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Organic Chemistry: 100 Must-Know Mechanisms
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About This Book
This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with explanations and additional information.
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Yes, you can access Organic Chemistry: 100 Must-Know Mechanisms by Roman Valiulin in PDF and/or ePUB format, as well as other popular books in Scienze fisiche & Chimica organica. We have over one million books available in our catalogue for you to explore.
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https://doi.org/10.1515/9783110608373-001
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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. ArndtâEistert Synthesis
- 11. BaeyerâVilliger Oxidation
- 12. Barton Decarboxylation
- 13. BaylisâHillman Reaction
- 14. Beckmann Rearrangement
- 15. Benzoin Condensation
- 16. Benzyne Mechanism
- 17. Bergman Cyclization
- 18. Birch Reduction
- 19. BischlerâNapieralski Cyclization
- 20. Brown Hydroboration
- 21. BuchwaldâHartwig Cross Coupling
- 22. Cannizzaro Reaction
- 23. ChanâEvansâLam 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. DessâMartin Oxidation
- 34. Diazotization (Diazonium Salt)
- 34. Diazotization (Diazonium Salt)
- 36. DiâĎâMethane Rearrangement
- 37. Favorskii Rearrangement
- 38. Fischer Indole Synthesis
- 39. FriedelâCrafts Acylation & Alkylation
- 40. Gabriel Synthesis
- 41. Gewald Reaction
- 42. GlaserâEglintonâHay Coupling
- 43. Grignard Reaction
- 44. Grob Fragmentation
- 45. Haloform Reaction
- 46. Heck Cross Coupling
- 47. HellâVolhardâZelinsky Reaction
- 48. Hiyama Cross Coupling
- 49. Hofmann Elimination
- 50. HornerâWadsworthâEmmons Olefination
- 51. Jones Oxidation
- 52. Kucherov Reaction
- 53. Kumada Cross Coupling
- 54. LeyâGriffith Oxidation
- 55. LiebeskindâSrogl Cross Coupling
- 56. Mannich Reaction
- 57. McMurry Coupling
- 58. MeerweinâPonndorfâVerley 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. PaalâKnorr Syntheses
- 72. PaternòâBĂźchi Reaction
- 73. PausonâKhand Reaction
- 74. Peptide (Amide) Coupling
- 75. PictetâSpengler Reaction
- 76. PinacolâPinacolone Rearrangement
- 77. Polonovski Reaction
- 78. Prilezhaev Epoxidation
- 79. Prins Reaction
- 80. Pummerer Rearrangement
- 81. RambergâBäcklund 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 ArylâAryl Coupling
- 93. Upjohn Dihydroxylation
- 94. VilsmeierâHaack Reaction
- 95. Wacker Oxidation
- 96. WagnerâMeerwein Rearrangement
- 97. Weinreb Ketone Synthesis
- 98. Wittig Reaction
- 99. WohlâZiegler Reaction
- 100. WolffâKishner Reduction
- Acknowledgments
- Bibliography and References