Overview

A comprehensive reference to nickel chemistry for every scientist working with organometallic catalysts Written by one of the world?s leading reseachers in the field, Nickel Catalysis in Organic Synthesis presents a comprehensive review of the high potential of modern nickel catalysis and its application in synthesis. Structured in a clear and assessible manner, the book offers a collection of various reaction types, such as cross-coupling reactions, reactions for the activation of unreactive bonds, carbon dioxide fixation, and many more. Nickel has been recognized as one of the most interesting transition metals for homogeneous catalysis. This book offers an overview to the recently developed new ligands, new reaction conditions, and new apparatus to control the reactivity of nickel catalysts, allowing scientists to apply nickel catalysts to a variety of bond-forming reactions. A must-read for anyone working with organometallic compounds and their application in organic synthesis, this important guide: -Reviews the numerous applications of nickel catalysis in synthesis -Explores the use of nickel as a relatively cheap and earth-abundant metal -Examines the versatility of nickel catalysis in reactions like cross-coupling reactions and CH activations -Offers a resource for academics and industry professionals Written for catalytic chemists, organic chemists, inorganic chemists, structural chemists, and chemists in industry, Nickel Catalysis in Organic Synthesis provides a much-needed overview of the most recent developments in modern nickel catalysis and its application in synthesis.

Full Product Details

Author:   Sensuke Ogoshi
Publisher:   Wiley-VCH Verlag GmbH
Imprint:   Blackwell Verlag GmbH
Dimensions:   Width: 17.30cm , Height: 2.30cm , Length: 24.90cm
Weight:   0.839kg
ISBN:  

9783527344079

ISBN 10:   3527344071
Pages:   352
Publication Date:   15 January 2020
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Out of stock  
The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available.

Table of Contents

Preface xi Part I Reactions via Nickelacycles 1 1 Formation of Nickelacycles and Reaction with Carbon Monoxide 3 Sensuke Ogoshi 1.1 Introduction 3 1.2 Formation of Hetero-nickelacycles from Nickel(0) 3 1.3 Stoichiometric Reaction of Hetero-nickelacycles with Carbon Monoxide 4 References 9 2 Transformation of Aldehydes via Nickelacycles 13 Yoichi Hoshimoto 2.1 Introduction and Scope ofThis Chapter 13 2.2 Catalytic Transformation of Aldehydes Through Three-Membered Oxanickelacycle Complexes 14 2.3 Catalytic Transformation of Aldehydes Through Five-Membered Oxanickelacycle Complexes 18 2.4 Catalytic Transformation of Aldehydes Through Seven-Membered Oxanickelacycle Complexes 22 2.5 Conclusion and Outlook 23 References 25 3 Transformation of Imines via Nickelacycles 29 Masato Ohashi 3.1 Introduction 29 3.2 [2+2+1] Carbonylative Cycloaddition of an Imine and Either an Alkyne or an Alkene Leading to γ-Lactams 29 3.3 [2+2+2] Cycloaddition Reaction of an Imine with Two Alkynes: Formation of 1,2-Dihydropyridine Derivatives 31 3.4 Three-Component Coupling and Cyclocondensation Reactions of an Imine, an Alkyne, and Alkylmetal Reagents 34 References 37 4 Asymmetric C—C Bond Formation Reactions via Nickelacycles 39 Ravindra Kumar and Sensuke Ogoshi 4.1 Introduction 39 4.2 Enantioselective Reactions Involving Nickelacycles 39 4.2.1 Nickel-Catalyzed Asymmetric Coupling of Alkynes and Aldehydes 39 4.2.1.1 Nickel-Catalyzed Asymmetric Reductive Coupling of Alkynes and Aldehydes 40 4.2.1.2 Nickel-Catalyzed Asymmetric Alkylative Coupling of Alkynes and Aldehydes 43 4.2.2 Nickel-Catalyzed Asymmetric Coupling of Alkynes and Imines 44 4.2.3 Nickel-Catalyzed Asymmetric Coupling of 1,3-Enynes and Aldehydes 45 4.2.4 Nickel-Catalyzed Asymmetric Coupling of 1,3-Enynes and Ketones 46 4.2.5 Nickel-Catalyzed Asymmetric Coupling of 1,3-Dienes and Aldehydes 47 4.2.6 Nickel-Catalyzed Asymmetric Coupling of Enones and Alkynes 50 4.2.6.1 Nickel-Catalyzed Asymmetric Alkylative Coupling of Enones and Alkynes 50 4.2.6.2 Nickel-Catalyzed Asymmetric Coupling of Enones and Alkynes 51 4.2.7 Nickel-Catalyzed Asymmetric Coupling of Arylenoates and Alkynes 55 4.2.8 Nickel-Catalyzed Asymmetric Coupling of Diynes with Ketenes 56 4.2.9 Nickel-Catalyzed Asymmetric Coupling of Allenes, Aldehydes, and Silanes 57 4.2.10 Nickel-Catalyzed Asymmetric Coupling of Allenes and Isocyanates 58 4.2.11 Nickel-Catalyzed Asymmetric Coupling of Alkenes, Aldehydes, and Silanes 59 4.2.12 Nickel-Catalyzed Asymmetric Coupling of Formamide and Alkene 61 4.2.13 Nickel-Catalyzed Asymmetric Coupling of Alkynes and Cyclopropyl Carboxamide 63 4.3 Miscellaneous 64 4.3.1 Nickel-Catalyzed Asymmetric Annulation of Pyridones via Hydroarylation to Alkenes 64 4.3.2 Nickel-Catalyzed Asymmetric Synthesis of Benzoxasilole 65 4.4 Overview and Future Perspective 66 References 67 Part II Functionalization of Unreactive Bonds 69 5 Recent Advances in Ni-Catalyzed Chelation-Assisted Direct Functionalization of Inert C—H Bonds 71 Yan-Hua Liu, Fang Hu, and Bing-Feng Shi 5.1 Introduction 71 5.2 Ni-Catalyzed Functionalization of Inert C—H Bonds Assisted by Bidentate Directing Groups 71 5.2.1 Arylation 72 5.2.2 Alkylation 76 5.2.3 Alkenylation 83 5.2.4 Alkynylation 85 5.2.5 Other C—C Bond Formation Reactions Directed by Bidentate Directing Group 88 5.2.6 C—N Bond Formation 89 5.2.7 C–Chalcogen (Chalcogen = O, S, Se) Bond Formation 89 5.2.8 C–Halogen Bond Formation 92 5.3 Ni-Catalyzed Functionalization of Inert C—H Bonds Assisted by Monodentate Directing Groups 94 5.3.1 Alkylation 94 5.3.2 Alkenylation 95 5.3.3 Alkynylation 96 5.3.4 C–Calcogen Bond Formation 97 5.4 Summary 98 References 98 6 C—C Bond Functionalization 103 Yoshiaki Nakao 6.1 Introduction 103 6.2 C—C Bond Functionalization of Three-Membered Rings 103 6.3 C—C Bond Functionalization of Four- and Five-Membered Rings 110 6.4 C—C Bond Functionalization of Less Strained Molecules 113 6.5 C—CN Bond Functionalization 115 6.6 Summary and Outlook 116 References 117 7 C—O Bond Transformations 123 Mamoru Tobisu 7.1 Introduction 123 7.2 C(aryl)—O Bond Cleavage 124 7.2.1 Aryl Esters, Carbamates, and Carbonates 124 7.2.2 Aryl Ethers 132 7.2.3 Arenols 136 7.3 C(benzyl)—O Bond Cleavage 138 7.3.1 Benzyl Esters and Carbamates 138 7.3.2 Benzyl Ethers 140 7.4 C(acyl)—O Bond Cleavage 141 7.5 Summary and Outlook 144 References 145 Part III Coupling Reactions via Ni(I) and/or Ni(III) 151 8 Photo-Assisted Nickel-Catalyzed Cross-Coupling Processes 153 Christophe Lévêque, Cyril Ollivier, and Louis Fensterbank 8.1 Introduction 153 8.2 Development of Visible-Light Photoredox/Nickel Dual Catalysis 154 8.2.1 For the Formation of Carbon–Carbon Bonds 154 8.2.1.1 Starting from Organotrifluoroborates 154 8.2.1.2 Starting from Carboxylates or Keto Acids or from Methylanilines 157 8.2.1.3 Starting from Alkylsilicates 160 8.2.1.4 Starting from 1,4-Dihydropyridines 166 8.2.1.5 Starting from Alkylsulfinates 168 8.2.1.6 Starting from Alkyl Bromides 168 8.2.1.7 Starting from Xanthates 169 8.2.1.8 Starting from Sp3 CH Bonds 169 8.2.2 For the Formation of Carbon–Heteroatom Bonds 170 8.2.2.1 Formation of C—O Bond 170 8.2.2.2 Formation of C—P Bond 171 8.2.2.3 Formation of C—S Bond 171 8.3 Energy-Transfer-Mediated Nickel Catalysis 173 8.4 Conclusion 175 References 176 9 Cross-Electrophile Coupling: Principles and New Reactions 183 Matthew M. Goldfogel, Liangbin Huang, and Daniel J. Weix 9.1 Introduction 183 9.2 Mechanistic Discussion of Cross-Electrophile Coupling 185 9.3 C(sp2)—C(sp3) Bond Formation 188 9.3.1 Cross-Electrophile Coupling of Aryl-X and Alkyl-X 188 9.3.2 Cross-Electrophile Coupling of ArX and Bn-X 195 9.3.3 Cross-Electrophile Coupling of ArX and Allyl-X 196 9.3.4 Vinyl-X with R-X 197 9.3.5 Acyl-X with Alkyl-X 199 9.4 C(sp2)–C(sp2) Coupling 201 9.4.1 Aryl-X/Vinyl-X+Aryl-X/Vinyl-X 201 9.4.2 Aryl-X+Acyl-X 202 9.5 C(sp3)–C(sp3) Coupling 203 9.6 C(sp)–C(sp3) Coupling 205 9.7 Multicomponent Reactions 206 9.8 Future of the Field 208 References 209 10 Organometallic Chemistry of High-Valent Ni(III) and Ni(IV) Complexes 223 Liviu M. Mirica, Sofia M. Smith, and Leonel Griego 10.1 Introduction 223 10.2 Organometallic Ni(III) Complexes 223 10.3 Organometallic Ni(IV) Complexes 234 10.4 Other High-Valent Ni Complexes 239 10.4.1 Additional NiIII Complexes 239 10.4.2 Additional NiIV Complexes 241 10.5 Conclusions and Outlook 243 References 244 Part IV Carbon Dioxide Fixation 249 11 Carbon Dioxide Fixation via Nickelacycle 251 Ryohei Doi and Yoshihiro Sato 11.1 Introduction: Carbon Dioxide as a C1 Building Block 251 11.2 Formation, Structure, and Reactivity of Nickelalactone 252 11.2.1 Formation and Characterization of Nickelalactone via Oxidative Cyclization with CO2 252 11.2.1.1 Reaction with Alkene 252 11.2.1.2 Reaction with Allene 255 11.2.1.3 Reaction with Diene 256 11.2.1.4 Reaction with Alkyne 257 11.2.1.5 Other Related Reactions 260 11.2.1.6 Generation of Nickelalactone Without CO2 261 11.2.2 Reactivity of Nickelalactone 261 11.2.2.1 Transmetalation with Organometallic Reagent 261 11.2.2.2 β-Hydride Elimination 263 11.2.2.3 Insertion of Another Unsaturated Molecule 264 11.2.2.4 Retro-cyclization 265 11.2.2.5 Nucleophilic Attack 265 11.2.2.6 Oxidation 267 11.2.2.7 Ligand Exchange 267 11.3 Catalytic Transformation via Nickelalactone 1: Reactions of Alkynes 268 11.3.1 Synthesis of Pyrone 268 11.3.1.1 Initial Finding 268 11.3.1.2 Reaction of Diynes with CO2 268 11.3.2 Synthesis of α,β-Unsaturated Ester 269 11.3.2.1 Electrochemical Reactions 269 11.3.2.2 Reduction with Organometallic Reagents 270 11.4 Catalytic Transformation via Nickelalactone 2: Reactions of Alkenes and Related Molecules 271 11.4.1 Transformation of Diene, Allene, and Substituted Alkene 271 11.4.1.1 Coupling of Diene with CO2 271 11.4.1.2 Electrochemical Process 272 11.4.1.3 Use of Reductant 272 11.4.2 Synthesis of Acrylic Acid from Ethylene and CO2 274 11.4.2.1 Before the Dawn 275 11.4.2.2 Development of Catalytic Reaction 276 11.5 Concluding Remarks 278 References 279 12 Relevance of Ni(I) in Catalytic Carboxylation Reactions 285 Rosie J. Somerville and Ruben Martin 12.1 Introduction 285 12.2 Mechanistic Building Blocks 287 12.2.1 Additives 287 12.2.2 Coordination of CO2 287 12.2.3 Insertion/C—C Bond Formation 288 12.2.4 Ligand Effects 289 12.2.5 Oxidative Addition 290 12.2.6 Oxidation State 290 12.2.7 Single Electron Transfer (SET) 290 12.2.8 Conclusion 290 12.3 Electrocarboxylation 291 12.3.1 Introduction 291 12.3.2 Phosphine Ligands 294 12.3.3 Bipyridine and Related α-Diimine Ligands 296 12.3.4 Salen Ligands 297 12.3.5 Conclusion 298 12.4 Non-electrochemical Methods 298 12.4.1 Aryl Halides 300 12.4.2 Benzyl Electrophiles 304 12.4.3 Carboxylation of Unactivated Alkyl Electrophiles 306 12.4.4 Carboxylation of Allyl Electrophiles 312 12.4.5 Unsaturated Systems 315 12.5 Conclusions 318 References 319 Index 331

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Sensuke Ogoshi, PhD, is Full Professor at Osaka University. His research is directed toward the discovery of new transition metal complexes that can act as key reaction intermediates in new transformation reactions of unsaturated compounds. Recently, he has focused on catalytic transformation reactions of unsaturated compounds via nickelacycles, as well as the development of the new synthetic methods of oragano-fluorine compounds by transition-metal catalysts.

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