Modern organic synthesis : an introduction / / George S. Zweifel, Michael H. Nantz, Peter Somfai |
Autore | Zweifel George S. |
Edizione | [Second edition.] |
Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2017 |
Descrizione fisica | 1 online resource (xiii, 390 pages) : illustrations |
Disciplina | 547/.2 |
Soggetto topico | Organic compounds - Synthesis |
ISBN |
1-119-08672-8
1-119-08676-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910809131603321 |
Zweifel George S. | ||
Hoboken, New Jersey : , : Wiley, , 2017 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Molecular encapsulation : organic reactions in constrained systems / / editors, Udo H. Brinker, Jean-Lue Mieusset |
Pubbl/distr/stampa | Chichester, England : , : Wiley, , 2010 |
Descrizione fisica | xix, 500 p |
Disciplina | 547/.2 |
Soggetto topico |
Nanochemistry
Microencapsulation |
Soggetto genere / forma | Electronic books. |
ISBN |
0-470-66487-8
9786613678744 1-280-76797-9 0-470-66488-6 1-119-95710-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910208843103321 |
Chichester, England : , : Wiley, , 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Molecular encapsulation : organic reactions in constrained systems / / editors, Udo H. Brinker, Jean-Lue Mieusset |
Pubbl/distr/stampa | Chichester, England : , : Wiley, , 2010 |
Descrizione fisica | xix, 500 p |
Disciplina | 547/.2 |
Soggetto topico |
Nanochemistry
Microencapsulation |
ISBN |
0-470-66487-8
9786613678744 1-280-76797-9 0-470-66488-6 1-119-95710-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Reaction control by molecular recognition-a survey from the photochemical perspective / Cheng Yang [and others] -- Cyclodextrins / Ronald Breslow -- Cyclodextrins as molecular reactors / Christopher J. Easton and Hideki Onagi -- Reactions mediated by cyclodextrins / Keiko Takahashi -- Reactions in zeolites / Stéphane Walspurger and Jean Sommer -- Chemistry in self-seembled nanoreactors / Jarl Ivar van der Vlugt [and others] -- Concave reagents / Ulrich Lüning -- Reactivity control by calixarenes / Luigi Mandolini, Roberta Cacciapaglia, and Stefano Di Stefano -- Reactions inside carcerands / Ralf Warmuth -- Encapsulation of reactive intermediates / Jean-Luc Mieusset and Udo H. Brinker -- Dye encapsulation / Jeremiah J. Gassensmith, Easwaran Arunkumar and Bradley D. Smith -- Organic cations in constrained systems / Werner Abraham and Lutz Grubert -- Proteins as host for enantioselective catalysis: artificial metalloenzymes based on the biotin-streptavidin technology / Jincheng Mao and Thomas R. Ward -- Chemical reactions with RNA and DNA enzymes / Andres Jäschke -- Reactions in supramolecular systems / Lucia Zakharova [and others] -- Encapsulation processes by bilayer vesicles / Marc C.A. Stuart and Jan B.F.N. Engberts -- Reactions in liposomes / Pasquale Stano and Pier Luigi Luisi. |
Record Nr. | UNINA-9910829875003321 |
Chichester, England : , : Wiley, , 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Molecular orbitals and organic chemical reactions [[electronic resource] /] / Ian Fleming |
Autore | Fleming Ian <1935-> |
Edizione | [Reference ed.] |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2010 |
Descrizione fisica | 1 online resource (529 p.) |
Disciplina |
541.28
547/.2 |
Soggetto topico |
Molecular orbitals
Chemical bonds Physical organic chemistry |
ISBN |
1-119-96467-9
1-282-55013-6 9786612550133 0-470-68949-8 0-470-68950-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
CONTENTS; Preface; 1 Molecular Orbital Theory; 1.1 The Atomic Orbitals of a Hydrogen Atom; 1.2 Molecules Made from Hydrogen Atoms; 1.3 C-H and C-C Bonds; 1.4 Conjugation-Hückel Theory; 1.5 Aromaticity; 1.6 Strained Bonds-Cyclopropanes and Cyclobutanes; 1.7 Heteronuclear Bonds, C-M, C-X and C=O; 1.8 The Tau Bond Model; 1.9 Spectroscopic Methods; 2 Molecular Orbitals and the Structures of Organic Molecules; 2.1 The Effects of Conjugation; 2.2 Hyperconjugation- Conjugation; 2.3 The Configurations and Conformations of Molecules; 2.4 The Effect of Conjugation on Electron Distribution
2.5 Other Noncovalent Interactions3 Chemical Reactions-How Far and How Fast; 3.1 Factors Affecting the Position of an Equilibrium; 3.2 The Principle of Hard and Soft Acids and Bases (HSAB); 3.3 Transition Structures; 3.4 The Perturbation Theory of Reactivity; 3.5 The Salem-Klopman Equation; 3.6 Hard and Soft Nucleophiles and Electrophiles; 3.7 Other Factors Affecting Chemical Reactivity; 4 Ionic Reactions-Reactivity; 4.1 Single Electron Transfer (SET) in Ionic Reactions; 4.2 Nucleophilicity; 4.3 Ambident Nucleophiles; 4.4 Electrophilicity; 4.5 Ambident Electrophiles; 4.6 Carbenes 5 Ionic Reactions-Stereochemistry5.1 The Stereochemistry of the FundamentalOrganic Reactions; 5.2 Diastereoselectivity; 6 Thermal Pericyclic Reactions; 6.1 The Four Classes of Pericyclic Reactions; 6.2 Evidence for the Concertedness of Bond Makingand Breaking; 6.3 Symmetry-allowed and Symmetry-forbidden Reactions; 6.4 Explanations for the Woodward-Hoffmann Rules; 6.5 Secondary Effects; 7 Radical Reactions; 7.1 Nucleophilic and Electrophilic Radicals; 7.2 The Abstraction of Hydrogen and Halogen Atoms; 7.3 The Addition of Radicals to Bonds 7.4 Synthetic Applications of the Chemoselectivity of Radicals7.5 Stereochemistry in some Radical Reactions; 7.6 Ambident Radicals; 7.7 Radical Coupling; 8 Photochemical Reactions; 8.1 Photochemical Reactions in General; 8.2 Photochemical Ionic Reactions; 8.3 Photochemical Pericyclic Reactions and Related Stepwise Reactions; 8.4 Photochemically Induced Radical Reactions; 8.5 Chemiluminescence; References; Index |
Record Nr. | UNINA-9910139364603321 |
Fleming Ian <1935-> | ||
Hoboken, N.J., : Wiley, 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Molecular rearrangements in organic synthesis / / edited by Christian M. Rojas ; contributors, Laura L. Anderson [and thirty-six others] |
Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2015 |
Descrizione fisica | 1 online resource (955 p.) |
Disciplina | 547/.2 |
Soggetto topico |
Rearrangements (Chemistry)
Organic compounds - Synthesis |
ISBN |
1-118-93988-3
1-118-93989-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | 1,2-migrations. Pinacol and semi-pinacol rearrangements in total synthesis -- Baeyer-Villiger (BV) oxidation/rearrangement in organic synthesis -- The Wolff rearrangement : tactics, strategies and recent applications in organic synthesis -- Alkyl and acyl azide rearrangements -- Beckmann rearrangements and fragmentations in organic synthesis -- Brook rearrangement. 1,2-migrations via three-membered rings. The quasi-favorskii rearrangement -- The Ramberg-Backlund reaction -- Applications of di-pi-methane and related rearrangement reactions in chemical synthesis. 1,3-transpositions. Payne rearrangement -- Vinylcyclopropane-cyclopentene rearrangement -- Ferrier carbocyclization reaction. [3,3]- and [2,3]-sigmatropic rearrangements. The Claisen rearrangement -- [3,3]-sigmatropic rearrangements with heteroatom-heteroatom bonds -- [2,3]-rearrangements of ammonium zwitterions -- Oxonium ylide rearrangements in synthesis -- The [2,3]-Wittig rearrangement -- The Mislow-Evans rearrangement. Ipso rearrangements. Smiles rearrangements -- Pummerer-type reactions as powerful tools in organic synthesis. |
Record Nr. | UNINA-9910208950703321 |
Hoboken, New Jersey : , : Wiley, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Molecular rearrangements in organic synthesis / / edited by Christian M. Rojas ; contributors, Laura L. Anderson [and thirty-six others] |
Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2015 |
Descrizione fisica | 1 online resource (955 p.) |
Disciplina | 547/.2 |
Soggetto topico |
Rearrangements (Chemistry)
Organic compounds - Synthesis |
ISBN |
1-118-93988-3
1-118-93989-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | 1,2-migrations. Pinacol and semi-pinacol rearrangements in total synthesis -- Baeyer-Villiger (BV) oxidation/rearrangement in organic synthesis -- The Wolff rearrangement : tactics, strategies and recent applications in organic synthesis -- Alkyl and acyl azide rearrangements -- Beckmann rearrangements and fragmentations in organic synthesis -- Brook rearrangement. 1,2-migrations via three-membered rings. The quasi-favorskii rearrangement -- The Ramberg-Backlund reaction -- Applications of di-pi-methane and related rearrangement reactions in chemical synthesis. 1,3-transpositions. Payne rearrangement -- Vinylcyclopropane-cyclopentene rearrangement -- Ferrier carbocyclization reaction. [3,3]- and [2,3]-sigmatropic rearrangements. The Claisen rearrangement -- [3,3]-sigmatropic rearrangements with heteroatom-heteroatom bonds -- [2,3]-rearrangements of ammonium zwitterions -- Oxonium ylide rearrangements in synthesis -- The [2,3]-Wittig rearrangement -- The Mislow-Evans rearrangement. Ipso rearrangements. Smiles rearrangements -- Pummerer-type reactions as powerful tools in organic synthesis. |
Record Nr. | UNINA-9910815830603321 |
Hoboken, New Jersey : , : Wiley, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Multicomponent reactions : concepts and applications for design and synthesis / / edited by Raquel P. Herrera, Eugenia Marques-Lopez ; contributors Juan V. Alegre-Requena [and seventeen others] |
Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2015 |
Descrizione fisica | 1 online resource (526 p.) |
Disciplina | 547/.2 |
Soggetto topico |
Chemical reactions
Catalysis Chemistry, Organic |
ISBN |
1-118-86397-6
1-118-86400-X 1-118-86399-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
""Title Page""; ""Copyright Page""; ""Contents""; ""List of Contributors""; ""Preface""; ""List of Abbreviations""; ""Chapter 1 Introduction: Multi-component Strategies""; ""General Introduction""; ""1.1 Basic Concepts""; ""1.1.1 Clarifying Terminology: One-Pot, Domino/Cascade, Tandem, and MCRs""; ""1.1.2 Using Rational Design to Discover New MCRs""; ""1.1.3 Discovering New MCRs with Automated Combinatorial Reaction Finding""; ""1.1.4 Computational and Analytical Tools to Study MCRs""; ""1.1.5 Diversity-Oriented Synthesis and Biology-Oriented Synthesis""; ""1.1.6 Optimization of MCRs""
""1.2 Catalysis in MCRs and Various Synthetic Approaches""""1.2.1 Organocatalysis in MCRs""; ""1.2.2 Organometallic Catalysis in MCRs""; ""1.2.3 Biocatalysis in MCRs""; ""1.2.4 Combining Different Types of Catalysis""; ""1.2.5 Other Methods""; ""1.3 Green Chemistry""; ""1.3.1 Atom Economy""; ""1.3.2 Using Green Solvents""; ""1.3.3 Solventless MCRs""; ""1.3.4 Heterogeneous Catalysis in MCRs""; ""1.4 Importance and Evolution""; ""References""; ""Chapter 2 Organocatalytic Asymmetric Multicomponent Reactions""; ""2.1 Introduction""; ""2.2 Three-Component Mannich Reaction"" ""2.3 Cycloaddition Reaction""""2.4 Organocatalytic Multicomponent Domino Asymmetric Reactions""; ""2.4.1 Michael-Type Multicomponent Process: Cyclic Carbon Frameworks""; ""2.4.2 Miscellaneous Domino Reactions""; ""2.5 Development of Drug Intermediates""; ""2.6 Miscellaneous Reaction""; ""2.7 Conclusions""; ""References""; ""Chapter 3 Metal-Catalyzed Multicomponent Reactions""; ""3.1 Introduction""; ""3.2 Palladium-Catalyzed MCRs""; ""3.2.1 Palladium-Catalyzed Carbonylation Reactions""; ""3.2.2 Palladium-Catalyzed MCRs Involving Isocyanides"" ""3.2.3 Carbopalladation of Unsaturated C�C π-Components""""3.2.4 Amines as Building Blocks""; ""3.3 Nickel-Catalyzed MCRs""; ""3.3.1 Nickel-Catalyzed Cross-Trimerization of Alkynes""; ""3.3.2 Nickel-Catalyzed π-Systems Couplings""; ""3.3.3 Ni-Catalyzed Reductive Conjugate Addition""; ""3.4 Group 11 Metal-Catalyzed MCRs""; ""3.4.1 Copper-Catalyzed Azide Alkyne Cycloaddition""; ""3.4.2 A3-Coupling""; ""3.4.3 Miscellaneous""; ""3.5 Rhodium-Catalyzed MCRs""; ""3.5.1 Rhodium-Catalyzed Mcrs via Onium Ylide Intermediates""; ""3.5.2 Rhodium-Catalyzed Three-Component Cross-Addition Reactions"" ""3.6 Group 8 Metal-Catalyzed MCRs""""3.6.1 Iron-Catalyzed MCRs""; ""3.6.2 Ruthenium-Catalyzed MCRs""; ""3.7 Conclusions""; ""References""; ""Chapter 4 Multicomponent Reactions with Organoboron Compounds""; ""4.1 Introduction""; ""4.2 Catalytic MCRs with Organoboron Compounds""; ""4.2.1 Cobalt-Catalyzed MCRs Containing Organoboron Compounds""; ""4.2.2 Palladium-Catalyzed MCRs Containing Organoboron Compounds""; ""4.3 Multicomponent Assembly of Organoboron Compounds: Efficient Approach to Supramolecular Chemistry""; ""4.4 Multicomponent Petasis-Borono Mannich Reaction"" ""4.4.1 Organocatalytic Enantioselective Petasis-Type Reaction"" |
Record Nr. | UNINA-9910131297203321 |
Hoboken, New Jersey : , : Wiley, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Multicomponent reactions : concepts and applications for design and synthesis / / edited by Raquel P. Herrera, Eugenia Marques-Lopez ; contributors Juan V. Alegre-Requena [and seventeen others] |
Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2015 |
Descrizione fisica | 1 online resource (526 p.) |
Disciplina | 547/.2 |
Soggetto topico |
Chemical reactions
Catalysis Chemistry, Organic |
ISBN |
1-118-86397-6
1-118-86400-X 1-118-86399-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
""Title Page""; ""Copyright Page""; ""Contents""; ""List of Contributors""; ""Preface""; ""List of Abbreviations""; ""Chapter 1 Introduction: Multi-component Strategies""; ""General Introduction""; ""1.1 Basic Concepts""; ""1.1.1 Clarifying Terminology: One-Pot, Domino/Cascade, Tandem, and MCRs""; ""1.1.2 Using Rational Design to Discover New MCRs""; ""1.1.3 Discovering New MCRs with Automated Combinatorial Reaction Finding""; ""1.1.4 Computational and Analytical Tools to Study MCRs""; ""1.1.5 Diversity-Oriented Synthesis and Biology-Oriented Synthesis""; ""1.1.6 Optimization of MCRs""
""1.2 Catalysis in MCRs and Various Synthetic Approaches""""1.2.1 Organocatalysis in MCRs""; ""1.2.2 Organometallic Catalysis in MCRs""; ""1.2.3 Biocatalysis in MCRs""; ""1.2.4 Combining Different Types of Catalysis""; ""1.2.5 Other Methods""; ""1.3 Green Chemistry""; ""1.3.1 Atom Economy""; ""1.3.2 Using Green Solvents""; ""1.3.3 Solventless MCRs""; ""1.3.4 Heterogeneous Catalysis in MCRs""; ""1.4 Importance and Evolution""; ""References""; ""Chapter 2 Organocatalytic Asymmetric Multicomponent Reactions""; ""2.1 Introduction""; ""2.2 Three-Component Mannich Reaction"" ""2.3 Cycloaddition Reaction""""2.4 Organocatalytic Multicomponent Domino Asymmetric Reactions""; ""2.4.1 Michael-Type Multicomponent Process: Cyclic Carbon Frameworks""; ""2.4.2 Miscellaneous Domino Reactions""; ""2.5 Development of Drug Intermediates""; ""2.6 Miscellaneous Reaction""; ""2.7 Conclusions""; ""References""; ""Chapter 3 Metal-Catalyzed Multicomponent Reactions""; ""3.1 Introduction""; ""3.2 Palladium-Catalyzed MCRs""; ""3.2.1 Palladium-Catalyzed Carbonylation Reactions""; ""3.2.2 Palladium-Catalyzed MCRs Involving Isocyanides"" ""3.2.3 Carbopalladation of Unsaturated C�C π-Components""""3.2.4 Amines as Building Blocks""; ""3.3 Nickel-Catalyzed MCRs""; ""3.3.1 Nickel-Catalyzed Cross-Trimerization of Alkynes""; ""3.3.2 Nickel-Catalyzed π-Systems Couplings""; ""3.3.3 Ni-Catalyzed Reductive Conjugate Addition""; ""3.4 Group 11 Metal-Catalyzed MCRs""; ""3.4.1 Copper-Catalyzed Azide Alkyne Cycloaddition""; ""3.4.2 A3-Coupling""; ""3.4.3 Miscellaneous""; ""3.5 Rhodium-Catalyzed MCRs""; ""3.5.1 Rhodium-Catalyzed Mcrs via Onium Ylide Intermediates""; ""3.5.2 Rhodium-Catalyzed Three-Component Cross-Addition Reactions"" ""3.6 Group 8 Metal-Catalyzed MCRs""""3.6.1 Iron-Catalyzed MCRs""; ""3.6.2 Ruthenium-Catalyzed MCRs""; ""3.7 Conclusions""; ""References""; ""Chapter 4 Multicomponent Reactions with Organoboron Compounds""; ""4.1 Introduction""; ""4.2 Catalytic MCRs with Organoboron Compounds""; ""4.2.1 Cobalt-Catalyzed MCRs Containing Organoboron Compounds""; ""4.2.2 Palladium-Catalyzed MCRs Containing Organoboron Compounds""; ""4.3 Multicomponent Assembly of Organoboron Compounds: Efficient Approach to Supramolecular Chemistry""; ""4.4 Multicomponent Petasis-Borono Mannich Reaction"" ""4.4.1 Organocatalytic Enantioselective Petasis-Type Reaction"" |
Record Nr. | UNINA-9910819294303321 |
Hoboken, New Jersey : , : Wiley, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Name reactions for carbocyclic ring formations [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2010 |
Descrizione fisica | 1 online resource (774 p.) |
Disciplina | 547/.2 |
Altri autori (Persone) |
LiJie Jack
CoreyE. J |
Collana | Wiley series on comprehensive name reactions |
Soggetto topico | Ring formation (Chemistry) |
ISBN |
1-299-31411-2
0-470-87221-7 0-470-87220-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Name Reactions for Carbocyclic Ring Formations; Contents; Foreword; Preface; Contributing Authors; Chapter 1 Three-Membered Carbocycles; 1.1 Freund Reaction; 1.2 Kishner Cyclopropane Synthesis; 1.3 Kulinovich Cyclopropanol Synthesis; 1.4 Simmons-Smith Cyclopropanation; Chapter 2 Four-Membered Carbocycles; 2.1 Staudinger Ketene Cycloaddition; Chapter 3 Five-Membered Carbocycles; 3.1 Danheiser Annulation; 3.2 Dieckmann Condensation; 3.3 Favorskii Rearrangement; 3.4 Nazarov Cyclization; 3.5 Pauson-Khand Reaction; 3.6 Weiss-Cook Reaction; Chapter 4 Six-Membered Carbocycles
4.1 Bardhan-Sengupta Pheantherene Synthesis4.2 Bergman Cyclization; 4.3 Bogert-Cook Reaction; 4.4 Bradsher Cycloaddition and Bradsher Reaction; 4.5 Bradsher Reaction; 4.6 Darzens Synthesis of Tetralin Derivatives; 4.7 Diels-Alder Reaction; 4.8 Dötz Benzannulation; 4.9 Elbs Reaction; 4.10 Fujimoto-Belleau Reaction; 4.11 Haworth Reaction; 4.12 Moore Cyclization; 4.13 Myers-Saito Cyclization; 4.14 Robinson Annulation; 4.15 Scholl Reaction; Chapter 5 Large-Ring Carbocycles; 5.1 Buchner Reaction; 5.2 de Mayo Reaction; 5.3 Ring-closing Metathesis (RCM); 5.4 Thorpe-Ziegler Reaction Chapter 6 Transformations of Carbocycles 6.1 Blanc Chloromethylation Reaction; 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present; 6.3 Houben-Hoesch Reaction; 6.4 Kolbe-Schmitt Reaction; 6.5 Vilsmeier-Haack Reaction; 6.6 von Richter Reaction; Appendices; 1, Contents Volume 1: Name Reactions in Heterocyclic Chemistry; 2, Contents Volume 2: Name Reactions for Functional Group Transformations; 3, Contents Volume 3: Name Reactions for Homologations-Part I; 4, Contents Volume 4: Name Reactions for Homologations-Part II; 5, Contents Volume 6: Name Reactions in Heterocyclic Chemistry-Part II Subject Index |
Record Nr. | UNINA-9910140873403321 |
Hoboken, N.J., : Wiley, c2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Name reactions for carbocyclic ring formations [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2010 |
Descrizione fisica | 1 online resource (774 p.) |
Disciplina | 547/.2 |
Altri autori (Persone) |
LiJie Jack
CoreyE. J |
Collana | Wiley series on comprehensive name reactions |
Soggetto topico | Ring formation (Chemistry) |
ISBN |
1-299-31411-2
0-470-87221-7 0-470-87220-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Name Reactions for Carbocyclic Ring Formations; Contents; Foreword; Preface; Contributing Authors; Chapter 1 Three-Membered Carbocycles; 1.1 Freund Reaction; 1.2 Kishner Cyclopropane Synthesis; 1.3 Kulinovich Cyclopropanol Synthesis; 1.4 Simmons-Smith Cyclopropanation; Chapter 2 Four-Membered Carbocycles; 2.1 Staudinger Ketene Cycloaddition; Chapter 3 Five-Membered Carbocycles; 3.1 Danheiser Annulation; 3.2 Dieckmann Condensation; 3.3 Favorskii Rearrangement; 3.4 Nazarov Cyclization; 3.5 Pauson-Khand Reaction; 3.6 Weiss-Cook Reaction; Chapter 4 Six-Membered Carbocycles
4.1 Bardhan-Sengupta Pheantherene Synthesis4.2 Bergman Cyclization; 4.3 Bogert-Cook Reaction; 4.4 Bradsher Cycloaddition and Bradsher Reaction; 4.5 Bradsher Reaction; 4.6 Darzens Synthesis of Tetralin Derivatives; 4.7 Diels-Alder Reaction; 4.8 Dötz Benzannulation; 4.9 Elbs Reaction; 4.10 Fujimoto-Belleau Reaction; 4.11 Haworth Reaction; 4.12 Moore Cyclization; 4.13 Myers-Saito Cyclization; 4.14 Robinson Annulation; 4.15 Scholl Reaction; Chapter 5 Large-Ring Carbocycles; 5.1 Buchner Reaction; 5.2 de Mayo Reaction; 5.3 Ring-closing Metathesis (RCM); 5.4 Thorpe-Ziegler Reaction Chapter 6 Transformations of Carbocycles 6.1 Blanc Chloromethylation Reaction; 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present; 6.3 Houben-Hoesch Reaction; 6.4 Kolbe-Schmitt Reaction; 6.5 Vilsmeier-Haack Reaction; 6.6 von Richter Reaction; Appendices; 1, Contents Volume 1: Name Reactions in Heterocyclic Chemistry; 2, Contents Volume 2: Name Reactions for Functional Group Transformations; 3, Contents Volume 3: Name Reactions for Homologations-Part I; 4, Contents Volume 4: Name Reactions for Homologations-Part II; 5, Contents Volume 6: Name Reactions in Heterocyclic Chemistry-Part II Subject Index |
Record Nr. | UNINA-9910820978603321 |
Hoboken, N.J., : Wiley, c2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|