LEADER 05543nam 2200685Ia 450 001 9910144286603321 005 20170810191421.0 010 $a1-282-30204-3 010 $a9786612302046 010 $a0-470-18730-1 010 $a0-470-18882-0 035 $a(CKB)1000000000376586 035 $a(EBL)469371 035 $a(OCoLC)609848038 035 $a(SSID)ssj0000388221 035 $a(PQKBManifestationID)11277293 035 $a(PQKBTitleCode)TC0000388221 035 $a(PQKBWorkID)10411636 035 $a(PQKB)10535733 035 $a(MiAaPQ)EBC469371 035 $a(EXLCZ)991000000000376586 100 $a19861103d1987 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aSynthesis of fused heterocycles$hPart 1$b[electronic resource] /$fG.P. Ellis 210 $aChichester [Sussex] ;$aNew York $cWiley$dc1987 215 $a1 online resource (675 p.) 225 1 $aThe chemistry of heterocyclic compounds ;$v47/1 300 $aDescription based upon print version of record. 311 $a0-471-91431-2 320 $aIncludes bibliographical references and indexes. 327 $aSYNTHESIS OF FUSED HETEROCYCLES; Contents; Preface; 1. Introduction; 2. Acetal or Aldehyde and Amine; 3. Acetal and Ring-carbon or Ring-nitrogen; 4. Acylamine and Aldehyde or Ketone; 5. Acylamine and Amine; 6. Acylamine or Carbamate and Carboxamide or Nitrile; 7. Acylamine and Carboxylic Acid or Ester; 8. Acylamine or Amine and Ether or Thioether; 9. Acylamine, Acylhydrazine or Amine and Halogen; 10. Acylamine or Amine and Hydroxy or Thiol; 11. Acylamine, Amine or Diazonium Salt and Lactam Carbonyl; 12. Acylamine or Amine and Methylene; 13. Acylamine or Amine and Nitrile 327 $a14. Acylamine, Acylhydrazine, Amine or Carbamate and Nitro15. Acylamine or Amine and Nitroso or N-oxide; 16. Acylamine, Acyloxy, Amine or Hydroxy and Phosphorane; 17. Acylamine or Acylhydrazine and Ring-carbon or Ring-sulphur; 18. Acylamine or Acylhydrazine and Ring-nitrogen; 19. Acylamine or Amine and Sulphonamide, Thioureide or Ureide; 20. Acylamine or Amine and Thiocyanate; 21. Acyl halide and Ring-carbon or Ring-nitrogen; 22. Aldehyde or Ketone and Alkene or Alkyne; 23. Aldehyde or Ketone and Azide; 24. Aldehyde or Ketone and Carbamate; 25. Aldehyde or Ketone and Carboxamide or Hydrazide 327 $a26. Aldehyde or Ketone and Carboxylic Acid or Ester27. Aldehyde or Ketone and Ether or Thioether; 28. Aldehyde or Ketone and Halogen; 29. Aldehyde and Hydroxy, Thiol or Thiocyanate; 30. Aldehyde and Ketone; Dialdehyde or Diketone; 31. Aldehyde or Ketone and Methylene; 32. Aldehyde or Ketone and Nitrile; 33. Aldehyde or Ketone and Nitro, Nitroso or N-Oxide; 34. Aldehyde or other Carbonyl and Phosphorane; 35. Aldehyde or Ketone and Ring-carbon; 36. Aldehyde or Ketone and Ring-nitrogen; 37. Alkene or Alkyne and Amine or Nitro; 38. Alkene or Alkyne and Carboxylic Acid or its Derivative 327 $a39. Alkene or Alkyne and Halogen40. Alkene or Alkyne and Hydroxy, Thiol or Ether; 41. Alkene, Methylene, Ring-carbon, or Ring-nitrogen and Lactam Carbonyl; 42. Alkene or Alkyne and Methylene, Ring-carbon or Ring-nitrogen; 43. Amidine and Amine, Carboxylic Acid, Ester, Hydroxy, Methylene or Nitro; 44. Amidine and Ring-carbon or Ring-nitrogen; 45. Amine and Azo or Diazo; 46. Amine and Carboxamide or Thiocarboxamide; 47. Amine and Carboxylic Acid; 48. Amine and Carboxylic Ester; 49. Amine and Enamine; 50. Amine and Hydrazide or Hydrazine; 51. Amine and Hydrazone or Imine; 52. Amine and Ketone 327 $a53. Amine and Ring-carbon or Ring-sulphur54. Amine and Ring-nitrogen; 55. Azide and Azo or Nitro; 56. Azide and a Carboxylic Acid or its Derivative; 57. Azide and Methyl, Methylene or Methine; 58. Azide and Ring-carbon; 59. Azide and Ring-nitrogen; 60. Azo or Triazene and Carbamate, Carboxylic Acid, Ester or Nitrile; 61. Carbamate or Ureide and Ring-carbon or Ring-nitrogen; 62. Carboxamide and another Carboxylic Acid Derivative; 63. Carboxamide or Sulphonamide and Diazonium Salt or Diazo; 64. Carboxamide, Hydroxamic Acid, Hydrazide, Nitrile or Ureide and Hydroxy or Ether 327 $a65. Carboxamide or Nitrile and Ring-carbon or Ring-nitrogen 330 $aThis book classifies methods of synthesizing a heterocyclic ring which is fused to another ring. Classification is based on the functional group or groups present in the substrate, each chapter being devoted to the reactions of a particular pair of groups. The groups are arranged alphabetically so that they can be found easily. The book enables the reader to locate references (over 2000 are included) to the conversion of a wide variety of functional groups into heterocyclic rings of five to eight atoms. Each cyclization is shown as an equation which contains concise details or reagents, condit 410 0$aChemistry of heterocyclic compounds ;$v47/1. 606 $aHeterocyclic chemistry 606 $aOrganic compounds$xSynthesis 606 $aHeterocyclic compounds 608 $aElectronic books. 615 0$aHeterocyclic chemistry. 615 0$aOrganic compounds$xSynthesis. 615 0$aHeterocyclic compounds. 676 $a547.59 676 $a547/.59 676 $a547/.59/05 700 $aEllis$b G. P$g(Gwynn Pennant)$095658 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910144286603321 996 $aSynthesis of fused heterocycles$92057878 997 $aUNINA LEADER 03279nam 2200589 450 001 9910792667303321 005 20230126214933.0 010 $a3-11-052170-9 024 7 $a10.1515/9783110524154 035 $a(CKB)3710000000984012 035 $a(MiAaPQ)EBC4804421 035 $a(DE-B1597)473926 035 $a(OCoLC)979733330 035 $a(DE-B1597)9783110524154 035 $a(Au-PeEL)EBL4804421 035 $a(CaPaEBR)ebr11344955 035 $a(CaONFJC)MIL984157 035 $a(OCoLC)973834407 035 $a(EXLCZ)993710000000984012 100 $a20170223h20162016 uy 0 101 0 $aeng 135 $aurcnu|||||||| 181 $2rdacontent 182 $2rdamedia 183 $2rdacarrier 200 10$aCognitive, social, and individual constraints on linguistic variation $ea case study of presentational 'haber' pluralization in Caribbean Spanish /$fJeroen Claes 210 1$aBerlin, Germany ;$aBoston, [Massachusetts] :$cDe Gruyter Mouton,$d2016. 210 4$dİ2016 215 $a1 online resource (262 pages) $cillustrations 225 1 $aCognitive Linguistics Research,$x1861-4132 ;$vVolume 60 311 $a3-11-052162-8 311 $a3-11-052415-5 320 $aIncludes bibliographical references and index. 327 $tFrontmatter -- $tAcknowledgements -- $tContents -- $tList of figures -- $tList of tables -- $tAbbreviations and other conventions -- $tChapter 1: Introduction -- $tChapter 2: Presentational haber pluralization -- $tChapter 3: Cognitive Construction Grammar and language variation -- $tChapter 4: Research questions and hypotheses -- $tChapter 5: Methodology -- $tChapter 6: Semantic and syntactic properties of presentational haber -- $tChapter 7: Cognitive constraints on presentational haber pluralization -- $tChapter 8: Social constraints on presentational haber pluralization -- $tChapter 9: Individual constraints on presentational haber pluralization -- $tChapter 10: Cognitive, social, and individual constraints on presentational haber pluralization -- $tReferences -- $tIndex -- $tAppendix A: Story-reading task -- $tAppendix B: Questionnaire-reading task 330 $aThe present volume tries to answer the question: What constrains morphosyntactic variation? By analyzing the variable agreement of presentational haber (?there to be?) in Caribbean Spanish with advanced statistical tools and theoretical constructs of Cognitive Sociolinguistics, psycholinguistics, and variationist sociolinguistics, it proposes an innovative theoretical model of the constraints that govern morphosyntactic variation. 410 0$aCognitive linguistics research ;$vVolume 60. 606 $aSpanish language$xVariation$zCaribbean Area 606 $aSpanish language$xMorphosyntax 606 $aCognitive grammar$xSocial aspects 607 $aCaribbean Area$2fast 615 0$aSpanish language$xVariation 615 0$aSpanish language$xMorphosyntax. 615 0$aCognitive grammar$xSocial aspects. 676 $a465 700 $aClaes$b Jeroen$01513780 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910792667303321 996 $aCognitive, social, and individual constraints on linguistic variation$93748426 997 $aUNINA LEADER 01116nam 2200361 450 001 9910795535203321 005 20230814215216.0 010 $a1-5475-2784-6 035 $a(CKB)5120000000157797 035 $a(MiAaPQ)EBC5509834 035 $a(Au-PeEL)EBL5509834 035 $a(OCoLC)1096531536 035 $a(EXLCZ)995120000000157797 100 $a20190417d2018 uy 0 101 0 $apor 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aPalavras confusas em ingle?s e vocabula?rio de ni?vel avanc?ado /$fSergio Casado Rodri?guez 210 1$a[Place of publication not identified] :$c[Sergio Casado],$d[2018] 215 $a1 online resource (45 pages) 606 $aVocabulary$vStudy guides 615 0$aVocabulary 676 $a428.1076 700 $aRodri?guez$b Sergio Casado$01501164 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910795535203321 996 $aPalavras confusas em ingle?s e vocabula?rio de ni?vel avanc?ado$93728254 997 $aUNINA