Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Copper catalysis in organic synthesis / / edited by Gopinathan Anilkumar, Salim Saranya
| Copper catalysis in organic synthesis / / edited by Gopinathan Anilkumar, Salim Saranya |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH, , [2020] |
| Descrizione fisica | 1 online resource (506 pages) |
| Disciplina | 546.652595 |
| Soggetto topico |
Organic compounds - Synthesis
Copper catalysts |
| ISBN |
3-527-82643-2
3-527-82642-4 3-527-82644-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Copper Catalysis / Salim Saranya, Gopinathan Anilkumar -- Cu-Catalyst in Reactions Involving Pyridinium and Indolizinium Moieties / Bianca Furdui, Andrea V Dediu, Rodica M Dinica -- Copper-Catalyzed Cross-Coupling Reactions of Organoboron Compounds / Jan Nekvinda, Webster L Santos -- Cu-Catalyzed Homocoupling Reactions / Ganesh C Nandi, Sundaresan Ravindra, Cholakkaparambil Irfana Jesin, Parameswaran Sasikumar, Kokkuvayil V Radhakrishnan -- Cu-Catalyzed Organic Reactions in Aqueous Media / Noel Nebra, Joaquín García-Álvarez -- Cu-Catalyzed Organic Reactions in Deep Eutectic Solvents (DESs) / Noel Nebra, Joaquín García-Álvarez -- Microwave-Assisted Cu-Catalyzed Organic Reactions / Bogdan Štefane, Helena Brodnik-Žugelj, Uroš Grošelj, Jurij Svete, Franc Požgan -- Cu-Catalyzed Asymmetric Synthesis / Hidetoshi Noda, Naoya Kumagai, Masakatsu Shibasaki -- Cu-Catalyzed Click Reactions / Rajagopal Ramkumar, Pazhamalai Anbarasan -- Cu-Catalyzed Multicomponent Reactions / Thachapully D Suja, Rajeev S Menon -- Copper-Catalyzed Aminations / Nissy Ann Harry, Rajenahally V Jagadeesh -- Cu-Catalyzed Carbonylation Reactions / Parameswaran Sasikumar, Thoppe S Priyadarshini, Sanjay Varma, Ganesh C Nandi, Kokkuvayil V Radhakrishnan -- Ligand-Free, Cu-Catalyzed Reactions / Muhammad F Jamali, Sanoop P Chandrasekharan, Kishor Mohanan -- Copper-Catalyzed Decarboxylative Coupling / Firas El-Hage, Jola Pospech -- Copper-Catalyzed C-H Activation / Xun-Xiang Guo -- Aerobic Cu-Catalyzed Organic Reactions / Ahmad A Almasalma, Esteban Mejia -- Copper-Catalyzed Trifluoromethylation Reactions / Dzmitry G Kananovich -- Cu-Catalyzed Reactions for Carbon-Heteroatom Bond Formations / Govindasamy Sekar, Subramani Sangeetha, Anuradha Nandy, Rajib Saha -- Cu-Assisted Cyanation Reactions / Sumanta Garai, Ganesh A Thakur -- Application of Cu-Mediated Reactions in the Synthesis of Natural Products / Anas Ansari, Ramesh Ramapanicker. |
| Record Nr. | UNINA-9910555298703321 |
| Weinheim, Germany : , : Wiley-VCH, , [2020] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Copper catalysis in organic synthesis / / edited by Gopinathan Anilkumar, Salim Saranya
| Copper catalysis in organic synthesis / / edited by Gopinathan Anilkumar, Salim Saranya |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH, , [2020] |
| Descrizione fisica | 1 online resource (506 pages) |
| Disciplina | 546.652595 |
| Soggetto topico |
Organic compounds - Synthesis
Copper catalysts |
| ISBN |
3-527-82643-2
3-527-82642-4 3-527-82644-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Copper Catalysis / Salim Saranya, Gopinathan Anilkumar -- Cu-Catalyst in Reactions Involving Pyridinium and Indolizinium Moieties / Bianca Furdui, Andrea V Dediu, Rodica M Dinica -- Copper-Catalyzed Cross-Coupling Reactions of Organoboron Compounds / Jan Nekvinda, Webster L Santos -- Cu-Catalyzed Homocoupling Reactions / Ganesh C Nandi, Sundaresan Ravindra, Cholakkaparambil Irfana Jesin, Parameswaran Sasikumar, Kokkuvayil V Radhakrishnan -- Cu-Catalyzed Organic Reactions in Aqueous Media / Noel Nebra, Joaquín García-Álvarez -- Cu-Catalyzed Organic Reactions in Deep Eutectic Solvents (DESs) / Noel Nebra, Joaquín García-Álvarez -- Microwave-Assisted Cu-Catalyzed Organic Reactions / Bogdan Štefane, Helena Brodnik-Žugelj, Uroš Grošelj, Jurij Svete, Franc Požgan -- Cu-Catalyzed Asymmetric Synthesis / Hidetoshi Noda, Naoya Kumagai, Masakatsu Shibasaki -- Cu-Catalyzed Click Reactions / Rajagopal Ramkumar, Pazhamalai Anbarasan -- Cu-Catalyzed Multicomponent Reactions / Thachapully D Suja, Rajeev S Menon -- Copper-Catalyzed Aminations / Nissy Ann Harry, Rajenahally V Jagadeesh -- Cu-Catalyzed Carbonylation Reactions / Parameswaran Sasikumar, Thoppe S Priyadarshini, Sanjay Varma, Ganesh C Nandi, Kokkuvayil V Radhakrishnan -- Ligand-Free, Cu-Catalyzed Reactions / Muhammad F Jamali, Sanoop P Chandrasekharan, Kishor Mohanan -- Copper-Catalyzed Decarboxylative Coupling / Firas El-Hage, Jola Pospech -- Copper-Catalyzed C-H Activation / Xun-Xiang Guo -- Aerobic Cu-Catalyzed Organic Reactions / Ahmad A Almasalma, Esteban Mejia -- Copper-Catalyzed Trifluoromethylation Reactions / Dzmitry G Kananovich -- Cu-Catalyzed Reactions for Carbon-Heteroatom Bond Formations / Govindasamy Sekar, Subramani Sangeetha, Anuradha Nandy, Rajib Saha -- Cu-Assisted Cyanation Reactions / Sumanta Garai, Ganesh A Thakur -- Application of Cu-Mediated Reactions in the Synthesis of Natural Products / Anas Ansari, Ramesh Ramapanicker. |
| Record Nr. | UNINA-9910830812003321 |
| Weinheim, Germany : , : Wiley-VCH, , [2020] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Copper(I)-catalyzed stereoselective borylation reactions : multisubstituted alkenyl and allylic boronates / / Yu Ozawa
| Copper(I)-catalyzed stereoselective borylation reactions : multisubstituted alkenyl and allylic boronates / / Yu Ozawa |
| Autore | Ozawa Yu |
| Edizione | [1st ed. 2023.] |
| Pubbl/distr/stampa | Singapore : , : Springer, , [2023] |
| Descrizione fisica | 1 online resource (236 pages) |
| Disciplina | 546.652595 |
| Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
| Soggetto topico |
Copper catalysts
Organoboron compounds - Synthesis |
| ISBN |
9789819910984
9789819910977 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | 1. General Introduction -- 2. Modification of QuinoxP*-Type Bisphosphine Ligands for High-Performance Asymmetric Boryl Substitution of Racemic Allyl Electrophiles -- 3. Allylcopper(I) Isomerization-Enabled Copper(I)-Catalyzed Intramolecular Alkylboration of Terminal Allenes -- 4. Intermolecular Alkylboration of gem-Disubstituted Allenes for Stereoselective Synthesis of Multi-Alkylated Allylic Boronates -- 5. Computational Investigation on Copper(I)-Catalyzed Enantioselective Radical Borylation of Benzyl Halides -- 6. Summary of This Thesis. |
| Record Nr. | UNINA-9910720074003321 |
Ozawa Yu
|
||
| Singapore : , : Springer, , [2023] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Copper-catalyzed asymmetric synthesis / / edited by Alexandre Alexakis, Norbert Krause, and Simon Woodward ; Shinya Adachi [and thirty-one others] ; contributors
| Copper-catalyzed asymmetric synthesis / / edited by Alexandre Alexakis, Norbert Krause, and Simon Woodward ; Shinya Adachi [and thirty-one others] ; contributors |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany : , : Wiley-VCH Verlag GmbH & Co., , 2014 |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
AlexakisAlexandre
KrauseNorbert WoodwardSimon AdachiShinya |
| Soggetto topico |
Asymmetric synthesis
Copper catalysts Organocopper compounds Organic compounds - Synthesis |
| ISBN |
3-527-66457-2
3-527-66459-9 3-527-66460-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Copper-Catalyzed Asymmetric Synthesis; Contents; List of Contributors; Introduction; Chapter 1 The Primary Organometallic in Copper-Catalyzed Reactions; 1.1 Scope and Introduction; 1.2 Terminal Organometallics Sources Available; 1.3 Coordination Motifs in Asymmetric Copper Chemistry; 1.3.1 Classical Cuprate Structure and Accepted Modes of Reaction; 1.3.1.1 Conjugate Addition; 1.3.1.2 SN2 Allylation Reactions; 1.3.2 Motifs in Copper-Main Group Bimetallics and Substrate Binding; 1.4 Asymmetric Organolithium-Copper Reagents; 1.5 Asymmetric Grignard-Copper Reagents
1.6 Asymmetric Organozinc-Copper Reagents1.7 Asymmetric Organoboron-Copper Reagents; 1.8 Asymmetric Organoaluminium-Copper Reagents; 1.9 Asymmetric Silane and Stannane Copper-Promoted Reagents; 1.10 Conclusions; References; Chapter 2 Copper-Catalyzed Asymmetric Conjugate Addition; 2.1 Introduction; 2.2 Conjugate Addition; 2.2.1 The Nucleophile; 2.2.2 The Copper Salt; 2.2.3 The Ligand; 2.2.4 Scope of Michael Acceptors; 2.2.4.1 Enones; 2.2.4.2 Enals; 2.2.4.3 Nitroalkenes; 2.2.4.4 α,β-Unsaturated Amide and Ester Derivatives; 2.2.4.5 Other Michael Acceptors 2.2.5 Formation of All-Carbon Quaternary Stereocenters2.3 Trapping of Enolates; References; Chapter 3 Copper-Catalyzed Asymmetric Conjugate Addition and Allylic Substitution of Organometallic Reagents to Extended Multiple-Bond Systems; 3.1 Introduction; 3.2 Copper-Catalyzed Asymmetric Conjugate Addition (ACA) to Polyconjugated Michael Acceptors; 3.2.1 Background; 3.2.2 1,6 Selectivity in ACA to Polyconjugated Systems; 3.2.3 1,4 Selectivity in ACA to Polyconjugated Systems; 3.3 Copper-Catalyzed Asymmetric Allylic Substitution on Extended Multiple-Bond Systems; 3.3.1 Background 3.3.2 Copper-Catalyzed Enantioselective Allylic Substitution on Extended Multiple-Bond Systems3.4 Conclusion; References; Chapter 4 Asymmetric Allylic Alkylation; 4.1 Introduction; 4.2 Nucleophiles in Enantioselective Process Development; 4.2.1 Grignard Nucleophiles; 4.2.2 Diorganozinc Nucleophiles; 4.2.3 Triorganoaluminium Nucleophiles; 4.2.4 Organoboranes Nucleophiles; 4.2.5 Organolithium Nucleophiles; 4.3 Functionalized Substrates; 4.3.1 Trisubstituted Substrates; 4.3.2 Ester Derivatives; 4.3.3 Heterofunctionalized Substrates; 4.3.4 Vinylic Boronates and Silanes 4.3.5 Substrates Bearing Two Leaving Groups (1,4 or 1,1')4.3.6 Enyne-Type Substrates; 4.4 Desymmetrization of meso-Allylic Substrates; 4.4.1 Polycyclic Hydrazines, Symmetric Allylic Epoxides, Oxabicyclic Alkenes; 4.4.2 Cyclic Allylic Bis(Diethyl phosphates); 4.4.3 Miscellaneous Desymmetrization; 4.5 Kinetic Resolution Processes; 4.5.1 Allylic Epoxides and Aziridines, Oxabicyclic Alkenes, Bicyclic Oxazines; 4.5.2 Stereodivergent Kinetic Resolution on Acyclic Allylic Halides; 4.6 Direct Enantioconvergent Transformation; 4.7 Conclusion and Perspectives; References Chapter 5 Ring Opening of Epoxides and Related Systems |
| Record Nr. | UNINA-9910138966103321 |
| Weinheim an der Bergstrasse, Germany : , : Wiley-VCH Verlag GmbH & Co., , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Copper-catalyzed asymmetric synthesis / / edited by Alexandre Alexakis, Norbert Krause, and Simon Woodward ; Shinya Adachi [and thirty-one others] ; contributors
| Copper-catalyzed asymmetric synthesis / / edited by Alexandre Alexakis, Norbert Krause, and Simon Woodward ; Shinya Adachi [and thirty-one others] ; contributors |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany : , : Wiley-VCH Verlag GmbH & Co., , 2014 |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
AlexakisAlexandre
KrauseNorbert WoodwardSimon AdachiShinya |
| Soggetto topico |
Asymmetric synthesis
Copper catalysts Organocopper compounds Organic compounds - Synthesis |
| ISBN |
3-527-66457-2
3-527-66459-9 3-527-66460-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Copper-Catalyzed Asymmetric Synthesis; Contents; List of Contributors; Introduction; Chapter 1 The Primary Organometallic in Copper-Catalyzed Reactions; 1.1 Scope and Introduction; 1.2 Terminal Organometallics Sources Available; 1.3 Coordination Motifs in Asymmetric Copper Chemistry; 1.3.1 Classical Cuprate Structure and Accepted Modes of Reaction; 1.3.1.1 Conjugate Addition; 1.3.1.2 SN2 Allylation Reactions; 1.3.2 Motifs in Copper-Main Group Bimetallics and Substrate Binding; 1.4 Asymmetric Organolithium-Copper Reagents; 1.5 Asymmetric Grignard-Copper Reagents
1.6 Asymmetric Organozinc-Copper Reagents1.7 Asymmetric Organoboron-Copper Reagents; 1.8 Asymmetric Organoaluminium-Copper Reagents; 1.9 Asymmetric Silane and Stannane Copper-Promoted Reagents; 1.10 Conclusions; References; Chapter 2 Copper-Catalyzed Asymmetric Conjugate Addition; 2.1 Introduction; 2.2 Conjugate Addition; 2.2.1 The Nucleophile; 2.2.2 The Copper Salt; 2.2.3 The Ligand; 2.2.4 Scope of Michael Acceptors; 2.2.4.1 Enones; 2.2.4.2 Enals; 2.2.4.3 Nitroalkenes; 2.2.4.4 α,β-Unsaturated Amide and Ester Derivatives; 2.2.4.5 Other Michael Acceptors 2.2.5 Formation of All-Carbon Quaternary Stereocenters2.3 Trapping of Enolates; References; Chapter 3 Copper-Catalyzed Asymmetric Conjugate Addition and Allylic Substitution of Organometallic Reagents to Extended Multiple-Bond Systems; 3.1 Introduction; 3.2 Copper-Catalyzed Asymmetric Conjugate Addition (ACA) to Polyconjugated Michael Acceptors; 3.2.1 Background; 3.2.2 1,6 Selectivity in ACA to Polyconjugated Systems; 3.2.3 1,4 Selectivity in ACA to Polyconjugated Systems; 3.3 Copper-Catalyzed Asymmetric Allylic Substitution on Extended Multiple-Bond Systems; 3.3.1 Background 3.3.2 Copper-Catalyzed Enantioselective Allylic Substitution on Extended Multiple-Bond Systems3.4 Conclusion; References; Chapter 4 Asymmetric Allylic Alkylation; 4.1 Introduction; 4.2 Nucleophiles in Enantioselective Process Development; 4.2.1 Grignard Nucleophiles; 4.2.2 Diorganozinc Nucleophiles; 4.2.3 Triorganoaluminium Nucleophiles; 4.2.4 Organoboranes Nucleophiles; 4.2.5 Organolithium Nucleophiles; 4.3 Functionalized Substrates; 4.3.1 Trisubstituted Substrates; 4.3.2 Ester Derivatives; 4.3.3 Heterofunctionalized Substrates; 4.3.4 Vinylic Boronates and Silanes 4.3.5 Substrates Bearing Two Leaving Groups (1,4 or 1,1')4.3.6 Enyne-Type Substrates; 4.4 Desymmetrization of meso-Allylic Substrates; 4.4.1 Polycyclic Hydrazines, Symmetric Allylic Epoxides, Oxabicyclic Alkenes; 4.4.2 Cyclic Allylic Bis(Diethyl phosphates); 4.4.3 Miscellaneous Desymmetrization; 4.5 Kinetic Resolution Processes; 4.5.1 Allylic Epoxides and Aziridines, Oxabicyclic Alkenes, Bicyclic Oxazines; 4.5.2 Stereodivergent Kinetic Resolution on Acyclic Allylic Halides; 4.6 Direct Enantioconvergent Transformation; 4.7 Conclusion and Perspectives; References Chapter 5 Ring Opening of Epoxides and Related Systems |
| Record Nr. | UNINA-9910824691103321 |
| Weinheim an der Bergstrasse, Germany : , : Wiley-VCH Verlag GmbH & Co., , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Copper-mediated cross-coupling reactions / / edited by Gwilherm Evano, Laboratoire de chimie organique, Service de chimie et physicochimie organiques, Université libre de Bruxelles, Brussels, Belgium, Nicolas Blanchard, Université de Strasbourg, École européenne de chimie, polymères et Matériaux, Laboratoire de chimie moléculaire associé au CNRS, Strasbourg, France
| Copper-mediated cross-coupling reactions / / edited by Gwilherm Evano, Laboratoire de chimie organique, Service de chimie et physicochimie organiques, Université libre de Bruxelles, Brussels, Belgium, Nicolas Blanchard, Université de Strasbourg, École européenne de chimie, polymères et Matériaux, Laboratoire de chimie moléculaire associé au CNRS, Strasbourg, France |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , [2014] |
| Descrizione fisica | 1 online resource (836 p.) |
| Disciplina | 546/.652595 |
| Altri autori (Persone) |
EvanoGwilherm
BlanchardNicolas |
| Soggetto topico |
Copper catalysts
Copper - Reactivity Chemical bonds Organic compounds - Synthesis |
| ISBN |
1-118-69047-8
1-118-69065-6 1-118-69068-0 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Machine generated contents note: Introduction Copper catalysis from an historical perspective: a legacy from the past Gwilherm Evano and Nicolas Blanchard PART 1 FORMATION OF C-HETEROATOM BONDS Chapter 1: Modern Ullmann-Goldberg Chemistry: Arylation of N-nucleophiles with Aryl Halides Yongwen Jiang and Dawei Ma Chapter 2: Ullmann condensation today: arylation of alcohols and thiols with aryl halides Anis Tlili and Marc Taillefer Chapter 3: Copper-Catalyzed Formation of C-P Bonds with Aryl Halides Carole Alayrac and Annie-Claude Gaumont Chapter 4: Alternative and Emerging Reagents for the Arylation of Heteronucleophiles Luc Neuville Chapter 5: Beyond Ullmann-Goldberg Chemistry: Vinylation, Alkynylation and Allenylation of Heteronucleophiles Kevin Jouvin and Gwilherm Evano Chapter 6: Aromatic/Vinylic Finkelstein Reaction Alicia Casitas and Xavi Ribas Chapter 7: Insights into the Mechanism of Modern Ullmann-Goldberg Coupling Reactions Alicia Casitas and Xavi Ribas PART 2 FORMATION OF C-C BONDS Chapter 8: Modern Copper-Catalyzed Hurtley Reaction: Efficient C-Arylation of CH-Acid Derivatives Irina P Beletskaya and Alexey Yu Fedorov Chapter 9: Copper-Catalyzed Cyanations of Aryl Halides and Related Compounds Thomas Schareina and Matthias Beller Chapter 10: Copper-Mediated Aryl-aryl Bond Formation Leading to Biaryls: A Century After Ullmann Breakthrough Yoshihiko Yamamoto Chapter 11: Copper-Catalyzed Alkynylation, Alkenylation and Allylation Reaction of Aryl Derivatives Ren-Jie Song and Jin-Heng Li Chapter 12: Copper-Catalyzed Alkynylation and Alkenylation Reaction of Alkynyl Derivatives: New Access to Diynes and Enynes Ruimao Hua Chapter 13: Copper-Mediated Alkenylation Reaction of Alkenyl Derivatives: a Straightforward Elaboration of 1,3-Dienes Hao Li, Songbai Liu, and Lanny S Liebeskind Chapter 14: Emerging Areas in Copper-Mediated Trifluoromethylations: Catalytic and Oxidative Cross-Coupling Processes Kevin Jouvin, Celine Guissart and Gwilherm Evano PART 3 APPLICATIONS OF COPPER CATALYZED CROSS COUPLING REACTIONS: HETEROCYCLES, NATURAL PRODUCTS, PROCESS AND SUSTAINABLE CHEMISTRY Chapter 15: Copper-Mediated Cyclization Reactions: New Entries to Heterocycles Daoshan Yang and Hua Fu Chapter 16: Copper-Mediated C-N Bond Forming Reactions: New Opportunities in Natural Product Synthesis Jihoon Lee and James S Panek Chapter 17: Natural Products and C-O/C-S Bond Forming Reactions: Copper Showed the Way Doron Pappo Chapter 18: Copper-Catalyzed C-C Bond Formation in Natural Product Synthesis: Elegant and Efficient Solutions to a Key Bond Disconnection Morgan Donnard and Nicolas Blanchard Chapter 19: Process Chemistry and Copper Catalysis Klaus Kunz and Norbert Lui Chapter 20: Reusable Catalysts for Copper-Mediated Coupling Reactions under Heterogeneous Conditions Zhiyong Wang, Changfeng Wan and Ye Wang. |
| Record Nr. | UNINA-9910139000803321 |
| Hoboken, New Jersey : , : Wiley, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Copper-mediated cross-coupling reactions / / edited by Gwilherm Evano, Laboratoire de chimie organique, Service de chimie et physicochimie organiques, Université libre de Bruxelles, Brussels, Belgium, Nicolas Blanchard, Université de Strasbourg, École européenne de chimie, polymères et Matériaux, Laboratoire de chimie moléculaire associé au CNRS, Strasbourg, France
| Copper-mediated cross-coupling reactions / / edited by Gwilherm Evano, Laboratoire de chimie organique, Service de chimie et physicochimie organiques, Université libre de Bruxelles, Brussels, Belgium, Nicolas Blanchard, Université de Strasbourg, École européenne de chimie, polymères et Matériaux, Laboratoire de chimie moléculaire associé au CNRS, Strasbourg, France |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , [2014] |
| Descrizione fisica | 1 online resource (836 p.) |
| Disciplina | 546/.652595 |
| Altri autori (Persone) |
EvanoGwilherm
BlanchardNicolas |
| Soggetto topico |
Copper catalysts
Copper - Reactivity Chemical bonds Organic compounds - Synthesis |
| ISBN |
1-118-69047-8
1-118-69065-6 1-118-69068-0 |
| Classificazione | SCI013050 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Machine generated contents note: Introduction Copper catalysis from an historical perspective: a legacy from the past Gwilherm Evano and Nicolas Blanchard PART 1 FORMATION OF C-HETEROATOM BONDS Chapter 1: Modern Ullmann-Goldberg Chemistry: Arylation of N-nucleophiles with Aryl Halides Yongwen Jiang and Dawei Ma Chapter 2: Ullmann condensation today: arylation of alcohols and thiols with aryl halides Anis Tlili and Marc Taillefer Chapter 3: Copper-Catalyzed Formation of C-P Bonds with Aryl Halides Carole Alayrac and Annie-Claude Gaumont Chapter 4: Alternative and Emerging Reagents for the Arylation of Heteronucleophiles Luc Neuville Chapter 5: Beyond Ullmann-Goldberg Chemistry: Vinylation, Alkynylation and Allenylation of Heteronucleophiles Kevin Jouvin and Gwilherm Evano Chapter 6: Aromatic/Vinylic Finkelstein Reaction Alicia Casitas and Xavi Ribas Chapter 7: Insights into the Mechanism of Modern Ullmann-Goldberg Coupling Reactions Alicia Casitas and Xavi Ribas PART 2 FORMATION OF C-C BONDS Chapter 8: Modern Copper-Catalyzed Hurtley Reaction: Efficient C-Arylation of CH-Acid Derivatives Irina P Beletskaya and Alexey Yu Fedorov Chapter 9: Copper-Catalyzed Cyanations of Aryl Halides and Related Compounds Thomas Schareina and Matthias Beller Chapter 10: Copper-Mediated Aryl-aryl Bond Formation Leading to Biaryls: A Century After Ullmann Breakthrough Yoshihiko Yamamoto Chapter 11: Copper-Catalyzed Alkynylation, Alkenylation and Allylation Reaction of Aryl Derivatives Ren-Jie Song and Jin-Heng Li Chapter 12: Copper-Catalyzed Alkynylation and Alkenylation Reaction of Alkynyl Derivatives: New Access to Diynes and Enynes Ruimao Hua Chapter 13: Copper-Mediated Alkenylation Reaction of Alkenyl Derivatives: a Straightforward Elaboration of 1,3-Dienes Hao Li, Songbai Liu, and Lanny S Liebeskind Chapter 14: Emerging Areas in Copper-Mediated Trifluoromethylations: Catalytic and Oxidative Cross-Coupling Processes Kevin Jouvin, Celine Guissart and Gwilherm Evano PART 3 APPLICATIONS OF COPPER CATALYZED CROSS COUPLING REACTIONS: HETEROCYCLES, NATURAL PRODUCTS, PROCESS AND SUSTAINABLE CHEMISTRY Chapter 15: Copper-Mediated Cyclization Reactions: New Entries to Heterocycles Daoshan Yang and Hua Fu Chapter 16: Copper-Mediated C-N Bond Forming Reactions: New Opportunities in Natural Product Synthesis Jihoon Lee and James S Panek Chapter 17: Natural Products and C-O/C-S Bond Forming Reactions: Copper Showed the Way Doron Pappo Chapter 18: Copper-Catalyzed C-C Bond Formation in Natural Product Synthesis: Elegant and Efficient Solutions to a Key Bond Disconnection Morgan Donnard and Nicolas Blanchard Chapter 19: Process Chemistry and Copper Catalysis Klaus Kunz and Norbert Lui Chapter 20: Reusable Catalysts for Copper-Mediated Coupling Reactions under Heterogeneous Conditions Zhiyong Wang, Changfeng Wan and Ye Wang. |
| Record Nr. | UNINA-9910814093603321 |
| Hoboken, New Jersey : , : Wiley, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
