Organic Chemistry: 100 Must-Know Mechanisms / / Roman Valiulin.
In chemistry, good problem-solving requires a balanced combination of scientific intuition andmethodical analysis. Additionally, thoughtfully presented diagrams and infographics can conveya large amount of complex information in a more intuitive and accessible manner. 100 Must-KnowMechanisms (Second...
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| Superior document: | Title is part of eBook package: De Gruyter DG Plus DeG Package 2023 Part 1 |
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| VerfasserIn: | |
| Place / Publishing House: | Berlin ;, Boston : : De Gruyter, , [2023] ©2023 |
| Year of Publication: | 2023 |
| Edition: | 2nd, Completely Revised Edition |
| Language: | English |
| Series: | De Gruyter Textbook
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| Online Access: | |
| Physical Description: | 1 online resource (XXII, 267 p.) |
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Table of Contents:
- Frontmatter
- Second Edition
- 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 and Malaprade Oxidation
- 30 CuAAC
- 31 Curtius Rearrangement
- 32 Darzens Condensation
- 33 Dess–Martin Oxidation
- 34 Diazotization (Diazonium Salt)
- 35 Diels–Alder Cycloaddition
- 36 Di-π-Methane Rearrangement
- 37 Favorskii Rearrangement
- 38 Fischer Indole Synthesis
- 39 Friedel–Crafts Acylation and 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 Fig.
- 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 and II Reactions
- 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 Fi
- 97 Weinreb Ketone Synthesis
- 98 Wittig Reaction
- 99 Wohl–Ziegler Reaction
- 100 Wolff–Kishner Reduction
- Acknowledgments
- Bibliography and References