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Advanced organic chemistry / Francis A. Carey, Richard J. Sundberg
Advanced organic chemistry / Francis A. Carey, Richard J. Sundberg
Autore Carey, Francis A.
Edizione [2nd ed.]
Pubbl/distr/stampa New York : Plenum Press, c1984
Descrizione fisica 2 v. : ill. ; 26 cm
Disciplina 547
Altri autori (Persone) Sundberg, Richard J.
Soggetto topico Chemistry, Organic
ISBN 0306410877
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Pt. A: Structure and mechanisms
Pt. B.: Reactions and synthesis
Record Nr. UNISALENTO-991003416959707536
Carey, Francis A.  
New York : Plenum Press, c1984
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Advanced organic chemistry : reactions, mechanisms, and structure / Jerry March
Advanced organic chemistry : reactions, mechanisms, and structure / Jerry March
Autore March, Jerry
Edizione [3rd ed.]
Pubbl/distr/stampa New York : John Wiley & Sons, c1985
Descrizione fisica xiii, 1346 p. : ill. ; 25 cm
Disciplina 547
Soggetto topico Chemistry, Organic
ISBN 0471888419
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991003417059707536
March, Jerry  
New York : John Wiley & Sons, c1985
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Advanced organic chemistry : reactions, mechanisms, and structure / Jerry March
Advanced organic chemistry : reactions, mechanisms, and structure / Jerry March
Autore March, Jerry
Edizione [2nd ed.]
Pubbl/distr/stampa New York : McGraw-Hill, c1977
Descrizione fisica xv, 1328 p. : ill. ; 24 cm
Disciplina 547
Collana McGraw-Hill series in advanced chemistry
Soggetto topico Chemistry, Organic
ISBN 0070402477
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991003417009707536
March, Jerry  
New York : McGraw-Hill, c1977
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Advanced organic chemistry [[electronic resource] /] / Deepa Sharma
Advanced organic chemistry [[electronic resource] /] / Deepa Sharma
Autore Sharma Deepa
Pubbl/distr/stampa Tunbridge Wells, : New Academic Science, c2012
Descrizione fisica xv, 456 p. : ill
Disciplina 547
Soggetto topico Chemistry, Organic
Chemistry
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910785887003321
Sharma Deepa  
Tunbridge Wells, : New Academic Science, c2012
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Advanced organic chemistry [[electronic resource] /] / Deepa Sharma
Advanced organic chemistry [[electronic resource] /] / Deepa Sharma
Autore Sharma Deepa
Edizione [1st ed.]
Pubbl/distr/stampa Tunbridge Wells, : New Academic Science, c2012
Descrizione fisica xv, 456 p. : ill
Disciplina 547
Soggetto topico Chemistry, Organic
Chemistry
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Preface -- Acknowledgements -- Contents -- Section-I Fundamentals of Organic Chemistry -- Chapter 1 Atomic Bonding -- 1.1 Introduction -- 1.2 Valence Bond Theory -- 1.3 Molecular Orbital Theory (MOT) -- 1.3.1 Formation of Bonding Molecular Orbital (Additive Overlapping of Two Atomic Orbitals) -- 1.3.2 Formation of Antibonding Molecular Orbital (ABMO)(Subtractive Overlapping of Two Atomic Orbitals) -- 1.3.3 Rules for Linear Combination of Atomic Orbitals -- 1.3.4 Rules for Filling up of Molecular Orbitals -- 1.3.5 MO Diagram -- 1.3.6 Bond Order or Bond Multiplicity -- 1.3.7 Difference between Atomic Orbitals and Molecular Orbitals -- 1.3.8 Similarities between Atomic Orbitals and Molecular Orbitals -- 1.4 VSEPR Theory -- 1.4.1 Postulates of VSEPR Theory -- 1.5 Metallic Crystal -- 1.5.1 Factors Favouring the Formation of Metallic Bond -- 1.5.2 Nature of Metallic Bond -- 1.5.3 Some of the Physical Properties of Metals and their Explanation on the Basis of Electron-gas Theory -- 1.6 Hydrogen Bond -- 1.6.1 What is Hydrogen Bond? -- 1.6.2 Types of Hydrogen Bonding -- 1.6.3 Nature and Formation of Hydrogen Bond -- 1.6.4 Conditions for the Formation of Hydrogen Bond -- 1.6.5 Strength of H-bond -- 1.6.6 Effect of Hydrogen Bonding on the Physical Properties of the Compounds Containing Hydrogen Bonds -- Chapter 2 Stereochemistry -- 2.1 Isomerism -- 2.1.1 Structural Isomerism -- 2.2 Stereoisomerism -- 2.2.1 General Terms Encountered in Stereochemistry or Causes of Optical Isomerism -- 2.3 Optical Isomerism and Chirality -- 2.3.1 Optical Activity -- 2.3.2 The Polarimeter -- 2.3.3 Calculation of Number of Optical Isomers -- 2.4 Compounds Containing More Than One Chiral Centres -- 2.5 Specific Configuration for Compounds Containing More than one Chiral Centre -- 2.6 Geometrical Isomerism or CIS-Trans Isomerism -- 2.7 Racemization.
2.8 Walden Inversion -- 2.9 To Assign 'E-Z' Configuration and 'R-S' Configuration on the Basis of Sequence Rule -- 2.10 Conversion of 3-Dimensional Structures to Fischer Projection Formula -- 2.11 Optically Active Compounds Without Chiral Centre -- 2.11.1 Chirality in Allenes -- 2.11.2 Chirality in Spirans -- 2.11.3 Chirality in Biphenyls -- 2.12 Conformational Analysis -- 2.12.1 Conformers of Ethane -- 2.12.2 Conformations of n-Butane -- 2.12.3 Conformations of 1,2-Dichloro Ethane -- Chapter 3 Reaction Intermediates and Factors Affecting Reactivity -- 3.1 Carbonium Ion or Carbocations -- 3.1.1 Classification of Carbonium Ions -- 3.1.2 Formation of Carbonium Ions -- 3.1.3 Order of Stability of Carbonium Ions -- 3.1.4 Structure of Carbonium Ion -- 3.2 Carbanions -- 3.2.1 Classification of Carbanions -- 3.2.2 Structure of Carbanions -- 3.2.3 Stability of Carbanions -- 3.2.4 Explanation for the Order of Stability of Carbanions -- 3.2.5 Properties of Carbanion -- 3.3 Free Radicals -- 3.3.1 Structure -- 3.3.2 Stability Order -- 3.3.3 Formation of Free Radicals -- 3.4 Carbenes -- 3.4.1 Structure of Carbenes -- 3.4.2 Carbenes as Reaction Intermediates -- 3.5 Nitrenes or Imidogens -- 3.6 Benzynes or Arynes -- 3.7 Factors Affecting Reactivity -- 3.8 Hyperconjugation -- 3.8.1 Theories of Hyperconjugation -- 3.8.2 Types of Hyperconjugation -- Section II Classification of Name Reactions on the Basis of Product Formed -- Chapter 1 Reactions Yielding Carbonyl Compounds -- 1.1 Aldol Condensation -- 1.2 Gattermann Synthesis -- 1.3 Rosenmund Reduction -- 1.4 Sommelet Reaction -- 1.5 Baker-Venkataraman Reaction -- 1.6 Carroll Rearrangement -- 1.7 NEF Reaction -- 1.8 Robinson Annulation -- 1.9 Friedel-Crafts Acylation -- 1.10 Mannich Reaction -- 1.11 Dieckmann Condensation -- Chapter 2 Reactions Yielding Alcohol/Hydroxy Carboxylic Acid/Phenols.
2.1 Meerwein-Ponndorf-Verley Reduction -- 2.2 Blanc Reaction (Blanc Chloromethylation) -- 2.3 Brown Hydroboration -- 2.4 Cannizzaro Reaction -- 2.5 Nozaki-Hiyama-Kishi Reaction -- 2.6 Oppenauer Oxidation -- 2.7 Grignard Reaction -- 2.8 Evans Aldol Reaction -- 2.9 Dienone-Phenol Rearrangement -- 2.10 Bamberger Rearrangement -- Chapter 3 Reactions Yielding Arenes -- 3.1 Friedel-Crafts Alkylation Reaction -- 3.2 Benzoin Condensation -- Chapter 4 Reactions Yielding Saturated and Unsaturated Hydrocarbons -- 4.1 Clemmensen Reduction -- 4.2 Wolff-Kishner Reduction -- 4.3 Kolbe Electrolytic Reaction -- 4.4 Chugaev Reaction -- 4.5 Cope Elimination Reaction -- 4.6 McMurry Coupling -- 4.7 Birch Reduction -- 4.8 Peterson Olefination -- 4.9 Shapiro Reaction -- 4.10 Hoffmann Elimination Reaction (Hoffmann Degradation) -- 4.11 Di-π Methane Rearrangement (Zimmerman Rearrangement) -- Chapter 5 Reactions Yielding Carboxylic Acids and Derivatives -- 5.1 Kolbe-Schmidt Reaction -- 5.2 Conjugated Carboxylic Acid: Knoevenagel Condensation -- 5.3 Perkin Reaction -- 5.4 Michael Reaction -- 5.5 Darzens Glycidic Ester Condensation -- 5.6 Stobbe Condensation -- 5.7 Yamaguchi Esterification -- 5.8 Reformatsky Reaction (Reformatskii Reaction) -- Chapter 6 Reactions Yielding Heterocyclic Compounds and Derivatives -- 6.1 Paterno-Buchi Reaction -- 6.2 Chichibabin Reaction (Amination of Nitrogen Heterocycles) -- 6.3 Bischler Napieralski Reaction -- 6.4 Fischer Indole Synthesis -- 6.5 Bartoli Reaction (Bartoli Indole Synthesis) -- 6.6 Hegedus Indole Synthesis -- Chapter 7 Reactions Yielding Halogen/Derivatives -- 7.1 Hydroboration -- 7.2 Wohl-Ziegler Bromination -- 7.3 Haloform Reaction -- 7.4 Hell-Volhard-Zelinsky Reaction -- Chapter 8 Miscellaneous Reactions -- 8.1 Wolff Rearrangement -- 8.2 Bucherer Reaction -- 8.3 Robinson-Gabriel Synthesis -- 8.4 Fishcer Oxazole Synthesis.
8.5 Smiles Rearrangement -- 8.6 Diazo Coupling (Diazo Compounds) -- 8.7 Claisen Ester Condensation -- 8.8 Sharpless Epoxidation (Epoxy Alcohol) -- 8.9 Chapmann Rearrangement -- 8.10 Overmann Rearrangement -- 8.11 Gabriel Synthesis -- 8.12 Diels-Alder Reaction -- 8.13 Ullmann Reaction -- Section III Rearrangements: Classification and Mechanism -- Chapter 1 Rearrangements Induced by Cationic or Electron Deficient Sites (Carbon) -- 1.1 Wagner-Meerwein Rearrangement -- 1.2 Pinacol Rearrangement -- 1.3 Tiffeneau-Demjanov Rearrangement -- 1.4 Allylic Rearrangement -- Chapter 2 Rearrangements to Electron Deficient Hetero Atom -- 2.1 Rearrangements to Cationic Oxygen -- 2.1.1 Baeyer-Villiger Oxidation -- 2.1.2 Darkin Rearrangement -- 2.2 Rearrangements to Electron Deficient Nitrogen -- 2.2.1 Beckmann Rearrangement -- 2.2.2 Hoffmann Rearrangement -- 2.2.3 Schmidt Rearrangement -- 2.2.4 Lossen Rearrangement -- 2.2.5 Curtius Rearrangement -- Chapter 3 Rearrangements to Acyl Carbenes -- 3.1 Criegee Rearrangement -- Chapter 4 Rearrangements Induced by Bases or Electron Rich Sites (Carbon) -- 4.1 Benzylic Acid Rearrangement -- 4.2 Wittig Rearrangement -- 4.3 Steven Rearrangement -- 4.4 Favorskii Rearrangement -- 4.5 Neber Rearrangement -- Chapter 5 Rearrangements Occurring by Addition-Elimination Mechanism -- 5.1 Payne Rearrangement -- 5.2 Grob Rearrangement/Grob Fragmentation -- 5.3 Sommelet Hauser Rearrangement -- Chapter 6 Rearrangements in Pericyclic Reactions -- 6.1 Cope Rearrangement -- 6.2 Claisen Rearrangement -- Chapter 7 Aromatic Rearrangements -- 7.1 Fries Rearrangement -- 7.2 Riemer-Tiemann Reaction -- 7.3 Benzidine Rearrangement -- Section IV Organic Reactions and Their Mechanisms -- Chapter 1 Substitution Reactions -- 1.1 Aliphatic Nucleophilic Substitution -- 1.2 Aromatic Nucleophilic Substitution -- 1.3 Electrophilic Aromatic Substitution.
1.4 Electrophilic Aliphatic Substitution -- 1.5 Free Radical Substitution Reaction -- 1.6 Neighbouring Group Participation -- Chapter 2 Elimination Reactions -- 2.1 Beta-Elimination Reactions-Bimolecular or E2 Elimination -- 2.2 Beta-Elimination Reactions-Unimolecular or E1 Elimination -- 2.3 E1cB Elimination Reaction-Conjugate Base Unimolecular Elimination -- 2.4 Internal Elimination (Ei) -- Chapter 3 Addition Reactions -- 3.1 Electrophilic Addition Reactions (Addition of Hydrogen Halides to Alkenes) -- Chapter 4 Pericyclic Reactions -- 4.1 Electrocyclic Reactions -- 4.2 Cycloadditions -- 4.3 Cheletropic Reactions -- 4.4 Sigmatropic Reactions or Rearrangements -- Appendix 1 Claisen and Cope Related Rearrangements -- Appendix 2 Claisen and Cope Related Rearrangements -- Index.
Record Nr. UNINA-9910817654703321
Sharma Deepa  
Tunbridge Wells, : New Academic Science, c2012
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Advanced organic chemistry of nucleic acids [[electronic resource] /] / Z. Shabarova, A. Bogdanov
Advanced organic chemistry of nucleic acids [[electronic resource] /] / Z. Shabarova, A. Bogdanov
Autore Shabarova Z (Zoe)
Pubbl/distr/stampa Weinheim ; ; New York, : VCH, c1994
Descrizione fisica 1 online resource (606 p.)
Disciplina 547.79
574.87328
Altri autori (Persone) BogdanovA (Alexey)
Soggetto topico Nucleic acids
Chemistry, Organic
Soggetto genere / forma Electronic books.
ISBN 1-281-75881-7
9786611758813
3-527-61593-8
3-527-61592-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Advanced Organic Chemistry of Nucleic Acids; Contents; 1 Structure of Nucleosides; 1.1 Introduction; 1.2 Pyrimidine and Purine Bases; 1.2.1 Pyrimidines; 1.2.2 Purines; 1.2.3 Nomenclature of Pyrimidines and Purines; 1.2.4 Abbreviations; 1.3 Carbohydrate Moieties of Nucleosides; 1.4 Bonding Between Carbohydrate Moiety and Heterocyclic Base; 1.4.1 Purine Nucleosides; 1.4.2 Pyrimidine Nucleosides; 1.5 Size of the Oxide Ring in the Sugar; 1.6 Configuration of the Glycoside (Anomeric) Center; 1.7 Nomenclature and Abridged Formulas of Nucleosides; 1.8 Minor Nucleosides; 1.9 Pseudouridine
1.10 Nucleoside Antibiotics1.10.1 Purine Nucleosides; 1.10.2 Pyrimidine Nucleosides; 1.11 Other Nucleosides; References; 2 Properties of Nucleosides; 2.1 Heterocyclic Bases; 2.1.1 General Concepts; 2.1.2 Tautomerism; 2.1.3 Reactions with Electrophilic Reagents; 2.1.4 Reactions with Nucleophilic Reagents; 2.1.5 Addition Reactions; 2.1.6 Reactions Involving Exocyclic Amino Groups; 2.2 Reactions at the Carbohydrate Moiety; 2.2.1 Substitution for Hydrogen Atoms in Hydroxyl Groups; 2.2.2 Oxidation; 2.3 Reactions Involving Heterocyclic Bases and the Carbohydrate Moiety
2.4 Stability of N-Glycosidic Bonds2.4.1 Effect of the Heterocyclic Base Species; 2.4.2 Effect of Substituents in the Carbohydrate Moiety; 2.4.3 Mechanism of Hydrolysis of N-Glycosidic Bonds; 2.5 Properties of Pseudouridine; References; 3 Structure of Nucleotides; 3.1 Introduction; 3.2 Nomenclature and Isomerism; 3.3 Structure of Nucleotides; 3.3.1 Nucleoside 5'-Phosphates; 3.3.2 Nucleoside 3'- and 2'-Phosphates; 3.3.3 Nucleoside Cyclic Phosphates; 3.3.4 Nucleoside 3'(2').5'-Diphosphates; 3.4 General Comments Regarding the Structure of Monomer Units in Nucleic Acids; References
4 Properties of Nucleotides4.1 Acid-Base Behavior; 4.1.1 Ionization of Bases; 4.1.2 Ionization of Hydroxyl Groups in Pentose; 4.1.3 Ionization of the Phosphate Group; 4.2 Formation of Derivatives with Metals; 4.3 Reactions at Heterocyclic Bases and Pentose; 4.4 Some Properties of the Phosphate Group (General Concepts); 4.4.1 Structure of the Phosphate Group and the Mechanism of Nucleophilic Substitution at the Phosphorus Atom; 4.4.2 Catalysis of Nucleophilic Substitution at the Phosphorus Atom; 4.4.3 Hydrolysis of Alkyl Phosphates; 4.4.4 Cyclic Phosphates; 4.4.5 B-Elimination Reactions
4.5 Reactions of Nucleotides Involving the Phosphate Group4.5.1 Chemical and Enzymatic Dephosphorylation; 4.5.2 Migration of the Phosphate Group; 4.5.3 Alkylation of the Phosphate Group; 4.5.4 Activation of the Phosphate Group in Nucleotides . Synthesis of Some Derivatives with Respect to the Phosphate Group; 4.5.5 Acylation of the Phosphate Group; 4.6 Properties of Nucleotide Derivatives with Substituents in the Phosphate Group; 4.6.1 Nucleoside Cyclic Phosphates; 4.6.2 Alkyl Esters of Nucleotides; 4.6.3 Mixed Anhydrides of Nucleotides; 4.6.4 Amides of Nucleotides
4.7 Hydrolysis of N-Glycosidic Bonds
Record Nr. UNINA-9910144008903321
Shabarova Z (Zoe)  
Weinheim ; ; New York, : VCH, c1994
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Advanced practical organic chemistry / J. Leonard, B. Lygo, G. Proctor
Advanced practical organic chemistry / J. Leonard, B. Lygo, G. Proctor
Autore Léonard, J.
Edizione [2nd ed.]
Pubbl/distr/stampa London ; New York : Blackie Academic & Professional, 1995
Descrizione fisica xiii, 298 p. : ill. ; 23 cm
Disciplina 547
Altri autori (Persone) Lygo, B.author
Proctor, G.
Soggetto topico Chemistry, Organic
ISBN 0751402001
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991003061169707536
Léonard, J.  
London ; New York : Blackie Academic & Professional, 1995
Materiale a stampa
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Agents of change : enzymes in milk and dairy products / / edited by Alan L. Kelly, Lotte Bach Larsen
Agents of change : enzymes in milk and dairy products / / edited by Alan L. Kelly, Lotte Bach Larsen
Edizione [1st ed. 2021.]
Pubbl/distr/stampa Cham, Switzerland : , : Springer, , [2021]
Descrizione fisica 1 online resource (VIII, 551 p. 57 illus., 35 illus. in color.)
Disciplina 910.5
Collana Food Engineering Series
Soggetto topico Chemistry, Organic
Enzymes
Food - Biotechnology
ISBN 3-030-55482-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1. Enzymology of Milk and Dairy Products: Overview -- 2. The plasmin system in milk and dairy products -- 3. Lysosomal and other indigenous non-plasmin proteases in bovine milk -- 4. Phosphatases in milk -- 5. Antimicrobial enzymes in milk, and their role in human milk -- 6. Enzymes associated with milk phospholipid membrane structures: Milk fat globule membranes and extracellular vesicles -- 7. Milk and other glycosidases -- 8. The enzymology of non-bovine milk -- 9. The enzymology of human milk -- 10. Lipases from milk and other sources -- 11. Heat-stable Microbial Peptidases Associated with the Microbiota of Raw Milk -- 12. The heat stability of indigenous and bacterial enzymes in milk -- 13. The role of proteases in the stability of UHT-treated Milk -- 14. Milk-clotting enzymes -- 15. Enzymology of cheese ripening -- 16. Enzyme modified cheese -- 17. Enzymatic Protein Cross-Linking in Dairy Science and Technology -- 18. The production of bioactive peptides from milk proteins -- 19. Reducing allergenicity by proteolysis -- 20. Final thoughts, future perspectives, and emerging enzymes. .
Record Nr. UNINA-9910483715903321
Cham, Switzerland : , : Springer, , [2021]
Materiale a stampa
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Agricultural and biological chemistry
Agricultural and biological chemistry
Pubbl/distr/stampa Tokyo, Japan, : Agricultural Chemical Society of Japan, 1961-1991
Descrizione fisica 1 online resource
Disciplina 574.192
Soggetto topico Biochemistry
Agricultural chemistry
Chemistry, Organic
Chemistry, Agricultural
biochemistry
Biochimie
Chimie agricole
Chimie organique
35.70 biochemistry: general
48.00 agricultural science: general
Biochemie
Landbouwkunde
Soggetto genere / forma Periodical
Internet resource
Periodicals.
ISSN 1881-1280
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910304558003321
Tokyo, Japan, : Agricultural Chemical Society of Japan, 1961-1991
Materiale a stampa
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Alicyclic Chemistry [[electronic resource] /] / by V.K. Ahluwalia, Renu Aggarwal
Alicyclic Chemistry [[electronic resource] /] / by V.K. Ahluwalia, Renu Aggarwal
Autore Ahluwalia V.K
Edizione [2nd ed. 2023.]
Pubbl/distr/stampa Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2023
Descrizione fisica 1 online resource (XIII, 222 p. 482 illus.)
Disciplina 541.39
Soggetto topico Reaction mechanisms (Chemistry)
Chemical structure
Chemistry, Organic
Reaction Mechanisms
Structure And Bonding
Organic Chemistry
ISBN 3-031-36068-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction -- Nomenclature of Cycloalkanes -- Synthesis of Cycloalkanes -- Properties of Cycloalkanes -- Chemistry of Small Rings -- Chemistry of Common Ring Compounds -- Chemistry of Medium Sized and Larger Rings -- Conformations of Cycloalkanes -- Cycloalkanes Containing an Heteroatom (Heterocyclic Compounds) -- Non-Benzenoid Aromatics -- Bridged Rings -- The Cage Molecules -- Tropones and Tropolones -- Fluxional Molecules -- Catenanes, Rotaxanes and Knots.
Record Nr. UNINA-9910734895103321
Ahluwalia V.K  
Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2023
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