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Basic Concepts Viewed from Frontier in Inorganic Coordination Chemistry / / edited by Takashiro Akitsu
Basic Concepts Viewed from Frontier in Inorganic Coordination Chemistry / / edited by Takashiro Akitsu
Pubbl/distr/stampa London, United Kingdom : , : IntechOpen, , 2018
Descrizione fisica 1 online resource (152 pages) : illustrations and some color
Disciplina 546
Soggetto topico Chemistry, Inorganic
Chemistry, Organic
ISBN 1-83881-835-9
1-78984-865-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910317771603321
London, United Kingdom : , : IntechOpen, , 2018
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Basic organic chemistry for the life sciences / / Hrvoj Vancik
Basic organic chemistry for the life sciences / / Hrvoj Vancik
Autore Vančik Hrvoj
Edizione [Second edition.]
Pubbl/distr/stampa Cham, Switzerland : , : Springer, , [2022]
Descrizione fisica 1 online resource (213 pages)
Disciplina 547
Soggetto topico Chemistry, Organic
Química orgànica
Soggetto genere / forma Llibres electrònics
ISBN 9783030924386
9783030924379
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910523799303321
Vančik Hrvoj  
Cham, Switzerland : , : Springer, , [2022]
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Beilstein journal of organic chemistry
Beilstein journal of organic chemistry
Pubbl/distr/stampa [Frankfurt, Germany], : Beilstein-Institut
Descrizione fisica 1 online resource
Soggetto topico Chemistry, Organic
Química orgànica
Soggetto genere / forma Periodical
Fulltext
Internet Resources.
Periodicals.
Revistes electròniques.
Soggetto non controllato Organic Chemistry
ISSN 1860-5397
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti BJOC
Record Nr. UNISA-996215494103316
[Frankfurt, Germany], : Beilstein-Institut
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Beilstein journal of organic chemistry
Beilstein journal of organic chemistry
Pubbl/distr/stampa [Frankfurt, Germany], : Beilstein-Institut
Descrizione fisica 1 online resource
Soggetto topico Chemistry, Organic
Química orgànica
Soggetto genere / forma Periodical
Fulltext
Internet Resources.
Periodicals.
Revistes electròniques.
Soggetto non controllato Organic Chemistry
ISSN 1860-5397
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti BJOC
Record Nr. UNINA-9910146207603321
[Frankfurt, Germany], : Beilstein-Institut
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Beyer / Walter organic chemistry : a comprehensive degree text and source book / [Hans Beyer], Wolfgang Walter ; translated and edited by Douglas Lloyd
Beyer / Walter organic chemistry : a comprehensive degree text and source book / [Hans Beyer], Wolfgang Walter ; translated and edited by Douglas Lloyd
Autore Beyer, Hans
Pubbl/distr/stampa Chichester : Albion Pub., c1997
Descrizione fisica xx, 1037 p. : ill. ; 24 cm
Disciplina 547
Altri autori (Persone) Walter, Wolfgangauthor
Collana Albion chemical science series
Soggetto topico Chemistry, Organic
ISBN 1898563373
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991003985549707536
Beyer, Hans  
Chichester : Albion Pub., c1997
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Bioorganic & medicinal chemistry
Bioorganic & medicinal chemistry
Pubbl/distr/stampa [Oxford] ; ; [New York], : Pergamon Press
Soggetto topico Bioorganic chemistry
Pharmaceutical chemistry
Bioorganic chemistry - Periodicals
Biochemistry
Clinical chemistry
Chemistry, Organic
Chemistry, Clinical
Chimie bio-organique - Périodiques
Chimie pharmaceutique
Chimie bio-organique
Biochimie
Chimie clinique
Chimie organique
biochemistry
organic chemistry
Physiologische Chemie
Zeitschrift
Online-Ressource
Soggetto genere / forma Periodicals.
Soggetto non controllato Biochemistry
ISSN 1464-3391
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Bioorganic and medicinal chemistry
Record Nr. UNINA-9910333248903321
[Oxford] ; ; [New York], : Pergamon Press
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Bioorganic & medicinal chemistry
Bioorganic & medicinal chemistry
Pubbl/distr/stampa [Oxford] ; ; [New York], : Pergamon Press
Soggetto topico Bioorganic chemistry
Pharmaceutical chemistry
Bioorganic chemistry - Periodicals
Biochemistry
Clinical chemistry
Chemistry, Organic
Chemistry, Clinical
Chimie bio-organique - Périodiques
Chimie pharmaceutique
Chimie bio-organique
Biochimie
Chimie clinique
Chimie organique
biochemistry
organic chemistry
Physiologische Chemie
Zeitschrift
Online-Ressource
Soggetto genere / forma Periodicals.
Soggetto non controllato Biochemistry
ISSN 1464-3391
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Bioorganic and medicinal chemistry
Record Nr. UNISA-996199886303316
[Oxford] ; ; [New York], : Pergamon Press
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Bioorganic & medicinal chemistry letters
Bioorganic & medicinal chemistry letters
Pubbl/distr/stampa [Oxford] ; ; [New York], : Pergamon Press
Soggetto topico Bioorganic chemistry
Pharmaceutical chemistry
Bioorganic chemistry - Periodicals
Biochemistry
Chemistry, Organic
Chemistry, Pharmaceutical
Chimie bio-organique - Périodiques
Chimie pharmaceutique
Chimie bio-organique
Biochimie
Chimie organique
biochemistry
organic chemistry
Klinische Chemie
Zeitschrift
Online-Ressource
Physiologische Chemie
Pharmazeutische Chemie
Soggetto genere / forma Periodicals.
ISSN 1464-3405
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Bioorganic and medicinal chemistry letters
Record Nr. UNINA-9910142680403321
[Oxford] ; ; [New York], : Pergamon Press
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Bioorganic & medicinal chemistry letters
Bioorganic & medicinal chemistry letters
Pubbl/distr/stampa [Oxford] ; ; [New York], : Pergamon Press
Soggetto topico Bioorganic chemistry
Pharmaceutical chemistry
Bioorganic chemistry - Periodicals
Biochemistry
Chemistry, Organic
Chemistry, Pharmaceutical
Chimie bio-organique - Périodiques
Chimie pharmaceutique
Chimie bio-organique
Biochimie
Chimie organique
biochemistry
organic chemistry
Klinische Chemie
Zeitschrift
Online-Ressource
Physiologische Chemie
Pharmazeutische Chemie
Soggetto genere / forma Periodicals.
ISSN 1464-3405
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Bioorganic and medicinal chemistry letters
Record Nr. UNISA-996204794903316
[Oxford] ; ; [New York], : Pergamon Press
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Biorganic synthesis : an introduction / / Gary W. Morrow
Biorganic synthesis : an introduction / / Gary W. Morrow
Autore Morrow Gary W. <1951->
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (xxi, 429 pages) : illustrations
Disciplina 572/.45
Collana Oxford scholarship online
Soggetto topico Organic compounds - Synthesis
Biosynthesis
Chemistry, Organic
Soggetto genere / forma Electronic books.
ISBN 0-19-756322-8
0-19-986052-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction -- The Unique Role of Carbon -- Distinguishing Primary Versus Secondary Metabolism -- Secondary Metabolites and Natural Products -- Natural Products in Organic Chemistry and Medicine -- The Organic Chemistry of Biosynthesis -- Goals and Structure of This Book -- Review of Functional Groups, Stereochemistry, and Conformational Analysis -- Prochiral Relationships: One Step from Chirality -- Prochiral it-Systems: "Two-Faced" Reaction Centers -- Diastereotopic Atoms and Groups: One Step from a Diasteroeomer -- Monosubstituted Cyclohexanes: Favoring Equatorial Positions -- Disubstituted Cyclohexanes: Equivalent and Nonequivalent Combinations -- Bicyclic Systems: Joining of Rings -- Heterocyclic Ring Systems: One Atom Makes All the Difference -- Bond Making and Breaking: Have Pair, Will Share; Need Two from You -- Bronsted Acid-Base Reactions: Proton Donors Gladly Accepted -- Acidity Trends: Why that Proton Is or Isn't Acidic --
Carbocations: Three Bonds to Carbon Can Be a Plus -- Radicals: Odd and Reactive -- Elimination Reactions: Introducing the Carbon-Carbon n-Bond -- Carbocations: Rearrangements and Fates -- Electrophilic Additions: n-Bonds as Nucleophilic Agents -- Nucleophilic Substitutions and Alkylations: Make or Break for C-X Bonds -- Nucleophilic Carbonyl Addition Reactions: C=O n-Bond under Attack -- Imine Formation: Making the Essential C=N Linkage -- Nucleophilic 1,4-(Conjugate) Addition Reactions: Remote Attack on Conjugated Carbonyls -- Nucleophilic Acyl Substitution Reactions: Turning One Acyl Compound into Another -- Looking Ahead -- Study Problems -- Enzymes: The Catalysts of Biological Organic Chemistry -- Cofactors: Enzyme Assistants in Bioorganic Reactions -- NADH/NADPH: Nature's Version of Sodium Borohydride for Carbonyl Reduction -- NAD+/NADP+: Nature's Version of PCC for Alcohol Oxidation -- FAD: Another Hydride Acceptor for Dehydrogenations --
The Significance of the Anomeric Carbon: Glycoside Formation -- UDP-Sugars and Glycoside Formation: SN2 Chemistry at Work -- Organic Reactions in Carbohydrate Chemistry: Overview of Glucose Metabolism -- Glycolysis: A 10-Step Program -- What Happens to the Pyruvic Acid from Glycolysis -- The Citric Acid Cycle: Another 10-Step Program -- The Pentose Phosphate Pathway: Seven Alternative Steps to Some Familiar Intermediates -- The Big Picture -- Amino Acids: More Important Primary Metabolite Building Blocks for Biosynthesis -- Biosynthesis of Serine: A Good Place to Start -- Peptides and Proteins: A Very Brief Review -- Putting Proteins and Carbohydrates Together: Glycoproteins Versus Protein Glycosylation -- Looking Ahead -- Study Problems -- Classification of Terpenes: How Many Isoprene Units? -- The Mevalonic Acid Route to DMAPP and IPP -- The Deoxyxylulose Phosphate Route to IPP and DMAPP -- Hemiterpenes: Just One Isoprene Unit --
Monoterpenes (C10) and Isoprene Linkage: Heads, IPP Wins; Tails, DMAPP Loses -- Geranyl PP to Neryl PP via Linalyl PP: The Importance of Alkene Stereochemistry -- Some Acyclic Monoterpenes and Their Uses -- Mono- and Bicyclic Monoterpenes via Cationic Cyclizations and Wagner-Meerwein Shifts -- What's that Smell? Limonene Derivatives as Flavor and Fragrance Compounds -- Irregular Monoterpenes: If Not Head-to-Tail, then How? -- Iridoids: From Catnip to Alkaloids -- Sesquiterpenes (C15): Linking of Different Starter Units -- Some FPP Cyclizations in Sesquiterpene Biosynthesis -- Trichodiene and the Trichothecenes: How to Trace a Rearrangement Pathway -- Diterpenes (C20): Taking it to the Next Level of Molecular Complexity and Diversity -- Cyclic Diterpenes: From Baseball and Plant Hormones to Anticancer Drugs -- Sesterterpenes (C25): Less Common, More Complex -- Triterpenes and Steroids: Another Case of Irregular Linkage of Terpene Units --
Oxidosqualene and Steroid Biosynthesis: Cyclization to Lanosterol and Beyond -- Conversion of Lanosterol (C30) to Cholesterol (C27): Where Did the Carbons Go? -- Conversions of Cholesterol: Production of the Sex Hormones -- Dehydrocholesterol, Sunshine, and Vitamin D3 Biosynthesis -- Tetraterpenes and Carotenoids: Tail-to-Tail Linkage of C20 Units -- Looking Ahead -- Study Problems -- Fatty Acids: Multiples of Two Carbons, Saturated or Unsaturated -- Saturated Fatty Acid Biosynthesis: It All Starts with Acetyl-CoA -- Branched Fatty Acids: Different Routes and Different Results -- Mono- and Polyunsaturated Fatty Acids: Putting in the "Essential" Double Bonds -- Aerobic Versus Anaerobic Routes to Desaturation -- Further Desaturation of Fatty Acids: Triple Bonds and Rings -- Prostaglandins, Thromboxanes, and Leukotrienes: The Power of Oxygenated FAs -- Polyketide Biosynthesis: More Starter Units and Extender Units, but with a Twist --
Aromatic Polyketide Natural Products: Phenols and Related Structures -- Isotopic Labeling Studies: Biosynthetic Insights via 13C NMR -- Further Modification of Polyketides: Alkylations, Oxidations, Reductions, and Decarboxylations -- Other Oxidative Modifications of Aromatic Rings: Expansion or Cleavage Processes -- Oxidative Coupling of Phenols: Formation of Aryl-Aryl Bonds -- The Use of Other Starter Groups: From Cancer Drugs and Antibiotics to Poison Ivy -- More on Polyketide Synthase (PKS) Systems: Increasing Product Diversity -- Modular Type I PKS Complexes and Macrolide Antibiotics: Erythromycin Biosynthesis -- Genetic Manipulation of Modular PKS Systems: Rational Drug Modification -- Some Final PKS Products of Medicinal Importance -- Looking Ahead -- Study Problems -- What Is Shikimic Acid? -- Shikimic, Chorismic, and Prephenic Acids at the Heart of the Pathway -- The Claisen Rearrangement: Allyl Vinyl Ethers in a Chair --
Conversion of Chorismic Acid to Prephenic Acid -- Conversion of Prephenic Acid to Phenylalanine or Tyrosine -- More Uses for Chorismic Acid -- Shikimic Acid Pathway Products from Phenylalanine and Tyrosine: An Overview -- Phenylpropanoids: A Large Family of Phenyl C3 Compounds -- Phenylpropanoids: Reduction of Acids to Phenyl C3 Aldehydes and Alcohols -- Reduction of Phenyl C3 Alcohols to Phenylpropenes -- Lignans and Lignin: Oxidative Phenolic Coupling with a Twist -- Coniferyl Alcohol Oxidative Coupling: Allyl C-Radical + Allyl C-Radical -- Coniferyl Alcohol Oxidative Coupling: Ortho C-Radical + Allyl C-Radical -- Coniferyl Alcohol Oxidative Coupling: O-Radical + Allyl C-Radical -- Lignin: A Plant Polymer and Major Source of Carbon -- Podophyllotoxin Biosynthesis: Aryltetralin Lignans from the American Mayapple -- Cleavage of Cinnamic Acids to Phenyl Cl Compounds: Different Routes, Similar Outcomes -- Coumarins: Sweet-Smelling Benzopyrones --
Combining the Shikimate, Polyketide, and Terpenoid Pathways -- Kavalactones: Natural Sedatives from the South Pacific -- Flavonoids: Structurally Diverse Plant Polyphenolics -- The Chalcone-to-Flavanone-to-Flavone Sequence: Formation of Apigenin -- The Flavanone-to-Dihydroflavonol-to-Anthocyanin Sequence: Formation of Pelargonidin -- The Flavanone-to-Isoflavanone-to-Isoflavone Sequence: Formation of Genistein -- Isoflavanoid Structural Modifications: Production of Antimicrobial Phytoalexins -- Rotenoids: Fish Poisons from Isoflavones -- Looking Ahead -- Study Problems -- Alkaloid Structure: The Importance of N-Heterocycles -- Alkaloids Not Derived from Amino Acids: Amination Reactions, Poisons, and Venoms -- Amino Acids and Mannich Reactions: Important Keys to Alkaloid Biosynthesis -- Alkaloids from Ornithine: Tropanes via the Mannich Reaction in Action -- Pyrrolizidine Alkaloids: Poison Plants and Insect Defense --
Piperidine-Type Alkaloids Derived from Lysine -- Quinolizidine Alkaloids: Livestock Poisons from Cadaverine -- Alkaloids from Phenylalanine: From Neurotransmitters to Decongestants and Narcotics -- Alkaloids from Tyrosine: The Pictet-Spengler Reaction in Alkaloid Biosynthesis -- (S)-Reticuline: A Versatile Pictet-Spengler-Derived Benzyltetrahydroisoquinoline -- Oxidative Coupling in Alkaloid Biosynthesis: Biosynthesis of Corytuberine and Morphine -- The Morphine Rule -- Alkaloids from Tryptophan: Adventures in Indole Alkaloid Structural Complexity -- Pictet-Spengler-Type Reactions of Tryptamine: p-Carbolines and Indole Terpene Alkaloids -- Alkaloids from Nicotinic Acid: Toxic Addictive Derivatives of a Common Nutrient -- Alkaloids from Anthranilic Acid: From Tryptophan to Quinolines and Acridines -- Alkaloids from Histidine: From Simple Amides to Glaucoma Drugs -- Purine Alkaloids: Addictive Stimulants in our Coffee, Tea, and Chocolate --
Cyclic and Macrocyclic Peptides: From Sweeteners to Antibiotics and Beyond -- Penicillins, Cephalosporins, and Carbapenums: The Essential p-Lactam Antibiotics -- A Final Look Ahead -- Study Problems -- Why We Synthesize Organic Compounds -- Synthetic Challenges: Total Synthesis -- Synthetic Challenges: Semisynthesis -- Synthetic Challenges: Biomimetic Synthesis -- Synthetic Challenges: Structural Revision or Confirmation -- Synthetic Challenges: Formal Synthesis -- Synthetic Challenges: Stereoselective Synthesis of Optically Pure Compounds -- Resolution of Enantiomers to Obtain Optically Pure Compounds -- Use of Chiral Pool Compounds for Synthesis of Optically Pure Natural Products -- Use of Chiral Reagents for Synthesis of Optically Pure Compounds -- Use of Chiral Substrate Control for Stereoselective Synthesis -- Use of Chiral Auxiliaries for Synthesis of Optically Pure Compounds -- Use of Chiral Catalysis for Synthesis of Optically Pure Compounds -- Use of Enzymes for Synthesis of Optically Pure Compounds: Biocatalysis -- Some Final Thoughts -- Study Problems.
Record Nr. UNINA-9910465672303321
Morrow Gary W. <1951->  
New York, New York : , : Oxford University Press, , 2016
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