{"text_format":"2","workbook":"xls","n_sheets":1,"sheets":["report2"],"not_rendered":{"charts":0,"images":0,"macros":0,"external_links":1,"defined_names":1,"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":25,"n_cols":5,"rows_kept":25,"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],[4,2,4,3],[8,2,8,3],[9,2,9,3],[10,2,10,3],[12,2,12,3],[13,2,13,3],[17,2,17,3]],"flags":["formulas_cached_only"]}
[null,"1.","Record Nr.",null,"UNINA9911019927203321"]
[null,null,"Titolo",null,"Quaternary stereocenters : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim, : Wiley-VCH"]
[{"$nulls":4},"Chichester, : John Wiley, c2005"]
[null,null,"ISBN",null,"1-280-85406-5"]
[{"$nulls":4},"9786610854066"]
[{"$nulls":4},"3-527-60685-8"]
[{"$nulls":4},"3-527-60697-1"]
[null,null,"Descrizione fisica",null,"1 online resource (362 p.)"]
[null,null,"Disciplina",null,"547.1223"]
[null,null,"Soggetti",null,"Stereochemistry"]
[{"$nulls":4},"Organic compounds - Synthesis"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"Quaternary Stereocenters; Contents; Foreword; Preface; List of Contributors; Symbols and Abbreviations; 1 Important Natural Products; 1.1 Introduction; 1.2 Alkylation of Tertiary Carbon Centers; 1.3 Cycloaddition to Alkenes; 1.3.1 Diels-Alder Reaction; 1.3.2 Other Types of Cycloaddition; 1.4 Rearrangement Reactions; 1.5 Carbometallation Reactions; 1.5.1 Addition of a Carbon Nucleophile to a β,β-Disubstituted α,β-Unsaturated Enone; 1.5.2 Asymmetric and Diastereomeric Addition of a Carbon Nucleophile to Unactivated Alkenes Catalyzed by Palladium [42]; 1.6 C-H Functionalization Reactions"]
[{"$nulls":4},"1.7 Asymmetric Modification of Enantiotopic/Diastereotopic Substituents of Quaternary Carbon Centers1.8 Summary; 2 Important Pharmaceuticals and Intermediates; 2.1 The Chirality of Drugs and Agrochemicals; 2.2 Steroids; 2.3 Pharmaceuticals and Agrochemicals Based on α-Dialkylated Amino Acids; 2.4 Azole Antimycotics; 2.5 Alkaloids; 2.6 HIV Inhibitors; 2.7 β-Lactam Antibiotics; 2.8 The Tetracyclines; 2.9 Summary and Outlook; 3 Aldol Reactions; 3.1 Introduction; 3.2 Metal Enolates; 3.2.1 Lithium Enolates; 3.2.2 Titanium and Zirconium Enolates; 3.2.3 Boron Enolates; 3.3 Catalytic Aldol Additions"]
[{"$nulls":4},"3.3.1 Fluoride-ion-mediated Aldol Addition3.3.2 Lewis-acid-mediated "]
[{"$nulls":4},"Mukaiyama-type Aldol Reactions; 3.3.3 Direct Aldol Additions; 3.3.4 Organocatalysis; 3.3.5 Enzyme and Antibody Catalysis; 3.4 Conclusions; 3.5 Note Added in Proof; 4 Michael Reactions and Conjugate Additions; 4.1 Introduction; 4.2 Chiral Brönstedt Bases; 4.2.1 Cinchona Alkaloids; 4.2.2 Polymer-bound Alkaloids; 4.2.3 Organocatalysis; 4.2.4 Miscellaneous Examples; 4.3 Chiral Metal Complexes; 4.3.1 Cobalt and Copper Catalysis; 4.3.2 Rhodium Catalysis; 4.3.3 Heterobimetallic Catalysis; 4.3.4 Miscellaneous Examples"]
[{"$nulls":4},"4.4 Chiral Auxiliaries4.4.1 α-Phenethylamine; 4.4.2 L-Valine Ester; 4.4.3 L-Valine Diethylamide; 4.4.4 Miscellaneous Examples; 5 Rearrangement Reactions; 5.1 Introduction; 5.2 Applications; 5.2.1 The Claisen Rearrangement; 5.2.2 The Overman Rearrangement; 5.2.3 The Cope Rearrangement; 5.2.4 The Wittig Rearrangement; 5.2.5 Semipinacol Rearrangements; 5.2.6 Miscellaneous; 5.3 Summary; 6 Cycloaddition Reactions; 6.1 Introduction; 6.2 [2+1] Cycloaddition Reactions; 6.3 [2+2] Cycloaddition Reactions; 6.4 1,3-Dipolar Cycloaddition Reactions; 6.4.1 Nitrone Cycloadditions"]
[{"$nulls":4},"6.4.2 Other 1,3-Dipolar Cycloadditions6.5 Diels-Alder Reactions; 6.6 Hetero-Diels-Alder Reactions; 6.6.1 The Carbonyl Group as Dienophile; 6.6.2 α,β-Unsaturated Carbonyl Derivatives as Heterodienes; 6.6.3 Imine Derivatives as Heterodienophiles; 6.7 Consecutive Cycloaddition Reactions; 7 Asymmetric Cross-coupling and Mizoroki-Heck Reactions; 7.1 The Asymmetric Heck Reaction; 7.1.1 Introduction; 7.1.2 Mizoroki-Heck Reaction Mechanism; 7.1.3 Asymmetric Formation of Quaternary Carbon Centers; 7.2 Metal-catalyzed Cross-coupling Reactions; 7.2.1 Palladium-catalyzed α-Arylation"]
[{"$nulls":4},"7.2.2 Palladium-catalyzed α-Vinylation"]
[null,null,null,"Sommario/riassunto","Filling the gap in the literature, this book presents everything there is to know about this topic. By comprehensively covering the quaternary stereocenters found in a range of important and useful molecules in pharmaceutical and medicinal applications, as well as in thousands of natural products, the book provides the know-how chemists need to synthesize challenging molecules with numerous applications.A must for organic chemists in academia, the pharmaceutical industry and medicine.From the Contents:Important Natural ProductsImportant Pharmaceuticals and Intermediates"]