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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 |
| ISBN |
0-19-062734-4
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-9910798672103321 |
Morrow Gary W. <1951->
|
||
| New York, New York : , : Oxford University Press, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
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 |
| ISBN |
0-19-062734-4
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-9910815132903321 |
|
Morrow Gary W. <1951->
|
||
| New York, New York : , : Oxford University Press, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Bioscience, biotechnology, and biochemistry
| Bioscience, biotechnology, and biochemistry |
| Pubbl/distr/stampa | Tokyo, Japan, : Japan Society for Bioscience, Biotechnology, and Agrochemistry |
| Descrizione fisica | : illustrations (black and white) |
| Disciplina | 574.19/2/05 |
| Soggetto topico |
Biochemistry
Chemistry, Organic Biotechnology Life sciences Biological Science Disciplines Biochimie Biotechnologie Chimie organique Sciences de la vie biochemistry biological sciences bioengineering Biochemie |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1347-6947 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-996212455303316 |
| Tokyo, Japan, : Japan Society for Bioscience, Biotechnology, and Agrochemistry | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Bioscience, biotechnology, and biochemistry
| Bioscience, biotechnology, and biochemistry |
| Pubbl/distr/stampa | Tokyo, Japan, : Japan Society for Bioscience, Biotechnology, and Agrochemistry |
| Descrizione fisica | : illustrations (black and white) |
| Disciplina | 574.19/2/05 |
| Soggetto topico |
Biochemistry
Chemistry, Organic Biotechnology Life sciences Biological Science Disciplines Biochimie Biotechnologie Chimie organique Sciences de la vie biochemistry biological sciences bioengineering Biochemie |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1347-6947 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910146478703321 |
| Tokyo, Japan, : Japan Society for Bioscience, Biotechnology, and Agrochemistry | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
BODIPY Dyes : A Privilege Molecular Scaffold with Tunable Properties / / edited by Jorge Bañuelos-Prieto and Rebeca Sola Llano
| BODIPY Dyes : A Privilege Molecular Scaffold with Tunable Properties / / edited by Jorge Bañuelos-Prieto and Rebeca Sola Llano |
| Pubbl/distr/stampa | London, United Kingdom : , : IntechOpen, , 2019 |
| Descrizione fisica | 1 online resource (100 pages) : illustrations some color |
| Disciplina | 667.25 |
| Soggetto topico |
Chemistry, Organic
Dyes and dyeing - Chemistry |
| ISBN |
1-83881-816-2
1-78985-082-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | BODIPY dyes |
| Record Nr. | UNINA-9910317765103321 |
| London, United Kingdom : , : IntechOpen, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Building blocks, catalysis and coupling chemistry [[electronic resource] /] / edited by Andrew B. Hughes
| Building blocks, catalysis and coupling chemistry [[electronic resource] /] / edited by Andrew B. Hughes |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Weinheim, Germany, : Wiley-VCH, 2011 |
| Descrizione fisica | 1 online resource (600 p.) |
| Disciplina | 547.7 |
| Altri autori (Persone) | HughesAndrew B |
| Collana | Amino acids, peptides and proteins in organic chemistry |
| Soggetto topico |
Amino acids
Catalysis Chemistry, Organic |
| ISBN |
3-527-63180-1
3-527-63181-X 9786613302366 1-283-30236-5 3-527-63305-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | pt. 1. Amino acids as building blocks -- pt. 2. Amino acids coupling chemistry. |
| Record Nr. | UNINA-9910265225603321 |
| Weinheim, Germany, : Wiley-VCH, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Bulletin of the Agricultural Chemical Society of Japan
| Bulletin of the Agricultural Chemical Society of Japan |
| Pubbl/distr/stampa | [Tokyo], : Agricultural Chemical Society of Japan, 1926-1960 |
| Descrizione fisica | 1 online resource |
| Disciplina | 572 |
| Soggetto topico |
Biochemistry
Agricultural chemistry Chemistry, Organic Biochimie Chimie agricole Chimie organique |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1881-1272 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910304555103321 |
| [Tokyo], : Agricultural Chemical Society of Japan, 1926-1960 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Carbohydrate research
| Carbohydrate research |
| Pubbl/distr/stampa | [Oxford], : Elsevier Science Ltd |
| Soggetto topico |
Carbohydrates
Chemistry, Organic Biochemistry Chimie organique Glucides Biochimie carbohydrate |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1873-426X |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910333132603321 |
| [Oxford], : Elsevier Science Ltd | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Carbohydrate research
| Carbohydrate research |
| Pubbl/distr/stampa | [Oxford], : Elsevier Science Ltd |
| Soggetto topico |
Carbohydrates
Chemistry, Organic Biochemistry Chimie organique Glucides Biochimie carbohydrate |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1873-426X |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-996208158703316 |
| [Oxford], : Elsevier Science Ltd | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Carbon Nanotubes : Polymer Nanocomposites / / edited by Siva Yellampalli
| Carbon Nanotubes : Polymer Nanocomposites / / edited by Siva Yellampalli |
| Pubbl/distr/stampa | Rijeka : , : IntechOpen, , 2011 |
| Descrizione fisica | 1 online resource (ix, 412 pages) : illustrations |
| Disciplina | 620.115 |
| Soggetto topico |
Chemistry, Organic
Carbon nanotubes |
| ISBN | 953-51-4458-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Carbon nanotubes |
| Record Nr. | UNINA-9910138254703321 |
| Rijeka : , : IntechOpen, , 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Soggetto topico
-
Chemistry, Organic
(671)
- Chemistry (98)
- Organic compounds - Synthesis (73)
- Organic reaction mechanisms (69)
- Chemical reactions (35)