Organic Chemistry: 100 Must-Know Mechanisms / / 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 exp...
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Superior document: | Title is part of eBook package: De Gruyter DG Ebook Package English 2020 |
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Place / Publishing House: | Berlin ;, Boston : : De Gruyter, , [2020] ©2020 |
Year of Publication: | 2020 |
Language: | English |
Series: | De Gruyter Textbook
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Online Access: | |
Physical Description: | 1 online resource (X, 239 p.) |
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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 |
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Summary: | 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. |
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. |