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The chemistry of chlorosulfonyl isocyanate [[electronic resource] /] / Durga Nath Dhar, Preeti Dhar
The chemistry of chlorosulfonyl isocyanate [[electronic resource] /] / Durga Nath Dhar, Preeti Dhar
Autore Dhar Durga Nath
Pubbl/distr/stampa River Edge, N.J., : World Scientific, c2002
Descrizione fisica 1 online resource (xvi, 377 p. ) : ill
Disciplina 661.894
Altri autori (Persone) DharPreeti
Soggetto topico Isocyanates
Chemistry, Organic
Chlorosulfonyl isocyanate
Soggetto genere / forma Electronic books.
ISBN 981-277-702-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Reactions: Alkenes; Dienes; Trienes; Tetraenes; Pentaene; Alcohols; Ketenes; Acetals; Acids; Amides; Oxygen Heterocycles; Heterocycles; Applications: Herbicides; Plant Protection Agents; Pesticides; Insecticides; Anticancer; Analgesics; Neuroleptics; Eye Disorders; Antibiotics; Inhibitors; Antibiotics; Cephem; Liquid Crystals; Textile; and other topics.
Record Nr. UNINA-9910450884403321
Dhar Durga Nath  
River Edge, N.J., : World Scientific, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The chemistry of chlorosulfonyl isocyanate [[electronic resource] /] / Durga Nath Dhar, Preeti Dhar
The chemistry of chlorosulfonyl isocyanate [[electronic resource] /] / Durga Nath Dhar, Preeti Dhar
Autore Dhar Durga Nath
Pubbl/distr/stampa River Edge, N.J., : World Scientific, c2002
Descrizione fisica 1 online resource (xvi, 377 p. ) : ill
Disciplina 661.894
Altri autori (Persone) DharPreeti
Soggetto topico Isocyanates
Chemistry, Organic
Chlorosulfonyl isocyanate
ISBN 981-277-702-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Reactions: Alkenes; Dienes; Trienes; Tetraenes; Pentaene; Alcohols; Ketenes; Acetals; Acids; Amides; Oxygen Heterocycles; Heterocycles; Applications: Herbicides; Plant Protection Agents; Pesticides; Insecticides; Anticancer; Analgesics; Neuroleptics; Eye Disorders; Antibiotics; Inhibitors; Antibiotics; Cephem; Liquid Crystals; Textile; and other topics.
Record Nr. UNINA-9910785100403321
Dhar Durga Nath  
River Edge, N.J., : World Scientific, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The chemistry of chlorosulfonyl isocyanate [[electronic resource] /] / Durga Nath Dhar, Preeti Dhar
The chemistry of chlorosulfonyl isocyanate [[electronic resource] /] / Durga Nath Dhar, Preeti Dhar
Autore Dhar Durga Nath
Pubbl/distr/stampa River Edge, N.J., : World Scientific, c2002
Descrizione fisica 1 online resource (xvi, 377 p. ) : ill
Disciplina 661.894
Altri autori (Persone) DharPreeti
Soggetto topico Isocyanates
Chemistry, Organic
Chlorosulfonyl isocyanate
ISBN 981-277-702-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Reactions: Alkenes; Dienes; Trienes; Tetraenes; Pentaene; Alcohols; Ketenes; Acetals; Acids; Amides; Oxygen Heterocycles; Heterocycles; Applications: Herbicides; Plant Protection Agents; Pesticides; Insecticides; Anticancer; Analgesics; Neuroleptics; Eye Disorders; Antibiotics; Inhibitors; Antibiotics; Cephem; Liquid Crystals; Textile; and other topics.
Record Nr. UNINA-9910807881703321
Dhar Durga Nath  
River Edge, N.J., : World Scientific, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The chemistry of double-bonded functional groups : Supplement A, Part 2 / / edited by Saul Patai
The chemistry of double-bonded functional groups : Supplement A, Part 2 / / edited by Saul Patai
Pubbl/distr/stampa London, England : , : John Wiley & Sons, Inc., , 1977
Descrizione fisica 1 online resource (1343 pages) : illustrations
Disciplina 2002
Collana Chemistry of functional groups
Soggetto topico Physical organic chemistry
Functional groups
Chemistry, Organic
ISBN 0-470-77842-3
0-470-77151-8
0-470-77181-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto [pt. 1.] Dipole moments, configurations and conformations of molecules containing X=Y groups -- Otto Exner -- Liquid crystals with X=Y groups -- J.P. Van Meter -- Thermochemistry of X=Y groups -- Robert Shaw -- Mechanisms of elimination and addition reactions involving the X=Y group -- Anthony F. Cockerill and Roger G. Harrison -- The electrochemistry of X=Y groups -- Albert J. Fry and Roberta Gable Reed -- 1,3-Dipolar cycloadditions involving X=Y groups -- Giorgio Bianchi, Carlo De Micheli and Remo Gandolfi -- Reactions of carbenes with X=Y groups -- Alan P. Marchand -- [pt. 2.] The formation of unsaturated groups by heterolytic fragmentation -- Konrad B. Becker and Cyril A. Grob -- Electrophilic additions to carbon-carbon double bonds -- George H. Schmid and Dennis G. Garratt -- The olefin metathesis reaction -- Nissim Calderon -- Oxidation of C=C and C=N groups -- P.M. Henry and G.L. Lange -- Transition metal catalysed carbonylation of olefins -- John K. Stille and David E. James -- Imidines and diamidides (1,3,5-triazapentadienes) -- John A. Elvidge and N.R. Barot.
Altri titoli varianti Double‐Bonded Functional Groups
Record Nr. UNINA-9910830016903321
London, England : , : John Wiley & Sons, Inc., , 1977
Materiale a stampa
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The Chemistry of Double-Bonded Functional Groups: Supplement A. Vol. 2
The Chemistry of Double-Bonded Functional Groups: Supplement A. Vol. 2
Autore Patai Saul E
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Incorporated, 1989
Descrizione fisica 1 online resource : illustrations
Disciplina 547
Altri autori (Persone) PataiSaul
Collana Chemistry of functional groups. Supplement
Soggetto topico Physical organic chemistry
Functional groups
Chemistry, Organic
ISBN 0-470-77888-1
0-470-77225-5
0-470-77236-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Vol. 2. 1989. [v. 2., pt. 1.] Complementary views on the homopolar double-bond structure -- Georges Trinquier and Jean-Paul Malrieu -- Mass spectrometry of the double bond -- Margaret N. Mruzek -- Nuclear magnetic resonance spectroscopy of C=C, C=O, C=N and N=N double bonds -- Poul Erik Hansen -- The photoelectron spectroscopy of double-bonded CC, CN, NN and CO groups -- L. Klasinc and S.P. McGlynn -- Directing and activating effects of doubly bonded groups -- Marvin Charton -- Double bonds from a biochemical perspective -- Alan H. Mehler -- Intramolecular 1,3-dipolar cycloadditions to double bonds -- O. Tsuge, T. Hatta and T. Hisano -- The ene reaction -- G.V. Boyd -- Radiation chemistry of double-bonded compounds -- Zeev B. Alfassi -- Asymmetric induction in additions to C=O and C=N bonds -- Joseph Klein -- Electrophilic additions to carbon-carbon double bonds --- George H. Schmid -- Mechanisms of base-catalyzed alkene-forming 1,2-eliminations -- Joseph R. Gandler -- [v. 2., pt. 2.] Carbonylation of main-group organometallic compounds -- Norma Nudelman -- Rearrangements involving allenes -- Samuel Braverman -- 1,1-Diarylalkenes -- William S. Murphy -- Fulvenes -- M. Neuenschwander -- The thiocarbonyl group -- Ernst Schaumann -- Cycloadditions of enones -- Janine Cossy, Pierre-Alain Carrupt and Pierre Vogel.
Record Nr. UNINA-9910830559403321
Patai Saul E  
[Place of publication not identified], : John Wiley & Sons Incorporated, 1989
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The Chemistry of Double-Bonded Functional Groups: Supplement A. Vol. 2
The Chemistry of Double-Bonded Functional Groups: Supplement A. Vol. 2
Autore Patai Saul E
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Incorporated, 1989
Descrizione fisica 1 online resource : illustrations
Disciplina 547
Altri autori (Persone) PataiSaul
Collana Chemistry of functional groups. Supplement
Soggetto topico Physical organic chemistry
Functional groups
Chemistry, Organic
ISBN 0-470-77888-1
0-470-77225-5
0-470-77236-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Vol. 2. 1989. [v. 2., pt. 1.] Complementary views on the homopolar double-bond structure -- Georges Trinquier and Jean-Paul Malrieu -- Mass spectrometry of the double bond -- Margaret N. Mruzek -- Nuclear magnetic resonance spectroscopy of C=C, C=O, C=N and N=N double bonds -- Poul Erik Hansen -- The photoelectron spectroscopy of double-bonded CC, CN, NN and CO groups -- L. Klasinc and S.P. McGlynn -- Directing and activating effects of doubly bonded groups -- Marvin Charton -- Double bonds from a biochemical perspective -- Alan H. Mehler -- Intramolecular 1,3-dipolar cycloadditions to double bonds -- O. Tsuge, T. Hatta and T. Hisano -- The ene reaction -- G.V. Boyd -- Radiation chemistry of double-bonded compounds -- Zeev B. Alfassi -- Asymmetric induction in additions to C=O and C=N bonds -- Joseph Klein -- Electrophilic additions to carbon-carbon double bonds --- George H. Schmid -- Mechanisms of base-catalyzed alkene-forming 1,2-eliminations -- Joseph R. Gandler -- [v. 2., pt. 2.] Carbonylation of main-group organometallic compounds -- Norma Nudelman -- Rearrangements involving allenes -- Samuel Braverman -- 1,1-Diarylalkenes -- William S. Murphy -- Fulvenes -- M. Neuenschwander -- The thiocarbonyl group -- Ernst Schaumann -- Cycloadditions of enones -- Janine Cossy, Pierre-Alain Carrupt and Pierre Vogel.
Record Nr. UNINA-9910840991003321
Patai Saul E  
[Place of publication not identified], : John Wiley & Sons Incorporated, 1989
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chemistry of natural compounds
Chemistry of natural compounds
Pubbl/distr/stampa London, : Kluwer/Plenum Publishers
Disciplina 547
Soggetto topico Chemistry, Organic
Chimie organique
ISSN 1573-8388
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996215985103316
London, : Kluwer/Plenum Publishers
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Chemistry of natural compounds
Chemistry of natural compounds
Pubbl/distr/stampa London, : Kluwer/Plenum Publishers
Disciplina 547
Soggetto topico Chemistry, Organic
Chimie organique
ISSN 1573-8388
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910141123403321
London, : Kluwer/Plenum Publishers
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chemistry of natural products : amino acids, peptides, proteins and enzymes / / V. K. Ahluwalia, Lalita S. Kumar, and Sanjiv Kumar
Chemistry of natural products : amino acids, peptides, proteins and enzymes / / V. K. Ahluwalia, Lalita S. Kumar, and Sanjiv Kumar
Autore Ahluwalia V. K.
Pubbl/distr/stampa Cham, Switzerland : , : Springer, , [2022]
Descrizione fisica 1 online resource (250 pages)
Disciplina 631
Soggetto topico Natural products
Chemistry, Organic
ISBN 3-030-86698-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intro -- Preface -- Contents -- About the Authors -- 1 Amino Acids -- 1.1 Introduction -- 1.2 Nomenclature of Amino Acids -- 1.2.1 Representation of Amino Acids -- 1.3 Classification of Amino Acids -- 1.3.1 Coded or Primary Protein Amino Acids -- 1.3.2 Secondary and Tertiary Protein Amino Acids -- 1.3.3 Non-coded or Non-protein Amino Acids -- 1.3.4 Essential Amino Acids -- 1.4 Stereochemical Aspects of α-Amino Acids -- 1.4.1 Absolute Configuration of α-Amino Acids -- 1.4.2 Amino Acids with Two Chiral Centres -- 1.5 Physical Properties of α-Amino Acids -- 1.5.1 General Physical Properties -- 1.5.2 Acid-Base Properties of Amino Acids -- 1.5.3 Spectral Properties of α-Amino Acids -- 1.6 Chemical Reactions of Amino Acids -- 1.6.1 Reactions Due to Amino Group -- 1.6.2 Reactions Due to Carboxyl Group -- 1.6.3 Reactions Due to Both Amino and Carboxyl Groups -- 1.7 Industrial Preparation of α-Amino Acids -- 1.8 Chemical Synthesis of α-Amino Acids -- 1.8.1 Enantiomeric Resolution of α-Amino Acids -- 1.8.2 Asymmetric Synthesis of α-Amino Acids -- 1.9 Industrial Applications of α-Amino Acids -- 2 Peptides -- 2.1 Introduction -- 2.2 Structure and Classification of Peptides -- 2.2.1 Structure of Peptide Bond -- 2.2.2 Classification of Peptides -- 2.3 Nomenclature of Peptides -- 2.3.1 Representation of Peptides and Polypeptides -- 2.4 Peptide Synthesis -- 2.4.1 Protection of Amino Group -- 2.4.2 Protection of Carboxyl Group -- 2.4.3 Protection of Side Chains -- 2.4.4 Coupling Methods -- 2.5 Solid-Phase Peptide Synthesis -- 2.5.1 Solid-Phase Peptide Synthesis Using t-Boc Protection (Merrifield Approach) -- 2.5.2 Solid-Phase Peptide Synthesis Using Fmoc Protection (Sheppard's Approach) -- 2.5.3 Limitations of Solid-Phase Peptide Synthesis -- 2.6 Some Biologically Important Peptides -- 2.6.1 Oxytocin -- 2.6.2 Glutathione -- 2.6.3 Insulin -- 2.6.4 Bradykinin.
2.6.5 Gramicidin S -- 3 Proteins -- 3.1 Introduction -- 3.2 Classification of Proteins -- 3.2.1 Classification on the Basis of Shape and Structure -- 3.2.2 Classification on the Basis of Products of Hydrolysis -- 3.2.3 Classification on the Basis of Biological Functions -- 3.3 Properties of Proteins -- 3.3.1 Molecular Weight -- 3.3.2 Amphoteric Nature -- 3.3.3 Solubility -- 3.3.4 Precipitation -- 3.3.5 Denaturation -- 3.3.6 Colour Reactions -- 3.4 Structural Organisation of Proteins -- 3.4.1 Covalent or Primary Structure of Proteins -- 3.4.2 Conformational Aspects of Proteins: Higher Order Structures -- 4 Enzymes -- 4.1 Introduction -- 4.2 Nomenclature and Classification of Enzymes -- 4.2.1 Systematic and Recommended Names -- 4.2.2 Classification Numbers and Code Names -- 4.3 Characteristics of Enzymes -- 4.3.1 Catalytic Power -- 4.3.2 Enzyme Specificity -- 4.3.3 Enzyme Regulation -- 4.4 Mechanism of Enzyme Action -- 4.5 Factors Affecting Enzyme Action -- 4.6 Chymotrypsin: An Enzyme in Action -- 4.6.1 Structure of Chymotrypsin -- 4.6.2 Important Amino Acid Residues of Chymotrypsin -- 4.6.3 Mechanism of Action -- 4.7 Cofactors (or Coenzymes) -- 4.7.1 Nicotinamide Adenine Dinucleotide (NAD+) and Nicotinamide Adenine Dinucleotide Phosphate (NADP+) -- 4.7.2 UDP-Glucose -- 4.7.3 Flavin Mononucleotide (FMN) and Flavin Adenine Dinucleotide (FAD) -- 4.7.4 Thiamine Pyrophosphate (TPP) -- 4.7.5 Cocarboxylase -- 4.7.6 Pyridoxal-5-Phosphate -- 4.8 Enzymes in Organic Synthesis -- 4.8.1 Enzymatic Oxidations -- 4.8.2 Enzymatic Hydroxylation -- 4.8.3 Enzymatic Hydrolysis -- 4.8.4 Enzymatic Reductions -- 4.8.5 Enzymatic Isomerisations -- 4.8.6 Pharmaceutical Applications of Enzymes -- Suggested Readings -- Glossary -- Index.
Record Nr. UNINA-9910633936903321
Ahluwalia V. K.  
Cham, Switzerland : , : Springer, , [2022]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chemistry of organo-hybrids : synthesis and characterization of functional nano-objects / / edited by Bernadette Charleux, Laboratoire de Chimie, Catalyse, Polymeres et Procedes, Universite Claude Bernard, Lyon 1, Villeurbanne Cedex, France, Christophe Copéret, Department of Chemistry, ETH Zurich, Zurich, Switzerland, Emmanuel Lacóte, Laboratoire C2P2, CNRS--CPE Lyon--Universite de Lyon, Villeurbanne Cedex, France
Chemistry of organo-hybrids : synthesis and characterization of functional nano-objects / / edited by Bernadette Charleux, Laboratoire de Chimie, Catalyse, Polymeres et Procedes, Universite Claude Bernard, Lyon 1, Villeurbanne Cedex, France, Christophe Copéret, Department of Chemistry, ETH Zurich, Zurich, Switzerland, Emmanuel Lacóte, Laboratoire C2P2, CNRS--CPE Lyon--Universite de Lyon, Villeurbanne Cedex, France
Pubbl/distr/stampa Hoboken, New Jersey : , : John Wiley & Sons, Inc., , [2015]
Descrizione fisica 1 online resource (548 p.)
Disciplina 661/.0681
Soggetto topico Chemistry, Organic
Physical organic chemistry
Nanostructured materials
ISBN 1-118-87006-9
1-118-87005-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chemistry of Organo-Hybrids; Contents; Preface; Contributors; 1 Covalent Organic Functionalization and Characterization of Carbon Nanotubes; 1.1 Introduction; 1.2 Covalent Functionalization of Carbon Nanotubes with Organic Molecules; 1.2.1 Defect-Site Chemistry; 1.2.2 Halogenation; 1.2.3 Arylation; 1.2.4 Cycloaddition Reactions; 1.2.5 Radical Addition; 1.2.6 Nucleophilic and Electrophilic Additions; 1.2.7 Plasma Functionalization and Mechanochemical Treatment; 1.3 Characterization of Functionalized Carbon Nanotubes; 1.3.1 Spectroscopic Techniques; 1.3.2 Microscopic Techniques
1.3.3 Thermal Techniques1.4 Conclusion; References; 2 Functionalized Graphenes; 2.1 Starting Materials; 2.2 Characterization; 2.3 Functionalization; 2.3.1 Functionalization on the Carbon Framework; 2.3.2 Functionalization Involving an Oxygenated Function; 2.4 Conclusion; References; 3 Nanodiamonds: Emergence of Functionalized Diamondoids and Their Unique Applications; 3.1 Introduction; 3.2 Historical Background: From the Synthesis of Detonation Nanodiamond to the Isolation and Characterization of Higher Diamondoids; 3.2.1 Nanodiamond versus Diamondoids: The Case of Polymantanes
3.2.2 Synthesis of Polymantanes versus Extraction from the Geosphere3.2.3 Diamondoid Nomenclature and Characterization; 3.3 Functionalization of Adamantane, Diamantane, and Higher Diamondoids; 3.3.1 Diamondoid Halides; 3.3.2 Hydroxylated Diamondoids; 3.3.3 Metallated Nucleophilic Diamondoids; 3.3.4 Amino and Nitro Diamondoids and Their Derivatives; 3.3.5 Polyfunctionalized Diamondoids with Different Reactive Functionalities; 3.3.6 Alkyl-, Aryl-, Olefin-, Phosphine-, Cyano-, and Thiol-Substituted Diamondoids; 3.4 Organohybrids Built on Nanodiamond and Diamondoids and Their Applications
3.4.1 Biological Applications of Nanodiamond and Diamondoid-Based Hybrids3.4.2 Polymeric Diamondoid Materials; 3.4.3 Molecular Mechanics and Electronics Innovations from Diamond Nanoassembly; 3.4.4 Synthetic and Catalytic Applications Associated to Modified Diamondoids; Abbreviations; References; 4 Titania-Based Hybrid Materials: From Molecular Precursors To The Controlled Design of Hierarchical Hybrid Materials; 4.1 Introduction; 4.2 Overview of the Reactivity of Precursors and Consequences on Structures at Large scale of Titanium-Based OXO-Polymers
4.2.1 The Real Nature of the Precursor Ti(OR)44.2.2 Chemical Additives as Inhibitors of Condensation; 4.3 Main Chemical Routes for the Synthesis of Titania-Based Hybrid Materials; 4.3.1 Route A; 4.3.2 Route B; 4.3.3 Route C; 4.3.4 Route D; 4.4 Titania-Based Hybrid Mesostructured Materials; 4.4.1 Overview; 4.4.2 Evaporation-Induced Self-Assembly (EISA); 4.4.3 Hybrid O-I Titania-Based POMTFs; 4.5 Conclusion; References; 5 Functionalization of Zirconium Oxide Surfaces; 5.1 Introduction; 5.2 Why Zirconia-organic Hybrids?; 5.2.1 Mechanical Properties; 5.2.2 Chemical Properties
5.2.3 Optical and Electrical Properties
Record Nr. UNINA-9910132285503321
Hoboken, New Jersey : , : John Wiley & Sons, Inc., , [2015]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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