Organic chemistry Books
Springer Silane Coupling Agents
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Springer Chemistry of Nucleosides and Nucleotides 002 Discontinued Chemistry of Nucleosides and Nucleotides
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Springer Carbonylation
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Springer New Methods for Polymer Synthesis
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Springer Micelles Theoretical and Applied Aspects Language of Science
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Springer Solid State NMR of Polymers International Conference Proceedings NATO Asi Ser. A Life Sciences 207
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Springer Cosmetic and Pharmaceutical Applications of Polymers Symposium Proceedings
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Springer Surface Phenomena and Additives in WaterBased Coatings and Printing Technology Proceedings of the International Symposium on Surface Phenomena and 2125 1990 in San Diego NATO Asi Series
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Springer Particles on Surfaces 3
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Springer Particle Technology and Surface Phenomena in Minerals and Petroleum Proceedings of an American Institute of Chemical Engineering Symposium Held in San Diego California August 2125 1991
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Springer The Steric Factor in Medicinal Chemistry Dissymmetric Probes of Pharmacological Receptors Critical Issues in Psychiatry
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Springer Synthesis Characterization and Theory of Polymeric Networks and Gels
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Springer Chemistry of Nucleosides and Nucleotides
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Springer Progress in Electrorheology Science and Technology of Electrorheological Materials
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Springer Asphaltenes Fundamentals and Applications
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Springer Mineral Scale Formation and Inhibition Proceedings of an American Chemical Society Symposium Held in Washington DC August 2126 1994
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Springer Polymers and Other Advanced Materials
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Springer Fundamental Principles of Molecular Modeling Proceedings of an International Workshop Held in Skukuza Kruger Park South Africa August 2025 1995 Emotions Personality and
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Springer Pioneering Ideas for the Physical and Chemical Sciences Josef Loschmidts Contributions and Modern Developments in Structural Organic Chemistry Atomistics and Statistical Mechanics
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Springer Polyampholytes Synthesis Characterization and Application
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Springer Flavonoids in Cell Function
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Springer In Situ Spectroscopy of Monomer and Polymer Synthesis
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Springer Asphaltenes Heavy Oils and Petroleomics
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Springer Inorganic and Organometallic Macromolecules Design and Applications
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Springer Carbonbased Membranes for Separation Processes
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Springer Carbohydrates
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Springer The Art of Writing Reasonable Organic Reaction Mechanisms
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Springer AdpRibosylation Reactions
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Springer Mesomolecules From Molecules to Materials 1 Structure Energetics and Reactivity in Chemistry Series
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Springer Food Enzymes Structure and Mechanism
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Springer Perfumes Cosmetics and Soaps Vol 3 Modern Cosmetics
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Springer Practical Inorganic Chemistry Preparations Reactions And Instrumental Methods Science Paperbacks 158
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Springer The Biosynthesis of Secondary Metabolites
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Springer The Flavonoids Advances in Research Since 1980
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Springer Microorganisms in Foods 5
Book SynopsisThe control of food safety in modern food processing relies upon HACCP and other systems that identify hazards and define processes to control them. These demand a thorough understanding of the properties of microbial pathogens under all the conditions that could be found in foods and the food processing environment.Table of ContentsIntroduction. Aeromonas Spp. Bacillus Cirrus. Brucella. Campylobacter, Clostrdium Botulinum. Clostridium Perfringens. Intestinally Pathogenic Escherichia Coli. Up Listeria Monocytogenes. Parasites: Aniszkidae. Parasites:Taenia. Parasites: Trichinella Spiralis. Plesiomonas. Pseudomonas Cocovenenans. Salmonellae. Seafood Toxins of Microbiological Origins. Shigella. Staphylococcus Aureus. Streptococcus. Toxigenic Fungi: Aspegillus. Toxigenic Fungi: Fusarium. Toxigenic Fungi: Penicillium. Vibrio Cholerae. Vibrio Parahaemolyticus. Vibrio Vulnificus. Viruses. Yersinia Enterocolitica. Index
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Springer Basic Concepts in Organic Chemistry A Programmed Learning Approach
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Springer Hydrocolloid Applications
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Springer Microbial Food Poisoning
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Springer The Mixing of Rubber
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Springer Cyclic Polymers
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Springer Food and Beverage Mycology
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Elsevier Science Nitrosation Reactions and the Chemistry of Nitric
Book Synopsis
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Springer Chemistry and Analysis of Volatile Organic Compounds in the Environment
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Springer The Chemistry of Natural Products
Book Synopsis1 Carbohydrates.- 1.1 Introduction.- 1.2 Recent developments in O-glycosidation methodology.- 1.3 Recent developments in C-glycoside synthesis.- 1.4 Synthesis of antibiotic sugars.- 1.5 Use of carbohydrates as chiral templates and reagents for asymmetric synthesis.- 1.6 Use of carbohydrates as chiral starting materials for the synthesis of enantiomerically pure natural products.- References.- 2 Aromatic compounds.- 2.1 Introduction.- 2.2 Benzenoids.- 2.3 Coumarins.- 2.4 Isocoumarins, chromanones, chromones and cannabinoids.- 2.5 Macrocyclic lactones.- 2.6 Pyrones, butenolides, lignans and benzofurans.- 2.7 Terphenyls.- 2.8 Flavonoids.- 2.9 Xanthones and benzophenones.- 2.10 Naphthalenes and naphthoquinones.- 2.11 Anthraquinones.- 2.12 Anthracyclines.- 2.13 Some other polycyclic antibiotics.- 2.14 Ansamycins.- References.- 3 Terpenoids.- 3.1 Introduction.- 3.2 Monoterpenoids.- 3.3 Sesquiterpenoids.- 3.4 Diterpenoids.- 3.5 Sesterterpenoids.- 3.6 Triterpenoids.- 3.7 Carotenoids.- ReferencTrade Review`The first editon of The Chemistry of Natural Products was published in 1985, and the various chapters then described progress in the ten years preceding 1982/3. This new edition covers the period between then and mid-1992, and in most respects it is a new book rather than a new edition of an existing test. Although the book has the same format as its predecessor, the detailed content and may of the authors of the individual chapters are different...Each chapter has a useful list of literature references. The book is well-produced and can be recommended as providing a varied, interesting, and useful account of progress in different aspects of natural product chemistry over the last ten years.' National Products Reports `This well written and presented book summarises much elegant chemistry which is accompanied by clearly drawn and well explained reaction schemes...it admirably achieves its purpose...' The Pharmaceutical Journal Table of Contents1 Carbohydrates.- 1.1 Introduction.- 1.2 Recent developments in O-glycosidation methodology.- 1.3 Recent developments in C-glycoside synthesis.- 1.4 Synthesis of antibiotic sugars.- 1.5 Use of carbohydrates as chiral templates and reagents for asymmetric synthesis.- 1.5.1 Asymmetric reduction.- 1.5.2 Enantioselective alkylation of carbohydrate derived nucleophiles.- 1.5.3 Enantioselective alkylation of carbohydrate derived electrophiles.- 1.5.4 Monosaccharides as chiral auxiliaries for cycloaddition reactions.- 1.6 Use of carbohydrates as chiral starting materials for the synthesis of enantiomerically pure natural products.- References.- 2 Aromatic compounds.- 2.1 Introduction.- 2.2 Benzenoids.- 2.3 Coumarins.- 2.4 Isocoumarins, chromanones, chromones and cannabinoids.- 2.5 Macrocyclic lactones.- 2.6 Pyrones, butenolides, lignans and benzofurans.- 2.7 Terphenyls.- 2.8 Flavonoids.- 2.9 Xanthones and benzophenones.- 2.10 Naphthalenes and naphthoquinones.- 2.11 Anthraquinones.- 2.12 Anthracyclines.- 2.13 Some other polycyclic antibiotics.- 2.14 Ansamycins.- References.- 3 Terpenoids.- 3.1 Introduction.- 3.2 Monoterpenoids.- 3.3 Sesquiterpenoids.- 3.4 Diterpenoids.- 3.5 Sesterterpenoids.- 3.6 Triterpenoids.- 3.7 Carotenoids.- References.- 4 Steroids.- 4.1 Introduction.- 4.2 Molecular rearrangement.- 4.3 Remote functionalisation.- 4.4 Photochemical reactions.- 4.5 Partial synthesis.- 4.5.1 Oestranes.- 4.5.2 Androstanes.- 4.5.3 Pregnanes.- 4.5.4 Cholanes.- 4.5.5 Cardenolides and bufadienolides.- 4.5.6 Vitamins D.- 4.5.7 Cholestanes and derivatives.- References.- 5 Amino acids, peptides and proteins.- 5.1 Introduction.- 5.2 Amino acids.- 5.2.1 Synthesis.- 5.2.2 New naturally occurring amino acids.- 5.3 Peptides.- 5.3.1 Synthesis.- 5.3.2 Synthesis of glycopeptides.- 5.3.3 Synthesis of phosphorylated peptides.- 5.3.4 Post-translational modifications.- 5.3.5 Design of peptide-based pharmaceuticals.- 5.3.6 New peptides from natural sources.- 5.4 Techniques for structural elucidation.- 5.4.1 X-ray crystallography.- 5.4.2 N.m.r. spectroscopy.- 5.4.3 Molecular modelling.- 5.5 Proteins.- 5.5.1 Incorporation of unnatural amino acids.- 5.5.2 Purification and analysis.- 5.5.3 Sequences, databases and protein folding.- 5.6 Appendix.- 5.6.1 Useful books.- 5.6.2 Databases.- References.- 6 Alkaloids.- 6.1 Introduction.- 6.2 Biomimetic studies.- 6.2.1 Biomimetic synthesis of Iboga and Aspidosperma alkaloids.- 6.2.2 Biomimetic routes to Daphniphyllum alkaloids.- 6.3 Synthesis.- 6.3.1 Reserpine.- 6.3.2 Other yohimbine and heteroyohimbine alkaloids.- 6.4 Marine alkaloids.- 6.4.1 The manzamines.- 6.4.2 Biosynthetic origin of manzamines.- 6.4.3 Total synthesis of manzamine C.- 6.4.4 Synthetic approaches to manzamine A.- References.- 7 Nucleosides, nucleotides and nucleic acids.- 7.1 Introduction.- 7.2 Nucleosides.- 7.2.1 Nucleoside synthesis: general methods.- 7.2.2 Nucleosides containing modified sugars.- 7.2.3 Other nucleosides of interest.- 7.2.4 Some useful and novel reactions.- 7.3 Nucleotides.- 7.3.1 Nucleoside monophosphates and their analogues.- 7.3.2 Cyclic nucleotides.- 7.3.3 Nucleoside polyphosphates and their analogues.- 7.4 Nucleic acids.- 7.4.1 Oligodeoxyribonucleotide synthesis.- 7.4.2 Oligoribonucleotide synthesis.- 7.4.3 Oligonucleotides containing modified internucleotidic links.- 7.4.4 Nucleic acid sequencing.- 7.5 Supplementary reading.- References.- 8 Porphyrins.- 8.1 General introduction.- 8.2 Macrocycle biosynthesis.- 8.2.1 Introduction.- 8.2.2 Substitution pattern of uroporphyrinogen III.- 8.2.3 Biosynthesis of vitamin B12.- 8.3 Haemoprotein model compounds.- 8.3.1 Introduction.- 8.3.2 Supramolecular effects in haemoprotein model compounds.- 8.3.3 Cytochrome P-450 models.- 8.4 Porphyrins with easily oxidisable substituents.- 8.4.1 Introduction.- 8.4.2 Mesotetrakis (3,5-di-t-butyl-4-hydroxyphenyl)porphyrin.- 8.4.3 Mesotetrakis (pyrogallyl) porphyrin.- 8.5 Utilisation of porphyrin excited states.- 8.5.1 Introduction.- 8.5.2 Modelling photosynthesis.- 8.5.3 Solar energy conversion.- 8.6 Porphyrins in photodynamic therapy.- 8.6.1 Introduction.- 8.6.2 Haematoporphyrin derivative, HpD.- 8.6.3 Second generation porphyrins.- 8.6.4 New approaches to photosensitiser delivery.- 8.6.5 Mechanism of photodynamic action.- 8.6.6 Photosensitising porphyrins as herbicides.- 8.7 DNA-porphyrin interactions.- 8.7.1 Introduction.- 8.7.2 DNA cleavage.- 8.7.3 DNA binding.- 8.8 Porphyrins as novel materials.- 8.8.1 Introduction: solid state and liquid crystalline phenomena.- 8.8.2 Porphyrins in molecular electronics.- 8.9 Porphyrins with liquid crystalline properties.- 8.9.1 Introduction.- 8.9.2 Porphyrins with discotic phases.- References.- 9 Aliphatic compounds.- 9.1 Introduction.- 9.2 Semiochemicals.- 9.2.1 Lepidopteran pheromones.- 9.2.2 Methyl substituted aliphatic pheromones.- 9.2.3 Unbridged spiroketals.- 9.3 Development of synthetic technology.- 9.3.1 Bridged spiroketal semiochemicals of bark beetles.- 9.3.2 Organosulphur semiochemicals.- 9.4 Marine natural products.- 9.4.1 Palytoxin.- 9.4.2 Okadaic acid, dinophysistoxins and acanthifolicin.- 9.4.3 Fused ring polyethers.- 9.5 Enyne-allene and enediyne antibiotics.- 9.5.1 Neocarzinostatin.- 9.5.2 Trisulphide triggered enediyne antibiotics: the esperamicins and calicheamicins.- 9.5.3 Dynemicins.- References.- Chemical abbreviations and acronyms.
£170.99
Springer The Chemical Industry
Book Synopsis1 Introduction.- 1.1 Development of the chemical industry.- 1.2 What the chemical industry does.- 1.3 Characteristics of the industry.- 1.4 Sectors of the industry.- 1.5 Conversion of chemicals into consumer products.- 1.6 The chemical industry.- 1.7 Quality and safety.- 1.8 Environmental aspects.- 1.9 The importance of team-work.- References.- 2 Quality and safety issues.- 2.1 Quality.- 2.2 Health and safety.- Acknowledgements.- References.- 3 Environmental issues.- 3.1 Introduction.- 3.2 Some environmental disasters.- 3.3 Public response to the disasters.- 3.4 The chemical companies' response.- 3.5 The way forward?.- 3.6 Conclusions.- References.- 4 Polymers.- 4.1 Introduction.- 4.2 Molecular weight of polymers.- 4.3 Chemistry of polymerization.- 4.4 Homopolymers and copolymers.- 4.5 Manufacture of polymers.- 4.6 Properties of polymers.- 4.7 Thermoset polymers and cross-linking.- 4.8 Elastomers (rubbers).- 4.9 Fibres.- 4.10 Present and future developments in polymer chemistry.- 5 DyeTrade Review`...I enjoyed the book and I believe students will also find it useful.' Chemistry & Industry Table of ContentsEditorial introduction to the first edition. Preface to the second edition. Introduction. Quality and safety issues. Environmental issues. Polymers. Dyestuffs. The sulphur, phosphorous, nitrogen and chlor-alkali industries. Agrochemicals. The pharmaceutical industry. Biological catalysis and biotechnology. The future. Index.
£85.49
Springer Process Analytical Chemistry
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£170.99
Springer Advanced Asymmetric Synthesis Stateoftheart and future trends in feature technology
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Springer Chemistry of BetaLactams
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£141.00