LEADER 05505nam 2200673Ia 450 001 9910841365203321 005 20230331005417.0 010 $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 $aHeterocyclic compounds 615 0$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 $a9910841365203321 996 $aSynthesis of fused heterocycles$94135097 997 $aUNINA