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Environmentally sustainable catalytic asymmetric oxidations / / Konstantin Bryliakov
Environmentally sustainable catalytic asymmetric oxidations / / Konstantin Bryliakov
Autore Bryliakov Konstantin
Edizione [1st ed.]
Pubbl/distr/stampa Boca Raton : , : Taylor & Francis, , [2015]
Descrizione fisica 1 online resource (160 p.)
Disciplina 547.23
547/.23
Soggetto topico Oxidation
Green chemistry
Chemistry, Organic
ISBN 0-429-16826-8
1-4665-8857-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Contents; Preface; Author; List of Abbreviations; Chapter 1: Introduction; Chapter 2: Transition Metal-Catalyzed Asymmetric Epoxidations; Chapter 3: Transition Metal-Catalyzed Asymmetric Sulfoxidations; Chapter 4: Miscellaneous Transition Metal-Catalyzed Asymmetric Oxidations; Chapter 5: Organocatalytic Asymmetric Oxidations; Chapter 6: Fe- and Mn-Based Synthetic Models of Non-Heme Oygenases : Stereospecific C-H Oxidations; Chapter 7: Active Species and Mechanisms of Non-Heme Fe- and Mn-Catalyzed Oxidations; Chapter 8: Industrial Perspective; Back Cover
Record Nr. UNINA-9910809672103321
Bryliakov Konstantin  
Boca Raton : , : Taylor & Francis, , [2015]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Enzyme catalysis in organic synthesis : a comprehensive handbook
Enzyme catalysis in organic synthesis : a comprehensive handbook
Pubbl/distr/stampa [Place of publication not identified], : Wiley VCH, 2002
Disciplina 660.6/34
Soggetto topico Enzymes - Biotechnology
Organic compounds - Synthesis
Enzymes - Industrial applications
Catalysis
Chemistry, Organic
Enzymes
Physicochemical Processes
Chemical Processes
Chemistry
Enzymes and Coenzymes
Natural Science Disciplines
Physicochemical Phenomena
Chemicals and Drugs
Chemical Phenomena
Phenomena and Processes
Disciplines and Occupations
Biomedical Engineering
Health & Biological Sciences
ISBN 3-527-61826-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-996197429503316
[Place of publication not identified], : Wiley VCH, 2002
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Essential organic chemistry / / Paula Yurkanis Bruice
Essential organic chemistry / / Paula Yurkanis Bruice
Autore Bruice Paula Yurkanis <1941->
Edizione [Third edition, global edition.]
Pubbl/distr/stampa Harlow, England : , : Pearson, , 2016
Descrizione fisica 1 online resource (761 pages) : illustration (some color), tables
Disciplina 547
Collana Always learning
Soggetto topico Chemistry, Organic
ISBN 1-292-08905-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright Page -- Brief Table of Contents -- Contents -- Preface -- About the Author -- Chapter 1 Remembering General Chemistry: Electronic Structure and Bonding -- Natural Organic Compounds Versus Synthetic Organic Compounds -- 1.1 The Structure of an Atom -- 1.2 How the Electrons in an Atom Are Distributed -- 1.3 Ionic and Covalent Bonds -- 1.4 How the Structure of a Compound Is Represented -- PROBLEM-SOLVING STRATEGY -- 1.5 Atomic Orbitals -- 1.6 How Atoms Form Covalent Bonds -- 1.7 How Single Bonds Are Formed in Organic Compounds -- 1.8 How a Double Bond Is Formed: The Bonds in Ethene -- Diamond, Graphite, Graphene, and Fullerenes: Substances that Contain Only Carbon Atoms -- 1.9 How a Triple Bond Is Formed: The Bonds in Ethyne -- 1.10 The Bonds in the Methyl Cation, the Methyl Radical, and the Methyl Anion -- 1.11 The Bonds in Ammonia and in the Ammonium Ion -- 1.12 The Bonds in Water -- Water-A Compound Central to Life -- 1.13 The Bond in a Hydrogen Halide -- 1.14 Summary: Hybridization, Bond Lengths, Bond Strengths, and Bond Angles -- PROBLEM-SOLVING STRATEGY -- 1.15 The Dipole Moments of Molecules -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- Chapter 2 Acids and Bases: Central to Understanding Organic Chemistry -- 2.1 An Introduction to Acids and Bases -- 2.2 pKa and pH -- Acid Rain -- 2.3 Organic Acids and Bases -- Poisonous Amines -- PROBLEM-SOLVING STRATEGY -- 2.4 How to Predict the Outcome of an Acid-Base Reaction -- 2.5 How to Determine the Position of Equilibrium -- 2.6 How the Structure of an Acid Affects Its pKa Value -- 2.7 How Substituents Affect the Strength of an Acid -- PROBLEM-SOLVING STRATEGY -- 2.8 An Introduction to Delocalized Electrons -- Fosamax Prevents Bones from Being Nibbled Away -- 2.9 A Summary of the Factors that Determine Acid Strength.
2.10 How pH Affects the Structure of an Organic Compound -- PROBLEM-SOLVING STRATEGY -- Aspirin Must Be in Its Basic Form to Be Physiologically Active -- 2.11 Buffer Solutions -- Blood: A Buffered Solution -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- TUTORIAL Acids and Bases -- Chapter 3 An Introduction to Organic Compounds -- 3.1 How Alkyl Substituents Are Named -- Bad-Smelling Compounds -- 3.2 The Nomenclature of Alkanes -- How is the Octane Number of Gasoline Determined? -- 3.3 The Nomenclature of Cycloalkanes Skeletal Structures -- PROBLEM-SOLVING STRATEGY -- 3.4 The Nomenclature of Alkyl Halides -- PROBLEM-SOLVING STRATEGY -- 3.5 The Classification of Alkyl Halides, Alcohols, and Amines -- Nitrosamines and Cancer -- 3.6 The Structures of Alkyl Halides, Alcohols, Ethers, and Amines -- 3.7 Noncovalent Interactions -- PROBLEM-SOLVING STRATEGY -- Drugs Bind to Their Receptors -- 3.8 Factors that Affect the Solubility of Organic Compounds -- Cell Membranes -- 3.9 Rotation Occurs About Carbon-Carbon Single Bonds -- 3.10 Some Cycloalkanes have Angle Strain -- Von Baeyer, Barbituric Acid, and Blue Jeans -- 3.11 Conformers of Cyclohexane -- 3.12 Conformers of Monosubstituted Cyclohexanes -- Starch and Cellulose-Axial and Equatorial -- 3.13 Conformers of Disubstituted Cyclohexanes -- PROBLEM-SOLVING STRATEGY -- 3.14 Fused Cyclohexane Rings -- Cholesterol and Heart Disease -- How High Cholesterol Is Treated Clinically -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- Chapter 4 Isomers: The Arrangement of Atoms in Space -- 4.1 CIS-Trans Isomers Result from Restricted Rotation -- Cis-Trans Interconversion in Vision -- 4.2 Designating Geometric Isomers Using the E,Z System -- PROBLEM-SOLVING STRATEGY -- 4.3 A Chiral Object Has a Nonsuperimposable Mirror Image -- 4.4 An Asymmetric Center Is a Cause of Chirality in a Molecule.
4.5 Isomers with One Asymmetric Center -- 4.6 How to Draw Enantiomers -- 4.7 Naming Enantiomers by the R,S System -- PROBLEM-SOLVING STRATEGY -- PROBLEM-SOLVING STRATEGY -- 4.8 Chiral Compounds Are Optically Active -- 4.9 How Specific Rotation Is Measured -- 4.10 Isomers with More than One Asymmetric Center -- 4.11 Stereoisomers of Cyclic Compounds -- PROBLEM-SOLVING STRATEGY -- 4.12 Meso Compounds Have Asymmetric Centers but Are Optically Inactive -- PROBLEM-SOLVING STRATEGY -- 4.13 Receptors -- The Enantiomers of Thalidomide -- 4.14 How Enantiomers Can Be Separated -- Chiral Drugs -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- Chapter 5 Alkenes -- Pheromones -- 5.1 The Nomenclature of Alkenes -- 5.2 How an Organic Compound Reacts Depends on its Functional Group -- 5.3 How Alkenes React . Curved Arrows Show the Flow of Electrons -- A Few Words About Curved Arrows -- 5.4 Thermodynamics: How Much Product Is Formed? -- 5.5 Increasing the Amount of Product Formed in a Reaction -- 5.6 Using ΔH° Values to Determine the Relative Stabilities of Alkenes -- PROBLEM-SOLVING STRATEGY -- Trans Fats -- 5.7 Kinetics: How Fast Is the Product Formed? -- 5.8 The Rate of a Chemical Reaction -- 5.9 The Reaction Coordinate Diagram for the Reaction of 2-Butene with HBr -- 5.10 Catalysis -- 5.11 Catalysis by Enzymes -- SOME IMPORTANT THINGS TO REMEMBER -- PROBLEMS -- TUTORIAL An Exercise in Drawing Curved Arrows: Pushing Electrons -- Chapter 6 The Reactions of Alkenes and Alkynes -- Green Chemistry: Aiming for Sustainability -- 6.1 The Addition of a Hydrogen Halide to an Alkene -- 6.2 Carbocation Stability Depends on the Number of Alkyl Groups Attached to the Positively Charged Carbon -- 6.3 Electrophilic Addition Reactions Are Regioselective -- Which Are More Harmful, Natural Pesticides or Synthetic Pesticides? -- PROBLEM-SOLVING STRATEGY.
6.4 A Carbocation will Rearrange if It Can Form a More Stable Carbocation -- 6.5 The Addition of Water to an Alkene -- 6.6 The Stereochemistry of Alkene Reactions -- PROBLEM-SOLVING STRATEGY -- 6.7 The Stereochemistry of Enzyme-Catalyzed Reactions -- 6.8 Enantiomers Can Be Distinguished by Biological Molecules -- 6.9 An Introduction to Alkynes -- Synthetic Alkynes Are Used to Treat Parkinson's Disease -- Why Are Drugs So Expensive? -- 6.10 The Nomenclature of Alkynes -- Synthetic Alkynes Are Used for Birth Control -- 6.11 The Structure of Alkynes -- 6.12 The Physical Properties of Unsaturated Hydrocarbons -- 6.13 The Addition of a Hydrogen Halide to an Alkyne -- 6.14 The Addition of Water to an Alkyne -- 6.15 The Addition of Hydrogen to an Alkyne -- SOME IMPORTANT THINGS TO REMEMBER -- SUMMARY OF REACTIONS -- PROBLEMS -- Chapter 7 Delocalized Electrons and Their Effect on Stability, pKa, and the Products of a Reaction Aromaticity and the Reactions of Benzene -- 7.1 Delocalized Electrons Explain Benzene's Structure -- Kekule's Dream -- 7.2 The Bonding in Benzene -- 7.3 Resonance Contributors and the Resonance Hybrid -- 7.4 How to Draw Resonance Contributors -- Electron Delocalization Affects the Three-Dimensional Shape of Proteins -- 7.5 The Predicted Stabilities of Resonance Contributors -- 7.6 Delocalization Energy Is the Additional Stability Delocalized Electrons Give to a Compound -- 7.7 Delocalized Electrons Increase Stability -- PROBLEM-SOLVING STRATEGY -- PROBLEM-SOLVING STRATEGY -- 7.8 Delocalized Electrons Affect pKa Values -- PROBLEM-SOLVING STRATEGY -- 7.9 Electronic Effects -- 7.10 Delocalized Electrons Can Affect the Product of a Reaction -- 7.11 Reactions of Dienes -- 7.12 The Diels-Alder Reaction Is a 1, 4-Addition Reaction -- 7.13 Benzene Is an Aromatic Compound -- 7.14 The Two Criteria for Aromaticity.
7.15 Applying the Criteria for Aromaticity -- Buckyballs -- 7.16 How Benzene Reacts -- 7.17 The Mechanism for Electrophilic Aromatic Substitution Reactions -- Thyroxine -- 7.18 Organizing What We Know About the Reactions of Organic Compounds -- SOME IMPORTANT THINGS TO REMEMBER -- SUMMARY OF REACTIONS -- PROBLEMS -- TUTORIAL: DRAWING RESONANCE CONTRIBUTORS -- Chapter 8 Substitution and Elimination Reactions of Alkyl Halides -- DDT: A Synthetic Organohalide That Kills Disease-Spreading Insects -- 8.1 The Mechanism for an SN2 Reaction -- 8.2 Factors That Affect SN2 Reactions -- Why Are Living Organisms Composed of Carbon Instead of Silicon? -- 8.3 The Mechanism for an SN1 Reaction -- 8.4 Factors That Affect SN1 Reactions -- 8.5 Comparing SN2 and SN1 Reactions -- PROBLEM-SOLVING STRATEGY -- Naturally Occurring Organohalides That Defend against Predators -- 8.6 Intermolecular versus Intramolecular Reactions -- PROBLEM-SOLVING STRATEGY -- 8.7 Elimination Reactions of Alkyl Halides -- 8.8 The Products of an Elimination Reaction -- 8.9 Relative Reactivities of Alkyl Halides Reactions -- The Nobel Prize -- 8.10 Does a Tertiary Alkyl Halide Undergo SN2/E2 Reactions or SN1/E1 Reactions? -- 8.11 Competition between Substitution and Elimination -- 8.12 Solvent Effects -- Solvation Efects -- 8.13 Substitution Reactions in Synthesis -- SOME IMPORTANT THINGS TO REMEMBER -- SUMMARY OF REACTIONS -- PROBLEMS -- Chapter 9 Reactions of Alcohols, Ethers, Epoxides, Amines, and Thiols -- 9.1 The Nomenclature of Alcohols -- Grain Alcohol and Wood Alcohol -- 9.2 Activating an Alcohol for Nucleophilic Substitution by Protonation -- 9.3 Activating an OH Group for Nucleophilic Substitution in a Cell -- The Inability to Perform an SN2 Reaction Causes a Severe Clinical Disorder -- 9.4 Elimination Reactions of Alcohols: Dehydration -- 9.5 Oxidation of Alcohols.
Blood Alcohol Content.
Record Nr. UNINA-9910154958003321
Bruice Paula Yurkanis <1941->  
Harlow, England : , : Pearson, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Esterification [[electronic resource] ] : methods, reactions, and applications
Esterification [[electronic resource] ] : methods, reactions, and applications
Autore Otera Junzo
Edizione [2nd ed.]
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2010
Descrizione fisica 1 online resource (388 p.)
Disciplina 547.27
Altri autori (Persone) NishikidoJoji
Soggetto topico Esterification
Chemistry, Organic
Soggetto genere / forma Electronic books.
ISBN 1-282-38025-7
9786612380259
3-527-62762-6
3-527-62763-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Esterification; Contents; Preface; Preface to the Second Edition; Introduction; Part One: Methodology; 1: Reaction of Alcohols with Carboxylic Acids and their Derivatives; 1.1 Reaction with Carboxylic Acids; 1.1.1 Without Activator; 1.1.2 Acid Catalysts; 1.1.2.1 Brønsted Acids; 1.1.2.2 Lewis Acids; 1.1.2.3 Solid Acids; 1.1.3 Base Activators; 1.1.4 Carbodiimide Activators; 1.1.5 The Mitsunobu Reaction; 1.1.6 Activation of Carboxylic Acids; 1.1.7 Enzymes; 1.1.8 π-Acids; 1.2 Reaction with Esters: Transesterification; 1.2.1 Without Activator; 1.2.2 Acid Catalysts; 1.2.2.1 Brønsted Acids
1.2.2.2 Lewis Acids1.2.2.3 Solid Acids; 1.2.3 Base Activators; 1.2.3.1 Metal Salts; 1.2.3.2 Amines; 1.2.3.3 Others; 1.2.4 Other Activators; 1.2.5 Enzymes; 1.3 Reaction with Acid Anhydrides; 1.3.1 Without Activator; 1.3.2 Acid Catalysts; 1.3.2.1 Brønsted Acids; 1.3.2.2 Lewis Acids; 1.3.2.3 Solid Acids; 1.3.3 Base Activators; 1.3.3.1 Metal Salts; 1.3.3.2 Amines; 1.3.3.3 Phosphines; 1.3.4 Enzymes; 1.3.5 Mixed Anhydrides; 1.4 Reaction with Acid Halides and Other Acyl Derivatives; 1.4.1 Without Activator; 1.4.2 Acid Catalysts; 1.4.2.1 Bønsted Acids; 1.4.2.2 Lewis Acids; 1.4.2.3 Solid Acids
1.4.3 Base Activators1.4.3.1 Metal Salts; 1.4.3.2 Amines; 1.4.3.3 Phase Transfer Catalyst; 1.4.4 Other Activators; 1.4.5 Enzymes; 2: Use of Tin and Other Metal Alkoxides; 3: Conversion of Carboxylic Acids into Esters without Use of Alcohols; 3.1 Reaction with Diazomethane; 3.2 Reaction with Alkyl Halides; 3.3 Treatment with Other Electrophiles; 4: Ester Interchange Reaction; Part Two: Synthetic Applications; 5: Kinetic Resolution; 5.1 Enzymatic Resolution; 5.2 Nonenzymatic Resolution; 5.3 Dynamic Kinetic Resolution; 5.4 Parallel Kinetic Resolution; 6: Asymmetric Desymmetrization
7: Miscellaneous Topics7.1 Selective Esterification; 7.1.1 Differentiation between Primary, Secondary, and Tertiary Alcohols, and Phenols; 7.1.2 Differentiation between Identical or Similar Functions; 7.2 Use of Theoretical Amounts of Reactants; 7.3 New Reaction Media; 7.4 New Technologies; 7.5 Application to Natural Products Synthesis; 8: Industrial Uses; 8.1 Ethyl Acetate; 8.2 Acrylic Esters; 8.2.1 Methyl Methacrylate (MMA); 8.2.2 Alkyl Acrylates; 8.3 Polyesters; 8.4 Oils and Fats; 8.4.1 Food Emulsifiers; 8.4.2 Soaps; 8.5 Biodiesel Fuel; 8.6 Amino Acid Esters; 8.7 Macrolides
8.8 Flavoring Agents and Fragrances8.9 Pyrethroids; Epilogue; References; Index
Record Nr. UNINA-9910139542603321
Otera Junzo  
Weinheim, : Wiley-VCH, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Esterification : methods, reactions, and applications
Esterification : methods, reactions, and applications
Autore Otera Junzo
Edizione [2nd ed.]
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2010
Descrizione fisica 1 online resource (388 p.)
Disciplina 547.27
Altri autori (Persone) NishikidoJoji
Soggetto topico Esterification
Chemistry, Organic
ISBN 1-282-38025-7
9786612380259
3-527-62762-6
3-527-62763-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Esterification; Contents; Preface; Preface to the Second Edition; Introduction; Part One: Methodology; 1: Reaction of Alcohols with Carboxylic Acids and their Derivatives; 1.1 Reaction with Carboxylic Acids; 1.1.1 Without Activator; 1.1.2 Acid Catalysts; 1.1.2.1 Brønsted Acids; 1.1.2.2 Lewis Acids; 1.1.2.3 Solid Acids; 1.1.3 Base Activators; 1.1.4 Carbodiimide Activators; 1.1.5 The Mitsunobu Reaction; 1.1.6 Activation of Carboxylic Acids; 1.1.7 Enzymes; 1.1.8 π-Acids; 1.2 Reaction with Esters: Transesterification; 1.2.1 Without Activator; 1.2.2 Acid Catalysts; 1.2.2.1 Brønsted Acids
1.2.2.2 Lewis Acids1.2.2.3 Solid Acids; 1.2.3 Base Activators; 1.2.3.1 Metal Salts; 1.2.3.2 Amines; 1.2.3.3 Others; 1.2.4 Other Activators; 1.2.5 Enzymes; 1.3 Reaction with Acid Anhydrides; 1.3.1 Without Activator; 1.3.2 Acid Catalysts; 1.3.2.1 Brønsted Acids; 1.3.2.2 Lewis Acids; 1.3.2.3 Solid Acids; 1.3.3 Base Activators; 1.3.3.1 Metal Salts; 1.3.3.2 Amines; 1.3.3.3 Phosphines; 1.3.4 Enzymes; 1.3.5 Mixed Anhydrides; 1.4 Reaction with Acid Halides and Other Acyl Derivatives; 1.4.1 Without Activator; 1.4.2 Acid Catalysts; 1.4.2.1 Bønsted Acids; 1.4.2.2 Lewis Acids; 1.4.2.3 Solid Acids
1.4.3 Base Activators1.4.3.1 Metal Salts; 1.4.3.2 Amines; 1.4.3.3 Phase Transfer Catalyst; 1.4.4 Other Activators; 1.4.5 Enzymes; 2: Use of Tin and Other Metal Alkoxides; 3: Conversion of Carboxylic Acids into Esters without Use of Alcohols; 3.1 Reaction with Diazomethane; 3.2 Reaction with Alkyl Halides; 3.3 Treatment with Other Electrophiles; 4: Ester Interchange Reaction; Part Two: Synthetic Applications; 5: Kinetic Resolution; 5.1 Enzymatic Resolution; 5.2 Nonenzymatic Resolution; 5.3 Dynamic Kinetic Resolution; 5.4 Parallel Kinetic Resolution; 6: Asymmetric Desymmetrization
7: Miscellaneous Topics7.1 Selective Esterification; 7.1.1 Differentiation between Primary, Secondary, and Tertiary Alcohols, and Phenols; 7.1.2 Differentiation between Identical or Similar Functions; 7.2 Use of Theoretical Amounts of Reactants; 7.3 New Reaction Media; 7.4 New Technologies; 7.5 Application to Natural Products Synthesis; 8: Industrial Uses; 8.1 Ethyl Acetate; 8.2 Acrylic Esters; 8.2.1 Methyl Methacrylate (MMA); 8.2.2 Alkyl Acrylates; 8.3 Polyesters; 8.4 Oils and Fats; 8.4.1 Food Emulsifiers; 8.4.2 Soaps; 8.5 Biodiesel Fuel; 8.6 Amino Acid Esters; 8.7 Macrolides
8.8 Flavoring Agents and Fragrances8.9 Pyrethroids; Epilogue; References; Index
Record Nr. UNINA-9910678056403321
Otera Junzo  
Weinheim, : Wiley-VCH, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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European journal of organic chemistry
European journal of organic chemistry
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH
Descrizione fisica 1 online resource
Disciplina 547
Soggetto topico Chemistry, Organic
Organic compounds - Synthesis
Bioorganic chemistry
Physical organic chemistry
Biochemistry
Chimie organique
Composés organiques - Synthèse
Chimie bio-organique
Chimie organique physique
Soggetto genere / forma Periodical
ISSN 1099-0690
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996200959603316
Weinheim, Germany, : Wiley-VCH
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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European journal of organic chemistry
European journal of organic chemistry
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH
Descrizione fisica 1 online resource
Disciplina 547
Soggetto topico Chemistry, Organic
Organic compounds - Synthesis
Bioorganic chemistry
Physical organic chemistry
Biochemistry
Chimie organique
Composés organiques - Synthèse
Chimie bio-organique
Chimie organique physique
Soggetto genere / forma Periodical
ISSN 1099-0690
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910145990203321
Weinheim, Germany, : Wiley-VCH
Materiale a stampa
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Fluorination / / Jinbo Hu, Teruo Umemoto, editors
Fluorination / / Jinbo Hu, Teruo Umemoto, editors
Edizione [1st ed. 2020.]
Pubbl/distr/stampa Singapore : , : Springer, , [2020]
Descrizione fisica 1 online resource (946 illus., 351 illus. in color. eReference.)
Disciplina 547
Collana Synthetic Organofluorine Chemistry
Soggetto topico Chemistry, Organic
Catalysis
Pharmaceutical technology
Compostos organofluorats
Soggetto genere / forma Llibres electrònics
ISBN 981-10-3896-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Monofluorination (synthesis of –CF and XF compounds) -- Synthesis of alkyl fluorides -- Synthesis of alkenyl fluorides -- Synthesis of aryl fluorides -- Synthesis of X-F compounds (X = heteroatom) -- Difluorination (synthesies of -CF2- and -CF2H compounds) -- Trifluorination -- Other polyfluorination [synthesies of –CF3, -CmFn (n > 3) and -XFn compounds].
Record Nr. UNINA-9910420950303321
Singapore : , : Springer, , [2020]
Materiale a stampa
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Fondamenti di chimica organica / John McMurry
Fondamenti di chimica organica / John McMurry
Autore McMurry, John
Edizione ["terza edizione italiana condotta sulla quinta edizione americana"]
Pubbl/distr/stampa Bologna : Zanichelli, 2005
Descrizione fisica xii, 484 p. : ill. ; 27 cm
Disciplina 547
Soggetto topico Chemistry, Organic
ISBN 9788808075390
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ita
Record Nr. UNISALENTO-991002386579707536
McMurry, John  
Bologna : Zanichelli, 2005
Materiale a stampa
Lo trovi qui: Univ. del Salento
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Fondamenti di chimica organica / Janice Gorzynski Smith
Fondamenti di chimica organica / Janice Gorzynski Smith
Autore Smith, Janice Gorzynski
Edizione ["edizione italiana / a cura di Antonella Capperucci, Stefano Menichetti"]
Pubbl/distr/stampa Milano : McGrawll-Hill, 2009
Descrizione fisica xxxii, 672 p. : ill. ; 28 cm
Altri autori (Persone) Capperucci, Antonella
Menichetti, Stefano
Soggetto topico Chemistry, Organic
ISBN 9788838664885
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ita
Record Nr. UNISALENTO-991002390279707536
Smith, Janice Gorzynski  
Milano : McGrawll-Hill, 2009
Materiale a stampa
Lo trovi qui: Univ. del Salento
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