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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
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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 : , : Springer International Publishing : , : Imprint : 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 Food science
Chemistry, Organic
Food—Microbiology
Food Science
Organic Chemistry
Food Microbiology
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 : , : Springer International Publishing : , : Imprint : 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
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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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