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Organic Chemistry: 100 Must-Know Mechanisms
Roman Valiulin
- 289 pages
- English
- ePUB (adapté aux mobiles)
- Disponible sur iOS et Android
Organic Chemistry: 100 Must-Know Mechanisms
Roman Valiulin
Ă propos de ce livre
In chemistry, good problem-solving requires a balanced combination of scientific intuition and
methodical analysis. Additionally, thoughtfully presented diagrams and infographics can convey
a large amount of complex information in a more intuitive and accessible manner. 100 Must-Know
Mechanisms (Second Edition) strives to be at the intersection of these two key principles. Its
thorough visualizations enable experienced readers to use it as a quick reference for specific
mechanisms of interest. At the same time, the book's breadth of covered reactions, from classic to
cutting-edge, make it a good study-aid for the developing chemist. A slow and consistent study of
the entire series of mechanisms can help set the foundation for good scientific intuition, while its
detailed infographics and careful navigation features encourage coming back to it frequently. This
edition includes over 40 new illustrations, numerous new mechanistic schemes, enhanced original
figures with a variety of real-case examples, and more
Foire aux questions
Informations
Table des matiĂšres
- Title Page
- Copyright
- Contents
- Second Edition
- List of Acronyms and Abbreviations
- 1âElectrophilic Addition Mechanism
- 2âNucleophilic Substitution Mechanism
- 3âAromatic Electrophilic Substitution Mechanism
- 4âAromatic Nucleophilic Substitution Mechanism
- 5âAromatic Radical Nucleophilic Substitution Mechanism
- 6âElimination Mechanism
- 7âAcyloin Condensation
- 8âAlkyne Zipper Reaction
- 9âArbuzov Reaction
- 10âArndtâEistert Synthesis
- 11âBaeyerâVilliger Oxidation
- 12âBarton Decarboxylation
- 13âBaylisâHillman Reaction
- 14âBeckmann Rearrangement
- 15âBenzoin Condensation
- 16âBenzyne Mechanism
- 17âBergman Cyclization
- 18âBirch Reduction
- 19âBischlerâNapieralski Cyclization
- 20âBrown Hydroboration
- 21âBuchwaldâHartwig Cross-Coupling
- 22âCannizzaro Reaction
- 23âChanâEvansâLam Cross-Coupling
- 24âChichibabin Amination
- 25âClaisen Condensation
- 26âClaisen Rearrangement
- 27âCope Elimination
- 28âCope Rearrangement
- 29âCriegee and Malaprade Oxidation
- 30âCuAAC
- 31âCurtius Rearrangement
- 32âDarzens Condensation
- 33âDessâMartin Oxidation
- 34âDiazotization (Diazonium Salt)
- 35âDielsâAlder Cycloaddition
- 36âDi-Ï-Methane Rearrangement
- 37âFavorskii Rearrangement
- 38âFischer Indole Synthesis
- 39âFriedelâCrafts Acylation and Alkylation
- 40âGabriel Synthesis
- 41âGewald Reaction
- 42âGlaserâEglintonâHay Coupling
- 43âGrignard Reaction
- 44âGrob Fragmentation
- 45âHaloform Reaction
- 46âHeck Cross-Coupling
- 47âHellâVolhardâZelinsky Reaction
- 48âHiyama Cross-Coupling
- 49âHofmann Elimination
- 50âHornerâWadsworthâEmmons Olefination
- 51âJones Oxidation
- 52âKucherov Reaction
- 53âKumada Cross-Coupling
- 54âLeyâGriffith Oxidation
- 55âLiebeskindâSrogl Cross-Coupling
- 56âMannich Reaction
- 57âMcMurry Coupling
- 58âMeerweinâPonndorfâVerley Reduction
- 59âMichael Addition
- 60âMinisci Reaction
- 61âMitsunobu Reaction
- 62âMiyaura Borylation
- 63âMukaiyama RedOx Hydration
- 64âNazarov Cyclization
- 65âNef Reaction
- 66âNegishi Cross-Coupling
- 67âNorrish Type I and II Reactions
- 68âOlefin (Alkene) Metathesis
- 69âOppenauer Oxidation
- 70âOzonolysis
- 71âPaalâKnorr Syntheses
- 72âPaternĂČâBĂŒchi Reaction
- 73âPausonâKhand Reaction
- 74âPeptide (Amide) Coupling
- 75âPictetâSpengler Reaction
- 76âPinacolâPinacolone Rearrangement
- 77âPolonovski Reaction
- 78âPrilezhaev Epoxidation
- 79âPrins Reaction
- 80âPummerer Rearrangement
- 81âRambergâBĂ€cklund Rearrangement
- 82âReformatsky Reaction
- 83âRobinson Annulation
- 84âShapiro Reaction
- 85âSonogashira Cross-Coupling
- 86âStaudinger Reaction
- 87âSteglich Esterification
- 88âStille Cross-Coupling
- 89âSuzuki Cross-Coupling
- 90âSwern Oxidation
- 91âUgi Reaction
- 92âUllmann ArylâAryl Coupling
- 93âUpjohn Dihydroxylation
- 94âVilsmeierâHaack Reaction
- 95âWacker Oxidation
- 96âWagnerâMeerwein Rearrangement
- 97âWeinreb Ketone Synthesis
- 98âWittig Reaction
- 99âWohlâZiegler Reaction
- 100âWolffâKishner Reduction
- Acknowledgments