Organic chemistry Books
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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£141.00
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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Springer Chemistry of Iron
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Springer Supercritical Fluid Extraction and its Use in Chromatographic Sample Preparation
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Springer Principles of Molecular Recognition
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Springer Modern Colorants Synthesis and Structure 3 Advances in Color Chemistry Series
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Springer Analysis of Sterols
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Springer New Methods of Polymer Synthesis Volume 2
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Springer Naturally Occurring Quinones IV Recent advances
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Springer Handbook of Phase Transfer Catalysis
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Springer Enzymatic Reactions in Organic Media
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Springer Specialist Surfactants
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Springer Handbook of Downstream Processing
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Springer Active Oxygen in Chemistry Structure Energetics and Reactivity in Chemistry Series 2
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Springer Energetics of Organic Free Radicals 4 Structure Energetics and Reactivity in Chemistry Series
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Springer Chemistry of Precious Metals
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Springer Acyclic Carbocyclic and LNucleosides
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Springer Pouchers Perfumes Cosmetics and Soaps
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Springer Nonlinear Optical Effects in Organic Polymers 162 Nato Science Series E
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Springer Selectivities in Lewis Acid Promoted Reactions Workshop Proceedings 289 Nato Science Series C
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Springer Crosslinking and Scission in Polymers Proceedings 292 Nato Science Series C
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Springer Calixarenes A Versatile Class of Macrocyclic Compounds 3 Topics in Inclusion Science
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Springer Conjugated Polymeric Materials Opportunities in Electronics Optoelectronics and Molecular Electronics 182 Nato Science Series E
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Springer Novel Biodegradable Microbial Polymers International Workshop Proceedings 186 Nato Science Series E
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Springer Basic Principles of Membrane Technology
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Springer Olefin Metathesis and Polymerization Catalysts Synthesis Mechanism and Utilization 326 Nato Science Series C
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Springer Inclusion Aspects of Membrane Chemistry 2 Topics in Inclusion Science
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Springer Metal Promoted Selectivity in Organic Synthesis 12 Catalysis by Metal Complexes
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Springer Inorganic and Organometallic Oligomers and Polymers Proceedings of the 33rd IUPAC Symposium on Macromolecules
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Springer Chemistry and Properties of Biomolecular Systems 8 Topics in Molecular Organization and Engineering
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Springer Spectral Atlas of Polycyclic Aromatic Compounds Including Information on Aquatic Toxicity Occurrence and Biological Activity 3
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