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Domino reactions in organic synthesis [[electronic resource] /] / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke
| Domino reactions in organic synthesis [[electronic resource] /] / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke |
| Autore | Tietze Lutz-Friedjan |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2006 |
| Descrizione fisica | 1 online resource (633 p.) |
| Disciplina | 547.1393 |
| Altri autori (Persone) |
BrascheGordon <1976->
GerickeKersten M. <1976-> |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-72267-3
9786610722679 3-527-60992-X 3-527-60868-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Domino Reactions in Organic Synthesis; Table of Contents; Preface; Abbreviations; Introduction; Classification; 1 Cationic Domino Reactions; 1.1 Cationic/Cationic Processes; 1.1.1 Cationic/Cationic/Cationic Processes; 1.2 Cationic/Pericyclic Processes; 1.3 Cationic/Reductive Processes; 2 Anionic Domino Reactions; 2.1 Anionic/Anionic Processes; 2.1.1 Anionic/Anionic/Anionic Processes; 2.1.2 Fourfold and Higher Anionic Processes; 2.1.3 Two- and Threefold Anionic Processes Followed by a Nonanionic Process; 2.2 Anionic/Radical Processes; 2.3 Anionic/Pericyclic Processes
2.3.1 Anionic/Pericyclic Processes Followed by Further Transformations2.4 Anionic/Transition Metal-Catalyzed Processes; 2.5 Anionic/Oxidative or Reductive Processes; 3 Radical Domino Reactions; 3.1 Radical/Cationic Domino Processes; 3.2 Radical/Anionic Domino Processes; 3.3 Radical/Radical Domino Processes; 3.3.1 Radical/Radical/Anionic Domino Processes; 3.3.2 Radical/Radical/Radical Domino Processes; 3.3.3 Radical/Radical/Pericyclic Domino Processes; 3.3.4 Radical/Radical/Oxidation Domino Processes; 3.4 Radical/Pericyclic Domino Processes; 4 Pericyclic Domino Reactions 4.1 Diels-Alder Reactions4.1.1 Diels-Alder/Diels-Alder Reactions; 4.1.2 Diels-Alder Reactions/Sigmatropic Rearrangements; 4.1.3 Diels-Alder/Retro-Diels-Alder Reactions; 4.1.4 Diels-Alder Reactions/Mixed Transformations; 4.1.5 Hetero-Diels-Alder Reactions; 4.2 1,3-Dipolar Cycloadditions; 4.3 [2+2] and Higher Cycloadditions; 4.4 Sigmatropic Rearrangements; 4.5 Electrocyclic Reactions; 4.6 Ene Reactions; 4.7 Retro-Pericyclic Reactions; 5 Photochemically Induced Domino Processes; 5.1 Photochemical/Cationic Domino Processes; 5.2 Photochemical/Anionic Domino Processes 5.3 Photochemical/Radical Domino Processes5.4 Photochemical/Pericyclic Domino Processes; 5.5 Photochemical/Photochemical Domino Processes; 5.6 Photochemical/Transition Metal-Catalyzed Domino Processes; 6 Transition Metal-Catalyzed Domino Reactions; 6.1 Palladium-Catalyzed Transformations; 6.1.1 The Heck Reaction; 6.1.1.1 Domino Heck Reactions; 6.1.1.2 Heck/Cross-Coupling Reactions; 6.1.1.3 Heck/Tsuji-Trost Reactions; 6.1.1.4 Heck Reactions/CO-Insertions; 6.1.1.5 Heck Reactions/C-H-Activations; 6.1.1.6 Heck Reactions: Pericyclic Transformations; 6.1.1.7 Heck Reactions/Mixed Transformations 6.1.2 Cross-Coupling Reactions6.1.2.1 Suzuki Reactions; 6.1.2.2 Stille Reactions; 6.1.2.3 Sonogashira Reactions; 6.1.2.4 Other Cross-Coupling Reactions; 6.1.3 Nucleophilic Substitution (Tsuji-Trost Reaction); 6.1.4 Reactions of Alkynes and Allenes; 6.1.5 Other Pd(0)-Catalyzed Transformations; 6.1.6 Pd(II)-Catalyzed Transformations; 6.2 Rhodium-Catalyzed Transformations; 6.2.1 Formation of Carbenes; 6.2.2 Hydroformylations; 6.2.3 Other Rhodium-Catalyzed Transformations; 6.3 Ruthenium-Catalyzed Transformations; 6.3.1 Metathesis Reactions; 6.3.1.1 Metathesis-Metathesis Processes 6.3.1.2 Metathesis/Heck Reaction/Pericyclic Reaction/Hydrogenation |
| Record Nr. | UNINA-9910144299003321 |
Tietze Lutz-Friedjan
|
||
| Weinheim, : Wiley-VCH, c2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Domino reactions in organic synthesis [[electronic resource] /] / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke
| Domino reactions in organic synthesis [[electronic resource] /] / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke |
| Autore | Tietze Lutz-Friedjan |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2006 |
| Descrizione fisica | 1 online resource (633 p.) |
| Disciplina | 547.1393 |
| Altri autori (Persone) |
BrascheGordon <1976->
GerickeKersten M. <1976-> |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions |
| ISBN |
1-280-72267-3
9786610722679 3-527-60992-X 3-527-60868-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Domino Reactions in Organic Synthesis; Table of Contents; Preface; Abbreviations; Introduction; Classification; 1 Cationic Domino Reactions; 1.1 Cationic/Cationic Processes; 1.1.1 Cationic/Cationic/Cationic Processes; 1.2 Cationic/Pericyclic Processes; 1.3 Cationic/Reductive Processes; 2 Anionic Domino Reactions; 2.1 Anionic/Anionic Processes; 2.1.1 Anionic/Anionic/Anionic Processes; 2.1.2 Fourfold and Higher Anionic Processes; 2.1.3 Two- and Threefold Anionic Processes Followed by a Nonanionic Process; 2.2 Anionic/Radical Processes; 2.3 Anionic/Pericyclic Processes
2.3.1 Anionic/Pericyclic Processes Followed by Further Transformations2.4 Anionic/Transition Metal-Catalyzed Processes; 2.5 Anionic/Oxidative or Reductive Processes; 3 Radical Domino Reactions; 3.1 Radical/Cationic Domino Processes; 3.2 Radical/Anionic Domino Processes; 3.3 Radical/Radical Domino Processes; 3.3.1 Radical/Radical/Anionic Domino Processes; 3.3.2 Radical/Radical/Radical Domino Processes; 3.3.3 Radical/Radical/Pericyclic Domino Processes; 3.3.4 Radical/Radical/Oxidation Domino Processes; 3.4 Radical/Pericyclic Domino Processes; 4 Pericyclic Domino Reactions 4.1 Diels-Alder Reactions4.1.1 Diels-Alder/Diels-Alder Reactions; 4.1.2 Diels-Alder Reactions/Sigmatropic Rearrangements; 4.1.3 Diels-Alder/Retro-Diels-Alder Reactions; 4.1.4 Diels-Alder Reactions/Mixed Transformations; 4.1.5 Hetero-Diels-Alder Reactions; 4.2 1,3-Dipolar Cycloadditions; 4.3 [2+2] and Higher Cycloadditions; 4.4 Sigmatropic Rearrangements; 4.5 Electrocyclic Reactions; 4.6 Ene Reactions; 4.7 Retro-Pericyclic Reactions; 5 Photochemically Induced Domino Processes; 5.1 Photochemical/Cationic Domino Processes; 5.2 Photochemical/Anionic Domino Processes 5.3 Photochemical/Radical Domino Processes5.4 Photochemical/Pericyclic Domino Processes; 5.5 Photochemical/Photochemical Domino Processes; 5.6 Photochemical/Transition Metal-Catalyzed Domino Processes; 6 Transition Metal-Catalyzed Domino Reactions; 6.1 Palladium-Catalyzed Transformations; 6.1.1 The Heck Reaction; 6.1.1.1 Domino Heck Reactions; 6.1.1.2 Heck/Cross-Coupling Reactions; 6.1.1.3 Heck/Tsuji-Trost Reactions; 6.1.1.4 Heck Reactions/CO-Insertions; 6.1.1.5 Heck Reactions/C-H-Activations; 6.1.1.6 Heck Reactions: Pericyclic Transformations; 6.1.1.7 Heck Reactions/Mixed Transformations 6.1.2 Cross-Coupling Reactions6.1.2.1 Suzuki Reactions; 6.1.2.2 Stille Reactions; 6.1.2.3 Sonogashira Reactions; 6.1.2.4 Other Cross-Coupling Reactions; 6.1.3 Nucleophilic Substitution (Tsuji-Trost Reaction); 6.1.4 Reactions of Alkynes and Allenes; 6.1.5 Other Pd(0)-Catalyzed Transformations; 6.1.6 Pd(II)-Catalyzed Transformations; 6.2 Rhodium-Catalyzed Transformations; 6.2.1 Formation of Carbenes; 6.2.2 Hydroformylations; 6.2.3 Other Rhodium-Catalyzed Transformations; 6.3 Ruthenium-Catalyzed Transformations; 6.3.1 Metathesis Reactions; 6.3.1.1 Metathesis-Metathesis Processes 6.3.1.2 Metathesis/Heck Reaction/Pericyclic Reaction/Hydrogenation |
| Record Nr. | UNINA-9910830246903321 |
|
Tietze Lutz-Friedjan
|
||
| Weinheim, : Wiley-VCH, c2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Domino reactions in organic synthesis / / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke
| Domino reactions in organic synthesis / / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke |
| Autore | Tietze Lutz-Friedjan |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2006 |
| Descrizione fisica | 1 online resource (633 p.) |
| Disciplina | 547.1393 |
| Altri autori (Persone) |
BrascheGordon <1976->
GerickeKersten M. <1976-> |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions |
| ISBN |
9786610722679
9781280722677 1280722673 9783527609925 352760992X 9783527608683 3527608680 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Domino Reactions in Organic Synthesis; Table of Contents; Preface; Abbreviations; Introduction; Classification; 1 Cationic Domino Reactions; 1.1 Cationic/Cationic Processes; 1.1.1 Cationic/Cationic/Cationic Processes; 1.2 Cationic/Pericyclic Processes; 1.3 Cationic/Reductive Processes; 2 Anionic Domino Reactions; 2.1 Anionic/Anionic Processes; 2.1.1 Anionic/Anionic/Anionic Processes; 2.1.2 Fourfold and Higher Anionic Processes; 2.1.3 Two- and Threefold Anionic Processes Followed by a Nonanionic Process; 2.2 Anionic/Radical Processes; 2.3 Anionic/Pericyclic Processes
2.3.1 Anionic/Pericyclic Processes Followed by Further Transformations2.4 Anionic/Transition Metal-Catalyzed Processes; 2.5 Anionic/Oxidative or Reductive Processes; 3 Radical Domino Reactions; 3.1 Radical/Cationic Domino Processes; 3.2 Radical/Anionic Domino Processes; 3.3 Radical/Radical Domino Processes; 3.3.1 Radical/Radical/Anionic Domino Processes; 3.3.2 Radical/Radical/Radical Domino Processes; 3.3.3 Radical/Radical/Pericyclic Domino Processes; 3.3.4 Radical/Radical/Oxidation Domino Processes; 3.4 Radical/Pericyclic Domino Processes; 4 Pericyclic Domino Reactions 4.1 Diels-Alder Reactions4.1.1 Diels-Alder/Diels-Alder Reactions; 4.1.2 Diels-Alder Reactions/Sigmatropic Rearrangements; 4.1.3 Diels-Alder/Retro-Diels-Alder Reactions; 4.1.4 Diels-Alder Reactions/Mixed Transformations; 4.1.5 Hetero-Diels-Alder Reactions; 4.2 1,3-Dipolar Cycloadditions; 4.3 [2+2] and Higher Cycloadditions; 4.4 Sigmatropic Rearrangements; 4.5 Electrocyclic Reactions; 4.6 Ene Reactions; 4.7 Retro-Pericyclic Reactions; 5 Photochemically Induced Domino Processes; 5.1 Photochemical/Cationic Domino Processes; 5.2 Photochemical/Anionic Domino Processes 5.3 Photochemical/Radical Domino Processes5.4 Photochemical/Pericyclic Domino Processes; 5.5 Photochemical/Photochemical Domino Processes; 5.6 Photochemical/Transition Metal-Catalyzed Domino Processes; 6 Transition Metal-Catalyzed Domino Reactions; 6.1 Palladium-Catalyzed Transformations; 6.1.1 The Heck Reaction; 6.1.1.1 Domino Heck Reactions; 6.1.1.2 Heck/Cross-Coupling Reactions; 6.1.1.3 Heck/Tsuji-Trost Reactions; 6.1.1.4 Heck Reactions/CO-Insertions; 6.1.1.5 Heck Reactions/C-H-Activations; 6.1.1.6 Heck Reactions: Pericyclic Transformations; 6.1.1.7 Heck Reactions/Mixed Transformations 6.1.2 Cross-Coupling Reactions6.1.2.1 Suzuki Reactions; 6.1.2.2 Stille Reactions; 6.1.2.3 Sonogashira Reactions; 6.1.2.4 Other Cross-Coupling Reactions; 6.1.3 Nucleophilic Substitution (Tsuji-Trost Reaction); 6.1.4 Reactions of Alkynes and Allenes; 6.1.5 Other Pd(0)-Catalyzed Transformations; 6.1.6 Pd(II)-Catalyzed Transformations; 6.2 Rhodium-Catalyzed Transformations; 6.2.1 Formation of Carbenes; 6.2.2 Hydroformylations; 6.2.3 Other Rhodium-Catalyzed Transformations; 6.3 Ruthenium-Catalyzed Transformations; 6.3.1 Metathesis Reactions; 6.3.1.1 Metathesis-Metathesis Processes 6.3.1.2 Metathesis/Heck Reaction/Pericyclic Reaction/Hydrogenation |
| Record Nr. | UNINA-9911019428603321 |
|
Tietze Lutz-Friedjan
|
||
| Weinheim, : Wiley-VCH, c2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Hydroformylation for Organic Synthesis / / edited by Maurizio Taddei, André Mann
| Hydroformylation for Organic Synthesis / / edited by Maurizio Taddei, André Mann |
| Edizione | [1st ed. 2013.] |
| Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 |
| Descrizione fisica | 1 online resource (VII, 229 p. 272 illus., 12 illus. in color.) |
| Disciplina | 547.1393 |
| Collana | Topics in Current Chemistry |
| Soggetto topico |
Chemistry, Organic
Catalysis Chemical engineering Organic Chemistry Industrial Chemistry/Chemical Engineering |
| ISBN | 3-642-45059-8 |
| Classificazione |
540
VA 1110 VK 5500 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | The role of metals and ligands in organic hydroformylation -- Hydroformylation in aqueous biphasic media assisted by molecular receptors -- Asymmetric hydroformylation -- Domino reactions triggered by hydroformylation -- Rhodium-catalyzed hydroformylation in fused azapolycycles synthesis -- Hydroformylation in natural product synthesis. |
| Record Nr. | UNINA-9910437803103321 |
| Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Introduzione ai meccanismi della chimica organica / Peter Sykes
| Introduzione ai meccanismi della chimica organica / Peter Sykes |
| Autore | Sykes, Peter |
| Pubbl/distr/stampa | Bologna : Zanichelli, 1997 |
| Descrizione fisica | x, 181 p. : ill. ; 24 cm |
| Disciplina | 547.1393 |
| Soggetto topico |
Organic chemistry
Chemical reactions |
| ISBN | 9788808088765 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNISALENTO-991002463449707536 |
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Sykes, Peter
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| Bologna : Zanichelli, 1997 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
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Metal-catalyzed Cross-coupling Reactions [[electronic resource]]
| Metal-catalyzed Cross-coupling Reactions [[electronic resource]] |
| Autore | Diederich Francois |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2008 |
| Descrizione fisica | 1 online resource (542 p.) |
| Disciplina |
547.1393
547.2 |
| Altri autori (Persone) | StangPeter |
| Soggetto topico |
Catalysis
Catalysis -- Industrial applications Metal catalysts -- Industrial applications Metal catalysts Organic compounds -- Synthesis Organometallic compounds Organic compounds - Synthesis Organic Chemistry Chemistry Physical Sciences & Mathematics |
| ISBN |
1-281-76389-6
9786611763893 3-527-61222-X 3-527-61220-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Metal-catalyzed Cross-coupling Reactions; Contents; 1 Palladium- or Nickel-catalyzed Cross-coupling with Organometals Containing Zinc, Magnesium, Aluminum, and Zirconium; 1.1 Introduction; 1.2 Systematic survey of palladium- or nickel-catalyzed cross-coupling; 1.2.1 Scope with respect to metal counterions and inhibition of catalysis by organolithiums; 1.2.2 Cross-coupling between two unsaturated carbon groups; 1.2.2.1 Palladium-catalyzed cross-coupling involving alkynylmetals and related alkynyl nucleophiles: alkynyl-aryl, alkynyl-alkenyl, and alkynyl-alkynyl coupling
1.2.2.2 Hydrometallation cross-coupling and carbometallation - cross-coupling tandem protocols and other alkenyl-aryl, alkenyl-alkenyl, and alkenyl- alkynyl coupling reactions: double metal catalysis1.2.2.3 Aryl-aryl coupling; 1.2.3 Palladium-catalyzed cross-coupling involving alkyl groups without proximal unsaturation.; 1.2.4 Cross-coupling involving allyl, benzyl, and propargyl groups; 1.2.4.1 Coupling reactions of alkenyl- and arylmetals with allyl, benzyl, and propargyl electrophiles; 1.2.4.2 Cross-coupling with allyl- and benzylmetals; 1.2.5 Cross-coupling involving carbonyl compounds 1.2.5.1 Palladium-catalyzed acylation of organometals with acyl halides1.2.5.2 Palladium-catalyzed allylation and related reactions of enolates; 1.2.5.3 a-Substitution of carbonyl compounds with unsaturated carbon groups; 1.2.6 Leaving groups; 1.2.7 Ligands; 1.3 Assymetric cross-coupling; 1.4 Palladium-catalyzed tandem processes involving cross-coupling reactions; 1.5 Mechanism of cross-coupling; 1.6 Conclusions; 1.7 Representative experimental procedures; 1.7.1 p.Methoxyphenylethyne (1) [42]; 1.7.1.1 Preparation of ethynylzinc chloride; 1.7.1.2 Preparation of p-methoxyphenylethyne 1.7.2 (7E,9E, 13E)-Retinol (vitamin A)1.7.3 a-Farnesene; 1.7.4 (Z)-1 -[ 1'-methyl-(E)-2'-heptenylidene]indan; Abbreviations .; References; 2 Cross-coupling Reactions of Organoboron Compounds with Organic Halides; 2.1 Introduction; 2.2 Preparation of organoboron compounds; 2.2.1 Hydroboration of alkenes and alkynes; 2.2.2 Haloboration of terminal alkynes; 2.2.3 Preparation from organolithium and magnesium reagents; 2.2.4 Miscellaneous methods; 2.3 Palladium-catalyzed reactions of organoboron compounds and their mechanism; 2.3.1 Cross-coupling reactions 2.3.2 Other reactions catalyzed by transition-metal complexes2.4 Cross-coupling reactions of organoboron compounds; 2.4.1 Coupling of 1 -alkenylboron derivatives: Synthesis of conjugated dienes; 2.4.2 Coupling of arylboron compounds: Synthesis of biaryls; 2.4.3 Coupling of alkyboron derivatives; 2.4.4 Reactions with triflates; 2.4.5 Carbonylative coupling; 2.5 Conclusions; 2.6 Experimental procedures; 2.6.1 Reaction of 1-alkenylboronates with vinylic halides: Synthesis of (lZ,3E) -1-phenyl- 1, 3-octadiene; 2.6.1.1 (E)- 1 -Hexenyl- 1.3, 2-benzodioxaborole 2.6.1.2 (1Z,3E - 1-Phenyl-1, 3-octadiene |
| Record Nr. | UNISA-996202133603316 |
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Diederich Francois
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| Hoboken, : Wiley, 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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