Inhaltsangabe
1. Abnormal Claisen rearrangement.- 2. Alder ene reaction.- 3. Aldol condensation.- 4. Allan-Robinson reaction.- 5. Alper carbonylation.- 6. Amadori rearrangement.- 7. Angeli-Rimini hydroxamic acid synthesis.- 8. ANRORC mechanism.- 9. Arndt-Eistert homologation.- 10. Auwers reaction.- 11. Baeyer-Drewson indigo synthesis.- 12. Baeyer-Villiger oxidation.- 13. Baker-Venkataraman rearrangement.- 14. Bamberger rearrangement.- 15. Bamford-Stevens reaction.- 16. Bargellini reaction.- 17. Bartoli indole synthesis.- 18. Barton decarboxylation.- 19. Barton-McCombie deoxygenation.- 20. Barton nitrite photolysis.- 21. Baylis-Hillman reaction.- 22. Beckmann rearrangement.- 23. Beirut reaction.- 24. Benzilic acid rearrangement.- 25. Benzoin condensation.- 26. Bergman cyclization.- 27. Biginelli pyrimidone synthesis.- 28. Birch reduction.- 29. Bischler-Möhlau indole synthesis.- 30. Bischler-Napieralski reaction.- 31. Blaise reaction.- 32. Blanc chloromethylation reaction.- 33. Boekelheide reaction.- 34. Boger pyridine synthesis.- 35. Boord reaction.- 36. Borsche-Drechsel cyclization.- 37. Boulton-Katritzky rearrangement.- 38. Bouveault aldehyde synthesis.- 39. Bouveault-Blanc reduction.- 40. Boyland-Sims oxidation.- 41. Bradsher reaction.- 42. Brook rearrangement.- 43. Brown hydroboration reaction.- 44. Bucherer carbazole synthesis.- 45. Bucherer reaction.- 46. Bucherer-Bergs reaction.- 47. Buchner-Curtius-Schlotterbeck reaction.- 48. Buchner method of ring expansion.- 49. Buchwald-Hartwig C-N bond and C-O bond formation reactions.- 50. Burgess dehydrating reagent.- 51. Cadiot-Chodkiewicz coupling.- 52. Cannizzaro dispropotionation reaction.- 53. Carroll rearrangement.- 54. Castro-Stephens coupling.- 55. Chapman rearrangement.- 56. Chichibabin amination reaction.- 57. Chichibabin pyridine synthesis.- 58. Chugaev reaction.- 59. Ciamician-Dennsted rearrangement.- 60. Claisen condensation.- 61. Claisen rearrangement.- 62. Clarke-Eschweiler reductive alkylation of amines.- 63. Clemmensen reduction.- 64. Combes quinoline synthesis.- 65. Conrad-Limpach reaction.- 66. Cook-Heilbron thiazole synthesis.- 67. Cope elimination reaction.- 68. Cope, oxy-Cope, and anionic oxy-Cope rearrangements.- 69. Corey-Bakshi-Shibata (CBS) reduction.- 70. Corey-Chaykovsky reaction.- 71. Corey-Fuchs reaction.- 72. Corey-Kim oxidation.- 73. Corey-Winter olefin synthesis.- 74. Cornforth rearrangement.- 75. Criegee glycol cleavage.- 76. Criegee mechanism of ozonolysis.- 77. Curtius rearrangement.- 78. Dakin oxidation.- 79. Dakin-West reaction.- 80. Danheiser annulation.- 81. Darzens glycidic ester condensation.- 82. Davis chiral oxaziridine reagent.- 83. de Mayo reaction.- 84. Demjanov rearrangement.- 85. Dess-Martin periodinane oxidation.- 86. Dieckmann condensation.- 87. Diels-Alder reaction.- 88. Dienone-phenol rearrangement.- 89. Di-?-methane rearrangement.- 90. Doebner reaction.- 91. Doebner-von Miller reaction.- 92. Doering-LaFlamme allene synthesis.- 93. Dornow-Wiehler isoxazole synthesis.- 94. Dötz reaction.- 95. Dowd ring expansion.- 96. Dutt-Wormall reaction.- 97. Eglinton reaction.- 98. Eschenmoser coupling reaction.- 99. Eschenmoser-Tanabe fragmentation.- 100. Etard reaction.- 101. Evans aldol reaction.- 102. Favorskii rearrangement and Quasi-Favorskii rearrangement.- 103. Feist-Bénary furan synthesis.- 104. Ferrier rearrangement.- 105. Finkelstein reaction.- 106. Fischer-Hepp rearrangement.- 107. Fischer indole synthesis.- 108. Fischer-Speier esterification.- 109. Fleming oxidation.- 110. Forster reaction.- 111. Frater-Seebach alkylation.- 112. Friedel-Crafts reaction.- 113. Friedländer synthesis.- 114. Fries rearrangement.- 115. Fritsch-Buttenberg-Wiechell rearrangement.- 116. Fujimoto-Belleau reaction.- 117. Fukuyama amine synthesis.- 118. Gabriel synthesis.- 119. Gassman indole synthesis.- 120. Gattermann-Koch reaction.- 121. Gewald aminothiophene synthesis.- 122. Glaser coupling.- 123. Gomberg-Bachmann reaction.- 124. Gribble indole reduction.- 125.
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