{"text_format":"2","workbook":"xls","n_sheets":1,"sheets":["report2"],"not_rendered":{"charts":0,"images":0,"macros":0,"external_links":1,"defined_names":1,"comments":0,"pivot_tables":0},"unopened":[],"bounds":{"document_bytes":16777216,"sheet_cells":100000,"run_cost":"one","rows_first":2000,"rows_last":500,"rows_between":2000,"halvings":0,"cell_chars":16384,"cell_head_chars":4096},"cells_cut":0,"cells_raw":0,"read":"whole","date_system":"1900","formulas":"cached_only"}

{"sheet":"report2","index":0,"n_rows":30,"n_cols":5,"rows_kept":30,"cut":false,"hidden":false,"merged":[[0,2,0,3],[0,4,0,5],[1,2,1,3],[1,4,1,5],[2,2,2,3],[2,4,2,5],[3,2,3,3],[4,2,4,3],[8,2,8,3],[9,2,9,3],[10,2,10,3],[13,2,13,3],[17,2,17,3],[18,2,18,3],[22,2,22,3]],"flags":["formulas_cached_only"]}
[null,"1.","Record Nr.",null,"UNINA9910144286503321"]
[null,null,"Autore",null,"Ellis G. P (Gwynn Pennant)"]
[null,null,"Titolo",null,"Synthesis of fused heterocycles . Part 2 [[electronic resource] /] / G.P. Ellis"]
[null,null,"Pubbl/distr/stampa",null,"Chichester [Sussex] ; ; New York, : Wiley, c1992"]
[null,null,"ISBN",null,"1-282-30632-4"]
[{"$nulls":4},"9786612306327"]
[{"$nulls":4},"0-470-18731-X"]
[{"$nulls":4},"0-470-18883-9"]
[null,null,"Descrizione fisica",null,"1 online resource (785 p.)"]
[null,null,"Collana",null,"The chemistry of heterocyclic compounds ; ; 47"]
[null,null,"Disciplina",null,"547.59"]
[{"$nulls":4},"547/.59"]
[{"$nulls":4},"547/.59/05"]
[null,null,"Soggetti",null,"Heterocyclic chemistry"]
[{"$nulls":4},"Organic compounds - Synthesis"]
[{"$nulls":4},"Heterocyclic compounds"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","\"A Wiley-Interscience publication.\""]
[null,null,null,"Nota di bibliografia","Includes bibliography and indexes."]
[null,null,"Nota di contenuto",null,"SYNTHESIS OF FUSED HETEROCYCLES; Contents; Preface; 1. Introduction; 2. Acetal or Aldehyde and Amine or Carboxamide; 3. Acetal and Ring-carbon or Ring-nitrogen; 4. Acylamine and Aldehyde or Ketone; 5. Acylamine or Carbamate and Amine or Hydrazine; 6. Acylamine and Carboxamide; 7. Acylamine and a Carboxylic Acid Derivative; 8. Acylamine or Amine and Ether; 9. Acylamine, Acylhydrazine. Amine or Isocyanate and Halogen; 10. Acylamine or Amine and Hydroxy; 11. Acylamine or Diazonium Salt and Lactam Carbonyl; 12. Acylamine or Imine and Methylene or Alkene; 13. Acylamine or Amine and Nitrile"]
[{"$nulls":4},"14. Acylamine, Amine or Imine and Nitro15. Acylamine or Amine and Nitroso or N-Oxide; 16. Acylamine, Acyloxy, Amine or Hydroxy and Phosphorane; 17. Acylamine or Acylhydrazine and Ring-carbon; 18. Acylamine or Acylhydrazine and Ring-nitrogen; 19. Acylamine or Amine and Sulphonamide or Thioureide; 20. Acylamine or Amine and Thiocyanate; 21. Acyl Halide and Ring-carbon or Ring-nitrogen; 22. Aldehyde or Ketone and Alkene or Alkyne; 23. Aldehyde or Ketone and Azide or Triazene; 24. Aldehyde or Ketone and Carbamate, "]
[{"$nulls":4},"Isothiocyanate or Thiourea; 25. Aldehyde or Ketone and Carboxamide or Sulphonamide"]
[{"$nulls":4},"26. Aldehyde or Ketone and Carboxylic Acid or Ester27. Aldehyde or Ketone and Ether; 28. Aldehyde or Ketone and Halogen; 29. Aldehyde, Ketone or Lactam Carbonyl and Hydroxy; 30. Aldehyde and Ketone: Dialdehyde or Diketone; 31. Aldehyde or Ketone and Methylene; 32. Aldehyde or Ketone and Nitrile; 33. Aldehyde or Ketone and Nitro, Nitroso or N-Oxide; 34. Aldehyde or Other Carbonyl and Phosphorane; 35. Aldehyde or Ketone and Ring-carbon; 36. Aldehyde, Ketone or Lactam Carbonyl and Ring-nitrogen; 37. Alkene or Alkyne and Amine, Azide or Nitro"]
[{"$nulls":4},"38. Alkene or Alkyne and Carboxylic Acid or its Derivative39. Alkene or Alkyne and Halogen; 40. Alkene or Alkyne and Hydroxy or Ether; 41. Alkene, Methylene or Ring-carbon and Lactam or Lactone Carbonyl; 42. Alkene or Alkyne and Methylene, Ring-carbon or Ring-nitrogen; 43. Amidine and Amine, Carboxylic Acid or its Derivative; 44. Amidine and Ring-carbon or Ring-nitrogen; 45. Amine and Azide, Azo or Diazo; 46. Amine or Phosphorane and Carboxamide; 47. Amine and Carboxylic Acid; 48. Amine and Carboxylic Ester; 49. Amine and Enamine or Oxime"]
[{"$nulls":4},"50. Amine or Diazonium Salt and Hydrazide or Hydrazine51. Amine and Hydrazone or Imine; 52. Amine and Ketone; 53. Amine and Ring-carbon; 54. Amine and Ring-nitrogen; 55. Azide and Azo or Nitro; 56. Azide or Isocyanate and a Carboxylic Acid Derivative; 57. Azide or Azo and Methyl or Methylene; 58. Azide or Azo and Ring-carbon; 59. Azide and Ring-nitrogen; 60. Azo and Carbamate; 61. Carbamate or Ureide and Ring-carbon or Ring-nitrogen; 62. Carbamate or Carboxamide and another Carboxylic Acid Derivative; 63. Carboxamide or Nitrile and Diazonium Salt"]
[{"$nulls":4},"64. Carboxamide, Nitrile or Ureide and Hydroxy or Ether"]
[null,null,null,"Sommario/riassunto","Partial table of contents:. Acetal or Aldehyde and Amine or Carboxamide. Acylamine and Carboxamide. Acylamine or Amine and Ether. Acyl Halide and Ring-Carbon or Ring-Nitrogen. Aldehyde or Ketone and Ether. Aldehyde or Ketone and Halogen. Amine and Azide, Azo or Diazo. Amine and Carboxylic Acid. Amine and Enamine or Oxime. Azide and Azo or Nitro. Azide or Azo and Methyl or Methylene. Azide and Ring-Nitrogen. Carboxamide or Nitrile and Diazonium Salt. Carboxylic Acid or Its Derivative and Halogen. Carboxylic Acid, Acyl Chloride or Ester and Hydroxy or Ether. Carboxylic Acid Halide or Ester and N"]