LEADER 04828nam 2200625 450 001 9910132344403321 005 20230807212133.0 010 $a3-527-67274-5 010 $a3-527-67270-2 010 $a3-527-67285-0 035 $a(CKB)3710000000264763 035 $a(EBL)1819344 035 $a(SSID)ssj0001407705 035 $a(PQKBManifestationID)11755962 035 $a(PQKBTitleCode)TC0001407705 035 $a(PQKBWorkID)11411374 035 $a(PQKB)10172615 035 $a(MiAaPQ)EBC1819344 035 $a(Au-PeEL)EBL1819344 035 $a(CaPaEBR)ebr10986564 035 $a(CaONFJC)MIL663053 035 $a(OCoLC)893739710 035 $a(EXLCZ)993710000000264763 100 $a20141202h20152015 uy| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCatalytic arylation methods $efrom the academic lab to industrial processes /$fAnthony J. Burke and Carolina Silva Marques 210 1$aWeinheim, Germany :$cWiley-VCH Verlag GmbH & KGaA,$d[2015] 210 4$dİ2015 215 $a1 online resource (1058 p.) 300 $aDescription based upon print version of record. 311 $a1-322-31771-2 311 $a3-527-33518-8 320 $aIncludes bibliographical references and index. 327 $aCover; Related Titles; Title Page; Copyright; Dedication; Preface; List of Abbreviations; Chapter 1: Cross-Coupling Arylations: Precedents and Rapid HistoricalReview of the Field; 1.1 Metal-Catalyzed Cross-Couplings: From Its Origins to the Nobel Prize and Beyond; 1.2 Arylation: What Is So Special?; 1.3 Recent New Developments; 1.4 Selected Experiments from the Literature; References; Chapter 2: Amine, Phenol, Alcohol, and Thiol Arylation; 2.1 Introduction; 2.2 Pd-Catalyzed Processes; 2.3 Cu-Catalyzed and Promoted Arylations: (CAr-N Bond Formation); 2.4 Fe-Catalyzed Arylations 327 $a2.5 Ni-Catalyzed Reactions2.6 Co-Catalyzed Arylations; 2.7 Mn-Catalyzed Arylations; 2.8 Cd-Catalyzed Arylations; 2.9 Bi(III) and Indium Oxide-Catalyzed Thiol Arylations; 2.10 Conclusions and Final Comment; 2.11 Selected Experiments from the Literature; References; Chapter 3: Decarboxylative Coupling Techniques; 3.1 Introduction; 3.2 Pd-Catalyzed Versions; 3.3 Other Metal-Catalyzed Versions; 3.4 Conclusions; 3.5 Selected Experiments; References; Chapter 4: C-H Bond Activation for Arylations; 4.1 Introduction; 4.2 C(sp2)-H Activations; 4.3 Conclusions 327 $a4.4 Selected Experiments from the LiteratureReferences; Chapter 5: Conjugate Additions; 5.1 Conjugate Additions: A Powerful Tool for Appending Organic Residues to Cyclic and Acyclic Substrates; 5.2 Applications of Rh Catalysts; 5.3 Applications of Pd Catalysts; 5.4 Applications of Ru and Other Catalysts; 5.5 Conclusions; 5.6 Selected Experiments; References; Chapter 6: Imine Arylations - Synthesis of Arylamines; 6.1 Arylation of C=N Bonds: Simple Access to Chiral Amine Units; 6.2 Application of Rh Catalysts; 6.3 Application of Pd Catalysts; 6.4 Application of Ru and Other Catalysts 327 $a6.5 The Petasis-Akritopoulou Reaction6.6 Conclusions; 6.7 Selected Experiments; References; Chapter 7: Carbonyl Group Arylation; 7.1 Introduction; 7.2 Application of Rh Catalysts; 7.3 Application of Pd Catalysts; 7.4 Application of Ru and Other Catalysts; 7.5 Conclusions; 7.6 Selected Experiments; References; Chapter 8: ?-Arylation Processes; 8.1 Introduction; 8.2 Arylation of Enolates and Equivalents; 8.3 Other Metal-Catalyzed ?-Arylations; 8.4 Conclusions; 8.5 Selected Experiments; References; Chapter 9: Catalytic Cycloaddition Aromatization Processes; 9.1 Introduction 327 $a9.2 Cycloaddition Events9.3 Radical-Based Cycloaromatization Processes; 9.4 Conclusions; 9.5 Selected Experiments from the Literature; References; Index; End User License Agreement 330 $aA current view of the challenging field of catalytic arylation reactions. Clearly structured, the chapters in this one-stop resource are arranged according to the reaction type, and focus on novel, efficient and sustainable processes, rather than the well-known and established cross-coupling methods.The entire contents are written by two authors with academic and industrial expertise to ensure consistent coverage of the latest developments in the field, as well as industrial applications, such as C-H activation, iron and gold-catalyzed coupling reactions, cycloadditions or novel methodologies 606 $aArylation 615 0$aArylation. 676 $a541.395 700 $aBurke$b Anthony J.$0994780 702 $aMarques$b Carolina Silva 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910132344403321 996 $aCatalytic arylation methods$92278565 997 $aUNINA LEADER 01266nas 2200421- 450 001 9910130573303321 005 20220322213019.0 011 $a2193-9020 035 $a(OCoLC)864929408 035 $a(CKB)3400000000085960 035 $a(CONSER)--2015247522 035 $a(DE-599)ZDB2687595-0 035 $a(MiAaPQ)2034730 035 $a(EXLCZ)993400000000085960 100 $a20060630b20122017 --- a 101 0 $aeng 135 $aur|n||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aIZA Journal of Labor & Development 210 1$aHeidelberg, Germany :$cSpringerOpen,$d2012- 215 $a1 online resource 517 1 $aIZA Journal of Labor and Development 517 1 $aIZAJOLD 531 $aJ LABOR DEV 531 1 $aIZA j. labor dev. 606 $aLabor market$zDeveloping countries$vPeriodicals 606 $aLabor market$2fast$3(OCoLC)fst00990036 607 $aDeveloping countries$2fast 608 $aPeriodicals.$2fast 615 0$aLabor market 615 7$aLabor market. 712 02$aIZA (Forschungsinstitut zur Zukunft der Arbeit), 906 $aJOURNAL 912 $a9910130573303321 996 $aIZA Journal of Labor & Development$92133072 997 $aUNINA