Cargando…
Advances in Transition-Metal Mediated Heterocyclic Synthesis /
Advances in Transition-Metal Mediated Heterocyclic Synthesis provides an overview of recent catalytic reactions involving transition metals�i�A�to produce heterocyclic compounds. The book is organized according to the type of transformation used to achieve the synthesis of the heterocyclic systems (...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
London :
Academic Press, An imprint of Elsevier,
[2018]
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000 i 4500 | ||
|---|---|---|---|
| 001 | SCIDIR_on1037272358 | ||
| 003 | OCoLC | ||
| 005 | 20231120010256.0 | ||
| 006 | m o d | ||
| 007 | cr cnu|||unuuu | ||
| 008 | 180524s2018 enka ob 001 0 eng d | ||
| 040 | |a N$T |b eng |e rda |e pn |c N$T |d N$T |d OPELS |d YDX |d EBLCP |d OCLCF |d STF |d MERER |d OCLCQ |d CNCGM |d OTZ |d NLE |d INT |d AU@ |d UKMGB |d OCLCQ |d U3W |d LVT |d OCLCQ |d D6H |d SNK |d LQU |d ABC |d OCLCQ |d S2H |d OCLCO |d OCLCQ |d OCLCO |d K6U |d OCLCQ |d SFB |d OCLCQ |d OCLCO | ||
| 066 | |c (S | ||
| 016 | 7 | |a 018880091 |2 Uk | |
| 019 | |a 1037808063 |a 1039404455 |a 1105189577 |a 1105573803 |a 1229491629 | ||
| 020 | |a 9780128116524 |q (electronic bk.) | ||
| 020 | |a 0128116528 |q (electronic bk.) | ||
| 020 | |z 9780128116517 | ||
| 020 | |z 012811651X | ||
| 035 | |a (OCoLC)1037272358 |z (OCoLC)1037808063 |z (OCoLC)1039404455 |z (OCoLC)1105189577 |z (OCoLC)1105573803 |z (OCoLC)1229491629 | ||
| 050 | 4 | |a QD400.5.S95 | |
| 072 | 7 | |a SCI |x 013040 |2 bisacsh | |
| 082 | 0 | 4 | |a 547.59 |2 23 |
| 245 | 0 | 0 | |a Advances in Transition-Metal Mediated Heterocyclic Synthesis / |c edited by Daniel Sol�e, Israel Fern�andez. |
| 264 | 1 | |a London : |b Academic Press, An imprint of Elsevier, |c [2018] | |
| 300 | |a 1 online resource : |b illustrations | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Online resource; title from PDF title page (EBSCO, viewed May 25, 2018). | |
| 520 | |a Advances in Transition-Metal Mediated Heterocyclic Synthesis provides an overview of recent catalytic reactions involving transition metals�i�A�to produce heterocyclic compounds. The book is organized according to the type of transformation used to achieve the synthesis of the heterocyclic systems (mainly aza- and oxa-heterocycles). As such, it covers recent applications on the synthesis of heterocycles, also describing the details of the novel transformations in a didactic manner to motivate readers in search of new catalytic processes. The editors have included state-of-the-art strategies, including transition-metal reactions involving unsaturated systems (reactions of allenes, new gold(I)-catalyzed reactions, and Prins reaction). Chapters highlight the versatility of organopalladium chemistry dealing with carbonylative transformations, C-H activation reactions, coupling processes, and the control of the ambiphilic character of organopalladium species. Finally, the book discusses new reactions leading to heterocycles based on C-H activation processes catalyzed by other metals (Rh, Ru, Co). Written by an outstanding team of authors who are leading experts in organometallic chemistry and organic synthesis, this book is a valuable resource not only for chemists mainly focused on synthesis, but also for those interested in reaction mechanisms involving transition metals. | ||
| 505 | 0 | |6 880-01 |a Front Cover; Advances in Transition-Metal Mediated Heterocyclic Synthesis; Copyright Page; Contents; List of Contributors; Foreword; 1 Metal-Mediated Synthesis of Nonaromatic Oxacycles From Allenols; 1.1 Introduction; 1.2 Silver-Catalyzed Reactions; 1.3 Gold-Catalyzed Reactions; 1.4 Platinum-Catalyzed Reactions; 1.5 Palladium-Catalyzed Reactions; 1.6 Lanthanum-Catalyzed Reactions; 1.7 Gallium-Catalyzed Reactions; 1.8 Conclusion; References; 2 Intramolecular Diamination of Alkenes; 2.1 Introduction. | |
| 505 | 8 | |a 2.2 Metal-Catalyzed Synthesis of Heterocycles Through the Oxidative Intramolecular Vicinal Diamination of Alkenes2.2.1 Palladium Catalysis; 2.2.2 Other Metal Catalysis Using Iodine(III) Oxidants; 2.2.3 Copper Catalysis; 2.3 Metal-Catalyzed Synthesis of Heterocycles Through the Oxidative Intra-/Intermolecular Vicinal Diamination of Alkenes; 2.3.1 Palladium Catalysis; 2.3.2 Copper Catalysis; 2.4 Metal-Catalyzed Synthesis of Heterocycles Through the Oxidative Intermolecular Vicinal Diamination of Alkenes; 2.5 Summary and Outlook; References. | |
| 505 | 8 | |a 3.2.2.2 With Halides Together With Nucleophilic Partners3.2.2.3 With Halides Together With Electrophilic Partners; 3.2.2.4 With Halides Together With Alkenes and Imines; 3.2.2.5 With Halides Together With Alkynes and Arynes; 3.2.2.6 With Other Substrates; 3.3 Palladium-Catalyzed Carbonylation Processes Leading to Heterocycles Without Incorporation of CO into the Cycle; 3.3.1 Under Oxidative Conditions; 3.3.1.1 Through Carbonylative Carbocyclization; 3.3.1.2 Through Heterocyclization-Alkoxycarbonylation; 3.3.1.3 Through Heterocyclization-Carbonylation-Cyclization Coupling. | |
| 505 | 8 | |a 3.3.1.4 Through Monocarbonylation of Terminal Alkynes Followed by Intramolecular Conjugate Addition3.3.2 Under Nonoxidative Conditions; 3.3.2.1 With Halides; 3.3.2.2 With Imine Derivatives; 3.3.2.3 With Functionalized Alkynes; 3.4 Conclusions and Perspectives; References; 4 Synthesis of Heterocyclic Compounds Based on Transition-Metal-Catalyzed Carbene Coupling Reactions; 4.1 Introduction; 4.2 Cyclization Prior to Metal Carbene Formation; 4.3 Cyclization Through Other Carbene Precursors; 4.4 Cyclization Through Reductive Elimination; 4.5 Cyclization Through Nucleophilic Displacement. | |
| 650 | 0 | |a Heterocyclic compounds. | |
| 650 | 0 | |a Transition metals. | |
| 650 | 0 | |a Transition metal catalysts. | |
| 650 | 2 | |a Heterocyclic Compounds |0 (DNLM)D006571 | |
| 650 | 6 | |a Compos�es h�et�erocycliques. |0 (CaQQLa)201-0006824 | |
| 650 | 6 | |a M�etaux de transition. |0 (CaQQLa)201-0011368 | |
| 650 | 6 | |a Catalyseurs �a base de m�etaux de transition. |0 (CaQQLa)201-0064129 | |
| 650 | 7 | |a SCIENCE |x Chemistry |x Organic. |2 bisacsh | |
| 650 | 7 | |a Heterocyclic compounds |2 fast |0 (OCoLC)fst00955736 | |
| 650 | 7 | |a Transition metal catalysts |2 fast |0 (OCoLC)fst01154758 | |
| 650 | 7 | |a Transition metals |2 fast |0 (OCoLC)fst01154781 | |
| 700 | 1 | |a Sol�e, Daniel, |e editor. | |
| 700 | 1 | |a Fern�andez, Israel, |e editor. | |
| 776 | 0 | 8 | |i Print version: |t Advances in Transition-Metal Mediated Heterocyclic Synthesis. |d London : Academic Press, An imprint of Elsevier, [2018] |z 012811651X |z 9780128116517 |w (OCoLC)1011519523 |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780128116517 |z Texto completo |
| 880 | 8 | |6 505-01/(S |a 3 Synthesis of Heterocycles by Palladium-Catalyzed Carbonylative Reactions3.1 Introduction; 3.2 Palladium-Catalyzed Cyclocarbonylations Leading to Heterocycles; 3.2.1 Under Oxidative Conditions; 3.2.1.1 With Alkyne and Alkene Derivatives (Without Direct C-H Activation); 3.2.1.2 With Acetylenic C-H Activation; 3.2.1.3 With Alkenylic C-H Activation; 3.2.1.4 With Aromatic C-H Activation; 3.2.1.5 With Aliphatic C-H Activation; 3.2.1.6 With Diols, β-Amino Alcohols, Diamines, and Related Compounds; 3.2.2 Under Nonoxidative Conditions; 3.2.2.1 With Functionalized Halides. | |