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De Gruyter Textbook Ser.
Organic Chemistry: 100 Must-Know Mechanisms / Roman Valiulin. — 1 online resource (X, 239 p.). — (De Gruyter Textbook Ser.). — In English. — <URL:http://elib.fa.ru/ebsco/2483378.pdf>.

Record create date: 5/5/2020

Subject: Chemistry, Organic.; Chemistry, Organic.

Collections: EBSCO

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Table of Contents

  • 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

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