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Informationen zum Autor Dr. Zerong Wang earned his Ph.D. at Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences. He went on to a postdoctoral at the University of California, Berkeley to study enolate chemistry followed by a second postdoctoral at York University to explore the synthesis of nucleoside analogues. Dr. Wang is currently an Associate Professor at the University of Houston-Clear Lake, with research interests in photochemistry, nucleosides, heterocycles, computational chemistry, and material science. Klappentext Jeder Eintrag enthält eine Beschreibung der Reaktion, ein Diagramm zum Reaktionsablauf, eine kurze Biografie zum Namensgeber der Reaktion, geläufige Vorgänge, Abwandlungen (wo vorhanden), Anwendungen, verwandte Reaktionen (wo vorhanden), Beispielexperimente, Querverweise. Mit mehreren Indizes (auch nach Reaktionstyp). Zusammenfassung With its coverage of 701 organic name reactions and reagents, this three-volume set is the largest, most up-to-date major reference work of its kind. It offers students and professional chemists a valuable resource for conducting experiments and performing a broad range of applications, from pharmaceuticals to plastics to pesticides. Inhaltsverzeichnis Preface. Acknowledgments. Autobiography. Chemical Abbreviations. PART ONE. 1. Abnormal Claisen Rearrangement. 2. Acetoacetic Ester Condensation. 3. Acetoacetic Ester Synthesis. 4. Acyloin Condensation. 5. Acyloin Rearrangement. 6. Adkins Catalyst. 7. Ainley and King Synthesis. 8. Akabori Amino Acid Reaction. 9. Albright-Goldman Oxidation. 10. Alder Ene Reaction. 11. Alder-Rickert Reaction. 12. Aldol Reaction and Aldol Condensation. 13. Algar-Flynn-Oyamada (AFO) Reaction. 14. Alkene Metathesis. 15. Allan-Robinson Condensation. 16. Allylic Rearrangement. 17. Amadori Rearrangement. 18. Andrussow Process. 19. Angeli-Remini Reaction. 20. ANRORC Rearrangement. 21. Anschutz Anthracene Synthesis. 22. Appel Reaction. 23. Arens-Van Dorp Reaction. 24. Arndt-Eistert Synthesis. 25. Asinger Reaction. 26. Aston-Greenburg Rearrangement. 27. Atherton-Todd Reaction. 28. Auwers-Skita Rule. 29. Aza-Claisen Rearrangement. 30. Baddeley Isomerization. 31. Baeyer Diarylmethane Synthesis. 32. Baeyer-Drewson Reaction. 33. Baeyer Indole Synthesis. 34. Baeyer Oxindole Synthesis. 35. Baeyer Pyridine Synthesis. 36. Baeyer-Villiger Oxidation. 37. Bailey Peptide Synthesis. 38. Bakelite Process. 39. Baker-Ollis Sydnones Synthesis. 40. Baker-Venkataraman Rearrangement. 41. Ball-Goodwin-Morton Oxidation. 42. Bally-Scholl Reaction. 43. Balsohn Alkylation. 44. Balz-Schiemann Reaction. 45. Bamberger Rearrangement. 46. Bamford-Stevens Reaction. 47. Barbier Reaction. 48. Barbier-Wieland Degradation. 49. Bardhan Sengupta Synthesis. 50. Bargellini Condensation. 51. Bart Reaction. 52. Bartoli Indole Synthesis. 53. Barton Decarboxylation. 54. Barton Deoxygenation. 55. Barton Reaction. 56. Barton-Kellogg Olefination. 57. Barton-Zard Pyrrole Synthesis. 58. Batcho-Leimgruber Indole Synthesis. 59. Baudisch Reaction. 60. Baumann-Fromm Thiophene Synthesis. 61. Baumgarten ¿-Amino Ketone Synthesis. 62. Baylis-Hillman Reaction. 63. B¿echamp Reduction. 64. Beckmann Rearrangement and Beckmann Fragmentation. 65. Bedoukian Halogenation. 66. B¿ehal-Sommelet Rearrangement. 67. Beirut Reaction. 68. Bellus-Claisen Rearrangement. 69. B¿enary Reaction. 70. Benkeser Reduction. 71. Benzidine Rearrangement. ...
