Organic chemistry Books
Springer Fachmedien Wiesbaden Organische Chemie: Chemie-Basiswissen II
Book SynopsisDie Reihe Chemie-Basiswissen stellt den gesamten Wissensstoff für das Bachelorstudium Chemie dar. Studenten mit Chemie im Nebenfach und Studierende des höheren Lehramtes dient sie zur Examensvorbereitung. Der Band II, Organische Chemie, präsentiert den Stoff dieses Gebietes in kurzer und übersichtlicher Form. Das didaktische Konzept und die am Curriculum orientierte Stoffauswahl haben das Buch bei Haupt- und Nebenfachstudenten der Chemie sowie Studierenden des höheren Lehramtes beliebt gemacht. Die 8. Auflage wurde vollständig durchgesehen und aktualisiert und um ein Kapitel über Chemikaliensicherheit und Gefahrstoffrecht erweitert. Ebenfalls neu hinzugekommen sind Übungsaufgaben mit Lösungen zu den einzelnen Kapiteln.Table of ContentsGrundwissen der organischen Chemie.- Chemische Bindung in organischen Verbindungen.- Allgemeine Grundbegriffe.- Gesättigte Kohlenwasserstoffe (Alkane).- Die radikalische Substitutions-Reaktion (SR).- Ungesättigte Kohlenwasserstoffe (Alkene, Alkine).- Additionen an Alkene und Alkine.- Aromatische Kohlenwasserstoffe (Arene).- Die aromatische Substitution (SAr).- Halogen-Verbindungen.- Die nucleophile Substitution (SN) am gesättigten C-Atom.- Die Eliminierungs-Reaktionen (E1, E2).- Sauerstoff-Verbindungen.- Schwefel-Verbindungen.- Stickstoff-Verbindungen.- Element-organische Verbindungen.- Aldehyde, Ketone und Chinone.- Reaktionen von Aldehyden und Ketonen.- Carbonsäuren.- Derivate der Carbonsäuren.- Reaktionen von Carbonsäurederivaten.- Kohlensäure und ihre Derivate.- Heterocyclen.- Wichtige Reaktionsmechanismen im Überblick.- Orbital-Symmetrie und Mehrzentrenreaktionen.- Stereochemie.- Photochemie.- Chemie von Naturstoffen und Biochemie.- Chemie und Biochemie.- Kohlenhydrate.- Aminosäuren, Peptide und Proteine.- Lipide.- Nucleotide und Nucleinsäuren.- Terpene und Carotinoide.- Steroide.- Alkaloide.- Natürliche Farbstoffe.- Angewandte Chemie.- Organische Grundstoffchemie.- Kunststoffe.- Farbstoffe.- Chemie im Alltag.- Methodenregister.- Literaturnachweis und Literaturauswahl an Lehrbüchern.
£42.74
Springer-Verlag Berlin and Heidelberg GmbH & Co. KG From the Maluku to Molecules
Book SynopsisYes, more than ever, because medicinal chemists draw creative inspiration for their syntheses from nature to develop the next blockbuster in medicine.Oliver Kayser tells the story of natural products and medicinal plants in this book in a highly informative and amusing way from a new perspective.
£55.68
Springer Verlag GmbH Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products
Book SynopsisFor centuries preparations containing resin from the root of Thapsia garganica L. (Fig. 1) have been used in Arabian and European medicine for treatment of pulmonary diseases, catarrh and as counterirritants for relief of rheumatic pains (1). The properties of the resin were described already by Theophrastos (372-287 B. C. ), Dioscorides (approximately A. D. 50), and Plinius (A. D. 24-79) (2). Radix Thapsiae and Resina Thapsiae have been included in several pharmacopoeias, the latest in the French pharmacopoeia from 1937. The two major active principles were about Fig. I. Thapsia garganica References, pp. 163-167 Sesquiterpenoids from Thapsia Species 131 Thapsigargin (1), Rl: Oct, R2= But Thapsigargicin (2), Rl= Hex, R2 = But Thapsitranstagin (3), Rl: iVai, R2= 2-MeBut Thapsivillosin A (4), Rl= Ang, R2= Sen Thapsivillosin B ( 5), Rl: Ang, R2= 2-MeBut Thapsivillosin C ( 6), Rl= Oct, R2= 2-MeBut Thapsivillosin D ( 7), Rl: 6-MeOct, R2= Sen Thapsivillosin E ( 8), Rl: 6-MeOct, R2= 2-MeBut Thapsivillosin G ( 9), Rl= 6-MeHcp, R2= 2-MeBut Thapsivillosin H ( 10), Rl or R2= Ang or Sen Thapsivillosin I ( 11), Rl= Ang, R2= But Thapsivillosin J ( 12), Rl: iVai, R2= But Thapsivillosin K ( 13), Rl: Sen, R2= 2-MeBut Chart 1. Hexaoxygenated thapsigargins found in Thapsia two decades ago found to be the sesquiterpene lactones thapsigargin (1) and thapsigargicin (2) (3).Table of ContentsThe Explosion of Structural Information on Insect Neuropeptides.- 1. Introduction.- 2. General Methods Used for Isolation, Identification and Characterization of Insect Neuropeptides.- 2.1. Biological Assays.- 2.1.1. Adipokinetic Bioassay.- 2.1.2. Myotropic Bioassay.- 2.2. Liquid Chromatography.- 2.3. Edman Degradation Sequencing, Mass Spectrometry and Peptide Synthesis.- 2.4. Immunological Techniques (RIA, ELISA, Immunocytochemistry).- 2.5. Molecular Biological Techniques.- 3. The Insect Neuropeptides.- 3.1. Peptides Involved in Homeostasis and Metabolism.- 3.1.1. Adipokinetic and Hypertrehalosaemic Peptides.- 3.1.2. Diuretic and Antidiuretic Peptides.- 3.2. Peptides Regulating Reproduction, Growth and Development.- 3.2.1. Pheromone Biosynthesis Activating Neuropeptides.- 3.2.2. Allatotropins and Allatostatins.- 3.2.2.1. Allatotropins.- 3.2.2.2. Allatostatins.- 3.2.3. Prothoracicotropic Hormone, Bombyxin and Other Insulin-Related Neuropeptides.- 3.2.3.1. Prothoracicotropic Hormone.- 3.2.3.2. Bombyxin.- 3.2.3.3. Locusta Insulin-Related Peptide.- 3.2.4. Eclosion Hormones.- 3.2.5. Peptides Affecting Gonad Activity.- 3.2.5.1. Ovary Maturating Peptide and Neuroparsin of Locusta migratoria.- 3.2.5.2. Oostatic Hormones of Diptera.- 3.2.6. Diapause Hormones.- 3.3. Peptides Modifying Spontaneous Muscle Contractions:Mytropic Peptides.- 3.3.1. Proctolin and Cardiostimulatory Peptides.- 3.3.2. Myokinins.- 3.3.3. Sulfakinins.- 3.3.4. Pyrokinins/Myotropins.- 3.3.5. Tachykinins.- 3.3.6. Periviscerokinin.- 3.3.7. Accessory Glands- and Midgut Myotropins and Others.- 3.3.8. Myoinhibitory Peptides and Other FMRF amide Related Peptides (FaRPs).- 3.4. Chromatotropic Factors in Insects.- 4. Conclusions.- Acknowledgments.- References.- Sesquiterpenoids from Thapsia Species and Medicinal Chemistry of the Thapsigargins.- 1. Introduction.- 2. Taxonomy of Thapsia.- 2.1. Thapsia garganica and Thapsia transtagana.- 2.2. Thapsia maxima.- 2.3. Thapsia villosa.- 2.4. Thapsia gymnesica.- 3. Elucidation of the Structure of Thapsigargin.- 4. Proazulenic Slovanolides.- 5. Non-lactonic Sesquiterpenoids from Thapsia.- 6. Pharmacological Activity of the Thapsigargins.- 7. Molecular Pharmacology.- 8. Chemistry of Thapsigargin.- 8.1. Changes at C(8).- 8.2. Changes at C(3).- 8.3. Changes of the Vicinal Diol.- 8.4. Changes of Lactone Carbonyl Group.- 8.5. Changes at O(10).- 9. Structure Activity Relationships.- 10. Metabolic Catabolism of Thapsigargin.- References.- Pregnane Glycosides.- 1. Introduction.- 2. Isolation and Identification.- 2.1. Thin Layer and Column Chromatography.- 2.2. Sephadex LH-20 Chromatography.- 2.3. Flash Chromatography.- 2.4. Low Pressure Liquid Chromatography (LPLC).- 2.5. High Performance Liquid Chromatography (HPLC).- 3. Structure Elucidation.- 3.1. One-Dimensional NMR Spectroscopy.- 3.2. Two-Dimensional NMR Spectroscopy.- 3.3. Mass Spectrometry.- 3.4. I.R. Spectroscopy.- 3.5. U.V. Spectroscopy.- 3.6. Optical Rotatory Dispersion.- 3.7. Hydrolysis of Pregnane Glycosides.- 4. Pregnane Aglycons.- 5. Sugars of Pregnane Glycosides.- 5.1. General and Monosaccharides.- 5.2. Disaccharides from Pregnane Glycosides.- 5.3. Trisaccharides from Pregnane Glycosides.- 6. Biosynthesis of Pregnane Glycosides.- 7. Biological Activity.- Acknowledgement.- References.- Author Index.
£80.99
Springer Verlag GmbH Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products
Table of ContentsChemistry of Synthetic Immunomodulant Muramyl Peptides.- I. From Freund’s Adjuvant to MDP.- II. Synthesis of N-acetyl-muramyl-L-alanyl-D-isoglutamine (MDP).- 1. Protected Dipeptide Derivatives.- 2. Protected N-acetyl-muramyl Derivatives.- 3. Coupling of Protected Muramic Acid and Dipeptide Derivatives.- 4. Deprotecting Procedures.- 5. Synthesis of Labelled MDP.- III. Synthesis of Other N-acetyl-muramyl-dipeptides, Analogues and Derivatives of MDP.- 1. Modifications of the Peptide Moiety.- 2. Modifications of the Carbohydrate Moiety.- IV. Synthesis of N-acetyl-muramyl-tri-, tetra-, and -pentapeptides, and of Some Analogs Bearing a Lipophilic Group at the C-terminal End.- 1. Substitution of the ?-amide Group of MDP by a Free or Amidated Amino Acid.- 2. Lengthening of the Peptide Chain at the Carboxyl Function of MDP.- 3. Lipophilic Derivatives of N-acetyl-muramyl-L-alanyl-D-isoglutaminyl-L-alanine.- V. Synthesis of N-acetyl-?-D-glucosaminyl-(1–4)-N-acetyl-muramyl-peptides.- VI. Synthesis of Oligomers and Conjugates of MDP.- 1. Synthesis of Oligomers of MDP.- 2. Synthesis of Conjugates of MDP.- VII. Mass Spectrometry of MDP and Analogues.- VIII. 13C-NMR Spectrometry of MDP and Derivatives.- IX. Analysis of MDP.- Addendum.- References.- Appendix: Leading References on Biological Activities of MDP and Derivatives.- The Chemistry of Longifolene and Its Derivatives..- I. Introduction.- II. Isolation, Occurrence.- III. Structure.- IV. Synthesis.- V. Isolongifolene.- 1. Structure.- 2. Synthesis.- 3. Mechanism of Rearrangement.- VI. Reactions of Longifolene.- 1. “Normal” Reactions.- a) Addition Reactions.- b) Substitution Reactions.- 2. Skeletal Rearrangements.- a) Simple Wagner-Meerwein Rearrangements.- b) Deep-Seated Rearrangements.- 3. Steric Diversion.- a) Electrophilic Additions.- b) Oxidations.- 4. Transannular Reactions.- a) Radical Reactions.- b) Ionic Reactions.- c) Lead Tetraacetate Oxidation of Longifolols.- 5. Conversions into Other Sesquiterpene Skeletons.- 6. Miscellaneous Transformations.- VII. Reactions of Isolongifolene.- 1. Epoxidation and Reactions of Epoxide.- 2. Addition of Halogens and Pseudo-Halogens.- VIII. Ultraviolet Absorption of Some Longifolene Derivatives.- IX. Biosynthesis.- X. Longifolene in Industry.- References.- Homoisoflavanones and Biogenetically Related Compounds..- 1. Introduction.- 2. Isolation and Identification.- 2.1. Isolation.- 2.2. Chromatography.- 3. Structure and Nomenclature.- 3.1. General Aspects and Nomenclature.- 3.2. Ultraviolet-Visible Spectroscopy.- 3.3. Infrared Spectroscopy.- 3.4. Nuclear Magnetic Resonance Spectroscopy.- 3.4.1. 1H-NMR Spectra.- 3.4.2. 13C-NMR Spectra.- 3.5. Mass Spectrometry.- 3.6. Optical Activity and Absolute Configuration.- 4. Chemical Transformations and Syntheses.- 4.1. Synthesis of the Skeleton.- 4.2. Routes to Eucomol.- 4.3. Isomerization and Hydrogenation Reactions of the 3(9)-Double Bond.- 4.4. Deuterium Exchange Reactions.- 4.5. Acylation and Deacylation Reactions.- 4.6. Alkylation and Dealkylation Reactions.- 4.7. Further Reactions of Eucomol.- 4.8. Chemistry of Brazilin and Hematoxylin.- 5. Biosynthesis.- 6. Biological Activity.- 7. Chemotaxonomy.- References.- Naturally Occurring Phenalenones and Related Compounds..- I. Introduction.- II. Phenalenones and Related Metabolites from Fungi.- A. Occurrence.- B. Structure and Chemistry.- C. Synthesis.- D. Biosynthesis.- E. Biological Activity.- III. Phenalenones and Related Metabolites in Higher Plants.- A. Occurrence.- B. Structure Determination.- C. Spectroscopic Methods.- D. Synthesis.- E. Biological Activity.- F. Biosynthesis.- References.- Molecular Mechanisms of Enzyme-Catalyzed Dioxygenation. (An Interdisciplinary Review.).- I. Introduction.- II. Some Basic Chemistry of Molecular Oxygen.- III. Precedents for Metal-Activation of Dioxygen.- 1. How Would an Iron- or Copper-Protein Interact with Molecular Oxygen?.- 2. Precedents for the Transfer of Dioxygen Within the Co-ordination Sphere.- 3. Precedents for the Reaction of Co-ordinated Dioxygen with Free Substrates.- 4. Free Forms of Activated Dioxygen Generated by Metals.- IV. Precedents for Metal Activation of Organic Substrates.- V. The Double Bond-Cleaving Dioxygenases.- 1. Ene-diol Cleaving Dioxygenases.- 2. Extradiol-Cleaving Dioxygenases.- 3. Other Double Bond-Cleaving Dioxygenases.- VI. The Luciferases.- VII. Peroxidizing Dioxygenases.- VIII. Miscellaneous Dioxygenases.- 1. External Flavoprotein Dioxygenases.- 2. Sulfur Oxidizing Dioxygenases.- 3. Inositol Dioxygenase.- 4. Nitropropane Dioxygenase.- 5. Carotene Dioxygenase.- 6. Ribulose Bisphosphate Carboxylate/Oxygenase.- IX. ?-Keto Carboxylic Acid Decarboxylating Dioxygenases.- X. Summary.- Acknowledgments.- References.- Author Index.
£40.49
Books on Demand Synthese unter Schutzgas: Ratgeber vom Praktiker
Book Synopsis
£8.91
S. Hirzel Verlag Beyer/Walter. Organische Chemie
Book Synopsis
£74.80
S. Hirzel Verlag Beyer/Walter_quickfit: Namensreaktionen: 120
Book Synopsis
£35.82
Spektrum Akademischer Verlag Lerntafel: Organische Chemie II im Überblick
Book Synopsis1 Oxidation und Reduktion.- 2 Carbonylverbindungen.- 3 Pericyclische Reaktionen und Umlagerungen. 4 Naturstoffe I.- 5 Naturstoffe II.- 6 Naturstoffe III
£7.88
Spektrum Akademischer Verlag Alle Grafiken Des Lehrbuchs Pflanzenphysiologie
Book Synopsis
£9.45
Logos Verlag Berlin GmbH Enzymatic Stabilization and Formation of Food
Book Synopsis
£53.79
Verlag G. Mainz Development of Methodologies in Organic Synthesis
Book SynopsisSynthetic organic chemistry aims toward the development of methods for the practical synthesis of important molecules such as bioactive ingredients, pesticides, dyes, and polymers. Although extraction of organic molecules from natural resources is possible, organic synthesis often provides a cheaper and more practical access to them from readily accessible starting materials, as well as the possibility to artificially modify the structure of naturally-occurring molecules to increase their activity or modulate their properties. In medicinal chemistry, a standard approach to find the most potent active ingredient is the so-called combinatorial sythesis strategy: after identification of a promising structure, often a small molecule found in nature, a library of compounds with different substitution patterns is prepared and tested to find the bist hit.
£37.39
Verlag G. Mainz Novel Concepts for Iron and Manganesecatalyzed
Book SynopsisTransition metal catalysis plays a crucial role in the development of new chemical transformations, which can be broadly applied in organic synthesis, medicinal chemistry, synthesis of biologically relevant molecules, pharmaceuticals and other related fields. In recent years, the need for application of sustainable methods is significantly growing due to the necessity of waste-free transformations. Plenty of industrially run processes still apply classical procedures, which often lead to production of tons of waste as a consequence of multistep synthesis. Thus, development of novel catalytic systems which would afford complex molecular structures via straightforward processes is still desired. Hence, metal-catalyzed transformations play a crucial role in the development of new synthetic strategies, as they can easily lead to the reduction of synthetic steps and, ipso facto, reduction of waste leading to atom-economic transformations. Application of transition metals particularly in
£37.39
Editorial Academica Espanola Conversión de aceite residual en Biodiesel
Book Synopsis
£89.52
S Chand & Co Ltd Organic Reactions, Conversions, Mechanisms and
Book Synopsis
£9.59
Anmol Publications Pvt Ltd A Textbook of Organic Reaction Mechanism
Book Synopsis
£11.25
ANE Books Organic Chemistry: Selected Topics
Book SynopsisThe text covers various topics such as Polynuclear Aromatic Hydrocarbons, Heterocyclic Aromatic Compounds, Drugs, Dyes, Polyness, and Alkaloids in a detailed and systematic manner. It is aimed at B.Sc III-year students of Delhi University but is also beneficial for graduate students in Indian Universities.
£8.49
Birkhauser Verlag AG Solution Structure and Solution Dynamics in
Book SynopsisThis book introduces some methods for the determination of the three-dimensional geometry of molecules in solution and the occurrence of dynamical processes (interaction with the solvent, rearrangements in the molecular geometry, interactions with other molecules) in several ytterbium complexes. An especial attention has been deserved to the study of some important catalysts that were recently developed in the scientific research. The determination of molecular geometry and dynamics in solution, even if it is generally a hard task, is often a crucial step to understand and rationalize the catalytic mechanism, as well to design new catalysts. The proposed methods are applied here to several systems, even chiral, and are founded on a detailed analysis of the paramagnetic and optical properties of the ytterbium ion, and combining several instrumental techniques (mainly Nuclear Magnetic Resonance and Circular Dichroism).
£14.99
IAEA The Radiation Chemistry of Polysaccharides
Book SynopsisThis publication provides the background and compiles the most recent research findings as well as details development activities relating to the development of radiation processed products made of natural polymers. Successes clearly indicate that radiation processing of natural polymers has emerged as an exciting area where the unique characteristics of these polymeric materials can be exploited for a variety of practical applications in agriculture, health care, industry and the environment.
£62.70
Universities Press Chemistry for CBSE Class IX
Book SynopsisChemistry for CBSE Class IX is an excellent preparatory book for students. This book provides class-tested material and practice problems that help students understand theories and concepts and, as a consequence, develop problem-solving skills to attempt exams with full confidence. The book is written in lucid language with a variety of solved examples, and aims to assist students in understanding the subject, even without the help of an instructor, as solutions are provided for most of the questions.
£14.99
Universities Press Chemistry for CBSE Class X
Book SynopsisChemistry for CBSE Class X is an excellent preparatory book for students. This book provides class-tested material and practice problems that help students understand the theory and concepts and, as a consequence, develop problem-solving skills to attempt exams with full confidence.
£21.84
Sunway University Press Essential Organic Chemistry
Book SynopsisEssential Organic Chemistry is a study guide that prepares students for the Cambridge International AS and A Level Chemistry (9701) examination. Covering the latest syllabus and with over 60 past-year questions, this book is an essential resource to enhance students' understanding and examination performance.Table of Contents Foreword How to use this book Chapter 1 Introduction to Organic Chemistry Chapter 2 Hydrocarbons Chapter 3 Halogenoalkanes Chapter 4 Alcohols Chapter 5 Carbonyl Compounds Chapter 6 Carboxylic Acids and Esters Chapter 7 Benzene and Methylbenzene Chapter 8 Phenol Chapter 9 Carboxylic Acids and Acyl Chlorides Chapter 10 Organic Nitrogen Compounds Chapter 11 Polymerisation
£23.36
Springer Verlag, Singapore Ionically Gelled Biopolysaccharide Based Systems
Book SynopsisThis volume provides a thorough insight into the chemistry and mechanism of ionic gelations of various ionic biopolysaccharides, like alginate, gellan gum, pectin, chitosan, carboxymethyl cellulose, etc., and the applications of various ionically gelled biopolysaccharides in drug delivery fields, with chapters emphasizing the recent advances in the field by the experts. This book will be of interest to graduate students and academic and industry researchers from pharmacy, biotechnology, bioengineering, biomedical and material sciences fields.Table of ContentsIonically gelled pectinates in drug delivery.- Ionically gelled alginates in drug delivery.- Ionically gelled gellan gum in drug delivery.- Ionically gelled chitosan in drug delivery.- Ionically gelled carboxymethyl polysaccharides in drug delivery.- Polyelectrolyte complex-based ionically gelled biopolymeric systems for sustained drug release.- Ionically gelled polysaccharide-based interpenetrating polymer network systems in drug delivery.- Ionically gelled polysaccharide-based multiple-units in drug delivery.- Ionically gelled polysaccharide-based floating drug delivery systems.
£116.99
Springer Verlag, Singapore Composites from the Aquatic Environment
Book SynopsisThis book provides a methodical compilation of deriving composites from the hidden treasure of the aquatic world.Continuous and rapid progress in the composite industries have increased the demand for resilient, economically viable, and sustainable composite materials having enhanced mechanical , thermal and electrical properties which better suits there respective applications.If the materials/organisms used for the production or conversion of composites are renewable, degradable and easily and abundantly available then it gives great opportunity to the researchers to work on different options or processes to make them a viable technology. This work describes the organisms and materials present in the aquatic environment for the production of composite materials. Elaborating the versatile green expedients and their potential applications in the field of composites. Since, growing ecological and environmental consciousness has driven efforts for development of new innovative materials for various end-use applications.Therefore the LCA an circular bio-economy will be discussed to be efficient and sustainable. This book is ideal for the students, academicians, researchers and industry players. It also cover the present scenario, applications and future perspectives of composites derived from aquatic organisms. This compiled book features chapters that discuss the conversion of different materials and organisms present in aquatic environment to composite materials like micro-algae, seaweeds, chitosan, collagen, agar cyanobacteria etc.in a viable manner.Table of ContentsOverview of composites from the aquatic environment.- LCA of microalgae biopolymer composites.- Microalgae based biopolymer composites: Role in circular bioeconomy.- Recent development in water hyacinth fiber composite and its application.- Characterization of water hyacinth biopolymer composites.- Chitosan (sea shell) based composites:Recent trends and future scope.- Preparation and characterization of chitosan biocomposites.- Development and characterization of agar biopolymer based composites.- Performance of Fish scale composites.- Development and characterization of collagen composites.- Recent advances in composites from seaweeds.- Nipah (nypa fruticans) palm fibre extraction process for nipah fibre reinforced polymer composites.- Starch/carrageenan blend based biocomposite as packaging materials.
£107.99
Springer Verlag, Singapore Immunity Boosting Medicinal Plants of the Western
Book SynopsisThis book presents a comprehensive guide to traditional immunity-boosting medicinal plants of the Himalayas, their traditional uses, phytochemistry, pharmacology, diversity, conversation, biotechnology, toxicology, as well as future prospective. All the chapters cover the latest advances in ethnobotany, phytochemistry, biochemistry, and biotechnology. The book offers a valuable asset for researchers and graduate students of chemistry, botany, biotechnology, microbiology, and the pharmaceutical sciences. The main purpose of the present book is to draw on the rich culture, folklore, and biodiversity of immunity-boosting medicinal plants of the Western Himalayas, with particular emphasis on the Indian Trans-Himalayan and Western Himalayan region. All the plants included in the present book are extensively used by the local tribes and people for their health-promoting properties from ancient times. This book will be a substantial contribution to the knowledge of the region and the country. Also, the book will be very useful to scientists, graduates, and undergraduates, along with researchers in the fields of natural products, herbal medicines, ethnobotany, pharmacology, chemistry, and biology. Further, it is an equally significant resource for a person working in different traditional medicinal systems; doctors (especially those engaged in Ayurveda, Chinese traditional medicinal system, Amchi, and allopathy); the pharmaceutical industry (for drug design and synthesis); biochemistry and biotechnology sciences; and the agricultural sciences. Table of Contents1. Introduction to Western Himalayas.- 2. Achillea millefolium L., Common Yarrow.- 3. Arisaema jacquemontii Blume, Jacquemont's Cobra Lily.- 4. Species of Arnebia genus found in the western Himalayas.- 5. Species of the Berberis genus found in the western Himalayas.- 6. Dactylorhiza hatagirea (D.Don) Soo – Himalayan Marsh Orchid.- 7. Fritillaria roylei Hook.f.: Himalayan Fritillary.- 8. Gentiana kurroo Royle: Himalayan Gentian.- 9. Habenaria intermedia D.Don and Habenaria edgeworthii Hook., f. ex Collett.: The Western Himalayan medicinal Plants.- 10. Humulus lupulus L.: Beer plant.- 11. Inula racemosa Hook. f. – Puskarmool: Its ethnobotanical uses, phytochemicals and pharmacological activities.- 12. Juniperus recurva Buch.-Ham. ex D.Don and Juniperus squamata D. Don: Himalayan Juniper.- 13. Lancea tibetica Hook.f. & Thomson: Ethnobotany, phytochemistry and pharmacology.- 14. Malaxis muscifera (Lindley) O. Kuntze. and Malaxis acuminata D. Don.: Jeevak.- 15. Picrorhiza kurroa Royle ex Benth.: Kutki.- 16. Species of the genus Polygonatum found in the Western Himalayas.- 17. Species of the genus Rhodiola found in the Western Himalayas.- 18. Saussurea lappa C.B. Clarke: Kushta/Kut.- 19. Saussurea lappa C.B. Clarke: Kushta/Kut.- 20. Species of the genus Selinum found in the western Himalayas.- 21. Swertia chirayita (Roxb. ex Flem.): Chirayata/Chiretta.- 22. Taxus wallichiana Zucc.: The Himalayan yew.- 23. Tribulus terrestris L.: Gokshur /Gokharu.- 24. Species the Genus Viola found in Western Himalayas.
£143.99
World Scientific Publishing Co Pte Ltd Crystal Engineering: A Textbook
Book SynopsisThis book is important because it is the first textbook in an area that has become very popular in recent times. There are around 250 research groups in crystal engineering worldwide today. The subject has been researched for around 40 years but there is still no textbook at the level of senior undergraduates and beginning PhD students. This book is expected to fill this gap.The writing style is simple, with an adequate number of exercises and problems, and the diagrams are easy to understand. This book consists major areas of the subject, including organic crystals and co-ordination polymers, and can easily form the basis of a 30 to 40 lecture course for senior undergraduates.Table of ContentsIntroduction; Intermolecular Interactions; Design Strategies; Crystallisation; Polymorphism; Solvates and Co-Crystals; Co-Ordination Polymers.
£73.80
Springer PalladiumCatalyzed Mechanochemical CrossCoupling
Book Synopsis1. General Introduction.- 2. Olefin Accelerated Solid State C N Cross Coupling Using Mechanochemistry.- 3. Solid State Suzuki-Miyaura Cross Coupling Reactions Using Mechanochemistry.- 4. Tackling Solubility Issues in Organic Synthesis: Solid State Cross Coupling of Insoluble Aryl Halides.- 5. Solid State Cross Coupling Reactions of Insoluble Aryl Halides Under Polymer Assisted Grinding Conditions.- 6. Mechanochemistry Directed Ligand Design: Development of a High Performance Phosphine Ligand for Palladium Catalyzed Suzuki Miyaura Cross Coupling Reactions.- 7. Mechanochemical Monoarylation of Dihaloarenes Enabled by In Situ Crystallization.- 8. Metallamechanoredox: Force induced Nickel Catalyzed Arylamination Using Ball Milling and Piezoelectric Materials.
£179.99
Nova Science Publishers Inc The Essential Guide to Alkaloids
Book Synopsis
£138.39
