{"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":45,"n_cols":5,"rows_kept":45,"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],[7,2,7,3],[8,2,8,3],[9,2,9,3],[11,2,11,3],[12,2,12,3],[16,2,16,3],[24,2,24,3],[24,4,24,5],[25,2,25,3],[25,4,25,5],[26,2,26,3],[26,4,26,5],[27,2,27,3],[28,2,28,3],[32,2,32,3],[33,2,33,3],[35,2,35,3],[36,2,36,3],[37,2,37,3],[38,2,38,3],[42,2,42,3]],"flags":["formulas_cached_only"]}
[null,"1.","Record Nr.",null,"UNINA9910137967603321"]
[null,null,"Titolo",null,"Organoselenium chemistry [[electronic resource] ] : synthesis and reactions / / edited by Thomas Wirth"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim, : Wiley-VCH, c2012"]
[null,null,"ISBN",null,"3-527-64195-5"]
[{"$nulls":4},"1-283-86988-8"]
[{"$nulls":4},"3-527-64196-3"]
[{"$nulls":4},"3-527-64194-7"]
[null,null,"Descrizione fisica",null,"1 online resource (464 p.)"]
[null,null,"Disciplina",null,"547.05724"]
[null,null,"Soggetti",null,"Organoselenium compounds"]
[{"$nulls":4},"Selenium compounds"]
[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,"Organoselenium Chemistry: Synthesis and Reactions; Contents; Preface; List of Contributors; 1: Electrophilic Selenium; 1.1 General Introduction; 1.1.1 Synthesis of Electrophilic Selenium Reagents; 1.1.2 Reactivity and Properties; 1.2 Addition Reactions to Double Bonds; 1.2.1 Addition Reaction Involving Oxygen-Centered Nucleophiles; 1.2.2 Addition Reaction Involving Nitrogen-Centered Nucleophiles; 1.2.3 Addition Reactions Involving Carbon-Centered Nucleophiles; 1.2.4 Addition Reaction Involving Chiral Nucleophiles or Chiral Substrates; 1.3 Selenocyclizations; 1.3.1 Oxygen Nucleophiles"]
[{"$nulls":4},"1.3.2 Nitrogen Nucleophiles1.3.3 Competition between Oxygen and Nitrogen Nucleophiles; 1.3.4 Carbon Nucleophiles; 1.3.5 Double Cyclization Reactions; References; 2: Nucleophilic Selenium; 2.1 Introduction; 2.1.1 Development of Nucleophilic Selenium Reagents; 2.1.2 Examples of Recent Applications; 2.2 Properties of Selenols and Selenolates; 2.2.1 Electronegativity of Selenium; 2.2.2 Tautomerism of Selenols; 2.2.3 Nucleophilicity of Selenolates; 2.3 Inorganic Nucleophilic Selenium Reagents; 2.3.1 Conventional Reagents; 2.3.2 New Reagents; 2.4 Organic Nucleophilic Selenium Reagents"]
[{"$nulls":4},"2.4.1 Preparation 2.4.2 Structure; 2.4.3 Ammonium Selenolates (NH4+); 2.4.4 Selenolates of Group 1 Elements (Li, Na, K, and Cs); 2.4.5 Selenolates of Group 2 Elements (Mg, Ca, and Ba); 2.4.6 Selenolates of Group 3 Elements (Sm, Ce, Pr, Nb, and U); 2.4.7 Selenolates of Group 4 "]
[{"$nulls":4},"Elements (Ti, Zr, and Hf); 2.4.8 Selenolates of Group 5 Elements (V, Nb, and Ta); 2.4.9 Selenolates of Group 6 Elements (Mo and W); 2.4.10 Selenolates of Group 7 Elements (Mn and Re); 2.4.11 Selenolates of Group 8 Elements (Fe, Ru, and Os); 2.4.12 Selenolates of Group 9 Elements (Co, Rh, and Ir)"]
[{"$nulls":4},"2.4.13 Selenolates of Group 10 Elements (Ni, Pd, and Pt)2.4.14 Selenolates of Group 11 Elements (Cu, Ag, and Au); 2.4.15 Selenolates of Group 12 Elements (Zn, Cd, and Hg); 2.4.16 Selenolates of Group 13 Elements (B, Al, Ga, and In); 2.4.17 Selenolates of Group 14 Elements (Si, Ge, Sn, and Pb); 2.4.18 Selenolates of Group 15 Elements (P, As, Sb, and Bi); References; 3: Selenium Compounds in Radical Reactions; 3.1 Homolytic Substitution at Selenium to Generate Radical Precursors; 3.1.1 Bimolecular SH2 Reactions: Synthetic Considerations; 3.1.1.1 Radical Reagents"]
[{"$nulls":4},"3.1.2 Alkyl Radicals from Selenide Precursors 3.1.3 Acyl Radicals from Acyl Selenide Precursors; 3.1.4 Imidoyl Radicals from Imidoyl Selenides; 3.1.5 Other Radicals from Selenide Precursors; 3.2 Selenide Building Blocks; 3.3 Solid-Phase Synthesis; 3.4 Selenide Precursors in Radical Domino Reactions; 3.5 Homolytic Substitution at Selenium for the Synthesis of Se-Containing Products; 3.5.1 Intermolecular SH2 onto Se; 3.5.2 Intramolecular SH2: Cyclization onto Se; 3.6 Seleno Group Transfer onto Alkenes and Alkynes; 3.6.1 Seleno-Selenation; 3.6.2 Seleno-Sulfonation; 3.6.3 Seleno-Alkylation"]
[{"$nulls":4},"3.7 PhSeH in Radical Reactions"]
[null,null,null,"Sommario/riassunto","Selenium-based methods in synthetic chemistry have developed rapidly over the past years and are now offering highly useful tools for organic synthesis. Filling the gap for a comprehensive handbook and ready reference, this book covers all modern developments within the field, including biochemical aspects. The chemistry chapters are organized according to the different reactivities of various selenium compounds and reagents, with each chapter dealing with a special reaction type. Also includes a table with 77Se NMR shifts to aid in practical problems.From the Contents"]
[null,"2.","Record Nr.",null,"UNINA9910789641103321"]
[null,null,"Autore",null,"Hietanen Mika"]
[null,null,"Titolo",null,"Paul's argumentation in Galatians : a pragma-dialectical analysis / / Mika Hietanen"]
[null,null,"Pubbl/distr/stampa",null,"London ; ; New York : , : T & T Clark, , 2007"]
[null,null,"ISBN",null,"0-567-66122-9"]
[{"$nulls":4},"1-283-27115-X"]
[{"$nulls":4},"9786613271150"]
[{"$nulls":4},"0-567-58124-1"]
[null,null,"Descrizione fisica",null,"1 online resource (241 p.)"]
[null,null,"Collana",null,"Library of New Testament studies ; ; 344. European studies on Christian origins"]
[{"$nulls":4},"T & T Clark library of biblical studies"]
[null,null,"Disciplina",null,"227.406"]
[null,null,"Soggetti",null,"Rhetoric, Ancient - History"]
[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 (pages 199-211) and indexes."]
[null,null,"Nota di contenuto",null,"Preface -- List of Figures -- List of Tables -- Part 1. Introduction: 1.1 General Presentation of the Task ; 1.2 Overview of Paul's Argumentation ; 1.3 Problems in the Argumentation in Galatians 3.1-5.12 1.4 Specific Presentation of the Task -- Part 2. The method: 2.1 Background ; 2.2 General Characteristics of the Method ; 2.3 Metatheoretical Premisses ; 2.4 Speech Act Theory ; 2.5 A Model for Critical Discussion ; 2.6 Reconstructing Argumentative Discourse -- Part 3. Analysis: 3.1 The Analytical Procedure ; 3.2 Higher-Order Conditions ; 3.3 The Stages of the Argumentation ; 3.4 Gal. 3.1-5, the Galatians' Reception of the Spirit ; 3.5 Gal. 3.6-14, Abraham's Faith ; 3.6 Gal. 3.15-18, Testamental Practice and Inheritance ; 3.7 Gal. 3.19-25, the Purpose and Function of the Law ; 3.8 Gal. 3.26-29, Equality 'in Christ' ; 3.9 Gal. 4.1-7, the Freedom of God's Children ; 3.10 Gal. 4.8-11, Paul's Concern for the Galatians ; 3.11 Gal. 4.12-20, Paul's Relationship with the Galatians ; 3.12 Gal. 4.21-31, an Allegory of Hagar and Sarah ; 3.13 Gal. 5.1-12, Freedom versus Circumcision -- Part 4- Overview and conclusion. 4.1 An Analytic Overview ; 4.2 Violation of Rules and Quality of Argumentation ; 4.3 Conclusion: Paul's Argumentation in Galatians."]
[null,null,null,"Sommario/riassunto","\"Galatians is a polemical letter which contains a substantial amount of argumentative passages. Paul evidently wanted to persuade by using "]
[{"$nulls":4},"the best arguments possible to convince his addressees. Using a state-of-the-art method from the discipline of argumentation analysis, Paul's argumentation can be analysed with a precision that standard exegetical methods cannot provide. The pragma-dialectical method developed in Amsterdam facilitates an analysis which is both descriptive and normative. On the one hand, Paul's argumentation can be described, such as the relationship between premisses and conclusions, the structure of the arguments, and features relating to rhetorical strategy. On the other hand, the method makes it possible to evaluate Paul's argumentation against a set of rules for sound reasoning. Fallacies and problematic arguments can be described accurately. The spiritual nature of Paul's matters do not relieve him of rationality, and Paul himself does not argue as if it did. Paul's argumentation is found problematic in several respects. There is a tension in the text: Paul works a great deal to argue his claims while at the same time giving the impression that he merely wants to declare his standpoints and does not want to carry out an argumentation at all. Many of the conclusions are presented as self-evident, even when they are not. Paul's style is far from an ideal model of the resolution of a dispute. Paul relies heavily on an argumentative strategy with maximal use of rhetorical devices. The analysis shows that a contemporary method of argumentation analysis provides tools necessary to adequately describe and understand both individual arguments and the overarching strategy of the argumentation in a Pauline text.\"--Bloomsbury Publishing."]