{"text_format":"2","workbook":"xls","n_sheets":1,"sheets":["report2"],"not_rendered":{"charts":0,"images":0,"macros":0,"external_links":1,"defined_names":2,"comments":0,"pivot_tables":0},"unopened":[],"bounds":{"document_bytes":16777216,"sheet_cells":100000,"run_cost":"one","rows_first":2000,"rows_last":500,"rows_between":2000,"halvings":0,"cell_chars":16384,"cell_head_chars":4096},"cells_cut":0,"cells_raw":0,"read":"whole","date_system":"1900","formulas":"cached_only"}

{"sheet":"report2","index":0,"n_rows":33,"n_cols":5,"rows_kept":33,"cut":false,"hidden":false,"merged":[[0,2,0,3],[0,4,0,5],[1,2,1,3],[1,4,1,5],[2,2,2,3],[3,2,3,3],[4,2,4,3],[5,2,5,3],[6,2,6,3],[7,2,7,3],[9,2,9,3],[9,4,9,5],[10,2,10,3],[10,4,10,5],[11,2,11,3],[13,2,13,3],[16,2,16,3],[17,2,17,3],[18,2,18,3],[20,2,20,3],[21,2,21,3],[25,2,25,3]],"flags":["formulas_cached_only"]}
[null,"1.","Record Nr.",null,"UNINA990007540870403321"]
[null,null,"Titolo",null,"Annual Report on Reforms and progress in Chosen (Korea) (1912 - 13) / compiled by Government general of Chosen"]
[null,null,"Pubbl/distr/stampa",null,"Keijo : s.n., 1914"]
[null,null,"Descrizione fisica",null,"XIII, 271 p., 4 c. geogr. ripieg., [35] c. di ill. ; 27 cm"]
[null,null,"Locazione",null,"ILFGE"]
[null,null,"Collocazione",null,"G-04-001"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,"2.","Record Nr.",null,"UNINA9910138988103321"]
[null,null,"Titolo",null,"Metal-catalyzed cross-coupling reactions and more / / edited by Armin de Meijere, Stefan Bräse, and Martin Oestreich"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014"]
[{"$nulls":4},"©2014"]
[null,null,"ISBN",null,"3-527-65560-3"]
[{"$nulls":4},"3-527-65558-1"]
[{"$nulls":4},"3-527-65561-1"]
[null,null,"Descrizione fisica",null,"1 online resource (3 volumes)"]
[null,null,"Disciplina",null,"547.2"]
[null,null,"Soggetti",null,"Organic compounds - Synthesis"]
[{"$nulls":4},"Metal catalysts"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record"]
[null,null,null,"Nota di bibliografia","Includes bibliographical references at the end of each chapters and index"]
[null,null,"Nota di contenuto",null,"Metal-Catalyzed Cross-Coupling Reactions and More; Contents to Volume 1; Preface; List of Contributors; Chapter 1 Mechanistic Aspects of Metal-Catalyzed C,C- and C,X-Bond Forming Reactions; 1.1 Mechanisms of Cross-Coupling Reactions; 1.1.1 The Earlier Mechanistic Proposal: The Stille Reaction; 1.1.2 The Oxidative Addition; 1.1.2.1 Cis-Complexes in the Oxidative Addition; 1.1.2.2 The Role of Alkene and Anionic Ligands; 1.1.2.3 Cross-Couplings in the Presence of Bulky Phosphines; 1.1.2.4 N-Heterocyclic Carbenes as Ligands; 1.1.2.5 Palladacycles as Catalysts"]
[{"$nulls":4},"1.1.2.6 Involvement of Pd(IV) in Catalytic Cycles 1.1.2.7 Oxidative Addition of Stannanes to Pd(0); 1.1.3 The Transmetallation in the Stille Reaction; 1.1.3.1 Isolation of the Transmetallation Step; 1.1.3.2 Dissociative Mechanistic Proposals; 1.1.3.3 Cyclic and Open Associative Transmetallation; 1.1.3.4 The Copper Effect; 1.1.3.5 Transmetallation in the Suzuki-Miyaura Reaction; 1.1.3.6 Transmetallation in the Negishi Reaction; 1.1.3.7 Transmetallation in the Hiyama Reaction; 1.1.3.8 Couplings Catalyzed by Copper and Gold; 1.1.3.9 Couplings Catalyzed by Iron and Cobalt"]
[{"$nulls":4},"1.1.4 Reductive Elimination 1.2 Palladium-Catalyzed α-Arylation of Carbonyl Compounds and Nitriles; 1.3 Formation of C-X (X = N, O, S) Bonds in Metal-Catalyzed Reactions; 1.3.1 Reductive Elimination to "]
[{"$nulls":4},"Generate C-N, C-O, and C-S Bonds from Organopalladium(II) Complexes; 1.3.2 Nickel- and Copper-Catalyzed Formation of C-X Bonds; 1.4 Summary and Outlook; List of Abbreviations; References; Chapter 2 State-of-the-Art in Metal-Catalyzed Cross-Coupling Reactions of Organoboron Compounds with Organic Electrophiles; 2.1 Introduction; 2.1.1 Catalytic Cycle"]
[{"$nulls":4},"2.1.2 Improvements toward More Efficient Cross-Coupling Conditions 2.1.2.1 Development of New Phosphine and NHC Ligands; 2.1.2.2 Usage of Masked Boron Derivatives as Cross-Coupling Partners; 2.1.2.3 Lewis Acids as Additives; 2.1.2.4 Adjusting the Nucleophilicity of Organoboron Cross-Coupling Partners; 2.1.2.5 Copper Salts as Additives; 2.2 Advances in Cross-Coupling Reactions for the Formation of C(sp2)-C(sp2) Bonds; 2.2.1 Background; 2.2.2 Recent Developments in the Use of New Electrophilic Coupling Partners; 2.2.2.1 Chlorides; 2.2.2.2 Fluorides; 2.2.2.3 Pseudohalides"]
[{"$nulls":4},"2.2.3 Recent Developments in Organoboron Cross-Coupling Partners 2.2.3.1 Trifluoroborate Salts; 2.2.3.2 N-Methyliminodiacetic Acid (MIDA) Boronates; 2.2.3.3 Other Organoboron Cross-Coupling Partners; 2.2.4 Synthesis of Enantiomerically Enriched Atropisomers; 2.3 Advances in the Cross-Coupling Reactions for the Formation of C(sp3)-C(sp2) or C(sp3)-C(sp3) Bonds; 2.3.1 Background; 2.3.1.1 Stereochemistry; 2.3.2 Cross-Couplings between Unsaturated sp2 Carbon Centers and sp3 Carbon Centers; 2.3.2.1 Cross-Couplings between sp3 Alkyl Halides and sp2 Alkenyl or Aryl Boron Derivatives"]
[{"$nulls":4},"2.3.2.2 Cross-Couplings between sp3 Alkyl Boron Derivatives with sp2 Alkenyl or Aryl Halides"]
[null,null,null,"Sommario/riassunto","This is the follow-up handbook to the bestselling Metal-Catalyzed Cross Coupling Reactions, the definitive reference in the field. In line with the enormous developments in this area, this is not so much a new edition, but rather a new book in three volumes with over 50% more content. This new content includes C-H activation, shifting the focus away from typical cross-coupling reactions, while those topics and chapters found in Diederich/de Meijere's book have been updated and expanded. With its highly experienced editor team and the authors reading like an international Who's-Who in"]