Details
| Title | De Gruyter Textbook Ser. — Organic Chemistry: 100 Must-Know Mechanisms |
|---|---|
| Creators | Valiulin Roman |
| Collection | Электронные книги зарубежных издательств ; Общая коллекция |
| Subjects | Chemistry, Organic. ; EBSCO eBooks |
| Document type | Other |
| File type | |
| Language | English |
| Rights | Доступ по паролю из сети Интернет (чтение, печать, копирование) |
| Record key | on1170464896 |
| Record create date | 5/5/2020 |
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- Preface and Overview
- Contents
- List of Acronyms and Abbreviations
- 1. Electrophilic Addition Mechanism
- 2. Nucleophilic Substitution Mechanism
- 3. Aromatic Electrophilic Substitution Mechanism
- 4. Aromatic Nucleophilic Substitution Mechanism
- 5. Aromatic Radical Nucleophilic Substitution Mechanism
- 6. Elimination Mechanism
- 7. Acyloin Condensation
- 8. Alkyne Zipper Reaction
- 9. Arbuzov Reaction
- 10. Arndt‒Eistert Synthesis
- 11. Baeyer‒Villiger Oxidation
- 12. Barton Decarboxylation
- 13. Baylis‒Hillman Reaction
- 14. Beckmann Rearrangement
- 15. Benzoin Condensation
- 16. Benzyne Mechanism
- 17. Bergman Cyclization
- 18. Birch Reduction
- 19. Bischler‒Napieralski Cyclization
- 20. Brown Hydroboration
- 21. Buchwald‒Hartwig Cross Coupling
- 22. Cannizzaro Reaction
- 23. Chan‒Evans‒Lam Cross Coupling
- 24. Chichibabin Amination
- 25. Claisen Condensation
- 26. Claisen Rearrangement
- 27. Cope Elimination
- 28. Cope Rearrangement
- 29. Criegee & Malaprade Oxidation
- 30. CuAAC
- 31. Curtius Rearrangement
- 32. Darzens Condensation
- 33. Dess‒Martin Oxidation
- 34. Diazotization (Diazonium Salt)
- 34. Diazotization (Diazonium Salt)
- 36. Di‒π‒Methane Rearrangement
- 37. Favorskii Rearrangement
- 38. Fischer Indole Synthesis
- 39. Friedel‒Crafts Acylation & Alkylation
- 40. Gabriel Synthesis
- 41. Gewald Reaction
- 42. Glaser–Eglinton–Hay Coupling
- 43. Grignard Reaction
- 44. Grob Fragmentation
- 45. Haloform Reaction
- 46. Heck Cross Coupling
- 47. Hell–Volhard–Zelinsky Reaction
- 48. Hiyama Cross Coupling
- 49. Hofmann Elimination
- 50. Horner–Wadsworth–Emmons Olefination
- 51. Jones Oxidation
- 52. Kucherov Reaction
- 53. Kumada Cross Coupling
- 54. Ley–Griffith Oxidation
- 55. Liebeskind–Srogl Cross Coupling
- 56. Mannich Reaction
- 57. McMurry Coupling
- 58. Meerwein–Ponndorf–Verley Reduction
- 59. Michael Addition
- 60. Minisci Reaction
- 61. Mitsunobu Reaction
- 62. Miyaura Borylation
- 63. Mukaiyama RedOx Hydration
- 64. Nazarov Cyclization
- 65. Nef Reaction
- 66. Negishi Cross Coupling
- 67. Norrish Type I & II Reaction
- 68. Olefin (Alkene) Metathesis
- 69. Oppenauer Oxidation
- 70. Ozonolysis
- 71. Paal–Knorr Syntheses
- 72. Paternò–Büchi Reaction
- 73. Pauson–Khand Reaction
- 74. Peptide (Amide) Coupling
- 75. Pictet–Spengler Reaction
- 76. Pinacol–Pinacolone Rearrangement
- 77. Polonovski Reaction
- 78. Prilezhaev Epoxidation
- 79. Prins Reaction
- 80. Pummerer Rearrangement
- 81. Ramberg–Bäcklund Rearrangement
- 82. Reformatsky Reaction
- 83. Robinson Annulation
- 84. Shapiro Reaction
- 85. Sonogashira Cross Coupling
- 86. Staudinger Reaction
- 87. Steglich Esterification
- 88. Stille Cross Coupling
- 89. Suzuki Cross Coupling
- 90. Swern Oxidation
- 91. Ugi Reaction
- 92. Ullmann Aryl–Aryl Coupling
- 93. Upjohn Dihydroxylation
- 94. Vilsmeier–Haack Reaction
- 95. Wacker Oxidation
- 96. Wagner–Meerwein Rearrangement
- 97. Weinreb Ketone Synthesis
- 98. Wittig Reaction
- 99. Wohl–Ziegler Reaction
- 100. Wolff–Kishner Reduction
- Acknowledgments
- Bibliography and References
