LEADER 04590oam 2200649I 450 001 9910781380503321 005 20231219112952.0 010 $a1-136-79093-4 010 $a1-283-24188-9 010 $a9786613241887 010 $a1-136-79094-2 010 $a0-203-82598-5 024 7 $a10.4324/9780203825983 035 $a(CKB)2550000000033246 035 $a(EBL)684002 035 $a(OCoLC)727133393 035 $a(SSID)ssj0000540854 035 $a(PQKBManifestationID)11351580 035 $a(PQKBTitleCode)TC0000540854 035 $a(PQKBWorkID)10492658 035 $a(PQKB)11328686 035 $a(MiAaPQ)EBC684002 035 $a(Au-PeEL)EBL684002 035 $a(CaPaEBR)ebr10466445 035 $a(CaONFJC)MIL324188 035 $a(EXLCZ)992550000000033246 100 $a20180706d2011 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aRethinking Gramsci /$fedited by Marcus E. Green 210 1$aMilton Park, Abingdon, Oxon, [England] ;$aNew York :$cRoutledge,$d2011. 215 $a1 online resource (345 p.) 225 1 $aRoutledge innovations in political theory ;$v37 300 $aDescription based upon print version of record. 311 $a0-415-82055-3 311 $a0-415-77973-1 320 $aIncludes bibliographical references and index. 327 $aFront Cover; Rethinking Gramsci; Copyright Page; Contents; Contributors; Acknowledgments; Introduction: Rethinking Marxism and rethinking Gramsci: Marcus E. Green; Part I: Culture and criticism; 1. Race, culture, and communications: Looking backward and forward at cultural studies: Stuart Hall; 2. Dante, Gramsci, and cultural criticism: Paul Bove?; 3. Bloom and Babbitt: A Gramscian view: Daniel O'Connell; 4. Socialist education today: Pessimism or optimism of the intellect?: Marcia Landy; Part II: Hegemony, subalternity, common sense 327 $a5. The sources for Gramsci's concept of hegemony: Derek Boothman6. Gramsci cannot speak: Presentations and interpretations of Gramsci's concept of the subaltern: Marcus E. Green; 7. Self-consciousness of the Dalits as 'subalterns': Reflections on Gramsci in South Asia: Cosimo Zene; 8. Gramscian politics and capitalist common sense: Evan Watkins; 9. Gramsci's theory of trade unionism: Frank R. Annunziato; 10. Production and its Others: Gramsci's "sexual question": Nelson Moe 327 $a11. Social forces in the struggle over hegemony: Neo-Gramscian perspectives in international political economy: Adam David Morton12. From ethico-political hegemony to post-Marxism: Richard Howson; Part III: Political Philosophy; 13. Gramsci, Marxism, and philosophy: Richard D. Wolff; 14. General will and democracy in Rousseau, Hegel, and Gramsci: Carlos Nelson Coutinho; 15. From Marx to Gramsci, from Gramsci to Marx: Historical materialism and the philosophy of praxis: Wolfgang Fritz Haug; 16. Gramsci and the dialectic: Resisting "enCrocement": Steven R. Mansfield 327 $a17. Gramsci's critical modernity: Esteve MoreraPart IV: On Gramsci's Prison Notebooks; 18. Unfinished business: Gramsci's Prison Notebooks: David F. Ruccio; 19. Of Prison Notebooks and the restoration of an archive: Joseph W. Childers; 20. The mammoth task of translating Gramsci: Peter Ives; 21. Cuvier's little bone: Joseph Buttigieg's English edition of Antonio Gramsci's Prison Notebooks: William V. Spanos; 22. The Prison Notebooks: Antonio Gramsci's work in progress: Joseph A. Buttigieg; Appendix; Bibliography; Index 330 $aThis edited volume provides a coherent and comprehensive assessment of Antonio Gramsci's significant contribution to the fields of political and cultural theory. It contains seminal contributions from a broad range of important political and cultural theorists from around the world and explains the origins, development and context for Gramsci's thought as well as analysing his continued relevance and influence to contemporary debates.It demonstrates the multidisciplinary nature of Gramscian thought to produce new insights into the intersection of economic, political, cultural, and so 410 0$aRoutledge innovations in political theory ;$v37. 606 $aPolitical science$xPhilosophy$xHistory$y20th century 615 0$aPolitical science$xPhilosophy$xHistory 676 $a320.53/2092 701 $aGreen$b Marcus E$01462334 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910781380503321 996 $aRethinking Gramsci$93671296 997 $aUNINA LEADER 05258nam 2200661Ia 450 001 9910830989303321 005 20230607214117.0 010 $a1-280-36683-4 010 $a9786610366835 010 $a0-470-31459-1 010 $a0-471-46143-1 010 $a0-471-24429-5 035 $a(CKB)111087027125450 035 $a(EBL)469254 035 $a(OCoLC)814413777 035 $a(SSID)ssj0000230934 035 $a(PQKBManifestationID)11173750 035 $a(PQKBTitleCode)TC0000230934 035 $a(PQKBWorkID)10197375 035 $a(PQKB)10408593 035 $a(MiAaPQ)EBC469254 035 $a(EXLCZ)99111087027125450 100 $a20020117d2002 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aThe pyrazines$hSupplement I$b[electronic resource] /$fD.J. Brown 210 $aNew York $cJohn Wiley & Sons$dc2002 215 $a1 online resource (575 p.) 225 1 $aChemistry of heterocyclic compounds ;$vv. 58 300 $a"An Interscience publication." 311 $a0-471-40382-2 320 $aIncludes bibliographical references (p. 461-513) and index. 327 $aTHE PYRAZINES Supplement I; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES FROM ALIPHATIC OR CARBOCYCLIC SYNTHONS; 1.1 From a Single Six-Atom Synthon; 1.1.1 By Completion of the N-C2 Bond; 1.1.1.1 From Appropriate w-Unsaturated Azaalkylamines; 1.1.1.2 From Appropriate w-Halogeno(azaalkylamines); 1.1.1.3 From Appropriate a,w-Diamino(azaalkanes); 1.1.1.4 From Appropriate w-Amino(azaalkanols); 1.1.1.5 From Appropriate w-Amino(azaalkanals); 1.1.1.6 From Appropriate w-Amino(azaalkanones) 327 $a1.1.1.7 From Appropriate w-Amino(azaalkanoic Acids)1.1.1.8 From Appropriate w-Amino(azaalkanoic Esters); 1.1.1.9 From Appropriate w-Amino(azaalkanamides); 1.1.1.10 From Appropriate w-Amino(azaalkanenitriles); 1.1.2 By Completion of the C2-C3 Bond; 1.2 From Two Synthons; 1.2.1 By Using a One-Atom and a Five-Atom Synthon; 1.2.1.1 Where the One-Atom Synthon Supplies N1; 1.2.1.2 Where the One-Atom Synthon Supplies C2; 1.2.2 By Using a Two-Atom and a Four-Atom Synthon; 1.2.2.1 Where the Two-Atom Synthon Supplies N1 + C2; 1.2.2.2 Where the Two-Atom Synthon Supplies C2 + C3 327 $a1.2.3 By Using Two Three-Atom Synthons1.2.3.1 Where Identical Synthons Provide N1 + C2 + C3 and N4 + C5 + C6; 1.2.3.2 Where Different Synthons Provide N1 + C2 + C3 and N4 + C5 + C6; 1.2.3.3 Where the Synthons Provide N1 + C2 + C6 and C3 + N4 + C5; 1.3 From Three Synthons; 1.4 From Four or More Synthons; 1.4.1 Where Synthons Provide N1, C2 + C3, N4, C5 + C6; 1.4.2 Where Synthons Provide N1 + C2, C3 + N4, C5, C6; 1.4.3 Where Synthons Provide N1 + C2, C3, N4 + C5, C6; 1.5 Appendix: Glance Index to Typical Pyrazine Derivatives Available from Aliphatic or Carbocyclic Synthons 327 $aCHAPTER 2 PRIMARY SYNTHESES FROM OTHER HETEROCYCLIC SYSTEMS2.1 Pyrazines from Other Heteromonocyclic Systems; 2.1.1 Azepines as Substrates; 2.1.2 Azetes as Substrates; 2.1.3 Azirines as Substrates; 2.1.4 Azocines as Substrates; 2.1.5 1,2-Diazepines as Substrates; 2.1.6 1,4-Diazepines as Substrates; 2.1.7 Furans as Substrates; 2.1.8 Imidazoles as Substrates; 2.1.9 Isoxazoles as Substrates; 2.1.10 Oxazoles as Substrates; 2.1.11 Oxirenes as Substrates; 2.1.12 Pyridazines as Substrates; 2.1.13 Pyridines as Substrates; 2.1.14 Pyrroles as Substrates; 2.1.15 1,2,5-Selenadiazoles as Substrates 327 $a2.1.16 1,2,5-Thiadiazoles as Substrates2.1.17 Thiirenes as Substrates; 2.2 Pyrazines from Heterobicyclic Systems; 2.2.1 1, 2-Diazabicyclo[2.2.0]hexanes as Substrates; 2.2.2 2,4,-Diazabicyclo[3.1.0]hexanes as Substrates; 2.2.3 2,3-Dioxa-5,7-diazabicyclo-[2.2.2]octanes as Substrates; 2.2.4 Furo[2,3-b]pyrazines as Substrates; 2.2.5 Imidazo[1,2-a]pyrazines as Substrates; 2.2.6 Indoles as Substrates; 2.2.7 Isoxazolo[2,3-a]pyrazines as Substrates; 2.2.8 Isoxazolo[4,5-b]pyrazines as Substrates; 2.2.9 Pteridines as Substrates; 2.2.10 Pyrazino[2,3-d][1,3]oxazines as Substrates 327 $a2.2.11 Pyrazino[2,3-e][1,3,4]thiadiazines as Substrates 330 $aThis book serves as a supplement to The Pyrazines, Volume 41 of the Chemistry of Heterocyclic Compounds series. It covers the literature published between 1979 and 2000, and-together with Volume 41-provides a complete, up-to-date reference for heterocyclic chemists. It emphasizes practical approaches to pyrazine chemistry, offers a full appendix of all simple pyrazines up to 2000, and features detailed coverage of the following topics:Systematic descriptions of all primary synthetic routes to pyrazinesOther preparative routes to alkylpyrazines and their reaction 410 0$aChemistry of heterocyclic compounds ;$vv. 58. 606 $aPyridazines 606 $aHeterocyclic compounds 615 0$aPyridazines. 615 0$aHeterocyclic compounds. 676 $a547.59 676 $a547/.59/05 676 $a547/.593 700 $aBrown$b D. J$0383088 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830989303321 996 $aThe pyrazines$94111444 997 $aUNINA