 'new variables' are based on Ligand
Efficiency Indices (LEIs) formulated in a way that permits mapping
Chemico-Biological Space (CBS) in an Atlas-like representation. It
provides a practical and timely discussion of the concepts, ideas,
applications and examples of efficiency-driven drug discovery. This
book emphasizes the use of a graphical representation and objective
numerical methods to drive drug discovery more effectively. It
presents the definition of LEIs and the corresponding efficiency
planes within an atlas-like environment to provide a robust
graphical and numerical framework for medicinal chemists and
drug-discoverers.
In this second edition methods are described to measure the synthesis of lipids such as the phosphoinositides, ceramides and sphingomyelin, as well as techniques to molecularly characterize the various kinases and phosphatases that regulate the intracellular metabolism of these lipids. Lipid Signaling Protocols, Second Edition guides readers through detailed experimental protocols, which are complimented by review chapters that highlight the technical considerations, challenges and potential pitfalls associated with using these laboratory-based approaches. Written for the Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Lipid Signaling Protocols, Second Edition aims to ensure successful results in the further study of this vital field.
In this volume, a detailed description of cutting-edge computational methods applied to protein modeling as well as specific applications are presented. Chapters include: the application of Car-Parrinello techniques to enzyme mechanisms, the outline and application of QM/MM methods, polarizable force fields, recent methods of ligand docking, molecular dynamics related to NMR spectroscopy, computer optimization of absorption, distribution, metabolism and excretion extended by toxicity for drugs, enzyme design and bioinformatics applied to protein structure prediction. A keen emphasis is laid on the clear presentation of complex concepts, since the book is primarily aimed at Ph.D. students, who need an insight in up-to-date protein modeling. The inclusion of descriptive, color figures will allow the reader to get a pictorial representation of complicated structural issues.
In his thesis, Xiaoyu Sun conducts the first total synthesis of all possible stereoisomers of plakortide E and also confirms the absolute configuration of natural plakortide E. Xiaoyu Sun subsequently converts Plakortide E methyl ester to plakortone B in a biomimetic conversion. Construction and functionalization of cyclic peroxides are notoriously difficult due to the very low O-O bond dissociation energy. Plaktoride E is isolated from the Jamaican marine sponge platorits halichondrioides and contains a five-membered peroxide ring, with oxygen atoms linked to tertiary C4 and C6 centers. The methodology used for synthesizing highly substituted cyclic peroxides is novel and useful, and not only extends the field of Pd-catalyzed reactions, but also provides a convenient synthetic approach for the preparation of the 1,2-dioxolanes series. Plakortide E and plakortone B are bioactive, which means that the synthetic studies on them and their analogs are pivotal in drug discovery.
The conventional solvents used in chemical, pharmaceutical, biomedical and separation processes represent a great challenge to green chemistry because of their toxicity and flammability. Since the beginning of "the 12 Principles of Green Chemistry" in 1998, a general effort has been made to replace conventional solvents with environmentally benign substitutes. Water has been the most popular choice so far, followed by ionic liquids, surfactant, supercritical fluids, fluorous solvents, liquid polymers, bio-solvents and switchable solvent systems. Green Solvents Volume I and II provides a throughout overview of the different types of solvents and discusses their extensive applications in fields such as extraction, organic synthesis, biocatalytic processes, production of fine chemicals, removal of hydrogen sulphide, biochemical transformations, composite material, energy storage devices and polymers. These volumes are written by leading international experts and cover all possible aspects of green solvents' properties and applications available in today's literature. Green Solvents Volume I and II is an invaluable guide to scientists, R&D industrial specialists, researchers, upper-level undergraduates and graduate students, Ph.D. scholars, college and university professors working in the field of chemistry and biochemistry. |
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