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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| 001 | 9783110608373 | ||
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| 100 | 1 | |a Valiulin, Roman, |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
| 245 | 1 | 0 | |a Organic Chemistry: 100 Must-Know Mechanisms / |c Roman Valiulin. |
| 264 | 1 | |a Berlin ; |a Boston : |b De Gruyter, |c [2020] | |
| 264 | 4 | |c ©2020 | |
| 300 | |a 1 online resource (X, 239 p.) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 347 | |a text file |b PDF |2 rda | ||
| 490 | 0 | |a De Gruyter Textbook | |
| 505 | 0 | 0 | |t Frontmatter -- |t Preface and Overview -- |t Contents -- |t List of Acronyms and Abbreviations -- |t 1. Electrophilic Addition Mechanism -- |t 2. Nucleophilic Substitution Mechanism -- |t 3. Aromatic Electrophilic Substitution Mechanism -- |t 4. Aromatic Nucleophilic Substitution Mechanism -- |t 5. Aromatic Radical Nucleophilic Substitution Mechanism -- |t 6. Elimination Mechanism -- |t 7. Acyloin Condensation -- |t 8. Alkyne Zipper Reaction -- |t 9. Arbuzov Reaction -- |t 10. Arndt‒Eistert Synthesis -- |t 11. Baeyer‒Villiger Oxidation -- |t 12. Barton Decarboxylation -- |t 13. Baylis‒Hillman Reaction -- |t 14. Beckmann Rearrangement -- |t 15. Benzoin Condensation -- |t 16. Benzyne Mechanism -- |t 17. Bergman Cyclization -- |t 18. Birch Reduction -- |t 19. Bischler‒Napieralski Cyclization -- |t 20. Brown Hydroboration -- |t 21. Buchwald‒Hartwig Cross Coupling -- |t 22. Cannizzaro Reaction -- |t 23. Chan‒Evans‒Lam Cross Coupling -- |t 24. Chichibabin Amination -- |t 25. Claisen Condensation -- |t 26. Claisen Rearrangement -- |t 27. Cope Elimination -- |t 28. Cope Rearrangement -- |t 29. Criegee & Malaprade Oxidation -- |t 30. CuAAC -- |t 31. Curtius Rearrangement -- |t 32. Darzens Condensation -- |t 33. Dess‒Martin Oxidation -- |t 34. Diazotization (Diazonium Salt) -- |t 34. Diazotization (Diazonium Salt) -- |t 36. Di‒π‒Methane Rearrangement -- |t 37. Favorskii Rearrangement -- |t 38. Fischer Indole Synthesis -- |t 39. Friedel‒Crafts Acylation & Alkylation -- |t 40. Gabriel Synthesis -- |t 41. Gewald Reaction -- |t 42. Glaser–Eglinton–Hay Coupling -- |t 43. Grignard Reaction -- |t 44. Grob Fragmentation -- |t 45. Haloform Reaction -- |t 46. Heck Cross Coupling -- |t 47. Hell–Volhard–Zelinsky Reaction -- |t 48. Hiyama Cross Coupling -- |t 49. Hofmann Elimination -- |t 50. Horner–Wadsworth–Emmons Olefination -- |t 51. Jones Oxidation -- |t 52. Kucherov Reaction -- |t 53. Kumada Cross Coupling -- |t 54. Ley–Griffith Oxidation -- |t 55. Liebeskind–Srogl Cross Coupling -- |t 56. Mannich Reaction -- |t 57. McMurry Coupling -- |t 58. Meerwein–Ponndorf–Verley Reduction -- |t 59. Michael Addition -- |t 60. Minisci Reaction -- |t 61. Mitsunobu Reaction -- |t 62. Miyaura Borylation -- |t 63. Mukaiyama RedOx Hydration -- |t 64. Nazarov Cyclization -- |t 65. Nef Reaction -- |t 66. Negishi Cross Coupling -- |t 67. Norrish Type I & II Reaction -- |t 68. Olefin (Alkene) Metathesis -- |t 69. Oppenauer Oxidation -- |t 70. Ozonolysis -- |t 71. Paal–Knorr Syntheses -- |t 72. Paternò–Büchi Reaction -- |t 73. Pauson–Khand Reaction -- |t 74. Peptide (Amide) Coupling -- |t 75. Pictet–Spengler Reaction -- |t 76. Pinacol–Pinacolone Rearrangement -- |t 77. Polonovski Reaction -- |t 78. Prilezhaev Epoxidation -- |t 79. Prins Reaction -- |t 80. Pummerer Rearrangement -- |t 81. Ramberg–Bäcklund Rearrangement -- |t 82. Reformatsky Reaction -- |t 83. Robinson Annulation -- |t 84. Shapiro Reaction -- |t 85. Sonogashira Cross Coupling -- |t 86. Staudinger Reaction -- |t 87. Steglich Esterification -- |t 88. Stille Cross Coupling -- |t 89. Suzuki Cross Coupling -- |t 90. Swern Oxidation -- |t 91. Ugi Reaction -- |t 92. Ullmann Aryl–Aryl Coupling -- |t 93. Upjohn Dihydroxylation -- |t 94. Vilsmeier–Haack Reaction -- |t 95. Wacker Oxidation -- |t 96. Wagner–Meerwein Rearrangement -- |t 97. Weinreb Ketone Synthesis -- |t 98. Wittig Reaction -- |t 99. Wohl–Ziegler Reaction -- |t 100. Wolff–Kishner Reduction -- |t Acknowledgments -- |t Bibliography and References |
| 506 | 0 | |a restricted access |u http://purl.org/coar/access_right/c_16ec |f online access with authorization |2 star | |
| 520 | |a 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. | ||
| 530 | |a Issued also in print. | ||
| 538 | |a Mode of access: Internet via World Wide Web. | ||
| 546 | |a In English. | ||
| 588 | 0 | |a Description based on online resource; title from PDF title page (publisher's Web site, viewed 27. Jan 2023) | |
| 650 | 4 | |a Organische Chemie. | |
| 650 | 4 | |a Organische Synthese. | |
| 650 | 4 | |a Reaktionsmechanismus. | |
| 650 | 7 | |a SCIENCE / Chemistry / Organic. |2 bisacsh | |
| 653 | |a Chemical Sythesis. | ||
| 653 | |a Organic Chemistry. | ||
| 653 | |a Reaction Mechanisms. | ||
| 773 | 0 | 8 | |i Title is part of eBook package: |d De Gruyter |t DG Ebook Package English 2020 |z 9783110696288 |
| 773 | 0 | 8 | |i Title is part of eBook package: |d De Gruyter |t DG Plus DeG Package 2020 Part 1 |z 9783110696271 |
| 773 | 0 | 8 | |i Title is part of eBook package: |d De Gruyter |t De Gruyter English eBooks 2020 - UC |z 9783110659061 |
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| 776 | 0 | |c EPUB |z 9783110608519 | |
| 776 | 0 | |c print |z 9783110608304 | |
| 856 | 4 | 0 | |u https://doi.org/10.1515/9783110608373 |
| 856 | 4 | 0 | |u https://www.degruyter.com/isbn/9783110608373 |
| 856 | 4 | 2 | |3 Cover |u https://www.degruyter.com/document/cover/isbn/9783110608373/original |
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