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C-H bond activation in organic synthesis / / edited by Jie Jack Li, University of San Francisco, California, USA
| C-H bond activation in organic synthesis / / edited by Jie Jack Li, University of San Francisco, California, USA |
| Pubbl/distr/stampa | Boca Raton : , : CRC Press, , [2015] |
| Descrizione fisica | 1 online resource (320 p.) |
| Disciplina |
547.27
547/.27 |
| Soggetto topico |
Organic compounds - Synthesis
Activation (Chemistry) Analytical chemistry Carbon Hydrogen |
| ISBN | 0-429-06948-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | chapter 1. Introduction / Marion H. Emmert -- chapter 2. Radical-mediated C-H bond activation / Adam M. Azman -- chapter 3. Pd-catalyzed C-H functionalization / Jesse D. Carrick -- chapter 4. Rhodium-catalyzed C-H activation / Micheal Fultz -- chapter 5. Nickel-catalyzed C-H activation / Andrew C. Williams -- chapter 6. Iron-catalyzed C-H activation / Narendra B. Ambhaikar -- chapter 7. Copper-mediated C-H activation / Nadia M. Ahmad -- chapter 8. Cobalt-catalyzed C-H activation / Nicole L. Snyder and Eric J. Medici -- chapter 9. Fluorination and trifluoromethylation of arenes and heteroarenes via C-H activation / Ji Zhang and Timothy T. Curran -- chapter 10. C-H activation of heteroaromatics / Donna A.A. Wilton. |
| Altri titoli varianti | Carbon-hydrogen bond activation in organic synthesis |
| Record Nr. | UNINA-9910788021903321 |
| Boca Raton : , : CRC Press, , [2015] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki
| Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2014 |
| Descrizione fisica | 1 online resource (673 p.) |
| Disciplina | 547/.27 |
| Altri autori (Persone) | NishiwakiNagatoshi <1963-> |
| Soggetto topico |
Organic compounds - Synthesis
Ring formation (Chemistry) |
| ISBN |
1-118-77820-0
1-118-77817-0 1-118-77818-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Methods and Applications of Cycloaddition Reactions in Organic Syntheses; Contents; Preface; Contributors; Part I: [2+1] Cycloaddition; 1 [2+1]-Type Cyclopropanation Reactions; 1.1 INTRODUCTION; 1.2 CYCLOPROPANATION REACTION VIA MICHAEL-INDUCED RING CLOSURE REACTION; 1.2.1 Introduction; 1.2.2 Halo-Substituted Nucleophiles in MIRC Reaction; 1.2.3 Ylides for Cyclopropanation; 1.3 SIMMONS-SMITH CYCLOPROPANATION AND RELATED REACTIONS; 1.3.1 Introduction; 1.3.2 The Simmons-Smith Reaction with Zinc Reagents; 1.4 DIAZOALKANES WITH TRANSITION METAL CATALYSTS; 1.4.1 Introduction
1.4.2 Rhodium-Catalyzed Reactions1.4.4 Ruthenium-Catalyzed Reactions; 1.4.5 Cobalt- and Iron-Catalyzed Reactions; 1.4.6 Other Transition Metal-Catalyzed Reactions; 1.4.7 Cyclopropanation Without Transition Metal Catalysts; 1.4.8 Cyclopropanation of Dihalocarbenes; 1.5 CYCLOISOMERIZATION WITH TRANSITION METAL CATALYSTS; 1.5.1 Introduction; 1.5.2 Gold Complex-Catalyzed Reactions; 1.5.3 Palladium Complex-Catalyzed Reactions; 1.5.4 Platinum Complex-Catalyzed Reactions; 1.5.5 Ruthenium Complex-Catalyzed Reactions; 1.5.6 Other Metal Complex-Catalyzed Reactions; 1.6 KULINKOVICH REACTIONS 1.6.1 Introduction1.6.2 The Kulinkovich Reaction to Esters, Ketones, and Amides; 1.6.3 Kulinkovich Reaction to Nitriles; 1.6.4 Other Ti-Mediated Cyclopropanation Reactions; 1.7 MISCELLANEOUS [2+1]-TYPE OF CYCLOPROPANATION REACTIONS; REFERENCES; 2 N1 Unit Transfer Reaction To C-C Double Bonds; 2.1 INTRODUCTION; 2.2 AZIRIDINATION WITH AZIDES; 2.3 AZIRIDINATION WITH IMINOIODINANES; 2.4 AZIRIDINATION WITH N-HALOAMINE SALTS; 2.5 AZIRIDINATION WITH OTHER N1 UNIT; 2.6 CONCLUSIONS; REFERENCES; Part II: [2+2] Cycloaddition; 3 Lewis Base Catalyzed Asymmetric Formal [2+2] Cycloadditions 3.1 INTRODUCTION3.2 β-LACTAMS: FORMAL [2+2] CYCLOADDITIONS INVOLVING IMINES; 3.3 β-LACTONES I: FORMAL [2+2] CYCLOADDITIONS INVOLVING ALDEHYDES/KETONES; 3.4 β-LACTONES II: FORMAL [2+2] CYCLOADDITION OF KETENES LEADING TO KETENE DIMERS; 3.4.1 Introduction or or; 3.4.2 Homodimerization; 3.4.3 Heterodimerization; 3.5 MISCELLANEOUS FORMAL [2+2] ASYMMETRIC CYCLOADDITION PROCESSES; 3.5.1 Other Heterocyclic Classes-Introduction; 3.5.2 Asymmetric Formal [2+2] Cycloadditions; 3.6 CONCLUSIONS; REFERENCES; Part III: [2+2] and [4+2]/[2+2] Cycloaddition; 4 Catalytic [2+2] Cycloaddition of Silyl Enol Ethers 4.1 INTRODUCTION4.2 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY LEWIS ACID CATALYST; 4.2.1 Introduction; 4.2.2 Intramolecular [2+2] Cycloaddition Reactions; 4.2.3 Intermolecular [2+2] Cycloaddition Reactions; 4.2.4 Asymmetric Catalytic [2+2] Cycloaddition Reaction with Silyl Enol Ethers; 4.3 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY BRØNSTED ACID; 4.3.1 Catalytic [2+2] Cycloaddition Reactions of Silyl Enol Ethers by Trifluoromethanesulfonimide; 4.3.2 Multigram Syntheses of Cyclobutanes and Cyclobutenes by [2+2] Cycloaddition Reactions 4.3.3 Analysis of the Mechanism for [2+2] Cycloaddition Reactions by Trifluoromethanesulfonimide |
| Record Nr. | UNINA-9910138976903321 |
| Hoboken, New Jersey : , : Wiley, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki
| Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2014 |
| Descrizione fisica | 1 online resource (673 p.) |
| Disciplina | 547/.27 |
| Altri autori (Persone) | NishiwakiNagatoshi <1963-> |
| Soggetto topico |
Organic compounds - Synthesis
Ring formation (Chemistry) |
| ISBN |
1-118-77820-0
1-118-77817-0 1-118-77818-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Methods and Applications of Cycloaddition Reactions in Organic Syntheses; Contents; Preface; Contributors; Part I: [2+1] Cycloaddition; 1 [2+1]-Type Cyclopropanation Reactions; 1.1 INTRODUCTION; 1.2 CYCLOPROPANATION REACTION VIA MICHAEL-INDUCED RING CLOSURE REACTION; 1.2.1 Introduction; 1.2.2 Halo-Substituted Nucleophiles in MIRC Reaction; 1.2.3 Ylides for Cyclopropanation; 1.3 SIMMONS-SMITH CYCLOPROPANATION AND RELATED REACTIONS; 1.3.1 Introduction; 1.3.2 The Simmons-Smith Reaction with Zinc Reagents; 1.4 DIAZOALKANES WITH TRANSITION METAL CATALYSTS; 1.4.1 Introduction
1.4.2 Rhodium-Catalyzed Reactions1.4.4 Ruthenium-Catalyzed Reactions; 1.4.5 Cobalt- and Iron-Catalyzed Reactions; 1.4.6 Other Transition Metal-Catalyzed Reactions; 1.4.7 Cyclopropanation Without Transition Metal Catalysts; 1.4.8 Cyclopropanation of Dihalocarbenes; 1.5 CYCLOISOMERIZATION WITH TRANSITION METAL CATALYSTS; 1.5.1 Introduction; 1.5.2 Gold Complex-Catalyzed Reactions; 1.5.3 Palladium Complex-Catalyzed Reactions; 1.5.4 Platinum Complex-Catalyzed Reactions; 1.5.5 Ruthenium Complex-Catalyzed Reactions; 1.5.6 Other Metal Complex-Catalyzed Reactions; 1.6 KULINKOVICH REACTIONS 1.6.1 Introduction1.6.2 The Kulinkovich Reaction to Esters, Ketones, and Amides; 1.6.3 Kulinkovich Reaction to Nitriles; 1.6.4 Other Ti-Mediated Cyclopropanation Reactions; 1.7 MISCELLANEOUS [2+1]-TYPE OF CYCLOPROPANATION REACTIONS; REFERENCES; 2 N1 Unit Transfer Reaction To C-C Double Bonds; 2.1 INTRODUCTION; 2.2 AZIRIDINATION WITH AZIDES; 2.3 AZIRIDINATION WITH IMINOIODINANES; 2.4 AZIRIDINATION WITH N-HALOAMINE SALTS; 2.5 AZIRIDINATION WITH OTHER N1 UNIT; 2.6 CONCLUSIONS; REFERENCES; Part II: [2+2] Cycloaddition; 3 Lewis Base Catalyzed Asymmetric Formal [2+2] Cycloadditions 3.1 INTRODUCTION3.2 β-LACTAMS: FORMAL [2+2] CYCLOADDITIONS INVOLVING IMINES; 3.3 β-LACTONES I: FORMAL [2+2] CYCLOADDITIONS INVOLVING ALDEHYDES/KETONES; 3.4 β-LACTONES II: FORMAL [2+2] CYCLOADDITION OF KETENES LEADING TO KETENE DIMERS; 3.4.1 Introduction or or; 3.4.2 Homodimerization; 3.4.3 Heterodimerization; 3.5 MISCELLANEOUS FORMAL [2+2] ASYMMETRIC CYCLOADDITION PROCESSES; 3.5.1 Other Heterocyclic Classes-Introduction; 3.5.2 Asymmetric Formal [2+2] Cycloadditions; 3.6 CONCLUSIONS; REFERENCES; Part III: [2+2] and [4+2]/[2+2] Cycloaddition; 4 Catalytic [2+2] Cycloaddition of Silyl Enol Ethers 4.1 INTRODUCTION4.2 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY LEWIS ACID CATALYST; 4.2.1 Introduction; 4.2.2 Intramolecular [2+2] Cycloaddition Reactions; 4.2.3 Intermolecular [2+2] Cycloaddition Reactions; 4.2.4 Asymmetric Catalytic [2+2] Cycloaddition Reaction with Silyl Enol Ethers; 4.3 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY BRØNSTED ACID; 4.3.1 Catalytic [2+2] Cycloaddition Reactions of Silyl Enol Ethers by Trifluoromethanesulfonimide; 4.3.2 Multigram Syntheses of Cyclobutanes and Cyclobutenes by [2+2] Cycloaddition Reactions 4.3.3 Analysis of the Mechanism for [2+2] Cycloaddition Reactions by Trifluoromethanesulfonimide |
| Record Nr. | UNINA-9910828347603321 |
| Hoboken, New Jersey : , : Wiley, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||