LEADER 03504nam 2200661Ia 450 001 9910785199603321 005 20230207213758.0 010 $a1-4696-0423-X 010 $a0-8078-9841-4 035 $a(CKB)2670000000037582 035 $a(EBL)565708 035 $a(OCoLC)656846650 035 $a(SSID)ssj0000415812 035 $a(PQKBManifestationID)11304577 035 $a(PQKBTitleCode)TC0000415812 035 $a(PQKBWorkID)10416123 035 $a(PQKB)11701602 035 $a(MiAaPQ)EBC565708 035 $a(OCoLC)966766042 035 $a(MdBmJHUP)muse48400 035 $a(Au-PeEL)EBL565708 035 $a(CaPaEBR)ebr10405063 035 $a(CaONFJC)MIL930453 035 $a(EXLCZ)992670000000037582 100 $a20090928d2010 ub 0 101 0 $aeng 135 $aur|||||||nn|n 181 $ctxt 182 $cc 183 $acr 200 14$aThe devil and commodity fetishism in South America$b[electronic resource] /$fMichael T. Taussig 205 $a30th anniversary ed. /$bwith a new chapter by the author. 210 $aChapel Hill [N.C.] $cUniversity of North Carolina Press$dc2010 215 $a1 online resource (315 p.) 300 $aDescription based upon print version of record. 311 $a0-8078-7133-8 320 $aIncludes bibliographical references (p. [267]-287) and index. 327 $aContents; Preface to the Thirtieth Anniversary Edition; Preface; PART I: Fetishism: The Master Trope; 1 Fetishism and Dialectical Deconstruction; 2 The Devil and Commodity Fetishism; PART II: The Plantations of the Cauca Valley, Colombia; 3 Slave Religion and the Rise of the Free Peasantry; 4 Owners and Fences; 5 The Devil and the Cosmogenesis of Capitalism; 6 Pollution, Contradiction, and Salvation; 7 The Baptism of Money and the Secret of Capital; PART III: The Bolivian Tin Mines; 8 The Devil in the Mines; 9 The Worship of Nature; 10 The Problem of Evil 327 $a11 The Iconography of Nature and Conquest 12 The Transformation of Mining and Mining Mythology; 13 Peasant Rites of Production; 14 Mining Magic: The Mediation of Commodity Fetishism; Conclusion; The Sun Gives without Receiving: A Reinterpretation of the Devil Stories; Bibliography; Index; 330 $aIn this classic book, Michael Taussig explores the social significance of the devil in the folklore of contemporary plantation workers and miners in South America. Grounding his analysis in Marxist theory, Taussig finds that the fetishization of evil, in the image of the devil, mediates the conflict between precapitalist and capitalist modes of objectifying the human condition. He links traditional narratives of the devil-pact, in which the soul is bartered for illusory or transitory power, with the way in which production in capitalist economies causes workers to become alienated from the com 606 $aEconomic development$xSocial aspects$vCase studies 606 $aPlantations$zColombia$zCauca River Valley 606 $aTin mines and mining$zBolivia 606 $aSuperstition$vCase studies 615 0$aEconomic development$xSocial aspects 615 0$aPlantations 615 0$aTin mines and mining 615 0$aSuperstition 676 $a330.98003 676 $a338.9 700 $aTaussig$b Michael T$0101224 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910785199603321 996 $aThe devil and commodity fetishism in South America$93813849 997 $aUNINA LEADER 05322nam 2200649Ia 450 001 9910830143403321 005 20170814190100.0 010 $a1-282-30140-3 010 $a9786612301407 010 $a0-470-18655-0 010 $a0-470-18805-7 035 $a(CKB)1000000000376514 035 $a(EBL)469913 035 $a(OCoLC)609848406 035 $a(SSID)ssj0000388223 035 $a(PQKBManifestationID)11938150 035 $a(PQKBTitleCode)TC0000388223 035 $a(PQKBWorkID)10411435 035 $a(PQKB)11327748 035 $a(MiAaPQ)EBC469913 035 $a(PPN)22224268X 035 $a(EXLCZ)991000000000376514 100 $a20750817d1953 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCondensed pyridazine and pyrazine rings$b[electronic resource] /$fJ.C.E. Simpson 210 $aNew York $cWiley$d1953 215 $a1 online resource (413 p.) 225 1 $aChemistry of heterocyclic compounds ;$v5 300 $aDescription based upon print version of record. 311 $a0-470-37620-1 320 $aIncludes bibliographical references and index. 327 $aCONDENSED PYRIDAZINE AND PYRAZINE RINGS (Cianolines, Phthalazines, and Quinoxalines); J. C. E. Simpson, 1908-1952; Preface; Contents; PART I. Cinnolines; I . General Introduction to Cinnoline Derivatives. Preparation and Properties of Cinnoline; 1. General Introduction to Cinnoline Derivatives; 2. Preparation and Properties of Cinnoline; II. 4-Aryl-, 4-Aeyl-, and 4-Carboxycinnolines; 1. 4-Arylcinnolines; 2. 4-Acylcinnolines; 3. 4-Carboxycinnolines (Cinnoline-4-carboxylic Acids); III. 4-Methylcinnolines; IV. 4-Hydroxycinnolines; 1. Methods of Preparation; A . Richter Synthesis 327 $aB . Pfannstiel and Janecke SynthesisC. Borsehe Synthesis; 2. Properties; A. 4-Hydroxycinnolines Other Than 4-Hydroxycinnoline-3-carboxylic Acids; B. 4-Hydroxycinnoline-3-carboxylic Acids; V. 4-Chloro-, 4-Alkoxy-, and 4-Phenoxycinnolines; 1. 4-Chlorocinnolines; 2. 4-Alkoxycinnoline; 3. 4-Phenoxycinnoline; VI. 4-Aminocinnolines; 1. Primary Amino Compounds; 2. Secondary Amino Compounds; A. 4-Arylaminocinnolines; B. 4-Dialkylaminoalkylaminocinnolines; C. 4-Hydroxylamino-7-acetylcinnolineoxime; VII. Cinnoline Quaternary Salts; A. Preparation; B. Structure; C. Reactions; VIII . Reduced Cinnolines 327 $a1. Reduced Cinnolines with Nonoxygenated RingsA . Dihydrocinnolines; B . Tetrahydrocinnoline; C . Hexahydrocinnolines; 2 . Reduced Cinnolines with Oxygenated Rings; A . Reduced 3- and 4-Hydroxycinnolines; B . 1-Methyl -4-keto-1,4-dihydrocinnolines; C . Methyl 4-Keto-4,6-dihydrocinnolyl-6-nitronates; D . 3-Acetoxy-2-aryl-6-keto-2,6-dihydrocinnolines; E. 2-Pheny1-3-keto-hydroxy-2,3,5,6,7,8-hexahydrocinnoline; IX . Cinnolines Containing Additional Fused Rings; 1. 3,4--Benzocinnolines; 2. Tetrahydro-3,4-benzocinnolines; 3. Other Cinnolines with Additional Aromatic Rings 327 $a4. Cinnolines Containing Bridged Rings5. Cinnolinea Containing Fused Heterocyclic Rings; PART II . Phthalazines; X . Phthalazines Unsubstituted in the Hetero Ring; 1. Phthalazine; 2. 5,6-Dihydroxyphthalazine; XI . 1-Alkyl-, 1-Aryl-, and 1,4-Diarylphthalazines; 1. 1-Alkyl- and 1-Arylphthalazines; 2 . 1,4-Diarylphthalazines; XIl. 1-Hydroxyphthalazines; A. Preparation; B . Properties.; Xlll. Alkyl, Aryl, and Acyl Derivatives of 4-(1-)Hydroxyphthalazines; 1. O-Derivatives; 2. N-Derivatives (3-Substituted-4-keto-3,4-hydrophthalazines); A . Compounds without a 1-Substituent 327 $a3Aryl-, 3-Alkyl-, and 3-Aralky-4-keto-3,4-dihydrophthalazinesB . Compounds with a 1-Substituent; 3. Derivatives of Unknown Structure; XIV. 1-Hydroxy-3-aryl-3,4-dihydrophthalazine- 4-acetic Acids; A . Preparation; B . Properties; XV. 3-Aryl-1-ketophthalazines; A . Preparation; B. Properties and Reactions; XVI . Methylated Derivatives of 3-Aryl-1-ketophthalazines; 1. Derivatives of Compounds Containing a Hydrogen Atom at C4; A. 1.Methoxy-4-alkoxy-3-aryl-3,4-dihydrophthalazines; B. 1-Methoxy-3-arylphthalazinium Perchlorates 327 $a2. Derivatives of Compounds Containing a Methyl Group at C4 : 1-Methoxy-3-aryl-4-methylene-3,4-dihydrophthalazines 330 $aA volume in the Chemistry of Heterocyclic Compounds series, this book provides a summary of the chemistry of each of the six naphthyridine systems along with tables of known simple derivatives with original references. Each of the six naphthyridine systems are described in valuable detail and coverage includes: Primary synthetic methods from non-naphthyridine substrates; Chemistry and properties of the parent heterocycle and its simple alkyl derivatives; Formation and reactions of halogeno derivatives; formation and reactions of hydroxy, oxo, alkoxy, and related derivatives. 410 0$aChemistry of heterocyclic compounds ;$v5. 606 $aHeterocyclic compounds 606 $aPyridazines 615 0$aHeterocyclic compounds. 615 0$aPyridazines. 676 $a547.1 676 $a547/.59/05 700 $aSimpson$b J. C. E$01640985 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830143403321 996 $aCondensed pyridazine and pyrazine rings$93984783 997 $aUNINA