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171028s2017 nju o 000 0 eng d |
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|a EBLCP
|b eng
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|d OCLCQ
|d UEJ
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|d OCLCF
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|a 9783527697632
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|a 547.215
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|a UAMI
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|a Ackermann, Lutz.
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|a Catalytic Hydroarylation of Carbon-Carbon Multiple Bonds.
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|a Newark :
|b John Wiley & Sons, Incorporated,
|c 2017.
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| 300 |
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|a 1 online resource (416 pages)
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
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|2 rdacarrier
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|a Print version record.
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|a Cover -- Title Page -- Copyright -- Contents -- Introduction and Preface -- References -- Chapter 1 Functionalization of Heteroaromatic Substrates using Groups 9 and 10 Catalysts -- 1.1 Introduction -- 1.2 Thiophenes, furans, and Related Heterocycles -- 1.3 Pyrroles, Indoles, Pyridines, and Imidazopyridines -- 1.4 Azoles and Other Miscellaneous Heterocycles -- 1.5 Summary -- References -- Chapter 2 Ruthenium Catalysts for the Alkylation of Functionalized Arenes and Heteroaromatic Substrates via Hydroarylation -- 2.1 Introduction
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|a 2.2 Alkylation by Ruthenium(0) Catalysts via Oxidative-Addition C-H Activation2.2.1 Alkylation by Ruthenium(II) Catalysts via Carboxylate-Assisted C-H Activation -- 2.3 Summary and Conclusions -- Abbreviations -- References -- Chapter 3 Alkylation of Arenes Without Chelation Assistance: Transition Metal Catalysts with d6 Electron Configurations -- 3.1 Transition Metal-Mediated Arene Alkylation: Overview -- 3.2 Octahedral d6 Transition Metal Catalysts for Olefin Hydroarylation: Scorpionate Supported Ru(II) Catalysts
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|a 3.2.1 Structureâ#x80;#x93;Activity Relationships with TpRu(L)(NCMe)Ph: Examination of Elementary Steps and Catalytic Hydrophenylation of Ethylene as a Function of Ligand L3.2.2 Ethylene Hydrophenylation Catalyzed by Cationic Ru(II) Complexes Ligated by Poly(pyrazolyl)alkanes -- 3.3 Olefin Hydroarylation Catalyzed by Octahedral d6 Ir(III) Supported by the Acetylacetonate Ligand -- 3.3.1 Mechanism of Catalytic Olefin Hydrophenylation using Ir(III) Supported by the Acetylacetonate Ligand -- 3.3.2 Other d6 Ir(III) Catalysts
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|a 3.4 Summary: Comparison of Ru(II) and Ir(III) Catalysts for Olefin Hydroarylation3.5 Future Outlook: Extension of Olefin Hydroarylation using Hydrocarbons to Earth Abundant Metals -- References -- Chapter 4 Hydroarylation of Olefins with Complexes Bearing d8 Metal Centers -- 4.1 Introduction -- 4.2 PtII Catalyzed Hydroarylation -- 4.2.1 PtII Hydroarylation Catalysts Bearing Anionic Bidentate (NN) Ligands -- 4.2.2 PtII Hydroarylation Catalysts Bearing Neutral Bidentate (NN) Ligands -- 4.2.3 PtII Hydroarylation Catalysts Supported by Nonnitrogen-based Ligands
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|a 4.2.4 Summary of PtII Catalyzed Hydroarylations4.3 RhI-Catalyzed Hydroarylation -- 4.3.1 Reactions of Unfunctionalized Arenes with RhI Complexes Proceeding via Hydroarylation-Like Mechanisms -- 4.3.2 Directed ortho-Hydroarylation Catalyzed by RhI Complexes -- 4.3.3 RhI-Catalyzed Hydroarylation with Fluorinated Arenes -- 4.3.4 Summary of RhI-Catalyzed Hydroarylation -- 4.4 Directed ortho-Hydroarylation Catalyzed by IrI Complexes -- 4.5 Hydroarylation with Ni0 Complexes via NiII Intermediates
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| 500 |
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|a ""4.6 Formal Hydroarylation Reactions with PdII Catalysts via Heck-Like Mechanisms""
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| 590 |
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|a ProQuest Ebook Central
|b Ebook Central Academic Complete
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| 650 |
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|a Catalysis.
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| 650 |
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|a Catalyse.
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| 650 |
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|a Catalysis
|2 fast
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| 700 |
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|a Gunnoe, T. Brent.
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| 700 |
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|a Habgood, Laurel Goj.
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| 758 |
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|i has work:
|a Catalytic hydroarylation of carbon-carbon multiple bonds (Text)
|1 https://id.oclc.org/worldcat/entity/E39PCFR4CjYvjQ6PyWHFXrf3pK
|4 https://id.oclc.org/worldcat/ontology/hasWork
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| 776 |
0 |
8 |
|i Print version:
|a Ackermann, Lutz.
|t Catalytic Hydroarylation of Carbon-Carbon Multiple Bonds.
|d Newark : John Wiley & Sons, Incorporated, ©2017
|z 9783527340132
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| 856 |
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|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=5105920
|z Texto completo
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|b EBLB
|n EBL5105920
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| 994 |
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|a 92
|b IZTAP
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