LEADER 03984oam 2200637 c 450 001 996571845703316 005 20220221094418.0 010 $a3-8394-0295-6 024 7 $a10.14361/transcript.9783839402955 035 $a(CKB)2550000001338466 035 $a(EBL)1918351 035 $a(SSID)ssj0001336305 035 $a(PQKBManifestationID)12546924 035 $a(PQKBTitleCode)TC0001336305 035 $a(PQKBWorkID)11314628 035 $a(PQKB)10152933 035 $a(MiAaPQ)EBC1918351 035 $a(DE-B1597)396073 035 $a(OCoLC)979879357 035 $a(DE-B1597)9783839402955 035 $a(transcript Verlag)9783839402955 035 $a(EXLCZ)992550000001338466 100 $a20220221d2014 uy 0 101 0 $ager 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aDer Logos des Spiegels$eStruktur und Sinn einer spekulativen Metapher$fJoachim Schickel, Hans Heinz Holz 205 $a1st ed. 210 $aBielefeld$ctranscript Verlag$d2014 215 $a1 online resource (371 p.) 225 0 $aEdition panta rei 300 $aDescription based upon print version of record. 311 $a3-89942-295-3 311 $a1-322-00501-X 327 $a1 Editorial 2 Inhalt 5 Vorwort des Lektors 7 Vorwort des Herausgebers 9 Vorwort des Autors 13 Leitsa?tze 15 I.1 Das Sehen des Spiegels 19 I.2 Modi des Spiegelblicks 43 I.3 Der Begriff der Reflexion 81 II.1 Das Zeigen des Spiegels 117 II.2 Modi des Spiegelbildes 153 II.3 Der Begriff der Intuition 217 Narziss oder die Erfindung der Malerei. Das Bild des Malers und das Bild des Spiegels 275 Ovid. Die Sinnlichkeit des Spiegels 291 U?ber Leibniz 303 Wittgenstein. Logik als Spiegeldenken 331 Mo Ti. Der Spiegel und das Licht 351 Werkkonzeption 365 367 330 $a»Spiegel: noch nie hat man wissend beschrieben, was ihr in euerem Wesen seid« (Rilke) - dieser Satz war Joachim Schickel (1924-2002) lebenslanger Antrieb zum Nachdenken. Mit hoher sprachlicher Pra?zision beschreibt er in »Der Logos des Spiegels« die Vorga?nge und Funktionen des Spiegelns und die Verwendung der Spiegel-Struktur in Zeugnissen aus Philosophie, Literatur und Kunst der europa?ischen, chinesischen und indischen Geistesgeschichte. Aus diesem Reichtum unerscho?pflichen Wissens fu?hrt er zu Denkmustern unserer Zeit, die dem systematischen Sinn des Spiegel-Verha?ltnisses verpflichtet sind. So entsteht schließlich am Bild des Spiegels die Mo?glichkeit, das Verha?ltnis des Menschen zu sich selbst und zur Welt auszulegen und zu begreifen. 330 1 $a»Neu an Schickels Buch ist, dass er zum einen die philosophische Katoptrik durch historisch-philosophisch-literarische Beispiele auf die Probe stellt, zum anderen die Bedeutungsvielfalt analogischer und metaphorischer Redeweisen im Einzelnen analysiert und wieder zusammenbringt.« Kaan Kangal, Widerspruch, 57 (2013) 410 0$aEdition panta rhei. 606 $aDialektik; Sprache; Spiegel; Philosophie; Ontologie; Logik; China; Indien; Antike; Bild; Metapher; Anthropologie; Sprachphilosophie; Deutsche Philosophiegeschichte; Language; Philosophy; Image; Philosophy of Language; German History of Philosophy; 610 $aChina. 610 $aGerman History of Philosophy. 610 $aImage. 610 $aPhilosophy of Language. 610 $aPhilosophy. 615 4$aDialektik; Sprache; Spiegel; Philosophie; Ontologie; Logik; China; Indien; Antike; Bild; Metapher; Anthropologie; Sprachphilosophie; Deutsche Philosophiegeschichte; Language; Philosophy; Image; Philosophy of Language; German History of Philosophy; 676 $a121.3 700 $aSchickel$b Joachim$4aut$0571208 702 $aHolz$b Hans Heinz$4edt 801 0$bDE-B1597 801 1$bDE-B1597 906 $aBOOK 912 $a996571845703316 996 $aDer Logos des Spiegels$93670366 997 $aUNISA LEADER 05256nam 2200673Ia 450 001 9911019993503321 005 20200520144314.0 010 $a9786612118500 010 $a9781282118508 010 $a1282118501 010 $a9783527627332 010 $a3527627332 035 $a(CKB)1000000000774668 035 $a(EBL)481887 035 $a(OCoLC)413003441 035 $a(SSID)ssj0000204230 035 $a(PQKBManifestationID)11172511 035 $a(PQKBTitleCode)TC0000204230 035 $a(PQKBWorkID)10196082 035 $a(PQKB)10724196 035 $a(MiAaPQ)EBC481887 035 $a(PPN)152499741 035 $a(Perlego)2771632 035 $a(EXLCZ)991000000000774668 100 $a20081027d2009 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aModern arylation methods /$fedited by Lutz Ackermann 210 $aWeinheim $cWiley-VCH$dc2009 215 $a1 online resource (563 p.) 300 $aDescription based upon print version of record. 311 08$a9783527627325 311 08$a3527627324 311 08$a9783527319374 311 08$a3527319379 320 $aIncludes bibliographical references and index. 327 $aModern Arylation Methods; Contents; Preface; List of Contributors; 1 Arylation Reactions: A Historical Perspective; 1.1 Structure and Bonding of Benzene; 1.2 Syntheses of Substituted (Hetero)Arenes, and the Contents of this Book; Abbreviations; References; 2 Metal-Catalyzed Coupling Reactions with Aryl Chlorides, Tosylates and Fluorides; 2.1 Introduction; 2.2 Coupling Reactions of Aryl Chlorides; 2.2.1 Nickel-Catalyzed Cross-Couplings of Aryl Chlorides; 2.2.2 Palladium-Catalyzed Cross-Coupling Reactions; 2.2.2.1 Suzuki Reaction; 2.2.2.2 Stille Reaction; 2.2.2.3 Hiyama Coupling 327 $a2.2.2.4 Negishi Coupling2.2.2.5 Kumada Coupling; 2.3 Coupling Reactions of Aryl Fluorides; 2.4 Coupling Reactions of Aryl Tosylates; 2.5 Conclusions; Abbreviations; References; 3 Palladium-Catalyzed Arylations of Amines and ?-C-H Acidic Compounds; 3.1 Introduction; 3.2 Palladium-Catalyzed Arylations of Amines; 3.2.1 Historical Development; 3.2.2 Catalytic Systems; 3.2.2.1 Palladium Sources; 3.2.2.2 Ligands; 3.2.2.3 Bases; 3.2.2.4 Solvents; 3.2.3 Aryl Halides; 3.2.4 Arylsulfonic Acid Esters; 3.2.5 Heteroaromatic Electrophiles; 3.2.6 Amines as Nucleophiles 327 $a3.2.7 Amine Derivatives as Nucleophiles3.2.8 Applications; 3.2.9 Mechanistic Aspects; 3.2.10 Chirality; 3.3 Palladium-Catalyzed Arylations of ?-C-H Acidic Compounds; 3.3.1 Historical Development; 3.3.2 Catalytic Systems; 3.3.3 ?-Arylations of Esters; 3.3.4 ?-Arylations of Malonates and ?-Cyano Esters; 3.3.5 ?-Arylations of Ketones; 3.3.6 ?-Arylations of Amides; 3.3.7 ?-Arylations of Nitriles; 3.4 Summary and Conclusions; Abbreviations; References; 4 Copper-Catalyzed Arylations of Amines and Alcohols with Boron-Based Arylating Reagents; 4.1 Introduction 327 $a4.2 Discovery and Development of a New O-H Bond Arylation Reaction: From Stoichiometric to Catalytic in Copper4.3 Mechanistic Considerations; 4.4 Miscellaneous Applications; 4.4.1 Additional Applications with ArB(OH)(2); 4.4.2 Alternatives to ArB(OH)(2); 4.4.3 Alternatives to Phenols; 4.5 Development of a New N-H Bond Arylation Reaction; 4.5.1 Stoichiometric in Copper; 4.5.2 Alternatives to Boronic Acids; 4.6 Development of a New N-H Bond Arylation Reaction: Catalytic in Copper; 4.6.1 Proposed Mechanism; 4.6.2 Additional Important Non-N-H Arylation Examples; 4.7 Summary and Conclusions 327 $aAbbreviationsReferences; 5 Metal-Catalyzed Arylations of Nonactivated Alkyl (Pseudo)Halides via Cross-Coupling Reactions; 5.1 Introduction; 5.2 Palladium-Catalyzed Arylations of Alkyl (Pseudo)Halides; 5.3 Nickel-Catalyzed Arylations of Alkyl (Pseudo)Halides; 5.4 Iron-Catalyzed Arylations of Alkyl (Pseudo)Halides; 5.5 Copper- and Cobalt-Catalyzed Arylations of Alkyl (Pseudo)Halides; Abbreviations; References; 6 Arylation Reactions of Alkynes: The Sonogashira Reaction; 6.1 Introduction; 6.2 Palladium-Catalyzed Reactions: Ligands and Reaction Protocols; 6.2.1 Phosphine-Based Ligands 327 $a6.2.1.1 Copper-Free Catalytic Systems 330 $aToday, arylation methods are belonging to the most important reaction types in organic synthesis. Lutz Ackermann, a young and ambitious professor has gathered a number of top international authors to present the first comprehensive book on the topic. Starting from a historical review, the book covers hot topics like Palladium-catalyzed arylation of N-H and alpha-C-H-acidic Bonds, Copper-catalyzed arylation of N-H and O-H Bonds, direct arylation reactions, carbanion aromatic synthesis, arylation reactions of alkenes, alkynes and much more. This compact source of high quality information 606 $aArylation 606 $aOrganic compounds$xSynthesis 615 0$aArylation. 615 0$aOrganic compounds$xSynthesis. 676 $a541.39 701 $aAckermann$b Lutz$01837868 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911019993503321 996 $aModern arylation methods$94416710 997 $aUNINA