Organic Chemistry: 100 Must-Know Mechanisms / / Roman Valiulin.

• Superior document: Title is part of eBook package: De Gruyter DG Ebook Package English 2020
• VerfasserIn: Valiulin, Roman,
• Place / Publishing House: Berlin ;, Boston : : De Gruyter, , [2020]; ©2020
• Year of Publication: 2020
• Language: English
• Series: De Gruyter Textbook
• Physical Description: 1 online resource (X, 239 p.)
• Other title: Frontmatter --; 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) --; 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
• Format: Mode of access: Internet via World Wide Web.
• ISBN: 9783110608373; 9783110696288; 9783110696271; 9783110659061; 9783110704716; 9783110704518; 9783110704754; 9783110704556
• DOI: 10.1515/9783110608373
• Access: restricted access
• Hierarchical level: Monograph
• Statement of Responsibility: Roman Valiulin.

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.