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Flash chemistry [[electronic resource] ] : fast organic synthesis in microsystems / / Jun-ichi Yoshida
| Flash chemistry [[electronic resource] ] : fast organic synthesis in microsystems / / Jun-ichi Yoshida |
| Autore | Yoshida Junʼichi <1952-> |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2008 |
| Descrizione fisica | 1 online resource (248 p.) |
| Disciplina |
547.2
547/.2 |
| Soggetto topico |
Organic compounds - Synthesis
Intermediates (Chemistry) Microreactors Organic reaction mechanisms |
| ISBN |
1-281-94011-9
9786611940119 0-470-72342-4 0-470-72341-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Flash Chemistry Fast Organic Synthesis in Microsystems; Contents; Preface; 1 Introduction; 1.1 Flask Chemistry; 1.2 Flash Chemistry; 1.3 Flask Chemistry or Flash Chemistry; References; 2 The Background to Flash Chemistry; 2.1 How do Chemical Reactions Take Place?; 2.1.1 Macroscopic View of Chemical Reactions; 2.1.2 Thermodynamic Equilibrium and Kinetics; 2.1.3 Kinetics; 2.1.4 Transition State Theory; 2.1.5 Femtosecond Chemistry and Reaction Dynamics; 2.1.6 Reactions for Dynamics and Reactions for Synthesis; 2.1.7 Bimolecular Reactions in the Gas Phase
2.1.8 Bimolecular Reactions in the Solution Phase2.1.9 Fast Chemical Synthesis Inspired by Reaction Dynamics; References; 3 What is Flash Chemistry?; 4 Why is Flash Chemistry Needed?; 4.1 Chemical Reaction, an Extremely Fast Process at Molecular Level; 4.2 Rapid Construction of Chemical Libraries; 4.3 Rapid Synthesis of Radioactive Positron Emission Tomography Probes; 4.4 On-demand Rapid Synthesis i n Industry 304.5 Conclusions; References; 5 Methods of Activating Molecules; 5.1 Thermal Activation of Organic Molecules; 5.1.1 High Temperature Reactions; 5.1.2 Flash Vacuum Pyrolysis 5.1.3 Microwave Reactions5.2 Photochemical Activation; 5.3 Electrochemical Activation; 5.4 Chemical Activation; 5.5 Accumulation of Reactive Species; 5.5.1 The Cation-pool Method; 5.6 Continuous Generation of Reactive Species in a Flow System; 5.7 Interconversion Between Reactive Species; 5.8 Conclusions; References; 6 Control of Extremely Fast Reactions; 6.1 Mixing; 6.1.1 How Does Mixing Take Place?; 6.1.2 Molecular Diffusion and Brownian Motion; 6.1.3 Disguised Chemical Selectivity; 6.1.4 Lowering the Reaction Temperature; 6.1.5 The High Dilution Method; 6.1.6 Micromixing 6.1.7 Friedel-Crafts Alkylation Using anN-acyliminium Ion Pool6.1.8 Micromixing as a Powerful Tool for Flash Chemistry; 6.1.9 Disguised Chemical Selectivity in Competitive Parallel Reactions; 6.2 Temperature Control; 6.2.1 Exothermicity of Fast Reactions; 6.2.2 Hammond's Postulate; 6.2.3 The Friedel-Crafts Reaction; 6.2.4 Solvent; 6.2.5 Heat Transfer; 6.2.6 Precise Temperature Control in Microflow Systems; 6.3 Residence Time Control; 6.3.1 The Discovery of Benzyne. The Concept of Reactive Intermediates; 6.3.2 o -Bromophenyllithi um; 6.4 Conclusions; References 7 Microfluidic Devices and Microflow Systems7.1 Brief History; 7.1.1 Microflow Systems for Chemical Analysis; 7.1.2 Microflow Systems for Chemical Synthesis; 7.2 Characteristic Features of Microflow Systems; 7.3 Microstructured Fluidic Devices; 7.3.1 Microchip Reactors; 7.3.2 Microtube Reactors; 7.3.3 Micromixer; 7.3.4 Passive Micromixers; 7.3.5 Microheat Exchanger; 7.3.6 Photochemical Microflow Reactor; 7.3.7 Electrochemical Microflow Reactor; 7.3.8 Catalyst-containing Microflow Reactor; 7.3.9 Microflow Reactors for High-pressure and High-temperature Conditions; 7.4 Conclusions; References 8 Applications of Flash Chemistry in Organic Synthesis |
| Record Nr. | UNINA-9910830745903321 |
Yoshida Junʼichi <1952->
|
||
| Hoboken, N.J., : Wiley, 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Flash chemistry [[electronic resource] ] : fast organic synthesis in microsystems / / Jun-ichi Yoshida
| Flash chemistry [[electronic resource] ] : fast organic synthesis in microsystems / / Jun-ichi Yoshida |
| Autore | Yoshida Junʼichi <1952-> |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2008 |
| Descrizione fisica | 1 online resource (248 p.) |
| Disciplina |
547.2
547/.2 |
| Soggetto topico |
Organic compounds - Synthesis
Intermediates (Chemistry) Microreactors Organic reaction mechanisms |
| ISBN |
1-281-94011-9
9786611940119 0-470-72342-4 0-470-72341-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Flash Chemistry Fast Organic Synthesis in Microsystems; Contents; Preface; 1 Introduction; 1.1 Flask Chemistry; 1.2 Flash Chemistry; 1.3 Flask Chemistry or Flash Chemistry; References; 2 The Background to Flash Chemistry; 2.1 How do Chemical Reactions Take Place?; 2.1.1 Macroscopic View of Chemical Reactions; 2.1.2 Thermodynamic Equilibrium and Kinetics; 2.1.3 Kinetics; 2.1.4 Transition State Theory; 2.1.5 Femtosecond Chemistry and Reaction Dynamics; 2.1.6 Reactions for Dynamics and Reactions for Synthesis; 2.1.7 Bimolecular Reactions in the Gas Phase
2.1.8 Bimolecular Reactions in the Solution Phase2.1.9 Fast Chemical Synthesis Inspired by Reaction Dynamics; References; 3 What is Flash Chemistry?; 4 Why is Flash Chemistry Needed?; 4.1 Chemical Reaction, an Extremely Fast Process at Molecular Level; 4.2 Rapid Construction of Chemical Libraries; 4.3 Rapid Synthesis of Radioactive Positron Emission Tomography Probes; 4.4 On-demand Rapid Synthesis i n Industry 304.5 Conclusions; References; 5 Methods of Activating Molecules; 5.1 Thermal Activation of Organic Molecules; 5.1.1 High Temperature Reactions; 5.1.2 Flash Vacuum Pyrolysis 5.1.3 Microwave Reactions5.2 Photochemical Activation; 5.3 Electrochemical Activation; 5.4 Chemical Activation; 5.5 Accumulation of Reactive Species; 5.5.1 The Cation-pool Method; 5.6 Continuous Generation of Reactive Species in a Flow System; 5.7 Interconversion Between Reactive Species; 5.8 Conclusions; References; 6 Control of Extremely Fast Reactions; 6.1 Mixing; 6.1.1 How Does Mixing Take Place?; 6.1.2 Molecular Diffusion and Brownian Motion; 6.1.3 Disguised Chemical Selectivity; 6.1.4 Lowering the Reaction Temperature; 6.1.5 The High Dilution Method; 6.1.6 Micromixing 6.1.7 Friedel-Crafts Alkylation Using anN-acyliminium Ion Pool6.1.8 Micromixing as a Powerful Tool for Flash Chemistry; 6.1.9 Disguised Chemical Selectivity in Competitive Parallel Reactions; 6.2 Temperature Control; 6.2.1 Exothermicity of Fast Reactions; 6.2.2 Hammond's Postulate; 6.2.3 The Friedel-Crafts Reaction; 6.2.4 Solvent; 6.2.5 Heat Transfer; 6.2.6 Precise Temperature Control in Microflow Systems; 6.3 Residence Time Control; 6.3.1 The Discovery of Benzyne. The Concept of Reactive Intermediates; 6.3.2 o -Bromophenyllithi um; 6.4 Conclusions; References 7 Microfluidic Devices and Microflow Systems7.1 Brief History; 7.1.1 Microflow Systems for Chemical Analysis; 7.1.2 Microflow Systems for Chemical Synthesis; 7.2 Characteristic Features of Microflow Systems; 7.3 Microstructured Fluidic Devices; 7.3.1 Microchip Reactors; 7.3.2 Microtube Reactors; 7.3.3 Micromixer; 7.3.4 Passive Micromixers; 7.3.5 Microheat Exchanger; 7.3.6 Photochemical Microflow Reactor; 7.3.7 Electrochemical Microflow Reactor; 7.3.8 Catalyst-containing Microflow Reactor; 7.3.9 Microflow Reactors for High-pressure and High-temperature Conditions; 7.4 Conclusions; References 8 Applications of Flash Chemistry in Organic Synthesis |
| Record Nr. | UNINA-9910841300003321 |
|
Yoshida Junʼichi <1952->
|
||
| Hoboken, N.J., : Wiley, 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green chemistry [[electronic resource] ] : microwave synthesis / / K.R. Desai ; foreword by V.R. Kanetkar
| Green chemistry [[electronic resource] ] : microwave synthesis / / K.R. Desai ; foreword by V.R. Kanetkar |
| Autore | Desai K. R |
| Edizione | [Rev. ed.] |
| Pubbl/distr/stampa | Mumbai [India], : Himalaya Pub. House, 2010 |
| Descrizione fisica | 1 online resource (138 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) | KanetkarV. R |
| Soggetto topico |
Organic compounds - Synthesis
Microwaves Microwave heating |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-81186-X
9786612811869 1-4416-6206-5 93-5043-184-X 600-00-2822-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | COVER; CONTENTS; CHAPTER 1 :MICROWAVE SYNTHESIS; CHAPTER 2 :MICROWAVE INDUCED ORGANIC REACTION; CHAPTER 3 :MICROWAVE ASSISTED ORGANIC SYNTHESIS (NAME REACTIONS); CHAPTER 4 :MICROWAVE HARDWARE; CHAPTER 5 :APPLICATION OF MICROWAVE HEATING; REFERENCES |
| Record Nr. | UNINA-9910459324003321 |
|
Desai K. R
|
||
| Mumbai [India], : Himalaya Pub. House, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green chemistry [[electronic resource] ] : microwave synthesis / / K.R. Desai ; foreword by V.R. Kanetkar
| Green chemistry [[electronic resource] ] : microwave synthesis / / K.R. Desai ; foreword by V.R. Kanetkar |
| Autore | Desai K. R |
| Edizione | [Rev. ed.] |
| Pubbl/distr/stampa | Mumbai [India], : Himalaya Pub. House, 2010 |
| Descrizione fisica | 1 online resource (138 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) | KanetkarV. R |
| Soggetto topico |
Organic compounds - Synthesis
Microwaves Microwave heating |
| ISBN |
1-282-81186-X
9786612811869 1-4416-6206-5 93-5043-184-X 600-00-2822-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | COVER; CONTENTS; CHAPTER 1 :MICROWAVE SYNTHESIS; CHAPTER 2 :MICROWAVE INDUCED ORGANIC REACTION; CHAPTER 3 :MICROWAVE ASSISTED ORGANIC SYNTHESIS (NAME REACTIONS); CHAPTER 4 :MICROWAVE HARDWARE; CHAPTER 5 :APPLICATION OF MICROWAVE HEATING; REFERENCES |
| Record Nr. | UNINA-9910784936903321 |
|
Desai K. R
|
||
| Mumbai [India], : Himalaya Pub. House, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green chemistry [[electronic resource] ] : microwave synthesis / / K.R. Desai ; foreword by V.R. Kanetkar
| Green chemistry [[electronic resource] ] : microwave synthesis / / K.R. Desai ; foreword by V.R. Kanetkar |
| Autore | Desai K. R |
| Edizione | [Rev. ed.] |
| Pubbl/distr/stampa | Mumbai [India], : Himalaya Pub. House, 2010 |
| Descrizione fisica | 1 online resource (138 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) | KanetkarV. R |
| Soggetto topico |
Organic compounds - Synthesis
Microwaves Microwave heating |
| ISBN |
1-282-81186-X
9786612811869 1-4416-6206-5 93-5043-184-X 600-00-2822-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | COVER; CONTENTS; CHAPTER 1 :MICROWAVE SYNTHESIS; CHAPTER 2 :MICROWAVE INDUCED ORGANIC REACTION; CHAPTER 3 :MICROWAVE ASSISTED ORGANIC SYNTHESIS (NAME REACTIONS); CHAPTER 4 :MICROWAVE HARDWARE; CHAPTER 5 :APPLICATION OF MICROWAVE HEATING; REFERENCES |
| Record Nr. | UNINA-9910823366303321 |
|
Desai K. R
|
||
| Mumbai [India], : Himalaya Pub. House, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green oxidation in organic synthesis / / edited by Ning Jiao (Peking University, Beijing, China), Shannon S. Stahl (University of Wisconsin-Madison, Madison, US)
| Green oxidation in organic synthesis / / edited by Ning Jiao (Peking University, Beijing, China), Shannon S. Stahl (University of Wisconsin-Madison, Madison, US) |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2019 |
| Descrizione fisica | 1 online resource (534 pages) |
| Disciplina | 547/.2 |
| Collana | THEi Wiley ebooks |
| Soggetto topico |
Organic compounds - Synthesis
Green chemistry Oxidation |
| ISBN |
1-119-30404-0
1-119-30449-0 1-119-30419-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910555042803321 |
| Hoboken, New Jersey : , : Wiley, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green oxidation in organic synthesis / / edited by Ning Jiao (Peking University, Beijing, China), Shannon S. Stahl (University of Wisconsin-Madison, Madison, US)
| Green oxidation in organic synthesis / / edited by Ning Jiao (Peking University, Beijing, China), Shannon S. Stahl (University of Wisconsin-Madison, Madison, US) |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2019 |
| Descrizione fisica | 1 online resource (534 pages) |
| Disciplina | 547/.2 |
| Collana | THEi Wiley ebooks |
| Soggetto topico |
Organic compounds - Synthesis
Green chemistry Oxidation |
| ISBN |
1-119-30404-0
1-119-30449-0 1-119-30419-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910822850903321 |
| Hoboken, New Jersey : , : Wiley, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of organopalladium chemistry for organic synthesis / / edited by Ei-ichi Negishi
| Handbook of organopalladium chemistry for organic synthesis / / edited by Ei-ichi Negishi |
| Pubbl/distr/stampa | New York, : Wiley Interscience, c2002 |
| Descrizione fisica | 1 online resource (3279 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | NegishiEi-ichi |
| Soggetto topico |
Organic compounds - Synthesis
Palladium catalysts |
| ISBN |
9786610344611
0-471-47381-2 1-280-34461-X 1-280-36693-1 9786610366934 0-470-35209-4 0-471-46155-5 0-471-21246-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
HANDBOOK OF ORGANOPALLADIUM CHEMISTRY FOR ORGANIC SYNTHESIS Volume 2; CONTENTS; PREFACE; CONTRIBUTORS; ABBREVIATIONS; V PALLADIUM-CATALYZED REACTIONS INVOLVING NUCLEOPHILIC ATTACK ON LIGANDS; V.1 Background for Part V; V.2 Palladium-Catalyzed Nucleophilic Substitution Involving Allylpalladium, Propargylpalladium, and Related Derivatives; V.2.1 The Tsuji-Trost Reaction and Related Carbon-Carbon Bond Formation Reactions; V.2.1.1 Overview of the Palladium-Catalyzed Carbon-Carbon Bond Formation via p-Allylpalladium and Propargylpalladium Intermediates
V.2.1.2 Synthetic Scope of the Tsuji-Trost Reaction with Allylic Halides, Carboxylates, Ethers, and Related Oxygen Nucleophiles as Starting CompoundsV.2.1.3 Palladium-Catalyzed Allylation with Allyl Carbonates; V.2.1.4 Palladium-Catalyzed Allylation and Related Substitution Reactions of Enolates and Related Derivatives of "Ordinary" Ketones, Aldehydes, and Other Carbonyl Compounds; V.2.1.5 Palladium-Catalyzed Substitution Reactions of Alkenyl Epoxides; V.2.1.6 Palladium-Catalyzed Substitution Reactions of Sulfur and Other Heavier Group 16 Atom-Containing Allylic Derivatives V.2.1.7 Palladium-Catalyzed Substitution Reactions of Nitrogen and Other Group 15 Atom-Containing Allylic DerivativesV.2.1.8 Palladium-Catalyzed Substitution Reactions with Propargyl and Related Electrophiles; V.2.1.9 Palladium-Catalyzed Reactions of Soft Carbon Nucleophiles with Dienes, Vinylcyclopropanes, and Related Compounds; V.2.2 Palladium-Catalyzed Allylic, Propargylic, and Allenic Substitution with Nitrogen, Oxygen, and Other Groups 15-17 Heteroatom Nucleophiles V.2.2.1 Palladium-Catalyzed Substitution Reactions of Allylic, Propargylic, and Related Electrophiles with Heteroatom NucleophilesV.2.2.2 C-O and C-N Bond Formation Involving Conjugated Dienes and Allylpalladium Intermediates; V.2.2.3 Use of Alkenes as Precursors to p-Allylpalladium Derivatives in Allylic Substitution with O, N and Other Heteroatom Nucleophiles; V.2.3 Palladium-Catalyzed Allylic, Propargylic, and Allenic Substitution with Hydrogen and Metal Nucleophiles; V.2.3.1 Palladium-Catalyzed Hydrogenolysis of Allyl and Related Derivatives V.2.3.2 Palladium-Catalyzed Deprotection of Allyl-Based Protecting GroupsV.2.3.3 Palladium-Catalyzed Allylic and Related Silylation and Other Metallations; V.2.3.4 Palladium-Catalyzed Reactions of Allyl and Related Derivatives with Organoelectrophiles; V.2.4 Palladium-Catalyzed Asymmetric Allylation and Related Reactions; V.2.5 Other Reactions of Allylpalladium and Related Derivatives; V.2.5.1 Elimination of Allylpalladium and Related Derivatives; V.2.5.2 Cycloaddition Reactions of Allylpalladium and Related Derivatives; V.2.5.3 Rearrangements of Allylpalladium and Related Derivatives V.2.6 Synthesis of Natural Products and Biologically Active Compounds via Allylpalladium and Related Derivatives |
| Record Nr. | UNINA-9910146073103321 |
| New York, : Wiley Interscience, c2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of organopalladium chemistry for organic synthesis / / edited by Ei-ichi Negishi
| Handbook of organopalladium chemistry for organic synthesis / / edited by Ei-ichi Negishi |
| Pubbl/distr/stampa | New York, : Wiley Interscience, c2002 |
| Descrizione fisica | 1 online resource (3279 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | NegishiEi-ichi |
| Soggetto topico |
Organic compounds - Synthesis
Palladium catalysts |
| ISBN |
9786610344611
0-471-47381-2 1-280-34461-X 1-280-36693-1 9786610366934 0-470-35209-4 0-471-46155-5 0-471-21246-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
HANDBOOK OF ORGANOPALLADIUM CHEMISTRY FOR ORGANIC SYNTHESIS Volume 2; CONTENTS; PREFACE; CONTRIBUTORS; ABBREVIATIONS; V PALLADIUM-CATALYZED REACTIONS INVOLVING NUCLEOPHILIC ATTACK ON LIGANDS; V.1 Background for Part V; V.2 Palladium-Catalyzed Nucleophilic Substitution Involving Allylpalladium, Propargylpalladium, and Related Derivatives; V.2.1 The Tsuji-Trost Reaction and Related Carbon-Carbon Bond Formation Reactions; V.2.1.1 Overview of the Palladium-Catalyzed Carbon-Carbon Bond Formation via p-Allylpalladium and Propargylpalladium Intermediates
V.2.1.2 Synthetic Scope of the Tsuji-Trost Reaction with Allylic Halides, Carboxylates, Ethers, and Related Oxygen Nucleophiles as Starting CompoundsV.2.1.3 Palladium-Catalyzed Allylation with Allyl Carbonates; V.2.1.4 Palladium-Catalyzed Allylation and Related Substitution Reactions of Enolates and Related Derivatives of "Ordinary" Ketones, Aldehydes, and Other Carbonyl Compounds; V.2.1.5 Palladium-Catalyzed Substitution Reactions of Alkenyl Epoxides; V.2.1.6 Palladium-Catalyzed Substitution Reactions of Sulfur and Other Heavier Group 16 Atom-Containing Allylic Derivatives V.2.1.7 Palladium-Catalyzed Substitution Reactions of Nitrogen and Other Group 15 Atom-Containing Allylic DerivativesV.2.1.8 Palladium-Catalyzed Substitution Reactions with Propargyl and Related Electrophiles; V.2.1.9 Palladium-Catalyzed Reactions of Soft Carbon Nucleophiles with Dienes, Vinylcyclopropanes, and Related Compounds; V.2.2 Palladium-Catalyzed Allylic, Propargylic, and Allenic Substitution with Nitrogen, Oxygen, and Other Groups 15-17 Heteroatom Nucleophiles V.2.2.1 Palladium-Catalyzed Substitution Reactions of Allylic, Propargylic, and Related Electrophiles with Heteroatom NucleophilesV.2.2.2 C-O and C-N Bond Formation Involving Conjugated Dienes and Allylpalladium Intermediates; V.2.2.3 Use of Alkenes as Precursors to p-Allylpalladium Derivatives in Allylic Substitution with O, N and Other Heteroatom Nucleophiles; V.2.3 Palladium-Catalyzed Allylic, Propargylic, and Allenic Substitution with Hydrogen and Metal Nucleophiles; V.2.3.1 Palladium-Catalyzed Hydrogenolysis of Allyl and Related Derivatives V.2.3.2 Palladium-Catalyzed Deprotection of Allyl-Based Protecting GroupsV.2.3.3 Palladium-Catalyzed Allylic and Related Silylation and Other Metallations; V.2.3.4 Palladium-Catalyzed Reactions of Allyl and Related Derivatives with Organoelectrophiles; V.2.4 Palladium-Catalyzed Asymmetric Allylation and Related Reactions; V.2.5 Other Reactions of Allylpalladium and Related Derivatives; V.2.5.1 Elimination of Allylpalladium and Related Derivatives; V.2.5.2 Cycloaddition Reactions of Allylpalladium and Related Derivatives; V.2.5.3 Rearrangements of Allylpalladium and Related Derivatives V.2.6 Synthesis of Natural Products and Biologically Active Compounds via Allylpalladium and Related Derivatives |
| Record Nr. | UNINA-9910676659203321 |
| New York, : Wiley Interscience, c2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of reagents for organic synthesis : reagents for heteroarene functionalization / / edited by André B. Charette
| Handbook of reagents for organic synthesis : reagents for heteroarene functionalization / / edited by André B. Charette |
| Pubbl/distr/stampa | West Sussex, England : , : Wiley, , 2015 |
| Descrizione fisica | 1 online resource (829 p.) |
| Disciplina | 547/.2 |
| Collana | Hdbk of Reagents for Organic Synthesis |
| Soggetto topico |
Organic compounds - Synthesis
Heterocyclic chemistry Chemical tests and reagents |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-118-72657-X
1-118-72655-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Handbook of Reagents for Organic Synthesis: Reagents for Heteroarene Functionalization; Contents; Preface; Introduction; Recent Review Articles and Monographs; Short Note on InChIs and InChIKeys; Acetic Anhydride; Acetyl Chloride; Aluminum Chloride; Aluminum Trifluoromethanesulfonate; Antimony Trifluoromethanesulfonate; Bathophenanthroline; 1,2-Benzodiazine; Benzopyrazole; Benzotriazole; Bis(allyl)di-μ-chlorodipalladium; Bis(benzonitrile)dichloropalladium(II); Bis(dibenzylideneacetone)palladium(0); Bis(1,10-phenanthroline)palladium Hexafluorophosphate
Bis[tris(1,1-dimethylethyl)-phosphine]palladiumBromine; N-Bromosuccinimide; n-Butyllithium; sec-Butyllithium; tert-Butyllithium; Butyllithium-Potassium tert-Butoxide; Cesium Acetate; N-Chlorosuccinimide; Copper(II) Acetate; Copper(II) Bromide; Copper(I) Chloride; Copper(II) Chloride; Copper(I) Iodide; Copper(II) Trifluoroacetate; Copper(II) Trifluoromethanesulfonate; N-Cyano-4-methyl-N-phenylbenzenesulfonamide; Dibenzofuran; Dibenzothiophene; 1,1-Di-tert-butyl Peroxide; Di-tert-butyl(methyl)phosphine; Di-tert-butyl(methyl)phosphonium Tetrafluoroborate; Dichlorobis(acetonitrile) Palladium Dichlorobis(triphenylphosphine)-palladium(II)Di-μ-chlorotetrakis[(1,2-η)-cyclooctene]diiridium; Di-μ-methoxobis(1,5-cyclooctadiene)diiridium(I); Dimethyl Diazomalonate; (2S,5S)-2-(1,1-Dimethylethyl)-3-methyl-5-(phenylmethyl)-4-imidazolidinone; Diphenyliodonium Hexafluorophosphate; Diphenyliodonium Triflate; Dysprosium Trifluoromethanesulfonate; N-fluoro-N-(phenylsulfonyl)-benzenesulfonamide; 1-Fluoro-2,4,6-trimethylpyridinium Tetrafluoroborate; Furan; Gallium(III) Trifluoromethanesulfonate (Gallium Triflate); Hafnium(IV) Trifluoromethanesulfonate; Hypofluorous Acid-Acetonitrile Complex Indium(III) TriflateIndolizine; Iron, Bis(pyridine)bis(2-pyridinecarboxylato-N1,O2); Isoindole; Isoquinoline; Lithium t-Butoxide; Lithium Dichloro(1-methylethyl)-magnesate; Lithium Dichloro(2,2,6,6-tetramethylpiperidinato)-zincate; Magnesium tert-butoxide; Manganese(III) Acetate; 4-Methoxypyridine N-oxide; 6-Methoxyquinoline-N-oxide; 2-Methylbenzothiazole; N-Methylimidazole; N-Methylindole; 1-[[(4-Methylphenyl)sulfonyl]amino]-pyridinium inner salt; Methyltrioxorhenium; Nitric Acid; 4,4,4,́4,́5,5,5,́5-́Octamethyl-2,2-́bi-1,3,2-dioxaborolane; 1,2,5-Oxadiazole; Oxalyl Chloride-Dimethylformamide OxazolePalladium(II) Acetate; Palladium(II) Bromide; Palladium(II) Chloride; Palladium(π-cinnamyl) Chloride Dimer; Palladium Pivalate; Pentamethylcyclopentadienylrhodium(III) chloride dimer; 1,10-Phenanthroline; 1,10-Phenanthroline, 1-Oxide; (1,10-Phenanthroline)(trifluoromethyl) (triphenylphosphine)copper; Pinacolborane; Pivalic Acid; Potassium Acetate; Propanoic acid, 2-Diazo-, 2-Methyl-1-(1-methylethyl)propyl ester; Pyridazine; Pyridazine N-Oxide; Pyridine; Pyridine N-Oxide; Pyrrole; Quinoline; Ruthenium Dodecacarbonyltri Triangulo; Scandium Trifluoromethanesulfonate; Silver(I) Acetate Silver(I) Carbonate |
| Record Nr. | UNINA-9910460536003321 |
| West Sussex, England : , : Wiley, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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