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A matter of density : exploring the electron density concept in the chemical, biological, and materials sciences / / edited by N. Sukumar
| A matter of density : exploring the electron density concept in the chemical, biological, and materials sciences / / edited by N. Sukumar |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2013 |
| Descrizione fisica | x, 318 p., [24] p. of plates : ill. (some col.) |
| Disciplina | 539.7/2112 |
| Soggetto topico | Electron distribution |
| ISBN |
1-283-60878-2
1-118-43174-X 9786613921239 1-118-43171-5 1-118-43172-3 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910830389503321 |
| Hoboken, New Jersey : , : Wiley, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Orbital interactions in chemistry [[electronic resource] /] / by Thomas A. Albright, Jeremy K. Burdett, Myung-Hwan Whangbo
| Orbital interactions in chemistry [[electronic resource] /] / by Thomas A. Albright, Jeremy K. Burdett, Myung-Hwan Whangbo |
| Autore | Albright Thomas A |
| Edizione | [2nd ed.] |
| Pubbl/distr/stampa | Hoboken, N.J., : John Wiley & Sons, c2013 |
| Descrizione fisica | 1 online resource (835 p.) |
| Disciplina | 541/.28 |
| Altri autori (Persone) |
BurdettJeremy K
WhangboMyung-Hwan |
| Soggetto topico | Molecular orbitals |
| ISBN |
1-118-55825-1
1-118-55840-5 1-118-55821-9 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Orbital Interactions In Chemistry; Contents; Preface; About the Authors; Chapter 1: Atomic and Molecular Orbitals; 1.1 Introduction; 1.2 Atomic Orbitals; 1.3 Molecular Orbitals; Problems; References; Chapter 2: Concepts of Bonding and Orbital Interaction; 2.1 Orbital Interaction Energy; 2.1.1 Degenerate Interaction; 2.1.2 Nondegenerate Interaction; 2.2 Molecular Orbital Coefficients; 2.2.1 Degenerate Interaction; 2.2.2 Nondegenerate Interaction; 2.3 The Two-Orbital Problem-Summary; 2.4 Electron Density Distribution; Problems; References; Chapter 3: Perturbational Molecular Orbital Theory
3.1 Introduction3.2 Intermolecular Perturbation; 3.3 Linear H3, HF, and the Three-Orbital Problem; 3.4 Degenerate Perturbation; Problems; References; Chapter 4: Symmetry; 4.1 Introduction; 4.2 Symmetry of Molecules; 4.3 Representations of Groups; 4.4 Symmetry Properties of Orbitals; 4.5 Symmetry-Adapted Wavefunctions; 4.6 Direct Products; 4.7 Symmetry Properties, Integrals, and the Noncrossing Rule; 4.8 Principles of Orbital Construction Using Symmetry Principles; 4.9 Symmetry Properties of Molecular Vibrations; Problems; References Chapter 5: Molecular Orbital Construction from Fragment Orbitals5.1 Introduction; 5.2 Triangular H3; 5.3 Rectangular and Square Planar H4; 5.4 Tetrahedral H4; 5.5 Linear H4; 5.6 Pentagonal H5 and Hexagonal H6; 5.7 Orbitals of Cyclic Systems; Problems; References; Chapter 6: Molecular Orbitals of Diatomic Molecules and Electronegativity Perturbation; 6.1 Introduction; 6.2 Orbital Hybridization; 6.3 Molecular Orbitals of Diatomic Molecules; 6.4 Electronegativity Perturbation; 6.5 Photoelectron Spectroscopy and Through-Bond Conjugation; Problems; References Chapter 7: Molecular Orbitals and Geometrical Perturbation7.1 Molecular Orbitals of AH2; 7.2 Geometrical Perturbation; 7.3 Walsh Diagrams; 7.4 Jahn-Teller Distortions; 7.4.1 First-Order Jahn-Teller Distortion; 7.4.2 Second-Order Jahn-Teller Distortion; 7.4.3 Three-Center Bonding; 7.5 Bond Orbitals and Photoelectron Spectra Of AH2 Molecules; Problems; References; Chapter 8: State Wavefunctions and State Energies; 8.1 Introduction; 8.2 The Molecular Hamiltonian and State Wavefunctions; 8.3 Fock Operator; 8.4 State Energy; 8.5 Excitation Energy; 8.6 Ionization Potential and Electron Affinity 8.7 Electron Density Distribution and Magnitudes of Coulomb and Exchange Repulsions8.8 Low versus High Spin States; 8.9 Electron-Electron Repulsion and Charged Species; 8.10 Configuration Interaction; 8.11 Toward More Quantitative Treatments; 8.12 The Density Functional Method; Problems; References; Chapter 9: Molecular Orbitals of Small Building Blocks; 9.1 Introduction; 9.2 The AH System; 9.3 Shapes of AH3 Systems; 9.4 π-Bonding Effects of Ligands; 9.5 The AH4 System; 9.6 The AHn Series-Some Generalizations; Problems; References; Chapter 10: Molecules with Two Heavy Atoms; 10.1 Introduction 10.2 A2H6 Systems |
| Record Nr. | UNINA-9910141639403321 |
Albright Thomas A
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| Hoboken, N.J., : John Wiley & Sons, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The Pauson-Khand reaction [[electronic resource] ] : scope, variations, and applications / / edited by Ramon Rios Torres
| The Pauson-Khand reaction [[electronic resource] ] : scope, variations, and applications / / edited by Ramon Rios Torres |
| Pubbl/distr/stampa | Chichester, West Sussex, : Wiley, 2012 |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina | 547/.412 |
| Altri autori (Persone) | Ríos TorresRamón |
| Soggetto topico |
Pauson-Khand reaction
Ring formation (Chemistry) |
| ISBN |
1-118-30863-8
1-280-59141-2 9786613621245 1-118-30862-X 1-119-94193-8 1-119-94192-X |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
The Pauson-Khand Reaction; Contents; List of Contributors; Foreword; Preface; 1. The Pauson-Khand Reaction - an Introduction; 1.1 The Discovery and Early Evolution of the Khand Reaction; 1.2 The Intermolecular Pauson-Khand Reaction; 1.2.1 Regioselectivity of Alkyne Insertion; 1.2.2 Regioselectivity of Alkene Insertion; 1.3 The Intramolecular Pauson-Khand Reaction; 1.4 Enhancing the Pauson-Khand Annulation by Reaction Promotion; 1.4.1 Dry State Adsorption; 1.4.2 Ultrasound Techniques; 1.4.3 Microwave Promotion; 1.4.4 Amine N-Oxide Additives; 1.4.5 Sulfide Promoters
1.5 Catalytic Pauson-Khand Protocols1.6 Concluding Remarks; Acknowledgements; References; 2. The Mechanism of the Pauson-Khand Reaction: Hypothesis, Experimental Facts, and Theoretical Investigations; 2.1 Introduction; 2.2 Stoichiometric Pauson-Khand Reaction; 2.2.1 The Ligand Substitution Steps; 2.2.2 Cobaltacycle Formation; 2.2.3 CO Insertion; 2.2.4 Reductive Elimination; 2.3 Catalytic Pauson-Khand Reaction; 2.4 Theoretical Studies; 2.4.1 General Approach to the Mechanism; 2.4.2 Regioselectivity. Early Steps of the Pauson-Khand Reaction; 2.4.3 Stereoselectivity; 2.5 Conclusions; References 3. Non Chiral Pauson-Khand Reaction3.1 History of Co-Mediated Pauson-Khand Reaction; 3.2 Mechanism of the Pauson-Khand Reaction; 3.3 An Early Example of Catalytic Reaction; 3.4 Catalytic Reactions by Aid of Additives; 3.5 Catalytic Reaction Using in-situ Generated Low-Valent Cobalt Complex; 3.6 Catalytic Reaction Using Multinuclear Cobalt Carbonyl Catalysts; 3.7 Catalytic Reaction Using Heterogeneous Catalysts; 3.8 Catalytic Reaction in Other Than Conventional Solvents; 3.9 Intramolecular Reaction of Carbodiimides with Alkynes; References 4. Diastereoselective Pauson-Khand Reaction using Chiral Pool Techniques (Chiral Substrates)4.1 Introduction and Background; 4.2 Intramolecular Diastereoselective Pauson-Khand Reaction; 4.3 Intermolecular Diastereoselective Pauson-Khand Reaction; 4.4 Conclusion; References; 5. Asymmetric Intra- and Intermolecular Pauson-Khand Reactions: The Chiral Auxiliary Approach; 5.1 Introduction; 5.2 Asymmetric Intramolecular PKRs with the Aid of Chiral Auxiliaries; 5.2.1 Chiral Alkoxyacetylenes; 5.2.2 Chiral Acetylene Thioethers; 5.2.3 Chiral 2-alkynoate Derivatives; 5.2.4 Chiral O-alkyl Enol Ethers 5.2.5 Alkenyl sulfoxides5.2.6 Asymmetric Intramolecular PKRs Mediated by Chiral Auxiliaries Located in the Enyne Tether; 5.3 Asymmetric Intermolecular PKRs with the Aid of Chiral Auxiliaries; 5.3.1 Chiral Alkoxyacetylenes; 5.3.2 Chiral Acetylene Thioethers; 5.3.3 Alkynyl Sulfoxides; 5.3.4 Chiral Ynamines and Ynamides; 5.3.5 Chiral 2-alkynoates; 5.3.6 Alkenyl Sulfoxides; 5.4 Chiral Reagents for the Kinetic Resolution of PK Cycloadducts; 5.5 Conclusion; Acknowledgements; References; 6. The Enantioselective Pauson-Khand Reaction; 6.1 Introduction 6.2 Mechanistic Considerations. Topology of Alkyne-Dicobalt Clusters |
| Record Nr. | UNINA-9910141292203321 |
| Chichester, West Sussex, : Wiley, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Pauson-Khand reaction [[electronic resource] ] : scope, variations, and applications / / edited by Ramon Rios Torres
| The Pauson-Khand reaction [[electronic resource] ] : scope, variations, and applications / / edited by Ramon Rios Torres |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Chichester, West Sussex, : Wiley, 2012 |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina | 547/.412 |
| Altri autori (Persone) | Ríos TorresRamón |
| Soggetto topico |
Pauson-Khand reaction
Ring formation (Chemistry) |
| ISBN |
1-118-30863-8
1-280-59141-2 9786613621245 1-118-30862-X 1-119-94193-8 1-119-94192-X |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
The Pauson-Khand Reaction; Contents; List of Contributors; Foreword; Preface; 1. The Pauson-Khand Reaction - an Introduction; 1.1 The Discovery and Early Evolution of the Khand Reaction; 1.2 The Intermolecular Pauson-Khand Reaction; 1.2.1 Regioselectivity of Alkyne Insertion; 1.2.2 Regioselectivity of Alkene Insertion; 1.3 The Intramolecular Pauson-Khand Reaction; 1.4 Enhancing the Pauson-Khand Annulation by Reaction Promotion; 1.4.1 Dry State Adsorption; 1.4.2 Ultrasound Techniques; 1.4.3 Microwave Promotion; 1.4.4 Amine N-Oxide Additives; 1.4.5 Sulfide Promoters
1.5 Catalytic Pauson-Khand Protocols1.6 Concluding Remarks; Acknowledgements; References; 2. The Mechanism of the Pauson-Khand Reaction: Hypothesis, Experimental Facts, and Theoretical Investigations; 2.1 Introduction; 2.2 Stoichiometric Pauson-Khand Reaction; 2.2.1 The Ligand Substitution Steps; 2.2.2 Cobaltacycle Formation; 2.2.3 CO Insertion; 2.2.4 Reductive Elimination; 2.3 Catalytic Pauson-Khand Reaction; 2.4 Theoretical Studies; 2.4.1 General Approach to the Mechanism; 2.4.2 Regioselectivity. Early Steps of the Pauson-Khand Reaction; 2.4.3 Stereoselectivity; 2.5 Conclusions; References 3. Non Chiral Pauson-Khand Reaction3.1 History of Co-Mediated Pauson-Khand Reaction; 3.2 Mechanism of the Pauson-Khand Reaction; 3.3 An Early Example of Catalytic Reaction; 3.4 Catalytic Reactions by Aid of Additives; 3.5 Catalytic Reaction Using in-situ Generated Low-Valent Cobalt Complex; 3.6 Catalytic Reaction Using Multinuclear Cobalt Carbonyl Catalysts; 3.7 Catalytic Reaction Using Heterogeneous Catalysts; 3.8 Catalytic Reaction in Other Than Conventional Solvents; 3.9 Intramolecular Reaction of Carbodiimides with Alkynes; References 4. Diastereoselective Pauson-Khand Reaction using Chiral Pool Techniques (Chiral Substrates)4.1 Introduction and Background; 4.2 Intramolecular Diastereoselective Pauson-Khand Reaction; 4.3 Intermolecular Diastereoselective Pauson-Khand Reaction; 4.4 Conclusion; References; 5. Asymmetric Intra- and Intermolecular Pauson-Khand Reactions: The Chiral Auxiliary Approach; 5.1 Introduction; 5.2 Asymmetric Intramolecular PKRs with the Aid of Chiral Auxiliaries; 5.2.1 Chiral Alkoxyacetylenes; 5.2.2 Chiral Acetylene Thioethers; 5.2.3 Chiral 2-alkynoate Derivatives; 5.2.4 Chiral O-alkyl Enol Ethers 5.2.5 Alkenyl sulfoxides5.2.6 Asymmetric Intramolecular PKRs Mediated by Chiral Auxiliaries Located in the Enyne Tether; 5.3 Asymmetric Intermolecular PKRs with the Aid of Chiral Auxiliaries; 5.3.1 Chiral Alkoxyacetylenes; 5.3.2 Chiral Acetylene Thioethers; 5.3.3 Alkynyl Sulfoxides; 5.3.4 Chiral Ynamines and Ynamides; 5.3.5 Chiral 2-alkynoates; 5.3.6 Alkenyl Sulfoxides; 5.4 Chiral Reagents for the Kinetic Resolution of PK Cycloadducts; 5.5 Conclusion; Acknowledgements; References; 6. The Enantioselective Pauson-Khand Reaction; 6.1 Introduction 6.2 Mechanistic Considerations. Topology of Alkyne-Dicobalt Clusters |
| Record Nr. | UNINA-9910827004603321 |
| Chichester, West Sussex, : Wiley, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Peptidomimetics in organic and medicinal chemistry / / Andrea Trabocchi and Antonio Guarna
| Peptidomimetics in organic and medicinal chemistry / / Andrea Trabocchi and Antonio Guarna |
| Autore | Guarna Antonio |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2014 |
| Descrizione fisica | 1 online resource (320 p.) |
| Disciplina | 615.1/9 |
| Soggetto topico |
Peptide drugs
Proteins - Therapeutic use Drugs - Design |
| ISBN |
1-118-68314-5
1-118-68303-X 1-118-68384-6 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; Preface; Abbreviations; Part I The Basics of Peptidomimetics; Chapter 1 The Basics of Peptidomimetics; 1.1 Introduction; 1.2 Definition and Classification; 1.3 Strategic Approaches to Peptidomimetic Design; 1.3.1 Modification of Amino Acids; 1.3.2 Compounds with Global Restrictions; 1.3.3 Molecular Scaffolds Mimicking the Peptidic Backbone; 1.4 Successful Examples of Peptidomimetic Drugs; 1.4.1 ACE Inhibitors; 1.4.2 Thrombin Inhibitors; 1.5 Conclusion; References; Chapter 2 Synthetic Approaches towards Peptidomimetic Design; 2.1 Introduction
2.2 Local Modifications2.2.1 Single Amino Acid Modifications; 2.2.2 Dipeptide Isosteres; 2.2.3 Retro-inverso Peptides; 2.2.4 N-Methylation of Peptides; 2.2.5 Azapeptides; 2.2.6 Peptoids; 2.3 Global Restrictions through Cyclic Peptidomimetics; 2.4 Peptidomimetic Scaffolds; 2.5 Conclusions; References; Part II Synthetic Methods and Molecules; Chapter 3 Peptidomimetic Bioisosteres; 3.1 Introduction; 3.2 Peptide Bond Isosteres; 3.2.1 Thioamides; 3.2.2 Esters; 3.2.3 Alkenes and Fluoroalkenes; 3.2.4 Transition-State Isosteres; 3.3 Side-Chain Isosteres 3.3.1 Guanidine Isosteres in Arginine Peptidomimetics3.3.2 Isosteres of Aspartic Acid and Glutamic Acid; 3.3.3 Tethered α-Amino Acids: Constraining the x-Space; 3.4 Dipeptide Isosteres; 3.4.1 δ-Amino Acids; 3.5 Tripeptide Isosteres; 3.6 Conclusion; References; Chapter 4 Solid-Phase Synthesis and Combinatorial Approaches to Peptidomimetics; 4.1 Introduction; 4.2 Solid-Phase Synthesis of Peptidomimetics; 4.2.1 Scaffolds from α-Amino Acids; 4.2.2 Scaffolds from Amino Aldehyde Intermediates; 4.2.3 Pyrrolidine-Containing Scaffolds; 4.3 Conclusion; References Chapter 5 Click Chemistry: The Triazole Ring as a Privileged Peptidomimetic Scaffold5.1 Introduction; 5.1.1 CuAAC Reaction; 5.1.2 Triazole Ring as a Peptidomimetic Isostere; 5.2 Triazole-Containing Peptidomimetics Elaborated through `Click Chemistry'; 5.2.1 Macrocycles; 5.2.2 Oligomers and Foldamers; 5.3 Relevant Applications in Drug Discovery; 5.3.1 AChE Inhibitors; 5.3.2 HIV Protease Inhibitors; 5.3.3 MMP Inhibitors; 5.3.4 Integrin Ligands; 5.4 Conclusions; Acknowledgements; References; Chapter 6 Peptoids; 6.1 Introduction and Basics of Peptoids; 6.2 Synthetic Methods 6.3 Macrocyclic Peptoids6.4 Conformational Analysis of Folded Peptoids; 6.5 Application of Peptoids as Antimicrobial Peptidomimetics; 6.6 Conclusions; References; Chapter 7 Sugar Amino Acids; 7.1 Introduction; 7.2 α-SAAs; 7.2.1 Furanoid α-SAAs; 7.2.2 Pyranoid α-SAAs; 7.3 β-SAAs; 7.3.1 Furanoid β-SAAs; 7.3.2 Pyranoid β-SAAs; 7.4 r-SAAs1; 7.5 δ-SAAs; 7.5.1 Furanoid δ-SAAs; 7.5.2 Pyranoid δ-SAAs; 7.6 Representative Applications in Medicinal Chemistry; 7.7 Conclusions; References; Chapter 8 Cyclic α-Amino Acids as Proline Mimetics; 8.1 Introduction; 8.2 Cyclic α-Amino Acids 8.2.1 3-Substituted Proline Derivatives |
| Record Nr. | UNINA-9910140270003321 |
|
Guarna Antonio
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| Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Peptidomimetics in organic and medicinal chemistry / / Andrea Trabocchi and Antonio Guarna
| Peptidomimetics in organic and medicinal chemistry / / Andrea Trabocchi and Antonio Guarna |
| Autore | Guarna Antonio |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2014 |
| Descrizione fisica | 1 online resource (320 p.) |
| Disciplina | 615.1/9 |
| Soggetto topico |
Peptide drugs
Proteins - Therapeutic use Drugs - Design |
| ISBN |
1-118-68314-5
1-118-68303-X 1-118-68384-6 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; Preface; Abbreviations; Part I The Basics of Peptidomimetics; Chapter 1 The Basics of Peptidomimetics; 1.1 Introduction; 1.2 Definition and Classification; 1.3 Strategic Approaches to Peptidomimetic Design; 1.3.1 Modification of Amino Acids; 1.3.2 Compounds with Global Restrictions; 1.3.3 Molecular Scaffolds Mimicking the Peptidic Backbone; 1.4 Successful Examples of Peptidomimetic Drugs; 1.4.1 ACE Inhibitors; 1.4.2 Thrombin Inhibitors; 1.5 Conclusion; References; Chapter 2 Synthetic Approaches towards Peptidomimetic Design; 2.1 Introduction
2.2 Local Modifications2.2.1 Single Amino Acid Modifications; 2.2.2 Dipeptide Isosteres; 2.2.3 Retro-inverso Peptides; 2.2.4 N-Methylation of Peptides; 2.2.5 Azapeptides; 2.2.6 Peptoids; 2.3 Global Restrictions through Cyclic Peptidomimetics; 2.4 Peptidomimetic Scaffolds; 2.5 Conclusions; References; Part II Synthetic Methods and Molecules; Chapter 3 Peptidomimetic Bioisosteres; 3.1 Introduction; 3.2 Peptide Bond Isosteres; 3.2.1 Thioamides; 3.2.2 Esters; 3.2.3 Alkenes and Fluoroalkenes; 3.2.4 Transition-State Isosteres; 3.3 Side-Chain Isosteres 3.3.1 Guanidine Isosteres in Arginine Peptidomimetics3.3.2 Isosteres of Aspartic Acid and Glutamic Acid; 3.3.3 Tethered α-Amino Acids: Constraining the x-Space; 3.4 Dipeptide Isosteres; 3.4.1 δ-Amino Acids; 3.5 Tripeptide Isosteres; 3.6 Conclusion; References; Chapter 4 Solid-Phase Synthesis and Combinatorial Approaches to Peptidomimetics; 4.1 Introduction; 4.2 Solid-Phase Synthesis of Peptidomimetics; 4.2.1 Scaffolds from α-Amino Acids; 4.2.2 Scaffolds from Amino Aldehyde Intermediates; 4.2.3 Pyrrolidine-Containing Scaffolds; 4.3 Conclusion; References Chapter 5 Click Chemistry: The Triazole Ring as a Privileged Peptidomimetic Scaffold5.1 Introduction; 5.1.1 CuAAC Reaction; 5.1.2 Triazole Ring as a Peptidomimetic Isostere; 5.2 Triazole-Containing Peptidomimetics Elaborated through `Click Chemistry'; 5.2.1 Macrocycles; 5.2.2 Oligomers and Foldamers; 5.3 Relevant Applications in Drug Discovery; 5.3.1 AChE Inhibitors; 5.3.2 HIV Protease Inhibitors; 5.3.3 MMP Inhibitors; 5.3.4 Integrin Ligands; 5.4 Conclusions; Acknowledgements; References; Chapter 6 Peptoids; 6.1 Introduction and Basics of Peptoids; 6.2 Synthetic Methods 6.3 Macrocyclic Peptoids6.4 Conformational Analysis of Folded Peptoids; 6.5 Application of Peptoids as Antimicrobial Peptidomimetics; 6.6 Conclusions; References; Chapter 7 Sugar Amino Acids; 7.1 Introduction; 7.2 α-SAAs; 7.2.1 Furanoid α-SAAs; 7.2.2 Pyranoid α-SAAs; 7.3 β-SAAs; 7.3.1 Furanoid β-SAAs; 7.3.2 Pyranoid β-SAAs; 7.4 r-SAAs1; 7.5 δ-SAAs; 7.5.1 Furanoid δ-SAAs; 7.5.2 Pyranoid δ-SAAs; 7.6 Representative Applications in Medicinal Chemistry; 7.7 Conclusions; References; Chapter 8 Cyclic α-Amino Acids as Proline Mimetics; 8.1 Introduction; 8.2 Cyclic α-Amino Acids 8.2.1 3-Substituted Proline Derivatives |
| Record Nr. | UNINA-9910821269603321 |
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Guarna Antonio
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| Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Quantum oscillators [[electronic resource] /] / Olivier Henri-Rousseau and Paul Blaise
| Quantum oscillators [[electronic resource] /] / Olivier Henri-Rousseau and Paul Blaise |
| Autore | Henri-Rousseau Olivier |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2011 |
| Descrizione fisica | 1 online resource (682 p.) |
| Disciplina | 541/.224 |
| Altri autori (Persone) | BlaisePaul |
| Soggetto topico |
Harmonic oscillators
Spectrum analysis Wave mechanics Hydrogen bonding |
| ISBN |
1-283-23969-8
9786613239693 1-118-01802-8 1-118-01801-X 1-118-01803-6 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | pt. 1. Basis required for quantum oscillator studies -- pt. 2. Single quantum harmonic oscillators -- pt. 3. Anharmonicity -- pt. 4. Oscillator populations in thermal equilibrium -- pt. 5. Quantum normal modes of vibration -- pt. 6. Damped harmonic oscillators -- pt. 7. Vibrational spectroscopy. |
| Record Nr. | UNINA-9910137864403321 |
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Henri-Rousseau Olivier
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| Hoboken, N.J., : Wiley, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Smart membranes and sensors : synthesis, characterization, and applications / / edited by Annarosa Gugliuzza ; cover design by Russell Richardson
| Smart membranes and sensors : synthesis, characterization, and applications / / edited by Annarosa Gugliuzza ; cover design by Russell Richardson |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Scrivener Publishing : , : Wiley, , 2014 |
| Descrizione fisica | 1 online resource (771 p.) |
| Disciplina | 681/.2 |
| Soggetto topico |
Smart materials
Membranes (Technology) Intelligent sensors |
| ISBN |
1-119-02862-0
1-119-02864-7 1-119-02863-9 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Machine generated contents note: Preface Part 1: Sensing Materials for Smart Membranes 1 1 Interfaces Based on Carbon Nanotubes, Ionic Liquids and Polymer Matrices for Sensing and Membrane Separation Applications 3 María Belen Serrano-Santos, Ana Corres Ortega, and Thomas Schafer 1.1 Introduction 3 1.2 Ionic Liquid-Carbon Nanotubes Composites for Sensing Interfaces 5 1.3 Ionic Liquid Interfaces for Detection and Separation of Gases and Solvents 11 1.4 Ionic Liquid-Polymer Interfaces for Membrane Separation Processes 16 1.5 Conclusions 18 Acknowledgement 19 References 19 . |
| Record Nr. | UNINA-9910132161503321 |
| Hoboken, New Jersey : , : Scrivener Publishing : , : Wiley, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Smart membranes and sensors : synthesis, characterization, and applications / / edited by Annarosa Gugliuzza ; cover design by Russell Richardson
| Smart membranes and sensors : synthesis, characterization, and applications / / edited by Annarosa Gugliuzza ; cover design by Russell Richardson |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Scrivener Publishing : , : Wiley, , 2014 |
| Descrizione fisica | 1 online resource (771 p.) |
| Disciplina | 681/.2 |
| Soggetto topico |
Smart materials
Membranes (Technology) Intelligent sensors |
| ISBN |
1-119-02862-0
1-119-02864-7 1-119-02863-9 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Machine generated contents note: Preface Part 1: Sensing Materials for Smart Membranes 1 1 Interfaces Based on Carbon Nanotubes, Ionic Liquids and Polymer Matrices for Sensing and Membrane Separation Applications 3 María Belen Serrano-Santos, Ana Corres Ortega, and Thomas Schafer 1.1 Introduction 3 1.2 Ionic Liquid-Carbon Nanotubes Composites for Sensing Interfaces 5 1.3 Ionic Liquid Interfaces for Detection and Separation of Gases and Solvents 11 1.4 Ionic Liquid-Polymer Interfaces for Membrane Separation Processes 16 1.5 Conclusions 18 Acknowledgement 19 References 19 . |
| Record Nr. | UNINA-9910678148403321 |
| Hoboken, New Jersey : , : Scrivener Publishing : , : Wiley, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Solid-phase organic synthesis [[electronic resource] ] : concepts, strategies, and applications / / edited by Patrick H. Toy, Yulin Lam
| Solid-phase organic synthesis [[electronic resource] ] : concepts, strategies, and applications / / edited by Patrick H. Toy, Yulin Lam |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, 2012 |
| Descrizione fisica | 1 online resource (562 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) |
ToyPatrick H
LamYulin |
| Soggetto topico |
Solid-phase synthesis
Organic compounds - Synthesis |
| ISBN |
1-283-40957-7
9786613409577 1-118-14163-6 1-118-14164-4 1-118-14162-8 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
SOLID-PHASE ORGANIC SYNTHESIS: Concepts, Strategies, and Applications; CONTENTS; Preface; Acknowledgments; Contributors; Part I: CONCEPTS AND STRATEGIES; 1 LINKER STRATEGIES IN MODERN SOLID-PHASE ORGANIC SYNTHESIS; 1.1 Introduction; 1.2 Classical Linker Strategies; 1.2.1 Acid and Base Cleavable Linker Units; 1.2.2 Cyclorelease Linker Units; 1.2.3 Traceless Linker Units; 1.2.4 Photolabile Linker Units; 1.2.5 Safety-Catch Linker Units; 1.3 Multifunctional Linker Strategies; 1.3.1 Nitrogen Linker Units; 1.3.1.1 Triazene Linker Units; 1.3.1.2 Hydrazone Linker Units
1.3.1.3 Benzotriazole Linker Units1.3.2 Sulfur Linker Units; 1.3.3 Phosphorus Linker Units; 1.3.4 Selenium and Tellurium Linker Units; 1.3.5 Silyl and Germyl Linker Units; 1.3.6 Boron and Stannane Linker Units; 1.3.7 Bismuth Linker Units; 1.3.8 Alkene Linker Units; 1.4 Conclusions; References; 2 COLORIMETRIC TEST FOR SOLID-PHASE ORGANIC SYNTHESIS; 2.1 Introduction; 2.2 Functional Group Tests; 2.2.1 Amine Groups; 2.2.1.1 Ninhydrin (Kaiser) Test; 2.2.1.2 TNBSA Test; 2.2.1.3 Bromophenol Blue Test; 2.2.1.4 Chloranil Test; 2.2.1.5 DABITC Test; 2.2.1.6 MGI Test; 2.2.1.7 Isatin Test 2.2.1.8 DESC Test2.2.1.9 NPIT Test; 2.2.1.10 NF31 Test; 2.2.1.11 Nondestructive NF31 Test; 2.2.1.12 Naphthol Test; 2.2.1.13 2-Amino-3-chloro-1,4-naphthoquinone Test; 2.2.2 Alcohols; 2.2.2.1 PNBP Test; 2.2.2.2 TCT-AliR and TCT-Fluorescein Test; 2.2.2.3 Diphenyldichlorosilane-Methyl Red Test; 2.2.2.4 9-Anthronylnitrile Test; 2.2.2.5 NMA Test; 2.2.2.6 Protecting Group NPB Test; 2.2.2.7 Methyl Red/DIC Test; 2.2.2.8 Other Methods; 2.2.3 Thiol Groups; 2.2.3.1 Ellman's Test; 2.2.3.2 Other Methods; 2.2.4 Halogen Groups; 2.2.4.1 Fluorescein Test; 2.2.4.2 Other Methods; 2.2.5 Carboxylic Acid Groups 2.2.5.1 Malachite Green Test2.2.5.2 PDAM Test; 2.2.6 Aldehyde and Ketone Groups; 2.2.6.1 Fluorescent Dansylhydrazine Test; 2.2.6.2 p-Anisaldehyde Test; 2.2.6.3 Purpald Test; 2.3 Conclusions; References; 3 PRACTICAL ASPECTS OF COMBINATORIAL SOLID-PHASE SYNTHESIS; 3.1 Introduction; 3.1.1 What Is Combinatorial Chemistry; 3.1.2 What Is Not Combinatorial Chemistry; 3.1.3 History of Combinatorial Chemistry: Breakthrough Discoveries That Shaped the Future of the Combinatorial Chemistry Field; 3.1.3.1 Solid-Phase Synthesis; 3.1.3.2 Pooling Strategy; 3.1.3.3 Parallel Synthesis 3.2 Strategies in Combinatorial Solid-Phase Synthesis3.2.1 Random Split-and-Pool Method; 3.2.1.1 One-Bead-One-Compound Concept; 3.2.1.2 Encoding Methods for the OBOC Technique; 3.2.1.3 Organized Mixtures; 3.2.2 Directed Split-and-Pool Method in Practice; 3.2.2.1 Formulation of Solid-Phase Supports for the Directed Split-and-Pool Technique; 3.2.2.2 Chemical History of the Resin Formulations; 3.3 Equipment and Instrumentation; 3.3.1 Manual Solid-Phase Synthesis; 3.3.2 Integrated Semiautomated Synthesis; 3.3.3 Fully Automated Synthesizers (Gone with the Wind); 3.3.4 Instruments for Sorting 3.4 Characterization and Purification |
| Record Nr. | UNINA-9910141164703321 |
| Hoboken, NJ, : Wiley, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
